Genome-wide significant association with seven novel multiple sclerosis risk loci

Journal of Medical Genetics

Volumn 52, Issue 12, 2015, Pages 848-855

  Lill, Christina M ^a,b,c   Luessi, Felix ^b   Alcina, Antonio ^d   Sokolova, Ekaterina A ^e,f   Ugidos, Nerea ^g,h   de la Hera, Belén ⁱ   Guillot Noël, Léna ^j   Malhotra, Sunny ^k   Reinthaler, Eva ^l   Schjeide, Brit Maren M ^c   Mescheriakova, Julia Y ^m   Mashychev, Andriy ^a   Wohlers, Inken ^a   Akkad, Denis A ⁿ   Aktas, Orhan ^o   Alloza, Iraide ^g,h,p   Antigüedad, Alfredo ^q   Arroyo, Rafa ⁱ   Astobiza, Ianire ^g,h   Blaschke, Paul ^r   Boyko, Alexei N ^s   Buttmann, Mathias ^t   Chan, Andrew ^u   Dörner, Thomas ^v   Epplen, Joerg T ^m,w   Favorova, Olga O ^s   Fedetz, Maria ^d   Fernández, Oscar ^x   García Martínez, Angel ⁱ   Gerdes, Lisa Ann ^y   Graetz, Christiane ^b   Hartung, Hans Peter ^o   Hoffjan, Sabine ⁿ   Izquierdo, Guillermo ^z   Korobko, Denis S ^aa   Kroner, Antje ^t,ab   Kubisch, Christian ^ac   Kümpfel, Tania ^y   Leyva, Laura ^x   Lohse, Peter ^ad,ae   Malkova, Nadezhda A ^aa,af   Montalban, Xavier ^k   Popova, Ekaterina V ^s   Rieckmann, Peter ^t,ag   Rozhdestvenskii, Alexei S ^ah   Schmied, Christiane ^l   Smagina, Inna V ^ai,aj   Tsareva, Ekaterina Y ^s   Winkelmann, Alexander ^r   Zettl, Uwe K ^r   Binder, Harald ^b   Cournu Rebeix, Isabelle ^j   Hintzen, Rogier ^m   Zimprich, Alexander ^l   Comabella, Manuel ^k   Fontaine, Bertrand ^j,ak   Urcelay, Elena ⁱ   Vandenbroeck, Koen ^g,h,p   Filipenko, Maxim ^e,f   Matesanz, Fuencisla ^d   Zipp, Frauke ^b   Bertram, Lars ^a,c,al   more..

^a UNIVERSITY OF LÜBECK   (Germany)

^b UNIVERSITY MEDICAL CENTER MAINZ   (Germany)

^c MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^d INSTITUTO DE PARASITOLOGÍA Y BIOMEDICINA LÓPEZ NEYRA   (Spain)

^e INSTITUTE OF CHEMICAL BIOLOGY AND FUNDAMENTAL MEDICINE   (Russian Federation)

^f NOVOSIBIRSK STATE UNIVERSITY   (Russian Federation)

^g UNIVERSITY OF THE BASQUE COUNTRY UPV EHU   (Spain)

^h ACHUCARRO BASQUE CENTER FOR NEUROSCIENCE   (Spain)

ⁱ HOSPITAL CLÍNICO SAN CARLOS   (Spain)

^j SORBONNE UNIVERSITÉ   (France)

^k HOSPITAL UNIVERSITARI VALL D HEBRON   (Spain)

^l MEDICAL UNIVERSITY OF VIENNA   (Austria)

^m ERASMUS MEDICAL CENTER   (Netherlands)

ⁿ RUHR UNIVERSITY BOCHUM   (Germany)

^o Department of Orthopedic Surgery   (Germany)

^p BASQUE FOUNDATION FOR SCIENCE   (Spain)

^q HOSPITAL DE BASURTO   (Spain)

^r UNIVERSITY OF ROSTOCK   (Germany)

^s PIROGOV RUSSIAN NATIONAL RESEARCH MEDICAL UNIVERSITY   (Russian Federation)

^t UNIVERSITY OF WÜRZBURG   (Germany)

^u ST JOSEF HOSPITAL   (Germany)

^v CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^w UNIVERSITY OF WITTEN HERDECKE   (Germany)

^x HOSPITAL REGIONAL UNIVERSITARIO DE MÁLAGA   (Spain)

^y LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^z HOSPITAL UNIVERSITARIO VIRGEN MACARENA   (Spain)

^aa State Novosibirsk Regional Clinical Hospital   (Russian Federation)

^ab MEDICAL COLLEGE OF WISCONSIN   (United States)

^ac UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^ad UNIVERSITY OF MUNICH   (Germany)

^ae CEGAT GMBH   (Germany)

^af NOVOSIBIRSK STATE MEDICAL UNIVERSITY   (Russian Federation)

^ag Sozialstiftung Bamberg Hospital   (Germany)

^ah Omsk State Pedagogic University   (Russian Federation)

^ai Territorial Clinical Hospital   (Russian Federation)

^aj ALTAI STATE MEDICAL UNIVERSITY   (Russian Federation)

^ak PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^al IMPERIAL COLLEGE LONDON   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUSTRIA; CD28 GENE; COMPUTER MODEL; CONTROLLED STUDY; DLEU1 GENE; ETS1 GENE; FRANCE; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; GERMANY; HUMAN; IFNGR2 GENE; LOC100506457 GENE; LPIN3 GENE; LPP GENE; MAJOR CLINICAL STUDY; MULTIPLE SCLEROSIS; NETHERLANDS; NEUROPATHOLOGY; PRIORITY JOURNAL; QUANTITATIVE TRAIT LOCUS; RUSSIAN FEDERATION; SINGLE NUCLEOTIDE POLYMORPHISM; SPAIN; CASE CONTROL STUDY; GENE FREQUENCY; GENE LOCUS; GENETIC PREDISPOSITION; GENETICS; GENOME-WIDE ASSOCIATION STUDY; RISK FACTOR;

CASE-CONTROL STUDIES; GENE FREQUENCY; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MULTIPLE SCLEROSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 84954285551     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmedgenet-2015-103442     Document Type: Article

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