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

A L Esserlind; Anne Francke  Christensen; H Le; M Kirchmann; A W Hauge; N M Toyserkani; Torben Lindskov Hansen; Niels Grarup; T Werge; S Steinberg; F Bettella; H Stefansson; Jes Olesen

doi:10.1111/ene.12055

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

A L Esserlind, Anne Francke Christensen, H Le, M Kirchmann, A W Hauge, N M Toyserkani, Torben Lindskov Hansen, Niels Grarup, T Werge, S Steinberg, F Bettella, H Stefansson, Jes Olesen

65 Citations (Scopus)

Abstract

BACKGROUND AND PURPOSE: Genetic factors contribute to the aetiology of the prevalent form of migraine without aura (MO) and migraine with typical aura (MTA). Due to the complex inheritance of MO and MTA, the genetic background is still not fully established. In a population-based genome-wide association study by Chasman et al. (Nat Genet 2011: 43: 695-698), three common variants were found to confer risk of migraine at a genome-wide significant level (P

Original language	English
Journal	European Journal of Neurology
Pages (from-to)	765-772
Number of pages	8
ISSN	1351-5101
DOIs	https://doi.org/10.1111/ene.12055
Publication status	Published - May 2013

Access to Document

10.1111/ene.12055

Cite this

Esserlind, A. L., Christensen, A. F., Le, H., Kirchmann, M., Hauge, A. W., Toyserkani, N. M., Hansen, T. L., Grarup, N., Werge, T., Steinberg, S., Bettella, F., Stefansson, H., & Olesen, J. (2013). Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine. European Journal of Neurology, 765-772. https://doi.org/10.1111/ene.12055

@article{28bceaa74cd3464cbbb6427be1d3e1b3,

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

abstract = "BACKGROUND AND PURPOSE: Genetic factors contribute to the aetiology of the prevalent form of migraine without aura (MO) and migraine with typical aura (MTA). Due to the complex inheritance of MO and MTA, the genetic background is still not fully established. In a population-based genome-wide association study by Chasman et al. (Nat Genet 2011: 43: 695-698), three common variants were found to confer risk of migraine at a genome-wide significant level (P ",

author = "Esserlind, {A L} and Christensen, {Anne Francke} and H Le and M Kirchmann and Hauge, {A W} and Toyserkani, {N M} and Hansen, {Torben Lindskov} and Niels Grarup and T Werge and S Steinberg and F Bettella and H Stefansson and Jes Olesen",

note = "{\textcopyright} 2013 The Author(s) European Journal of Neurology {\textcopyright} 2013 EFNS.",

year = "2013",

month = may,

doi = "10.1111/ene.12055",

language = "English",

pages = "765--772",

journal = "European Journal of Neurology",

issn = "1351-5101",

publisher = "Wiley-Blackwell Publishing Ltd",

}

TY - JOUR

T1 - Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine

AU - Esserlind, A L

AU - Christensen, Anne Francke

AU - Le, H

AU - Kirchmann, M

AU - Hauge, A W

AU - Toyserkani, N M

AU - Hansen, Torben Lindskov

AU - Grarup, Niels

AU - Werge, T

AU - Steinberg, S

AU - Bettella, F

AU - Stefansson, H

AU - Olesen, Jes

PY - 2013/5

Y1 - 2013/5

N2 - BACKGROUND AND PURPOSE: Genetic factors contribute to the aetiology of the prevalent form of migraine without aura (MO) and migraine with typical aura (MTA). Due to the complex inheritance of MO and MTA, the genetic background is still not fully established. In a population-based genome-wide association study by Chasman et al. (Nat Genet 2011: 43: 695-698), three common variants were found to confer risk of migraine at a genome-wide significant level (P

AB - BACKGROUND AND PURPOSE: Genetic factors contribute to the aetiology of the prevalent form of migraine without aura (MO) and migraine with typical aura (MTA). Due to the complex inheritance of MO and MTA, the genetic background is still not fully established. In a population-based genome-wide association study by Chasman et al. (Nat Genet 2011: 43: 695-698), three common variants were found to confer risk of migraine at a genome-wide significant level (P

U2 - 10.1111/ene.12055

DO - 10.1111/ene.12055

M3 - Journal article

C2 - 23294458

SN - 1351-5101

SP - 765

EP - 772

JO - European Journal of Neurology

JF - European Journal of Neurology

ER -

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

Abstract

Access to Document

Fingerprint

Cite this