Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Published:2016-07-25 Issue:9 Volume:48 Page:1043-1048
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

van Rheenen Wouter, ,Shatunov Aleksey,Dekker Annelot M,McLaughlin Russell L,Diekstra Frank P,Pulit Sara L,van der Spek Rick A A,Võsa Urmo,de Jong Simone,Robinson Matthew R,Yang Jian^ORCID,Fogh Isabella,van Doormaal Perry TC,Tazelaar Gijs H P,Koppers Max,Blokhuis Anna M,Sproviero William^ORCID,Jones Ashley R,Kenna Kevin P,van Eijk Kristel R,Harschnitz Oliver,Schellevis Raymond D,Brands William J^ORCID,Medic Jelena,Menelaou Androniki,Vajda Alice,Ticozzi Nicola,Lin Kuang,Rogelj Boris^ORCID,Vrabec Katarina,Ravnik-Glavač Metka,Koritnik Blaž^ORCID,Zidar Janez,Leonardis Lea,Grošelj Leja Dolenc,Millecamps Stéphanie,Salachas François,Meininger Vincent,de Carvalho Mamede,Pinto Susana,Mora Jesus S,Rojas-García Ricardo,Polak Meraida,Chandran Siddharthan,Colville Shuna,Swingler Robert,Morrison Karen E,Shaw Pamela J,Hardy John,Orrell Richard W,Pittman Alan,Sidle Katie,Fratta Pietro,Malaspina Andrea,Topp Simon^ORCID,Petri Susanne,Abdulla Susanne,Drepper Carsten,Sendtner Michael,Meyer Thomas,Ophoff Roel A,Staats Kim A,Wiedau-Pazos Martina,Lomen-Hoerth Catherine,Van Deerlin Vivianna M^ORCID,Trojanowski John Q,Elman Lauren,McCluskey Leo,Basak A Nazli,Tunca Ceren,Hamzeiy Hamid,Parman Yesim,Meitinger Thomas,Lichtner Peter,Radivojkov-Blagojevic Milena,Andres Christian R,Maurel Cindy,Bensimon Gilbert,Landwehrmeyer Bernhard,Brice Alexis,Payan Christine A M,Saker-Delye Safaa,Dürr Alexandra,Wood Nicholas W,Tittmann Lukas,Lieb Wolfgang,Franke Andre,Rietschel Marcella,Cichon Sven,Nöthen Markus M,Amouyel Philippe^ORCID,Tzourio Christophe,Dartigues Jean-François,Uitterlinden Andre G,Rivadeneira Fernando^ORCID,Estrada Karol,Hofman Albert,Curtis Charles,Blauw Hylke M,van der Kooi Anneke J,de Visser Marianne,Goris An^ORCID,Weber Markus,Shaw Christopher E,Smith Bradley N,Pansarasa Orietta,Cereda Cristina,Del Bo Roberto,Comi Giacomo P,D'Alfonso Sandra,Bertolin Cinzia,Sorarù Gianni,Mazzini Letizia,Pensato Viviana,Gellera Cinzia,Tiloca Cinzia,Ratti Antonia,Calvo Andrea,Moglia Cristina,Brunetti Maura,Arcuti Simona,Capozzo Rosa,Zecca Chiara,Lunetta Christian,Penco Silvana,Riva Nilo,Padovani Alessandro,Filosto Massimiliano,Muller Bernard,Stuit Robbert Jan,Blair Ian,Zhang Katharine,McCann Emily P,Fifita Jennifer A,Nicholson Garth A,Rowe Dominic B,Pamphlett Roger^ORCID,Kiernan Matthew C,Grosskreutz Julian,Witte Otto W,Ringer Thomas,Prell Tino,Stubendorff Beatrice,Kurth Ingo^ORCID,Hübner Christian A,Leigh P Nigel,Casale Federico,Chio Adriano,Beghi Ettore,Pupillo Elisabetta,Tortelli Rosanna,Logroscino Giancarlo,Powell John,Ludolph Albert C,Weishaupt Jochen H,Robberecht Wim,Van Damme Philip,Franke Lude^ORCID,Pers Tune H,Brown Robert H,Glass Jonathan D,Landers John E,Hardiman Orla,Andersen Peter M,Corcia Philippe,Vourc'h Patrick,Silani Vincenzo,Wray Naomi R^ORCID,Visscher Peter M^ORCID,de Bakker Paul I W,van Es Michael A,Pasterkamp R Jeroen^ORCID,Lewis Cathryn M^ORCID,Breen Gerome,Al-Chalabi Ammar,van den Berg Leonard H,Veldink Jan H, , , , ,

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.3622.pdf

Reference32 articles.

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2. Al-Chalabi, A. et al. An estimate of amyotrophic lateral sclerosis heritability using twin data. J. Neurol. Neurosurg. Psychiatry 81, 1324–1326 (2010).

3. van Es, M.A. et al. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat. Genet. 41, 1083–1087 (2009).

4. Laaksovirta, H. et al. Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. Lancet Neurol. 9, 978–985 (2010).

5. Shatunov, A. et al. Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. Lancet Neurol. 9, 986–994 (2010).

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