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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
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
Effect of interleukin-17A and interleukin-17F gene polymorphisms on the risk of gastric cancer in a Chinese population
Contribution of PTPN22, CD28, CTLA-4 and ZAP-70 variants to the risk of type 1 diabetes in Tunisians
CRY2 Genetic Variants Associate with Dysthymia