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Association of Candidate Gene Polymorphisms with Chronic Kidney Disease: Results of a Case-Control Analysis in the Nefrona Cohort
Association between the BANK1 rs3733197 polymorphism and polymyositis/dermatomyositis in a Chinese Han population
Genome‐wide association study of statin‐induced myopathy in patients recruited using the UK clinical practice research datalink
Cytokine Genetic Variants and Health-Related Quality of Life in Crohn’s Disease: An Exploratory Study
STX1A gene variations contribute to the susceptibility of children attention-deficit/hyperactivity disorder: a case–control association study
Genetic aspects of idiopathic paediatric uveitis and juvenile idiopathic arthritis associated uveitis in Chinese Han
Investigating the role of microRNA-27a gene polymorphisms and its interactive effect with risk factors in gastrointestinal cancers
Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export
PNPLA3 rs738409 is not associated with the risk of hepatocellular carcinoma and persistent infection of hepatitis B virus (HBV) in HBV-related subjects: A case-control study and meta-analysis on Asians
Association of Polymorphisms in the Kisspeptin/GPR54 Pathway Genes With Risk of Early Puberty in Chinese Girls