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A systematic survey of loss-of-function variants in human protein-coding genes
A case-parent triad assessment of folate metabolic genes and the risk of childhood acute lymphoblastic leukemia
Decreased expression of repulsive guidance molecule member A by DNA methylation in colorectal cancer is related to tumor progression
Association study of a common variant near IRS1 with type 2 diabetes mellitus in Chinese Han population
Association of CDX1 binding site of periostin gene with bone mineral density and vertebral fracture risk
Genetic Variations in Stem Cell-Related Genes and Colorectal Cancer Prognosis
Identification of genetic associations of SP110/MYBBP1A/RELA with pulmonary tuberculosis in the Chinese Han population
Specific genetic polymorphisms of IL10-592 AA and IL10-819 TT genotypes lead to the key role for inducing docetaxel-induced liver injury in breast cancer patients
Mutation profiling identifies numerous rare drug targets and distinct mutation patterns in different clinical subtypes of breast cancers
Evidence from case-control and longitudinal studies supports associations of genetic variation in APOE, CETP, and IL6 with human longevity