Mohd Khairul Nizam Mohd Khalid

Ministry of Health — Malaysia

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index983citations41works0.82yr avg
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Research Topics

CRISPR and Genetic Engineering(7), Leptospirosis research and findings(6), Lysosomal Storage Disorders Research(4), Parasitic Infections and Diagnostics(4), Glycogen Storage Diseases and Myoclonus(4)

Publications41 total

Smartphone applications for early screening of retinoblastoma: a scoping review
BMC Ophthalmology·2026Open Access
Generalizable features of pegRNA design for prime editing of inherited retinal diseases
Ophthalmic Genetics·2025Open Access
Novel HBB:c.375_376delAC mutation in a Malay patient with HbE beta-thalassemia intermedia: A case report
Medicine·2025Open Access
A novel PNP variant causes lymphopenia, hypouricemia and neurological deficit
Paediatrica Indonesiana·2025Open Access
Mutation analysis of BCR-ABL1 kinase domain in chronic myeloid leukemia patients with tyrosine kinase inhibitors resistance: a Malaysian cohort study
BMC Research Notes·2024· 4 citedOpen Access
Resurgence of Dengue Virus Serotype 4 in Malaysia: A Comprehensive Clinicodemographic and Genomic Analysis
Tropical Medicine and Infectious Disease·2023· 6 citedOpen Access
Genotype, phenotype and treatment outcomes of 17 Malaysian patients with infantile-onset Pompe disease and the identification of 3 novel GAA variants
Orphanet Journal of Rare Diseases·2023· 4 citedOpen Access
Application of Multilocus Sequence Typing for the Characterization of Leptospira Strains in Malaysia
Tropical Medicine and Infectious Disease·2023· 2 citedOpen Access
The VEGAS Platform Is Unsuitable for Mammalian Directed Evolution
ACS Synthetic Biology·2022· 12 cited
Molecular, Biochemical, and Clinical Characterization of Thirteen Patients with Glycogen Storage Disease 1a in Malaysia
Genetics Research·2022· 5 citedOpen Access
Genotype, phenotype and treatment outcomes of 17 Malaysian patients with infantile-onset Pompe disease and the identification of 3 novel GAA variants
Research Square (Research Square)·2022Open Access
“Cheater” particles render the VEGAS platform unsuitable for mammalian directed evolution
2022
CRISPR/Cas-Mediated Knock-in of Genetically Encoded Fluorescent Biosensors into the AAVS1 Locus of Human-Induced Pluripotent Stem Cells
Methods in molecular biology·2021· 6 cited
Engineering domain-inlaid SaCas9 adenine base editors with reduced RNA off-targets and increased on-target DNA editing
Nature Communications·2020· 74 citedOpen Access
Performance comparison of EasyFix G26 and HYDRASYS 2 SCAN for the detection of serum monoclonal proteins
Journal of Clinical Laboratory Analysis·2020· 3 citedOpen Access
Utility of Self-Destructing CRISPR/Cas Constructs for Targeted Gene Editing in the Retina
Human Gene Therapy·2019· 24 cited
CRISPR/Cas-mediated base editing of the AMD high-risk Y402H complement factor H variant
Investigative Ophthalmology & Visual Science·2019Open Access
Clinical, biochemical and genetic profiles of patients with mucopolysaccharidosis type IVA (Morquio A syndrome) in Malaysia: the first national natural history cohort study
Orphanet Journal of Rare Diseases·2019· 21 citedOpen Access
Revisiting the taxonomy and evolution of pathogenicity of the genus Leptospira through the prism of genomics
PLoS neglected tropical diseases·2019· 587 citedOpen Access
Lafora disease in a Malaysian with a rare mutation in the EPM2A gene
Seizure·2019· 3 cited
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Frequent Co-authors

Yusnita Yakob(10), Alex W. Hewitt(8), Siti Nursheena Mohd Zain(8), Lock Hock Ngu(7), Ernie Zuraida Ali(7), Minh Thuan Nguyen Tran(6), Huey Yin Leong(6), Alice Pébay(5), Douadi Benacer(5), Anthony L. Cook(5), Siti Aishah Abdul Wahab(5), Sandy Hung(4), Guei‐Sheung Liu(4), Farah Haziqah Meor Termizi(4), Rohaidah Hashim(4), Julaina Abdul Jalil(4), Fairuz Amran(3), Kwai Lin Thong(3), Nor Azimah Abdul Azize(3), P. Chandrawathani(3)