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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 disorder
Bridget A Fernandez, Wendy Roberts, Brian Chung, et al.
Molecular Psychiatry
|
November 18, 2015
Psychiatric gene discoveries shape evidence on ADHD's biology
A 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 disorder
Dita Mušálková, Anna Přistoupilová, Ivana Jedličková, et al.
Nature Genetics
|
November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
E Belloni, M Muenke, E Roessler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 31, 2020
Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Journal of Clinical Epidemiology
|
April 26, 2023
CONSORT Harms 2022 statement, explanation, and elaboration: updated guideline for the reporting of harms in randomized trials
Daniela R Junqueira, Liliane Zorzela, Susan Golder, et al.
Journal of Neurodevelopmental Disorders
|
February 9, 2019
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
Gregory Costain, Susan Walker, Bob Argiropoulos, et al.
Translational Psychiatry
|
June 6, 2022
Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder
André Luíz Teles E Silva, Talita Glaser, Karina Griesi-Oliveira, et al.
American Journal of Human Genetics
|
November 22, 2016
Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5A
Chanshuai Han, Reem Alkhater, Tawfiq Froukh, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 10, 2025
Gene dosage architecture across complex traits
Sayeh Kazem, Kuldeep Kumar, Martineau Jean-Louis, et al.
Page
of 92
Search research articles
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Showing results (671-680 of 915) with videos related to
Sort By:
Page
of 92
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 disorder
Bridget A Fernandez, Wendy Roberts, Brian Chung, et al.
Molecular Psychiatry
|
November 18, 2015
Psychiatric gene discoveries shape evidence on ADHD's biology
A 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 disorder
Dita Mušálková, Anna Přistoupilová, Ivana Jedličková, et al.
Nature Genetics
|
November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
E Belloni, M Muenke, E Roessler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 31, 2020
Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Journal of Clinical Epidemiology
|
April 26, 2023
CONSORT Harms 2022 statement, explanation, and elaboration: updated guideline for the reporting of harms in randomized trials
Daniela R Junqueira, Liliane Zorzela, Susan Golder, et al.
Journal of Neurodevelopmental Disorders
|
February 9, 2019
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
Gregory Costain, Susan Walker, Bob Argiropoulos, et al.
Translational Psychiatry
|
June 6, 2022
Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder
André Luíz Teles E Silva, Talita Glaser, Karina Griesi-Oliveira, et al.
American Journal of Human Genetics
|
November 22, 2016
Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5A
Chanshuai Han, Reem Alkhater, Tawfiq Froukh, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 10, 2025
Gene dosage architecture across complex traits
Sayeh Kazem, Kuldeep Kumar, Martineau Jean-Louis, et al.
Page
of 92