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Susan Walker

Showing results (181-190 of 260) with videos related to

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Journal of Neurodevelopmental Disorders|February 9, 2019
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disordersGregory Costain, Susan Walker, Bob Argiropoulos, et al.
Archives of Women'S Mental Health|February 9, 2021
Prenatal attachment: using measurement invariance to test the validity of comparisons across eight culturally diverse countriesSarah Foley, Claire Hughes, Aja Louise Murray, et al.
American Journal of Human Genetics|November 22, 2016
Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5AChanshuai Han, Reem Alkhater, Tawfiq Froukh, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
High-dimensional multiomics reveals perturbations to IL-6/IL-6R axis and RUNX3 in CD4+ T cells during third trimester pregnancyJennifer Habel, Thi H O Nguyen, Natasha de Alwis, et al.
Archives of Women'S Mental Health|April 15, 2021
Correction to: Prenatal attachment: Using measurement invariance to test the validity of comparisons across eight culturally diverse countriesSarah Foley, Claire Hughes, Aja Louise Murray, et al.
Hepatology (Baltimore, Md.)|October 31, 2017
The circulating microbiome signature and inferred functional metagenomics in alcoholic hepatitisPuneet Puri, Suthat Liangpunsakul, Jeffrey E Christensen, et al.
Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
American Journal of Medical Genetics. Part A|June 23, 2021
Genome sequencing for detection of pathogenic deep intronic variation: A clinical case report illustrating opportunities and challengesSusan Walker, Sylvia Lamoureux, Tayyaba Khan, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Elife|February 13, 2019
<i>CNTN5</i><sup>-</sup><i></i>or <i>EHMT2</i><sup>-</sup><i></i>human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networksEric Deneault, Muhammad Faheem, Sean H White, et al.
Pageof 26

Showing results (181-190 of 260) with videos related to

Sort By:
Pageof 26
Journal of Neurodevelopmental Disorders|February 9, 2019
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disordersGregory Costain, Susan Walker, Bob Argiropoulos, et al.
Archives of Women'S Mental Health|February 9, 2021
Prenatal attachment: using measurement invariance to test the validity of comparisons across eight culturally diverse countriesSarah Foley, Claire Hughes, Aja Louise Murray, et al.
American Journal of Human Genetics|November 22, 2016
Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5AChanshuai Han, Reem Alkhater, Tawfiq Froukh, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
High-dimensional multiomics reveals perturbations to IL-6/IL-6R axis and RUNX3 in CD4+ T cells during third trimester pregnancyJennifer Habel, Thi H O Nguyen, Natasha de Alwis, et al.
Archives of Women'S Mental Health|April 15, 2021
Correction to: Prenatal attachment: Using measurement invariance to test the validity of comparisons across eight culturally diverse countriesSarah Foley, Claire Hughes, Aja Louise Murray, et al.
Hepatology (Baltimore, Md.)|October 31, 2017
The circulating microbiome signature and inferred functional metagenomics in alcoholic hepatitisPuneet Puri, Suthat Liangpunsakul, Jeffrey E Christensen, et al.
Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
American Journal of Medical Genetics. Part A|June 23, 2021
Genome sequencing for detection of pathogenic deep intronic variation: A clinical case report illustrating opportunities and challengesSusan Walker, Sylvia Lamoureux, Tayyaba Khan, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Elife|February 13, 2019
<i>CNTN5</i><sup>-</sup><i></i>or <i>EHMT2</i><sup>-</sup><i></i>human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networksEric Deneault, Muhammad Faheem, Sean H White, et al.
Pageof 26