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The CYP19A1 rs3751592 variant confers susceptibility to Alzheimer disease in the Chinese Han population
Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population
Two-stage additional evidence support association of common variants in the HDAC3 with the increasing risk of schizophrenia susceptibility
Interaction of Multiple Gene Variants and their Effects on Schizophrenia Phenotypes
Polymorphisms in UGT1A1 gene predispose South Indians to pigmentous gallstones
Lack of association between SREBF-1c gene polymorphisms and risk of non-alcoholic fatty liver disease in a Chinese Han population
IGF2BP2 rs11705701 polymorphisms are associated with prediabetes in a Chinese population: A population-based case-control study
Whole exome sequencing of extreme age-related macular degeneration phenotype
Loss-of-function variants influence the human serum metabolome
A Population-Based Genomic Study of Inherited Metabolic Diseases Detected Through Newborn Screening