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Genetic Variants on 3q21 and in the Sp8 Transcription Factor Gene (SP8) as Susceptibility Loci for Psychotic Disorders: A Genetic Association Study
Family environment and adult resilience: contributions of positive parenting and the oxytocin receptor gene
Fc Gamma Receptor 3A Polymorphism and Risk for HIV-Associated Cryptococcal Disease
Fine-Mapping an Association of FSHR with Preterm Birth in a Finnish Population
Functional Properties of Rare Missense Variants of Human CDH13 Found in Adult Attention Deficit/Hyperactivity Disorder (ADHD) Patients
Effects of polymorphisms in nucleotide excision repair genes on glioma risk in a Chinese population
Eleven Candidate Susceptibility Genes for Common Familial Colorectal Cancer
Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian Population
Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss
Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathy