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SLC6A1 gene involvement in susceptibility to attention-deficit/hyperactivity disorder: A case-control study and gene-environment interaction
SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility—A Joint Analysis in Four European Populations
Rare coding variants in PLCG2, ABI3, and TREM2implicate microglial-mediated innate immunity in Alzheimer’s disease
Rare mutations and potentially damaging missense variants in genes encoding fibrillar collagens and proteins involved in their production are candidates for risk for preterm premature rupture of membranes
Polymorphisms of protamine genes contribute to male infertility susceptibility in the Chinese Han population
Polymorphisms of xenobiotic-metabolizing genes and colorectal cancer risk in patients with lynch syndrome: A retrospective cohort study in Taiwan
Polymorphisms of CYP2C8, CYP2C9 and CYP2C19 and risk of coronary heart disease in Russian population
Polymorphisms of RAD51B are associated with rheumatoid arthritis and erosion in rheumatoid arthritis patients
Post-operative atrial fibrillation examined using whole-genome RNA sequencing in human left atrial tissue
Potentially functional variants in lncRNAs are associated with breast cancer risk in a Chinese population