Maria Chiara Meschini

967 total citations
23 papers, 637 citations indexed

About

Maria Chiara Meschini is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Maria Chiara Meschini has authored 23 papers receiving a total of 637 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Maria Chiara Meschini's work include Mitochondrial Function and Pathology (17 papers), ATP Synthase and ATPases Research (11 papers) and Metabolism and Genetic Disorders (11 papers). Maria Chiara Meschini is often cited by papers focused on Mitochondrial Function and Pathology (17 papers), ATP Synthase and ATPases Research (11 papers) and Metabolism and Genetic Disorders (11 papers). Maria Chiara Meschini collaborates with scholars based in Italy, Mexico and Portugal. Maria Chiara Meschini's co-authors include Filippo M. Santorelli, Rosalba Carrozzo, Claudia Nesti, Carlo Dionisi‐Vici, Fiorella Piemonte, Enrico Bertini, Teresa Rizza, Cristiano Rizzo, Stefano Doccini and Federica Deodato and has published in prestigious journals such as Nature Cell Biology, Brain and Neurology.

In The Last Decade

Maria Chiara Meschini

23 papers receiving 634 citations

Peers

Countries citing papers authored by Maria Chiara Meschini

Since Specialization

Citations

This map shows the geographic impact of Maria Chiara Meschini'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 Maria Chiara Meschini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Chiara Meschini more than expected).

Fields of papers citing papers by Maria Chiara Meschini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Chiara Meschini. 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 Maria Chiara Meschini. The network helps show where Maria Chiara Meschini may publish in the future.

Co-authorship network of co-authors of Maria Chiara Meschini

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Chiara Meschini. A scholar is included among the top collaborators of Maria Chiara Meschini 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 Maria Chiara Meschini. Maria Chiara Meschini 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	Converging Role for REEP1/SPG31 in Oxidative Stress 2023 ·International Journal of Molecular Sciences ·(unknown), Maria Chiara Meschini, Alessandra Tessa, Federica Morani, (unknown), Asahi Ogi, Maria Marchese, Michela Ori, Filippo M. Santorelli, Stefano Doccini	3
2	CLN8 is an endoplasmic reticulum cargo receptor that regulates lysosome biogenesis 2018 ·Nature Cell Biology ·Alberto di Ronza, Lakshya Bajaj, Jai Prakash Sharma, Deepthi Sanagasetti, Parisa Lotfi, Carolyn J. Adamski, John R. Collette, Michela Palmieri, (unknown), Lauren Popp, (unknown), Maria Chiara Meschini, Hon-Chiu Eastwood Leung, Laura Segatori, Alessandro Simonati, Richard N. Sifers, Filippo M. Santorelli, Marco Sardiello	83
3	Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28 2016 ·Journal of the Neurological Sciences ·Andrea Mignarri, Anna Rubegni, Alessandra Tessa, (unknown), Alessandro Malandrini, Elena Cardaioli, Maria Chiara Meschini, Maria Laura Stromillo, Stefano Doccini, Antonio Federico, Filippo M. Santorelli, Maria Teresa Dotti	20
4	Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy 2015 ·Human Molecular Genetics ·Claudia Nesti, Maria Chiara Meschini, Brigitte Meunier, Michele Sacchini, Stefano Doccini, Alessandro Romano, Sara Petrillo, Ilaria Pezzini, Nabila Seddiki, Anna Rubegni, Fiorella Piemonte, Maria Alice Donati, Gaël Brasseur, Filippo M. Santorelli	14
5	Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndrome 2015 ·Neurological Sciences ·Stefano Doccini, Maria Chiara Meschini, Davide Mei, Renzo Guerrini, Federico Sicca, Filippo M. Santorelli	7
6	Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay 2015 ·Journal of Neurology ·Chiara Criscuolo, Claudio Procaccini, Maria Chiara Meschini, Alessandra Cianflone, (unknown), Stefano Doccini, David Devos, Claudia Nesti, (unknown), Mario Pellegrino, Alessandro Filla, Giuseppe De Michele, Giuseppe Matarese, Filippo M. Santorelli	42
7	Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease 2014 ·Neurology ·Roberto Di Fabio, Francesca Moro, (unknown), Maria Chiara Meschini, Francesco Pezzini, Stefano Doccini, Carlo Casali, Francesco Pierelli, Alessandro Simonati, Filippo M. Santorelli	23
8	A Novel SUCLA2 Mutation in a Portuguese Child Associated With “Mild” Methylmalonic Aciduria 2014 ·Journal of Child Neurology ·Célia Nogueira, Maria Chiara Meschini, Claudia Nesti, Paula Garcia, Luísa Diogo, Carla Valongo, (unknown), Arnaldo Videira, Laura Vilarinho, Filippo M. Santorelli	13
9	Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency 2013 ·Neurogenetics ·Célia Nogueira, José Barros, María José Sá, Luı́sa Azevedo, Ricardo Taipa, Alessandra Torraco, Maria Chiara Meschini, Daniela Verrigni, Claudia Nesti, Teresa Rizza, João Paulo Teixeira, Rosalba Carrozzo, Manuel Melo Pires, Laura Vilarinho, Filippo M. Santorelli	35
10	Dopamine-agonist responsive Parkinsonism in a patient with the SANDO syndrome caused by POLG mutation 2013 ·BMC Medical Genetics ·M. Poggio, Claudia Nesti, Claudio Bruno, Maria Chiara Meschini, Angelo Schenone, Filippo M. Santorelli	20
11	TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesis 2012 ·Neurogenetics ·Alessandra Torraco, Daniela Verrigni, Teresa Rizza, Maria Chiara Meschini, (unknown), Diego Martinelli, Marzia Bianchi, Fiorella Piemonte, Carlo Dionisi‐Vici, Filippo M. Santorelli, Enrico Bertini, Rosalba Carrozzo	22
12	TRPV4 mutations in children with congenital distal spinal muscular atrophy 2012 ·Neurogenetics ·Chiara Fiorillo, Francesca Moro, Giacomo Brisca, Guja Astrea, Claudia Nesti, Zoltán Bálint, Andrea Olschewski, Maria Chiara Meschini, Christian Guelly, Michaela Auer‐Grumbach, Roberta Battini, Marina Pedemonte, Alessandro Romano, Valeria Menchise, Roberta Biancheri, Filippo M. Santorelli, Claudio Bruno	28
13	Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1 2011 ·Neurogenetics ·(unknown), Alessandra Torraco, Teresa Rizza, Fabiana Fattori, Maria Chiara Meschini, (unknown), Nancy E. Go, Frank E. Nargang, Margarida Duarte, Fiorella Piemonte, Carlo Dionisi‐Vici, Arnaldo Videira, Laura Vilarinho, Filippo M. Santorelli, Rosalba Carrozzo, Enrico Bertini	39
14	Cardiolipin content in mitochondria from cultured skin fibroblasts harboring mutations in the mitochondrial ATP6 gene 2011 ·Journal of Bioenergetics and Biomembranes ·Mohammed El‐Hafidi, Maria Chiara Meschini, Teresa Rizza, Filippo M. Santorelli, Enrico Bertini, Rosalba Carrozzo, (unknown)	5
15	Assaying ATP synthesis in cultured cells: A valuable tool for the diagnosis of patients with mitochondrial disorders 2009 ·Biochemical and Biophysical Research Communications ·Teresa Rizza, (unknown), Maria Chiara Meschini, Marzia Bianchi, Giulia Tozzi, Claudia Nesti, Fiorella Piemonte, Enrico Bertini, Filippo M. Santorelli, Rosalba Carrozzo	21
16	Cellular and functional analysis of four mutations located in the mitochondrial ATPase6 gene 2009 ·Journal of Cellular Biochemistry ·(unknown), Teresa Rizza, Maria Chiara Meschini, Claudia Nesti, Filippo M. Santorelli, Rosalba Carrozzo	16
17	Urine acylcarnitine analysis by ESI–MS/MS: A new tool for the diagnosis of peroxisomal biogenesis disorders 2008 ·Clinica Chimica Acta ·Guglielmo Duranti, Sara Boenzi, Cristiano Rizzo, Lucilla Ravà, Vincenzo Di Ciommo, Rosalba Carrozzo, Maria Chiara Meschini, David W. Johnson, Carlo Dionisi‐Vici	20
18	Infantile Mitochondrial Disorders 2007 ·Bioscience Reports ·Rosalba Carrozzo, Fiorella Piemonte, Alessandra Tessa, S. Lucioli, Teresa Rizza, Maria Chiara Meschini, Fabiana Fattori, Filippo M. Santorelli	5
19	SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness 2007 ·Brain ·Rosalba Carrozzo, Carlo Dionisi‐Vici, Ulrike Steuerwald, S. Lucioli, Federica Deodato, Silvia Di Giandomenico, Enrico Bertini, Barbara Franke, Leo A. J. Kluijtmans, Maria Chiara Meschini, Cristiano Rizzo, Fiorella Piemonte, Richard J. Rodenburg, René Santer, Filippo M. Santorelli, Arno van Rooij, (unknown), Éva Morava, Ron A. Wevers	146
20	A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy 2006 ·Biochemical and Biophysical Research Communications ·Denise Cassandrini, Maria Grazia Calevo, Alessandra Tessa, Giovanni Manfredi, Fabiana Fattori, Maria Chiara Meschini, Rosalba Carrozzo, E. Tonoli, Marina Pedemonte, Carlo Minetti, Federico Zara, Filippo M. Santorelli, Claudio Bruno	30

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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