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Association Between Vitamin D Receptor Gene Polymorphism rs2228570 and Allergic Rhinitis
Identification of Recurrent Variants in BRCA1 and BRCA2 across Multiple Cancers in the Chinese Population
Oncogene HSPH1 modulated by the rs2280059 genetic variant diminishes EGFR-TKIs efficiency in advanced lung adenocarcinoma
Androgen receptor-reduced sensitivity is associated with increased mortality and poorer glycaemia in men with type 2 diabetes mellitus: a prospective cohort study
Genetics and Age-Related Eye Disease Study Formulation Interaction in Neovascular Age-Related Macular Degeneration
A novel genetic variant associated with benign paroxysmal positional vertigo within the LOXL1
Use of Genomewide Association Studies to Evaluate Genetic Predisposition to Testicular Germ Cell Tumors
SAP30BP gene is associated with the susceptibility of rotator cuff tear: a case-control study based on Han Chinese population
RNF213 gene polymorphism rs9916351 and rs8074015 significantly associated with moyamoya disease in Chinese population
EBNA-1 titer gradient in families with multiple sclerosis indicates a genetic contribution