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Genetic variations in MOV10 and CACNB2 are associated with hypertension in a Chinese Han population
Gastric Inhibitory Polypeptide Receptor Methylation in Newly Diagnosed, Drug-NaÃ¯ve Patients with Type 2 Diabetes: A Case-Control Study
Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts
Genetic and microbial factors modulating the ubiquitin proteasome system in inflammatory bowel disease
Genome-wide association analysis identifies new susceptibility loci for BehÃ§et’s disease and epistasis between HLA-B*51 and ERAP1
Genetic and Non-Genetic Determinants of Raltegravir Penetration into Cerebrospinal Fluid: A Single Arm Pharmacokinetic Study
Genome-Wide Association Study Identifies a Novel Canine Glaucoma Locus
Genetic association of PLCE1, C11orf92-C11orf93, and NOC3L with colorectal cancer risk in the Han population
Genetic Association Study betweenSTK39 and CCDC62/HIP1R and Parkinsonâ€™s Disease
Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss