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Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disability
The association between rs1260326 with the risk of NAFLD and the mediation effect of triglyceride on NAFLD in the elderly Chinese Han population
Genetic predisposition of Alopecia Areata in Jordanians: A case-control study
Associations between Gene-Gene Interaction and Overweight/Obesity of 12-Month-Old Chinese Infants
The Relationship Between Low-Density Lipoprotein Cholesterol and Progression of Mild Cognitive Impairment: The Influence of rs6859 in PVRL2
Association Between Dystonia-Related Genetic Loci and Parkinson’s Disease in Eastern China
Association of polymorphisms of FOLR1 gene and FOLR2 gene and maternal folic acid supplementation with risk of ventricular septal defect: a case-control study
HUMAN STUDY COMT and DRD3 haplotype-associated pain intensity and acute care utilization in adult sickle cell disease
Compound heterozygous variants in DYNC2H1 in a foetus with type III short rib-polydactyly syndrome and situs inversus totalis
The interaction between glycemic index, glycemic load, and the genetic variant ADIPOQ T45G (rs2241766) in the risk of colorectal cancer: a case–control study in a Korean population