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Rare and common genetic variants underlying the risk of Hirschsprung’s disease
Plasma myeloperoxidase interactions with cadmium, lead, arsenic, and selenium and their impact on chronic kidney disease
SCN10A gene polymorphism is associated with pain sensitivity and postoperative analgesic effects in patients undergoing gynecological laparoscopy
Association between ESR1 and COL1A1 gene polymorphisms and skeletal fluorosis in Tibetan, Kazakh, Mongolian and Russian populations, China
The Impact of Adverse Childhood Experiences on the Development of Adolescent Risk-Taking: The Mediating Effect of Self-Control and Moderating Effect of Genetic Variations
Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years
A Functional Variant rs2122031 in ATG7 Is Associated with the Risk of Radiation Pneumonitis
The associations between CYP19A1 polymorphisms and serum 17ß-estradiol levels in Chinese patients with Alzheimer’s disease
Preclinical and clinical study on type 3 metabotropic glutamate receptors in Parkinson’s disease
The evaluation of targeted exome sequencing of candidate genes in a Han Chinese population with primary open-angle glaucoma