Matthew Hoi Kin Chau

13PUBLICATIONS
27CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Gene mapping
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Publications (13)

|Aug 24, 2026
Genetic Investigation of X-Linked Defects with Optimized Targeted Long-Read Sequencing.

|Jun 15, 2026
Underrecognized triploidy and genome-wide uniparental disomy in human blastocysts revealed by a concurrent preimplantation genetic testing approach.

|Jun 12, 2026
Prenatal-Onset Recessive Titinopathies: Clinical Spectrum, Genotype-Phenotype Correlations, and Outcomes.

|Feb 18, 2026
NONO-Related Syndromic X-Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal Cohort.

Yilin Zhao, Gang Zou, Mengmeng Shi

|Nov 10, 2025
Clinical validation of artificial intelligence-assisted karyotyping on peripheral blood in a cytogenetic diagnostic laboratory.

Yujie Zhu, Matthew Hoi Kin Chau, Huilin Wang

|Jan 03, 2025
Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage.

Matthew Hoi Kin Chau, Stephanie A Anderson, Rodger Song

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Frequent Collaborators

10 joint publications

Kwong Wai Choy

7 joint publications

Zirui Dong

6 joint publications

Tak Yeung Leung

5 joint publications

Ye Cao