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Ny Hoang

Showing results (11-20 of 28) with videos related to

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NPJ Genomic Medicine|June 27, 2017
Variable phenotype expression in a family segregating microdeletions of the <i>NRXN1</i> and <i>MBD5</i> autism spectrum disorder susceptibility genesMarc Woodbury-Smith, Rob Nicolson, Mehdi Zarrei, et al.
NPJ Genomic Medicine|December 22, 2017
Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosageBreanne Dale, Bonnie MacKinnon Modi, Sanne Jilderda, et al.
NPJ Genomic Medicine|May 3, 2019
Expanding the neurodevelopmental phenotypes of individuals with de novo <i>KMT2A</i> variantsAda J S Chan, Cheryl Cytrynbaum, Ny Hoang, et al.
Molecular Autism|November 21, 2017
Mutations in <i>RAB39B</i> in individuals with intellectual disability, autism spectrum disorder, and macrocephalyMarc Woodbury-Smith, Eric Deneault, Ryan K C Yuen, et al.
NPJ Genomic Medicine|November 29, 2025
UBR5 loss-of-function variants in autism spectrum disorder and intellectual disability: case series and review of the literatureMiriam S Reuter, Nelson Bautista Salazar, Jennifer L Howe, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 5, 2024
Autistic traits in youth with familial adenomatous polyposis: A Dutch-Canadian case-control studyPolina Perlman Danieli, Ny Hoang, Thanuja Selvanayagam, et al.
Journal of Neurodevelopmental Disorders|July 5, 2024
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructureJane Summers, Danielle Baribeau, Polina Perlman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2020
Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2019
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Nature Reviews. Genetics|April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorderChristian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

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Pageof 3
NPJ Genomic Medicine|June 27, 2017
Variable phenotype expression in a family segregating microdeletions of the <i>NRXN1</i> and <i>MBD5</i> autism spectrum disorder susceptibility genesMarc Woodbury-Smith, Rob Nicolson, Mehdi Zarrei, et al.
NPJ Genomic Medicine|December 22, 2017
Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosageBreanne Dale, Bonnie MacKinnon Modi, Sanne Jilderda, et al.
NPJ Genomic Medicine|May 3, 2019
Expanding the neurodevelopmental phenotypes of individuals with de novo <i>KMT2A</i> variantsAda J S Chan, Cheryl Cytrynbaum, Ny Hoang, et al.
Molecular Autism|November 21, 2017
Mutations in <i>RAB39B</i> in individuals with intellectual disability, autism spectrum disorder, and macrocephalyMarc Woodbury-Smith, Eric Deneault, Ryan K C Yuen, et al.
NPJ Genomic Medicine|November 29, 2025
UBR5 loss-of-function variants in autism spectrum disorder and intellectual disability: case series and review of the literatureMiriam S Reuter, Nelson Bautista Salazar, Jennifer L Howe, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 5, 2024
Autistic traits in youth with familial adenomatous polyposis: A Dutch-Canadian case-control studyPolina Perlman Danieli, Ny Hoang, Thanuja Selvanayagam, et al.
Journal of Neurodevelopmental Disorders|July 5, 2024
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructureJane Summers, Danielle Baribeau, Polina Perlman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2020
Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2019
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
Nature Reviews. Genetics|April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorderChristian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
Pageof 3