Ernie Z. Ali

Shah Alam, 40170, Malaysia

Last Updated: 09/26/2026

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Found 13 publications

Smartphone applications for early screening of retinoblastoma: a scoping review.

Smartphone applications for early screening of retinoblastoma: a scoping review.

Journal: BMC ophthalmology
Published: November 19, 2025

Clinical and Genetic Characterization of Isolated Methylmalonic Acidemia in Malaysian Children: Identification of Two Novel MMUT Variants.

Clinical and Genetic Characterization of Isolated Methylmalonic Acidemia in Malaysian Children: Identification of Two Novel MMUT Variants.

Journal: Diagnostics (Basel, Switzerland)
Published: November 07, 2025

Novel HBB:c.375_376delAC mutation in a Malay patient with HbE beta-thalassemia intermedia: A case report.

Novel HBB:c.375_376delAC mutation in a Malay patient with HbE beta-thalassemia intermedia: A case report.

Journal: Medicine
Published: January 16, 2025

Clinical Significance of Early-Onset Alzheimer's Mutations in Asian and Western Populations: A Scoping Review.

Clinical Significance of Early-Onset Alzheimer's Mutations in Asian and Western Populations: A Scoping Review.

Journal: Genes
Published: December 20, 2024

Resurgence of Dengue Virus Serotype 4 in Malaysia: A Comprehensive Clinicodemographic and Genomic Analysis.

Resurgence of Dengue Virus Serotype 4 in Malaysia: A Comprehensive Clinicodemographic and Genomic Analysis.

Journal: Tropical medicine and infectious disease
Published: July 07, 2023

Impact of GSK199 and GSK106 binding on protein arginine deiminase IV stability and flexibility: A computational approach.

Impact of GSK199 and GSK106 binding on protein arginine deiminase IV stability and flexibility: A computational approach.

Journal: Computational biology and chemistry
Published: June 15, 2023

Genotype, phenotype and treatment outcomes of 17 Malaysian patients with infantile-onset Pompe disease and the identification of 3 novel GAA variants.

Genotype, phenotype and treatment outcomes of 17 Malaysian patients with infantile-onset Pompe disease and the identification of 3 novel GAA variants.

Journal: Orphanet journal of rare diseases
Published: June 03, 2022

Identification of mutations in Malaysian patients with argininosuccinate lyase (ASL) deficiency.

Identification of mutations in Malaysian patients with argininosuccinate lyase (ASL) deficiency.

Journal: Molecular genetics and metabolism reports
Published: July 29, 2019

Fourteen new mutations of BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease (MSUD) in Malaysian population.

Fourteen new mutations of BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease (MSUD) in Malaysian population.

Journal: Molecular genetics and metabolism reports
Published: June 06, 2018

Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene.

Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene.

Journal: BioMed research international
Published: February 14, 2018

Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability.

Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability.

Journal: The Malaysian journal of pathology
Published: September 04, 2017

Carbamoylphosphate synthetase 1 (CPS1) deficiency: clinical, biochemical, and molecular characterization in Malaysian patients.

Carbamoylphosphate synthetase 1 (CPS1) deficiency: clinical, biochemical, and molecular characterization in Malaysian patients.

Journal: European journal of pediatrics
Published: August 22, 2015
Showing 1-12 of 13

Last Updated: 09/26/2026