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Hsa-mir-499 rs3746444 T/C Polymorphism is Associated with Increased Risk of Coronary Artery Disease in a Chinese Population
Multilocus Analysis Reveals Three Candidate Genes for Chinese Migraine Susceptibility
Gene-centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility
Genome-wide association study identifies COL2A1 locus involved in the hand development failure of Kashin-Beck disease
Polymorphisms in Telomere Length Associated TERC and TERT predispose for Ischemic Stroke in a Chinese Han population
Association of Polymorphisms in three pri-miRNAs that Target Pepsinogen C with the Risk and Prognosis of Gastric Cancer
The autoimmune risk gene ZMIZ1 is a vitamin D responsive marker of a molecular phenotype of multiple sclerosis
Single Nucleotide Variants of Candidate Genes in Aggrecan Metabolic Pathway Are Associated with Lumbar Disc Degeneration and Modic Changes
Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease
IL1A rs1800587 associates with chronic noncrisis pain in sickle cell disease