De novo mutations in histone-modifying genes in congenital heart disease.
Research Articles
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.
Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells.
Rett syndrome: Genes, synapses, circuits, and therapeutics.
Zebrafish homologs of genes within 16p11.2, a genomic region associated with brain disorders, are active during brain development, and include two deletion dosage sensor genes.
The autism sequencing consortium: Large-scale, high-throughput sequencing in autism spectrum disorders.
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism.
Drosophila neuroligin 2 is required presynaptically and postsynaptically for proper synaptic differentiation and synaptic transmission.
Preprocessing and quality control strategies for Illumina DASL assay-based brain gene expression studies with semi-degraded samples.
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.
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