Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

Author:

Mitrovič Mitja,Patsopoulos Nikolaos A.,Beecham Ashley H.,Dankowski Theresa,Goris An,Dubois Bénédicte,D’hooghe Marie B.,Lemmens Robin,Van Damme Philip,Søndergaard Helle Bach,Sellebjerg Finn,Sorensen Per Soelberg,Ullum Henrik,Thørner Lise W.,Werge Thomas,Saarela Janna,Cournu-Rebeix Isabelle,Damotte Vincent,Fontaine Bertrand,Guillot-Noel Lena,Lathrop Mark,Vukusik Sandra,Gourraud Pierre-Antoine,Andlauer Till F.M.,Pongratz Viola,Buck Dorothea,Gasperi Christiane,Bayas Antonios,Heesen Christoph,Kümpfel Tania,Linker Ralf,Paul Friedemann,Stangel Martin,Tackenberg Björn,Bergh Florian Then,Warnke Clemens,Wiendl Heinz,Wildemann Brigitte,Zettl Uwe,Ziemann Ulf,Tumani Hayrettin,Gold Ralf,Grummel Verena,Hemmer Bernhard,Knier Benjamin,Lill Christina M.,Luessi Felix,Dardiotis Efthimios,Agliardi Cristina,Barizzone Nadia,Mascia Elisabetta,Bernardinelli Luisa,Comi Giancarlo,Cusi Daniele,Esposito Federica,Ferrè Laura,Comi Cristoforo,Galimberti Daniela,Leone Maurizio A.,Sorosina Melissa,Mescheriakova Julia,Hintzen Rogier,van Duijn Cornelia,Teunissen Charlotte E.,Bos Steffan D.,Myhr Kjell-Morten,Celius Elisabeth G.,Lie Benedicte A.,Spurkland Anne,Comabella Manuel,Montalban Xavier,Alfredsson Lars,Stridh Pernilla,Hillert Jan,Jagodic Maja,Piehl Fredrik,Jelčić Ilijas,Martin Roland,Sospedra Mireia,Ban Maria,Hawkins Clive,Hysi Pirro,Kalra Seema,Karpe Fredrik,Khadake Jyoti,Lachance Genevieve,Neville Matthew,Santaniello Adam,Caillier Stacy J.,Calabresi Peter A.,Cree Bruce A.C.,Cross Anne,Davis Mary F.,Haines Jonathan L.,de Bakker Paul I.W.,Delgado Silvia,Dembele Marieme,Edwards Keith,Fitzgerald Kathryn C.,Hakonarson Hakon,Konidari Ioanna,Lathi Ellen,Manrique Clara P.,Pericak-Vance Margaret A.,Piccio Laura,Schaefer Cathy,McCabe Cristin,Weiner Howard,Goldstein Jacqueline,Olsson Tomas,Hadjigeorgiou Georgios,Taylor Bruce,Tajouri Lotti,Charlesworth Jac,Booth David R.,Harbo Hanne F.,Ivinson Adrian J.,Hauser Stephen L.,Compston Alastair,Stewart Graeme,Zipp Frauke,Barcellos Lisa F.,Baranzini Sergio E.,Martinelli-Boneschi Filippo,D’Alfonso Sandra,Ziegler Andreas,Oturai Annette,McCauley Jacob L.,Sawcer Stephen J.,Oksenberg Jorge R.,De Jager Philip L.,Kockum Ingrid,Hafler David A.,Cotsapas Chris

Funder

NHMRC

Research Fund KU Leuven

Research Foundation Flanders

National Institutes of Health

German Ministry for Education and Research

BMBF

Munich Cluster for Systems Neurology

Heinz Nixdorf Foundation Germany

Deutsche Forschungsgemeinschaft

Italian Foundation for Multiple Sclerosis

Fondazione Cariplo

Oslo MS Association

Bergen MS Society

Odda MS Society

Research Council of Norway

Swedish Medical Research Council

Swedish Research Council for Health, Working Life, and Welfare

Knut and Alice Wallenberg Foundation

AFA

Swedish Brain Foundation

Swedish Association for Persons with Neurological Disabilities

AstraZeneca

Wellcome Trust

Medical Research Council

Cambridge National Institute for Health Research (NIHR) Biomedical Research Centre

UK Medical Research Council

UK MS Society

European Union

US National Multiple Sclerosis Society

NIH

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3