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Pathway Analysis Using Genome-Wide Association Study Data for Coronary Restenosis â€“ A Potential Role for the PARVB Gene
Patrilineal Background of Esophageal Cancer and Gastric Cardia Cancer Patients in a Chaoshan High-Risk Area in China
Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III)
Meta-analysis identifies BACH2 and RAD51B as rheumatoid arthritis susceptibility loci
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing
Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression
Genome-wide genotype-based risk model for survival in acute myeloid leukaemia patients with normal karyotype
Human Candidate Polymorphisms in Sympatric Ethnic Groups Differing in Malaria Susceptibility in Mali
Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study
IL10 polymorphisms associated with BehÃ§et’s disease in Chinese Han