Valeriy Levandovskiy

Author

Hospital for Sick Children

Also Known As

V. Levandovskiy, Valeriy Levandovskiy

Publications

873

Citations

H-Index

Concepts

All Affiliations

Hospital for Sick Children University of Toronto Canada Research Chairs SickKids Foundation

About

Valeriy Levandovskiy is an author at Hospital for Sick Children specializing in medicine, metabolism, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	665
2	Biochemistry	6	6	457
3	Health Sciences	4	4	80
4	Natural Sciences	4	4	433
5	Social Sciences	1	1	22

Valeriy Levandovskiy

Publications

873

Citations

H-Index

Page 1

	Year	Citations
Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes Jessie M. Cameron, Alexandre Janer, Valeriy Levandovskiy, The American Journal of Human Genetics Fatal DeficiencyBiochemistryIron MetabolismGeneticsNatural Sciences	2011	270
Identification of a novel mutation in GYS1 (muscle-specific glycogen synthase) resulting in sudden cardiac death, that is diagnosable from skin fibroblasts Jessie M. Cameron, Valeriy Levandovskiy, Nevena MacKay, Molecular Genetics and Metabolism Cardiac MuscleCardiomyopathyFibrosisPathologySudden Cardiac Death	2009	81
Disruption of a mitochondrial RNA-binding protein gene results in decreased cytochrome <i>b</i> expression and a marked reduction in ubiquinol–cytochrome <i>c</i> reductase activity in mouse heart mitochondria Fenghao Xu, Cameron Ackerley, Mary C. Maj, Biochemical Journal Heart FailureMolecular BiologyMitochondrial BiologyMetabolic RemodelingRedox Biology	2008	79
Pyruvate Dehydrogenase Phosphatase Deficiency: Identification of the First Mutation in Two Brothers and Restoration of Activity by Protein Complementation Mary C. Maj, Neviana MacKay, Valeriy Levandovskiy, The Journal of Clinical Endocrinology & Metabolism	2005	64
Novel mutations in dihydrolipoamide dehydrogenase deficiency in two cousins with borderline‐normal PDH complex activity Jessie M. Cameron, Valeriy Levandovskiy, Neviana MacKay, American Journal of Medical Genetics Part A	2006	57
Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization Jessie M. Cameron, Valeriy Levandovskiy, Nevena MacKay, Mitochondrion ChromatinMitochondrial FunctionMitochondrial DynamicNatural SciencesMolecular Biology	2010	45
Deficiency of pyruvate dehydrogenase caused by novel and known mutations in the E<sub>1</sub>α subunit Jessie M. Cameron, Valeriy Levandovskiy, Neviana MacKay, American Journal of Medical Genetics Part A	2004	44
Mitochondrial citrate synthase crystals: Novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations Komudi Siriwardena, Nevena MacKay, Valeriy Levandovskiy, Molecular Genetics and Metabolism MitophagySignal TransductionMitochondrial FunctionBiochemistryNatural Sciences	2012	39
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotype Jessie M. Cameron, Mary C. Maj, Valeriy Levandovskiy, Human Genetics Developmental BiologyBiochemistryGenetic DisorderGeneticsMolecular Genetics	2009	33
Intermittent peripheral weakness as the presenting feature of pyruvate dehydrogenase deficiency F.G. Debray, Marie Lambert, Michel Vanasse, European Journal of Pediatrics Metabolic SyndromeEnergy MetabolismPyruvate Dehydrogenase DeficiencyPhysiologyPresenting Feature	2006	29

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