Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
Biological Psychiatry|December 24, 2014
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Pauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Biological Psychiatry|June 11, 2013
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous traitPauline Chaste, Lambertus Klei, Stephan J Sanders, et al.
Autism Research : Official Journal of the International Society for Autism Research|January 21, 2020
Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART StudyCarolyn E B McCormick, Brian C Kavanaugh, Danielle Sipsock, et al.
Molecular Autism|October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autismLambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Neuron|June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autismStephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
Pageof 4