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Michael E Talkowski

Showing results (91-100 of 184) with videos related to

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Biorxiv : the Preprint Server for Biology|November 24, 2025
CRISPR-engineered deletion of <i>POGZ</i> alters transcription factor binding at promoters of genes involved in synaptic signalingMariana Moyses-Oliveira, Yating Liu, Serkan Erdin, et al.
HGG Advances|July 11, 2026
CRISPR-engineered deletion of POGZ alters transcription factor binding at promoters of genes involved in synaptic signalingMariana Moyses-Oliveira, Yating Liu, Serkan Erdin, et al.
Nature Genetics|October 25, 2022
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16pDaniel J Weiner, Emi Ling, Serkan Erdin, et al.
Biological Psychiatry|December 29, 2022
Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived NeuronsEuan Parnell, Lorenza Culotta, Marc P Forrest, et al.
American Journal of Human Genetics|October 25, 2022
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal modelsKiana Mohajeri, Rachita Yadav, Eva D'haene, et al.
American Journal of Human Genetics|November 9, 2024
Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assemblyYulia Mostovoy, Philip M Boone, Yongqing Huang, et al.
Gut|July 12, 2020
Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBDShixian Hu, Arnau Vich Vila, Ranko Gacesa, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Transcriptomic profiling uncovers mis-splicing and gene fusions in amyotrophic lateral sclerosisHuilin Xu, Tiziana Petrozziello, Adel Boudi, et al.
Circulation|December 28, 2018
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial InfarctionAmit V Khera, Mark Chaffin, Seyedeh M Zekavat, et al.
Pageof 19

Showing results (91-100 of 184) with videos related to

Sort By:
Pageof 19
Biorxiv : the Preprint Server for Biology|November 24, 2025
CRISPR-engineered deletion of <i>POGZ</i> alters transcription factor binding at promoters of genes involved in synaptic signalingMariana Moyses-Oliveira, Yating Liu, Serkan Erdin, et al.
HGG Advances|July 11, 2026
CRISPR-engineered deletion of POGZ alters transcription factor binding at promoters of genes involved in synaptic signalingMariana Moyses-Oliveira, Yating Liu, Serkan Erdin, et al.
Nature Genetics|October 25, 2022
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16pDaniel J Weiner, Emi Ling, Serkan Erdin, et al.
Biological Psychiatry|December 29, 2022
Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived NeuronsEuan Parnell, Lorenza Culotta, Marc P Forrest, et al.
American Journal of Human Genetics|October 25, 2022
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal modelsKiana Mohajeri, Rachita Yadav, Eva D'haene, et al.
American Journal of Human Genetics|November 9, 2024
Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assemblyYulia Mostovoy, Philip M Boone, Yongqing Huang, et al.
Gut|July 12, 2020
Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBDShixian Hu, Arnau Vich Vila, Ranko Gacesa, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Transcriptomic profiling uncovers mis-splicing and gene fusions in amyotrophic lateral sclerosisHuilin Xu, Tiziana Petrozziello, Adel Boudi, et al.
Circulation|December 28, 2018
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial InfarctionAmit V Khera, Mark Chaffin, Seyedeh M Zekavat, et al.
Pageof 19