Catherine Owen

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

Manuela Fanciulli, Penny J. Norsworthy, Enrico Petretto et al. · Nature Genetics · 2007 · 462 citations · Full text

Immunogenetics, Autoimmune Disease, Autoantibody Production +9

The Codon 620 Tryptophan Allele of the Lymphoid Tyrosine Phosphatase (LYP) Gene Is a Major Determinant of Graves’ Disease

Marija Velaga, Valerie Wilson, Claire Jennings et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 460 citations · Full text

Analysis of DAX1 (NR0B1) and Steroidogenic Factor-1 (NR5A1) in Children and Adults with Primary Adrenal Failure: Ten Years’ Experience

Lin Lin, Wen-Xia Gu, Wing S. To et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 216 citations · Full text

Genomic Polymorphism at the Interferon-Induced Helicase (IFIH1) Locus Contributes to Graves’ Disease Susceptibility

Alison Sutherland, Jocelyn Davies, Catherine Owen et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 113 citations · Full text

Mutational Analysis of the FOXP3 Gene and Evidence for Genetic Heterogeneity in the Immunodysregulation, Polyendocrinopathy, Enteropathy Syndrome

Catherine Owen, Claire Jennings, Helen Imrie et al. · The Journal of Clinical Endocrinology & Metabolism · 2003 · 105 citations · Full text