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Molecular Autism|May 27, 2014
Rare deleterious mutations of the gene EFR3A in autism spectrum disordersAbha R Gupta, Michelle Pirruccello, Feng Cheng, et al.American Journal of Medical Genetics. Part A|October 7, 2008
Molecular characterization of a patient with 3p deletion syndrome and a review of the literatureThomas V Fernandez, I J García-González, Christopher E Mason, et al.Nature Communications|December 6, 2023
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHDSheng Wang, Belinda Wang, Vanessa Drury, et al.Neuron|May 5, 2017
De Novo Coding Variants Are Strongly Associated with Tourette DisorderA Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, et al.Plos Genetics|January 27, 2015
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or ContactinsJohn D Murdoch, Abha R Gupta, Stephan J Sanders, et al.Molecular Autism|April 11, 2017
Neurogenetic analysis of childhood disintegrative disorderAbha R Gupta, Alexander Westphal, Daniel Y J Yang, et al.Biological Psychiatry|December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autismThomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.Cell Reports|September 27, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|August 14, 2021
Investigation of gene-environment interactions in relation to tic severityMohamed Abdulkadir, Dongmei Yu, Lisa Osiecki, et al.European Archives of Psychiatry and Clinical Neuroscience|May 31, 2017
Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approachMohamed Abdulkadir, Douglas Londono, Derek Gordon, et al.Pageof 6