Home / Resources / Publication Library

Search Results for: Hereditary Genetics

Search All publications

How recent?

Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)
Parkinson’s disease susceptibility variants and severity of Lewy body pathology
Patrilineal background of the She minority population from Chaoshan Fenghuang Mountain, an isolated mountain region, in China
Polymorphism of TNIP1 was associated with atherosclerotic ischemic stroke in southern Han Chinese but unrelated with telomere
Polymorphisms in autophagy related genes and the coal workers’ pneumoconiosis in a Chinese population
Polymorphisms in Epithelial-Mesenchymal Transition-Related Genes and the Prognosis of Surgically Treated Non-small Cell Lung Cancer
Polymorphisms in the SRNPN gene are associated with obesity susceptibility among Spanish population
Polymorphisms in POLG were associated with the prognosis and mtDNA content in hepatocellular carcinoma patients
N370S-GBA1 mutation causes lysosomal cholesterol accumulation in Parkinson’s disease
Neuropeptide S (NPS) variants modify the signaling and risk effects of NPS Receptor 1 (NPSR1) variants in asthma