Identification of independent risk loci for Graves’ disease within the MHC in the Japanese population

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study

(2010) Paul R Newby et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Rare Variants Create Synthetic Genome-Wide Associations

(2010) Samuel P. Dickson et al.   PLOS BIOLOGY

Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease

(2009) O. J. Brand et al.   HUMAN MOLECULAR GENETICS

Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse

(2009) Hirofumi Nakaoka et al.   JOURNAL OF HUMAN GENETICS

A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians

(2009) Yoichiro Kamatani et al.   NATURE GENETICS

Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

(2009) et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genetic developments in autoimmune thyroid disease: an evolutionary process

(2008) Abigail A. Zeitlin et al.   CLINICAL ENDOCRINOLOGY

ZFAT expression in B and T lymphocytes and identification of ZFAT-regulated genes

(2008) Midori Koyanagi et al.   GENOMICS

Autoimmune diseases: insights from genome-wide association studies

(2008) G. Lettre et al.   HUMAN MOLECULAR GENETICS

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

(2008) Hiroyuki Unoki et al.   NATURE GENETICS

Susceptibility loci for intracranial aneurysm in European and Japanese populations

(2008) Kaya Bilguvar et al.   NATURE GENETICS

Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis

(2008) Michelle M. A. Fernando et al.   PLoS Genetics