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Proceedings of the National Academy of Sciences of the United States of America
|
August 8, 2006
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia
Lyudmila Georgieva, Valentina Moskvina, Tim Peirce, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 6, 2005
Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays
Malek Faham, Jianbiao Zheng, Martin Moorhead, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
July 25, 2021
Visual Evoked Potential Abnormalities in Phelan-McDermid Syndrome
Paige M Siper, Mikaela A Rowe, Sylvia B Guillory, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
September 20, 2017
PTSD Blood Transcriptome Mega-Analysis: Shared Inflammatory Pathways across Biological Sex and Modes of Trauma
Michael S Breen, Daniel S Tylee, Adam X Maihofer, et al.
Molecular Autism
|
March 8, 2014
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
Li Liu, Jing Lei, Stephan J Sanders, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 19, 2022
Gene-based therapeutics for rare genetic neurodevelopmental psychiatric disorders
Beverly L Davidson, Guangping Gao, Elizabeth Berry-Kravis, et al.
Nature Neuroscience
|
May 27, 2024
Regulation of cell distancing in peri-plaque glial nets by Plexin-B1 affects glial activation and amyloid compaction in Alzheimer's disease
Yong Huang, Minghui Wang, Haofei Ni, et al.
Human Molecular Genetics
|
April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Robert A Kozol, Holly N Cukier, Bing Zou, et al.
American Journal on Intellectual and Developmental Disabilities
|
August 26, 2025
Genetic Subtypes of Phelan-McDermid Syndrome Exhibit Similar Rates of Change Despite Differences in Level of Impairment in Developmental Constructs
Tess Levy, Cristan Farmer, Siddharth Srivastava, et al.
Human Molecular Genetics
|
September 24, 2021
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium
Tess Levy, Jennifer H Foss-Feig, Catalina Betancur, et al.
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of 37
Search research articles
Search
Showing results (251-260 of 361) with videos related to
Sort By:
Page
of 37
Proceedings of the National Academy of Sciences of the United States of America
|
August 8, 2006
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia
Lyudmila Georgieva, Valentina Moskvina, Tim Peirce, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 6, 2005
Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays
Malek Faham, Jianbiao Zheng, Martin Moorhead, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
July 25, 2021
Visual Evoked Potential Abnormalities in Phelan-McDermid Syndrome
Paige M Siper, Mikaela A Rowe, Sylvia B Guillory, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
September 20, 2017
PTSD Blood Transcriptome Mega-Analysis: Shared Inflammatory Pathways across Biological Sex and Modes of Trauma
Michael S Breen, Daniel S Tylee, Adam X Maihofer, et al.
Molecular Autism
|
March 8, 2014
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
Li Liu, Jing Lei, Stephan J Sanders, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 19, 2022
Gene-based therapeutics for rare genetic neurodevelopmental psychiatric disorders
Beverly L Davidson, Guangping Gao, Elizabeth Berry-Kravis, et al.
Nature Neuroscience
|
May 27, 2024
Regulation of cell distancing in peri-plaque glial nets by Plexin-B1 affects glial activation and amyloid compaction in Alzheimer's disease
Yong Huang, Minghui Wang, Haofei Ni, et al.
Human Molecular Genetics
|
April 18, 2015
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Robert A Kozol, Holly N Cukier, Bing Zou, et al.
American Journal on Intellectual and Developmental Disabilities
|
August 26, 2025
Genetic Subtypes of Phelan-McDermid Syndrome Exhibit Similar Rates of Change Despite Differences in Level of Impairment in Developmental Constructs
Tess Levy, Cristan Farmer, Siddharth Srivastava, et al.
Human Molecular Genetics
|
September 24, 2021
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium
Tess Levy, Jennifer H Foss-Feig, Catalina Betancur, et al.
Page
of 37