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Joseph D Buxbaum

Showing results (291-300 of 361) with videos related to

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American Journal of Human Genetics|August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with PhenotypeMichael S Breen, Paras Garg, Lara Tang, et al.
Scientific Data|September 26, 2019
CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar DisorderGabriel E Hoffman, Jaroslav Bendl, Georgios Voloudakis, et al.
Nature Neuroscience|July 18, 2017
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorderElaine T Lim, Mohammed Uddin, Silvia De Rubeis, et al.
Nature Genetics|September 26, 2022
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroupsManuel Mattheisen, Jakob Grove, Thomas D Als, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial EndpointsLatha Valluripalli Soorya, Camille W Brune, Cristan A Farmer, 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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 23, 2016
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African AmericansJesse Mez, Jaeyoon Chung, Gyungah Jun, et al.
Cell Reports|April 9, 2020
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal CortexDonna M Werling, Sirisha Pochareddy, Jinmyung Choi, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Brain : a Journal of Neurology|August 18, 2022
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASDLisa Pavinato, Andrea Delle Vedove, Diana Carli, et al.
Pageof 37

Showing results (291-300 of 361) with videos related to

Sort By:
Pageof 37
American Journal of Human Genetics|August 8, 2020
Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with PhenotypeMichael S Breen, Paras Garg, Lara Tang, et al.
Scientific Data|September 26, 2019
CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar DisorderGabriel E Hoffman, Jaroslav Bendl, Georgios Voloudakis, et al.
Nature Neuroscience|July 18, 2017
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorderElaine T Lim, Mohammed Uddin, Silvia De Rubeis, et al.
Nature Genetics|September 26, 2022
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroupsManuel Mattheisen, Jakob Grove, Thomas D Als, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial EndpointsLatha Valluripalli Soorya, Camille W Brune, Cristan A Farmer, 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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 23, 2016
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African AmericansJesse Mez, Jaeyoon Chung, Gyungah Jun, et al.
Cell Reports|April 9, 2020
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal CortexDonna M Werling, Sirisha Pochareddy, Jinmyung Choi, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Brain : a Journal of Neurology|August 18, 2022
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASDLisa Pavinato, Andrea Delle Vedove, Diana Carli, et al.
Pageof 37