Massimo Zeviani - Concepedia

Author

Massimo Zeviani

Fondazione IRCCS Istituto Neurologico Carlo Besta ORCID

Also Known As

G. Uziel, M Zeviani, M. Zeviani, MASSIMO ZEVIANI, Massimo ZEVIANI, Massimo Zeviani, Zeviani M., Zeviani Massimo, Zeviani, M, Zeviani, Massimo

755

Publications

51.2K

Citations

116

H-Index

217

Concepts

All Affiliations

Fondazione IRCCS Istituto Neurologico Carlo Besta MRC Mitochondrial Biology Unit University of Padua Istituti di Ricovero e Cura a Carattere Scientifico University of Cambridge

About

Massimo Zeviani is an author at Fondazione IRCCS Istituto Neurologico Carlo Besta specializing in medicine, genetics, and mitochondrial function.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	83	181	26.5K
2	Natural Sciences	43	59	8.7K
3	Health Sciences	10	10	1.1K
4	Arts	5	5	818
5	Engineering	1	1	35

Massimo Zeviani

359

Publications

43.3K

Citations

107

H-Index

Page 1

	Year	Citations
Identification and characterization of a spinal muscular atrophy-determining gene Suzie Lefebvre, Lydie Bürglen, Sophie Reboullet, Cell GeneticsGene CharacterizationMolecular GeneticsDisease Gene IdentificationGenomics	1995	3.9K
Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome Carlos T. Moraes, Salvatore DiMauro, Massimo Zeviani, New England Journal of Medicine	1989	1K
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria Johannes N. Spelbrink, Fang-Yuan Li, Valeria Tiranti, Nature Genetics Mitochondrial BiogenesisMitochondrial FunctionMitochondrial DynamicNatural SciencesGenetics	2001	879
Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease Giorgio Casari, Maurizio De Fusco, Sonia Ciarmatori, Cell Mitochondrial FunctionOxphos ImpairmentGeneticsMedicineSpastic Paraplegia	1998	824
Oxygen sensing requires mitochondrial ROS but not oxidative phosphorylation Joslyn K. Brunelle, Eric L. Bell, N.M. Quesada, Cell Metabolism Redox SignalingBiochemistryMitochondrial FunctionMitochondrial RosReactive Oxygen Specie	2005	752
Deletions of mitochondrial DNA in Kearns‐Sayre syndrome Massimo Zeviani, Carlos T. Moraes, S. DiMauro, Neurology Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGenetic DisorderNatural Sciences	1988	735
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region Massimo Zeviani, Serenella Servidei, Cinzia Gellera, Nature Mendelian DisorderGenetic DisorderGeneticsMultiple DeletionsDna Replication	1989	637
Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance Jyrki Kaukonen, Jukka K. Juselius, Valeria Tiranti, Science	2000	630
A Direct Repeat Is a Hotspot for Large-Scale Deletion of Human Mitochondrial DNA Eric A. Schon, Rosario Rizzuto, Carlos T. Moraes, Science Kearns-sayre SyndromeDnaGeneticsDna AnalysisMolecular Biology	1989	579
Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides Xavier Estivill, Nancy Govea, Anna Barceló, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseAudiology	1998	547

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