Daniele Ghezzi

7.4k total citations
91 papers, 3.2k citations indexed

About

Daniele Ghezzi is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Daniele Ghezzi has authored 91 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 43 papers in Clinical Biochemistry and 20 papers in Cellular and Molecular Neuroscience. Recurrent topics in Daniele Ghezzi's work include Mitochondrial Function and Pathology (71 papers), Metabolism and Genetic Disorders (43 papers) and ATP Synthase and ATPases Research (35 papers). Daniele Ghezzi is often cited by papers focused on Mitochondrial Function and Pathology (71 papers), Metabolism and Genetic Disorders (43 papers) and ATP Synthase and ATPases Research (35 papers). Daniele Ghezzi collaborates with scholars based in Italy, United Kingdom and Germany. Daniele Ghezzi's co-authors include Massimo Zeviani, Costanza Lamperti, Federica Invernizzi, Daria Diodato, Pio D’Adamo, Barbara Garavaglia, Valeria Tiranti, Alessia Nasca, Eleonora Lamantea and Graziella Uziel and has published in prestigious journals such as Nature Communications, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Daniele Ghezzi

89 papers receiving 3.2k citations

Peers

Countries citing papers authored by Daniele Ghezzi

Since Specialization

Citations

This map shows the geographic impact of Daniele Ghezzi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Daniele Ghezzi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniele Ghezzi more than expected).

Fields of papers citing papers by Daniele Ghezzi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniele Ghezzi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Daniele Ghezzi. The network helps show where Daniele Ghezzi may publish in the future.

Co-authorship network of co-authors of Daniele Ghezzi

This figure shows the co-authorship network connecting the top 25 collaborators of Daniele Ghezzi. A scholar is included among the top collaborators of Daniele Ghezzi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Daniele Ghezzi. Daniele Ghezzi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	De Novo DNM1L Pathogenic Variant Associated with Lethal Encephalocardiomyopathy—Case Report and Literature Review 2025 ·International Journal of Molecular Sciences ·(unknown), Luisa Zupin, Eleonora Lamantea, Enrico Baruffini, Daniele Ghezzi, Andrea Legati, Fulvio Celsi, (unknown), Valeria Capaci, Maurizio Pinamonti, Rossana Bussani, Marco Carrozzi, Cristina Dallabona, Massimo Zeviani, Maria Teresa Bonati	1
2	Bioinformatics Tools for NGS-Based Identification of Single Nucleotide Variants and Large-Scale Rearrangements in Mitochondrial DNA 2025 ·BioTech ·(unknown), (unknown), (unknown), Andrea Zauli, Eleonora Lamantea, Leonardo Caporali, Daniele Ghezzi, Andrea Legati	1
3	De Novo DNM1L Mutation in a Patient with Encephalopathy, Cardiomyopathy and Fatal Non-Epileptic Paroxysmal Refractory Vomiting 2024 ·International Journal of Molecular Sciences ·Beatrice Berti, Daniela Verrigni, Alessia Nasca, Michela Di Nottia, Daniela Leone, Alessandra Torraco, Teresa Rizza, Emanuele Bellacchio, (unknown), Concetta Palermo, Silvia Marchet, Costanza Lamperti, Antonio Novelli, Eugenio Mercuri, Enrico Bertini, Marika Pane, Daniele Ghezzi, Rosalba Carrozzo	2
4	Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and Dopamine 2023 ·Movement Disorders ·Elisabetta Indelicato, Sylvia Boesch, Niccolò E. Mencacci, Daniele Ghezzi, Holger Prokisch, Juliane Winkelmann, Michael Zech	3
5	NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia 2023 ·Genes ·Federica Invernizzi, (unknown), (unknown), Andrea Legati, Nadia Zanetti, Barbara Garavaglia, Eleonora Lamantea, Lorenzo Peverelli, Anna Ardissone, Isabella Moroni, Lorenzo Maggi, Silvia Bonanno, Laura M. Fiori, Daniele Velardo, Francesca Magri, Giacomo P. Comi, Dario Ronchi, Daniele Ghezzi, Costanza Lamperti	3
6	PPAR-gamma agonist pioglitazone recovers mitochondrial quality control in fibroblasts from PITRM1-deficient patients 2023 ·Frontiers in Pharmacology ·(unknown), (unknown), Marta Giacomello, Chiara Frascarelli, (unknown), Laurence A. Bindoff, (unknown), Paul Renbaum, Filippo M. Santorelli, Giulia Massaro, Carlo Viscomi, Massimo Zeviani, Daniele Ghezzi, Emanuela Bottani, Dario Brunetti	5
7	Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNA 2021 ·Journal of Molecular Diagnostics ·Andrea Legati, Nadia Zanetti, Alessia Nasca, (unknown), Costanza Lamperti, Eleonora Lamantea, Daniele Ghezzi	26
8	Clinical, imaging, biochemical and molecular features in Leigh syndrome: a study from the Italian network of mitochondrial diseases 2021 ·Orphanet Journal of Rare Diseases ·Anna Ardissone, Claudio Bruno, Daria Diodato, Alice Donati, Daniele Ghezzi, Eleonora Lamantea, Costanza Lamperti, Michelangelo Mancuso, Diego Martinelli, Guido Primiano, Elena Procopio, Anna Rubegni, Filippo M. Santorelli, Maria Cristina Schiaffino, Serenella Servidei, (unknown), Enrico Bertini, Isabella Moroni	17
9	New missense variants of NDUFA11 associated with late‐onset myopathy 2019 ·Muscle & Nerve ·Lorenzo Peverelli, Andrea Legati, Eleonora Lamantea, Alessia Nasca, (unknown), (unknown), Daniele Ghezzi, Costanza Lamperti	8
10	New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies 2016 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Andrea Legati, Aurelio Reyes, Alessia Nasca, Federica Invernizzi, Eleonora Lamantea, Valeria Tiranti, Barbara Garavaglia, Costanza Lamperti, Anna Ardissone, Isabella Moroni, Alan J. Robinson, Daniele Ghezzi, Massimo Zeviani	71
11	Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes 2016 ·Journal of Neurology ·Alessandra Torraco, Anna Ardissone, Federica Invernizzi, Teresa Rizza, Giuseppe Fiermonte, Marcello Niceta, Nadia Zanetti, Diego Martinelli, Angelo Vozza, Daniela Verrigni, Michela Di Nottia, Eleonora Lamantea, Daria Diodato, Marco Tartaglia, Carlo Dionisi‐Vici, Isabella Moroni, Laura Farina, Enrico Bertini, Daniele Ghezzi, Rosalba Carrozzo	34
12	RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy 2015 ·The American Journal of Human Genetics ·Aurelio Reyes, Laura Melchionda, Alessia Nasca, Franco Carrara, Eleonora Lamantea, (unknown), Costanza Lamperti, Mingyan Fang, Jianguo Zhang, Dario Ronchi, Sara Bonato, Gigliola Fagiolari, Maurizio Moggio, Daniele Ghezzi, Massimo Zeviani	80
13	Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature 2015 ·JIMD Reports ·Anna Ardissone, Tiziana Granata, Andrea Legati, Daria Diodato, Laura Melchionda, Eleonora Lamantea, Barbara Garavaglia, Daniele Ghezzi, Isabella Moroni	13
14	Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations 2014 ·Frontiers in Genetics ·Federica Invernizzi, Anna Ardissone, Eleonora Lamantea, Barbara Garavaglia, Massimo Zeviani, Laura Farina, Daniele Ghezzi, Isabella Moroni	40
15	Assembly Factors of Human Mitochondrial Respiratory Chain Complexes: Physiology and Pathophysiology 2012 ·Advances in experimental medicine and biology ·Daniele Ghezzi, Massimo Zeviani	110
16	Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor 2010 ·The American Journal of Human Genetics ·Daniele Ghezzi, Irina F. Sevrioukova, Federica Invernizzi, Costanza Lamperti, Marina Mora, Pio D’Adamo, Francesca Novara, Orsetta Zuffardi, Graziella Uziel, Massimo Zeviani	171
17	Sym1, the yeast ortholog of the MPV17 human disease protein, is a stress-induced bioenergetic and morphogenetic mitochondrial modulator 2009 ·Human Molecular Genetics ·Cristina Dallabona, Renè Massimiliano Marsano, (unknown), Daniele Ghezzi, Patrizia Mancini, Massimo Zeviani, Iliana Ferrero, Claudia Donnini	59
18	FASTKD2 Nonsense Mutation in an Infantile Mitochondrial Encephalomyopathy Associated with Cytochrome C Oxidase Deficiency 2008 ·The American Journal of Human Genetics ·Daniele Ghezzi, Ann Saada, Pio D’Adamo, Erika Fernández‐Vizarra, Paolo Gasparini, Valeria Tiranti, Orly Elpeleg, Massimo Zeviani	86
19	Myoclonus–dystonia syndrome: Clinical presentation, disease course, and genetic features in 11 families 2007 ·Movement Disorders ·Nardo Nardocci, Giovanna Zorzi, Chiara Barzaghi, Federica Zibordi, (unknown), Daniele Ghezzi, Barbara Garavaglia	58
20	Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease 2006 ·Movement Disorders ·Roberta Marongiu, Daniele Ghezzi, Tàmara Ialongo, Francesco Soleti, Antonio Emanuele Elia, (unknown), Alberto Albanese, Maria Concetta Altavista, Paolo Barone, Livia Brusa, Pietro Cortelli, Lucia Petrozzi, Cesa Scaglione, Paolo Stanzione, Michèle Tinazzi, Massimo Zeviani, Bruno Dallapiccola, Anna Rita Bentivoglio, Enza Maria Valente, Barbara Garavaglia	22

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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