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Bernie Devlin

Showing results (141-150 of 165) with videos related to

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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.
Molecular Psychiatry|June 11, 2021
Genome-wide association identifies the first risk loci for psychosis in Alzheimer diseaseMary Ann A DeMichele-Sweet, Lambertus Klei, Byron Creese, et al.
Bipolar Disorders|October 21, 2009
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophreniaHader A Mansour, Michael E Talkowski, Joel Wood, et al.
Nature Genetics|June 21, 2011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsyGünter U Höglinger, Nadine M Melhem, Dennis W Dickson, et al.
American Journal of Human Genetics|August 18, 2023
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesChelsea Lowther, Elise Valkanas, Jessica L Giordano, et al.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, 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.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Nature Neuroscience|September 27, 2016
Gene expression elucidates functional impact of polygenic risk for schizophreniaMenachem Fromer, Panos Roussos, Solveig K Sieberts, et al.
Pageof 17

Showing results (141-150 of 165) with videos related to

Sort By:
Pageof 17
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.
Molecular Psychiatry|June 11, 2021
Genome-wide association identifies the first risk loci for psychosis in Alzheimer diseaseMary Ann A DeMichele-Sweet, Lambertus Klei, Byron Creese, et al.
Bipolar Disorders|October 21, 2009
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophreniaHader A Mansour, Michael E Talkowski, Joel Wood, et al.
Nature Genetics|June 21, 2011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsyGünter U Höglinger, Nadine M Melhem, Dennis W Dickson, et al.
American Journal of Human Genetics|August 18, 2023
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesChelsea Lowther, Elise Valkanas, Jessica L Giordano, et al.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, 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.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Nature Neuroscience|September 27, 2016
Gene expression elucidates functional impact of polygenic risk for schizophreniaMenachem Fromer, Panos Roussos, Solveig K Sieberts, et al.
Pageof 17