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Cell|November 26, 2013
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autismA Jeremy Willsey, Stephan J Sanders, Mingfeng Li, et al.Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.Nature|April 13, 2012
De novo mutations revealed by whole-exome sequencing are strongly associated with autismStephan J Sanders, Michael T Murtha, Abha R Gupta, et al.Science (New York, N.Y.)|May 23, 2024
Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brainCindy Wen, Michael Margolis, Rujia Dai, et al.Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brainCindy Wen, Michael Margolis, Rujia Dai, et al.Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.Nature Genetics|January 6, 2009
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association studyMark S Silverberg, Judy H Cho, John D Rioux, et al.Psychological Medicine|September 15, 2012
Persistent infection with neurotropic herpes viruses and cognitive impairmentA M M Watson, K M Prasad, L Klei, et al.Cell|January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of AutismF Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.Pageof 47