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Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.

Authors :
Yannick Allanore
Mohamad Saad
Philippe Dieudé
Jérôme Avouac
Jorg H W Distler
Philippe Amouyel
Marco Matucci-Cerinic
Gabriella Riemekasten
Paolo Airo
Inga Melchers
Eric Hachulla
Daniele Cusi
H-Erich Wichmann
Julien Wipff
Jean-Charles Lambert
Nicolas Hunzelmann
Kiet Tiev
Paola Caramaschi
Elisabeth Diot
Otylia Kowal-Bielecka
Gabriele Valentini
Luc Mouthon
László Czirják
Nemanja Damjanov
Erika Salvi
Costanza Conti
Martina Müller
Ulf Müller-Ladner
Valeria Riccieri
Barbara Ruiz
Jean-Luc Cracowski
Luc Letenneur
Anne Marie Dupuy
Oliver Meyer
André Kahan
Arnold Munnich
Catherine Boileau
Maria Martinez
Source :
PLoS Genetics, Vol 7, Iss 7, p e1002091 (2011)
Publication Year :
2011
Publisher :
Public Library of Science (PLoS), 2011.

Abstract

Systemic sclerosis (SSc) is an orphan, complex, inflammatory disease affecting the immune system and connective tissue. SSc stands out as a severely incapacitating and life-threatening inflammatory rheumatic disease, with a largely unknown pathogenesis. We have designed a two-stage genome-wide association study of SSc using case-control samples from France, Italy, Germany, and Northern Europe. The initial genome-wide scan was conducted in a French post quality-control sample of 564 cases and 1,776 controls, using almost 500 K SNPs. Two SNPs from the MHC region, together with the 6 loci outside MHC having at least one SNP with a P

Subjects

Subjects :
Genetics
QH426-470

Details

Language :
English
ISSN :
15537390 and 15537404
Volume :
7
Issue :
7
Database :
Directory of Open Access Journals
Journal :
PLoS Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.83d5482598b498ea785808a1da0a951
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.pgen.1002091