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Caleb Webber

Showing results (21-30 of 76) with videos related to

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Human Molecular Genetics|December 15, 2010
Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromesTamim H Shaikh, Chad Haldeman-Englert, Elizabeth A Geiger, et al.
Genome Research|August 9, 2008
Reduced purifying selection prevails over positive selection in human copy number variant evolutionDuc-Quang Nguyen, Caleb Webber, Jayne Hehir-Kwa, et al.
Stem Cell Reports|June 6, 2020
Pro-maturational Effects of Human iPSC-Derived Cortical Astrocytes upon iPSC-Derived Cortical NeuronsAnne Hedegaard, Jimena Monzón-Sandoval, Sarah E Newey, et al.
Plos One|September 30, 2010
Elusive copy number variation in the mouse genomeAvigail Agam, Binnaz Yalcin, Amarjit Bhomra, et al.
Elife|June 26, 2014
Diagnostically relevant facial gestalt information from ordinary photosQuentin Ferry, Julia Steinberg, Caleb Webber, et al.
Biological Psychiatry Global Open Science|April 22, 2026
Spatial Mapping of Genetic Liability to Psychiatric Disorders in the Adult Human HippocampusYusuf Baran, Darren Cameron, Adele Pryce-Roberts, et al.
Elife|October 28, 2025
Changes in neural progenitor lineage composition during astrocytic differentiation of human iPSCsZongze Li, Lucia Fernandez Cardo, Michal Rokicki, et al.
Biological Psychiatry|September 23, 2022
Single-Nuclei RNA Sequencing of 5 Regions of the Human Prenatal Brain Implicates Developing Neuron Populations in Genetic Risk for SchizophreniaDarren Cameron, Da Mi, Ngoc-Nga Vinh, et al.
Plos Genetics|June 27, 2009
Forging links between human mental retardation-associated CNVs and mouse gene knockout modelsCaleb Webber, Jayne Y Hehir-Kwa, Duc-Quang Nguyen, et al.
Genome Research|April 19, 2015
The clustering of functionally related genes contributes to CNV-mediated diseaseTallulah Andrews, Frantisek Honti, Rolph Pfundt, et al.
Pageof 8

Showing results (21-30 of 76) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|December 15, 2010
Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromesTamim H Shaikh, Chad Haldeman-Englert, Elizabeth A Geiger, et al.
Genome Research|August 9, 2008
Reduced purifying selection prevails over positive selection in human copy number variant evolutionDuc-Quang Nguyen, Caleb Webber, Jayne Hehir-Kwa, et al.
Stem Cell Reports|June 6, 2020
Pro-maturational Effects of Human iPSC-Derived Cortical Astrocytes upon iPSC-Derived Cortical NeuronsAnne Hedegaard, Jimena Monzón-Sandoval, Sarah E Newey, et al.
Plos One|September 30, 2010
Elusive copy number variation in the mouse genomeAvigail Agam, Binnaz Yalcin, Amarjit Bhomra, et al.
Elife|June 26, 2014
Diagnostically relevant facial gestalt information from ordinary photosQuentin Ferry, Julia Steinberg, Caleb Webber, et al.
Biological Psychiatry Global Open Science|April 22, 2026
Spatial Mapping of Genetic Liability to Psychiatric Disorders in the Adult Human HippocampusYusuf Baran, Darren Cameron, Adele Pryce-Roberts, et al.
Elife|October 28, 2025
Changes in neural progenitor lineage composition during astrocytic differentiation of human iPSCsZongze Li, Lucia Fernandez Cardo, Michal Rokicki, et al.
Biological Psychiatry|September 23, 2022
Single-Nuclei RNA Sequencing of 5 Regions of the Human Prenatal Brain Implicates Developing Neuron Populations in Genetic Risk for SchizophreniaDarren Cameron, Da Mi, Ngoc-Nga Vinh, et al.
Plos Genetics|June 27, 2009
Forging links between human mental retardation-associated CNVs and mouse gene knockout modelsCaleb Webber, Jayne Y Hehir-Kwa, Duc-Quang Nguyen, et al.
Genome Research|April 19, 2015
The clustering of functionally related genes contributes to CNV-mediated diseaseTallulah Andrews, Frantisek Honti, Rolph Pfundt, et al.
Pageof 8