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Variants of the OLIG2 Gene are Associated with Cerebral Palsy in Chinese Han Infants with Hypoxic–Ischemic Encephalopathy
Circulating ceruloplasmin, ceruloplasmin‐associated genes and the incidence of venous thromboembolism in the Atherosclerosis Risk in Communities study
A functional variant in SLC1A3 influences ADHD risk by disrupting a hsa‐miR‐3171 binding site: A two‐stage association study
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
Polymorphisms in potential mercury transporter ABCC2 and neurotoxic symptoms in populations exposed to mercury vapor from goldmining
VEGF gene polymorphism interactions with dietary trace elements intake in determining the risk of metabolic syndrome
TRIB1 rs17321515 and rs2954029 gene polymorphisms increase the risk of non-alcoholic fatty liver disease in Chinese Han population
Role of polygenic risk in susceptibility to accelerated pubertal onset following chronic stress exposure