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Functional Role of NRF2 in Cervical Carcinogenesis
Synergy of two human endogenous retroviruses in multiple myeloma
PTEN gene polymorphisms and susceptibility to oral squamous cell carcinoma in a Chinese Han population
Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: Results from a multicenter study in Italy
Chronic Fatigue Syndrome and DNA Hypomethylation of the Glucocorticoid Receptor Gene Promoter 1F Region: Associations With Hypothalamic-Pituitary-Adrenal Axis Hypofunction and Childhood Trauma
No association of FAM47E rs6812193, SCARB2 rs6825004 and STX1B rs4889603 polymorphisms with Parkinson’s disease in a Chinese Han population
Let-7 related genetic variation and risk of metabolic syndrome in a Chinese population
Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal
Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus
A Pooled Genome-Wide Association Study of Asperger Syndrome