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Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans
Download from www.nature.comDAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
Download from link.springer.comGenetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
Download from www.hal.inserm.frIntellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism
Download from www.ncbi.nlm.nih.govHigh rate of disease-related copy number variations in childhood onset schizophrenia
Download from www.ncbi.nlm.nih.govDe novo mutations in histone modifying genes in congenital heart disease
Download from www.ncbi.nlm.nih.govUsing whole exome sequencing to identify inherited causes of autism
Download from www.ncbi.nlm.nih.govCopy-Number Disorders Are a Common Cause of Congenital Kidney Malformations
Download from www.ncbi.nlm.nih.govMutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy
Download from www.ncbi.nlm.nih.govA complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder
Download from www.researchgate.netDe novo mutations revealed by whole exome sequencing are strongly associated with autism
Download from www.nature.comCommon genetic variants, acting additively, are a major source of risk for autism
Download from dx.doi.orgMissing publications? Search for publications with a matching author name.