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Genetic variations at the human growth hormone receptor (GHR) gene locus are associated with idiopathic short stature
Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population
Genetic variations in sterol regulatory element binding protein cleavage-activating protein (SCAP) are associated with blood pressure in overweight/obese Chinese children
Genetic variants of PTGS2, TXA2R and TXAS1 are associated with carotid plaque vulnerability, platelet activation and TXA2 levels in ischemic stroke patients
Genome-wide analysis of ivermectin response by Onchocerca volvulus reveals that genetic drift and soft selective sweeps contribute to loss of drug sensitivity
Genome-wide association analysis for chronic venous disease identifies EFEMP1and KCNH8 as susceptibility loci
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Geographic-genetic analysis of Plasmodium falciparum parasite populations from surveys of primary school children in Western Kenya
GLIS3 and TYK2 Single Nucleotide Polymorphisms Are Not Associated with Dermatomyositis/Polymyositis in Chinese Han Population
Genetic risk for schizophrenia and psychosis in Alzheimer disease