Catarina M. Quinzii
Columbia University Irving Medical Center(US)
Publications by Year
Research Areas
Coenzyme Q10 studies and effects, Mitochondrial Function and Pathology, Advanced battery technologies research, Biochemical Acid Research Studies, Metabolism and Genetic Disorders
Most-Cited Works
- → Leigh Syndrome with Nephropathy and CoQ10 Deficiency Due to decaprenyl diphosphate synthase subunit 2 (PDSS2) Mutations(2006)389 cited
- → A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase (COQ2) Causes Primary Coenzyme Q10 Deficiency(2006)344 cited
- → The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene(2007)318 cited
- → ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q10 Deficiency(2008)318 cited
- → Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease(2013)230 cited
- → A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease(2009)216 cited
- → Heterogeneity of Coenzyme Q10Deficiency(2012)213 cited
- → HDAC inhibitors elicit metabolic reprogramming by targeting super-enhancers in glioblastoma models(2020)202 cited
- → Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: A CoQ10-responsive condition(2005)189 cited
- → Human Coenzyme Q10 Deficiency(2006)185 cited