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Journal of Autism and Developmental Disorders|January 4, 2021
DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental DisordersMichelle T Siu, Sarah J Goodman, Isaac Yellan, et al.Developmental Cell|January 6, 2015
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentDenis Gallagher, Anastassia Voronova, Mark A Zander, et al.Nature Genetics|June 30, 2001
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemiaZ Ma, S W Morris, V Valentine, et al.Clinical Genetics|December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorderM T Carter, S M Nikkel, B A Fernandez, et al.G3 (Bethesda, Md.)|September 19, 2015
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion SyndromeDaniele Merico, Mehdi Zarrei, Gregory Costain, et al.Brain : a Journal of Neurology|September 11, 2012
Early-onset Lafora body diseaseJulie Turnbull, Jean-Marie Girard, Hannes Lohi, et al.Clinical Epigenetics|July 18, 2019
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variantsM T Siu, D T Butcher, A L Turinsky, et al.Journal of Medical Genetics|September 17, 2009
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorderBridget A Fernandez, Wendy Roberts, Brian Chung, et al.Molecular Psychiatry|November 18, 2015
Psychiatric gene discoveries shape evidence on ADHD's biologyA Thapar, J Martin, E Mick, et al.Genes, Brain, and Behavior|February 15, 2024
Increased burden of rare protein-truncating variants in constrained, brain-specific and synaptic genes in extremely impulsively violent males with antisocial personality disorderDita Mušálková, Anna Přistoupilová, Ivana Jedličková, et al.Pageof 88