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Racial and ethnic differences in the relationship between aspirin use and non–small cell lung cancer risk and survival
Effects and interactions of myostatin and callipyge mutations: I. Growth and carcass traits
Association of BET1L and TNRC6B with uterine leiomyoma risk and its relevant clinical features in Han Chinese population
Folic acid modulates VPO1 DNA methylation levels and alleviates oxidative stress-induced apoptosis in vivo and in vitro
Common Variants in ALPL Gene Contribute to the Risk of Kidney Stones in the Han Chinese Population
CRISPR/Cas9‐mediated gene knockout for DNA methyltransferase Dnmt3a in CHO cells displays enhanced transgenic expression and long‐term stability
Genetic variation in the von Willebrand factor gene in Swedish von Willebrand disease patients
Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course
Neurexin gene family variants as risk factors for autism spectrum disorder
Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects