Sze Chern Lim

1.4k total citations
13 papers, 899 citations indexed

About

Sze Chern Lim is a scholar working on Molecular Biology, Clinical Biochemistry and Renewable Energy, Sustainability and the Environment. According to data from OpenAlex, Sze Chern Lim has authored 13 papers receiving a total of 899 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 2 papers in Renewable Energy, Sustainability and the Environment. Recurrent topics in Sze Chern Lim's work include Mitochondrial Function and Pathology (12 papers), ATP Synthase and ATPases Research (7 papers) and Metabolism and Genetic Disorders (7 papers). Sze Chern Lim is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), ATP Synthase and ATPases Research (7 papers) and Metabolism and Genetic Disorders (7 papers). Sze Chern Lim collaborates with scholars based in Australia, United Kingdom and Japan. Sze Chern Lim's co-authors include Matthew McKenzie, David R. Thorburn, Alison G. Compton, John Christodoulou, Elena J. Tucker, Vamsi K. Mootha, Damien L. Bruno, Adrienne Laskowski, Shangtao Liu and Daniel S. Lieber and has published in prestigious journals such as Journal of Molecular Biology, Scientific Reports and The FASEB Journal.

In The Last Decade

Sze Chern Lim

13 papers receiving 886 citations

Peers

Sze Chern Lim

MB

CB

GENET

CR

RESE

Elisa Fassone Italy

Valeriy Levandovskiy Canada

Nicole J. Lake United States

Woranontee Weraarpachai Canada

Manuèle Miné France

Johan Van Hove United States

Nevena MacKay Canada

Jorge Asin-Cayuela Sweden

Irene De Biase United States

Elliot Surgenor Australia

Elisa Fassone Italy

Sze Chern Lim

705 ×0.9

MB

365 ×1.0

CB

48 ×0.5

GENET

46 ×0.6

CR

28 ×0.5

RESE

Citations per year, relative to Sze Chern Lim Sze Chern Lim (= 1×) peers Elisa Fassone

Countries citing papers authored by Sze Chern Lim

Since Specialization

Citations

This map shows the geographic impact of Sze Chern Lim'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 Sze Chern Lim with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sze Chern Lim more than expected).

Fields of papers citing papers by Sze Chern Lim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sze Chern Lim. 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 Sze Chern Lim. The network helps show where Sze Chern Lim may publish in the future.

Co-authorship network of co-authors of Sze Chern Lim

This figure shows the co-authorship network connecting the top 25 collaborators of Sze Chern Lim. A scholar is included among the top collaborators of Sze Chern Lim 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 Sze Chern Lim. Sze Chern Lim is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

1.

Tsuruoka, Tomoko, Masaru Shimura, Makiko Tajika, et al.. (2022). Severe spinal cord hypoplasia due to a novel ATAD3A compound heterozygous deletion. Molecular Genetics and Metabolism Reports. 33. 100912–100912. 4 indexed citations

2.

Ziemann, Mark, Sze Chern Lim, Yilin Kang, et al.. (2021). MicroRNA-101-3p Modulates Mitochondrial Metabolism via the Regulation of Complex II Assembly. Journal of Molecular Biology. 434(2). 167361–167361. 14 indexed citations

3.

Borna, Nurun Nahar, Yoshihito Kishita, Masakazu Kohda, et al.. (2019). Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome. Neurogenetics. 20(1). 9–25. 44 indexed citations

4.

Lim, Sze Chern, Makiko Tajika, Masaru Shimura, et al.. (2018). Loss of the Mitochondrial Fatty Acid β-Oxidation Protein Medium-Chain Acyl-Coenzyme A Dehydrogenase Disrupts Oxidative Phosphorylation Protein Complex Stability and Function. Scientific Reports. 8(1). 55 indexed citations

5.

McKenzie, Matthew, Sze Chern Lim, & Michael R. Duchen. (2017). Simultaneous Measurement of Mitochondrial Calcium and Mitochondrial Membrane Potential in Live Cells by Fluorescent Microscopy. Journal of Visualized Experiments. 21 indexed citations

6.

McKenzie, Matthew, Sze Chern Lim, & Michael R. Duchen. (2017). Simultaneous Measurement of Mitochondrial Calcium and Mitochondrial Membrane Potential in Live Cells by Fluorescent Microscopy. Journal of Visualized Experiments. 6 indexed citations

7.

Lim, Sze Chern, Jana Hroudová, Nicole J. Van Bergen, et al.. (2016). Loss of mitochondrial DNA‐encoded protein ND1 results in disruption of complex I biogenesis during early stages of assembly. The FASEB Journal. 30(6). 2236–2248. 47 indexed citations

8.

Lim, Sze Chern, et al.. (2015). Anti-cancer analogues ME-143 and ME-344 exert toxicity by directly inhibiting mitochondrial NADH: ubiquinone oxidoreductase (Complex I).. PubMed. 5(2). 689–701. 45 indexed citations

9.

McKenzie, Matthew, Jana Hroudová, M. Isabel G. Lopez Sanchez, et al.. (2014). Capture of Somatic mtDNA Point Mutations with Severe Effects on Oxidative Phosphorylation in Synaptosome Cybrid Clones from Human Brain. Human Mutation. 35(12). 1476–1484. 12 indexed citations

10.

Lim, Sze Chern, Katherine R. Smith, David A. Stroud, et al.. (2014). A Founder Mutation in PET100 Causes Isolated Complex IV Deficiency in Lebanese Individuals with Leigh Syndrome. The American Journal of Human Genetics. 94(2). 209–222. 54 indexed citations

11.

Lim, Sze Chern, Justine E. Marum, Elena J. Tucker, et al.. (2013). Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes. Human Molecular Genetics. 22(22). 4460–4473. 81 indexed citations

12.

Calvo, Sarah E., Alison G. Compton, Steven G. Hershman, et al.. (2012). Molecular Diagnosis of Infantile Mitochondrial Disease with Targeted Next-Generation Sequencing. Science Translational Medicine. 4(118). 118ra10–118ra10. 343 indexed citations

13.

Riley, Lisa G., Sandra T. Cooper, Peter F. Hickey, et al.. (2010). Mutation of the Mitochondrial Tyrosyl-tRNA Synthetase Gene, YARS2, Causes Myopathy, Lactic Acidosis, and Sideroblastic Anemia—MLASA Syndrome. The American Journal of Human Genetics. 87(1). 52–59. 173 indexed citations

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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