Whole exome sequencing identifies rare protein-coding variants in Behçet's disease-Reference-Cited by-同舟云学术

Whole exome sequencing identifies rare protein-coding variants in Behçet's disease

Published:2015-12 Issue: Volume: Page:n/a-n/a
ISSN:2326-5191
Container-title:Arthritis & Rheumatology
language:en
Short-container-title:Arthritis & Rheumatology

Author:

Ognenovski Mikhail¹,Renauer Paul¹,Gensterblum Elizabeth¹,Kötter Ina²,Xenitidis Theodoros³,Henes Jörg C³,Casali Bruno⁴,Salvarani Carlo⁵,Direskeneli Haner⁶,Kaufman Kenneth M⁷⁸,Sawalha Amr H¹⁹

Affiliation:

1. Division of Rheumatology, Department of Internal Medicine; University of Michigan; Ann Arbor Michigan USA

2. Asklepios Clinic Altona; Department of Internal Medicine 4; Hamburg Germany

3. Centre for Interdisciplinary Clinical Immunology, Rheumatology and Auto-inflammatory Diseases-INDIRA and Department of Internal Medicine II; University of Tübingen; Tübingen Germany

4. Molecular Biology Laboratory; Azienda Ospedaliera Arcispedale Santa Maria Nuova, Istituto di Ricovero e Cura a Carattere Scientifico; Reggio Emilia Italy

5. Rheumatology Unit, Department of Internal Medicine, Azienda Ospedaliera Arcispedale Santa Maria Nuova; Istituto di Ricovero e Cura a Carattere Scientifico; Reggio Emilia Italy

6. Department of Rheumatology, Faculty of Medicine; Marmara University; Istanbul Turkey

7. Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center; Cincinnati Ohio USA

8. Cincinnati VA Medical Center; Cincinnati Ohio USA

9. Center for Computational Medicine and Bioinformatics, University of Michigan; Ann Arbor Michigan USA

Funder

NHLBI GO Exome Sequencing Project

Lung GO Sequencing Project

WHI Sequencing Project

Broad GO Sequencing Project

Seattle GO Sequencing Project

Heart GO Sequencing Project

Publisher