Arn van den Maagdenberg
Hoogleraar Moleculaire en functionele neurogenetica
- Naam
- Prof.dr. A.M.J.M. van den Maagdenberg
- Telefoon
- +31 71 526 9460
- a.van_den_maagdenberg@lumc.nl
- ORCID iD
- 0000-0002-9310-5535
Arn M.J.M. van den Maagdenberg is hoogleraar moleculaire en functionele neurogenetica bij de afdelingen Humane Genetica en Neurologie van het Leids Universitair Medisch Centrum (LUMC). Daarnaast is hij lid management van research theme Neuroscience van het LUMC. Hij is ook aanvoerder van het Medical Delta programma ‘Medical NeuroDelta’, vicevoorzitter van het ‘International Headache Genetics Consortium’, en heeft een ‘honorary contract’ bij Stichting Epilepsie Instellingen Nederland (SEIN) in Heemstede.
Meer informatie over Arn van den Maagdenberg
Arn M.J.M. van den Maagdenberg is hoogleraar moleculaire en functionele neurogenetica bij de afdelingen Humane Genetica en Neurologie van het Leids Universitair Medisch Centrum (LUMC). Daarnaast is hij lid management van research theme Neuroscience van het LUMC. Hij is ook aanvoerder van het Medical Delta programma ‘Medical NeuroDelta’, vicevoorzitter van het ‘International Headache Genetics Consortium’, en heeft een ‘honorary contract’ bij Stichting Epilepsie Instellingen Nederland (SEIN) in Heemstede.
Genetisch en functionieel hersenonderzoek
De hersenen zijn ons meest complexe orgaan. Het is intrigerend waarom in patiënten soms een kortsluiting in de hersenen lijkt te bestaan waardoor herhaald aanvallen van migraine and epilepsie kunnen ontstaan. Het is grotendeels onbegrepen waarom en waardoor tijdelijk de vatbaarheid voor het krijgen van zo’n aanval is vergroot. Het ontrafelen van de moleculaire en neurobiologische mechanismen die leiden tot zulke aanvallen om betere behandelingsmethoden te vinden is de grootste uitdaging.
Mijn genetisch en functionele hersenonderzoek geeft duidelijke aanwijzingen dat de functie van hersencellen en de communicatie met bloedvaten niet optimaal is. De zoektocht naar een betere behandeling van patiënten met een aanvalsgewijze aandoening wordt met deze kennis langs verschillende paden ingezet. Met gerenommeerde hoofdpijnspecialisten in het LUMC wordt patiëntgebonden onderzoek, zoals het monitoren en moduleren van hersenactiviteit in de klinische setting en, op termijn, de thuissituatie, maar basaal onderzoek met geavanceerde diermodellen, ontwikkeld binnen het LUMC. Meer recent wordt gebruik gemaakt van gekweekte humane orgaanstructuren om een meer directe vertaling naar de kliniek te garanderen. Zo’n combinatie van modellen zal antwoorden geven waar de patiënt uiteindelijk wat aan heeft. Deze translationele aanpak van onderzoek past uitstekend bij de uitgangspunten van de Nationale Wetenschapsagenda (NWA) om ontregelde hersenfunctie vanuit een ‘personalised medicine’ aanpak te benaderen.
Wetenschappelijke carrière
Arn M.J.M. van den Maagdenberg heeft zijn opleiding Biologie gedaan aan de Katholieke Universiteit Nijmegen en vervolgens zijn promotieonderzoek uitgevoerd aan de Universiteit van Leiden. De titel van zijn proefschrift (28 oktober 1993) luidt ‘Genetic and functional analysis of apolipoprotein E’. Vervolgens bekwaamde van den Maagdenberg zich verder in genetisch en functioneel onderzoek van verschillende ziekten bij achtereenvolgens de afdeling celbiologie en histologie van de Radbouduniversiteit in Nijmegen en de afdelingen humane genetica en neurologie in Leiden. Hij werd in 2011 benoemd tot hoogleraar Neurogenetica van het Leids Universiteit Medisch Centrum. De titel van zijn oratie (23 maart 2012) is ‘Samenwerken is hersenwerk’.
Al meer dan 25 jaar doet van den Maagdenberg onderzoek naar de moleculaire en functionele mechanismen van aanvalsgewijze hersenaandoeningen, met name migraine, epilepsie en beroerte. Hij heeft meer dan 350 wetenschappelijke publicaties, waaronder diverse invloedrijke reviews, en heeft meerdere boekhoofdstukken op zijn naam staan. Hij is (mede)aanvoerder/lid van verschillende consortia en wetenschappelijke adviesraden, zowel voor nationale initiatieven, teweten het Nederlands Epilepsiefonds, Medical NeuroDelta, als internationale initiatieven, waaronder het ‘International Headache Genetics Consortium’ (IHGC),
Prijzen en eervolle benoemingen
Van den Maagdenberg is winnaar van de C.J. Kok Award 2004 (LUMC): “Migraine: from patient to mice ….. and back again” en de "Migraine Trust Lecture" tijdens de ‘European Headache and Migraine Trust International Congress’ 2010 (EHMTIC; Nice): "Genetics in Migraine: from Genes to Phenotypes". Hij ontving in 2014 en 2017 ook de MFLS-LUMC Onderzoeksprijs Medische Genetica als beste module biomedische wetenschappen. Daarnaast won hij in 2010 de Publieksprijs voor “In de aanval”, een jaarlijkse competitie voor beste communicatie van wetenschap naar het Nederlands publiek (Academische Jaarprijs), als onderdeel van het LUMC migraine team.
Hoogleraar Moleculaire en functionele neurogenetica
- Faculteit Geneeskunde
- Divisie 4
- Humane Genetica
- Aydogmus, H.; Hu, M.C.; Ivancevic, L.; Frimat, J.P.; Maagdenberg, A.M.J.M. van den; Sarro, P.M. & Mastrangeli, M. (2023), An organ-on-chip device with integrated charge sensors and recording microelectrodes, Scientific Reports 13(1).
- Irene de Boer, Aster V E Harder, Michel D Ferrari, Arn M J M van den Maagdenberg & Gisela M Terwindt (2023), Genetics of migraine: Delineation of contemporary understanding of the genetic underpinning of migraine, Handbook of Clinical Neurology 198.
- Mehta, D.; Boer, I. de; Sutherland, H.G.; Pijpers, J.A.; Bron, C.; Bainomugisa, C.; Haupt, L.M.; Maagdenberg, A.M.J.M. van den; Griffiths, L.R.; Nyholt, D.R. & Terwindt, G.M. (2023), Alterations in DNA methylation associate with reduced migraine and headache days after medication withdrawal treatment in chronic migraine patients, Clinical Epigenetics 15(1).
- Winsvold, B.S.; Harder, A.V.E.; Ran, C.; Chalmer, M.A.; Dalmasso, M.C.; Ferkingstad, E.; Tripathi, K.P.; Bacchelli, E.; Borte, S.; Fourier, C.; Petersen, A.S.; Vijfhuizen, L.S.; Magnusson, S.H.; O'Connor, E.; Bjornsdottir, G.; Häppölä, P.; Wang, Y.F.; Callesen, I.; Kelderman, T.; Gallardo, V.J.; Boer, I. de; Olofsgård, F.J.; Heinze, K.; Lund, N.; Thomas, L.F.; Hsu, C.L.; Pirinen, M.; Hautakangas, H.; Ribasés, M.; Guerzoni, S.; Sivakumar, P.; Yip, J.; Heinze, A.; Küçükali, F.; Ostrowski, S.R.; Pedersen, O.B.; Kristoffersen, E.S.; Martinsen, A.E.; Artigas, M.S.; Lagrata, S.; Cainazzo, M.M.; Adebimpe, J.; Quinn, O.; Göbel, C.; Cirkel, A.; Volk, A.E.; Heilmann-Heimbach, S.; Skogholt, A.H.; Gabrielsen, M.E.; Wilbrink, L.A.; Danno, D.; Mehta, D.; Guobjartsson, D.F.; Rosendaal, F.R.; Dijk, K.W. van; Fronczek, R.; Wagner, M.; Scherer, M.; Göbel, H.; Sleegers, K.; Sveinsson, O.A.; Pani, L.; Zoli, M.; Ramos-Quiroga, J.A.; Dardiotis, E.; Steinberg, A.; Riedel-Heller, S.; Sjöstrand, C.; Thorgeirsson, T.E.; Stefansson, H.; Southgate, L.; Trembath, R.C.; Vandrovcova, J.; Noordam, R.; Paemeleire, K.; Stefansson, K.; Fann, C.S.J.; Waldenlind, E.; Tronvik, E.; Jensen, R.H.; Chen, S.P.; Houlden, H.; Terwindt, G.M.; Kubisch, C.; Maestrini, E.; Vikelis, M.; Pozo-Rosich, P.; Belin, A.C.; Matharu, M.; Maagdenberg, A.M.J.M. van den; Hansen, T.F.; Ramirez, A.; Zwart, J.A.; HUNT All Headache; Int Headache Genetics Consortium; Genomic Consortium & Int Consortium Cluster Headache (2023), Cluster headache genomewide association study and meta-analysis identifies eight loci and implicates smoking as causal risk factor, Annals of Neurology 94(4).
- Pelzer, N.; Boer, I. de; Maagdenberg, A.M.J.M. van den & Terwindt, G.M. (2023), Neurological and psychiatric comorbidities of migraine: Concepts and future perspectives, Cephalalgia 43(6).
- Dehghani, A.; Schenke, M.; Heiningen, S.H. van; Karatas, H.; Tolner, E.A. & Maagdenberg, A.M.J.M. van den (2023), Optogenetic cortical spreading depolarization induces headache-related behaviour and neuroinflammatory responses some prolonged in familial hemiplegic migraine type 1 mice, Journal of Headache and Pain 24(1).
- Maksemous, N.; Harder, A.V.E.; Ibrahim, O.; Vijfhuizen, L.S.; Sutherland, H.; Pelzer, N.; Boer, I. de; Terwindt, G.M.; Lea, R.A.; Maagdenberg, A.M.J.M. van den & Griffiths, L.R. (2023), Whole exome sequencing of hemiplegic migraine patients shows an increased burden of missense variants in CACNA1H and CACNA1I genes, Molecular Neurobiology 60(6): 3034-3043.
- Hu, M.H.Y.; Frimat, J.P.; Rijkers, K.; Schijns, O.E.M.G.; Maagdenberg, A.M.J.M. van den; Dings, J.T.A.; Luttge, R. & Hoogland, G. (2023), Spontaneous Epileptic Recordings from hiPSC-Derived Cortical Neurons Cultured with a Human Epileptic Brain Biopsy on a Multi Electrode Array, Applied Sciences 13(3).
- Buijsen, R.A.M.; Hu, M.C.; Saez-Gonzalez, M.; Notopoulou, S.; Mina, E.; Koning, W.; Gardiner, S.L.; Graaf, L. van der; Daoutsali, E.; Pepers, B.A.; Mei, H.L.; Dis, V. van; Frimat, J.P.; Maagdenberg, A.M.J.M. van den; Petrakis, S. & Roon-Mom, W.M.C. van (2023), Spinocerebellar Ataxia Type 1 Characteristics in Patient-Derived Fibroblast and iPSC-Derived Neuronal Cultures, Movement Disorders.
- Onderwater, G.L.J.; Dongen, R.M. van; Harms, A.C.; Zielman, R.; Oosterhout, W.P.J. van; Klinken, J.B. van; Goeman, J.J.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Hankemeier, T. & Ferrari, M.D. (2023), Cerebrospinal fluid and plasma amine profiles in interictal migraine, Annals of Neurology 93(4).
- Giniatullin, R.; Khazipov, R.; Maagdenberg, A.M.J.M. van den & Jolkkonen, J. (2023), Common and distinct mechanisms of migraine and stroke, Frontiers in Cellular Neuroscience 17.
- Depienne, C.; Maagdenberg, A.M.J.M. van den; Kuhnel, T.; Ishiura, H.; Corbett, M.A. & Tsuji, S. (2023), Insights into familial adult myoclonus epilepsy pathogenesis: How the same repeat expansion in six unrelated genes may lead to cortical excitability, Epilepsia 64: S31-S38.
- Welander, N.Z.; Rukh, G.; Rask-Andersen, M.; Harder, A.V.E.; Maagdenberg, A.M.J.M. van den; Schioth, H.B.; Mwinyi, J. & Int Headache Genetics Consortium (2023), Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study, Headache: The Journal of Head and Face Pain.
- Pietra, A. della; Krivoshein, G.; Ivanov, K.; Giniatullina, R.; Jyrkkanen, H.K.; Leinonen, V.; Lehtonen, M.; Maagdenberg, A.M.J.M. van den; Savinainen, J. & Giniatullin, R. (2023), Potent dual MAGL/FAAH inhibitor AKU-005 engages endocannabinoids to diminish meningeal nociception implicated in migraine pain, Journal of Headache and Pain 24(1).
- Zhao, L.; Zhao, W.H.; Cao, J. & Tu, Y.H. (2023), Causal relationships between migraine and microstructural white matter: a Mendelian randomization study, Journal of Headache and Pain 24(1).
- Mehta, D.; Boer, I. de; Sutherland, H.G.; Pijpers, J.A.; Bron, C.; Bainomugisa, C.; Haupt, L.M.; Maagdenberg, A.M.J.M. van den; Griffiths, L.R.; Nyholt, D.R. & Terwindt, G.M. (2023), Alterations in DNA methylation associate with reduced migraine and headache days after medication withdrawal treatment in chronic migraine patients, Clinical Epigenetics 15(1).
- Winsvold, B.S.; Harder, A.V.E.; Ran, C.; Chalmer, M.A.; Dalmasso, M.C.; Ferkingstad, E.; Tripathi, K.P.; Bacchelli, E.; Borte, S.; Fourier, C.; Petersen, A.S.; Vijfhuizen, L.S.; Magnusson, S.H.; O'Connor, E.; Bjornsdottir, G.; Häppölä, P.; Wang, Y.F.; Callesen, I.; Kelderman, T.; Gallardo, V.J.; Boer, I. de; Olofsgård, F.J.; Heinze, K.; Lund, N.; Thomas, L.F.; Hsu, C.L.; Pirinen, M.; Hautakangas, H.; Ribasés, M.; Guerzoni, S.; Sivakumar, P.; Yip, J.; Heinze, A.; Küçükali, F.; Ostrowski, S.R.; Pedersen, O.B.; Kristoffersen, E.S.; Martinsen, A.E.; Artigas, M.S.; Lagrata, S.; Cainazzo, M.M.; Adebimpe, J.; Quinn, O.; Göbel, C.; Cirkel, A.; Volk, A.E.; Heilmann-Heimbach, S.; Skogholt, A.H.; Gabrielsen, M.E.; Wilbrink, L.A.; Danno, D.; Mehta, D.; Guobjartsson, D.F.; Rosendaal, F.R.; Dijk, K.W. van; Fronczek, R.; Wagner, M.; Scherer, M.; Göbel, H.; Sleegers, K.; Sveinsson, O.A.; Pani, L.; Zoli, M.; Ramos-Quiroga, J.A.; Dardiotis, E.; Steinberg, A.; Riedel-Heller, S.; Sjöstrand, C.; Thorgeirsson, T.E.; Stefansson, H.; Southgate, L.; Trembath, R.C.; Vandrovcova, J.; Noordam, R.; Paemeleire, K.; Stefansson, K.; Fann, C.S.J.; Waldenlind, E.; Tronvik, E.; Jensen, R.H.; Chen, S.P.; Houlden, H.; Terwindt, G.M.; Kubisch, C.; Maestrini, E.; Vikelis, M.; Pozo-Rosich, P.; Belin, A.C.; Matharu, M.; Maagdenberg, A.M.J.M. van den; Hansen, T.F.; Ramirez, A.; Zwart, J.A.; HUNT All Headache; Int Headache Genetics Consortium; Genomic Consortium & Int Consortium Cluster Headache (2023), Cluster headache genomewide association study and meta-analysis identifies eight loci and implicates smoking as causal risk factor, Annals of Neurology 94(4).
- Bakker, M.K.; Kanning, J.P.; Abraham, G.; Martinsen, A.E.; Winsvold, B.S.; Zwart, J.A.; Bourcier, R.; Sawada, T.; Koido, M.; Kamatani, Y.; Morel, S.; Amouyel, P.; Debette, S.; Bijlenga, P.; Berrandou, T.; Ganesh, S.K.; Bouatia-Naji, N.; Jones, G.; Bown, M.; HUNT All In Stroke; CADISP Grp; Int Consortium Blood Pressure; Int Headache Genetics Consortium; ISGC; Intracranial Aneurysm Working Grp; Rinkel, G.J.E.; Veldink, J.H. & Ruigrok, Y.M. (2023), Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity, Stroke 54(3): 810-818.
- Dehghani, A.; Schenke, M.; Heiningen, S.H. van; Karatas, H.; Tolner, E.A. & Maagdenberg, A.M.J.M. van den (2023), Optogenetic cortical spreading depolarization induces headache-related behaviour and neuroinflammatory responses some prolonged in familial hemiplegic migraine type 1 mice, Journal of Headache and Pain 24(1).
- Pelzer, N.; Boer, I. de; Maagdenberg, A.M.J.M. van den & Terwindt, G.M. (2023), Neurological and psychiatric comorbidities of migraine: Concepts and future perspectives, Cephalalgia 43(6).
- Zhang, W.Q.; Zhang, L.; Yang, L.; Xiao, C.H.; Wu, X.Y.; Yan, P.J.; Cui, H.J.; Yang, C.; Zhu, J.W.; Wu, X.; Tang, M.S.; Wang, Y.T.; Chen, L.; Liu, Y.J.; Zou, Y.Q.; Zhang, L.; Yang, C.X.; Yao, Y.Q.; Li, J.Y.; Liu, Z.M.; Zhang, B.; Jiang, X. & Int Headache Genetics Consortium (2023), Migraine, chronic kidney disease and kidney function: observational and genetic analyses, Human Genetics.
- Zhao, L.; Zhao, W.H.; Cao, J. & Tu, Y.H. (2023), Causal relationships between migraine and microstructural white matter: a Mendelian randomization study, Journal of Headache and Pain 24(1).
- Bakker, M.K.; Kanning, J.P.; Abraham, G.; Martinsen, A.E.; Winsvold, B.S.; Zwart, J.A.; Bourcier, R.; Sawada, T.; Koido, M.; Kamatani, Y.; Morel, S.; Amouyel, P.; Debette, S.; Bijlenga, P.; Berrandou, T.; Ganesh, S.K.; Bouatia-Naji, N.; Jones, G.; Bown, M.; HUNT All In Stroke; CADISP Grp; Int Consortium Blood Pressure; Int Headache Genetics Consortium; ISGC; Intracranial Aneurysm Working Grp; Rinkel, G.J.E.; Veldink, J.H. & Ruigrok, Y.M. (2023), Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity, Stroke 54(3): 810-818.
- Zhang, W.Q.; Zhang, L.; Yang, L.; Xiao, C.H.; Wu, X.Y.; Yan, P.J.; Cui, H.J.; Yang, C.; Zhu, J.W.; Wu, X.; Tang, M.S.; Wang, Y.T.; Chen, L.; Liu, Y.J.; Zou, Y.Q.; Zhang, L.; Yang, C.X.; Yao, Y.Q.; Li, J.Y.; Liu, Z.M.; Zhang, B.; Jiang, X. & Int Headache Genetics Consortium (2023), Migraine, chronic kidney disease and kidney function: observational and genetic analyses, Human Genetics.
- Welander, N.Z.; Rukh, G.; Rask-Andersen, M.; Harder, A.V.E.; Maagdenberg, A.M.J.M. van den; Schioth, H.B.; Mwinyi, J. & Int Headache Genetics Consortium (2023), Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study, Headache: The Journal of Head and Face Pain.
- Giniatullin, R.; Khazipov, R.; Maagdenberg, A.M.J.M. van den & Jolkkonen, J. (2023), Common and distinct mechanisms of migraine and stroke, Frontiers in Cellular Neuroscience 17.
- Pietra, A. della; Krivoshein, G.; Ivanov, K.; Giniatullina, R.; Jyrkkanen, H.K.; Leinonen, V.; Lehtonen, M.; Maagdenberg, A.M.J.M. van den; Savinainen, J. & Giniatullin, R. (2023), Potent dual MAGL/FAAH inhibitor AKU-005 engages endocannabinoids to diminish meningeal nociception implicated in migraine pain, Journal of Headache and Pain 24(1).
- Depienne, C.; Maagdenberg, A.M.J.M. van den; Kuhnel, T.; Ishiura, H.; Corbett, M.A. & Tsuji, S. (2023), Insights into familial adult myoclonus epilepsy pathogenesis: How the same repeat expansion in six unrelated genes may lead to cortical excitability, Epilepsia 64: S31-S38.
- Hu, M.H.Y.; Frimat, J.P.; Rijkers, K.; Schijns, O.E.M.G.; Maagdenberg, A.M.J.M. van den; Dings, J.T.A.; Luttge, R. & Hoogland, G. (2023), Spontaneous Epileptic Recordings from hiPSC-Derived Cortical Neurons Cultured with a Human Epileptic Brain Biopsy on a Multi Electrode Array, Applied Sciences 13(3).
- Aydogmus, H.; Hu, M.C.; Ivancevic, L.; Frimat, J.P.; Maagdenberg, A.M.J.M. van den; Sarro, P.M. & Mastrangeli, M. (2023), An organ-on-chip device with integrated charge sensors and recording microelectrodes, Scientific Reports 13(1).
- Buijsen, R.A.M.; Hu, M.C.; Saez-Gonzalez, M.; Notopoulou, S.; Mina, E.; Koning, W.; Gardiner, S.L.; Graaf, L. van der; Daoutsali, E.; Pepers, B.A.; Mei, H.L.; Dis, V. van; Frimat, J.P.; Maagdenberg, A.M.J.M. van den; Petrakis, S. & Roon-Mom, W.M.C. van (2023), Spinocerebellar Ataxia Type 1 Characteristics in Patient-Derived Fibroblast and iPSC-Derived Neuronal Cultures, Movement Disorders.
- Maksemous, N.; Harder, A.V.E.; Ibrahim, O.; Vijfhuizen, L.S.; Sutherland, H.; Pelzer, N.; Boer, I. de; Terwindt, G.M.; Lea, R.A.; Maagdenberg, A.M.J.M. van den & Griffiths, L.R. (2023), Whole exome sequencing of hemiplegic migraine patients shows an increased burden of missense variants in CACNA1H and CACNA1I genes, Molecular Neurobiology 60(6): 3034-3043.
- He, Q.; Wang, W.J.; Xiong, Y.; Tao, C.Y.; Ma, L.; Ma, J.P.; You, C. & Int Headache Genetics Consortium (2023), A causal effects of gut microbiota in the development of migraine, The Journal of Headache and Pain 24(1).
- Ferrari, M.D.; Goadsby, P.J.; Burstein, R.; Kurth, T.; Ayata, C.; Charles, A.; Ashina, M.; Maagdenberg, A.M.J.M. van den & Dodick, D.W. (2022), Migraine, Nature Reviews Disease Primers 8(1).
- Krivoshein, G.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den & Giniatullin, R.A. (2022), Migraine-relevant sex-dependent activation of mouse meningeal afferents by TRPM3 agonists (vol 23, 4, 2022), Journal of Headache and Pain 23(1).
- Hautakangas, H.; Winsvold, B.S.; Ruotsalainen, S.E.; Bjornsdottir, G.; Harder, A.V.E.; Kogelman, L.J.A.; Thomas, L.F.; Noordam, R.; Benner, C.; Gormley, P.; Artto, V.; Banasik, K.; Bjornsdottir, A.; Boomsma, D.I.; Brumpton, B.; Burgdorf, K.S.; Buring, J.E.; Chalmer, M.A.; Boer, I. de; Dichgans, M.; Erikstrup, C.; Farkkila, M.; Garbrielsen, M.E.; Ghanbari, M.; Hagen, K.; Happola, P.; Hottenga, J.J.; Hrafnsdottir, M.G.; Hveem, K.; Johnsen, M.B.; Kahonen, M.; Kristoffersen, E.S.; Kurth, T.; Lehtimaki, T.; Lighart, L.; Magnusson, S.H.; Malik, R.; Pedersen, O.B.; Pelzer, N.; Penninx, B.W.J.H.; Ran, C.; Ridker, P.M.; Rosendaal, F.R.; Sigurdardottir, G.R.; Skogholt, A.H.; Sveinsson, O.A.; Thorgeirsson, T.E.; Ullum, H.; Vijfhuizen, L.S.; Widen, E.; Dijk, K.W. van; Aromaa, A.; Belin, A.C.; Freilinger, T.; Ikram, M.A.; Jarvelin, M.R.; Raitakari, O.T.; Terwindt, G.M.; Kallela, M.; Wessman, M.; Olesen, J.; Chasman, D.I.; Nyholt, D.R.; Stefansson, H.; Stefansson, K.; Maagdenberg, A.M.J.M. van den; Hansen, T.F.; Ripatti, S.; Zwart, J.A.; Palotie, A.; Pirinen, M.; Int Headache Genetics Consortium; HUNT All-in Headache & Danish Blood Donor Study Genomic C (2022), Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles, Nature Genetics 54.
- Loonen, I.C.M.; Kohler, I.; Ghorasaini, M.; Giera, M.; Maagdenberg, A.M.J.M. van den; Mayboroda, O.A. & Tolner, E.A. (2022), Changes in plasma lipid levels following cortical spreading depolarization in a transgenic mouse model of familial hemiplegic migraine, Metabolites 12(3).
- Hoogstraten, W.S. van; Lute, M.C.C.; Nusselder, H.; Kros, L.; Maagdenberg, A.M.J.M. van den & Zeeuw, C.I. de (2022), cATR tracing approach to Identify individual intermediary neurons based on their input and output , Cells 11(19).
- Terpollili, N.A.; Dolp, R.; Waehner, K.; Schwarzmaier, S.M.; Rumbler, E.; Todorov, B.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Plesnila, N. (2022), Ca(V)2.1 channel mutations causing familial hemiplegic migraine type 1 increase the susceptibility for cortical spreading depolarizations and seizures and worsen outcome after experimental traumatic brain injury, eLife 11.
- Krivoshein, G.; Bakreen, A.; Maagdenberg, A.M.J.M. van den; Malm, T.; Giniatullin, R. & Jolkkonen, J. (2022), Activation of Meningeal Afferents Relevant to Trigeminal Headache Pain after Photothrombotic Stroke Lesion, International Journal of Molecular Sciences 23(20).
- Moskowitz, M.A.; Dodick, D.W.; Scher, A.I. & Maagdenberg, A.M.J.M. van den (2022), Migraine research comes of age in the 21st century, The Lancet Neurology 21(11): 955-958.
- He, B.S.; , X.Y. di; Guled, F.; Harder, A.V.E.; Maagdenberg, A.M.J.M. van den; Terwindt, G.M.; Krekels, E.H.J.; Kohler, I.; Harms, A.; Ramautar, R. & Hankemeier, T. (2022), Quantification of endocannabinoids in human cerebrospinal fluid using a novel micro-flow liquid chromatography-mass spectrometry method, Analytica Chimica Acta 1210: 339888.
- Mitchell, B.L.; Diaz-Torres, S.; Bivol, S.; Cuellar-Partida, G.; Gerring, Z.F.; Martin, N.G.; Medland, S.E.; Grasby, K.L.; Nyholt, D.R.; Renteria, M.E. & Int Headache Genetics Consortium (2022), Elucidating the relationship between migraine risk and brain structure using genetic data, Brain 145(9): 3214-3224.
- Hu, M.; Frega, M.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den; Frimat, J.P. & Feber, J. le (2022), MEA-ToolBox, Neuroinformatics 20.
- Kasi, D.G.; Graaf, M.N.S. de; Motreuil-Ragot, P.A.; Frimat, J.P.M.S.; Ferrari, M.D.; Sarro, P.M.; Mastrangeli, M.; Maagdenberg, A.M.J.M. van den; Mummery, C.L. & Orlova, V.V. (2022), Rapid prototyping of organ-on-a-chip devices using maskless photolithography, Micromachines 13(1).
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- Jansen, N.A.; Schenke, M.; Voskuyl, R.A.; Thijs, R.D.; Maagdenberg, A.M.J.M. van den & Tolner, E.A. (2019), Apnea Associated with Brainstem Seizures in Cacna1a(S218L) Mice Is Caused by Medullary Spreading Depolarization, Journal of Neuroscience 39(48): 9633-9644.
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- Maagdenberg, A.M.J.M. van den; Nyholt, D.R. & Anttila, V. (2019), Novel hypotheses emerging from GWAS in migraine?, Journal of Headache and Pain 20.
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- Chung, D.Y.; Sadeghian, H.; Qin, T.; Lule, S.; Lee, H.; Karakaya, F.; Goins, S.; Oka, F.; Yaseen, M.A.; Houben, T.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den; Whalen, M.J.; Sakadzic, S. & Ayata, C. (2019), Determinants of Optogenetic Cortical Spreading Depolarizations, Cerebral Cortex 29(3): 1150-1161.
- Yalcin, N.; Chen, S.P.; Yu, E.S.; Liu, T.T.; Yen, J.C.; Atalay, Y.B.; Qin, T.; Celik, F.; Maagdenberg, A.M.J.M. van den; Moskowitz, M.A.; Ayata, C. & Eikermann-Haerter, K. (2019), Caffeine does not affect susceptibility to cortical spreading depolarization in mice, Journal of Cerebral Blood Flow and Metabolism 39(4): 740-750.
- Magni, G.; Boccazzi, M.; Bodini, A.; Abbracchio, M.P.; Maagdenberg, A.M.J.M. van den & Ceruti, S. (2019), Basal astrocyte and microglia activation in the central nervous system of Familial Hemiplegic Migraine Type I mice, Cephalalgia 39(14): 1809-1817.
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- Eroli, F.; Loonen, I.C.M.; Maagdenberg, A.M.J.M. van den; Tolner, E.A. & Nistri, A. (2018), Differential neuromodulatory role of endocannabinoids in the rodent trigeminal sensory ganglion and cerebral cortex relevant to pain processing, Neuropharmacology 131: 39-50.
- MaassenVandenBrink, A.; Terwindt, G.M. & Maagdenberg, A.M.J.M. van den (2018), Calcitonin gene-related peptide (receptor) antibodies: an exciting avenue for migraine treatment, Genome Medicine 10.
- Pelzer, N.; Haan, J.; Stam, A.H.; Vijfhuizen, L.S.; Koelewijn, S.C.; Smagge, A.; Vries, B. de; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Terwindt, G.M. (2018), Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation, Neurology 90(7): E575-E582.
- Yang, Y.H.; Zhao, H.Y.; Boomsma, D.I.; Ligthart, L.; Belin, A.C.; Smith, G.D.; Esko, T.; Freilinger, T.M.; Hansen, T.F.; Ikram, M.A.; Kallela, M.; Kubisch, C.; Paraskevi, C.; Strachan, D.P.; Wessman, M.; Maagdenberg, A.M.J.M. van den; Terwindt, G.M.; Nyholt, D.R. & Int Headache Genetics Consortium (2018), Molecular genetic overlap between migraine and major depressive disorder, European Journal of Human Genetics 26(8): 1202-1216.
- Noga, M.J.; Zielman, R.; Dongen, R.M. van; Bos, S.; Harms, A.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Hankemeier, T. & Ferrari, M.D. (2018), Strategies to assess and optimize stability of endogenous amines during cerebrospinal fluid sampling, Metabolomics 14(4).
- Winsvold, B.S.; Palta, P.; Eising, E.; Page, C.M.; Maagdenberg, A.M.J.M. van den; Palotie, A.; Zwart, J.A. & Int Headache Genetics Consortium (2018), Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study, Cephalalgia 38(2): 312-322.
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- Jepma, M.; Brown, S.B.R.E.; Murphy, P.R.; Koelewijn, S.C.; Vries, B. de; Maagdenberg, A.M. van den & Nieuwenhuis, S. (2018), Noradrenergic and Cholinergic Modulation of Belief Updating, Journal of Cognitive Neuroscience 30(12): 1803-1820.
- Gormley, P.; Kurki, M.I.; Hiekkala, M.E.; Veerapen, K.; Happola, P.; Mitchell, A.A.; Lal, D.; Palta, P.; Surakka, I.; Kaunisto, M.A.; Hamalainen, E.; Vepsalainen, S.; Havanka, H.; Harno, H.; Ilmavirta, M.; Nissila, M.; Sako, E.; Sumelahti, M.L.; Liukkonen, J.; Sillanpaa, M.; Metsahonkala, L.; Koskinen, S.; Lehtimaki, T.; Raitakari, O.; Mannikko, M.; Ran, C.; Belin, A.C.; Jousilahti, P.; Anttila, V.; Salomaa, V.; Artto, V.; Farkkila, M.; Runz, H.; Daly, M.J.; Neale, B.M.; Ripatti, S.; Kallela, M.; Wessman, M.; Palotie, A.; 23me Res Team & Int Headache Genetics Consortium (2018), Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families, Neuron 98(4): 743-+.
- Gormley, P.; Kurki, M.I.; Hiekkala, M.E.; Veerapen, K.; Happola, P.; Mitchell, A.A.; Lal, D.; Palta, P.; Surakka, I.; Kaunisto, M.A.; Hamalainen, E.; Vepsalainen, S.; Havanka, H.; Harno, H.; Ilmavirta, M.; Nissila, M.; Sako, E.; Sumelahti, M.L.; Liukkonen, J.; Sillanpaa, M.; Metsahonkala, L.; Koskinen, S.; Lehtimaki, T.; Raitakari, O.; Mannikko, M.; Ran, C.; Belin, A.C.; Jousilahti, P.; Anttila, V.; Salomaa, V.; Artto, V.; Farkkila, M.; Runz, H.; Daly, M.J.; Neale, B.M.; Ripatti, S.; Kallela, M.; Wessman, M.; Palotie, A.; 23 Me Res Team & IHGC (2018), Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (vol 98, pg 743, 2018), Neuron 99(5): 1098-1098.
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- Boer, I. de; Stam, A.H.; Buntinx, L.; Zielman, R.; Steen, I. van der; Maagdenberg, A.M.J.M. van den; Koning, E.J.P. de; Ferrari, M.D.; Hoon, J.N. de & Terwindt, G.M. (2018), RVCL-S and CADASIL display distinct impaired vascular function, Neurology 91(10): E956-E963.
- Noga, M.J.; Zielman, R.; Dongen, R.M. van; Bos, S.; Harms, A.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Hankemeier, T. & Ferrari, M.D. (2018), Strategies to assess and optimize stability of endogenous amines during cerebrospinal fluid sampling, Metabolomics 14(4).
- Winsvold, B.S.; Palta, P.; Eising, E.; Page, C.M.; Maagdenberg, A.M.J.M. van den; Palotie, A.; Zwart, J.A. & Int Headache Genetics Consortium (2018), Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study, Cephalalgia 38(2): 312-322.
- Eroli, F.; Loonen, I.C.M.; Maagdenberg, A.M.J.M. van den; Tolner, E.A. & Nistri, A. (2018), Differential neuromodulatory role of endocannabinoids in the rodent trigeminal sensory ganglion and cerebral cortex relevant to pain processing, Neuropharmacology 131: 39-50.
- Pelzer, N.; Haan, J.; Stam, A.H.; Vijfhuizen, L.S.; Koelewijn, S.C.; Smagge, A.; Vries, B. de; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Terwindt, G.M. (2018), Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation, Neurology 90(7): E575-E582.
- MaassenVandenBrink, A.; Terwindt, G.M. & Maagdenberg, A.M.J.M. van den (2018), Calcitonin gene-related peptide (receptor) antibodies: an exciting avenue for migraine treatment, Genome Medicine 10.
- Kantae V., Ogino S., Noga M.J., Harms A.C., Dongen R.M. van, Onderwater G.L.J., Maagdenberg A.M.J.M. van den, Terwindt G.M., Stelt M. van der, Ferrari M.D. & Hankemeier T. (2017), Quantitative profiling of endocannabinoids and related N-acylethanolamines in human CSF using nano LC-MS/MS, Journal of Lipid Research 2017(58): 615-624.
- Rootselaar, A.F. van; Groffen, A.J.; Vries, B. de; Callenbach, P.M.C.; Santen, G.W.E.; Koelewijn, S.; Vijfhuizen, L.S.; Buijink, A.; Tijssen, M.A.J. & Maagdenberg, A.M.J.M. van den (2017), delta-Catenin (CTNND2) missense mutation in familial cortical myoclonic tremor and epilepsy, Neurology 89(23): 2341-2350.
- Lubbert, M.; Goral, R.O.; Satterfield, R.; Putzke, T.; Maagdenberg, A.M.J.M. van den; Kamasawa, N. & Young, S.M. (2017), A novel region in the Ca(v)2.1 alpha(1) subunit C-terminus regulates fast synaptic vesicle fusion and vesicle docking at the mammalian presynaptic active zone, eLife 6.
- Khaiboullina, S.F.; Mendelevich, E.G.; Shigapova, L.H.; Shagimardanova, E.; Gazizova, G.; Nikitin, A.; Martynova, E.; Davidyuk, Y.N.; Bogdanov, E.I.; Gusev, O.; Maagdenberg, A.M.J.M. van den; Giniatullin, R.A. & Rizvanov, A.A. (2017), Cerebellar Arophy and changes in Cytokines Associated with the CACNA1A R583Q Mutation in a Russian Familial Hemiplegic Migraine Type 1 Family, FRONTIERS IN CELLULAR NEUROSCIENCE 11.
- Eroli, F.; Vilotti, S.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2017), HYPERPOLARIZATION-ACTIVATED CURRENT /(H) IN MOUSE TRIGEMINAL SENSORY NEURONS IN A TRANSGENIC MOUSE MODEL OF FAMILIAL HEMIPLEGIC MIGRAINE TYPE-1, Neuroscience 351: 47-64.
- Mulder, I.A.; Khmelinskii, A.; Dzyubachyk, O.; Jong, S. de; Rieff, N.; Wermer, M.H.; Hoehn, M.; Lelieveldt, B.P.F. & Maagdenberg, A.M.J.M. van den (2017), Automated Ischemic Lesion Segmentation in MRI Mouse Brain Data after Transient Middle Cerebral Artery Occlusion, Frontiers in Neuroinformatics 11.
- Chen, S.P.; Qin, T.; Seidel, J.L.; Zheng, Y.; Eikermann, M.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Moskowitz, M.A.; Ayata, C. & Eikermann-Haerter, K. (2017), Inhibition of the P2X7-PANX1 complex suppresses spreading depolarization and neuroinflammation, Brain 140: 1643-1656.
- Dongen, R.M. van; Zielman, R.; Noga, M.; Dekkers, O.M.; Hankemeier, T.; Maagdenberg, A.M.J.M. van den; Terwindt, G.M. & Ferrari, M.D. (2017), Migraine biomarkers in cerebrospinal fluid: A systematic review and meta-analysis, Cephalalgia 37(1): 49-63.
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- Kantae, V.; Ogino, S.; Noga, M.; Harms, A.C.; Dongen, R.M. van; Onderwater, G.L.J.; Maagdenberg, A.M.J.M. van den; Terwindt, G.M.; Stelt, M. van der; Ferrari, M.D. & Hankemeier, T. (2017), Quantitative profiling of endocannabinoids and related N-acylethanolamines in human CSF using nano LC-MS/MS, Journal of Lipid Research 58(3): 615-624.
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- Pelzer, N.; Blom, D.E.; Stam, A.H.; Vijfhuizen, L.S.; Hageman, A.T.M.; Vliet, J.A. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Haan, J. & Terwindt, G.M. (2017), Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation, Cephalalgia 37(8): 737-755.
- Hamming, A.M.; Toorn, A. van der; Rudrapatna, U.S.; Ma, L.; Os, H.J.A. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Zwet, E. van; Poinsatte, K.; Stowe, A.M.; Dijkhuizen, R.M. & Wermer, M.J.H. (2017), Valproate Reduces Delayed Brain Injury in a Rat Model of Subarachnoid Hemorrhage, Stroke 48(2): 452-458.
- Pelzer, N.; Bijkerk, R.; Reinders, M.E.J.; Zonneveld, A.J. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Eikenboom, J. & Terwindt, G.M. (2017), Circulating Endothelial Markers in Retinal Vasculopathy With Cerebral Leukoencephalopathy and Systemic Manifestations, Stroke 48(12): 3301-3307.
- Winsvold, B.S.; Bettella, F.; Witoelar, A.; Anttila, V.; Gormley, P.; Kurth, T.; Terwindt, G.M.; Freilinger, T.M.; Frei, O.; Shadrin, A.; Wang, Y.P.; Dale, A.M.; Maagdenberg, A.M.J.M. van den; Chasman, D.I.; Nyholt, D.R.; Palotie, A.; Andreassen, O.A.; Zwart, J.A. & Int Headache Genetics Consortium (2017), Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants, PLoS ONE 12(9).
- Mulder, I.A.; Khmelinskii, A.; Dzyubachyk, O.; Jong, S. de; Wermer, M.J.H.; Hoehn, M.; Lelieveldt, B.P.F. & Maagdenberg, A.M.J.M. van den (2017), MRI Mouse Brain Data of Ischemic Lesion after Transient Middle Cerebral Artery Occlusion, Frontiers in Neuroinformatics 11.
- Nowodworska, A.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Fabbretti, E. (2017), In situ imaging reveals properties of purinergic signalling in trigeminal sensory ganglia in vitro, Purinergic Signalling 13(4): 511-520.
- Eising, E.; Shyti, R.; Hoen, P.A.C. 't; Vijfhuizen, L.S.; Huisman, S.M.H.; Broos, L.A.M.; Mahfouz, A.; Reinders, M.J.T.; Ferrari, M.D.; Tolner, E.A.; Vries, B. de & Maagdenberg, A.M.J.M. van den (2017), Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine, Molecular Neurobiology 54(4): 2986-2996.
- Eising, E.; Pelzer, N.; Vijfhuizen, L.S.; Vries, B. de; Ferrari, M.D.; Hoen, P.A.C. 't; Terwindt, G.M. & Maagdenberg, A.M.J.M. van den (2017), Identifying a gene expression signature of cluster headache in blood, Scientific Reports 7.
- Cain, S.M.; Bohnet, B.; Ledue, J.; Yung, A.C.; Garcia, E.; Tyson, J.R.; Alles, S.R.A.; Han, H.L.; Maagdenberg, A.M.J.M. van den; Kozlowski, P.; MacVicar, B.A. & Snutch, T.P. (2017), In vivo imaging reveals that pregabalin inhibits cortical spreading depression and propagation to subcortical brain structures, Proceedings of the National Academy of Sciences 114(9): 2401-2406.
- Rodero, M.P.; Decalf, J.; Bondet, V.; Hunt, D.; Rice, G.I.; Werneke, S.; McGlasson, S.L.; Alyanakian, M.A.; Bader-Meunier, B.; Barnerias, C.; Bellon, N.; Belot, A.; Bodemer, C.; Briggs, T.A.; Desguerre, I.; Fremond, M.L.; Hully, M.; Maagdenberg, A.M.J.M. van den; Melki, I.; Meyts, I.; Musset, L.; Pelzer, N.; Quartier, P.; Terwindt, G.M.; Wardlaw, J.; Wiseman, S.; Rieux-Laucat, F.; Rose, Y.; Neven, B.; Hertel, C.; Hayday, A.; Albert, M.L.; Rozenberg, F.; Crow, Y.J. & Duffy, D. (2017), Detection of interferon alpha protein reveals differential levels and cellular sources in disease, Journal of Experimental Medicine 214(5): 1547-1555.
- Dongen, R.M. van; Zielman, R.; Noga, M.; Dekkers, O.M.; Hankemeier, T.; Maagdenberg, A.M.J.M. van den; Terwindt, G.M. & Ferrari, M.D. (2017), Migraine biomarkers in cerebrospinal fluid: A systematic review and meta-analysis, Cephalalgia 37(1): 49-63.
- Lubbert, M.; Goral, R.O.; Satterfield, R.; Putzke, T.; Maagdenberg, A.M.J.M. van den; Kamasawa, N. & Young, S.M. (2017), A novel region in the Ca(v)2.1 alpha(1) subunit C-terminus regulates fast synaptic vesicle fusion and vesicle docking at the mammalian presynaptic active zone, eLife 6.
- Eising, E.; Pelzer, N.; Vijfhuizen, L.S.; Vries, B. de; Ferrari, M.D.; Hoen, P.A.C. 't; Terwindt, G.M. & Maagdenberg, A.M.J.M. van den (2017), Identifying a gene expression signature of cluster headache in blood, Scientific Reports 7.
- Chen, S.P.; Qin, T.; Seidel, J.L.; Zheng, Y.; Eikermann, M.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Moskowitz, M.A.; Ayata, C. & Eikermann-Haerter, K. (2017), Inhibition of the P2X7-PANX1 complex suppresses spreading depolarization and neuroinflammation, Brain 140: 1643-1656.
- Mulder, I.A.; Khmelinskii, A.; Dzyubachyk, O.; Jong, S. de; Wermer, M.J.H.; Hoehn, M.; Lelieveldt, B.P.F. & Maagdenberg, A.M.J.M. van den (2017), MRI Mouse Brain Data of Ischemic Lesion after Transient Middle Cerebral Artery Occlusion, Frontiers in Neuroinformatics 11.
- Winsvold, B.S.; Bettella, F.; Witoelar, A.; Anttila, V.; Gormley, P.; Kurth, T.; Terwindt, G.M.; Freilinger, T.M.; Frei, O.; Shadrin, A.; Wang, Y.P.; Dale, A.M.; Maagdenberg, A.M.J.M. van den; Chasman, D.I.; Nyholt, D.R.; Palotie, A.; Andreassen, O.A.; Zwart, J.A. & Int Headache Genetics Consortium (2017), Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants, PLoS ONE 12(9).
- Cain, S.M.; Bohnet, B.; Ledue, J.; Yung, A.C.; Garcia, E.; Tyson, J.R.; Alles, S.R.A.; Han, H.L.; Maagdenberg, A.M.J.M. van den; Kozlowski, P.; MacVicar, B.A. & Snutch, T.P. (2017), In vivo imaging reveals that pregabalin inhibits cortical spreading depression and propagation to subcortical brain structures, Proceedings of the National Academy of Sciences 114(9): 2401-2406.
- Houben, T.; Loonen, I.C.M.; Baca, S.M.; Schenke, M.; Meijer, J.H.; Ferrari, M.D.; Terwindt, G.M.; Voskuyl, R.A.; Charles, A.; Maagdenberg, A.M.J.M. van den & Tolner, E.A. (2017), Optogenetic induction of cortical spreading depression in anesthetized and freely behaving mice, Journal of Cerebral Blood Flow and Metabolism 37(5): 1641-1655.
- Kantae, V.; Ogino, S.; Noga, M.; Harms, A.C.; Dongen, R.M. van; Onderwater, G.L.J.; Maagdenberg, A.M.J.M. van den; Terwindt, G.M.; Stelt, M. van der; Ferrari, M.D. & Hankemeier, T. (2017), Quantitative profiling of endocannabinoids and related N-acylethanolamines in human CSF using nano LC-MS/MS, Journal of Lipid Research 58(3): 615-624.
- Pelzer, N.; Blom, D.E.; Stam, A.H.; Vijfhuizen, L.S.; Hageman, A.T.M.; Vliet, J.A. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Haan, J. & Terwindt, G.M. (2017), Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation, Cephalalgia 37(8): 737-755.
- Khaiboullina, S.F.; Mendelevich, E.G.; Shigapova, L.H.; Shagimardanova, E.; Gazizova, G.; Nikitin, A.; Martynova, E.; Davidyuk, Y.N.; Bogdanov, E.I.; Gusev, O.; Maagdenberg, A.M.J.M. van den; Giniatullin, R.A. & Rizvanov, A.A. (2017), Cerebellar Arophy and changes in Cytokines Associated with the CACNA1A R583Q Mutation in a Russian Familial Hemiplegic Migraine Type 1 Family, FRONTIERS IN CELLULAR NEUROSCIENCE 11.
- Pelzer, N.; Bijkerk, R.; Reinders, M.E.J.; Zonneveld, A.J. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Eikenboom, J. & Terwindt, G.M. (2017), Circulating Endothelial Markers in Retinal Vasculopathy With Cerebral Leukoencephalopathy and Systemic Manifestations, Stroke 48(12): 3301-3307.
- Eising, E.; Shyti, R.; Hoen, P.A.C. 't; Vijfhuizen, L.S.; Huisman, S.M.H.; Broos, L.A.M.; Mahfouz, A.; Reinders, M.J.T.; Ferrari, M.D.; Tolner, E.A.; Vries, B. de & Maagdenberg, A.M.J.M. van den (2017), Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine, Molecular Neurobiology 54(4): 2986-2996.
- Rootselaar, A.F. van; Groffen, A.J.; Vries, B. de; Callenbach, P.M.C.; Santen, G.W.E.; Koelewijn, S.; Vijfhuizen, L.S.; Buijink, A.; Tijssen, M.A.J. & Maagdenberg, A.M.J.M. van den (2017), delta-Catenin (CTNND2) missense mutation in familial cortical myoclonic tremor and epilepsy, Neurology 89(23): 2341-2350.
- Rodero, M.P.; Decalf, J.; Bondet, V.; Hunt, D.; Rice, G.I.; Werneke, S.; McGlasson, S.L.; Alyanakian, M.A.; Bader-Meunier, B.; Barnerias, C.; Bellon, N.; Belot, A.; Bodemer, C.; Briggs, T.A.; Desguerre, I.; Fremond, M.L.; Hully, M.; Maagdenberg, A.M.J.M. van den; Melki, I.; Meyts, I.; Musset, L.; Pelzer, N.; Quartier, P.; Terwindt, G.M.; Wardlaw, J.; Wiseman, S.; Rieux-Laucat, F.; Rose, Y.; Neven, B.; Hertel, C.; Hayday, A.; Albert, M.L.; Rozenberg, F.; Crow, Y.J. & Duffy, D. (2017), Detection of interferon alpha protein reveals differential levels and cellular sources in disease, Journal of Experimental Medicine 214(5): 1547-1555.
- Eroli, F.; Vilotti, S.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2017), HYPERPOLARIZATION-ACTIVATED CURRENT /(H) IN MOUSE TRIGEMINAL SENSORY NEURONS IN A TRANSGENIC MOUSE MODEL OF FAMILIAL HEMIPLEGIC MIGRAINE TYPE-1, Neuroscience 351: 47-64.
- Hamming, A.M.; Toorn, A. van der; Rudrapatna, U.S.; Ma, L.; Os, H.J.A. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Zwet, E. van; Poinsatte, K.; Stowe, A.M.; Dijkhuizen, R.M. & Wermer, M.J.H. (2017), Valproate Reduces Delayed Brain Injury in a Rat Model of Subarachnoid Hemorrhage, Stroke 48(2): 452-458.
- Dreier, J.P.; Fabricius, M.; Ayata, C.; Sakowitz, O.W.; Shuttleworth, C.W.; Dohmen, C.; Graf, R.; Vajkoczy, P.; Helbok, R.; Suzuki, M.; Schiefecker, A.J.; Major, S.; Winkler, M.K.L.; Kang, E.J.; Milakara, D.; Oliveira-Ferreira, A.I.; Reiffurth, C.; Revankar, G.S.; Sugimoto, K.; Dengler, N.F.; Hecht, N.; Foreman, B.; Feyen, B.; Kondziella, D.; Friberg, C.K.; Piilgaard, H.; Rosenthal, E.S.; Westover, M.B.; Maslarova, A.; Santos, E.; Hertle, D.; Sanchez-Porras, R.; Jewell, S.L.; Balanca, B.; Platz, J.; Hinzman, J.M.; Luckl, J.; Schoknecht, K.; Scholl, M.; Drenckhahn, C.; Feuerstein, D.; Eriksen, N.; Horst, V.; Bretz, J.S.; Jahnke, P.; Scheel, M.; Bohner, G.; Rostrup, E.; Pakkenberg, B.; Heinemann, U.; Claassen, J.; Carlson, A.P.; Kowoll, C.M.; Lublinsky, S.; Chassidim, Y.; Shelef, I.; Friedman, A.; Brinker, G.; Reiner, M.; Kirov, S.A.; Andrew, R.D.; Farkas, E.; Guresir, E.; Vatter, H.; Chung, L.S.; Brennan, K.C.; Lieutaud, T.; Marinesco, S.; Maas, A.I.R.; Sahuquillo, J.; Dahlem, M.A.; Richter, F.; Herreras, O.; Boutelle, M.G.; Okonkwo, D.O.; Bullock, M.R.; Witte, O.W.; Martus, P.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Dijkhuizen, R.M.; Shutter, L.A.; Andaluz, N.; Schulte, A.P.; MacVicar, B.; Watanabe, T.; Woitzik, J.; Lauritzen, M.; Strong, A.J. & Hartings, J.A. (2017), Recording, analysis, and interpretation of spreading depolarizations in neurointensive care: Review and recommendations of the COSBID research group, Journal of Cerebral Blood Flow and Metabolism 37(5): 1595-1625.
- Nowodworska, A.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Fabbretti, E. (2017), In situ imaging reveals properties of purinergic signalling in trigeminal sensory ganglia in vitro, Purinergic Signalling 13(4): 511-520.
- Mulder, I.A.; Khmelinskii, A.; Dzyubachyk, O.; Jong, S. de; Rieff, N.; Wermer, M.H.; Hoehn, M.; Lelieveldt, B.P.F. & Maagdenberg, A.M.J.M. van den (2017), Automated Ischemic Lesion Segmentation in MRI Mouse Brain Data after Transient Middle Cerebral Artery Occlusion, Frontiers in Neuroinformatics 11.
- Esteve, C.; Tolner, E.A.; Shyti, R.; Maagdenberg, A.M.J.M. van den & McDonnell, L.A. (2016), Mass spectrometry imaging of amino neurotransmitters: a comparison of derivatization methods and application in mouse brain tissue, Metabolomics 12(2).
- Cassese, A.; Ellis, S.R.; Potocnik, N.O.; Burgermeister, E.; Eber, M.; Walch, A.; Maagdenberg, A.M.J.M. van den; McDonnell, L.A.; Heeren, R.M.A. & Balluff, B. (2016), Spatial Autocorrelation in Mass Spectrometry Imaging, Analytical Chemistry 88(11): 5871-5878.
- Stam, A.H.; Kothari, P.H.; Shaikh, A.; Gschwendter, A.; Jen, J.C.; Hodgkinson, S.; Hardy, T.A.; Hayes, M.; Kempster, P.A.; Kotschet, K.E.; Bajema, I.M.; Duinen, S.G. van; Maat-Schieman, M.L.C.; Jong, P.T.V.M. de; Smet, M.D. de; Wolff-Rouendaal, D. de; Dijkman, G.; Pelzer, N.; Kolar, G.R.; Schmidt, R.E.; Lacey, J.; Joseph, D.; Fintak, D.R.; Grand, M.G.; Brunt, E.M.; Liapis, H.; Hajj-Ali, R.A.; Kruit, M.C.; Buchem, M.A. van; Dichgans, M.; Frants, R.R.; Maagdenberg, A.M.J.M. van den; Haan, J.; Baloh, R.W.; Atkinson, J.P.; Terwindt, G.M. & Ferrari, M.D. (2016), Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, Brain 139: 2909-2922.
- Eising, E.; Huisman, S.M.H.; Mahfouz, A.; Vijfhuizen, L.S.; Anttila, V.; Winsvold, B.S.; Kurth, T.; Ikram, M.A.; Freilinger, T.; Kaprio, J.; Boomsma, D.I.; Duijn, C.M. van; Jarvelin, M.R.R.; Zwart, J.A.; Quaye, L.; Strachan, D.P.; Kubisch, C.; Dichgans, M.; Smith, G.D.; Stefansson, K.; Palotie, A.; Chasman, D.I.; Ferrari, M.D.; Terwindt, G.M.; Vries, B. de; Nyholt, D.R.; Lelieveldt, B.P.F.; Maagdenberg, A.M.J.M. van den & Reinders, M.J.T. (2016), Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas, Human Genetics 135(4): 425-439.
- Zhao, H.Y.; Eising, E.; Vries, B. de; Vijfhuizen, L.S.; Anttila, V.; Winsvold, B.S.; Kurth, T.; Stefansson, H.; Kallela, M.; Malik, R.; Stam, A.H.; Ikram, M.A.; Ligthart, L.; Freilinger, T.; Alexander, M.; Muller-Myhsok, B.; Schreiber, S.; Meitinger, T.; Aromas, A.; Eriksson, J.G.; Boomsma, D.I.; Duijn, C.M. van; Zwart, J.A.; Quaye, L.; Kubisch, C.; Dichgans, M.; Wessman, M.; Stefansson, K.; Chasman, D.I.; Palotie, A.; Martin, N.G.; Montgomery, G.W.; Ferrari, M.D.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Nyholt, D.R. & Int Headache Genetics Consortium (2016), Gene-based pleiotropy across migraine with aura and migraine without aura patient groups, Cephalalgia 36(7): 648-657.
- Eising, E.; Leeuw, C. de; Min, J.L.; Anttila, V.; Verheijen, M.H.G.; Terwindt, G.M.; Dichgans, M.; Freilinger, T.; Kubisch, C.; Ferrari, M.D.; Smit, A.B.; Vries, B. de; Palotie, A.; Maagdenberg, A.M.J.M. van den; Posthuma, D. & Int Headache Genetics Consortium (2016), Involvement of astrocyte and oligodendrocyte gene sets in migraine, Cephalalgia 36(7): 640-647.
- Gormley, P.; Anttila, V.; Winsvold, B.S.; Palta, P.; Esko, T.; Pers, T.H.; Farh, K.H.; Cuenca-Leon, E.; Muona, M.; Furlotte, N.A.; Kurth, T.; Ingason, A.; McMahon, G.; Ligthart, L.; Terwindt, G.M.; Kallela, M.; Freilinger, T.M.; Ran, C.; Gordon, S.G.; Stam, A.H.; Steinberg, S.; Borck, G.; Koiranen, M.; Quaye, L.; Adams, H.H.H.; Lehtimaki, T.; Sarin, A.P.; Wedenoja, J.; Hinds, D.A.; Buring, J.E.; Schurks, M.; Ridker, P.M.; Hrafnsdottir, M.G.; Stefansson, H.; Ring, S.M.; Hottenga, J.J.; Penninx, B.W.J.H.; Farkkila, M.; Artto, V.; Kaunisto, M.; Vepsalainen, S.; Malik, R.; Heath, A.C.; Madden, P.A.F.; Martin, N.G.; Montgomery, G.W.; Kurki, M.I.; Kals, M.; Magi, R.; Parn, K.; Hamalainen, E.; Huang, H.L.; Byrnes, A.E.; Franke, L.; Huang, J.; Stergiakouli, E.; Lee, P.H.; Sandor, C.; Webber, C.; Cader, Z.; Muller-Myhsok, B.; Schreiber, S.; Meitinger, T.; Eriksson, J.G.; Salomaa, V.; Heikkila, K.; Loehrer, E.; Uitterlinden, A.G.; Hofman, A.; Duijn, C.M. van; Cherkas, L.; Pedersen, L.M.; Stubhaug, A.; Nielsen, C.S.; Mannikko, M.; Mihailov, E.; Milani, L.; Gobel, H.; Esserlind, A.L.; Christensen, A.F.; Hansen, T.F.; Werge, T.; Kaprio, J.; Aromaa, A.J.; Raitakari, O.; Ikram, M.A.; Spector, T.; Jarvelin, M.R.; Metspalu, A.; Kubisch, C.; Strachan, D.P.; Ferrari, M.D.; Belin, A.C.; Dichgans, M.; Wessman, M.; Maagdenberg, A.M.J.M. van den; Zwart, J.A.; Boomsma, D.I.; Smith, G.D.; Stefansson, K.; Eriksson, N.; Daly, M.J.; Neale, B.M.; Olesen, J.; Chasman, D.I.; Nyholt, D.R.; Palotie, A. & Int Headache Genetics Consortium (2016), Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine, Nature Genetics 48(8): 856-+.
- Vries, B. de; Anttila, V.; Freilinger, T.; Wessman, M.; Kaunisto, M.A.; Kallela, M.; Artto, V.; Vijfhuizen, L.S.; Gobel, H.; Dichgans, M.; Kubisch, C.; Ferrari, M.D.; Palotie, A.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den & Int Headache Genetics Consortium (2016), Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set, Cephalalgia 36(7): 604-614.
- Zielman, R.; Postma, R.; Verhoeven, A.; Bakels, F.; Oosterhout, W.P.J. van; Meissner, A.; Maagdenberg, A.M.J.M. van den; Terwindt, G.M.; Mayboroda, O.A. & Ferrari, M.D. (2016), Metabolomic changes in CSF of migraine patients measured with H-1-NMR spectroscopy, Molecular BioSystems 12(12): 3674-3682.
- Lugtenberg, D.; Reijnders, M.R.F.; Fenckova, M.; Bijlsma, E.K.; Bernier, R.; Bon, B.W.M. van; Smeets, E.; Vulto-van Silfhout, A.T.; Bosch, D.; Eichler, E.E.; Mefford, H.C.; Carvill, G.L.; Bongers, E.M.H.F.; Schuurs-Hoeijmakers, J.H.M.; Ruivenkamp, C.A.; Santen, G.W.E.; Maagdenberg, A.M.J.M. van den; Peeters-Scholte, C.M.P.C.D.; Kuenen, S.; Verstreken, P.; Pfundt, R.; Yntema, H.G.; Vries, P.F. de; Veltman, J.A.; Hoischen, A.; Gilissen, C.; Vries, B.B.A. de; Schenck, A.; Kleefstra, T. & Vissers, L.E.L.M. (2016), De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila, European Journal of Human Genetics 24(8): 1145-1153.
- Khennouf, L.; Gesslein, B.; Lind, B.L.; Maagdenberg, A.M.J.M. van den & Lauritzen, M. (2016), Activity-Dependent Calcium, Oxygen, and Vascular Responses in a Mouse Model of Familial Hemiplegic Migraine Type 1, Annals of Neurology 80(2): 219-232.
- Nyholt, D.R. & Maagdenberg, A.M.J.M. van den (2016), Genome-wide association studies in migraine: current state and route to follow, Current Opinion in Neurology 29(3): 302-308.
- Vilotti, S.; Vana, N.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2016), Expression and function of calcitonin gene-related peptide (CGRP). receptors in trigeminal ganglia of R192Q Cacna1a knock-in mice, Neuroscience Letters 620: 104-110.
- Marchenkova, A.; Vilotti, S.; Ntamati, N.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2016), Inefficient constitutive inhibition of P2X3 receptors by brain natriuretic peptide system contributes to sensitization of trigeminal sensory neurons in a genetic mouse model of familial hemiplegic migraine, Molecular Pain 12.
- Marchenkova, A.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2016), LOSS OF INHIBITION BY BRAIN NATRIURETIC PEPTIDE OVER P2X3 RECEPTORS CONTRIBUTES TO ENHANCED SPIKE FIRING OF TRIGEMINAL GANGLION NEURONS IN A MOUSE MODEL OF FAMILIAL HEMIPLEGIC MIGRAINE TYPE-1, Neuroscience 331: 197-205.
- Maagdenberg, A.M.J.M. van den (2016), Migraine genetics: New opportunities, new challenges, Cephalalgia 36(7): 601-603.
- Hamming, A.M.; Wermer, M.J.H.; Rudrapatna, S.U.; Lanier, C.; Os, H.J.A. van; Bergh, W.M. van den; Ferrari, M.D.; Toorn, A. van der; Maagdenberg, A.M.J.M. van den; Stowe, A.M. & Dijkhuizen, R.M. (2016), Spreading depolarizations increase delayed brain injury in a rat model of subarachnoid hemorrhage, Journal of Cerebral Blood Flow and Metabolism 36(7): 1224-1231.
- Mulder, I.A.; Esteve, C.; Wermer, M.J.H.; Hoehn, M.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den & McDonnell, L.A. (2016), Funnel-freezing versus heat-stabilization for the visualization of metabolites by mass spectrometry imaging in a mouse stroke model, Proteomics 16(11-12): 1652-1659.
- Zielman, R.; Postma, R.; Verhoeven, A.; Bakels, F.; Oosterhout, W.P.J. van; Meissner, A.; Maagdenberg, A.M.J.M. van den; Terwindt, G.M.; Mayboroda, O.A. & Ferrari, M.D. (2016), Metabolomic changes in CSF of migraine patients measured with H-1-NMR spectroscopy, Molecular BioSystems 12(12): 3674-3682.
- Vries, B. de; Anttila, V.; Freilinger, T.; Wessman, M.; Kaunisto, M.A.; Kallela, M.; Artto, V.; Vijfhuizen, L.S.; Gobel, H.; Dichgans, M.; Kubisch, C.; Ferrari, M.D.; Palotie, A.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den & Int Headache Genetics Consortium (2016), Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set, Cephalalgia 36(7): 604-614.
- Stam, A.H.; Kothari, P.H.; Shaikh, A.; Gschwendter, A.; Jen, J.C.; Hodgkinson, S.; Hardy, T.A.; Hayes, M.; Kempster, P.A.; Kotschet, K.E.; Bajema, I.M.; Duinen, S.G. van; Maat-Schieman, M.L.C.; Jong, P.T.V.M. de; Smet, M.D. de; Wolff-Rouendaal, D. de; Dijkman, G.; Pelzer, N.; Kolar, G.R.; Schmidt, R.E.; Lacey, J.; Joseph, D.; Fintak, D.R.; Grand, M.G.; Brunt, E.M.; Liapis, H.; Hajj-Ali, R.A.; Kruit, M.C.; Buchem, M.A. van; Dichgans, M.; Frants, R.R.; Maagdenberg, A.M.J.M. van den; Haan, J.; Baloh, R.W.; Atkinson, J.P.; Terwindt, G.M. & Ferrari, M.D. (2016), Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, Brain 139: 2909-2922.
- Maagdenberg, A.M.J.M. van den (2016), Migraine genetics: New opportunities, new challenges, Cephalalgia 36(7): 601-603.
- Gormley, P.; Anttila, V.; Winsvold, B.S.; Palta, P.; Esko, T.; Pers, T.H.; Farh, K.H.; Cuenca-Leon, E.; Muona, M.; Furlotte, N.A.; Kurth, T.; Ingason, A.; McMahon, G.; Ligthart, L.; Terwindt, G.M.; Kallela, M.; Freilinger, T.M.; Ran, C.; Gordon, S.G.; Stam, A.H.; Steinberg, S.; Borck, G.; Koiranen, M.; Quaye, L.; Adams, H.H.H.; Lehtimaki, T.; Sarin, A.P.; Wedenoja, J.; Hinds, D.A.; Buring, J.E.; Schurks, M.; Ridker, P.M.; Hrafnsdottir, M.G.; Stefansson, H.; Ring, S.M.; Hottenga, J.J.; Penninx, B.W.J.H.; Farkkila, M.; Artto, V.; Kaunisto, M.; Vepsalainen, S.; Malik, R.; Heath, A.C.; Madden, P.A.F.; Martin, N.G.; Montgomery, G.W.; Kurki, M.I.; Kals, M.; Magi, R.; Parn, K.; Hamalainen, E.; Huang, H.L.; Byrnes, A.E.; Franke, L.; Huang, J.; Stergiakouli, E.; Lee, P.H.; Sandor, C.; Webber, C.; Cader, Z.; Muller-Myhsok, B.; Schreiber, S.; Meitinger, T.; Eriksson, J.G.; Salomaa, V.; Heikkila, K.; Loehrer, E.; Uitterlinden, A.G.; Hofman, A.; Duijn, C.M. van; Cherkas, L.; Pedersen, L.M.; Stubhaug, A.; Nielsen, C.S.; Mannikko, M.; Mihailov, E.; Milani, L.; Gobel, H.; Esserlind, A.L.; Christensen, A.F.; Hansen, T.F.; Werge, T.; Kaprio, J.; Aromaa, A.J.; Raitakari, O.; Ikram, M.A.; Spector, T.; Jarvelin, M.R.; Metspalu, A.; Kubisch, C.; Strachan, D.P.; Ferrari, M.D.; Belin, A.C.; Dichgans, M.; Wessman, M.; Maagdenberg, A.M.J.M. van den; Zwart, J.A.; Boomsma, D.I.; Smith, G.D.; Stefansson, K.; Eriksson, N.; Daly, M.J.; Neale, B.M.; Olesen, J.; Chasman, D.I.; Nyholt, D.R.; Palotie, A. & Int Headache Genetics Consortium (2016), Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine, Nature Genetics 48(8): 856-+.
- Marchenkova, A.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2016), LOSS OF INHIBITION BY BRAIN NATRIURETIC PEPTIDE OVER P2X3 RECEPTORS CONTRIBUTES TO ENHANCED SPIKE FIRING OF TRIGEMINAL GANGLION NEURONS IN A MOUSE MODEL OF FAMILIAL HEMIPLEGIC MIGRAINE TYPE-1, Neuroscience 331: 197-205.
- Eising, E.; Leeuw, C. de; Min, J.L.; Anttila, V.; Verheijen, M.H.G.; Terwindt, G.M.; Dichgans, M.; Freilinger, T.; Kubisch, C.; Ferrari, M.D.; Smit, A.B.; Vries, B. de; Palotie, A.; Maagdenberg, A.M.J.M. van den; Posthuma, D. & Int Headache Genetics Consortium (2016), Involvement of astrocyte and oligodendrocyte gene sets in migraine, Cephalalgia 36(7): 640-647.
- Marchenkova, A.; Vilotti, S.; Ntamati, N.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2016), Inefficient constitutive inhibition of P2X3 receptors by brain natriuretic peptide system contributes to sensitization of trigeminal sensory neurons in a genetic mouse model of familial hemiplegic migraine, Molecular Pain 12.
- Hamming, A.M.; Wermer, M.J.H.; Rudrapatna, S.U.; Lanier, C.; Os, H.J.A. van; Bergh, W.M. van den; Ferrari, M.D.; Toorn, A. van der; Maagdenberg, A.M.J.M. van den; Stowe, A.M. & Dijkhuizen, R.M. (2016), Spreading depolarizations increase delayed brain injury in a rat model of subarachnoid hemorrhage, Journal of Cerebral Blood Flow and Metabolism 36(7): 1224-1231.
- Nyholt, D.R. & Maagdenberg, A.M.J.M. van den (2016), Genome-wide association studies in migraine: current state and route to follow, Current Opinion in Neurology 29(3): 302-308.
- Eising, E.; Huisman, S.M.H.; Mahfouz, A.; Vijfhuizen, L.S.; Anttila, V.; Winsvold, B.S.; Kurth, T.; Ikram, M.A.; Freilinger, T.; Kaprio, J.; Boomsma, D.I.; Duijn, C.M. van; Jarvelin, M.R.R.; Zwart, J.A.; Quaye, L.; Strachan, D.P.; Kubisch, C.; Dichgans, M.; Smith, G.D.; Stefansson, K.; Palotie, A.; Chasman, D.I.; Ferrari, M.D.; Terwindt, G.M.; Vries, B. de; Nyholt, D.R.; Lelieveldt, B.P.F.; Maagdenberg, A.M.J.M. van den & Reinders, M.J.T. (2016), Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas, Human Genetics 135(4): 425-439.
- Zhao, H.Y.; Eising, E.; Vries, B. de; Vijfhuizen, L.S.; Anttila, V.; Winsvold, B.S.; Kurth, T.; Stefansson, H.; Kallela, M.; Malik, R.; Stam, A.H.; Ikram, M.A.; Ligthart, L.; Freilinger, T.; Alexander, M.; Muller-Myhsok, B.; Schreiber, S.; Meitinger, T.; Aromas, A.; Eriksson, J.G.; Boomsma, D.I.; Duijn, C.M. van; Zwart, J.A.; Quaye, L.; Kubisch, C.; Dichgans, M.; Wessman, M.; Stefansson, K.; Chasman, D.I.; Palotie, A.; Martin, N.G.; Montgomery, G.W.; Ferrari, M.D.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Nyholt, D.R. & Int Headache Genetics Consortium (2016), Gene-based pleiotropy across migraine with aura and migraine without aura patient groups, Cephalalgia 36(7): 648-657.
- Vilotti, S.; Vana, N.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2016), Expression and function of calcitonin gene-related peptide (CGRP). receptors in trigeminal ganglia of R192Q Cacna1a knock-in mice, Neuroscience Letters 620: 104-110.
- Lugtenberg, D.; Reijnders, M.R.F.; Fenckova, M.; Bijlsma, E.K.; Bernier, R.; Bon, B.W.M. van; Smeets, E.; Vulto-van Silfhout, A.T.; Bosch, D.; Eichler, E.E.; Mefford, H.C.; Carvill, G.L.; Bongers, E.M.H.F.; Schuurs-Hoeijmakers, J.H.M.; Ruivenkamp, C.A.; Santen, G.W.E.; Maagdenberg, A.M.J.M. van den; Peeters-Scholte, C.M.P.C.D.; Kuenen, S.; Verstreken, P.; Pfundt, R.; Yntema, H.G.; Vries, P.F. de; Veltman, J.A.; Hoischen, A.; Gilissen, C.; Vries, B.B.A. de; Schenck, A.; Kleefstra, T. & Vissers, L.E.L.M. (2016), De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila, European Journal of Human Genetics 24(8): 1145-1153.
- Khennouf, L.; Gesslein, B.; Lind, B.L.; Maagdenberg, A.M.J.M. van den & Lauritzen, M. (2016), Activity-Dependent Calcium, Oxygen, and Vascular Responses in a Mouse Model of Familial Hemiplegic Migraine Type 1, Annals of Neurology 80(2): 219-232.
- Mulder, I.A.; Esteve, C.; Wermer, M.J.H.; Hoehn, M.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den & McDonnell, L.A. (2016), Funnel-freezing versus heat-stabilization for the visualization of metabolites by mass spectrometry imaging in a mouse stroke model, Proteomics 16(11-12): 1652-1659.
- Esteve, C.; Tolner, E.A.; Shyti, R.; Maagdenberg, A.M.J.M. van den & McDonnell, L.A. (2016), Mass spectrometry imaging of amino neurotransmitters: a comparison of derivatization methods and application in mouse brain tissue, Metabolomics 12(2).
- Cassese, A.; Ellis, S.R.; Potocnik, N.O.; Burgermeister, E.; Eber, M.; Walch, A.; Maagdenberg, A.M.J.M. van den; McDonnell, L.A.; Heeren, R.M.A. & Balluff, B. (2016), Spatial Autocorrelation in Mass Spectrometry Imaging, Analytical Chemistry 88(11): 5871-5878.
- Shyti R., Kohler I., Schoenmaker B., Derks R.J., Ferrari M.D., Tolner E.A., Mayboroda O.A. & Maagdenberg A.M.J.M. van den (2015), Plasma metabolic profiling after cortical spreading depression in a transgenic mouse model of hemiplegic migraine by capillary electrophoresis--mass spectrometry, Molecular Biosystems 11(5): 1462-1471.
- Rutten, J.W.; Klever, R.R.; Hegeman, I.M.; Poole, D.S.; Dauwerse, H.G.; Broos, L.A.M.; Breukel, C.; Aartsma-Rus, A.M.; Verbeek, J.S.; Weerd, L. van der; Duinen, S.G. van; Maagdenberg, A.M.J.M. van den & Oberstein, S.A.J.L. (2015), The NOTCH3 score: a pre-clinical CADASIL biomarker in a novel human genomic NOTCH3 transgenic mouse model with early progressive vascular NOTCH3 accumulation, Acta Neuropathologica Communications 3.
- Sar, S.A. van der; Zielman, R.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Deelder, A.M.; Mayboroda, O.A.; Meissner, A. & Ferrari, M.D. (2015), Ethanol contamination of cerebrospinal fluid during standardized sampling and its effect on H-1-NMR metabolomics, Analytical and Bioanalytical Chemistry 407(16): 4835-4839.
- Mulder, I.A.; Esteve, C.; Carreira, R.J.; Rieff, N.; Broos, L.A.M.; Wermer, M.J.H.; Ferrari, M.D.; Tolner, E.A.; McDonnell, L.A. & Maagdenberg, A.M.J.M. van den (2015), Application of maldi mass spectrometry imaging for analysis of biomolecular profiles after experimental stroke in a migraine mouse model, Cephalalgia 35: 234-234.
- Kaja, S.; Payne, A.J.; Nielsen, E.O.; Thompson, C.L.; Maagdenberg, A.M.J.M. van den; Koulen, P. & Snutch, T.P. (2015), DIFFERENTIAL CEREBELLAR GABA(A) RECEPTOR EXPRESSION IN MICE WITH MUTATIONS IN CAV2.1 (P/Q-TYPE) CALCIUM CHANNELS, Neuroscience 304: 198-208.
- Shyti, R.; Kohler, I.; Schoenmaker, B.; Derks, R.J.E.; Ferrari, M.D.; Tolner, E.A.; Mayboroda, O.A. & Maagdenberg, A.M.J.M. van den (2015), Plasma metabolic profiling after cortical spreading depression in a transgenic mouse model of hemiplegic migraine by capillary electrophoresis mass spectrometry.
- Vecchia, D.; Tottene, A.; Maagdenberg, A.M.J.M. van den & Pietrobon, D. (2015), Abnormal cortical synaptic transmission in Ca(V)2.1 knockin mice with the S218L missense mutation which causes a severe familial hemiplegic migraine syndrome in humans, Frontiers in Cellular Neuroscience 9.
- LaBianca, S.; Jensen, R.; Maagdenberg, A.M.J.M. van den; Baandrup, L. & Bendtsen, L. (2015), Familial Hemiplegic Migraine and Recurrent Episodes of Psychosis: A Case Report, Headache 55(7): 1004-1007.
- Kros, L.; Rooda, O.H.J.E.; Spanke, J.K.; Alva, P.; Dongen, M.N. van; Karapatis, A.; Tolner, E.A.; Strydis, C.; Davey, N.; Winkelman, B.H.J.; Negrello, M.; Serdijn, W.A.; Steuber, V.; Maagdenberg, A.M.J.M. van den; Zeeuw, C.I. de & Hoebeek, F.E. (2015), Cerebellar output controls generalized spike-and-wave discharge occurrence, Annals of Neurology 77(6): 1027-1049.
- Eikermann-Haerter, K.; Lee, J.H.; Yalcin, N.; Yu, E.S.; Daneshmand, A.; Wei, Y.; Zheng, Y.; Can, A.; Sengul, B.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Ayata, C. (2015), Migraine Prophylaxis, Ischemic Depolarizations, and Stroke Outcomes in Mice, Stroke 46(1): 229-236.
- Shyti, R.; Eikermann-Haerter, K.; Heiningen, S.H. van; Meijer, O.C.; Ayata, C.; Joels, M.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Tolner, E.A. (2015), Stress hormone corticosterone enhances susceptibility to cortical spreading depression in familial hemiplegic migraine type 1 mutant mice, Experimental Neurology 263: 214-220.
- Heijs, B.; Carreira, R.J.; Tolner, E.A.; Ru, A.H. de; Maagdenberg, A.J.M. van den; Veelen, P.A. van & McDonnell, L.A. (2015), Comprehensive Analysis of the Mouse Brain Proteome Sampled in Mass Spectrometry Imaging, Analytical Chemistry 87(3): 1867-1875.
- Demirkan, A.; Henneman, P.; Verhoeven, A.; Dharuri, H.; Amin, N.; Klinken, J.B. van; Karssen, L.C.; Vries, B. de; Meissner, A.; Goraler, S.; Maagdenberg, A.M.J.M. van den; Deelder, A.M.; t' Hoen, P.A.C.; Duijn, C.M. van & Dijk, K.W. van (2015), Insight in Genome-Wide Association of Metabolite Quantitative Traits by Exome Sequence Analyses, PLoS Genetics 11(1).
- Jacobsen, K.K.; Nievergelt, C.M.; Zayats, T.; Greenwood, T.A.; Anttila, V.; Akiskal, H.S.; Haavik, J.; Fasmer, O.B.; Kelsoe, J.R.; Johansson, S.; Oedegaard, K.J. & BiGs Consortium IHG Consortium (2015), Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder, Journal of Affective Disorders 172: 453-461.
- Sadeghian, H.; Harms, C.; Qin, T.; Ferrari, M.; Maagdenberg, A. van den; Endres, M. & Ayata, C. (2015), Increased Susceptibility to Hypoxic/ischemic Injury in FHM1 Mutant Mice, Headache 55: 170-170.
- Odijk, M.; Wouden, E.J. van der; Olthuis, W.; Ferrari, M.D.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den & Berg, A. van den (2015), Microfabricated solid-state ion-selective electrode probe for measuring potassium in the living rodent brain: Compatibility with DC-EEG recordings to study spreading depression, Sensors and Actuators B: Chemical 207: 945-953.
- Nyholt, D.R.; Anttila, V.; Winsvold, B.S.; Kurth, T.; Stefansson, H.; Kallela, M.; Malik, R.; Vries, B. de; Terwindt, G.M.; Ikram, M.A.; Stam, A.H.; Ligthart, L.; Freilinger, T.; Alexander, M.; Muller-Myhsok, B.; Schreiber, S.; Meitinger, T.; Aromaa, A.; Eriksson, J.G.; Kaprio, J.; Boomsma, D.I.; Duijn, C. van; Raitakari, O.; Jarvelin, M.R.; Zwart, J.A.; Quaye, L.; Strachan, D.P.; Kubisch, C.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Dichgans, M.; Wessman, M.; Smith, G.D.; Stefansson, K.; Chasman, D.I.; Palotie, A. & Int Headache Genetics Consortium (2015), Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies, Cephalalgia 35(6): 489-499.
- Ferrari, M.D.; Klever, R.R.; Terwindt, G.M.; Ayata, C. & Maagdenberg, A.M.J.M. van den (2015), Migraine pathophysiology: lessons from mouse models and human genetics, Lancet Neurology 14(1): 65-80.
- Tolner, E.A.; Houben, T.; Terwindt, G.M.; Vries, B. de; Ferrari, M.D. & Maagdenberg, A.M.J.M. van den (2015), From migraine genes to mechanisms, PAIN 156(4): S64-S74.
- Weller, C.M.; Leen, W.G.; Neville, B.G.R.; Duncan, J.S.; Vries, B. de; Geilenkirchen, M.A.; Haan, J.; Kamsteeg, E.J.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Willemsen, M.A.A.P.; Scheffer, H. & Terwindt, G.M. (2015), A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood, Cephalalgia 35(1): 10-15.
- Panagiotakaki, E.; Grandis, E. de; Stagnaro, M.; Heinzen, E.L.; Fons, C.; Sisodiya, S.; Vries, B. de; Goubau, C.; Weckhuysen, S.; Kemlink, D.; Scheffer, I.; Lesca, G.; Rabilloud, M.; Klich, A.; Ramirez-Camacho, A.; Ulate-Campos, A.; Campistol, J.; Giannotta, M.; Moutard, M.L.; Doummar, D.; Hubsch-Bonneaud, C.; Jaffer, F.; Cross, H.; Gurrieri, F.; Tiziano, D.; Nevsimalova, S.; Nicole, S.; Neville, B.; Maagdenberg, A.M.J.M. van den; Mikati, M.; Goldstein, D.B.; Vavassori, R.; Arzimanoglou, A.; IBAHC Consortium; French AHC Consortium & Int AHC Consortium (2015), Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients, Orphanet Journal of Rare Diseases 10.
- Carreira, R.J.; Shyti, R.; Balluff, B.; Abdelmoula, W.M.; Heiningen, S.H. van; Zeijl, R.J. van; Dijkstra, J.; Ferrari, M.D.; Tolner, E.A.; McDonnell, L.A. & Maagdenberg, A.M.J.M. van den (2015), Large-Scale Mass Spectrometry Imaging Investigation of Consequences of Cortical Spreading Depression in a Transgenic Mouse Model of Migraine, Journal of The American Society for Mass Spectrometry 26(6): 853-861.
- Heijs, B.; Tolner, E.A.; Bovee, J.V.M.G.; Maagdenberg, A.M.J.M. van den & McDonnell, L.A. (2015), Brain Region-Specific Dynamics of On-Tissue Protein Digestion Using MALDI Mass Spectrometry Imaging, Journal of Proteome Research 14(12): 5348-5354.
- Louter, M.A.; Fernandez-Morales, J.; Vries, B. de; Winsvold, B.; Anttila, V.; Fernandez-Cadenas, I.; Vila-Pueyo, M.; Sintas, C.; Duijn, C.M. van; Cormand, B.; Alvarez-Sabin, J.; Montaner, J.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Palotie, A.; Zwart, J.A.; Macaya, A.; Terwindt, G.M. & Pozo-Rosich, P. (2015), Candidate-gene association study searching for genetic factors involved in migraine chronification, Cephalalgia 35(6): 500-507.
- Weller, C.M.; Wilbrink, L.A.; Houwing-Duistermaat, J.J.; Koelewijn, S.C.; Vijfhuizen, L.S.; Haan, J.; Ferrari, M.D.; Terwindt, G.M.; Maagdenberg, A.M. van den & Vries, B. de (2015), Cluster headache and the hypocretin receptor 2 reconsidered: A genetic association study and meta-analysis, Cephalalgia 35(9): 741-747.
- Roqueiro, D.; Witteveen, M.J.; Anttila, V.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den & Borgwardt, K. (2015), In silico phenotyping via co-training for improved phenotype prediction from genotype, Bioinformatics 31(12): 303-310.
- Malik, R.; Freilinger, T.; Anttila, V.; Vander Heiden, J.; Traylor, M.; Vries, B. de; Holliday, E.G.; Terwindt, G.M.; Sturm, J.; Bis, J.C.; Hopewell, J.C.; Ferrari, M.D.; Rannikmae, K.; Wessman, M.; Kallela, M.; Kubisch, C.; Fornage, M.; Meschia, J.F.; Lehtimaki, T.; Sudlow, C.; Clarke, R.; Chasman, D.I.; Mitchell, B.D.; Maguire, J.; Kaprio, J.; Farrall, M.; Raitakari, O.T.; Kurth, T.; Ikram, M.A.; Reiner, A.P.; Longstreth, W.T.; Rothwell, P.M.; Strachan, D.P.; Sharma, P.; Seshadri, S.; Quaye, L.; Cherkas, L.; Schurks, M.; Rosand, J.; Ligthart, L.; Boncoraglio, G.B.; Smith, G.D.; Duijn, C.M. van; Stefansson, K.; Worrall, B.B.; Nyholt, D.R.; Markus, H.S.; Maagdenberg, A.M.J.M. van den; Cotsapas, C.; Zwart, J.A.; Palotie, A.; Dichgans, M.; Int Headache Genetics Consortium & METASTROKE Collaboration Int Strok (2015), Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants, Neurology 84(21): 2132-2145.
- Loonen, I.C.M.; Houben, M.B.; Schenke, M.; Heiningen, S.H. van; Broos, L.A.M.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Tolner, E.A. (2015), The use of optogenetic stimulation for non-invasive induction of cortical spreading depression in anaesthetized and freely behaving mice, Cephalalgia 35: 230-231.
- Eikermann-Haerter, K.; Arbel-Ornath, M.; Yalcin, N.; Yu, E.S.; Kuchibhotla, K.V.; Yuzawa, I.; Hudry, E.; Willard, C.R.; Climov, M.; Keles, F.; Belcher, A.M.; Sengul, B.; Negro, A.; Rosen, I.A.; Arreguin, A.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Bacskai, B.J. & Ayata, C. (2015), Abnormal synaptic Ca2+ homeostasis and morphology in cortical neurons of familial hemiplegic migraine type 1 mutant mice, Annals of Neurology 78(2): 193-210.
- Inchauspe, C.G.; Pilati, N.; Guilmi, M.N. di; Urbano, F.J.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Forsythe, I.D. & Uchitel, O.D. (2015), Familial hemiplegic migraine type-1 mutated ca(v)2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice, Hearing Research 319: 56-68.
- Dilekoz, E.; Houben, T.; Eikermann-Haerter, K.; Balkaya, M.; Lenselink, A.M.; Whalen, M.J.; Spijker, S.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Ayata, C. (2015), Migraine Mutations Impair Hippocampal Learning Despite Enhanced Long-Term Potentiation, Journal of Neuroscience 35(8): 3397-3402.
- Sadeghian, H.; Harms, C.; Qin, T.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Endres, M. & Ayata, C. (2015), Increased susceptibility to hypoxic/ischemic injury in FHM1 mutant mice, Cephalalgia 35: 234-235.
- Kaja, S.; Payne, A.J.; Nielsen, E.O.; Thompson, C.L.; Maagdenberg, A.M.J.M. van den; Koulen, P. & Snutch, T.P. (2015), DIFFERENTIAL CEREBELLAR GABA(A) RECEPTOR EXPRESSION IN MICE WITH MUTATIONS IN CAV2.1 (P/Q-TYPE) CALCIUM CHANNELS, Neuroscience 304: 198-208.
- Shyti, R.; Eikermann-Haerter, K.; Heiningen, S.H. van; Meijer, O.C.; Ayata, C.; Joels, M.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Tolner, E.A. (2015), Stress hormone corticosterone enhances susceptibility to cortical spreading depression in familial hemiplegic migraine type 1 mutant mice, Experimental Neurology 263: 214-220.
- Panagiotakaki, E.; Grandis, E. de; Stagnaro, M.; Heinzen, E.L.; Fons, C.; Sisodiya, S.; Vries, B. de; Goubau, C.; Weckhuysen, S.; Kemlink, D.; Scheffer, I.; Lesca, G.; Rabilloud, M.; Klich, A.; Ramirez-Camacho, A.; Ulate-Campos, A.; Campistol, J.; Giannotta, M.; Moutard, M.L.; Doummar, D.; Hubsch-Bonneaud, C.; Jaffer, F.; Cross, H.; Gurrieri, F.; Tiziano, D.; Nevsimalova, S.; Nicole, S.; Neville, B.; Maagdenberg, A.M.J.M. van den; Mikati, M.; Goldstein, D.B.; Vavassori, R.; Arzimanoglou, A.; IBAHC Consortium; French AHC Consortium & Int AHC Consortium (2015), Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients, Orphanet Journal of Rare Diseases 10.
- Heijs, B.; Tolner, E.A.; Bovee, J.V.M.G.; Maagdenberg, A.M.J.M. van den & McDonnell, L.A. (2015), Brain Region-Specific Dynamics of On-Tissue Protein Digestion Using MALDI Mass Spectrometry Imaging, Journal of Proteome Research 14(12): 5348-5354.
- Kros, L.; Rooda, O.H.J.E.; Spanke, J.K.; Alva, P.; Dongen, M.N. van; Karapatis, A.; Tolner, E.A.; Strydis, C.; Davey, N.; Winkelman, B.H.J.; Negrello, M.; Serdijn, W.A.; Steuber, V.; Maagdenberg, A.M.J.M. van den; Zeeuw, C.I. de & Hoebeek, F.E. (2015), Cerebellar output controls generalized spike-and-wave discharge occurrence, Annals of Neurology 77(6): 1027-1049.
- Malik, R.; Freilinger, T.; Anttila, V.; Vander Heiden, J.; Traylor, M.; Vries, B. de; Holliday, E.G.; Terwindt, G.M.; Sturm, J.; Bis, J.C.; Hopewell, J.C.; Ferrari, M.D.; Rannikmae, K.; Wessman, M.; Kallela, M.; Kubisch, C.; Fornage, M.; Meschia, J.F.; Lehtimaki, T.; Sudlow, C.; Clarke, R.; Chasman, D.I.; Mitchell, B.D.; Maguire, J.; Kaprio, J.; Farrall, M.; Raitakari, O.T.; Kurth, T.; Ikram, M.A.; Reiner, A.P.; Longstreth, W.T.; Rothwell, P.M.; Strachan, D.P.; Sharma, P.; Seshadri, S.; Quaye, L.; Cherkas, L.; Schurks, M.; Rosand, J.; Ligthart, L.; Boncoraglio, G.B.; Smith, G.D.; Duijn, C.M. van; Stefansson, K.; Worrall, B.B.; Nyholt, D.R.; Markus, H.S.; Maagdenberg, A.M.J.M. van den; Cotsapas, C.; Zwart, J.A.; Palotie, A.; Dichgans, M.; Int Headache Genetics Consortium & METASTROKE Collaboration Int Strok (2015), Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants, Neurology 84(21): 2132-2145.
- Ferrari, M.D.; Klever, R.R.; Terwindt, G.M.; Ayata, C. & Maagdenberg, A.M.J.M. van den (2015), Migraine pathophysiology: lessons from mouse models and human genetics, Lancet Neurology 14(1): 65-80.
- Louter, M.A.; Fernandez-Morales, J.; Vries, B. de; Winsvold, B.; Anttila, V.; Fernandez-Cadenas, I.; Vila-Pueyo, M.; Sintas, C.; Duijn, C.M. van; Cormand, B.; Alvarez-Sabin, J.; Montaner, J.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Palotie, A.; Zwart, J.A.; Macaya, A.; Terwindt, G.M. & Pozo-Rosich, P. (2015), Candidate-gene association study searching for genetic factors involved in migraine chronification, Cephalalgia 35(6): 500-507.
- Weller, C.M.; Leen, W.G.; Neville, B.G.R.; Duncan, J.S.; Vries, B. de; Geilenkirchen, M.A.; Haan, J.; Kamsteeg, E.J.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Willemsen, M.A.A.P.; Scheffer, H. & Terwindt, G.M. (2015), A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood, Cephalalgia 35(1): 10-15.
- Eikermann-Haerter, K.; Lee, J.H.; Yalcin, N.; Yu, E.S.; Daneshmand, A.; Wei, Y.; Zheng, Y.; Can, A.; Sengul, B.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Ayata, C. (2015), Migraine Prophylaxis, Ischemic Depolarizations, and Stroke Outcomes in Mice, Stroke 46(1): 229-236.
- Demirkan, A.; Henneman, P.; Verhoeven, A.; Dharuri, H.; Amin, N.; Klinken, J.B. van; Karssen, L.C.; Vries, B. de; Meissner, A.; Goraler, S.; Maagdenberg, A.M.J.M. van den; Deelder, A.M.; t' Hoen, P.A.C.; Duijn, C.M. van & Dijk, K.W. van (2015), Insight in Genome-Wide Association of Metabolite Quantitative Traits by Exome Sequence Analyses, PLoS Genetics 11(1).
- Eikermann-Haerter, K.; Arbel-Ornath, M.; Yalcin, N.; Yu, E.S.; Kuchibhotla, K.V.; Yuzawa, I.; Hudry, E.; Willard, C.R.; Climov, M.; Keles, F.; Belcher, A.M.; Sengul, B.; Negro, A.; Rosen, I.A.; Arreguin, A.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Bacskai, B.J. & Ayata, C. (2015), Abnormal synaptic Ca2+ homeostasis and morphology in cortical neurons of familial hemiplegic migraine type 1 mutant mice, Annals of Neurology 78(2): 193-210.
- Nyholt, D.R.; Anttila, V.; Winsvold, B.S.; Kurth, T.; Stefansson, H.; Kallela, M.; Malik, R.; Vries, B. de; Terwindt, G.M.; Ikram, M.A.; Stam, A.H.; Ligthart, L.; Freilinger, T.; Alexander, M.; Muller-Myhsok, B.; Schreiber, S.; Meitinger, T.; Aromaa, A.; Eriksson, J.G.; Kaprio, J.; Boomsma, D.I.; Duijn, C. van; Raitakari, O.; Jarvelin, M.R.; Zwart, J.A.; Quaye, L.; Strachan, D.P.; Kubisch, C.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Dichgans, M.; Wessman, M.; Smith, G.D.; Stefansson, K.; Chasman, D.I.; Palotie, A. & Int Headache Genetics Consortium (2015), Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies, Cephalalgia 35(6): 489-499.
- LaBianca, S.; Jensen, R.; Maagdenberg, A.M.J.M. van den; Baandrup, L. & Bendtsen, L. (2015), Familial Hemiplegic Migraine and Recurrent Episodes of Psychosis: A Case Report, Headache 55(7): 1004-1007.
- Loonen, I.C.M.; Houben, M.B.; Schenke, M.; Heiningen, S.H. van; Broos, L.A.M.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Tolner, E.A. (2015), The use of optogenetic stimulation for non-invasive induction of cortical spreading depression in anaesthetized and freely behaving mice, Cephalalgia 35: 230-231.
- Roqueiro, D.; Witteveen, M.J.; Anttila, V.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den & Borgwardt, K. (2015), In silico phenotyping via co-training for improved phenotype prediction from genotype, Bioinformatics 31(12): 303-310.
- Shyti, R.; Kohler, I.; Schoenmaker, B.; Derks, R.J.E.; Ferrari, M.D.; Tolner, E.A.; Mayboroda, O.A. & Maagdenberg, A.M.J.M. van den (2015), Plasma metabolic profiling after cortical spreading depression in a transgenic mouse model of hemiplegic migraine by capillary electrophoresis mass spectrometry.
- Mulder, I.A.; Esteve, C.; Carreira, R.J.; Rieff, N.; Broos, L.A.M.; Wermer, M.J.H.; Ferrari, M.D.; Tolner, E.A.; McDonnell, L.A. & Maagdenberg, A.M.J.M. van den (2015), Application of maldi mass spectrometry imaging for analysis of biomolecular profiles after experimental stroke in a migraine mouse model, Cephalalgia 35: 234-234.
- Odijk, M.; Wouden, E.J. van der; Olthuis, W.; Ferrari, M.D.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den & Berg, A. van den (2015), Microfabricated solid-state ion-selective electrode probe for measuring potassium in the living rodent brain: Compatibility with DC-EEG recordings to study spreading depression, Sensors and Actuators B: Chemical 207: 945-953.
- Tolner, E.A.; Houben, T.; Terwindt, G.M.; Vries, B. de; Ferrari, M.D. & Maagdenberg, A.M.J.M. van den (2015), From migraine genes to mechanisms, PAIN 156(4): S64-S74.
- Weller, C.M.; Wilbrink, L.A.; Houwing-Duistermaat, J.J.; Koelewijn, S.C.; Vijfhuizen, L.S.; Haan, J.; Ferrari, M.D.; Terwindt, G.M.; Maagdenberg, A.M. van den & Vries, B. de (2015), Cluster headache and the hypocretin receptor 2 reconsidered: A genetic association study and meta-analysis, Cephalalgia 35(9): 741-747.
- Sadeghian, H.; Harms, C.; Qin, T.; Ferrari, M.; Maagdenberg, A. van den; Endres, M. & Ayata, C. (2015), Increased Susceptibility to Hypoxic/ischemic Injury in FHM1 Mutant Mice, Headache 55: 170-170.
- Sadeghian, H.; Harms, C.; Qin, T.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Endres, M. & Ayata, C. (2015), Increased susceptibility to hypoxic/ischemic injury in FHM1 mutant mice, Cephalalgia 35: 234-235.
- Heijs, B.; Carreira, R.J.; Tolner, E.A.; Ru, A.H. de; Maagdenberg, A.J.M. van den; Veelen, P.A. van & McDonnell, L.A. (2015), Comprehensive Analysis of the Mouse Brain Proteome Sampled in Mass Spectrometry Imaging, Analytical Chemistry 87(3): 1867-1875.
- Inchauspe, C.G.; Pilati, N.; Guilmi, M.N. di; Urbano, F.J.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Forsythe, I.D. & Uchitel, O.D. (2015), Familial hemiplegic migraine type-1 mutated ca(v)2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice, Hearing Research 319: 56-68.
- Carreira, R.J.; Shyti, R.; Balluff, B.; Abdelmoula, W.M.; Heiningen, S.H. van; Zeijl, R.J. van; Dijkstra, J.; Ferrari, M.D.; Tolner, E.A.; McDonnell, L.A. & Maagdenberg, A.M.J.M. van den (2015), Large-Scale Mass Spectrometry Imaging Investigation of Consequences of Cortical Spreading Depression in a Transgenic Mouse Model of Migraine, Journal of The American Society for Mass Spectrometry 26(6): 853-861.
- Vecchia, D.; Tottene, A.; Maagdenberg, A.M.J.M. van den & Pietrobon, D. (2015), Abnormal cortical synaptic transmission in Ca(V)2.1 knockin mice with the S218L missense mutation which causes a severe familial hemiplegic migraine syndrome in humans, Frontiers in Cellular Neuroscience 9.
- Dilekoz, E.; Houben, T.; Eikermann-Haerter, K.; Balkaya, M.; Lenselink, A.M.; Whalen, M.J.; Spijker, S.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Ayata, C. (2015), Migraine Mutations Impair Hippocampal Learning Despite Enhanced Long-Term Potentiation, Journal of Neuroscience 35(8): 3397-3402.
- Sar, S.A. van der; Zielman, R.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Deelder, A.M.; Mayboroda, O.A.; Meissner, A. & Ferrari, M.D. (2015), Ethanol contamination of cerebrospinal fluid during standardized sampling and its effect on H-1-NMR metabolomics, Analytical and Bioanalytical Chemistry 407(16): 4835-4839.
- Rutten, J.W.; Klever, R.R.; Hegeman, I.M.; Poole, D.S.; Dauwerse, H.G.; Broos, L.A.M.; Breukel, C.; Aartsma-Rus, A.M.; Verbeek, J.S.; Weerd, L. van der; Duinen, S.G. van; Maagdenberg, A.M.J.M. van den & Oberstein, S.A.J.L. (2015), The NOTCH3 score: a pre-clinical CADASIL biomarker in a novel human genomic NOTCH3 transgenic mouse model with early progressive vascular NOTCH3 accumulation, Acta Neuropathologica Communications 3.
- Jacobsen, K.K.; Nievergelt, C.M.; Zayats, T.; Greenwood, T.A.; Anttila, V.; Akiskal, H.S.; Haavik, J.; Fasmer, O.B.; Kelsoe, J.R.; Johansson, S.; Oedegaard, K.J. & BiGs Consortium IHG Consortium (2015), Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder, Journal of Affective Disorders 172: 453-461.
- Hullugundi, S.K.; Ansuini, A.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2014), A HYPEREXCITABILITY PHENOTYPE IN MOUSE TRIGEMINAL SENSORY NEURONS EXPRESSING THE R192Q CACNA1A MISSENSE MUTATION OF FAMILIAL HEMIPLEGIC MIGRAINE TYPE-1, Neuroscience 266: 244-254.
- Vries, B. de; Eising, E.; Broos, L.A.M.; Koelewijn, S.C.; Todorov, B.; Frants, R.R.; Boer, J.M.; Ferrari, M.D.; Hoen, P.A.C. 't & Maagdenberg, A.M.J.M. van den (2014), RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice, Cephalalgia 34(3): 174-182.
- Pelzer, N.; Vries, B. de; Kamphorst, J.T.; Vijfhuizen, L.S.; Ferrari, M.D.; Haan, J.; Maagdenberg, A.M.J.M. van den & Terwindt, G.M. (2014), PRRT2 AND HEMIPLEGIC MIGRAINE: A COMPLEX ASSOCIATION, Neurology 83(3): 288-290.
- Weller, C.M.; Pelzer, N.; Vries, B. de; Lopez, M.A.; Fabregues, O. de; Pascual, J.; Arroyo, M.A.R.; Koelewijn, S.C.; Stam, A.H.; Haan, J.; Ferrari, M.D.; Terwindt, G.M. & Maagdenberg, A.M.J.M. van den (2014), Two novel SCNIA mutations identified in families with familial hemiplegic migraine, Cephalalgia 34(13): 1062-1069.
- Chen, S.; Qin, T.; Seidel, J.; Ferrari, M.; Maagden, A. van den; Ayata, C. & Eikermann-Haerter, K. (2014), Inhibition of the p2x7 Receptor-Pannexin1 Pore Suppresses Spreading Depression and Inflammatory Downstream Mechanisms, Headache 54: 2-2.
- Park, J.; Moon, H.; Akerman, S.; Holland, P.R.; Lasalandra, M.P.; Andreou, A.P.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Goadsby, P.J. (2014), Differential trigeminovascular nociceptive responses in the thalamus in the familial hemiplegic migraine 1 knock-in mouse: A Fos protein study, Neurobiology of Disease 64: 1-7.
- Vaarhorst, A.A.M.; Verhoeven, A.; Weller, C.M.; Bohringer, S.; Goraler, S.; Meissner, A.; Decider, A.M.; Henneman, P.; Gorgels, A.P.M.; Brandt, P.A. van den; Schouten, L.J.; Greevenbroek, M.M. van; Merry, A.H.H.; Verschuren, W.M.M.; Maagdenberg, A.M.J.M. van den; Dijk, K.W. van; Isaacs, A.; Boomsma, D.; Oostra, B.A.; Duijn, C.M. van; Jukema, J.W.; Boer, J.M.A.; Feskens, E.; Heijmans, B.T. & Slagboom, P.E. (2014), A metabolomic profile is associated with the risk of incident coronary heart disease, American Heart Journal 168(1): 45-52.
- Guilmi, M.N. di; Wang, T.T.; Inchauspe, C.G.; Forsythe, I.D.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Borst, G.G. & Uchitel, O.D. (2014), Synaptic Gain-of-Function Effects of Mutant Ca(v)2.1 Channels in a Mouse Model of Familial Hemiplegic Migraine Are Due to Increased Basal [Ca2+](i), Journal of Neuroscience 34(21): 7047-7058.
- Heinzen, E.L.; Arzimanoglou, A.; Brashear, A.; Clapcote, S.J.; Gurrieri, F.; Goldstein, D.B.; Johannesson, S.H.; Mikati, M.A.; Neville, B.; Nicole, S.; Ozelius, L.J.; Poulsen, H.; Schyns, T.; Sweadner, K.J.; Maagdenberg, A. van den; Vilsen, B. & ATP1A3 Working Grp (2014), Distinct neurological disorders with ATP1A3 mutations, Lancet Neurology 13(5): 503-514.
- Vecchia, D.; Tottene, A.; Maagdenberg, A.M.J.M. van den & Pietrobon, D. (2014), Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in Ca(V)2.1 knockin migraine mice, Neurobiology of Disease 69: 225-234.
- Rose, S.J.; Kriener, L.H.; Heinzer, A.K.; Fan, X.L.; Raike, R.S.; Maagdenberg, A.M.J.M. van den & Hess, E.J. (2014), The first knockin mouse model of episodic ataxia type 2, Experimental Neurology 261: 553-562.
- Abdelmoula, W.M.; Skraskova, K.; Balluff, B.; Carreira, R.J.; Tolner, E.A.; Lelieveldt, B.P.F.; Maaten, L. van der; Morreau, H.; Maagdenberg, A.M.J.M. van den; Heeren, R.M.A.; McDonnell, L.A. & Dijkstra, J. (2014), Automatic Generic Registration of Mass Spectrometry Imaging Data to Histology Using Nonlinear Stochastic Embedding, Analytical Chemistry 86(18): 9204-9211.
- Pelzer, N.; Stam, A.H.; Carpay, J.A.; Vries, B. de; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Haan, J. & Terwindt, G.M. (2014), Familial hemiplegic migraine treated by sodium valproate and lamotrigine, Cephalalgia 34(9): 708-711.
- Abdelmoula, W.M.; Carreira, R.J.; Shyti, R.; Balluff, B.; Zeijl, R.J.M. van; Tolner, E.A.; Lelieveldt, B.F.P.; Maagdenberg, A.M.J.M. van den; McDonnell, L.A. & Dijkstra, J. (2014), Automatic Registration of Mass Spectrometry Imaging Data Sets to the Allen Brain Atlas, Analytical Chemistry 86(8): 3947-3954.
- Chen, S.; Qin, T.; Seidel, J.; Ferrari, M.; Maagden, A. van den; Ayata, C. & Eikermann-Haerter, K. (2014), Inhibition of the p2x7 Receptor-Pannexin1 Pore Suppresses Spreading Depression and Inflammatory Downstream Mechanisms, Headache 54: 2-2.
- Weller, C.M.; Pelzer, N.; Vries, B. de; Lopez, M.A.; Fabregues, O. de; Pascual, J.; Arroyo, M.A.R.; Koelewijn, S.C.; Stam, A.H.; Haan, J.; Ferrari, M.D.; Terwindt, G.M. & Maagdenberg, A.M.J.M. van den (2014), Two novel SCNIA mutations identified in families with familial hemiplegic migraine, Cephalalgia 34(13): 1062-1069.
- Hullugundi, S.K.; Ansuini, A.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2014), A HYPEREXCITABILITY PHENOTYPE IN MOUSE TRIGEMINAL SENSORY NEURONS EXPRESSING THE R192Q CACNA1A MISSENSE MUTATION OF FAMILIAL HEMIPLEGIC MIGRAINE TYPE-1, Neuroscience 266: 244-254.
- Vaarhorst, A.A.M.; Verhoeven, A.; Weller, C.M.; Bohringer, S.; Goraler, S.; Meissner, A.; Decider, A.M.; Henneman, P.; Gorgels, A.P.M.; Brandt, P.A. van den; Schouten, L.J.; Greevenbroek, M.M. van; Merry, A.H.H.; Verschuren, W.M.M.; Maagdenberg, A.M.J.M. van den; Dijk, K.W. van; Isaacs, A.; Boomsma, D.; Oostra, B.A.; Duijn, C.M. van; Jukema, J.W.; Boer, J.M.A.; Feskens, E.; Heijmans, B.T. & Slagboom, P.E. (2014), A metabolomic profile is associated with the risk of incident coronary heart disease, American Heart Journal 168(1): 45-52.
- Rose, S.J.; Kriener, L.H.; Heinzer, A.K.; Fan, X.L.; Raike, R.S.; Maagdenberg, A.M.J.M. van den & Hess, E.J. (2014), The first knockin mouse model of episodic ataxia type 2, Experimental Neurology 261: 553-562.
- Vries, B. de; Eising, E.; Broos, L.A.M.; Koelewijn, S.C.; Todorov, B.; Frants, R.R.; Boer, J.M.; Ferrari, M.D.; Hoen, P.A.C. 't & Maagdenberg, A.M.J.M. van den (2014), RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice, Cephalalgia 34(3): 174-182.
- Abdelmoula, W.M.; Skraskova, K.; Balluff, B.; Carreira, R.J.; Tolner, E.A.; Lelieveldt, B.P.F.; Maaten, L. van der; Morreau, H.; Maagdenberg, A.M.J.M. van den; Heeren, R.M.A.; McDonnell, L.A. & Dijkstra, J. (2014), Automatic Generic Registration of Mass Spectrometry Imaging Data to Histology Using Nonlinear Stochastic Embedding, Analytical Chemistry 86(18): 9204-9211.
- Abdelmoula, W.M.; Carreira, R.J.; Shyti, R.; Balluff, B.; Zeijl, R.J.M. van; Tolner, E.A.; Lelieveldt, B.F.P.; Maagdenberg, A.M.J.M. van den; McDonnell, L.A. & Dijkstra, J. (2014), Automatic Registration of Mass Spectrometry Imaging Data Sets to the Allen Brain Atlas, Analytical Chemistry 86(8): 3947-3954.
- Park, J.; Moon, H.; Akerman, S.; Holland, P.R.; Lasalandra, M.P.; Andreou, A.P.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Goadsby, P.J. (2014), Differential trigeminovascular nociceptive responses in the thalamus in the familial hemiplegic migraine 1 knock-in mouse: A Fos protein study, Neurobiology of Disease 64: 1-7.
- Heinzen, E.L.; Arzimanoglou, A.; Brashear, A.; Clapcote, S.J.; Gurrieri, F.; Goldstein, D.B.; Johannesson, S.H.; Mikati, M.A.; Neville, B.; Nicole, S.; Ozelius, L.J.; Poulsen, H.; Schyns, T.; Sweadner, K.J.; Maagdenberg, A. van den; Vilsen, B. & ATP1A3 Working Grp (2014), Distinct neurological disorders with ATP1A3 mutations, Lancet Neurology 13(5): 503-514.
- Pelzer, N.; Stam, A.H.; Carpay, J.A.; Vries, B. de; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Haan, J. & Terwindt, G.M. (2014), Familial hemiplegic migraine treated by sodium valproate and lamotrigine, Cephalalgia 34(9): 708-711.
- Vecchia, D.; Tottene, A.; Maagdenberg, A.M.J.M. van den & Pietrobon, D. (2014), Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in Ca(V)2.1 knockin migraine mice, Neurobiology of Disease 69: 225-234.
- Pelzer, N.; Vries, B. de; Kamphorst, J.T.; Vijfhuizen, L.S.; Ferrari, M.D.; Haan, J.; Maagdenberg, A.M.J.M. van den & Terwindt, G.M. (2014), PRRT2 AND HEMIPLEGIC MIGRAINE: A COMPLEX ASSOCIATION, Neurology 83(3): 288-290.
- Guilmi, M.N. di; Wang, T.T.; Inchauspe, C.G.; Forsythe, I.D.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Borst, G.G. & Uchitel, O.D. (2014), Synaptic Gain-of-Function Effects of Mutant Ca(v)2.1 Channels in a Mouse Model of Familial Hemiplegic Migraine Are Due to Increased Basal [Ca2+](i), Journal of Neuroscience 34(21): 7047-7058.
- Anttila, V.; Winsvold, B.S.; Gormley, P.; Kurth, T.; Bettella, F.; McMahon, G.; Kallela, M.; Malik, R.; Vries, B. de; Terwindt, G.; Medland, S.E.; Todt, U.; McArdle, W.L.; Quaye, L.; Koiranen, M.; Ikram, M.A.; Lehtimaki, T.; Stam, A.H.; Ligthart, L.; Wedenoja, J.; Dunham, I.; Neale, B.M.; Palta, P.; Hamalainen, E.; Schurks, M.; Rose, L.M.; Buring, J.E.; Ridker, P.M.; Steinberg, S.; Stefansson, H.; Jakobsson, F.; Lawlor, D.A.; Evans, D.M.; Ring, S.M.; Farkkila, M.; Artto, V.; Kaunisto, M.A.; Freilinger, T.; Schoenen, J.; Frants, R.R.; Pelzer, N.; Weller, C.M.; Zielman, R.; Heath, A.C.; Madden, P.A.F.; Montgomery, G.W.; Martin, N.G.; Borck, G.; Gobel, H.; Heinze, A.; Heinze-Kuhn, K.; Williams, F.M.K.; Hartikainen, A.L.; Pouta, A.; Ende, J. van den; Uitterlinden, A.G.; Hofman, A.; Amin, N.; Hottenga, J.J.; Vink, J.M.; Heikkila, K.; Alexander, M.; Muller-Myhsok, B.; Schreiber, S.; Meitinger, T.; Wichmann, H.E.; Aromaa, A.; Eriksson, J.G.; Traynor, B.J.; Trabzuni, D.; Rossin, E.; Lage, K.; Jacobs, S.B.R.; Gibbs, J.R.; Birney, E.; Kaprio, J.; Penninx, B.W.; Boomsma, D.I.; Duijn, C. van; Raitakari, O.; Jarvelin, M.R.; Zwart, J.A.; Cherkas, L.; Strachan, D.P.; Kubisch, C.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Dichgans, M.; Wessman, M.; Smith, G.D.; Stefansson, K.; Daly, M.J.; Nyholt, D.R.; Chasman, D.I.; Palotie, A.; North Amer Brain Expression; UK Brain Expression Consortium & Int Headache Genetics Consortium (2013), Genome-wide meta-analysis identifies new susceptibility loci for migraine, Nature Genetics 45(8): 912-U255.
- Raike, R.S.; Pizoli, C.E.; Weisz, C.; Maagdenberg, A.M.J.M. van den; Jinnah, H.A. & Hess, E.J. (2013), Limited regional cerebellar dysfunction induces focal dystonia in mice, Neurobiology of Disease 49: 200-210.
- Rossignol, E.; Kruglikov, I.; Maagdenberg, A.M.J.M. van den; Rudy, B. & Fishell, G. (2013), Ca(V)2.1 Ablation in Cortical Interneurons Selectively Impairs Fast-Spiking Basket Cells and Causes Generalized Seizures, Annals of Neurology 74(2): 209-222.
- Galliano, E.; Gao, Z.Y.; Schonewille, M.; Todorov, B.; Simons, E.; Pop, A.S.; D'Angelo, E.; Maagdenberg, A.M.J.M. van den; Hoebeek, F.E. & Zeeuw, C.I. de (2013), Silencing the Majority of Cerebellar Granule Cells Uncovers Their Essential Role in Motor Learning and Consolidation, Cell Reports 3(4): 1239-1251.
- Dibbens, L.M.; Vries, B. de; Donatello, S.; Heron, S.E.; Hodgson, B.L.; Chintawar, S.; Crompton, D.E.; Hughes, J.N.; Bellows, S.T.; Klein, K.M.; Callenbach, P.M.C.; Corbett, M.A.; Gardner, A.E.; Kivity, S.; Iona, X.; Regan, B.M.; Weller, C.M.; Crimmins, D.; O'Brien, T.J.; Guerrero-Lopez, R.; Mulley, J.C.; Dubeau, F.; Licchetta, L.; Bisulli, F.; Cossette, P.; Thomas, P.Q.; Gecz, J.; Serratosa, J.; Brouwer, O.F.; Andermann, F.; Andermann, E.; Maagdenberg, A.M.J.M. van den; Pandolfo, M.; Berkovic, S.F. & Scheffer, I.E. (2013), Mutations in DEPDC5 cause familial focal epilepsy with variable foci, Nature Genetics 45(5): 546-U123.
- Raike, R.S.; Weisz, C.; Hoebeek, F.E.; Terzi, M.C.; Zeeuw, C.I. de; Maagdenberg, A.M. van den; Jinnah, H.A. & Hess, E.J. (2013), Stress, caffeine and ethanol trigger transient neurological dysfunction through shared mechanisms in a mouse calcium channelopathy, Neurobiology of Disease 50: 151-159.
- Franceschini, A.; Hullugundi, S.K.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Fabbretti, E. (2013), Effects of LPS on P2X3 receptors of trigeminal sensory neurons and macrophages from mice expressing the R192Q Cacna1a gene mutation of familial hemiplegic migraine-1, Purinergic Signalling 9(1): 7-13.
- Swarts, H.G.P.; Weigand, K.M.; Venselaar, H.; Maagdenberg, A.M.J.M. van den; Russel, F.G.M. & Koenderink, J.B. (2013), Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions, BBA - Molecular Basis of Disease 1832(12): 2173-2179.
- Stam, A.H.; Weller, C.M.; Janssens, A.C.J.W.; Aulchenko, Y.S.; Oostra, B.A.; Frants, R.R.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Duijn, C.M. van & Terwindt, G.M. (2013), Migraine is not associated with enhanced atherosclerosis, Cephalalgia 33(4): 228-235.
- Eising, E.; Vries, B. de; Ferrari, M.D.; Terwindt, G.M. & Maagdenberg, A.M.J.M. van den (2013), Pearls and pitfalls in genetic studies of migraine, Cephalalgia 33(8): 614-625.
- Hullugundi, S.K.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2013), The Mechanism of Functional Up-Regulation of P2X3 Receptors of Trigeminal Sensory Neurons in a Genetic Mouse Model of Familial Hemiplegic Migraine Type 1 (FHM-1), PLoS ONE 8(4).
- Franceschini, A.; Vilotti, S.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Fabbretti, E. (2013), TNF alpha Levels and Macrophages Expression Reflect an Inflammatory Potential of Trigeminal Ganglia in a Mouse Model of Familial Hemiplegic Migraine, PLoS ONE 8(1).
- Chanda, M.L.; Tuttle, A.H.; Baran, I.; Atlin, C.; Guindi, D.; Hathaway, G.; Israelian, N.; Levenstadt, J.; Low, D.; Macrae, L.; O'Shea, L.; Silver, A.; Zendegui, E.; Lenselink, A.M.; Spijker, S.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Mogil, J.S. (2013), Behavioral evidence for photophobia and stress-related ipsilateral head pain in transgenic Cacna1a mutant mice, PAIN 154(8): 1254-1262.
- Mallmann, R.T.; Elgueta, C.; Sleman, F.; Castonguay, J.; Wilmes, T.; Maagdenberg, A. van den & Klugbauer, N. (2013), Ablation of Ca(V)2.1 Voltage-Gated Ca2+ Channels in Mouse Forebrain Generates Multiple Cognitive Impairments, PLoS ONE 8(10).
- Pelzer, N.; Vries, B. de; Boon, E.M.J.; Kruit, M.C.; Haan, J.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Terwindt, G.M. (2013), Heterozygous TREX1 mutations in early-onset cerebrovascular disease, Journal of Neurology 260(8): 2188-2190.
- Eising, E.; Datson, N.A.; Maagdenberg, A.M.J.M. van den & Ferrari, M.D. (2013), Epigenetic mechanisms in migraine: a promising avenue?, BMC Medicine 11.
- Gnanasekaran, A.; Bele, T.; Hullugundi, S.; Simonetti, M.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Fabbretti, E. (2013), Mutated Ca(V)2.1 channels dysregulate CASK/P2X3 signaling in mouse trigeminal sensory neurons of R192Q Cacna1a knock-in mice, Molecular Pain 9.
- Deboer, T.; Diepen, H.C. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Meijer, J.H. (2013), Reduced Sleep and Low Adenosinergic Sensitivity in Cacna1a R192Q Mutant Mice, SLEEP 36(1): 127-136.
- Pelzer, N.; Vries, B. de; Boon, E.M.J.; Kruit, M.C.; Haan, J.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Terwindt, G.M. (2013), Heterozygous TREX1 mutations in early-onset cerebrovascular disease, Journal of Neurology 260(8): 2188-2190.
- Stam, A.H.; Weller, C.M.; Janssens, A.C.J.W.; Aulchenko, Y.S.; Oostra, B.A.; Frants, R.R.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Duijn, C.M. van & Terwindt, G.M. (2013), Migraine is not associated with enhanced atherosclerosis, Cephalalgia 33(4): 228-235.
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- Eising, E.; Vries, B. de; Ferrari, M.D.; Terwindt, G.M. & Maagdenberg, A.M.J.M. van den (2013), Pearls and pitfalls in genetic studies of migraine, Cephalalgia 33(8): 614-625.
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- Galliano, E.; Gao, Z.Y.; Schonewille, M.; Todorov, B.; Simons, E.; Pop, A.S.; D'Angelo, E.; Maagdenberg, A.M.J.M. van den; Hoebeek, F.E. & Zeeuw, C.I. de (2013), Silencing the Majority of Cerebellar Granule Cells Uncovers Their Essential Role in Motor Learning and Consolidation, Cell Reports 3(4): 1239-1251.
- Raike, R.S.; Weisz, C.; Hoebeek, F.E.; Terzi, M.C.; Zeeuw, C.I. de; Maagdenberg, A.M. van den; Jinnah, H.A. & Hess, E.J. (2013), Stress, caffeine and ethanol trigger transient neurological dysfunction through shared mechanisms in a mouse calcium channelopathy, Neurobiology of Disease 50: 151-159.
- Hullugundi, S.K.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Nistri, A. (2013), The Mechanism of Functional Up-Regulation of P2X3 Receptors of Trigeminal Sensory Neurons in a Genetic Mouse Model of Familial Hemiplegic Migraine Type 1 (FHM-1), PLoS ONE 8(4).
- Mallmann, R.T.; Elgueta, C.; Sleman, F.; Castonguay, J.; Wilmes, T.; Maagdenberg, A. van den & Klugbauer, N. (2013), Ablation of Ca(V)2.1 Voltage-Gated Ca2+ Channels in Mouse Forebrain Generates Multiple Cognitive Impairments, PLoS ONE 8(10).
- Chanda, M.L.; Tuttle, A.H.; Baran, I.; Atlin, C.; Guindi, D.; Hathaway, G.; Israelian, N.; Levenstadt, J.; Low, D.; Macrae, L.; O'Shea, L.; Silver, A.; Zendegui, E.; Lenselink, A.M.; Spijker, S.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Mogil, J.S. (2013), Behavioral evidence for photophobia and stress-related ipsilateral head pain in transgenic Cacna1a mutant mice, PAIN 154(8): 1254-1262.
- Rossignol, E.; Kruglikov, I.; Maagdenberg, A.M.J.M. van den; Rudy, B. & Fishell, G. (2013), Ca(V)2.1 Ablation in Cortical Interneurons Selectively Impairs Fast-Spiking Basket Cells and Causes Generalized Seizures, Annals of Neurology 74(2): 209-222.
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- Swarts, H.G.P.; Weigand, K.M.; Venselaar, H.; Maagdenberg, A.M.J.M. van den; Russel, F.G.M. & Koenderink, J.B. (2013), Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions, BBA - Molecular Basis of Disease 1832(12): 2173-2179.
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- Gnanasekaran, A.; Bele, T.; Hullugundi, S.; Simonetti, M.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Fabbretti, E. (2013), Mutated Ca(V)2.1 channels dysregulate CASK/P2X3 signaling in mouse trigeminal sensory neurons of R192Q Cacna1a knock-in mice, Molecular Pain 9.
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- Gao, Z.Y.; Todorov, B.; Barrett, C.F.; Dorp, S. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Zeeuw, C.I. de & Hoebeek, F.E. (2012), Cerebellar Ataxia by Enhanced Ca(V)2.1 Currents Is Alleviated by Ca2+-Dependent K+-Channel Activators in Cacna1a(S218L) Mutant Mice, Journal of Neuroscience 32(44): 15533-15546.
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- Ceruti, S.; Villa, G.; Fumagalli, M.; Colombo, L.; Magni, G.; Zanardelli, M.; Fabbretti, E.; Verderio, C.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Abbracchio, M.P. (2012), Crosstalk between the purinergic system and known algogenic mediators in mouse trigeminal ganglia: implications for basic mechanisms of migraine pain, Purinergic Signalling 8(1): 131-132.
- Franceschini, A.; Nair, A.; Bele, T.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Fabbretti, E. (2012), Functional crosstalk in culture between macrophages and trigeminal sensory neurons of a mouse genetic model of migraine, BMC Neuroscience 13: -.
- Todorov, B.; Kros, L.; Shyti, R.; Plak, P.; Haasdijk, E.D.; Raike, R.S.; Frants, R.R.; Hess, E.J.; Hoebeek, F.E.; Zeeuw, C.I. de & Maagdenberg, A.M.J.M. van den (2012), Purkinje Cell-Specific Ablation of Ca(V)2.1 Channels is Sufficient to Cause Cerebellar Ataxia in Mice, Cerebellum 11(1): 246-258.
- Jones, E.A.; Shyti, R.; Zeijl, R.J.M. van; Heiningen, S.H. van; Ferrari, M.D.; Deelder, A.M.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den & McDonnell, L.A. (2012), Imaging mass spectrometry to visualize biomolecule distributions in mouse brain tissue following hemispheric cortical spreading depression.
- Inchauspe, C.G.; Urbano, F.J.; Guilmi, M.N. di; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Forsythe, I.D. & Uchitel, O.D. (2012), Presynaptic Ca(v)2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held, Journal of Neurophysiology 108(11): 2967-2976.
- Vries, B. de; Callenbach, P.M.C.; Kamphorst, J.T.; Weller, C.M.; Koelewijn, S.C.; Houten, R. ten; Coo, I.F.M. de; Brouwer, O.F. & Maagdenberg, A.M.J.M. van den (2012), PRRT2 MUTATION CAUSES BENIGN FAMILIAL INFANTILE CONVULSIONS, Neurology 79(21): 2154-2155.
- Garza-Lopez, E.; Sandoval, A.; Gonzalez-Ramirez, R.; Gandini, M.A.; Maagdenberg, A. van den; Waard, M. de & Felix, R. (2012), Familial hemiplegic migraine type 1 mutations W1684R and V1696I alter G protein-mediated regulation of Ca(V)2.1 voltage-gated calcium channels, BBA - Molecular Basis of Disease 1822(8): 1238-1246.
- Rooijen, D.E. van; Roelen, D.L.; Verduijn, W.; Haasnoot, G.W.; Huygen, F.J.P.M.; Perez, R.S.G.M.; Claas, F.H.J.; Marinus, J.; Hilten, J.J. van & Maagdenberg, A.M.J.M. van den (2012), Genetic HLA Associations in Complex Regional Pain Syndrome With and Without Dystonia, Journal of Pain 13(8): 784-789.
- Eikermann-Haerter, K.; Lee, J.H.; Yuzawa, I.; Liu, C.H.; Zhou, Z.P.; Shin, H.K.; Zheng, Y.; Qin, T.; Kurth, T.; Waeber, C.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Moskowitz, M.A. & Ayata, C. (2012), Migraine Mutations Increase Stroke Vulnerability by Facilitating Ischemic Depolarizations, Circulation 125(2): 335-U345.
- Ramautar, R.; Shyti, R.; Schoenmaker, B.; Groote, L. de; Derks, R.J.E.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Deelder, A.M. & Mayboroda, O.A. (2012), Metabolic profiling of mouse cerebrospinal fluid by sheathless CE-MS, Analytical and Bioanalytical Chemistry 404(10): 2895-2900.
- Ramautar, R.; Shyti, R.; Schoenmaker, B.; Groote, L. de; Derks, R.J.E.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Deelder, A.M. & Mayboroda, O.A. (2012), Metabolic profiling of mouse cerebrospinal fluid by sheathless CE-MS, Analytical and Bioanalytical Chemistry 404(10): 2895-2900.
- Rooijen, D.E. van; Roelen, D.L.; Verduijn, W.; Haasnoot, G.W.; Huygen, F.J.P.M.; Perez, R.S.G.M.; Claas, F.H.J.; Marinus, J.; Hilten, J.J. van & Maagdenberg, A.M.J.M. van den (2012), Genetic HLA Associations in Complex Regional Pain Syndrome With and Without Dystonia, Journal of Pain 13(8): 784-789.
- Jones, E.A.; Shyti, R.; Zeijl, R.J.M. van; Heiningen, S.H. van; Ferrari, M.D.; Deelder, A.M.; Tolner, E.A.; Maagdenberg, A.M.J.M. van den & McDonnell, L.A. (2012), Imaging mass spectrometry to visualize biomolecule distributions in mouse brain tissue following hemispheric cortical spreading depression.
- Franceschini, A.; Nair, A.; Bele, T.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Fabbretti, E. (2012), Functional crosstalk in culture between macrophages and trigeminal sensory neurons of a mouse genetic model of migraine, BMC Neuroscience 13: -.
- Inchauspe, C.G.; Urbano, F.J.; Guilmi, M.N. di; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Forsythe, I.D. & Uchitel, O.D. (2012), Presynaptic Ca(v)2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held, Journal of Neurophysiology 108(11): 2967-2976.
- Todorov, B.; Kros, L.; Shyti, R.; Plak, P.; Haasdijk, E.D.; Raike, R.S.; Frants, R.R.; Hess, E.J.; Hoebeek, F.E.; Zeeuw, C.I. de & Maagdenberg, A.M.J.M. van den (2012), Purkinje Cell-Specific Ablation of Ca(V)2.1 Channels is Sufficient to Cause Cerebellar Ataxia in Mice, Cerebellum 11(1): 246-258.
- Ceruti, S.; Villa, G.; Fumagalli, M.; Colombo, L.; Magni, G.; Zanardelli, M.; Fabbretti, E.; Verderio, C.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Abbracchio, M.P. (2012), Crosstalk between the purinergic system and known algogenic mediators in mouse trigeminal ganglia: implications for basic mechanisms of migraine pain, Purinergic Signalling 8(1): 131-132.
- Gao, Z.Y.; Todorov, B.; Barrett, C.F.; Dorp, S. van; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Zeeuw, C.I. de & Hoebeek, F.E. (2012), Cerebellar Ataxia by Enhanced Ca(V)2.1 Currents Is Alleviated by Ca2+-Dependent K+-Channel Activators in Cacna1a(S218L) Mutant Mice, Journal of Neuroscience 32(44): 15533-15546.
- Heinzen, E.L.; Swoboda, K.J.; Hitomi, Y.; Gurrieri, F.; Nicole, S.; Vries, B. de; Tiziano, F.D.; Fontaine, B.; Walley, N.M.; Heavin, S.; Panagiotakaki, E.; Fiori, S.; Abiusi, E.; Pietro, L. di; Sweney, M.T.; Newcomb, T.M.; Viollet, L.; Huff, C.; Jorde, L.B.; Reyna, S.P.; Murphy, K.J.; Shianna, K.V.; Gumbs, C.E.; Little, L.; Silver, K.; Ptacek, L.J.; Haan, J.; Ferrari, M.D.; Bye, A.M.; Herkes, G.K.; Whitelaw, C.M.; Webb, D.; Lynch, B.J.; Uldall, P.; King, M.D.; Scheffer, I.E.; Neri, G.; Arzimanoglou, A.; Maagdenberg, A.M.J.M. van den; Sisodiya, S.M.; Mikati, M.A.; Goldstein, D.B.; European Alternating Hemiplegia; Biobanca Registro Clinico & European Network Res Alternating (2012), De novo mutations in ATP1A3 cause alternating hemiplegia of childhood, Nature Genetics 44(9): 1030-+.
- Garza-Lopez, E.; Sandoval, A.; Gonzalez-Ramirez, R.; Gandini, M.A.; Maagdenberg, A. van den; Waard, M. de & Felix, R. (2012), Familial hemiplegic migraine type 1 mutations W1684R and V1696I alter G protein-mediated regulation of Ca(V)2.1 voltage-gated calcium channels, BBA - Molecular Basis of Disease 1822(8): 1238-1246.
- Freilinger, T.; Anttila, V.; Vries, B. de; Malik, R.; Kallela, M.; Terwindt, G.M.; Pozo-Rosich, P.; Winsvold, B.; Nyholt, D.R.; Oosterhout, W.P.J. van; Artto, V.; Todt, U.; Hamalainen, E.; Fernandez-Morales, J.; Louter, M.A.; Kaunisto, M.A.; Schoenen, J.; Raitakari, O.; Lehtimaki, T.; Vila-Pueyo, M.; Gobel, H.; Wichmann, E.; Sintas, C.; Uitterlinden, A.G.; Hofman, A.; Rivadeneira, F.; Heinze, A.; Tronvik, E.; Duijn, C.M. van; Kaprio, J.; Cormand, B.; Wessman, M.; Frants, R.R.; Meitinger, T.; Muller-Myhsok, B.; Zwart, J.A.; Farkkila, M.; Macaya, A.; Ferrari, M.D.; Kubisch, C.; Palotie, A.; Dichgans, M.; Maagdenberg, A.M.J.M. van den & Int Headache Genetics Consortium (2012), Genome-wide association analysis identifies susceptibility loci for migraine without aura, Nature Genetics 44(7): 777-U205.
- Eikermann-Haerter, K.; Lee, J.H.; Yuzawa, I.; Liu, C.H.; Zhou, Z.P.; Shin, H.K.; Zheng, Y.; Qin, T.; Kurth, T.; Waeber, C.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Moskowitz, M.A. & Ayata, C. (2012), Migraine Mutations Increase Stroke Vulnerability by Facilitating Ischemic Depolarizations, Circulation 125(2): 335-U345.
- Vries, B. de; Callenbach, P.M.C.; Kamphorst, J.T.; Weller, C.M.; Koelewijn, S.C.; Houten, R. ten; Coo, I.F.M. de; Brouwer, O.F. & Maagdenberg, A.M.J.M. van den (2012), PRRT2 MUTATION CAUSES BENIGN FAMILIAL INFANTILE CONVULSIONS, Neurology 79(21): 2154-2155.
- Shyti, R.; Vries, B. de & Maagdenberg, A. van den (2011), Migraine Genes and the Relation to Gender, Headache 51(6): 880-890.
- Chasman, D.I.; Schurks, M.; Anttila, V.; Vries, B. de; Schminke, U.; Launer, L.J.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Fendrich, K.; Volzke, H.; Ernst, F.; Griffiths, L.R.; Buring, J.E.; Kallela, M.; Freilinger, T.; Kubisch, C.; Ridker, P.M.; Palotie, A.; Ferrari, M.D.; Hoffmann, W.; Zee, R.Y.L.; Kurth, T. & IHGC (2011), Genome-wide association study reveals three susceptibility loci for common migraine in the general population, Nature Genetics 43(7): 695-U116.
- Stam, A.H.; Louter, M.A.; Haan, J.; Vries, B. de; Maagdenberg, A.M.J.M. van den; Frants, R.R.; Ferrari, M.D. & Terwindt, G.M. (2011), A long-term follow-up study of 18 patients with sporadic hemiplegic migraine.
- Mathew, R.; Andreou, A.P.; Chami, L.; Bergerot, A.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D. & Goadsby, P.J. (2011), Immunohistochemical characterization of calcitonin gene-related peptide in the trigeminal system of the familial hemiplegic migraine 1 knock-in mouse.
- Eikermann-Haerter, K.; Yuzawa, I.; Qin, T.; Wang, Y.M.; Baek, K.; Kim, Y.R.; Hoffmann, U.; Dilekoz, E.; Waeber, C.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Moskowitz, M.A. & Ayata, C. (2011), Enhanced Subcortical Spreading Depression in Familial Hemiplegic Migraine Type 1 Mutant Mice, Journal of Neuroscience 31(15): 5755-5763.
- Ceruti, S.; Villa, G.; Fumagalli, M.; Colombo, L.; Magni, G.; Zanardelli, M.; Fabbretti, E.; Verderio, C.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Abbracchio, M.P. (2011), Calcitonin Gene-Related Peptide-Mediated Enhancement of Purinergic Neuron/Glia Communication by the Algogenic Factor Bradykinin in Mouse Trigeminal Ganglia from Wild-Type and R192Q Ca(v)2.1 Knock-In Mice: Implications for Basic Mechanisms of Migraine Pain, Journal of Neuroscience 31(10): 3638-3649.
- Fioretti, B.; Catacuzzeno, L.; Sforna, L.; Gerke-Duncan, M.B.; Maagdenberg, A.M.J.M. van den; Franciolini, F.; Connor, M. & Pietrobon, D. (2011), Trigeminal ganglion neuron subtype-specific alterations of CaV2.1 calcium current and excitability in a Cacna1a mouse model of migraine, JOURNAL OF PHYSIOLOGY-LONDON 589(23): 5879-5895.
- Gnanasekaran, A.; Sundukova, M.; Maagdenberg, A.M.J.M. van den; Fabbretti, E. & Nistri, A. (2011), Lipid rafts control P2X3 receptor distribution and function in trigeminal sensory neurons of a transgenic migraine mouse model.
- Ligthart, L.; Vries, B. de; Smith, A.V.; Ikram, M.A.; Amin, N.; Hottenga, J.J.; Koelewijn, S.C.; Kattenberg, V.M.; Moor, M.H.M. de; Janssens, A.C.J.W.; Aulchenko, Y.S.; Oostra, B.A.; Geus, E.J.C. de; Smit, J.H.; Zitman, F.G.; Uitterlinden, A.G.; Hofman, A.; Willemsen, G.; Nyholt, D.R.; Montgomery, G.W.; Terwindt, G.M.; Gudnason, V.; Penninx, B.W.J.H.; Breteler, M.; Ferrari, M.D.; Launer, L.J.; Duijn, C.M. van; Maagdenberg, A.M.J.M. van den; Boomsma, D.I. & Dutch Icelandic Migraine Genetics (2011), Meta-analysis of genome-wide association for migraine in six population-based European cohorts, European Journal of Human Genetics 19(8): 901-907.
- Stam, A.H.; Louter, M.A.; Haan, J.; Vries, B. de; Maagdenberg, A.M.J.M. van den; Frants, R.R.; Ferrari, M.D. & Terwindt, G.M. (2011), A long-term follow-up study of 18 patients with sporadic hemiplegic migraine.
- Ceruti, S.; Villa, G.; Fumagalli, M.; Colombo, L.; Magni, G.; Zanardelli, M.; Fabbretti, E.; Verderio, C.; Maagdenberg, A.M.J.M. van den; Nistri, A. & Abbracchio, M.P. (2011), Calcitonin Gene-Related Peptide-Mediated Enhancement of Purinergic Neuron/Glia Communication by the Algogenic Factor Bradykinin in Mouse Trigeminal Ganglia from Wild-Type and R192Q Ca(v)2.1 Knock-In Mice: Implications for Basic Mechanisms of Migraine Pain, Journal of Neuroscience 31(10): 3638-3649.
- Fioretti, B.; Catacuzzeno, L.; Sforna, L.; Gerke-Duncan, M.B.; Maagdenberg, A.M.J.M. van den; Franciolini, F.; Connor, M. & Pietrobon, D. (2011), Trigeminal ganglion neuron subtype-specific alterations of CaV2.1 calcium current and excitability in a Cacna1a mouse model of migraine, JOURNAL OF PHYSIOLOGY-LONDON 589(23): 5879-5895.
- Gnanasekaran, A.; Sundukova, M.; Maagdenberg, A.M.J.M. van den; Fabbretti, E. & Nistri, A. (2011), Lipid rafts control P2X3 receptor distribution and function in trigeminal sensory neurons of a transgenic migraine mouse model.
- Shyti, R.; Vries, B. de & Maagdenberg, A. van den (2011), Migraine Genes and the Relation to Gender, Headache 51(6): 880-890.
- Ligthart, L.; Vries, B. de; Smith, A.V.; Ikram, M.A.; Amin, N.; Hottenga, J.J.; Koelewijn, S.C.; Kattenberg, V.M.; Moor, M.H.M. de; Janssens, A.C.J.W.; Aulchenko, Y.S.; Oostra, B.A.; Geus, E.J.C. de; Smit, J.H.; Zitman, F.G.; Uitterlinden, A.G.; Hofman, A.; Willemsen, G.; Nyholt, D.R.; Montgomery, G.W.; Terwindt, G.M.; Gudnason, V.; Penninx, B.W.J.H.; Breteler, M.; Ferrari, M.D.; Launer, L.J.; Duijn, C.M. van; Maagdenberg, A.M.J.M. van den; Boomsma, D.I. & Dutch Icelandic Migraine Genetics (2011), Meta-analysis of genome-wide association for migraine in six population-based European cohorts, European Journal of Human Genetics 19(8): 901-907.
- Mathew, R.; Andreou, A.P.; Chami, L.; Bergerot, A.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D. & Goadsby, P.J. (2011), Immunohistochemical characterization of calcitonin gene-related peptide in the trigeminal system of the familial hemiplegic migraine 1 knock-in mouse.
- Chasman, D.I.; Schurks, M.; Anttila, V.; Vries, B. de; Schminke, U.; Launer, L.J.; Terwindt, G.M.; Maagdenberg, A.M.J.M. van den; Fendrich, K.; Volzke, H.; Ernst, F.; Griffiths, L.R.; Buring, J.E.; Kallela, M.; Freilinger, T.; Kubisch, C.; Ridker, P.M.; Palotie, A.; Ferrari, M.D.; Hoffmann, W.; Zee, R.Y.L.; Kurth, T. & IHGC (2011), Genome-wide association study reveals three susceptibility loci for common migraine in the general population, Nature Genetics 43(7): 695-U116.
- Eikermann-Haerter, K.; Yuzawa, I.; Qin, T.; Wang, Y.M.; Baek, K.; Kim, Y.R.; Hoffmann, U.; Dilekoz, E.; Waeber, C.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Moskowitz, M.A. & Ayata, C. (2011), Enhanced Subcortical Spreading Depression in Familial Hemiplegic Migraine Type 1 Mutant Mice, Journal of Neuroscience 31(15): 5755-5763.
- Vries, B. de; Steup-Beekman, G.M.; Haan, J.; Bollen, E.L.; Luyendijk, J.; Frants, R.R.; Terwindt, G.M.; Buchem, M.A. van; Huizinga, T.W.J.; Maagdenberg, A.M.J.M. van den & Ferrari, M.D. (2010), TREX1 gene variant in neuropsychiatric systemic lupus erythematosus, Annals of the Rheumatic Diseases 69(10): 1886-1887.
- Nair, A.; Simonetti, M.; Birsa, N.; Ferrari, M.D.; deb Maagdenberg, A.M.J.M. van; Giniatullin, R.; Nistri, A. & Fabbretti, E. (2010), Familial hemiplegic migraine Ca(V)2.1 channel mutation R192Q enhances ATP-gated P2X3 receptor activity of mouse sensory ganglion neurons mediating trigeminal pain, Molecular Pain 6.
- Adams, P.J.; Rungta, R.L.; Garcia, E.; Maagdenberg, A.M.J.M. van den; MacVicar, B.A. & Snutch, T.P. (2010), Contribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel, Proceedings of the National Academy of Sciences 107(43): 18694-18699.
- Langford, D.J.; Bailey, A.L.; Chanda, M.L.; Clarke, S.E.; Drummond, T.E.; Echols, S.; Glick, S.; Ingrao, J.; Klassen-Ross, T.; LaCroix-Fralish, M.L.; Matsumiya, L.; Sorge, R.E.; Sotocinal, S.G.; Tabaka, J.M.; Wong, D.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Craig, K.D. & Mogil, J.S. (2010), Coding of facial expressions of pain in the laboratory mouse, Nature Methods 7(6): 447U52.
- Klychnikov, O.I.; Li, K.W.; Sidorov, I.A.; Loos, M.; Spijker, S.; Broos, L.A.M.; Frants, R.R.; Ferrari, M.D.; Mayboroda, O.A.; Deelder, A.M.; Smit, A.B. & Maagdenberg, A.M.J.M. van den (2010), Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(v)2.1 calcium channels, Proteomics 10(13): 2531-2535.
- Anttila, V.; Stefansson, H.; Kallela, M.; Todt, U.; Terwindt, G.M.; Calafato, M.S.; Nyholt, D.R.; Dimas, A.S.; Freilinger, T.; Muller-Myhsok, B.; Artto, V.; Inouye, M.; Alakurtti, K.; Kaunisto, M.A.; Hamalainen, E.; Vries, B. de; Stam, A.H.; Weller, C.M.; Heinze, A.; Heinze-Kuhn, K.; Goebel, I.; Borck, G.; Gobel, H.; Steinberg, S.; Wolf, C.; Bjornsson, A.; Gudmundsson, G.; Kirchmann, M.; Hauge, A.; Werge, T.; Schoenen, J.; Eriksson, J.G.; Hagen, K.; Stovner, L.; Wichmann, E.; Meitinger, T.; Alexander, M.; Moebus, S.; Schreiber, S.; Aulchenko, Y.S.; Breteler, M.M.B.; Uitterlinden, A.G.; Hofman, A.; Duijn, C.M. van; Tikka-Kleemola, P.; Vepsalainen; Lucae, S.; Tozzi, F.; Muglia, P.; Barrett, J.; Kaprio, J.; Farkkila, M.; Peltonen, L.; Stefansson, K.; Zwart, J.A.; Ferrari, M.D.; Olesen, J.; Daly, M.; Wessman, M.; Maagdenberg, A.M.J.M. van den; Dichgans, M.; Kubisch, C.; Dermitzakis, E.T.; Frants, R.R.; Palotie, A. & Int Headache Genetics Consortium (2010), Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1, Nature Genetics 42(10): 869+.
- Huehne, K.; Schaal, U.; Leis, S.; Uebe, S.; Gosso, M.F.; Maagdenberg, A.M.J.M. van den; Maihofner, C.; Birklein, F.; Rautenstrauss, B. & Winterpacht, A. (2010), Lack of genetic association of neutral endopeptidase (NEP) with complex regional pain syndrome (CRPS), Neuroscience Letters 472(1): 19-23.
- Panagiotakaki, E.; Gobbi, G.; Neville, B.; Ebinger, F.; Campistol, J.; Nevsimalova, S.; Laan, L.; Casaer, P.; Spiel, G.; Giannotta, M.; Fons, C.; Ninan, M.; Sange, G.; Schyns, T.; Vavassori, R.; Poncelin, D.; Arzimanoglou, A. & ENRAH Consortium (2010), Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults, Brain 133: 3598-3610.
- Kaja, S.; Ven, R.C.G. van de; Broos, L.A.M.; Frants, R.R.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Plomp, J.J. (2010), Severe and Progressive Neurotransmitter Release Aberrations in Familial Hemiplegic Migraine Type 1 Cacna1a S218L Knock-in Mice, Journal of Neurophysiology 104(3): 1445-1455.
- Inchauspe, C.G.; Urbano, F.J.; Guilmi, M.N. di; Forsythe, I.D.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Uchitel, O.D. (2010), Gain of Function in FHM-1 Ca(v)2.1 Knock-In Mice Is Related to the Shape of the Action Potential, Journal of Neurophysiology 104(1): 291-299.
- Koek, M.M.; Bakels, F.; Engel, W.; Maagdenberg, A. van den; Ferrari, M.D.; Coulier, L. & Hankemeier, T. (2010), Metabolic Profiling of Ultrasmall Sample Volumes with GC/MS: From Microliter to Nanoliter Samples, Analytical Chemistry 82(1): 156-162.
- Stam, A.H.; Vries, B. de; Janssens, A.C.J.W.; Vanmolkot, K.R.J.; Aulchenko, Y.S.; Henneman, P.; Oostra, B.A.; Frants, R.R.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Duijn, C.M. van & Terwindt, G.M. (2010), Shared genetic factors in migraine and depression Evidence from a genetic isolate Evidence from a genetic isolate, Neurology 74(4): 288-294.
- Rooij, A.M. de; Gosso, M.F.; Alsina-Sanchis, E.; Marinus, J.; Hilten, J.J. van & Maagdenberg, A.M.J.M. van den (2010), No mutations in the voltage-gated Na(V)1.7 sodium channel alpha 1 subunit gene SCN9A in familial complex regional pain syndrome, European Journal of Neurology 17(6): 808-814.
- Gosso, M.F.; Rooij, A.M. de; Alsina-Sanchis, E.; Kamphorst, J.T.; Marinus, J.; Hilten, J.J. van & Maagdenberg, A.M.J.M. van den (2010), Systematic mutation analysis of seven dystonia genes in complex regional pain syndrome with fixed dystonia, Journal of Neurology 257(5): 820-824.
- Maagdenberg, A.M.J.M. van den; Pizzorusso, T.; Kaja, S.; Terpolilli, N.; Shapovalova, M.; Hoebeek, F.E.; Barrett, C.F.; Gherardini, L.; Ven, R.C.G. van de; Todorov, B.; Broos, L.A.M.; Tottene, A.; Gao, Z.Y.; Fodor, M.; Zeeuw, C.I. de; Frants, R.R.; Plesnila, N.; Plomp, J.J.; Pietrobon, D. & Ferrari, M.D. (2010), High Cortical Spreading Depression Susceptibility and Migraine-Associated Symptoms in Ca(V)2.1 S218L Mice, Annals of Neurology 67(1): 85-98.
- Vries, B. de; Steup-Beekman, G.M.; Haan, J.; Bollen, E.L.; Luyendijk, J.; Frants, R.R.; Terwindt, G.M.; Buchem, M.A. van; Huizinga, T.W.J.; Maagdenberg, A.M.J.M. van den & Ferrari, M.D. (2010), TREX1 gene variant in neuropsychiatric systemic lupus erythematosus, Annals of the Rheumatic Diseases 69(10): 1886-1887.
- Koek, M.M.; Bakels, F.; Engel, W.; Maagdenberg, A. van den; Ferrari, M.D.; Coulier, L. & Hankemeier, T. (2010), Metabolic Profiling of Ultrasmall Sample Volumes with GC/MS: From Microliter to Nanoliter Samples, Analytical Chemistry 82(1): 156-162.
- Maagdenberg, A.M.J.M. van den; Pizzorusso, T.; Kaja, S.; Terpolilli, N.; Shapovalova, M.; Hoebeek, F.E.; Barrett, C.F.; Gherardini, L.; Ven, R.C.G. van de; Todorov, B.; Broos, L.A.M.; Tottene, A.; Gao, Z.Y.; Fodor, M.; Zeeuw, C.I. de; Frants, R.R.; Plesnila, N.; Plomp, J.J.; Pietrobon, D. & Ferrari, M.D. (2010), High Cortical Spreading Depression Susceptibility and Migraine-Associated Symptoms in Ca(V)2.1 S218L Mice, Annals of Neurology 67(1): 85-98.
- Adams, P.J.; Rungta, R.L.; Garcia, E.; Maagdenberg, A.M.J.M. van den; MacVicar, B.A. & Snutch, T.P. (2010), Contribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel, Proceedings of the National Academy of Sciences 107(43): 18694-18699.
- Huehne, K.; Schaal, U.; Leis, S.; Uebe, S.; Gosso, M.F.; Maagdenberg, A.M.J.M. van den; Maihofner, C.; Birklein, F.; Rautenstrauss, B. & Winterpacht, A. (2010), Lack of genetic association of neutral endopeptidase (NEP) with complex regional pain syndrome (CRPS), Neuroscience Letters 472(1): 19-23.
- Anttila, V.; Stefansson, H.; Kallela, M.; Todt, U.; Terwindt, G.M.; Calafato, M.S.; Nyholt, D.R.; Dimas, A.S.; Freilinger, T.; Muller-Myhsok, B.; Artto, V.; Inouye, M.; Alakurtti, K.; Kaunisto, M.A.; Hamalainen, E.; Vries, B. de; Stam, A.H.; Weller, C.M.; Heinze, A.; Heinze-Kuhn, K.; Goebel, I.; Borck, G.; Gobel, H.; Steinberg, S.; Wolf, C.; Bjornsson, A.; Gudmundsson, G.; Kirchmann, M.; Hauge, A.; Werge, T.; Schoenen, J.; Eriksson, J.G.; Hagen, K.; Stovner, L.; Wichmann, E.; Meitinger, T.; Alexander, M.; Moebus, S.; Schreiber, S.; Aulchenko, Y.S.; Breteler, M.M.B.; Uitterlinden, A.G.; Hofman, A.; Duijn, C.M. van; Tikka-Kleemola, P.; Vepsalainen; Lucae, S.; Tozzi, F.; Muglia, P.; Barrett, J.; Kaprio, J.; Farkkila, M.; Peltonen, L.; Stefansson, K.; Zwart, J.A.; Ferrari, M.D.; Olesen, J.; Daly, M.; Wessman, M.; Maagdenberg, A.M.J.M. van den; Dichgans, M.; Kubisch, C.; Dermitzakis, E.T.; Frants, R.R.; Palotie, A. & Int Headache Genetics Consortium (2010), Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1, Nature Genetics 42(10): 869+.
- Panagiotakaki, E.; Gobbi, G.; Neville, B.; Ebinger, F.; Campistol, J.; Nevsimalova, S.; Laan, L.; Casaer, P.; Spiel, G.; Giannotta, M.; Fons, C.; Ninan, M.; Sange, G.; Schyns, T.; Vavassori, R.; Poncelin, D.; Arzimanoglou, A. & ENRAH Consortium (2010), Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults, Brain 133: 3598-3610.
- Rooij, A.M. de; Gosso, M.F.; Alsina-Sanchis, E.; Marinus, J.; Hilten, J.J. van & Maagdenberg, A.M.J.M. van den (2010), No mutations in the voltage-gated Na(V)1.7 sodium channel alpha 1 subunit gene SCN9A in familial complex regional pain syndrome, European Journal of Neurology 17(6): 808-814.
- Gosso, M.F.; Rooij, A.M. de; Alsina-Sanchis, E.; Kamphorst, J.T.; Marinus, J.; Hilten, J.J. van & Maagdenberg, A.M.J.M. van den (2010), Systematic mutation analysis of seven dystonia genes in complex regional pain syndrome with fixed dystonia, Journal of Neurology 257(5): 820-824.
- Langford, D.J.; Bailey, A.L.; Chanda, M.L.; Clarke, S.E.; Drummond, T.E.; Echols, S.; Glick, S.; Ingrao, J.; Klassen-Ross, T.; LaCroix-Fralish, M.L.; Matsumiya, L.; Sorge, R.E.; Sotocinal, S.G.; Tabaka, J.M.; Wong, D.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Craig, K.D. & Mogil, J.S. (2010), Coding of facial expressions of pain in the laboratory mouse, Nature Methods 7(6): 447U52.
- Nair, A.; Simonetti, M.; Birsa, N.; Ferrari, M.D.; deb Maagdenberg, A.M.J.M. van; Giniatullin, R.; Nistri, A. & Fabbretti, E. (2010), Familial hemiplegic migraine Ca(V)2.1 channel mutation R192Q enhances ATP-gated P2X3 receptor activity of mouse sensory ganglion neurons mediating trigeminal pain, Molecular Pain 6.
- Klychnikov, O.I.; Li, K.W.; Sidorov, I.A.; Loos, M.; Spijker, S.; Broos, L.A.M.; Frants, R.R.; Ferrari, M.D.; Mayboroda, O.A.; Deelder, A.M.; Smit, A.B. & Maagdenberg, A.M.J.M. van den (2010), Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(v)2.1 calcium channels, Proteomics 10(13): 2531-2535.
- Kaja, S.; Ven, R.C.G. van de; Broos, L.A.M.; Frants, R.R.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Plomp, J.J. (2010), Severe and Progressive Neurotransmitter Release Aberrations in Familial Hemiplegic Migraine Type 1 Cacna1a S218L Knock-in Mice, Journal of Neurophysiology 104(3): 1445-1455.
- Stam, A.H.; Vries, B. de; Janssens, A.C.J.W.; Vanmolkot, K.R.J.; Aulchenko, Y.S.; Henneman, P.; Oostra, B.A.; Frants, R.R.; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; Duijn, C.M. van & Terwindt, G.M. (2010), Shared genetic factors in migraine and depression Evidence from a genetic isolate Evidence from a genetic isolate, Neurology 74(4): 288-294.
- Inchauspe, C.G.; Urbano, F.J.; Guilmi, M.N. di; Forsythe, I.D.; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den & Uchitel, O.D. (2010), Gain of Function in FHM-1 Ca(v)2.1 Knock-In Mice Is Related to the Shape of the Action Potential, Journal of Neurophysiology 104(1): 291-299.
- (2009), The 3D Moore-Rayleigh Test for the Quantitative Groupwise Comparison of MR Brain Images.
- de Vries B, Mamsa H, Stam AH, Wan JJ, Bakker SLM, Vanmolkot KRJ, Haan J, Terwindt GM, Boon EMJ & Howard BD (2009), Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake (vol 66, pg 97, 2009), Archives of Neurology -Chigago- 66(4): 497-497.
- de Rooij AM, de Mos M, van Hilten JJ, Sturkenboom MC, Gosso MF, van den Maagdenberg AM & Marinus J (2009), Increased risk of complex regional pain syndrome in siblings of patients?
- de Vries B, Mamsa H, Stam AH, Wan JJ, Bakker SLM, Vanmolkot KRJ, Haan J, Terwindt GM, Boon EMJ & Howard BD (2009), Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake (vol 66, pg 97, 2009), Archives of Neurology -Chigago- 66(4): 497-497.
- (2009), The 3D Moore-Rayleigh Test for the Quantitative Groupwise Comparison of MR Brain Images.
- de Rooij AM, de Mos M, van Hilten JJ, Sturkenboom MC, Gosso MF, van den Maagdenberg AM & Marinus J (2009), Increased risk of complex regional pain syndrome in siblings of patients?
- Deboer T, Oosterman JE, Ferrari MD, van den Maagdenberg AM & Meijer JH (2008), Effect of sleep deprivation on sleep and the sleep EEG in R192Q Ca(v)2.1 migraine mice, SLEEP 31.
- van den Maagdenberg AMJM (2008), Genetically modified animals to study migraine, European Journal of Neurology 15.
- Vanmolkot KRJ, Terwindt GM, Frants RR, Haan J, van den Maagdenberg A & Ferrari MD (2008), A gene for a new monogenic neurovascular migraine syndrome: A next step in unravelling molecular pathways for migraine?, Cephalalgia 28(5).
- Haan J, Terwindt GM, van den Maagdenberg AMJM, Stam AH & Ferrari MD (2008), A review of the genetic relation between migraine and epilepsy, Cephalalgia 28(2).
- van Oosterhout F, Michel S, Deboer T, Houben T, van de Ven RCG, Albus H, Westerhout J, Vansteensel MJ, Ferrari MD, van den Maagdenberg AMJM & Meijer JH (2008), Enhanced circadian phase resetting in R192Q Ca(v)2.1 calcium channel migraine mice, Annals of Neurology 64(3).
- Stam AH, van den Maagdenberg AMJM, Haan J, Terwindt GM & Ferrari MD (2008), Genetics of migraine: an update with special attention to genetic comorbidity, Current Opinion in Neurology 21(3).
- Graves TD, Imbrici P, Kors EE, Terwindt GM, Eunson LH, Frants RR, Haan J, Ferrari MD, Goadsby PJ, Hanna MG, van den Maagdenberg AMJM & Kullmann DM (2008), Premature stop codons in a facilitating EF-hand splice variant of Ca(v)2.1 cause episodic ataxia type 2, Neurobiology of Disease 32(1).
- Kahlig KM, Rhodes TH, Pusch M, Freilinger T, Pereira-Monteiro JM, Ferrari MD, van den Maagdenberg AMJM, Dichgans M & George AL (2008), Divergent sodium channel defects in familial hemiplegic migraine, Proceedings of the National Academy of Sciences 105(28).
- Castro MJ, Nunes B, de Vries B, Lemos C, Vanmolkot KRJ, van den Heuvel JJMW, Temudo T, Barros J, Sequeiros J, Frants RR, Koenderink JB, Pereira-Monteiro JM & van den Maagdenberg AMJM (2008), Two novel functional mutations in the Na+,K+-ATPase alpha 2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes, Clinical Genetics 73(1).
- de Vries B, Stam AH, Beker F, van den Maagdenberg AMJM, Vanmolkot KRJ, Laan LAEM, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM & Ferrari MD (2008), CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood, Cephalalgia 28(8).
- Kaja S, van de Ven RCG, Frants RR, Ferrari MD, van den Maagdenberg AMJM & Plomp JJ (2008), Reduced ACh release at neuromuscular synapses of Heterozygous leaner Ca(v)2.1-mutant mice, Synapse 62(5).
- Stam AH, Vanmolkot KRJ, Kremer HPH, Gartner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AMJM & Terwindt GM (2008), CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine, Clinical Genetics 74(5).
- van Oosterhout F, Michel S, Deboer T, Houben T, van de Ven RCG, Albus H, Westerhout J, Vansteensel MJ, Ferrari MD, van den Maagdenberg AMJM & Meijer JH (2008), Enhanced circadian phase resetting in R192Q Ca(v)2.1 calcium channel migraine mice, Annals of Neurology 64(3): 315-324.
- Stam AH, Vanmolkot KRJ, Kremer HPH, Gartner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AMJM & Terwindt GM (2008), CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine, Clinical Genetics 74(5).
- Vanmolkot KRJ, Terwindt GM, Frants RR, Haan J, van den Maagdenberg A & Ferrari MD (2008), A gene for a new monogenic neurovascular migraine syndrome: A next step in unravelling molecular pathways for migraine?, Cephalalgia 28(5).
- Kahlig KM, Rhodes TH, Pusch M, Freilinger T, Pereira-Monteiro JM, Ferrari MD, van den Maagdenberg AMJM, Dichgans M & George AL (2008), Divergent sodium channel defects in familial hemiplegic migraine, Proceedings of the National Academy of Sciences 105(28).
- Graves TD, Imbrici P, Kors EE, Terwindt GM, Eunson LH, Frants RR, Haan J, Ferrari MD, Goadsby PJ, Hanna MG, van den Maagdenberg AMJM & Kullmann DM (2008), Premature stop codons in a facilitating EF-hand splice variant of Ca(v)2.1 cause episodic ataxia type 2, Neurobiology of Disease 32(1).
- Stam AH, van den Maagdenberg AMJM, Haan J, Terwindt GM & Ferrari MD (2008), Genetics of migraine: an update with special attention to genetic comorbidity, Current Opinion in Neurology 21(3).
- Kaja S, van de Ven RCG, Frants RR, Ferrari MD, van den Maagdenberg AMJM & Plomp JJ (2008), Reduced ACh release at neuromuscular synapses of Heterozygous leaner Ca(v)2.1-mutant mice, Synapse 62(5).
- Deboer T, Oosterman JE, Ferrari MD, van den Maagdenberg AM & Meijer JH (2008), Effect of sleep deprivation on sleep and the sleep EEG in R192Q Ca(v)2.1 migraine mice, SLEEP 31.
- van Oosterhout F, Michel S, Deboer T, Houben T, van de Ven RCG, Albus H, Westerhout J, Vansteensel MJ, Ferrari MD, van den Maagdenberg AMJM & Meijer JH (2008), Enhanced circadian phase resetting in R192Q Ca(v)2.1 calcium channel migraine mice, Annals of Neurology 64(3): 315-324.
- Castro MJ, Nunes B, de Vries B, Lemos C, Vanmolkot KRJ, van den Heuvel JJMW, Temudo T, Barros J, Sequeiros J, Frants RR, Koenderink JB, Pereira-Monteiro JM & van den Maagdenberg AMJM (2008), Two novel functional mutations in the Na+,K+-ATPase alpha 2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes, Clinical Genetics 73(1).
- Haan J, Terwindt GM, van den Maagdenberg AMJM, Stam AH & Ferrari MD (2008), A review of the genetic relation between migraine and epilepsy, Cephalalgia 28(2).
- van Oosterhout F, Michel S, Deboer T, Houben T, van de Ven RCG, Albus H, Westerhout J, Vansteensel MJ, Ferrari MD, van den Maagdenberg AMJM & Meijer JH (2008), Enhanced circadian phase resetting in R192Q Ca(v)2.1 calcium channel migraine mice, Annals of Neurology 64(3).
- van den Maagdenberg AMJM (2008), Genetically modified animals to study migraine, European Journal of Neurology 15.
- de Vries B, Stam AH, Beker F, van den Maagdenberg AMJM, Vanmolkot KRJ, Laan LAEM, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM & Ferrari MD (2008), CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood, Cephalalgia 28(8).
- Bajaj N, de Vries B, Ferrari MD, Frants RR, Haan J, Koenderink JB, Raman A, Stam AH, Terwindt GM, van den Boogerd EH, van den Heuvel JJMW, van den Maagdenberg AMJM, van Vark J, Vanmolkot K & Vanmolkot KRJ (2007), First case of compound heterozygosity in familial hemiplegic migraine: two mutations in Na,K-ATPase gene ATP1A2, Cephalalgia 27(6).
- Albus H, Deboer T, Ferrari M, Meijer J, Michel S, van den Maagdenberg A & van Oosterhout F (2007), FHM1 R192Q Cacna1a mutant mice show enhanced adjustment to advanced shifts of the light-dark cycle: a molecular basis to chronobiology in migraine?, Cephalalgia 27(6).
- Ferrari MD, Frants RR, Ginjaar HB, Haan J, Luijckx GJ, Poll-The BT, Stam A, Terwindt GM & van den Maagdenberg AMJM (2007), FHM1 S218L mutation associated with trauma triggered delayed cerebral coma and seizures in sporadic cases, Cephalalgia 27(6).
- van den Maagdenberg A, Terwindt G, Dichgans M, Frants R, Baloh R, Atkinson J, Ferrari M, Richards A, Jen J, Kavanagh D, Vanmolkot K, De Vries B, Stam A, Haan J & De Jong P (2007), Novel gene causing retinal Vasculopathy with cerebral leukodystrophy, Raynaud's phenomenon and migraine, Cephalalgia 27(10).
- Bakker E, Beker F, De Vries B, de Vries B, Ferrari MD, Frants RR, Haan J, Haas JP, Lauffer H, Stam AH, Terwindt GM, Van den Maagdenberg AMJM & Vanmolkot KRJ (2007), Novel CACNA1A mutation: genetic evidence for shared etiology of AHC and FHM, Cephalalgia 27(6).
- Kaja S, Van de Ven RCG, Broos LAM, Frants RR, Ferrari MD, Van den Maagdenberg AMJM & Plomp JJ (2007), Characterization of acetylcholine release and the compensatory contribution of non-Ca(v)2.1 channels at motor nerve terminals of leaner Ca(v)2.1-mutant mice, Neuroscience 144(4).
- Kaja S, van de Ven RCG, van Dijk JG, Verschuuren JJGM, Arahata K, Frants RR, Ferrari MD, van den Maagdenberg AMJM & Plomp JJ (2007), Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya, European Journal of Neuroscience 25(7).
- Kaja S, Todorov B, de Ven RCGV, Ferrari MD, Frants RR, van den Maagdenberg AMJM & Plomp JJ (2007), Redundancy of Ca(v)2.1 channel accessory subunits in transmitter release at the mouse neuromuscular junction, Brain Research 1143.
- Vanmolkot KRJ, Stam AH, Raman A, Koenderink JB, de Vries B, van den Boogerd EH, van Vark J, van den Heuvel JJMW, Bajaj N, Terwindt GM, Haan J, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2007), First case of compound heterozygosity in Na, K-ATPase gene ATP1A2 in familial hemiplegic migraine, European Journal of Human Genetics 15(8).
- Richards A, van den Maagdenberg AMJM, Jen JC, Kavanagh D, Bertram P, Spitzer D, Liszewski MK, Barilla-LaBarca ML, Terwindt GM, Kasai Y, McLellan M, Grand MG, Vanmolkot KRJ, de Vries B, Wan J, Kane MJ, Mamsa H, Schafer R, Stam AH, Haan J, Paulus TVMDJ, Storimans CW, van Schooneveld MJ, Oosterhuis JA, Gschwendter A, Dichgans M, Kotschet KE, Hodgkinson S, Hardy TA, Delatycki MB, Hajj-Ali RA, Kothari PH, Nelson SF, Frants RR, Baloh RW, Ferrari MD & Atkinson JP (2007), C-terminal truncations in human 3 '-5 ' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy, Nature Genetics 39(9).
- van den Maagdenberg AMJM, Haan J, Terwindt GM & Ferrari MD (2007), Migraine: gene mutations and functional consequences, Current Opinion in Neurology 20(3).
- van de Ven RCG, Kaja S, Plomp JJ, Frants RR, van den Maagdenberg AMJM & Ferrari MD (2007), Genetic models of migraine, Archives of Neurology -Chigago- 64(5).
- Mehrotra S, Vanmolkot KRJ, Frants RR, van den Maagdenberg AMJM, Ferrari MD & MaassenVanDenBrink A (2007), The Phe-124-Cys and A-161T variants of the human 5-HT1B receptor gene are not major determinants of the clinical response to sumatriptan, Headache 47(5).
- van de Ven RCG, Hogers B, van den Maagdenberg AMJM, de Groot HJM, Ferrari MD, Frants RR, Poelmann RE, van der Weerd L & Kiihne SR (2007), T-1 relaxation in in vivo mouse brain at ultra-high field, Magnetic Resonance in Medicine 58(2).
- Castro MJ, Stam AH, Lemos C, Barros J, Gouveia RG, Martins IP, Koenderink JB, Vanmolkot KRJ, Mendes AP, Frants RR, Ferrari MD, Sequeiros J, Pereira-Monteiro JM & van den Maagdenberg AMJM (2007), Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine, Journal of Human Genetics 52(12).
- de Vries B, Freilinger T, Vanmolkot KRJ, Koenderink JB, Stam AH, Terwindt GM, Babini E, van den Boogerd EH, van den Heuvel JJMW, Frants RR, Haan J, Pusch M, van den Maagdenberg AMJM, Ferrari MD & Dichgans M (2007), Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine, Neurology 69(23).
- Vanmolkot KRJ, Stam AH, Raman A, Koenderink JB, de Vries B, van den Boogerd EH, van Vark J, van den Heuvel JJMW, Bajaj N, Terwindt GM, Haan J, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2007), First case of compound heterozygosity in Na, K-ATPase gene ATP1A2 in familial hemiplegic migraine, European Journal of Human Genetics 15(8).
- Bajaj N, de Vries B, Ferrari MD, Frants RR, Haan J, Koenderink JB, Raman A, Stam AH, Terwindt GM, van den Boogerd EH, van den Heuvel JJMW, van den Maagdenberg AMJM, van Vark J, Vanmolkot K & Vanmolkot KRJ (2007), First case of compound heterozygosity in familial hemiplegic migraine: two mutations in Na,K-ATPase gene ATP1A2, Cephalalgia 27(6).
- Castro MJ, Stam AH, Lemos C, Barros J, Gouveia RG, Martins IP, Koenderink JB, Vanmolkot KRJ, Mendes AP, Frants RR, Ferrari MD, Sequeiros J, Pereira-Monteiro JM & van den Maagdenberg AMJM (2007), Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine, Journal of Human Genetics 52(12).
- Ferrari MD, Frants RR, Ginjaar HB, Haan J, Luijckx GJ, Poll-The BT, Stam A, Terwindt GM & van den Maagdenberg AMJM (2007), FHM1 S218L mutation associated with trauma triggered delayed cerebral coma and seizures in sporadic cases, Cephalalgia 27(6).
- van de Ven RCG, Hogers B, van den Maagdenberg AMJM, de Groot HJM, Ferrari MD, Frants RR, Poelmann RE, van der Weerd L & Kiihne SR (2007), T-1 relaxation in in vivo mouse brain at ultra-high field, Magnetic Resonance in Medicine 58(2).
- Kaja S, Van de Ven RCG, Broos LAM, Frants RR, Ferrari MD, Van den Maagdenberg AMJM & Plomp JJ (2007), Characterization of acetylcholine release and the compensatory contribution of non-Ca(v)2.1 channels at motor nerve terminals of leaner Ca(v)2.1-mutant mice, Neuroscience 144(4).
- Kaja S, Todorov B, de Ven RCGV, Ferrari MD, Frants RR, van den Maagdenberg AMJM & Plomp JJ (2007), Redundancy of Ca(v)2.1 channel accessory subunits in transmitter release at the mouse neuromuscular junction, Brain Research 1143.
- Bakker E, Beker F, De Vries B, de Vries B, Ferrari MD, Frants RR, Haan J, Haas JP, Lauffer H, Stam AH, Terwindt GM, Van den Maagdenberg AMJM & Vanmolkot KRJ (2007), Novel CACNA1A mutation: genetic evidence for shared etiology of AHC and FHM, Cephalalgia 27(6).
- Mehrotra S, Vanmolkot KRJ, Frants RR, van den Maagdenberg AMJM, Ferrari MD & MaassenVanDenBrink A (2007), The Phe-124-Cys and A-161T variants of the human 5-HT1B receptor gene are not major determinants of the clinical response to sumatriptan, Headache 47(5).
- van den Maagdenberg A, Terwindt G, Dichgans M, Frants R, Baloh R, Atkinson J, Ferrari M, Richards A, Jen J, Kavanagh D, Vanmolkot K, De Vries B, Stam A, Haan J & De Jong P (2007), Novel gene causing retinal Vasculopathy with cerebral leukodystrophy, Raynaud's phenomenon and migraine, Cephalalgia 27(10).
- de Vries B, Freilinger T, Vanmolkot KRJ, Koenderink JB, Stam AH, Terwindt GM, Babini E, van den Boogerd EH, van den Heuvel JJMW, Frants RR, Haan J, Pusch M, van den Maagdenberg AMJM, Ferrari MD & Dichgans M (2007), Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine, Neurology 69(23).
- Richards A, van den Maagdenberg AMJM, Jen JC, Kavanagh D, Bertram P, Spitzer D, Liszewski MK, Barilla-LaBarca ML, Terwindt GM, Kasai Y, McLellan M, Grand MG, Vanmolkot KRJ, de Vries B, Wan J, Kane MJ, Mamsa H, Schafer R, Stam AH, Haan J, Paulus TVMDJ, Storimans CW, van Schooneveld MJ, Oosterhuis JA, Gschwendter A, Dichgans M, Kotschet KE, Hodgkinson S, Hardy TA, Delatycki MB, Hajj-Ali RA, Kothari PH, Nelson SF, Frants RR, Baloh RW, Ferrari MD & Atkinson JP (2007), C-terminal truncations in human 3 '-5 ' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy, Nature Genetics 39(9).
- Kaja S, van de Ven RCG, van Dijk JG, Verschuuren JJGM, Arahata K, Frants RR, Ferrari MD, van den Maagdenberg AMJM & Plomp JJ (2007), Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya, European Journal of Neuroscience 25(7).
- Albus H, Deboer T, Ferrari M, Meijer J, Michel S, van den Maagdenberg A & van Oosterhout F (2007), FHM1 R192Q Cacna1a mutant mice show enhanced adjustment to advanced shifts of the light-dark cycle: a molecular basis to chronobiology in migraine?, Cephalalgia 27(6).
- van den Maagdenberg AMJM, Haan J, Terwindt GM & Ferrari MD (2007), Migraine: gene mutations and functional consequences, Current Opinion in Neurology 20(3).
- van de Ven RCG, Kaja S, Plomp JJ, Frants RR, van den Maagdenberg AMJM & Ferrari MD (2007), Genetic models of migraine, Archives of Neurology -Chigago- 64(5).
- Scher AI, Terwindt GM, Verschuren WMM, Kruit MC, Blom HJ, Kowa H, Frants RR, van den Maagdenberg AMJM, van Buchem M, Ferrari MD & Launer LJ (2006), MTHFR C677T polymorphism and migraine with aura - Reply, Annals of Neurology 60(5).
- Kaja S, Van de Ven RCG, Ferrari MD, Frants RR, Van den Maagdenberg AMJM & Plomp JJ (2006), Compensatory contribution of Ca(v)2.3 channels to acetylcholine release at the neuromuscular junction of Tottering mice, Journal of Neurophysiology 95(4).
- Bergerot A, Holland PR, Akerman S, Bartsch T, Ahn AH, MaassenVanDenBrink A, Reuter U, Tassorelli C, Schoenen J, Mitsikostas DD, van den Maagdenberg AMJM & Goadsby PJ (2006), Animal models of migraine: looking at the component parts of a complex disorder, European Journal of Neuroscience 24(6).
- Bakker MJ, van Dijk JG, van den Maagdenberg AMJM & Tijssen MAJ (2006), Startle syndromes, Lancet Neurology 5(6).
- Scher AI, Terwindt GM, Verschuren WMM, Kruit MC, Blom HJ, Kowa H, Frants RR, van den Maagdenberg AMJM, van Buchem M, Ferrari MD & Launer LJ (2006), Migraine and MTHFR C677T genotype in a population-based sample, Annals of Neurology 59(2).
- Todorov B, de Ven RCGV, Kaja S, Broos LAM, Verbeek SJ, Plomp JJ, Ferrari MD, Frants RR & van den Maagdenberg AMJM (2006), Conditional inactivation of the Cacna1a gene in transgenic mice, genesis 44(12).
- Vanmolkot KR, Kors EE, Turk U, Turkdogan D, Keyser A, Broos LA, Kia SK, van den Heuvel JJ, Black DF, Haan J, Frants RR, Barone V, Ferrari MD, Casari G, Koenderink JB & van den Maagdenberg AM (2006), Two de novo mutations in the Na, K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine, European Journal of Human Genetics 14(5).
- Vanmolkot KRJ, Stroink H, Koenderink JB, Kors EE, van den Heuvel JJMW, van den Boogerd EH, Stam AH, Haan J, de Vries BBA, Terwindt GM, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2006), Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation, Annals of Neurology 59(2).
- Lopes LR, Peres MFP, Vanmolkot KRJ, Tobo PR, Zukerman E, Frants RR, Van den Maagdenberg AMJM & Moreira CA (2006), Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families, Arquivos de Neuro-Psiquiatria 64(3A).
- Rees MI, Harvey K, Pearce BR, Chung SK, Duguid IC, Thomas P, Beatty S, Graham GE, Armstrong L, Shiang R, Abbott KJ, Zuberi SM, Stephenson JBP, Owen MJ, Tijssen MAJ, van den Maagdenberg AMJM, Smart TG, Supplisson S & Harvey RJ (2006), Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease, Nature Genetics 38(7).
- De Vries B, Haan J, Frants RR, Van den Maagdenberg AMJM & Ferrari MD (2006), Genetic biomarkers for migraine, Headache 46(7).
- Gupta S, Akerman S, van den Maagdenberg AMJM, Saxena PR, Goadsby PJ & van den Brink AM (2006), Intravital microscopy on a closed cranial window in mice: a model to study trigeminovascular mechanisms involved in migraine, Cephalalgia 26(11).
- De Vries B, Haan J, Frants RR, Van den Maagdenberg AMJM & Ferrari MD (2006), Genetic biomarkers for migraine, Headache 46(7).
- Scher AI, Terwindt GM, Verschuren WMM, Kruit MC, Blom HJ, Kowa H, Frants RR, van den Maagdenberg AMJM, van Buchem M, Ferrari MD & Launer LJ (2006), MTHFR C677T polymorphism and migraine with aura - Reply, Annals of Neurology 60(5).
- Todorov B, de Ven RCGV, Kaja S, Broos LAM, Verbeek SJ, Plomp JJ, Ferrari MD, Frants RR & van den Maagdenberg AMJM (2006), Conditional inactivation of the Cacna1a gene in transgenic mice, genesis 44(12).
- Gupta S, Akerman S, van den Maagdenberg AMJM, Saxena PR, Goadsby PJ & van den Brink AM (2006), Intravital microscopy on a closed cranial window in mice: a model to study trigeminovascular mechanisms involved in migraine, Cephalalgia 26(11).
- Bergerot A, Holland PR, Akerman S, Bartsch T, Ahn AH, MaassenVanDenBrink A, Reuter U, Tassorelli C, Schoenen J, Mitsikostas DD, van den Maagdenberg AMJM & Goadsby PJ (2006), Animal models of migraine: looking at the component parts of a complex disorder, European Journal of Neuroscience 24(6).
- Vanmolkot KRJ, Stroink H, Koenderink JB, Kors EE, van den Heuvel JJMW, van den Boogerd EH, Stam AH, Haan J, de Vries BBA, Terwindt GM, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2006), Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation, Annals of Neurology 59(2).
- Lopes LR, Peres MFP, Vanmolkot KRJ, Tobo PR, Zukerman E, Frants RR, Van den Maagdenberg AMJM & Moreira CA (2006), Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families, Arquivos de Neuro-Psiquiatria 64(3A).
- Vanmolkot KR, Kors EE, Turk U, Turkdogan D, Keyser A, Broos LA, Kia SK, van den Heuvel JJ, Black DF, Haan J, Frants RR, Barone V, Ferrari MD, Casari G, Koenderink JB & van den Maagdenberg AM (2006), Two de novo mutations in the Na, K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine, European Journal of Human Genetics 14(5).
- Bakker MJ, van Dijk JG, van den Maagdenberg AMJM & Tijssen MAJ (2006), Startle syndromes, Lancet Neurology 5(6).
- Rees MI, Harvey K, Pearce BR, Chung SK, Duguid IC, Thomas P, Beatty S, Graham GE, Armstrong L, Shiang R, Abbott KJ, Zuberi SM, Stephenson JBP, Owen MJ, Tijssen MAJ, van den Maagdenberg AMJM, Smart TG, Supplisson S & Harvey RJ (2006), Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease, Nature Genetics 38(7).
- Kaja S, Van de Ven RCG, Ferrari MD, Frants RR, Van den Maagdenberg AMJM & Plomp JJ (2006), Compensatory contribution of Ca(v)2.3 channels to acetylcholine release at the neuromuscular junction of Tottering mice, Journal of Neurophysiology 95(4).
- Scher AI, Terwindt GM, Verschuren WMM, Kruit MC, Blom HJ, Kowa H, Frants RR, van den Maagdenberg AMJM, van Buchem M, Ferrari MD & Launer LJ (2006), Migraine and MTHFR C677T genotype in a population-based sample, Annals of Neurology 59(2).
- Scher, A.I.; Terwindt, G.M.; Verschuren, M.W.M.M.; Kruit, M.C.; Blom, H.J.; Kowa, H.; Maagdenberg, A.M.J.M. van den; Buchem, M. van; Ferrari, M.D. & Launer, L.J. (2005), The association of migraine with aura with the methylenetetrahydrofolate reductase (MTHFR) C677T variant and the homocysteine metabolic pathway in the general population, Cephalalgia 25(10).
- Callenbach PMC, van den Boogerd EH, de Coo RFM, ten Houten R, Oosterwijk JC, Hageman G, Frants RR, Brouwer OF & van den Maagdenberg AMJM (2005), Refinement of the chromosome 16 locus for benign familial infantile convulsions, Clinical Genetics 67(6).
- Kaja S, Van de Ven RCG, Broos LAM, Veldman H, Van Dijk JG, Verschuuren JJGM, Frants RR, Ferrari MD, Van den Maagdenberg AMJM & Plomp JJ (2005), Gene dosage-dependent transmitter release changes at neuromuscular synapses of Cacna1a R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness, Neuroscience 135(1).
- Wirtz PW, Lang B, Graus F, van den Maagdenberg AMJM, Saiz A, Gans PAD, Twijnstra A & Verschuuren JJGM (2005), P/Q-type calcium channel antibodies, Lambert-Eaton myasthenic syndrome and survival in small cell lung cancer, Journal of Neuroimmunology 164(1-2).
- van Rootselaar AF, van Schaik IN, van den Maagdenberg AMJM, Koelman JHTM, Callenbach PMC & Tijssen MAJ (2005), Familial cortical myoclonic tremor with epilepsy: A single syndromic classification for a group of pedigrees bearing common features, Movement Disorders 20(6).
- Dichgans M, Freilinger T, Eckstein G, Babini E, Lorenz-Depiereux B, Biskup S, Ferrari MD, Herzog J, van den Maagdenberg AMJM, Pusch M & Strom TM (2005), Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine, Lancet 366(9483).
- Spacey SD, Vanmolkot KRJ, Murphy C, van den Maagdenberg AMJM & Hsiung RGY (2005), Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family, Headache 45(9).
- Tottene A, Pivotto F, Fellin T, Cesetti T, van den Maagdenberg AMJM & Pietrobon D (2005), Specific kinetic alterations of human Ca(V)2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma, Journal of Biological Chemistry 280(18).
- Hottenga JJ, Vanmolkot KRJ, Kors EE, Kia SK, de Jong PTVM, Haan J, Terwindt GM, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2005), The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine, Cephalalgia 25(12).
- Hoebeek FE, Stahl JS, van Alphen AM, Schonewille M, Luo C, Rutteman M, van den Maagdenberg AMJM, Molenaar R, Goossens HHLM, Frens MA & De Zeeuw CI (2005), Increased noise level of Purkinje cell activities minimizes impact of their modulation during sensorimotor control, Neuron 45(6).
- Wirtz PW, Lang B, Graus F, van den Maagdenberg AMJM, Saiz A, Gans PAD, Twijnstra A & Verschuuren JJGM (2005), P/Q-type calcium channel antibodies, Lambert-Eaton myasthenic syndrome and survival in small cell lung cancer, Journal of Neuroimmunology 164(1-2).
- Scher, A.I.; Terwindt, G.M.; Verschuren, M.W.M.M.; Kruit, M.C.; Blom, H.J.; Kowa, H.; Maagdenberg, A.M.J.M. van den; Buchem, M. van; Ferrari, M.D. & Launer, L.J. (2005), The association of migraine with aura with the methylenetetrahydrofolate reductase (MTHFR) C677T variant and the homocysteine metabolic pathway in the general population, Cephalalgia 25(10).
- Callenbach PMC, van den Boogerd EH, de Coo RFM, ten Houten R, Oosterwijk JC, Hageman G, Frants RR, Brouwer OF & van den Maagdenberg AMJM (2005), Refinement of the chromosome 16 locus for benign familial infantile convulsions, Clinical Genetics 67(6).
- Hottenga JJ, Vanmolkot KRJ, Kors EE, Kia SK, de Jong PTVM, Haan J, Terwindt GM, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2005), The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine, Cephalalgia 25(12).
- Kaja S, Van de Ven RCG, Broos LAM, Veldman H, Van Dijk JG, Verschuuren JJGM, Frants RR, Ferrari MD, Van den Maagdenberg AMJM & Plomp JJ (2005), Gene dosage-dependent transmitter release changes at neuromuscular synapses of Cacna1a R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness, Neuroscience 135(1).
- Hoebeek FE, Stahl JS, van Alphen AM, Schonewille M, Luo C, Rutteman M, van den Maagdenberg AMJM, Molenaar R, Goossens HHLM, Frens MA & De Zeeuw CI (2005), Increased noise level of Purkinje cell activities minimizes impact of their modulation during sensorimotor control, Neuron 45(6).
- van Rootselaar AF, van Schaik IN, van den Maagdenberg AMJM, Koelman JHTM, Callenbach PMC & Tijssen MAJ (2005), Familial cortical myoclonic tremor with epilepsy: A single syndromic classification for a group of pedigrees bearing common features, Movement Disorders 20(6).
- Dichgans M, Freilinger T, Eckstein G, Babini E, Lorenz-Depiereux B, Biskup S, Ferrari MD, Herzog J, van den Maagdenberg AMJM, Pusch M & Strom TM (2005), Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine, Lancet 366(9483).
- Tottene A, Pivotto F, Fellin T, Cesetti T, van den Maagdenberg AMJM & Pietrobon D (2005), Specific kinetic alterations of human Ca(V)2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma, Journal of Biological Chemistry 280(18).
- Spacey SD, Vanmolkot KRJ, Murphy C, van den Maagdenberg AMJM & Hsiung RGY (2005), Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family, Headache 45(9).
- Kors EE, Melberg A, Vanmolkot KRJ, Kumlien E, Haan J, Raininko R, Flink R, Ginjaar HB, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2004), Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation, Neurology 63(6).
- Hottenga JJ, Kors EE, Kia S, Vanmolkot KRJ, Haan J, Terwindt GM, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2004), The hereditary vascular retinopathy (HVR) 3p21 locus contains a susceptibility gene for migraine and Raynaud, Cephalalgia 24(2).
- van den Maagdenberg AMJM, Pietrobon D, Pizzorusso T, Kaja S, Broos LAM, Cesetti T, van de Ven RCG, Tottene A, van der Kaa J, Plomp JJ, Frants RR & Ferrari MD (2004), A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression, Neuron 41(5).
- Mullner C, Broos LAM, van den Maagdenberg AMJM & Striessnig J (2004), Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Ca(v)2.1 Ca2+ channel gating - Evidence for beta-subunit isoform-specific effects, Journal of Biological Chemistry 279(50).
- Kors EE, Vanmolkot KRJ, Haan J, Kia SK, Stroink H, Laan LAEM, Gill DS, Pascual J, van den Maagdenberg AMJM, Frants RR & Ferrari MD (2004), Alternating hemiplegia of childhood: No mutations in the second familial hemiplegic migraine gene ATP1A2, Neuropediatrics 35(5).
- Kaunisto MA, Harno H, Vanmolkot KRJ, Gargus JJ, Sun G, Hamalainen E, Liukkonen E, Kallela M, van den Maagdenberg AMJM, Frants RR, Farkkila M, Palotie A & Wessman M (2004), A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2, neurogenetics 5(2).
- Kors EE, Vanmolkot KRJ, Haan J, Frants RR, van den Maagdenberg AM & Ferrari MD (2004), Recent findings in headache genetics, Current Opinion in Neurology 17(3).
- Kors EE, Vanmolkot KRJ, Haan J, Frants RR, van den Maagdenberg AM & Ferrari MD (2004), Recent findings in headache genetics, Current Opinion in Neurology 17(3).
- Kors EE, Vanmolkot KRJ, Haan J, Kia SK, Stroink H, Laan LAEM, Gill DS, Pascual J, van den Maagdenberg AMJM, Frants RR & Ferrari MD (2004), Alternating hemiplegia of childhood: No mutations in the second familial hemiplegic migraine gene ATP1A2, Neuropediatrics 35(5).
- Mullner C, Broos LAM, van den Maagdenberg AMJM & Striessnig J (2004), Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Ca(v)2.1 Ca2+ channel gating - Evidence for beta-subunit isoform-specific effects, Journal of Biological Chemistry 279(50).
- Hottenga JJ, Kors EE, Kia S, Vanmolkot KRJ, Haan J, Terwindt GM, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2004), The hereditary vascular retinopathy (HVR) 3p21 locus contains a susceptibility gene for migraine and Raynaud, Cephalalgia 24(2).
- Kaunisto MA, Harno H, Vanmolkot KRJ, Gargus JJ, Sun G, Hamalainen E, Liukkonen E, Kallela M, van den Maagdenberg AMJM, Frants RR, Farkkila M, Palotie A & Wessman M (2004), A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2, neurogenetics 5(2).
- Kors EE, Melberg A, Vanmolkot KRJ, Kumlien E, Haan J, Raininko R, Flink R, Ginjaar HB, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2004), Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation, Neurology 63(6).
- van den Maagdenberg AMJM, Pietrobon D, Pizzorusso T, Kaja S, Broos LAM, Cesetti T, van de Ven RCG, Tottene A, van der Kaa J, Plomp JJ, Frants RR & Ferrari MD (2004), A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression, Neuron 41(5).
- Vanmolkot KRJ, Kors EE, Hottenga JJ, Terwindt GM, Haan J, Hoefnagels WAJ, Black DF, Sandkuijl LA, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2003), Novel mutations in the Na+,K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions, Annals of Neurology 54(3).
- Vanmolkot KRJ, van den Maagdenberg AMJM, Haan J & Ferrari MD (2003), New discoveries about the second gene for familial hemiplegic migraine, ATP1A2, Lancet Neurology 2(12).
- van den Maagdenberg AMJM & Plomp JJ (2003), Neuromuscular synapse function in typical migraine, Cephalalgia 23(2).
- Kors EE, Haan J, Giffin NJ, Pazdera L, Schnittger C, Lennox GG, Terivindt GM, Vermeulen FLMJ, Van den Maagdenberg AMJM, Frants RR & Ferrari MD (2003), Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation, Archives of Neurology -Chigago- 60(5).
- Callenbach PMC, van den Maagdenberg AMJM, Hottenga JJ, van den Boogerd EH, de Coo RFM, Lindhout D, Frants RR, Sandkuijl LA & Brouwer OF (2003), Familial partial epilepsy with variable foci in a Dutch family: Clinical characteristics and confirmation of linkage to chromosome 22q, Epilepsia 44(10).
- Plomp JJ, Van Den Maagdenberg AM, Ferrari MD, Frants RR & Molenaar PC (2003), Transmitter release deficits at the neuromuscular synapse of mice with mutations in the Ca(v)2.1 (alpha(1A)) subunit of the P/Q-type Ca2+ channel, Annals of the New York Academy of Sciences 998.
- Callenbach PMC, van den Maagdenberg AMJM, Hottenga JJ, van den Boogerd EH, de Coo RFM, Lindhout D, Frants RR, Sandkuijl LA & Brouwer OF (2003), Familial partial epilepsy with variable foci in a Dutch family: Clinical characteristics and confirmation of linkage to chromosome 22q, Epilepsia 44(10).
- Vanmolkot KRJ, van den Maagdenberg AMJM, Haan J & Ferrari MD (2003), New discoveries about the second gene for familial hemiplegic migraine, ATP1A2, Lancet Neurology 2(12).
- Vanmolkot KRJ, Kors EE, Hottenga JJ, Terwindt GM, Haan J, Hoefnagels WAJ, Black DF, Sandkuijl LA, Frants RR, Ferrari MD & van den Maagdenberg AMJM (2003), Novel mutations in the Na+,K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions, Annals of Neurology 54(3).
- Kors EE, Haan J, Giffin NJ, Pazdera L, Schnittger C, Lennox GG, Terivindt GM, Vermeulen FLMJ, Van den Maagdenberg AMJM, Frants RR & Ferrari MD (2003), Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation, Archives of Neurology -Chigago- 60(5).
- Plomp JJ, Van Den Maagdenberg AM, Ferrari MD, Frants RR & Molenaar PC (2003), Transmitter release deficits at the neuromuscular synapse of mice with mutations in the Ca(v)2.1 (alpha(1A)) subunit of the P/Q-type Ca2+ channel, Annals of the New York Academy of Sciences 998.
- van den Maagdenberg AMJM & Plomp JJ (2003), Neuromuscular synapse function in typical migraine, Cephalalgia 23(2).
- Terwindt G, Kors E, Haan J, Vermeulen F, van den Maagdenberg A, Frants R & Ferrari M (2002), Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine, Archives of Neurology -Chigago- 59(6).
- Kors EE, van den Maagdenberg AMJM, Plomp JJ, Frants RR & Ferrari MD (2002), Calcium channel mutations and migraine, Current Opinion in Neurology 15(3).
- van den Maagdenberg AMJM, Kors EE, Brunt ER, van Paesschen W, Pascual J, Ravine D, Keeling S, Vanmolkot KRJ, Vermeulen FLMG, Terwindt GM, Haan J, Frants RR & Ferrari MD (2002), Episodic ataxia type 2 - Three novel truncating mutations and one novel missense mutation in the CACNA1A gene, Journal of Neurology 249(11).
- Terwindt G, Kors E, Haan J, Vermeulen F, van den Maagdenberg A, Frants R & Ferrari M (2002), Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine, Archives of Neurology -Chigago- 59(6).
- Kors EE, van den Maagdenberg AMJM, Plomp JJ, Frants RR & Ferrari MD (2002), Calcium channel mutations and migraine, Current Opinion in Neurology 15(3).
- van den Maagdenberg AMJM, Kors EE, Brunt ER, van Paesschen W, Pascual J, Ravine D, Keeling S, Vanmolkot KRJ, Vermeulen FLMG, Terwindt GM, Haan J, Frants RR & Ferrari MD (2002), Episodic ataxia type 2 - Three novel truncating mutations and one novel missense mutation in the CACNA1A gene, Journal of Neurology 249(11).
- Ophoff RA, DeYoung J, Service SK, Joose M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AMJM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB & Frants RR (2001), Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3, American Journal of Human Genetics 69(2).
- Haan J, van Vliet JA, Kors EE, Terwindt GM, Vermeulen FLMG, van den Maagdenberg AMJM, Frants RR & Ferrari MD (2001), No involvement of the calcium channel gene (CACNA1A) in a family with cluster headache, Cephalalgia 21(10).
- Kors EE, Terwindt GM, Vermeulen FLMG, Fitzsimons RB, Jardine PE, Heywood P, Love S, van den Maagdenberg AMJM, Haan J, Frants RR & Ferrari MD (2001), Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine, Annals of Neurology 49(6).
- Ophoff RA, van den Maagdenberg AMJM, Roon KI, Ferrari MD & Frants RR (2001), The impact of pharmacogenetics for migraine, European Journal of Pharmacology 413(1).
- Ophoff RA, DeYoung J, Service SK, Joose M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AMJM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB & Frants RR (2001), Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3, American Journal of Human Genetics 69(2).
- Kors EE, Terwindt GM, Vermeulen FLMG, Fitzsimons RB, Jardine PE, Heywood P, Love S, van den Maagdenberg AMJM, Haan J, Frants RR & Ferrari MD (2001), Delayed cerebral edema and fatal coma after minor head trauma: Role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine, Annals of Neurology 49(6).
- Ophoff RA, van den Maagdenberg AMJM, Roon KI, Ferrari MD & Frants RR (2001), The impact of pharmacogenetics for migraine, European Journal of Pharmacology 413(1).
- Haan J, van Vliet JA, Kors EE, Terwindt GM, Vermeulen FLMG, van den Maagdenberg AMJM, Frants RR & Ferrari MD (2001), No involvement of the calcium channel gene (CACNA1A) in a family with cluster headache, Cephalalgia 21(10).
- Haan J, Kors EE, Terwindt GM, Vermeulen FLMG, Vergouwe MN, van den Maagdenberg AMJM, Gill DS, Pascual J, Ophoff RA, Frants RR & Ferrari MD (2000), Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene, Cephalalgia 20(8).
- Plomp JJ, Vergouwe MN, Van den Maagdenberg AM, Ferrari MD, Frants RR & Molenaar PC (2000), Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca2+ channel mutation.
- Haan J, Kors EE, Terwindt GM, Vermeulen FLMG, Vergouwe MN, van den Maagdenberg AMJM, Gill DS, Pascual J, Ophoff RA, Frants RR & Ferrari MD (2000), Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene, Cephalalgia 20(8).
- Plomp JJ, Vergouwe MN, Van den Maagdenberg AM, Ferrari MD, Frants RR & Molenaar PC (2000), Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca2+ channel mutation.
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