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American Journal of Medical Genetics. Part A
|
July 11, 2017
A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings
Catarina M Seabra, Nicholas Szoko, Serkan Erdin, et al.
Endocrinology
|
June 14, 2021
Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem Cells
Kim 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 libraries
Xander 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 families
Jessica 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 vitro
Maria 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 Infertility
Samantha 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 variant
Christelle 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 editing
Dahlia 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 samples
Michael E Talkowski, Hader Mansour, Kodavali V Chowdari, et al.
Nature
|
July 12, 2018
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations
Po-Ru Loh, Giulio Genovese, Robert E Handsaker, et al.
Page
of 19
Search research articles
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Showing results (31-40 of 184) with videos related to
Sort By:
Page
of 19
American Journal of Medical Genetics. Part A
|
July 11, 2017
A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings
Catarina M Seabra, Nicholas Szoko, Serkan Erdin, et al.
Endocrinology
|
June 14, 2021
Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem Cells
Kim 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 libraries
Xander 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 families
Jessica 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 vitro
Maria 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 Infertility
Samantha 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 variant
Christelle 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 editing
Dahlia 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 samples
Michael E Talkowski, Hader Mansour, Kodavali V Chowdari, et al.
Nature
|
July 12, 2018
Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations
Po-Ru Loh, Giulio Genovese, Robert E Handsaker, et al.
Page
of 19