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David Hunt

Showing results (171-180 of 182) with videos related to

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Nature Methods|May 7, 2024
Author Correction: brainlife.io: a decentralized and open-source cloud platform to support neuroscience researchSoichi Hayashi, Bradley A Caron, Anibal Sólon Heinsfeld, et al.
Nature Methods|April 11, 2024
brainlife.io: a decentralized and open-source cloud platform to support neuroscience researchSoichi Hayashi, Bradley A Caron, Anibal Sólon Heinsfeld, et al.
Arxiv|June 19, 2023
<i>brainlife.io</i>: A decentralized and open source cloud platform to support neuroscience researchSoichi Hayashi, Bradley A Caron, Anibal Sólon Heinsfeld, et al.
American Journal of Human Genetics|December 28, 2019
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental DisorderRaphael Carapito, Ekaterina L Ivanova, Aurore Morlon, et al.
American Journal of Human Genetics|January 15, 2019
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental DisorderRaphael Carapito, Ekaterina L Ivanova, Aurore Morlon, et al.
American Journal of Human Genetics|September 21, 2022
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndromeSanaa Choufani, Vanda McNiven, Cheryl Cytrynbaum, et al.
American Journal of Human Genetics|August 8, 2025
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndromeSanaa Choufani, Vanda McNiven, Cheryl Cytrynbaum, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 31, 2024
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorderNour Elkhateeb, Renarta Crookes, Michael Spiller, et al.
Molecular Psychiatry|November 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental conditionElizabeth E Palmer, Michael Pusch, Alessandra Picollo, et al.
Neurology. Genetics|November 18, 2021
<i>PURA-</i>Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic SpectrumKatrine M Johannesen, Elena Gardella, Cathrine E Gjerulfsen, et al.
Pageof 19

Showing results (171-180 of 182) with videos related to

Sort By:
Pageof 19
Nature Methods|May 7, 2024
Author Correction: brainlife.io: a decentralized and open-source cloud platform to support neuroscience researchSoichi Hayashi, Bradley A Caron, Anibal Sólon Heinsfeld, et al.
Nature Methods|April 11, 2024
brainlife.io: a decentralized and open-source cloud platform to support neuroscience researchSoichi Hayashi, Bradley A Caron, Anibal Sólon Heinsfeld, et al.
Arxiv|June 19, 2023
<i>brainlife.io</i>: A decentralized and open source cloud platform to support neuroscience researchSoichi Hayashi, Bradley A Caron, Anibal Sólon Heinsfeld, et al.
American Journal of Human Genetics|December 28, 2019
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental DisorderRaphael Carapito, Ekaterina L Ivanova, Aurore Morlon, et al.
American Journal of Human Genetics|January 15, 2019
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental DisorderRaphael Carapito, Ekaterina L Ivanova, Aurore Morlon, et al.
American Journal of Human Genetics|September 21, 2022
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndromeSanaa Choufani, Vanda McNiven, Cheryl Cytrynbaum, et al.
American Journal of Human Genetics|August 8, 2025
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndromeSanaa Choufani, Vanda McNiven, Cheryl Cytrynbaum, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 31, 2024
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorderNour Elkhateeb, Renarta Crookes, Michael Spiller, et al.
Molecular Psychiatry|November 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental conditionElizabeth E Palmer, Michael Pusch, Alessandra Picollo, et al.
Neurology. Genetics|November 18, 2021
<i>PURA-</i>Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic SpectrumKatrine M Johannesen, Elena Gardella, Cathrine E Gjerulfsen, et al.
Pageof 19