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PRM1 variant rs35576928 (Arg>Ser) is associated with defective spermatogenesis in the Chinese Han population
Association of single nucleotide polymorphisms in the genes ATM, GSTP1, SOD2, TGFB1, XPD and XRCC1 with risk of severe erythema after breast conserving radiotherapy
Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
Epigenetic Regulation of Cancer Stem Cell Genes in Triple-Negative Breast Cancer
Polymorphisms in the glutamate decarboxylase 1 gene associated with heroin dependence
Detection of pathogenic mutations and the mechanism of a rare chromosomal rearrangement in a Chinese family with Becker muscular dystrophy
Analysis of the genotype of diacylglycerol kinase delta single-nucleotide polymorphisms in Parkinson disease in the Han Chinese population
Stemness of the Organ of Corti Relates to the Epigenetic Status of Sox2 Enhancers
ESR1, HK3 and BRSK1 gene variants are associated with both age at natural menopause and premature ovarian failure
Methylation Defect in Imprinted Genes Detected in Patients with an Albright’s Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction