Brian Y. Chung

21 Sassoon Road
Hong Kong, China

Last Updated: 09/26/2026

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Found 86 publications

Socio-economic burden and health-related quality of life in patients with rare diseases during the COVID-19 pandemic: abridged secondary publication.

Socio-economic burden and health-related quality of life in patients with rare diseases during the COVID-19 pandemic: abridged secondary publication.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: March 04, 2026

Bridging the Functional Gap by Synergy of Exome/Genome and RNA Sequencing: A Systematic Semi-quantitative Review Demonstrating Enhanced Diagnostic Yield in Genetic Diagnostics.

Bridging the Functional Gap by Synergy of Exome/Genome and RNA Sequencing: A Systematic Semi-quantitative Review Demonstrating Enhanced Diagnostic Yield in Genetic Diagnostics.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 05, 2025

Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies.

Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies.

Journal: American journal of human genetics

Published: July 17, 2025

Fragile X syndrome: genetic and clinical profile in the Hong Kong Chinese population.

Fragile X syndrome: genetic and clinical profile in the Hong Kong Chinese population.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: June 05, 2025

Determining the value of genomics in healthcare.

Determining the value of genomics in healthcare.

Journal: Nature medicine

Published: March 27, 2025

Identification of technically challenging variants: Whole-genome sequencing improves diagnostic yield in patients with high clinical suspicion of rare diseases.

Identification of technically challenging variants: Whole-genome sequencing improves diagnostic yield in patients with high clinical suspicion of rare diseases.

Journal: HGG advances

Published: March 07, 2025

Integrated genomic and transcriptomic profiling of glioblastoma reveals ecDNA-driven heterogeneity and microenvironmental reprogramming.

Integrated genomic and transcriptomic profiling of glioblastoma reveals ecDNA-driven heterogeneity and microenvironmental reprogramming.

Journal: Cell reports

Published: February 28, 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

Effect of communicating genetic risk of type 2 diabetes and wearable technologies on wearable device-measured behavioural outcomes in East Asians: protocol of a randomised controlled trial.

Effect of communicating genetic risk of type 2 diabetes and wearable technologies on wearable device-measured behavioural outcomes in East Asians: protocol of a randomised controlled trial.

Journal: BMJ open

Published: December 04, 2024

Long-surviving Neu-Laxova syndrome confirmed by whole exome sequencing: a case report.

Long-surviving Neu-Laxova syndrome confirmed by whole exome sequencing: a case report.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: May 29, 2024

A step forward in genetic counselling: defining practice and ethics through the Genetic Counselling Practice Consortium in Hong Kong.

A step forward in genetic counselling: defining practice and ethics through the Genetic Counselling Practice Consortium in Hong Kong.

Journal: Journal of human genetics

Published: March 05, 2024

Genome-wide DNA methylation profiling for central nervous system embryonal tumours in children: abridged secondary publication.

Genome-wide DNA methylation profiling for central nervous system embryonal tumours in children: abridged secondary publication.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: February 27, 2024

Showing 1-12 of 86

Last Updated: 09/26/2026