A. A. Annuar

发表

The first Malay database toward the ethnic-specific target molecular variation

R. Zain, B. Zilfalil, M. F. Johan, 2015, BMC Research Notes.

Rare homozygous PRKN exon 8 and 9 deletion in Malay familial early-onset Parkinson's disease.

A. Tan, Shen-Yang Lim, A. A. Annuar, 2021, Annals of the Academy of Medicine, Singapore.

Genetic Analysis of the Cytoplasmic Dynein Subunit Families

E. Fisher, H. Hummerich, E. Fisher, 2006, PLoS genetics.

Diversity in Parkinson's disease genetics research: current landscape and future directions

S. Lesage, S. Bardien, I. Mata, 2021, medRxiv.

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

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

Exercise induced cramps and myoglobinuria in dystrophinopathy - A report of three Malaysian patients

K. Wong, M. Thong, A. A. Annuar, 2010 .

Evaluation of novel Parkinson's disease candidate genes in the Chinese population

H. Liany, Jianjun Liu, V. Mok, 2019, Neurobiology of Aging.

Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.

M. Nalls, C. Blauwendraat, W. Koh, 2020, JAMA neurology.

The frequency of common mitochondrial DNA mutations in a cohort of Malaysian patients with specifi c mitochondrial encephalomyopathy syndromes

K. Wong, A. A. Annuar, J. Chong, 2011 .

Experimental spinal cord trauma: a review of mechanically induced spinal cord injury in rat models

A. A. Annuar, J. Sanusi, D. Abdullahi, 2017, Reviews in the neurosciences.

Single mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO) and Kearns-Sayre syndrome (KSS) patients from a multiethnic Asian population

K. Wong, M. Thong, A. A. Annuar, 2014 .

Exome sequencing in Asian populations identifies rare deficient SMPD1 alleles that increase risk of Parkinson's disease

C. Khor, J. Wiggs, L. Robak, 2023, medRxiv.

Improved β-catenin detection in spinal cord tissue sections: autofluorescence quenching

A. A. Annuar, J. Sanusi, D. Abdullahi, 2020, Neuroscience Research Notes.

Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry

J. Foo, Shen-Yang Lim, A. A. Annuar, 2024, Journal of movement disorders.

Dystrophin gene analysis in Duchenne / Becker dystrophy in a Malaysian population using multiplex polymerase chain reaction 1

K. Wong, A. A. Annuar, K. Goh, 2010 .