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Association of the DISC1 and NRG1 Genetic Polymorphisms with Schizophrenia in a Chinese Population
Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits
Analysis of receptor tyrosine kinase genetics identifies two novel risk loci in GAS6 and PROS1 in Behçet’s disease
Clinical Significance of Long Non-Coding RNA CASC8 rs10505477 Polymorphism in Lung Cancer Susceptibility, Platinum-Based Chemotherapy Response, and Toxicity
The Sp1-mediaded allelic regulation of MMP13 expression by an ESCC susceptibility SNP rs2252070
CYP gene family variants as a potential risk factors in drug addiction in Han Chinese
Complement factor H and LOC387715/ARMS2/HTRA1 variant’s frequencies and phenotypic associations in neovascular age-related macular degeneration, a pilot study
Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate
A candidate gene approach identifies six SNPs in tenascin-C (TNC) associated with degenerative rotator cuff tears
Multiple genetic imaging study of the association between cholesterol metabolism and brain functional alterations in individuals with risk factors for Alzheimer’s disease