Lock Hock Ngu

1.9k total citations
59 papers, 899 citations indexed

About

Lock Hock Ngu is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Lock Hock Ngu has authored 59 papers receiving a total of 899 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 27 papers in Clinical Biochemistry and 15 papers in Physiology. Recurrent topics in Lock Hock Ngu's work include Metabolism and Genetic Disorders (27 papers), Mitochondrial Function and Pathology (11 papers) and Lysosomal Storage Disorders Research (11 papers). Lock Hock Ngu is often cited by papers focused on Metabolism and Genetic Disorders (27 papers), Mitochondrial Function and Pathology (11 papers) and Lysosomal Storage Disorders Research (11 papers). Lock Hock Ngu collaborates with scholars based in Malaysia, Netherlands and Australia. Lock Hock Ngu's co-authors include Wee Teik Keng, Bushra Afroze, Michael Fietz, Arjan P.M. de Brouwer, Nicholas T. Gorden, Tjitske Kleefstra, Stef J.F. Letteboer, Erwin van Wijk, Ronald Roepman and Karlien L. M. Coene and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Lock Hock Ngu

57 papers receiving 889 citations

Peers

Countries citing papers authored by Lock Hock Ngu

Since Specialization

Citations

This map shows the geographic impact of Lock Hock Ngu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Lock Hock Ngu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lock Hock Ngu more than expected).

Fields of papers citing papers by Lock Hock Ngu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lock Hock Ngu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Lock Hock Ngu. The network helps show where Lock Hock Ngu may publish in the future.

Co-authorship network of co-authors of Lock Hock Ngu

This figure shows the co-authorship network connecting the top 25 collaborators of Lock Hock Ngu. A scholar is included among the top collaborators of Lock Hock Ngu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lock Hock Ngu. Lock Hock Ngu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Cost-Effectiveness Analysis of Idursulfase for the Long-Term Treatment of Hunter Syndrome Using a Partitioned-Survival Model Approach in R 2025 ·Value in Health Regional Issues ·(unknown), Asrul Akmal Shafie, Lock Hock Ngu, (unknown)	0
2	Genotype, phenotype and treatment outcomes of 17 Malaysian patients with infantile-onset Pompe disease and the identification of 3 novel GAA variants 2023 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), (unknown), (unknown), (unknown), Mohd Khairul Nizam Mohd Khalid, (unknown), (unknown), (unknown), Lock Hock Ngu	4
3	A Comparison of Self-evaluated Survey and Work Sampling Approach for Estimating Patient-care Unit Cost Multiplier in Genetic Nursing Activities 2022 ·Asian Nursing Research ·(unknown), Asrul Akmal Shafie, Lock Hock Ngu	1
4	Rare disease in Malaysia: Challenges and solutions 2020 ·PLoS ONE ·Asrul Akmal Shafie, (unknown), Mohamed Azmi Hassali, Lock Hock Ngu, Meow‐Keong Thong, (unknown), Nathorn Chaiyakunapruk	26
5	RANBP2 susceptibility to infection-induced encephalopathy: Clinicoradiologic and molecular description in a Malaysian family 2020 ·Molecular Genetics and Metabolism Reports ·(unknown), Lock Hock Ngu	4
6	Intron retention is among six unreported AGL mutations identified in Malaysian GSD III patients 2019 ·Genes & Genomics ·(unknown), (unknown), (unknown), Lock Hock Ngu, (unknown), (unknown), Zulqarnain Mohamed	1
7	Identification of mutations in Malaysian patients with argininosuccinate lyase (ASL) deficiency 2019 ·Molecular Genetics and Metabolism Reports ·(unknown), (unknown), Lock Hock Ngu	2
8	Selective screening for detection of mucopolysaccharidoses in Malaysia; A two-year study (2014–2016) 2019 ·Molecular Genetics and Metabolism Reports ·(unknown), (unknown), (unknown), Lock Hock Ngu, (unknown)	4
9	Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability. 2017 ·PubMed ·(unknown), (unknown), (unknown), (unknown), Zunita Zakaria, Lock Hock Ngu, Wee Teik Keng	6
10	Case report of treatment experience with idursulfase beta (Hunterase) in an adolescent patient with MPS II 2017 ·Molecular Genetics and Metabolism Reports ·Lock Hock Ngu, (unknown), (unknown), (unknown)	13
11	Fructose-1,6-bisphosphatase deficiency as a cause of recurrent hypoglycemia and metabolic acidosis: Clinical and molecular findings in Malaysian patients 2017 ·Pediatrics & Neonatology ·(unknown), (unknown), (unknown), (unknown), Wee Teik Keng, (unknown), Lock Hock Ngu	17
12	AB168. Novel DYM compound heterozygous mutations in a Malaysian boy with Dyggve-Melchior-Clausen syndrome 2015 ·Annals of Translational Medicine ·Winnie Ong, (unknown), (unknown), (unknown), (unknown), Lock Hock Ngu, Nisha Patel, Mais Hashem, Fowzan S. Alkuraya, Wee Teik Keng	1
13	Mutation analysis of glycine decarboxylase, aminomethyltransferase and glycine cleavage system protein-H genes in 13 unrelated families with glycine encephalopathy 2014 ·Journal of Human Genetics ·(unknown), (unknown), Zulhabri Othman, (unknown), (unknown), (unknown), Anand Mohan, (unknown), Syed Zulkifli Syed Zakaria, Lock Hock Ngu	19
14	Two Novel Gross Deletions of TSC2 in Malaysian Patients with Tuberous Sclerosis Complex and TSC2/PKD1 Contiguous Deletion Syndrome 2014 ·Japanese Journal of Clinical Oncology ·(unknown), (unknown), (unknown), (unknown), Fatemeh Hayati, (unknown), (unknown), (unknown), (unknown), Wee Teik Keng, Lock Hock Ngu, Teguh Haryo Sasongko	11
15	Treatment of Lesch–Nyhan disease with S-adenosylmethionine: Experience with five young Malaysians, including a girl 2013 ·Brain and Development ·(unknown), Shanti Balasubramaniam, (unknown), John P. O’Neill, (unknown), Wee Teik Keng, Lock Hock Ngu, John A. Duley	26
16	Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region 2012 ·Molecular Genetics and Metabolism ·Wuh‐Liang Hwu, Torayuki Okuyama, (unknown), (unknown), Xuefan Gu, Joannie Hui, Motomichi Kosuga, Shuan‐Pei Lin, Lock Hock Ngu, (unknown), Akemi Tanaka, Meow‐Keong Thong, Duangrurdee Wattanasirichaigoon, Pornswan Wasant, Jim McGill	5
17	A catalytic defect in mitochondrial respiratory chain complex I due to a mutation in NDUFS2 in a patient with Leigh syndrome 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Lock Hock Ngu, Leo Nijtmans, Felix Distelmaier, Hanka Venselaar, Sjenet E. van Emst‐de Vries, Mariël A.M. van den Brand, (unknown), Liesbeth T. Wintjes, Peter H.G.M. Willems, Lambertus P. van den Heuvel, Jan Smeıtınk, Richard J. Rodenburg	27
18	Clinical and Biochemical Profiles of Maple Syrup Urine Disease in Malaysian Children 2011 ·JIMD Reports ·(unknown), (unknown), (unknown), (unknown), Lock Hock Ngu	18
19	Mowat-Wilson syndrome: the first two Malaysian cases. 2010 ·PubMed ·Shanti Balasubramaniam, (unknown), Lock Hock Ngu, (unknown), (unknown)	5
20	Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene 2010 ·Journal of Medical Genetics ·Merel S. Ebberink, Bernadett Csányi, W.K. Chong, (unknown), P. J. Sharp, Petra A.W. Mooijer, Conny Dekker, (unknown), Lock Hock Ngu, (unknown), Ronald J. A. Wanders, Michael Fietz, Peter T. Clayton, Hans R. Waterham, Sacha Ferdinandusse	68

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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