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Michael E Talkowski

Showing results (31-40 of 184) with videos related to

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American Journal of Medical Genetics. Part A|July 11, 2017
A novel microduplication of ARID1B: Clinical, genetic, and proteomic findingsCatarina M Seabra, Nicholas Szoko, Serkan Erdin, et al.
Endocrinology|June 14, 2021
Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem CellsKim L Keen, Andrew J Petersen, Alexander G Figueroa, et al.
Cell Reports Methods|December 13, 2023
Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR librariesXander Nuttle, Nicholas D Burt, Benjamin Currall, et al.
Psychiatric Genetics|December 21, 2011
Genetic associations between neuregulin-1 SNPs and neurocognitive function in multigenerational, multiplex schizophrenia familiesJessica L Yokley, Konasale M Prasad, Kodavali V Chowdari, et al.
Nature Communications|May 19, 2021
16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitroMaria Sundberg, Hannah Pinson, Richard S Smith, et al.
American Journal of Human Genetics|December 24, 2019
SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male InfertilitySamantha L P Schilit, Shreya Menon, Corinna Friedrich, et al.
Nature|May 19, 2012
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variantChristelle Golzio, Jason Willer, Michael E Talkowski, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editingDahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.
Biological Psychiatry|August 9, 2006
Novel, replicated associations between dopamine D3 receptor gene polymorphisms and schizophrenia in two independent samplesMichael E Talkowski, Hader Mansour, Kodavali V Chowdari, et al.
Nature|July 12, 2018
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterationsPo-Ru Loh, Giulio Genovese, Robert E Handsaker, et al.
Pageof 19

Showing results (31-40 of 184) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics. Part A|July 11, 2017
A novel microduplication of ARID1B: Clinical, genetic, and proteomic findingsCatarina M Seabra, Nicholas Szoko, Serkan Erdin, et al.
Endocrinology|June 14, 2021
Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem CellsKim L Keen, Andrew J Petersen, Alexander G Figueroa, et al.
Cell Reports Methods|December 13, 2023
Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR librariesXander Nuttle, Nicholas D Burt, Benjamin Currall, et al.
Psychiatric Genetics|December 21, 2011
Genetic associations between neuregulin-1 SNPs and neurocognitive function in multigenerational, multiplex schizophrenia familiesJessica L Yokley, Konasale M Prasad, Kodavali V Chowdari, et al.
Nature Communications|May 19, 2021
16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitroMaria Sundberg, Hannah Pinson, Richard S Smith, et al.
American Journal of Human Genetics|December 24, 2019
SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male InfertilitySamantha L P Schilit, Shreya Menon, Corinna Friedrich, et al.
Nature|May 19, 2012
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variantChristelle Golzio, Jason Willer, Michael E Talkowski, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editingDahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.
Biological Psychiatry|August 9, 2006
Novel, replicated associations between dopamine D3 receptor gene polymorphisms and schizophrenia in two independent samplesMichael E Talkowski, Hader Mansour, Kodavali V Chowdari, et al.
Nature|July 12, 2018
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterationsPo-Ru Loh, Giulio Genovese, Robert E Handsaker, et al.
Pageof 19