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Common variants in PERK, JNK, BIP and XBP1 genes are associated with the risk of prediabetes or diabetes-related phenotypes in a Chinese population
Common vitamin D pathway gene variants reveal contrasting effects on serum vitamin D levels in African Americans and European Americans
Compound HRAS/PIK3CA Mutations in Chinese Patients with Alveolar Rhabdomyosarcomas
Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations
Comprehensive interrogation of CpG island methylation in the gene encoding COMT, a key estrogen and catecholamine regulator
Correlation Analysis of FPGS rs10760502G>A Polymorphism with Prognosis and MTX-related Toxicity in Pediatric B-cell Acute Lymphoblastic Leukemia
CREM Variants rs4934540 and rs2295415 Conferred Susceptibility to Non-Obstructive Azoospermia Risk in the Chinese Population
Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Mark
Designing a High-Throughput Somatic Mutation Profiling Panel Specifically for Gynaecological Cancers
Bovine CLEC7A genetic variants and their association with seropositivity in Johne’s disease ELISA