photo of Dr Chern Lim

Dr Chern Lim

Dr Chern Lim

Details

Role Clinical Analyst (Medical Scientist)
Group TGU Clinical Genomics

Top Publications

  • Lim, SC, Tajika, M, Shimura, M, Carey, KT, Stroud, DA, Murayama, K, Ohtake, A, McKenzie, M. 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) : 153 2024
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  • Lim, SC, Hroudová, J, Van Bergen, NJ, Sanchez, MIGL, Trounce, IA, McKenzie, M. 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 2016
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  • McKenzie, M, Chiotis, M, Hroudová, J, Sanchez, MIGL, Lim, SC, Cook, MJ, McKelvie, P, Cotton, RGH, Murphy, M, St John, JC, et al. 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 2014
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  • Lim, SC, Smith, KR, Stroud, DA, Compton, AG, Tucker, EJ, Dasvarma, A, Gandolfo, LC, Marum, JE, McKenzie, M, Peters, HL, et al. A Founder Mutation in PET100 Causes Isolated Complex IV Deficiency in Lebanese Individuals with Leigh Syndrome. American Journal of Human Genetics 94(2) : 209 -222 2014
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  • Lim, SC, Friemel, M, Marum, JE, Tucker, EJ, Bruno, DL, Riley, LG, Christodoulou, J, Kirk, EP, Boneh, A, DeGennaro, CM, et al. Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes. Human Molecular Genetics 22(22) : 4460 -4473 2013
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