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Genome-wide association analysis identifies susceptibility loci for migraine without aura.

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Genome-wide association analysis identifies susceptibility loci for migraine without aura. / Freilinger, Tobias; Anttila, Verneri; de Vries, Boukje; Malik, Rainer; Kallela, Mikko; Terwindt, Gisela M; Pozo-Rosich, Patricia; Winsvold, Bendik; Nyholt, Dale R; Oosterhout, van; Willebrordus, P J; Artto, Ville; Todt, Unda; Hämäläinen, Eija; Fernández-Morales, Jèssica; Louter, Mark A; Kaunisto, Mari A; Schoenen, Jean; Raitakari, Olli; Lehtimäki, Terho; Vila-Pueyo, Marta; Göbel, Hartmut; Wichmann, Erich; Sintas, Cèlia; Uitterlinden, Andre G; Hofman, Albert; Rivadeneira, Fernando; Heinze, Axel; Tronvik, Erling; Duijn, van; Cornelia, M; Kaprio, Jaakko; Cormand, Bru; Wessman, Maija; Frants, Rune R; Meitinger, Thomas; Müller-Myhsok, Bertram; Zwart, John-Anker; Färkkilä, Markus; Kubisch, Christian; Ferrari, Michel D; Palotie, Aarno; Dichgans, Martin; Maagdenberg, van den; Arn, M J M; Consortium, International Headache Genetics.

In: NAT GENET, Vol. 44, No. 7, 7, 2012, p. 777-782.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Freilinger, T, Anttila, V, de Vries, B, Malik, R, Kallela, M, Terwindt, GM, Pozo-Rosich, P, Winsvold, B, Nyholt, DR, Oosterhout, V, Willebrordus, PJ, Artto, V, Todt, U, Hämäläinen, E, Fernández-Morales, J, Louter, MA, Kaunisto, MA, Schoenen, J, Raitakari, O, Lehtimäki, T, Vila-Pueyo, M, Göbel, H, Wichmann, E, Sintas, C, Uitterlinden, AG, Hofman, A, Rivadeneira, F, Heinze, A, Tronvik, E, Duijn, V, Cornelia, M, Kaprio, J, Cormand, B, Wessman, M, Frants, RR, Meitinger, T, Müller-Myhsok, B, Zwart, J-A, Färkkilä, M, Kubisch, C, Ferrari, MD, Palotie, A, Dichgans, M, Maagdenberg, VD, Arn, MJM & Consortium, IHG 2012, 'Genome-wide association analysis identifies susceptibility loci for migraine without aura.', NAT GENET, vol. 44, no. 7, 7, pp. 777-782. <http://www.ncbi.nlm.nih.gov/pubmed/22683712?dopt=Citation>

APA

Freilinger, T., Anttila, V., de Vries, B., Malik, R., Kallela, M., Terwindt, G. M., Pozo-Rosich, P., Winsvold, B., Nyholt, D. R., Oosterhout, V., Willebrordus, P. J., Artto, V., Todt, U., Hämäläinen, E., Fernández-Morales, J., Louter, M. A., Kaunisto, M. A., Schoenen, J., Raitakari, O., ... Consortium, I. H. G. (2012). Genome-wide association analysis identifies susceptibility loci for migraine without aura. NAT GENET, 44(7), 777-782. [7]. http://www.ncbi.nlm.nih.gov/pubmed/22683712?dopt=Citation

Vancouver

Freilinger T, Anttila V, de Vries B, Malik R, Kallela M, Terwindt GM et al. Genome-wide association analysis identifies susceptibility loci for migraine without aura. NAT GENET. 2012;44(7):777-782. 7.

Bibtex

@article{1cc3a8ba4cbf436e85a61185a2c15bb9,
title = "Genome-wide association analysis identifies susceptibility loci for migraine without aura.",
abstract = "Migraine without aura is the most common form of migraine, characterized by recurrent disabling headache and associated autonomic symptoms. To identify common genetic variants associated with this migraine type, we analyzed genome-wide association data of 2,326 clinic-based German and Dutch individuals with migraine without aura and 4,580 population-matched controls. We selected SNPs from 12 loci with 2 or more SNPs associated with P values of",
keywords = "Adult, Humans, Male, Female, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Case-Control Studies, Genetic Loci, Genome-Wide Association Study/methods, Microfilament Proteins/genetics, Low Density Lipoprotein Receptor-Related Protein-1/genetics, MADS Domain Proteins/genetics, Migraine without Aura/*genetics, Myogenic Regulatory Factors/genetics, Protein-Serine-Threonine Kinases/genetics, Receptors, Transforming Growth Factor beta/genetics, TRPM Cation Channels/genetics, Adult, Humans, Male, Female, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Case-Control Studies, Genetic Loci, Genome-Wide Association Study/methods, Microfilament Proteins/genetics, Low Density Lipoprotein Receptor-Related Protein-1/genetics, MADS Domain Proteins/genetics, Migraine without Aura/*genetics, Myogenic Regulatory Factors/genetics, Protein-Serine-Threonine Kinases/genetics, Receptors, Transforming Growth Factor beta/genetics, TRPM Cation Channels/genetics",
author = "Tobias Freilinger and Verneri Anttila and {de Vries}, Boukje and Rainer Malik and Mikko Kallela and Terwindt, {Gisela M} and Patricia Pozo-Rosich and Bendik Winsvold and Nyholt, {Dale R} and van Oosterhout and Willebrordus, {P J} and Ville Artto and Unda Todt and Eija H{\"a}m{\"a}l{\"a}inen and J{\`e}ssica Fern{\'a}ndez-Morales and Louter, {Mark A} and Kaunisto, {Mari A} and Jean Schoenen and Olli Raitakari and Terho Lehtim{\"a}ki and Marta Vila-Pueyo and Hartmut G{\"o}bel and Erich Wichmann and C{\`e}lia Sintas and Uitterlinden, {Andre G} and Albert Hofman and Fernando Rivadeneira and Axel Heinze and Erling Tronvik and van Duijn and M Cornelia and Jaakko Kaprio and Bru Cormand and Maija Wessman and Frants, {Rune R} and Thomas Meitinger and Bertram M{\"u}ller-Myhsok and John-Anker Zwart and Markus F{\"a}rkkil{\"a} and Christian Kubisch and Ferrari, {Michel D} and Aarno Palotie and Martin Dichgans and Maagdenberg, {van den} and Arn, {M J M} and Consortium, {International Headache Genetics}",
year = "2012",
language = "English",
volume = "44",
pages = "777--782",
journal = "NAT GENET",
issn = "1061-4036",
publisher = "NATURE PUBLISHING GROUP",
number = "7",

}

RIS

TY - JOUR

T1 - Genome-wide association analysis identifies susceptibility loci for migraine without aura.

AU - Freilinger, Tobias

AU - Anttila, Verneri

AU - de Vries, Boukje

AU - Malik, Rainer

AU - Kallela, Mikko

AU - Terwindt, Gisela M

AU - Pozo-Rosich, Patricia

AU - Winsvold, Bendik

AU - Nyholt, Dale R

AU - Oosterhout, van

AU - Willebrordus, P J

AU - Artto, Ville

AU - Todt, Unda

AU - Hämäläinen, Eija

AU - Fernández-Morales, Jèssica

AU - Louter, Mark A

AU - Kaunisto, Mari A

AU - Schoenen, Jean

AU - Raitakari, Olli

AU - Lehtimäki, Terho

AU - Vila-Pueyo, Marta

AU - Göbel, Hartmut

AU - Wichmann, Erich

AU - Sintas, Cèlia

AU - Uitterlinden, Andre G

AU - Hofman, Albert

AU - Rivadeneira, Fernando

AU - Heinze, Axel

AU - Tronvik, Erling

AU - Duijn, van

AU - Cornelia, M

AU - Kaprio, Jaakko

AU - Cormand, Bru

AU - Wessman, Maija

AU - Frants, Rune R

AU - Meitinger, Thomas

AU - Müller-Myhsok, Bertram

AU - Zwart, John-Anker

AU - Färkkilä, Markus

AU - Kubisch, Christian

AU - Ferrari, Michel D

AU - Palotie, Aarno

AU - Dichgans, Martin

AU - Maagdenberg, van den

AU - Arn, M J M

AU - Consortium, International Headache Genetics

PY - 2012

Y1 - 2012

N2 - Migraine without aura is the most common form of migraine, characterized by recurrent disabling headache and associated autonomic symptoms. To identify common genetic variants associated with this migraine type, we analyzed genome-wide association data of 2,326 clinic-based German and Dutch individuals with migraine without aura and 4,580 population-matched controls. We selected SNPs from 12 loci with 2 or more SNPs associated with P values of

AB - Migraine without aura is the most common form of migraine, characterized by recurrent disabling headache and associated autonomic symptoms. To identify common genetic variants associated with this migraine type, we analyzed genome-wide association data of 2,326 clinic-based German and Dutch individuals with migraine without aura and 4,580 population-matched controls. We selected SNPs from 12 loci with 2 or more SNPs associated with P values of

KW - Adult

KW - Humans

KW - Male

KW - Female

KW - Genetic Predisposition to Disease

KW - Polymorphism, Single Nucleotide

KW - Case-Control Studies

KW - Genetic Loci

KW - Genome-Wide Association Study/methods

KW - Microfilament Proteins/genetics

KW - Low Density Lipoprotein Receptor-Related Protein-1/genetics

KW - MADS Domain Proteins/genetics

KW - Migraine without Aura/genetics

KW - Myogenic Regulatory Factors/genetics

KW - Protein-Serine-Threonine Kinases/genetics

KW - Receptors, Transforming Growth Factor beta/genetics

KW - TRPM Cation Channels/genetics

KW - Adult

KW - Humans

KW - Male

KW - Female

KW - Genetic Predisposition to Disease

KW - Polymorphism, Single Nucleotide

KW - Case-Control Studies

KW - Genetic Loci

KW - Genome-Wide Association Study/methods

KW - Microfilament Proteins/genetics

KW - Low Density Lipoprotein Receptor-Related Protein-1/genetics

KW - MADS Domain Proteins/genetics

KW - Migraine without Aura/genetics

KW - Myogenic Regulatory Factors/genetics

KW - Protein-Serine-Threonine Kinases/genetics

KW - Receptors, Transforming Growth Factor beta/genetics

KW - TRPM Cation Channels/genetics

M3 - SCORING: Journal article

VL - 44

SP - 777

EP - 782

JO - NAT GENET

JF - NAT GENET

SN - 1061-4036

IS - 7

M1 - 7

ER -