Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus

A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis

(2010) P G Bronson et al.   GENES AND IMMUNITY

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility

(2010) Rebecca L. Zuvich et al.   HUMAN GENETICS

CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis

(2010) Paola G. Bronson et al.   HUMAN MOLECULAR GENETICS

A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis

(2009) B. Skinningsrud et al.   ANNALS OF THE RHEUMATIC DISEASES

Chromosomal region 16p13: further evidence of increased predisposition to immune diseases

(2009) A Martinez et al.   ANNALS OF THE RHEUMATIC DISEASES

Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15− Crohn's disease patients

(2009) Ana Márquez et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis

(2009) Ilse A Hoppenbrouwers et al.   JOURNAL OF HUMAN GENETICS

Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus

(2009) Devindri Perera et al.   JOURNAL OF NEUROIMMUNOLOGY

Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes

(2009) S. Nejentsev et al.   SCIENCE

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

(2008) J P Rubio et al.   GENES AND IMMUNITY

The expanding genetic overlap between multiple sclerosis and type I diabetes

(2008)   GENES AND IMMUNITY

Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia

(2008) M Zoledziewska et al.   GENES AND IMMUNITY

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

(2008) Frank Dudbridge   HUMAN HEREDITY

Polymorphisms inCLEC16AandCIITAat 16p13 Are Associated with Primary Adrenal Insufficiency

(2008) Beate Skinningsrud et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM