Search Results - "Selvanayagam T"

UBR5 loss-of-function variants in autism spectrum disorder and intellectual disability: case series and review of the literature.

Authors: Reuter MS Salazar NB Howe JL et al.

Source: NPJ genomic medicine [NPJ Genom Med] 2025 Nov 29; Vol. 11 (1), pp. 1. Date of Electronic Publication: 2025 Nov 29.

Publication Type: Journal Article

Journal Info: Publisher: Springer Nature in partnership with the Center of Excellence in Genomic Medicine Research at King Abdulaziz University Country of Publication: England NLM ID: 101685193 Publication Model: Electronic Cited Medium: Internet ISSN: 2056-7944 (Electronic) Linking ISSN: 20567944 NLM ISO Abbreviation: NPJ Genom Med Subsets: PubMed not MEDLINE

An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism.

Authors: Bradley CA Ko SY Tian M et al.

Source: Nature [Nature] 2026 May 13. Date of Electronic Publication: 2026 May 13.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-4687 (Electronic) Linking ISSN: 00280836 NLM ISO Abbreviation: Nature Subsets: MEDLINE

Autistic traits in youth with familial adenomatous polyposis: A Dutch-Canadian case-control study.

Authors: Danieli PP Hoang N Selvanayagam T et al.

Source: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Genet] 2024 Dec; Vol. 195 (8), pp. e32999. Date of Electronic Publication: 2024 Jul 05.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235742 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-485X (Electronic) Linking ISSN: 15524841 NLM ISO Abbreviation: Am J Med Genet B Neuropsychiatr Genet Subsets: MEDLINE

Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia.

Authors: Murthy H Hoang N Stark JC et al.

Source: Brain : a journal of neurology [Brain] 2026 Jan 08; Vol. 149 (1), pp. 252-261.

Publication Type: Journal Article

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Clinical utility of genome sequencing in autism: illustrative examples from a genomic research study.

Authors: Selvanayagam T Hoang N Sarikaya E et al.

Source: Journal of medical genetics [J Med Genet] 2025 May 27; Vol. 62 (6), pp. 413-421. Date of Electronic Publication: 2025 May 27.

Publication Type: Journal Article

Journal Info: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure.

Authors: Summers J Baribeau D Perlman P et al.

Source: Journal of neurodevelopmental disorders [J Neurodev Disord] 2024 Jul 05; Vol. 16 (1), pp. 37. Date of Electronic Publication: 2024 Jul 05.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101483832 Publication Model: Electronic Cited Medium: Internet ISSN: 1866-1955 (Electronic) Linking ISSN: 18661947 NLM ISO Abbreviation: J Neurodev Disord Subsets: MEDLINE

Genomic architecture of autism from comprehensive whole-genome sequence annotation.

Authors: Trost B Thiruvahindrapuram B Chan AJS et al.

Source: Cell [Cell] 2022 Nov 10; Vol. 185 (23), pp. 4409-4427.e18.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0413066 Publication Model: Print Cited Medium: Internet ISSN: 1097-4172 (Electronic) Linking ISSN: 00928674 NLM ISO Abbreviation: Cell Subsets: MEDLINE

Developmental implications of genetic testing for physical indications.

Authors: Baribeau DA Hoang N Selvanayagam T et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2022 Nov; Vol. 30 (11), pp. 1297-1300. Date of Electronic Publication: 2022 Sep 06.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.

Authors: Selvanayagam T Walker S Gazzellone MJ et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2018 Nov; Vol. 26 (11), pp. 1588-1596. Date of Electronic Publication: 2018 Jul 05.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Copy number variation in Han Chinese individuals with autism spectrum disorder.

Authors: Gazzellone MJ Zhou X Lionel AC et al.

Source: Journal of neurodevelopmental disorders [J Neurodev Disord] 2014; Vol. 6 (1), pp. 34. Date of Electronic Publication: 2014 Aug 23.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101483832 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1866-1947 (Print) Linking ISSN: 18661947 NLM ISO Abbreviation: J Neurodev Disord Subsets: PubMed not MEDLINE