Hui-lin X. Chin

Singapore, Singapore

Last Updated: 09/26/2026

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Found 43 publications

GENEKIDS-PRO: genomic enhancement and patient engagement in nephrology through multidisciplinary kidney genetics clinic implementation and integration in Singapore - a study protocol using a process evaluation framework.

GENEKIDS-PRO: genomic enhancement and patient engagement in nephrology through multidisciplinary kidney genetics clinic implementation and integration in Singapore - a study protocol using a process evaluation framework.

Journal: BMC nephrology
Published: March 07, 2026

Implementation of spinal muscular atrophy screening for newborns at a Singapore tertiary hospital.

Implementation of spinal muscular atrophy screening for newborns at a Singapore tertiary hospital.

Journal: Annals of the Academy of Medicine, Singapore
Published: March 03, 2026

Scoping Review of Global Kidney Genetics Clinic Models and Outcomes.

Scoping Review of Global Kidney Genetics Clinic Models and Outcomes.

Journal: Kidney international reports
Published: February 19, 2026

McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure: A Case Report and Literature Review.

McCune-Albright Syndrome as a Rare Cause of Fanconi Syndrome and Kidney Failure: A Case Report and Literature Review.

Journal: Kidney medicine
Published: January 09, 2026

Case Report: Infant with vaccine-associated paralytic poliomyelitis unveils global disparities in care for inborn errors of immunity.

Case Report: Infant with vaccine-associated paralytic poliomyelitis unveils global disparities in care for inborn errors of immunity.

Journal: Frontiers in immunology
Published: November 21, 2025

Expanding the phenotypic spectrum associated with ZIC1 variants: A neurodevelopmental disorder with and without craniosynostosis.

Expanding the phenotypic spectrum associated with ZIC1 variants: A neurodevelopmental disorder with and without craniosynostosis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 16, 2025

Beyond epistaxis: cascade screening and presymptomatic treatment of hereditary hemorrhagic telangiectasia.

Beyond epistaxis: cascade screening and presymptomatic treatment of hereditary hemorrhagic telangiectasia.

Journal: BMC pediatrics
Published: September 01, 2025

Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophy.

Case Report: Incidental diagnosis of cystic fibrosis via whole genome sequencing alters HSCT planning in a child with cerebral X-linked adrenoleukodystrophy.

Journal: Frontiers in pediatrics
Published: June 20, 2025

Case Report: Evaluation of COL4A5 non-canonical splicing variants in two families.

Case Report: Evaluation of COL4A5 non-canonical splicing variants in two families.

Journal: Frontiers in medicine
Published: April 14, 2025

Clinical Implementation of Nephrologist-Led Genomic Testing for Glomerular Diseases in Singapore: Rationale and Protocol.

Clinical Implementation of Nephrologist-Led Genomic Testing for Glomerular Diseases in Singapore: Rationale and Protocol.

Journal: American journal of nephrology
Published: October 01, 2024

Pathogenic variants in the Alport genes are prevalent in the Singapore multiethnic population with highest frequency in the Chinese.

Pathogenic variants in the Alport genes are prevalent in the Singapore multiethnic population with highest frequency in the Chinese.

Journal: Scientific reports
Published: August 28, 2024

Atypical Presentation of an LMNB1 Duplication Involving the Silencer Region: Beyond Classical Autosomal-Dominant Leukodystrophy.

Atypical Presentation of an LMNB1 Duplication Involving the Silencer Region: Beyond Classical Autosomal-Dominant Leukodystrophy.

Journal: Neurology. Genetics
Published: July 08, 2024
Showing 1-12 of 43

Last Updated: 09/26/2026