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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
Family environment and adult resilience: contributions of positive parenting and the oxytocin receptor gene
CRY2 Genetic Variants Associate with Dysthymia
Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis
Defining the Contribution of CNTNAP2 to Autism Susceptibility