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W Scherer

Showing results (881-890 of 915) with videos related to

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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 phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.
Nature|February 21, 2014
Epigenomic alterations define lethal CIMP-positive ependymomas of infancyS 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 signatureDmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Nature|November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autismSilvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Molecular Psychiatry|September 21, 2022
Rare copy number variation in posttraumatic stress disorderAdam X Maihofer, Worrawat Engchuan, Guillaume Huguet, et al.
Science (New York, N.Y.)|April 12, 2003
Human chromosome 7: DNA sequence and biologyStephen 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 subgroupsDavid J H Shih, Paul A Northcott, Marc Remke, et al.
Cell|November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett 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 disordersDalila 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 DisordersJacob Ellegood, Antoine Beauchamp, Yohan Yee, et al.
Pageof 92

Showing results (881-890 of 915) with videos related to

Sort By:
Pageof 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 phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.
Nature|February 21, 2014
Epigenomic alterations define lethal CIMP-positive ependymomas of infancyS 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 signatureDmitrijs Rots, Eric Chater-Diehl, Alexander J M Dingemans, et al.
Nature|November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autismSilvia De Rubeis, Xin He, Arthur P Goldberg, et al.
Molecular Psychiatry|September 21, 2022
Rare copy number variation in posttraumatic stress disorderAdam X Maihofer, Worrawat Engchuan, Guillaume Huguet, et al.
Science (New York, N.Y.)|April 12, 2003
Human chromosome 7: DNA sequence and biologyStephen 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 subgroupsDavid J H Shih, Paul A Northcott, Marc Remke, et al.
Cell|November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett 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 disordersDalila 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 DisordersJacob Ellegood, Antoine Beauchamp, Yohan Yee, et al.
Pageof 92