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The Potential Role of Clock Genes in Children Attention-deficit/hyperactivity Disorder
Neural network correlates of high‐altitude adaptive genetic variants in Tibetans: A pilot, exploratory study
Rare variants and biological pathways identified in treatment‐refractory depression
Variants of INSR rs2963 is Associated With Gestational Diabetes Mellitus and Iron Storage
Fibroblast growth factor 23 genotype and cardiovascular disease in patients undergoing hemodialysis
The role of kynurenine pathway and kynurenic aminotransferase alleles in postpartum depression following cesarean section in Chinese women
Variants in RETN gene are associated with steroid-induced osteonecrosis of the femoral head risk among Han Chinese people.
Association of heme oxygenase-1 single nucleotide polymorphisms with susceptibility to tuberculosis in Chinese Han population.
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease.