Canny Sugiana - Concepedia

Author

Canny Sugiana

Royal Children's Hospital

Also Known As

C Sugiana, C. Sugiana, Canny Sugiana

Publications

3.8K

Citations

H-Index

Concepts

All Affiliations

Royal Children's Hospital The University of Melbourne Murdoch Children's Research Institute Victorian Clinical Genetics Services La Trobe University

About

Canny Sugiana is an author at Royal Children's Hospital specializing in mitochondrial function, molecular biology, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	3.4K
2	Natural Sciences	3	3	2.3K
3	Cell Biology	1	1	952
4	Cellular Physiology	1	1	952
5	Immunology	1	1	952

Canny Sugiana

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology David J. Pagliarini, Sarah E. Calvo, Betty Chang, Cell Mitochondrial FunctionMedicineNatural SciencesMolecular BiologyMolecular Genetics	2008	2K
BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosis Kate McArthur, Lachlan Whitehead, John M. Heddleston, Science MitophagyApoptosisImmunologyPathologyMolecular Biology	2018	952
Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause disease Christopher J.R. Dunning, Matthew McKenzie, Canny Sugiana, The EMBO Journal Mitochondrial FunctionNatural SciencesGeneticsMolecular BiologyDna Replication	2007	190
NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency Denise M. Kirby, Renato Salemi, Canny Sugiana, Journal of Clinical Investigation	2004	186
Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease Canny Sugiana, David J. Pagliarini, Matthew McKenzie, The American Journal of Human Genetics Genome InstabilityMitochondrial FunctionMedicineGeneticsMolecular Biology	2008	177
Respiratory chain complex I deficiency caused by mitochondrial DNA mutations Helen Swalwell, Denise M. Kirby, Emma L. Blakely, European Journal of Human Genetics Mitochondrial MyopathyRespiratory Chain ComplexMendelian DisorderMitochondrial BiogenesisMitochondrial Function	2011	125
NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency Denise M. Kirby, Renato Salemi, Canny Sugiana, Journal of Clinical Investigation	2004	19
Molecular diagnosis of mitochondrial respiratory chain disorders in <scp>J</scp>apan: Focusing on mitochondrial <scp>DNA</scp> depletion syndrome Taro Yamazaki, Kei Murayama, Alison G. Compton, Pediatrics International	2013	18

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