Associated Papers
Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population.
Yamada Y et al.
Biomedical Reports, 2018
Deep Resequencing of Ulcerative Colitis-Associated Genes Identifies Novel Variants in Candidate Genes in the Korean Population.
Moon CM et al.
Inflammatory Bowel Diseases, 2018
RXRB Is an MHC-Encoded Susceptibility Gene Associated with Anti-Topoisomerase I Antibody-Positive Systemic Sclerosis.
Oka A et al.
The Journal of Investigative Dermatology, 2017
Familial vs. sporadic sarcoidosis: BTNL2 polymorphisms, clinical presentations, and outcomes in a French cohort.
Pacheco Y et al.
Orphanet Journal of Rare Diseases, 2016
Identification of novel hereditary cancer genes by whole exome sequencing.
Sokolenko AP et al.
Cancer Letters, 2015
Genetic predisposition to prostate cancer: Update and future perspectives.
Demichelis F et al.
Urologic Oncology, 2015
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
Prescott NJ et al.
Plos Genetics, 2015
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.
Goldstein JI et al.
Nature Communications, 2014
25187353 (PubMed )
Supplement: NIHMS614937-supplement-1.pdf
Germline missense variants in the BTNL2 gene are associated with prostate cancer susceptibility.
Fitzgerald LM et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2013
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