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Rare mutations and potentially damaging missense variants in genes encoding fibrillar collagens and proteins involved in their production are candidates for risk for preterm premature rupture of membranes
Replication of a genome-wide association study on essential hypertension in Mongolians
Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L/MOpsin Interchange Mutations
Role of interleukin-10 polymorphisms and haplotypes in polycystic ovary syndrome risk
Roles of IL-4 genetic polymorphisms and haplotypes in the risk of gastric cancer and their interaction with environmental factors
Rs12970134 near MC4R is associated with appetite and beverage intake in overweight and obese children: A family-based association study in Chinese population
SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon.
Scanning indels in the 5q22.1 region and identification of the TMEM232 susceptibility gene that is associated with atopic dermatitis in the Chinese Han population
Serum concentrations of vitamin E and carotenoids are altered in Alzheimer’s disease: A case-control study
Serum high-sensitive C-reactive protein (hsCRP) level and CRP genetic polymorphisms are associated with abdominal aortic aneurysm