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Molecular and Cellular Neurosciences|March 27, 2007
A macromolecular complex involving the amyloid precursor protein (APP) and the cytosolic adapter FE65 is a negative regulator of axon branchingAnnat F Ikin, Shasta L Sabo, Lorene M Lanier, et al.
American Journal of Human Genetics|April 4, 2020
Co-localization between Sequence Constraint and Epigenomic Information Improves Interpretation of Whole-Genome Sequencing DataDanqing Xu, Chen Wang, Krzysztof Kiryluk, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 13, 2014
Expression profiling associates blood and brain glucocorticoid receptor signaling with trauma-related individual differences in both sexesNikolaos P Daskalakis, Hagit Cohen, Guiqing Cai, et al.
Molecular Autism|December 28, 2019
Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literatureAlexander Kolevzon, Elsa Delaby, Elizabeth Berry-Kravis, et al.
Journal of Autism and Developmental Disorders|April 27, 2011
Brief report: the Autism Mental Status Examination: development of a brief autism-focused examDavid Grodberg, Paige M Weinger, Alexander Kolevzon, et al.
Nature Genetics|July 21, 2014
Most genetic risk for autism resides with common variationTrent Gaugler, Lambertus Klei, Stephan J Sanders, et al.
Nature Genetics|February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samplesJack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
American Journal of Human Genetics|April 19, 2016
A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control StudiesCorneliu A Bodea, Benjamin M Neale, Stephan Ripke, et al.
Human Genetics|April 17, 2007
Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generationBernie Devlin, Lambertus Klei, Marina Myles-Worsley, et al.
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