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Human Molecular Genetics
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January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
Anath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.
Nature
|
February 21, 2014
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
S C Mack, H Witt, R M Piro, et al.
American Journal of Human Genetics
|
April 28, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Molecular Psychiatry
|
September 21, 2022
Rare copy number variation in posttraumatic stress disorder
Adam X Maihofer, Worrawat Engchuan, Guillaume Huguet, et al.
Science (New York, N.Y.)
|
April 12, 2003
Human chromosome 7: DNA sequence and biology
Stephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
February 5, 2014
Cytogenetic prognostication within medulloblastoma subgroups
David J H Shih, Paul A Northcott, Marc Remke, et al.
Cell
|
November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotation
Brett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.
American Journal of Human Genetics
|
April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Dalila Pinto, Elsa Delaby, Daniele Merico, et al.
Biorxiv : the Preprint Server for Biology
|
June 26, 2025
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders
Jacob Ellegood, Antoine Beauchamp, Yohan Yee, et al.
Page
of 92
Search research articles
Search
Showing results (881-890 of 915) with videos related to
Sort By:
Page
of 92
Human Molecular Genetics
|
January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
Anath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.
Nature
|
February 21, 2014
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
S C Mack, H Witt, R M Piro, et al.
American Journal of Human Genetics
|
April 28, 2021
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature
Dmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Nature
|
November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Molecular Psychiatry
|
September 21, 2022
Rare copy number variation in posttraumatic stress disorder
Adam X Maihofer, Worrawat Engchuan, Guillaume Huguet, et al.
Science (New York, N.Y.)
|
April 12, 2003
Human chromosome 7: DNA sequence and biology
Stephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
February 5, 2014
Cytogenetic prognostication within medulloblastoma subgroups
David J H Shih, Paul A Northcott, Marc Remke, et al.
Cell
|
November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotation
Brett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.
American Journal of Human Genetics
|
April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Dalila Pinto, Elsa Delaby, Daniele Merico, et al.
Biorxiv : the Preprint Server for Biology
|
June 26, 2025
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders
Jacob Ellegood, Antoine Beauchamp, Yohan Yee, et al.
Page
of 92