Tsan Yuk Hospital

Recent papers from Tsan Yuk Hospital

1. IBD in transition: a decade of data from the Malaysian Kinta Valley cohortInflammatory Bowel Diseases · 2026
2. Artificial intelligence in electrocardiogram-based prediction of heart failure: a systematic review and meta-analysisFrontiers in Cardiovascular Medicine · 2026
3. Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centersAmerican Journal of Medical Genetics Part A · 2024
4. Revealing parental mosaicism: the hidden answer to the recurrence of apparent de novo variantsHuman Genomics · 2023
5. Epidemiology of Diabetes and Atherosclerotic Cardiovascular Disease Among Asian American Adults: Implications, Management, and Future Directions: A Scientific Statement From the American Heart AssociationCirculation · 2023
6. Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-conceptnpj Genomic Medicine · 2022
7. Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies—Experience from a Local Prenatal Diagnostic LaboratoryHealthcare · 2022
8. Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural AnomaliesGenes · 2022
9. Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinesenpj Genomic Medicine · 2022
10. First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal TestingGenes · 2021
11. Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal DiagnosisFrontiers in Genetics · 2021
12. Expanded Carrier Screening in Chinese Population – A Survey on Views and Acceptance of Pregnant and Non-Pregnant WomenFrontiers in Genetics · 2020
13. Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literatureAmerican Journal of Medical Genetics Part A · 2020
14. Generation of genomic-integration-free human induced pluripotent stem cells and the derived cardiomyocytes of X-linked dilated cardiomyopathy from DMD gene mutationStem Cell Research · 2020
15. The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypesMolecular Genetics & Genomic Medicine · 2020
16. A Small‐Molecule AIE Chromosome Periphery Probe for Cytogenetic StudiesAngewandte Chemie International Edition · 2020
17. A Small‐Molecule AIE Chromosome Periphery Probe for Cytogenetic StudiesAngewandte Chemie · 2020
18. Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong KongBMC Pregnancy and Childbirth · 2020
19. Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong KongAmerican Journal of Medical Genetics Part C Seminars in Medical Genetics · 2019
20. Exome sequencing identifies molecular diagnosis in children with drug‐resistant epilepsyEpilepsia Open · 2018