Ny V. Hoang

Toronto, ON, Canada

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 31 publications

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

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

Journal: NPJ genomic medicine
Published: March 05, 2025

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

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

Journal: Nature
Published: December 10, 2024

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

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

Journal: Journal of medical genetics
Published: October 25, 2024

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

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

Journal: Brain : a journal of neurology
Published: June 25, 2024

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

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

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: March 04, 2024

Global developmental delay and a de novo deletion of the 16p13.13 region.

Global developmental delay and a de novo deletion of the 16p13.13 region.

Journal: BMJ case reports
Published: February 29, 2024

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

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

Journal: Journal of neurodevelopmental disorders
Published: September 28, 2023

Support to caregivers who have received genetic information about neurodevelopmental and psychiatric vulnerability in their young children: A narrative review.

Support to caregivers who have received genetic information about neurodevelopmental and psychiatric vulnerability in their young children: A narrative review.

Journal: Clinical genetics
Published: March 19, 2023

The Phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples.

The Phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples.

Journal: Journal of medical genetics
Published: July 21, 2022

Developmental implications of genetic testing for physical indications.

Developmental implications of genetic testing for physical indications.

Journal: European journal of human genetics : EJHG
Published: May 09, 2022

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

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

Journal: Cell
Published: May 05, 2022

Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplication.

Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplication.

Journal: American journal of medical genetics. Part A
Published: March 18, 2022
Showing 1-12 of 31

Last Updated: 09/26/2026