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Thanuja Selvanayagam

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European Journal of Human Genetics : EJHG|September 6, 2022
Developmental implications of genetic testing for physical indicationsDanielle A Baribeau, Ny Hoang, Thanuja Selvanayagam, et al.
European Journal of Human Genetics : EJHG|July 7, 2018
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesityThanuja Selvanayagam, Susan Walker, Matthew J Gazzellone, et al.
Journal of Medical Genetics|April 1, 2025
Clinical utility of genome sequencing in autism: illustrative examples from a genomic research studyThanuja Selvanayagam, Ny Hoang, Ege Sarikaya, 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|August 30, 2014
Copy number variation in Han Chinese individuals with autism spectrum disorderMatthew J Gazzellone, Xue Zhou, Anath C Lionel, 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.
Brain : a Journal of Neurology|July 28, 2025
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatoniaHarsha Murthy, Ny Hoang, Jamie C Stark, et al.
Nature|May 13, 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autismClarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.
Cell|November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
European Journal of Human Genetics : EJHG|September 6, 2022
Developmental implications of genetic testing for physical indicationsDanielle A Baribeau, Ny Hoang, Thanuja Selvanayagam, et al.
European Journal of Human Genetics : EJHG|July 7, 2018
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesityThanuja Selvanayagam, Susan Walker, Matthew J Gazzellone, et al.
Journal of Medical Genetics|April 1, 2025
Clinical utility of genome sequencing in autism: illustrative examples from a genomic research studyThanuja Selvanayagam, Ny Hoang, Ege Sarikaya, 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|August 30, 2014
Copy number variation in Han Chinese individuals with autism spectrum disorderMatthew J Gazzellone, Xue Zhou, Anath C Lionel, 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.
Brain : a Journal of Neurology|July 28, 2025
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatoniaHarsha Murthy, Ny Hoang, Jamie C Stark, et al.
Nature|May 13, 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autismClarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.
Cell|November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.
Pageof 1