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Family history of type 1 and type 2 diabetes and risk of latent autoimmune diabetes in adults (LADA)
Genetic modifiers of multiple sclerosis progression, severity and onset
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population
Genetic polymorphisms of C-type lectin receptors in Behcet’s disease in a Chinese Han population
Feasibility of multiplexed gene mutation detection in plasma samples of colorectal cancer patients by mass spectrometric genotyping
Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population
Filaggrin gene polymorphism associated with Epstein–Barr virus-associated tumors in China
FOXA1 hypermethylation: link between parity and ER-negative breast cancer in African American women?
Frequency and significance of rare RNF213 variants in patients with adult moyamoya disease
Gene Variations of Sixth Complement Component Affecting Tacrolimus Metabolism in Patients with Liver Transplantation for Hepatocellular Carcinoma