A family-based genome-wide association study reveals an association of spondyloarthritis withMAPK14

Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci

(2016) David Ellinghaus et al.   NATURE GENETICS

Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13

(2015) Félicie Costantino et al.   ANNALS OF THE RHEUMATIC DISEASES

Prevalence of spondyloarthritis in reference to HLA-B27 in the French population: results of the GAZEL cohort

(2013) Félicie Costantino et al.   ANNALS OF THE RHEUMATIC DISEASES

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

(2013) Adrian Cortes et al.   NATURE GENETICS

Association between the IL-1 family gene cluster and spondyloarthritis

(2012) Dominique Monnet et al.   ANNALS OF THE RHEUMATIC DISEASES

Investigating the genetic association betweenERAP1and spondyloarthritis

(2012) Amir Kadi et al.   ANNALS OF THE RHEUMATIC DISEASES

Are spondylarthritides related but distinct conditions or a single disease with a heterogeneous phenotype?

(2012) Dominique Baeten et al.   ARTHRITIS AND RHEUMATISM

Prevalence of axial spondylarthritis in the United States: Estimates from a cross-sectional survey

(2012) John D. Reveille et al.   ARTHRITIS CARE & RESEARCH

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

(2011) David M Evans et al.   NATURE GENETICS

The Assessment in Spondyloarthritis International Society (ASAS) classification criteria for peripheral spondyloarthritis and for spondyloarthritis in general: the spondyloarthritis concept in progress

(2010) H. Zeidler et al.   ANNALS OF THE RHEUMATIC DISEASES

METAL: fast and efficient meta-analysis of genomewide association scans

(2010) C. J. Willer et al.   BIOINFORMATICS

Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci

(2010) John D Reveille et al.   NATURE GENETICS

Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila

(2010) C. J. Schoen et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Family-based genome-wide association studies

(2009) Beben Benyamin et al.   PHARMACOGENOMICS

Recurrence of spondylarthropathy among first-degree relatives of patients: a systematic cross-sectional study

(2008) E Dernis et al.   ANNALS OF THE RHEUMATIC DISEASES

Likelihood-Based Association Analysis for Nuclear Families and Unrelated Subjects with Missing Genotype Data

(2008) Frank Dudbridge   HUMAN HEREDITY