Costanza Lamperti - Concepedia

Author

Costanza Lamperti

Fondazione IRCCS Istituto Neurologico Carlo Besta ORCID

Also Known As

C Lamperti, C. Lamperti, Costanza Lamperti, Lamperti, Costanza, Tiziana Granata

164

Publications

7.4K

Citations

H-Index

107

Concepts

All Affiliations

Fondazione IRCCS Istituto Neurologico Carlo Besta University of Milan Istituti di Ricovero e Cura a Carattere Scientifico MRC Mitochondrial Biology Unit Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

About

Costanza Lamperti 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	27	35	2.8K
2	Health Sciences	6	6	329
3	Natural Sciences	3	3	258
4	Engineering	2	2	90
5	Public Health	1	1	69

Costanza Lamperti

Publications

6.6K

Citations

H-Index

Page 1

	Year	Citations
Multi-system neurological disease is common in patients with OPA1 mutations Patrick Yu‐Wai‐Man, Philip G. Griffiths, Gráinne S. Gorman, Brain	2010	437
NAD+-Dependent Activation of Sirt1 Corrects the Phenotype in a Mouse Model of Mitochondrial Disease Raffaele Cerutti, Eija Pirinen, Costanza Lamperti, Cell Metabolism	2014	339
Transcription Factor EB Controls Metabolic Flexibility during Exercise Gelsomina Mansueto, Andrea Armani, Carlo Viscomi, Cell Metabolism	2016	318
In Vivo Correction of COX Deficiency by Activation of the AMPK/PGC-1α Axis Carlo Viscomi, Emanuela Bottani, Gabriele Civiletto, Cell Metabolism	2011	284
Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor Daniele Ghezzi, Irina F. Sevrioukova, Federica Invernizzi, The American Journal of Human Genetics MitophagyMitochondrial FunctionGeneticsApoptosisAutophagy	2010	225
Opa1 Overexpression Ameliorates the Phenotype of Two Mitochondrial Disease Mouse Models Gabriele Civiletto, Tatiana Varanita, Raffaele Cerutti, Cell Metabolism	2015	214
Cerebellar ataxia and coenzyme Q10 deficiency Costanza Lamperti, Ali Naini, Michio Hirano, Neurology Mendelian DisorderCoq10 SupplementationMedicineGeneticsGenetic Disorder	2003	204
Novel (ovario) leukodystrophy related to <i>AARS2</i> mutations Cristina Dallabona, Daria Diodato, Sietske H. Kevelam, Neurology	2014	201
Recurrent De Novo and Biallelic Variation of ATAD3A , Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes Tamar Harel, Wan Hee Yoon, Caterina Garone, The American Journal of Human Genetics Distinct Neurological SyndromesNeurodegenerative DiseasesRecurrent De NovoMitochondrial FunctionGenetics	2016	186
Clinical implementation of RNA sequencing for Mendelian disease diagnostics Vicente A. Yépez, Mirjana Gušić, Robert Kopajtich, Genome Medicine	2022	184

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