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A rare genetic defect of MBL2 increased the risk for progression of IgA nephropathy
Ehlers-Danlos Syndrome is associated with Idiopathic Urticaria–a Retrospective Study
Relationship among ETV1 genetic polymorphisms, PFS, and microRNA in gastrointestinal stromal tumors.
Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization
The research of ion channel‐related gene polymorphisms with atrial fibrillation in the Chinese Han population
3′ UTR variants of TNS3, PHLDB1, NTN4, and GNG2 genes are associated with IgA nephropathy risk in Chinese Han population
Genetic variants in the ITPR2 gene are associated with Kashin‐Beck Disease in Tibetan
FKBP5 Gene Variants May Modulate Depressive Features in Bipolar Disorder
Associations of the IL-17A rs2275913 and IL-17F rs763780 polymorphisms with the risk of digestive system neoplasms: A meta-analysis
Association of ENAM, TUFT1, MMP13, IL1B, IL10 and IL1RN gene polymorphism and dental caries susceptibility in Chinese children