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Next-Generation Sequencing for Cystic Fibrosis: Florida Newborn Screening Experience
Maternal vitamin D and genetic variants determine cord blood vitamin D levels in newborn
A MGMT Enhancer Variant is Associated with Glioma Susceptibility and Progression
High-grade glioma, IDH-and H3-wildtype in young adults: a rare condition with a distinct epigenetic landscape
Identification of rare genetic variants in familial forms and unrelated cases of bisphosphonates-associated atypical femur fracture
Association of inflammatory susceptibility genes with myopia in Chinese children
Association of single-nucleotide polymorphisms in SLC2A9, SLC22A12 and SLC22A11 genes with hyperuricemia in the Chinese Tibetan population
Genetic polymorphisms associated with metabolic dysfunction-associated steatotic liver disease and cardiometabolic risk susceptibility in the Chinese Han population
CYP2C9 polymorphism is associated with susceptibility to ischemic stroke in a Chinese population
Multiple polygenic score approach in colorectal cancer risk prediction