Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine-Reference-Cited by-同舟云学术

Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine

Published:2013-01-07 Issue:5 Volume:20 Page:765-772
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Esserlind A.-L.¹,Christensen A. F.¹,Le H.¹,Kirchmann M.¹,Hauge A. W.¹,Toyserkani N. M.¹,Hansen T.,Grarup N.²,Werge T.³,Steinberg S.⁴,Bettella F.⁴,Stefansson H.⁴,Olesen J.¹

Affiliation:

1. Department of Neurology; The Danish Headache Center; Glostrup Hospital; University of Copenhagen; Glostrup; Denmark

2. The Novo Nordisk Foundation Center for Basic Metabolic Research; Faculty of Health and Medical Sciences; University of Copenhagen; Denmark

3. Institute of Biological Psychiatry; Mental Health Center Sct. Hans; University of Copenhagen; Roskilde; Denmark

4. deCODE Genetics; Sturlugata 8 IS-101; Reykjavik; Iceland

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ene.12055/fullpdf

Reference33 articles.

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2. Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine;Dichgans;Lancet,2005

3. A gene for familial hemiplegic migraine maps to chromosome 19;Joutel;Nat Genet,1993

4. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4;Ophoff;Cell,1996

5. Increased familial risk and evidence of genetic factor in migraine;Russell;BMJ,1995

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