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Effect of the -2081G/A Polymorphism of the TLR4 Gene and Its Interaction with Helicobacter pylori Infection on the Risk of Gastric Cancer in Chinese Individuals
Clinical and non-targeted metabolomic profiling of homozygous carriers of Transcription Factor 7-like 2 variant rs7903146
Combination of hearing screening and genetic screening for deafness-susceptibility genes in newborns
Combining TNFSF15 and ASCA IgA can be used as a predictor for the stenosis/perforating phenotype of Crohn’s disease
Common Genetic Variation in the Human CTF1 Locus, Encoding Cardiotrophin-1, Determines Insulin Sensitivity
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
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
Detection of Copy Number Variation (CNV) by SNP-Allelotyping