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Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
Selenium Drives a Transcriptional Adaptive Program to Block Ferroptosis and Treat Stroke
Functional impact of global rare copy number variation in autism spectrum disorders
Common genetic variants, acting additively, are a major source of risk for autism
Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage
Chromosome conformation elucidates regulatory relationships in developing human brain.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Human Disease Variation in the Light of Population Genomics
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
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