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Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population
Family history of type 1 and type 2 diabetes and risk of latent autoimmune diabetes in adults (LADA)
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population
Filaggrin gene polymorphism associated with Epstein–Barr virus-associated tumors in China
Gene Variations of Sixth Complement Component Affecting Tacrolimus Metabolism in Patients with Liver Transplantation for Hepatocellular Carcinoma
Gene-by-environment interactions of the CLOCK, PEMT, and GHRELIN loci with average sleep duration in relation to obesity traits using a cohort of 643 New Zealand European children
Frequency and significance of rare RNF213 variants in patients with adult moyamoya disease
Gene-gene and gene-environment interactions influence platinum-based chemotherapy response and toxicity in non-small cell lung cancer patients
Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson’s Disease
Genetic Diagnosis of Deafness