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

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Standard

Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine. / Esserlind, A-L; Christensen, A F; Le, H; Kirchmann, M; Hauge, A W; Toyserkani, N M; Hansen, Torben; Grarup, Niels; Werge, T; Steinberg, S; Bettella, F; Stefansson, H; Olesen, J.

I: European Journal of Neurology, Bind 20, Nr. 5, 05.2013, s. 765-772.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Esserlind, A-L, Christensen, AF, Le, H, Kirchmann, M, Hauge, AW, Toyserkani, NM, Hansen, T, 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, bind 20, nr. 5, s. 765-772. https://doi.org/10.1111/ene.12055

APA

Esserlind, A-L., Christensen, A. F., Le, H., Kirchmann, M., Hauge, A. W., Toyserkani, N. M., Hansen, T., 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, 20(5), 765-772. https://doi.org/10.1111/ene.12055

Vancouver

Esserlind A-L, Christensen AF, Le H, Kirchmann M, Hauge AW, Toyserkani NM o.a. Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine. European Journal of Neurology. 2013 maj;20(5):765-772. https://doi.org/10.1111/ene.12055

Author

Esserlind, A-L ; Christensen, A F ; Le, H ; Kirchmann, M ; Hauge, A W ; Toyserkani, N M ; Hansen, Torben ; Grarup, Niels ; Werge, T ; Steinberg, S ; Bettella, F ; Stefansson, H ; Olesen, J. / Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine. I: European Journal of Neurology. 2013 ; Bind 20, Nr. 5. s. 765-772.

Bibtex

@article{17be071ffc1744a28a11c6e5d908c3c8,

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

abstract = "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 <5 × 10(-8) ). We aimed to evaluate the top association single nucleotide polymorphisms (SNPs) from the discovery set by Chasman et al. in a primarily clinic-based Danish and Icelandic cohort.",

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

volume = "20",

pages = "765--772",

journal = "European Journal of Neurology",

issn = "1351-5101",

publisher = "Wiley-Blackwell",

number = "5",

}

RIS

TY - JOUR

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

AU - Esserlind, A-L

AU - Christensen, A F

AU - Le, H

AU - Kirchmann, M

AU - Hauge, A W

AU - Toyserkani, N M

AU - Hansen, Torben

AU - Grarup, Niels

AU - Werge, T

AU - Steinberg, S

AU - Bettella, F

AU - Stefansson, H

AU - Olesen, J

PY - 2013/5

Y1 - 2013/5

N2 - 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 <5 × 10(-8) ). We aimed to evaluate the top association single nucleotide polymorphisms (SNPs) from the discovery set by Chasman et al. in a primarily clinic-based Danish and Icelandic cohort.

AB - 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 <5 × 10(-8) ). We aimed to evaluate the top association single nucleotide polymorphisms (SNPs) from the discovery set by Chasman et al. in a primarily clinic-based Danish and Icelandic cohort.

U2 - 10.1111/ene.12055

DO - 10.1111/ene.12055

M3 - Journal article

C2 - 23294458

VL - 20

SP - 765

EP - 772

JO - European Journal of Neurology

JF - European Journal of Neurology

SN - 1351-5101

IS - 5

ER -

ID: 48610525