Chun Y. Mak

Sar, China

Last Updated: 09/26/2026

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Found 21 publications

Mendelian randomisation reveals modifiable pathways and epigenetic markers from childhood maltreatment to neuropsychiatric disorders.

Mendelian randomisation reveals modifiable pathways and epigenetic markers from childhood maltreatment to neuropsychiatric disorders.

Journal: The British journal of psychiatry : the journal of mental science

Published: November 04, 2025

Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory.

Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory.

Journal: Healthcare (Basel, Switzerland)

Published: October 27, 2022

Functional Evaluation and Genetic Landscape of Children and Young Adults Referred for Assessment of Bronchiectasis.

Functional Evaluation and Genetic Landscape of Children and Young Adults Referred for Assessment of Bronchiectasis.

Journal: Frontiers in genetics

Published: April 30, 2022

Analytical validity and clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis: abridged secondary publication.

Analytical validity and clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis: abridged secondary publication.

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

Published: March 09, 2022

Multicentre study of hospitalised patients with sports- and recreational cycling-related traumatic brain injury in Hong Kong.

Multicentre study of hospitalised patients with sports- and recreational cycling-related traumatic brain injury in Hong Kong.

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

Published: October 28, 2021

Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.

Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.

Journal: NPJ genomic medicine

Published: August 06, 2021

Tattoo-associated uveitis.

Tattoo-associated uveitis.

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

Published: June 25, 2021

Perception of personalized medicine, pharmacogenomics, and genetic testing among undergraduates in Hong Kong.

Perception of personalized medicine, pharmacogenomics, and genetic testing among undergraduates in Hong Kong.

Journal: Human genomics

Published: May 27, 2021

Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction.

Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction.

Journal: Circulation. Genomic and precision medicine

Published: November 16, 2020

Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis.

Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis.

Journal: Frontiers in genetics

Published: October 22, 2020

Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population.

Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population.

Journal: PLoS genetics

Published: August 12, 2020

Actionable secondary findings in 1116 Hong Kong Chinese based on exome sequencing data.

Actionable secondary findings in 1116 Hong Kong Chinese based on exome sequencing data.

Journal: Journal of human genetics

Published: June 05, 2020

Showing 1-12 of 21

Last Updated: 09/26/2026