Large genome-wide association study identifies three novel risk variants for restless legs syndrome

Didriksen, Nawaz, et al. identify three novel genetic risk variants for restless legs syndrome and confirm 19 out of 20 previously reported variants through a genome-wide association meta-analysis including nearly half a million individuals. Using expression QTL analysis, they also find that a subse...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Maria Didriksen, Muhammad Sulaman Nawaz, Joseph Dowsett, Steven Bell, Christian Erikstrup, Ole B. Pedersen, Erik Sørensen, Poul J. Jennum, Kristoffer S. Burgdorf, Brendan Burchell, Adam S. Butterworth, Nicole Soranzo, David B. Rye, Lynn Marie Trotti, Prabhjyot Saini, Lilja Stefansdottir, Sigurdur H. Magnusson, Gudmar Thorleifsson, Thordur Sigmundsson, Albert P. Sigurdsson, Katja Van Den Hurk, Franke Quee, Michael W. T. Tanck, Willem H. Ouwehand, David J. Roberts, Eric J. Earley, Michael P. Busch, Alan E. Mast, Grier P. Page, John Danesh, Emanuele Di Angelantonio, Hreinn Stefansson, Henrik Ullum, Kari Stefansson
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2020
Materias:
Acceso en línea:https://doaj.org/article/b804eef352554c768c94ad94c5a8a74a
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:b804eef352554c768c94ad94c5a8a74a
record_format dspace
spelling oai:doaj.org-article:b804eef352554c768c94ad94c5a8a74a2021-12-02T16:19:51ZLarge genome-wide association study identifies three novel risk variants for restless legs syndrome10.1038/s42003-020-01430-12399-3642https://doaj.org/article/b804eef352554c768c94ad94c5a8a74a2020-11-01T00:00:00Zhttps://doi.org/10.1038/s42003-020-01430-1https://doaj.org/toc/2399-3642Didriksen, Nawaz, et al. identify three novel genetic risk variants for restless legs syndrome and confirm 19 out of 20 previously reported variants through a genome-wide association meta-analysis including nearly half a million individuals. Using expression QTL analysis, they also find that a subset of these loci may have a causal effect on nearby gene expression.Maria DidriksenMuhammad Sulaman NawazJoseph DowsettSteven BellChristian ErikstrupOle B. PedersenErik SørensenPoul J. JennumKristoffer S. BurgdorfBrendan BurchellAdam S. ButterworthNicole SoranzoDavid B. RyeLynn Marie TrottiPrabhjyot SainiLilja StefansdottirSigurdur H. MagnussonGudmar ThorleifssonThordur SigmundssonAlbert P. SigurdssonKatja Van Den HurkFranke QueeMichael W. T. TanckWillem H. OuwehandDavid J. RobertsEric J. EarleyMichael P. BuschAlan E. MastGrier P. PageJohn DaneshEmanuele Di AngelantonioHreinn StefanssonHenrik UllumKari StefanssonNature PortfolioarticleBiology (General)QH301-705.5ENCommunications Biology, Vol 3, Iss 1, Pp 1-9 (2020)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Maria Didriksen
Muhammad Sulaman Nawaz
Joseph Dowsett
Steven Bell
Christian Erikstrup
Ole B. Pedersen
Erik Sørensen
Poul J. Jennum
Kristoffer S. Burgdorf
Brendan Burchell
Adam S. Butterworth
Nicole Soranzo
David B. Rye
Lynn Marie Trotti
Prabhjyot Saini
Lilja Stefansdottir
Sigurdur H. Magnusson
Gudmar Thorleifsson
Thordur Sigmundsson
Albert P. Sigurdsson
Katja Van Den Hurk
Franke Quee
Michael W. T. Tanck
Willem H. Ouwehand
David J. Roberts
Eric J. Earley
Michael P. Busch
Alan E. Mast
Grier P. Page
John Danesh
Emanuele Di Angelantonio
Hreinn Stefansson
Henrik Ullum
Kari Stefansson
Large genome-wide association study identifies three novel risk variants for restless legs syndrome
description Didriksen, Nawaz, et al. identify three novel genetic risk variants for restless legs syndrome and confirm 19 out of 20 previously reported variants through a genome-wide association meta-analysis including nearly half a million individuals. Using expression QTL analysis, they also find that a subset of these loci may have a causal effect on nearby gene expression.
format article
author Maria Didriksen
Muhammad Sulaman Nawaz
Joseph Dowsett
Steven Bell
Christian Erikstrup
Ole B. Pedersen
Erik Sørensen
Poul J. Jennum
Kristoffer S. Burgdorf
Brendan Burchell
Adam S. Butterworth
Nicole Soranzo
David B. Rye
Lynn Marie Trotti
Prabhjyot Saini
Lilja Stefansdottir
Sigurdur H. Magnusson
Gudmar Thorleifsson
Thordur Sigmundsson
Albert P. Sigurdsson
Katja Van Den Hurk
Franke Quee
Michael W. T. Tanck
Willem H. Ouwehand
David J. Roberts
Eric J. Earley
Michael P. Busch
Alan E. Mast
Grier P. Page
John Danesh
Emanuele Di Angelantonio
Hreinn Stefansson
Henrik Ullum
Kari Stefansson
author_facet Maria Didriksen
Muhammad Sulaman Nawaz
Joseph Dowsett
Steven Bell
Christian Erikstrup
Ole B. Pedersen
Erik Sørensen
Poul J. Jennum
Kristoffer S. Burgdorf
Brendan Burchell
Adam S. Butterworth
Nicole Soranzo
David B. Rye
Lynn Marie Trotti
Prabhjyot Saini
Lilja Stefansdottir
Sigurdur H. Magnusson
Gudmar Thorleifsson
Thordur Sigmundsson
Albert P. Sigurdsson
Katja Van Den Hurk
Franke Quee
Michael W. T. Tanck
Willem H. Ouwehand
David J. Roberts
Eric J. Earley
Michael P. Busch
Alan E. Mast
Grier P. Page
John Danesh
Emanuele Di Angelantonio
Hreinn Stefansson
Henrik Ullum
Kari Stefansson
author_sort Maria Didriksen
title Large genome-wide association study identifies three novel risk variants for restless legs syndrome
title_short Large genome-wide association study identifies three novel risk variants for restless legs syndrome
title_full Large genome-wide association study identifies three novel risk variants for restless legs syndrome
title_fullStr Large genome-wide association study identifies three novel risk variants for restless legs syndrome
title_full_unstemmed Large genome-wide association study identifies three novel risk variants for restless legs syndrome
title_sort large genome-wide association study identifies three novel risk variants for restless legs syndrome
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/b804eef352554c768c94ad94c5a8a74a
work_keys_str_mv AT mariadidriksen largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT muhammadsulamannawaz largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT josephdowsett largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT stevenbell largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT christianerikstrup largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT olebpedersen largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT eriksørensen largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT pouljjennum largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT kristoffersburgdorf largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT brendanburchell largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT adamsbutterworth largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT nicolesoranzo largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT davidbrye largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT lynnmarietrotti largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT prabhjyotsaini largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT liljastefansdottir largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT sigurdurhmagnusson largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT gudmarthorleifsson largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT thordursigmundsson largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT albertpsigurdsson largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT katjavandenhurk largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT frankequee largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT michaelwttanck largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT willemhouwehand largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT davidjroberts largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT ericjearley largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT michaelpbusch largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT alanemast largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT grierppage largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT johndanesh largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT emanuelediangelantonio largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT hreinnstefansson largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT henrikullum largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
AT karistefansson largegenomewideassociationstudyidentifiesthreenovelriskvariantsforrestlesslegssyndrome
_version_ 1718384193819377664