Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Céline Bellenguez; Steve Bevan; Andreas Gschwendtner; Chris C. A. Spencer; A I Burgess; Matti Pirinen; Caroline Jackson; Matthew Traylor; Amy Strange; Zhan Su; Gavin Band; Paul D. Syme; Rainer Malik; Joanna Pera; Bo Norrving; Robin Lemmens; Colin L. Freeman; Renata Schanz; Tom James; Deborah Poole; Lee Murphy; Helen Segal; Lynelle Cortellini; Yu‐Ching Cheng; Daniel Woo; Michael A. Nalls; Bertram Müller‐Myhsok; Christa Meisinger; Udo Seedorf; Helen Ross‐Adams; Steven Boonen; Dorota Włoch-Kopeć; Valerie Valant; Julia Slark; Karen L. Furie; Hossein Delavaran; Cordelia Langford; Panos Deloukas; Sarah Edkins; Sarah Hunt; Emma Gray; Serge Dronov; Leena Peltonen; Sólveig Grétarsdóttir; Gudmar Thorleifsson; Unnur Þorsteinsdóttir; Kāri Stefánsson; Giorgio B. Boncoraglio; Eugenio Parati; John Attia; Elizabeth Holliday; Christopher Levi; Maria-Grazia Franzosi; Anuj Goel; Anna Helgadóttir; Jenefer M. Blackwell; Elvira Bramon; Matthew A. Brown; Juan P. Casas; Aiden Corvin; Audrey Duncanson; Janusz Jankowski; Christopher G. Mathew; Colin N A Palmer; Robert Plomin; Anna Rautanen; Stephen Sawcer; Richard C. Trembath; Ananth C. Viswanathan; Nicholas Wood; Bradford B. Worrall; Steven J. Kittner; Braxton D. Mitchell; Brett Kissela; James F. Meschia; Vincent Thijs; Arne Lindgren; Mary Joan MacLeod; Agnieszka Słowik; James Walters; Jonathan Rosand; Pankaj Sharma; Martin Farrall; Cathie Sudlow; Peter M. Rothwell; Martin Dichgans; Peter Donnelly; Hugh S. Markus

doi:10.1038/ng.1081

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Céline Bellenguez(Centre for Human Genetics), Steve Bevan(St George's, University of London), Andreas Gschwendtner(Ludwig-Maximilians-Universität München), Chris C. A. Spencer(Centre for Human Genetics), A I Burgess(University of Oxford), Matti Pirinen(Centre for Human Genetics), Caroline Jackson(University of Edinburgh), Matthew Traylor(St George's, University of London), Amy Strange(Centre for Human Genetics), Zhan Su(Centre for Human Genetics), Gavin Band(Centre for Human Genetics), Paul D. Syme(University of Aberdeen), Rainer Malik(Ludwig-Maximilians-Universität München), Joanna Pera(Jagiellonian University), Bo Norrving(Lund University), Robin Lemmens(Vlaams Instituut voor Biotechnologie), Colin L. Freeman(Centre for Human Genetics), Renata Schanz(Imperial College London), Tom James(St George's, University of London), Deborah Poole(University of Oxford), Lee Murphy(Western General Hospital), Helen Segal(University of Oxford), Lynelle Cortellini(Broad Institute), Yu‐Ching Cheng(University of Maryland, Baltimore), Daniel Woo(University of Cincinnati Medical Center), Michael A. Nalls(National Institute on Aging), Bertram Müller‐Myhsok(Max Planck Institute of Psychiatry), Christa Meisinger(Helmholtz Zentrum München), Udo Seedorf(University of Münster), Helen Ross‐Adams(Jagiellonian University), Steven Boonen(KU Leuven), Dorota Włoch-Kopeć(Jagiellonian University), Valerie Valant(Broad Institute), Julia Slark(Imperial College London), Karen L. Furie(Massachusetts General Hospital), Hossein Delavaran(Lund University), Cordelia Langford(Wellcome Sanger Institute), Panos Deloukas(Wellcome Sanger Institute), Sarah Edkins(Wellcome Sanger Institute), Sarah Hunt(Wellcome Sanger Institute), Emma Gray(Wellcome Sanger Institute), Serge Dronov(Wellcome Sanger Institute), Leena Peltonen(Wellcome Sanger Institute), Sólveig Grétarsdóttir(deCODE Genetics (Iceland)), Gudmar Thorleifsson(deCODE Genetics (Iceland)), Unnur Þorsteinsdóttir(deCODE Genetics (Iceland)), Kāri Stefánsson(deCODE Genetics (Iceland)), Giorgio B. Boncoraglio(Istituti di Ricovero e Cura a Carattere Scientifico), Eugenio Parati(Istituti di Ricovero e Cura a Carattere Scientifico), John Attia(Hunter Medical Research Institute), Elizabeth Holliday(Hunter Medical Research Institute), Christopher Levi(Hunter Medical Research Institute), Maria-Grazia Franzosi(Mario Negri Institute for Pharmacological Research), Anuj Goel(Centre for Human Genetics), Anna Helgadóttir(deCODE Genetics (Iceland)), Jenefer M. Blackwell(The University of Western Australia), Elvira Bramon(King's College London), Matthew A. Brown(The University of Queensland), Juan P. Casas(London School of Hygiene & Tropical Medicine), Aiden Corvin(Trinity College Dublin), Audrey Duncanson(Wellcome Trust), Janusz Jankowski(University of Oxford), Christopher G. Mathew(Guy's Hospital), Colin N A Palmer(Ninewells Hospital), Robert Plomin(King's College London), Anna Rautanen(Centre for Human Genetics), Stephen Sawcer(University of Cambridge), Richard C. Trembath(Guy's Hospital), Ananth C. Viswanathan(National Health Service), Nicholas Wood(National Hospital for Neurology and Neurosurgery), Bradford B. Worrall(University of Virginia), Steven J. Kittner(University of Maryland, Baltimore), Braxton D. Mitchell(University of Maryland, Baltimore), Brett Kissela(University of Cincinnati Medical Center), James F. Meschia(Mayo Clinic in Florida), Vincent Thijs(Vlaams Instituut voor Biotechnologie), Arne Lindgren(Lund University), Mary Joan MacLeod(University of Aberdeen), Agnieszka Słowik(Jagiellonian University), James Walters(University of Glasgow), Jonathan Rosand(Broad Institute), Pankaj Sharma(Imperial College London), Martin Farrall(Centre for Human Genetics), Cathie Sudlow(University of Edinburgh), Peter M. Rothwell(University of Oxford), Martin Dichgans(Ludwig-Maximilians-Universität München), Peter Donnelly(Centre for Human Genetics), Hugh S. Markus(St George's, University of London)

Nature Genetics

February 5, 2012

10.1038/ng.1081

Cited by 417Open Access

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