N. A. Murad

Characterising the genetic risk for type 2 diabetes in a Malaysian multi- ethnic cohort Running head: Type 2 diabetes genetics in Malaysia

R. Scott, C. Oldmeadow, J. Attia, 2016 .

Advancement in the diagnosis of mitochondrial diseases

S. A. Sulaiman, Zam Zureena Mohd Rani, Fara Zela Mohd Radin, 2020, Journal of Translational Genetics and Genomics.

Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)

G. Francis, Qian Wang, D. Gaudet, 2021, The Lancet.

Glucocerebrosidase genetic variants in Malays with early and late-onset Parkinson’s disease

N. Ibrahim, S. Syafruddin, Shen-Yang Lim, 2020 .

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

Chelsea X Alvarado, D. Hernandez, M. Nalls, 2023, The Lancet Neurology.

HLA-B*15: 02 screening in epileptic patients using a high resolution melting-real time PCR (HRM-QPCR) method

Zam Zureena Mohd Rani, R. A. Ali, A. R. Jamal, 2018 .

Development of a HLA-B*58: 01 Allele Screening System for Allopurinol-Induced Severe Cutaneous Adverse Reactions Detection

Gan Kok Beng, Kim Soon Chong, Anusha Devi Nawoor, 2020, IEEE Access.

Mitochondrial dysfunction in a novel form of autosomal recessive ataxia.

T. Dörk, N. Gueven, M. Lavin, 2013, Mitochondrion.

Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC).

G. Francis, Qian Wang, D. Gaudet, 2021, Lancet.