Mariantonietta Capristo

Author

University of Bologna ORCID

Also Known As

Capristo, Mariantonietta <1981>, M. Capristo, Mariantonietta Capristo

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

University of Bologna Istituto delle Scienze Neurologiche di Bologna Istituti di Ricovero e Cura a Carattere Scientifico IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola Sapienza University of Rome

About

Mariantonietta Capristo is an author at University of Bologna specializing in medicine, pathology, and mitochondrial medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	410
2	Cell Biology	3	3	164
3	Engineering	1	1	99
4	Public Health	1	1	17
5	Gastroenterology	1	1	17

Mariantonietta Capristo

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy Sarah L. Stenton, Claudia B. Catarino, N.A. Andreeva, Journal of Clinical Investigation	2021	144
The genetic and metabolic signature of oncocytic transformation implicates HIF1α destabilization Anna Maria Porcelli, Anna Ghelli, Claudio Ceccarelli, Human Molecular Genetics	2009	120
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene <i>MTND1</i> , an <i>Oncojanus</i> Function Giuseppe Gasparre, Ivana Kurelac, Mariantonietta Capristo, Cancer Research	2011	99
Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment Luisa Iommarini, Ivana Kurelac, Mariantonietta Capristo, Human Molecular Genetics EngineeringTumor ProgressionPathologyOsteosarcoma CellsDifferent Mtdna Mutations	2013	99
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy Roberto De Giorgio, Loris Pironi, Rita Rinaldi, Annals of Neurology GeneticsImmunologyPathologyThymidine Phosphorylase ReplacementTranslational Medicine	2016	92
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells Claudia Calabrese, Luisa Iommarini, Ivana Kurelac, Cancer & Metabolism	2013	87
Expanding and validating the biomarkers for mitochondrial diseases Alessandra Maresca, Valentina Del Dotto, Martina Romagnoli, Journal of Molecular Medicine Metabolic DisorderPathologyNeurochemical BiomarkersOxidative StressMetabolic Syndrome	2020	66
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy Leonardo Caporali, Luisa Iommarini, Chiara La Morgia, PLoS Genetics	2018	58
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome Chiara La Morgia, Alessandra Maresca, Giulia Amore, Scientific Reports	2020	50
ATPase Domain <scp><i>AFG3L2</i></scp> Mutations Alter <scp>OPA1</scp> Processing and Cause Optic Neuropathy Leonardo Caporali, Stefania Magri, Andrea Legati, Annals of Neurology	2020	48

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