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Variants in RETN gene are associated with steroid-induced osteonecrosis of the femoral head risk among Han Chinese people.
Precision therapy of 6‐mercaptopurine in Chinese children with acute lymphoblastic leukemia
Association of heme oxygenase-1 single nucleotide polymorphisms with susceptibility to tuberculosis in Chinese Han population.
Methylation of the LEP gene promoter in blood at 12 months and BMI at 4 years of age—a population-based cohort study
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease.
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells
Development of a set of SNP markers for population genetics of the red gorgonian (Paramuricea clavata), an emblematic species of the Mediterranean coralligenous
Association of SCN1A, SCN2A, and UGT2B7 Polymorphisms with Responsiveness to Valproic Acid in the Treatment of Epilepsy
Primary qualities evoked by quinine, sucrose, and capsaicin associate with PROP bitterness, but not TAS2R38 genotype
Genetic determinants of gestational diabetes mellitus: a case–control study in two independent populations