Breana M. Cham
Singapore, Singapore
Last Updated: 09/26/2026
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Found 17 publications
Genetic counselling and testing for inherited glomerular kidney diseases: A single-centre experience.
Journal: Annals of the Academy of Medicine, Singapore
Published: January 06, 2026
Three Years of a New Multidisciplinary Adult Neurogenetics Clinic in Singapore.
Journal: Neurology. Genetics
Published: October 02, 2025
Deep phenotyping of patients with citrin deficiency in Singapore- single centre experience.
Journal: Molecular genetics and metabolism
Published: February 25, 2025
Clinical Implementation of Nephrologist-Led Genomic Testing for Glomerular Diseases in Singapore: Rationale and Protocol.
Journal: American journal of nephrology
Published: October 01, 2024
Rapid exome sequencing to aid diagnostics in genetic disorders: Implementation and challenges in the Singapore context.
Journal: Annals of the Academy of Medicine, Singapore
Published: January 02, 2023
Stakes of Assessments in Residency: Influence on Previous and Current Self-Regulated Learning and Co-Regulated Learning in Early Career Specialists.
Journal: Perspectives on medical education
Published: December 22, 2022
Inactivation of DRG1, encoding a translation factor GTPase, causes a recessive neurodevelopmental disorder.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 11, 2022
Novel Variants and Clinical Characteristics of 16 Patients from Southeast Asia with Genetic Variants in Neurofibromin-1.
Journal: Journal of pediatric genetics
Published: January 25, 2021
Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management.
Journal: Archives of disease in childhood
Published: March 19, 2020
Genetic landscape of congenital disorders in patients from Southeast Asia: results from sequencing using a gene panel for Mendelian phenotypes.
Journal: Archives of disease in childhood
Published: March 17, 2020
Germline AGO2 mutations impair RNA interference and human neurological development.
Journal: Nature communications
Published: December 28, 2019
Coffin-Siris Syndrome-1: Report of five cases from Asian populations with truncating mutations in the ARID1B gene.
Journal: Journal of the neurological sciences
Published: June 18, 2019
Last Updated: 09/26/2026