Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

Migraine is a common episodic neurological disorder, typically presenting with recurrent attacks of severe headache and autonomic dysfunction. Apart from rare monogenic subtypes, no genetic or molecular markers for migraine have been convincingly established. We identified the minor allele of rs1835...

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Main Authors: Anttila, Verneri, Stefansson, Hreinn, Kallela, Mikko, Todt, Unda, Terwindt, Gisela M, Calafato, M Stella, Nyholt, Dale R, Dimas, Antigone S, Freilinger, Tobias, Müller-Myhsok, Bertram, Artto, Ville, Inouye, Michael, Alakurtti, Kirsi, Kaunisto, Mari A, Hämäläinen, Eija, de Vries, Boukje, Stam, Anine H, Weller, Claudia M, Heinze, Axel, Heinze-Kuhn, Katja, Goebel, Ingrid, Borck, Guntram, Göbel, Hartmut, Steinberg, Stacy, Wolf, Christiane, Björnsson, Asgeir, Gudmundsson, Gretar, Kirchmann, Malene, Hauge, Anne, Werge, Thomas, Schoenen, Jean, Eriksson, Johan G, Hagen, Knut, Stovner, Lars, Wichmann, H-Erich, Meitinger, Thomas, Alexander, Michael, Moebus, Susanne, Schreiber, Stefan, Aulchenko, Yurii S, Breteler, Monique M B, Uitterlinden, Andre G, Hofman, Albert, van Duijn, Cornelia M, Tikka-Kleemola, Päivi, Vepsäläinen, Salli, Lucae, Susanne, Tozzi, Federica, Muglia, Pierandrea, Barrett, Jeffrey, Kaprio, Jaakko, Färkkilä, Markus, Peltonen, Leena, Stefansson, Kari, Zwart, John-Anker, Ferrari, Michel D, Olesen, Jes, Daly, Mark, Wessman, Maija, van den Maagdenberg, Arn M J M, Dichgans, Martin, Kubisch, Christian, Dermitzakis, Emmanouil T, Frants, Rune R, Palotie, Aarno
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2948563/
https://ncbi.nlm.nih.gov/pubmed/20802479
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.652
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