Works by van den Maagdenberg, Arn M. J. M.


Results: 99
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    Migraine genetics: an update.

    Published in:
    2005
    By:
    • Haan, J.;
    • Kors, E.;
    • Vanmolkot, Kaate;
    • Maagdenberg, Arn;
    • Frants, Rune;
    • Ferrari, M.;
    • Kors, E E;
    • Vanmolkot, Kaate R J;
    • van den Maagdenberg, Arn M J M;
    • Frants, Rune R;
    • Ferrari, M D
    Publication type:
    journal article
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    Spinocerebellar Ataxia Type 1 Characteristics in Patient‐Derived Fibroblast and iPSC‐Derived Neuronal Cultures.

    Published in:
    Movement Disorders, 2023, v. 38, n. 8, p. 1428, doi. 10.1002/mds.29446
    By:
    • Buijsen, Ronald A.M.;
    • Hu, Michel;
    • Sáez‐González, Maria;
    • Notopoulou, Sofia;
    • Mina, Eleni;
    • Koning, Winette;
    • Gardiner, Sarah L.;
    • van der Graaf, Linda M.;
    • Daoutsali, Elena;
    • Pepers, Barry A.;
    • Mei, Hailiang;
    • van Dis, Vera;
    • Frimat, Jean‐Philippe;
    • van den Maagdenberg, Arn M. J. M.;
    • Petrakis, Spyros;
    • van Roon‐Mom, Willeke M.C.
    Publication type:
    Article
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    HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study.

    Published in:
    Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-61628-9
    By:
    • Qu, Kang;
    • Li, Ming-xi;
    • Yu, Peng;
    • Palotie, Aarno;
    • Pressman, Alice;
    • Belin, Andrea C.;
    • Bjornsdottir, Anna;
    • van den Maagdenberg, Arn M. J. M.;
    • Harder, Aster V. E.;
    • Winsvold, Bendik S.;
    • Müller-Myhsok, Bertram;
    • Cormand, Bru;
    • Ran, Caroline;
    • Northover, Carrie;
    • Kubisch, Christian;
    • van Duijn, Cornelia;
    • Nyholt, Dale R.;
    • Chasman, Daniel I.;
    • Posthuma, Danielle;
    • Lessel, Davor
    Publication type:
    Article
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    Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

    Published in:
    Journal of Human Genetics, 2007, v. 52, n. 12, p. 990, doi. 10.1007/s10038-007-0205-7
    By:
    • Castro, Maria-José;
    • Stam, Anine H.;
    • Lemos, Carolina;
    • Barros, José;
    • Gouveia, Raquel G.;
    • Martins, Isabel Pavão;
    • Koenderink, Jan B.;
    • Vanmolkot, Kaate R. J.;
    • Mendes, Alexandre P.;
    • Frants, Rune R.;
    • Ferrari, Michel D.;
    • Sequeiros, Jorge;
    • Pereira-Monteiro, José M.;
    • van den Maagdenberg, Arn M. J. M.
    Publication type:
    Article
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    First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.

    Published in:
    European Journal of Human Genetics, 2007, v. 15, n. 8, p. 884, doi. 10.1038/sj.ejhg.5201841
    By:
    • Vanmolkot, Kaate R. J.;
    • Stam, Anine H.;
    • Raman, Ashok;
    • Koenderink, Jan B.;
    • de Vries, Boukje;
    • van den Boogerd, Eelke H.;
    • van Vark, Judith;
    • van den Heuvel, Jeroen J. M. W.;
    • Bajaj, Nin;
    • Terwindt, Gisela M.;
    • Haan, Joost;
    • Frants, Rune R.;
    • Ferrari, Michel D.;
    • van den Maagdenberg, Arn M. J. M.
    Publication type:
    Article
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    Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.

    Published in:
    European Journal of Human Genetics, 2006, v. 14, n. 5, p. 555, doi. 10.1038/sj.ejhg.5201607
    By:
    • Vanmolkot, Kaate R J;
    • Kors, Esther E;
    • Turk, Ulku;
    • Turkdogan, Dylsad;
    • Keyser, Antoine;
    • Broos, Ludo A M;
    • Kia, Sima Kheradmand;
    • van den Heuvel, Jeroen J M W;
    • Black, David F;
    • Haan, Joost;
    • Frants, Rune R;
    • Barone, Virginia;
    • Ferrari, Michel D;
    • Casari, Giorgio;
    • Koenderink, Jan B;
    • van den Maagdenberg, Arn M J M
    Publication type:
    Article
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    Migraine and epilepsy: genetically linked?

    Published in:
    Expert Review of Neurotherapeutics, 2008, v. 8, n. 9, p. 1307, doi. 10.1586/14737175.8.9.1307
    By:
    • Haan, Joost;
    • van den Maagdenberg, Arn M. J. M.;
    • Brouwer, Oebele F.;
    • Ferrari, Michel D.
    Publication type:
    Article
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    Genome-wide association study reveals three susceptibility loci for common migraine in the general population.

    Published in:
    Nature Genetics, 2011, v. 43, n. 7, p. 695, doi. 10.1038/ng.856
    By:
    • Chasman, Daniel I.;
    • Schürks, Markus;
    • Anttila, Verneri;
    • de Vries, Boukje;
    • Schminke, Ulf;
    • Launer, Lenore J.;
    • Terwindt, Gisela M.;
    • van den Maagdenberg, Arn M. J. M.;
    • Fendrich, Konstanze;
    • Völzke, Henry;
    • Ernst, Florian;
    • Griffiths, Lyn R.;
    • Buring, Julie E.;
    • Kallela, Mikko;
    • Freilinger, Tobias;
    • Kubisch, Christian;
    • Ridker, Paul M.;
    • Palotie, Aarno;
    • Ferrari, Michel D.;
    • Hoffmann, Wolfgang
    Publication type:
    Article
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    C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.

    Published in:
    Nature Genetics, 2007, v. 39, n. 9, p. 1068, doi. 10.1038/ng2082
    By:
    • Richards, Anna;
    • van den Maagdenberg, Arn M. J. M.;
    • Jen, Joanna C.;
    • Kavanagh, David;
    • Bertram, Paula;
    • Spitzer, Dirk;
    • Liszewski, M. Kathryn;
    • Barilla-LaBarca, Maria-Louise;
    • Terwindt, Gisela M.;
    • Kasai, Yumi;
    • McLellan, Mike;
    • Grand, Mark Gilbert;
    • Vanmolkot, Kaate R. J.;
    • de Vries, Boukje;
    • Jijun Wan;
    • Kane, Michael J.;
    • Mamsa, Hafsa;
    • Schäfer, Ruth;
    • Stam, Anine H.;
    • Haan, Joost
    Publication type:
    Article
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    Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.

    Published in:
    Nature Genetics, 2006, v. 38, n. 7, p. 801, doi. 10.1038/ng1814
    By:
    • Rees, Mark I.;
    • Harvey, Kirsten;
    • Pearce, Brian R.;
    • Seo-Kyung Chung;
    • Duguid, Ian C.;
    • Thomas, Philip;
    • Beatty, Sarah;
    • Graham, Gail E.;
    • Armstrong, Linlea;
    • Shiang, Rita;
    • Abbott, Kim J.;
    • Zuberi, Sameer M.;
    • Stephenson, John B. P.;
    • Owen, Michael J.;
    • Tijssen, Marina A. J.;
    • van den Maagdenberg, Arn M. J. M.;
    • Smart, Trevor G.;
    • Supplisson, Stéphane;
    • Harvey, Robert J.
    Publication type:
    Article
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    Caffeine does not affect susceptibility to cortical spreading depolarization in mice.

    Published in:
    Journal of Cerebral Blood Flow & Metabolism, 2019, v. 39, n. 4, p. 740, doi. 10.1177/0271678X18768955
    By:
    • Yalcin, Nilufer;
    • Chen, Shih-Pin;
    • Yu, Esther S.;
    • Liu, Tzu-Ting;
    • Yen, Jiin-Cherng;
    • Atalay, Yahya B.;
    • Qin, Tao;
    • Celik, Furkan;
    • van den Maagdenberg, Arn M. J. M.;
    • Moskowitz, Michael A.;
    • Ayata, Cenk;
    • Eikermann-Haerter, Katharina
    Publication type:
    Article
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    Insight in Genome-Wide Association of Metabolite Quantitative Traits by Exome Sequence Analyses.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 1, p. 1, doi. 10.1371/journal.pgen.1004835
    By:
    • Demirkan, Ayşe;
    • Henneman, Peter;
    • Verhoeven, Aswin;
    • Dharuri, Harish;
    • Amin, Najaf;
    • van Klinken, Jan Bert;
    • Karssen, Lennart C.;
    • de Vries, Boukje;
    • Meissner, Axel;
    • Göraler, Sibel;
    • van den Maagdenberg, Arn M. J. M.;
    • Deelder, André M.;
    • C ’t Hoen, Peter A.;
    • van Duijn, Cornelia M.;
    • van Dijk, Ko Willems
    Publication type:
    Article
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    The NOTCH3 score: a pre-clinical CADASIL biomarker in a novel human genomic NOTCH3 transgenic mouse model with early progressive vascular NOTCH3 accumulation.

    Published in:
    Acta Neuropathologica Communications, 2015, v. 3, p. 1, doi. 10.1186/s40478-015-0268-1
    By:
    • Rutten, Julie W.;
    • Klever, Roselin R.;
    • Hegeman, Ingrid M.;
    • Poole, Dana S.;
    • Dauwerse, Hans G.;
    • Broos, Ludo A. M.;
    • Breukel, Cor;
    • Aartsma-Rus, Annemieke M.;
    • Verbeek, J. Sjef;
    • van der Weerd, Louise;
    • van Duinen, Sjoerd G.;
    • van den Maagdenberg, Arn M. J. M.;
    • Oberstein, Saskia A. J. Lesnik
    Publication type:
    Article
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    Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants.

    Published in:
    PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0185663
    By:
    • Winsvold, Bendik S.;
    • Bettella, Francesco;
    • Witoelar, Aree;
    • Anttila, Verneri;
    • Gormley, Padhraig;
    • Kurth, Tobias;
    • Terwindt, Gisela M.;
    • Freilinger, Tobias M.;
    • Frei, Oleksander;
    • Shadrin, Alexey;
    • Wang, Yunpeng;
    • Dale, Anders M.;
    • van den Maagdenberg, Arn M. J. M.;
    • Chasman, Daniel I.;
    • Nyholt, Dale R.;
    • Palotie, Aarno;
    • Andreassen, Ole A.;
    • Zwart, John-Anker;
    • null, null
    Publication type:
    Article
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    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<sub>v</sub>2.1 Knock-In Mice: Implications for Basic Mechanisms of Migraine Pain

    Published in:
    Journal of Neuroscience, 2011, v. 31, n. 10, p. 3638, doi. 10.1523/JNEUROSCI.6440-10.2011
    By:
    • Ceruti, Stefania;
    • Villa, Giovanni;
    • Fumagalli, Marta;
    • Colombo, Laura;
    • Magni, Giulia;
    • Zanardelli, Matteo;
    • Fabbretti, Elsa;
    • Verderio, Claudia;
    • van den Maagdenberg, Arn M. J. M.;
    • Nistri, Andrea;
    • Abbracchio, Maria P.
    Publication type:
    Article
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    Migraine and MTHFR C677T genotype in a population‐based sample.

    Published in:
    Annals of Neurology, 2006, v. 59, n. 2, p. 372
    By:
    • Ann I. Scher;
    • Gisela M. Terwindt;
    • W. M. Monique Verschuren;
    • Mark C. Kruit;
    • Henk J. Blom;
    • Hisanori Kowa;
    • Rune R. Frants;
    • Arn M. J. M. van den Maagdenberg;
    • Mark van Buchem;
    • Michel D. Ferrari;
    • Lenore J. Launer
    Publication type:
    Article
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