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Associations of ATP-Sensitive Potassium Channel’s Gene Polymorphisms With Type 2 Diabetes and Related Cardiovascular Phenotypes
Study of KIAA0319, DYXIC1 and DCDC2 Gene Polymorphisms in Children with Dyslexia in Indian Population
SNP rs7130280 in lncRNA NONHSAT159216.1 confers susceptibility to Behcet’s disease in a Chinese Han population
Association between RAC1 gene variation, redox homeostasis and type 2 diabetes mellitus
Relationship between rs7586085, GALNT3 and CCDC170 gene polymorphisms and the risk of osteoporosis among the Chinese Han population
Genetic variation at the catalytic subunit of glutamate cysteine ligase contributes to the susceptibility to sporadic colorectal cancer: a pilot study
PAM variants were associated with type 2 diabetes mellitus risk in the Chinese population
Association of the MARCO polymorphism rs6761637 with hepatocellular carcinoma susceptibility and clinical characteristics
A genetic variant in IL-6 lowering its expression is protective for critical patients with COVID-19
Impact of COMT, PRODH and DISC1 Genetic Variants on Cognitive Performance of Patients with Schizophrenia