Lucia Valente

846 total citations
11 papers, 644 citations indexed

About

Lucia Valente is a scholar working on Molecular Biology, Clinical Biochemistry and Epidemiology. According to data from OpenAlex, Lucia Valente has authored 11 papers receiving a total of 644 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 1 paper in Epidemiology. Recurrent topics in Lucia Valente's work include Mitochondrial Function and Pathology (9 papers), ATP Synthase and ATPases Research (4 papers) and Metabolism and Genetic Disorders (4 papers). Lucia Valente is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), ATP Synthase and ATPases Research (4 papers) and Metabolism and Genetic Disorders (4 papers). Lucia Valente collaborates with scholars based in Italy, United Kingdom and Switzerland. Lucia Valente's co-authors include Massimo Zeviani, Valeria Tiranti, Erika Fernández‐Vizarra, Angela Berardinelli, Andrea Martinuzzi, Eleonora Napoli, Maura Floreani, Federica Dabbeni‐Sala, Luca De Gioia and Claudio Castellan and has published in prestigious journals such as Brain, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Lucia Valente

11 papers receiving 633 citations

Peers

Countries citing papers authored by Lucia Valente

Since Specialization

Citations

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

Fields of papers citing papers by Lucia Valente

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lucia Valente. 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 Lucia Valente. The network helps show where Lucia Valente may publish in the future.

Co-authorship network of co-authors of Lucia Valente

This figure shows the co-authorship network connecting the top 25 collaborators of Lucia Valente. A scholar is included among the top collaborators of Lucia Valente 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 Lucia Valente. Lucia Valente is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

#	Work	Indexed citations
1	A multi-center comparison of diagnostic methods for the biochemical evaluation of suspected mitochondrial disorders 2012 ·Mitochondrion ·Richard J. Rodenburg, (unknown), Valeria Tiranti, Robert W. Taylor, Agnès Rötig, Lucia Valente, Federica Invernizzi, Dominique Chrétien, L. He, (unknown), Kirstin Janssen, Patrick F. Chinnery, Hubert J.M. Smeets, I.F.M. de Coo, Lambertus P. van den Heuvel	15
2	Characterization of the first adult de novo case of 46,X,der(Y)t(X;Y)(p22.3;q11.2) 2012 ·Gene ·Nenad Bukvić, (unknown), (unknown), Marianna Bruno, (unknown), (unknown), (unknown), Lucia Valente, (unknown), (unknown)	3
3	The R336Q mutation in human mitochondrial EFTu prevents the formation of an active mt-EFTu·GTP·aa-tRNA ternary complex 2009 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Lucia Valente, (unknown), Tsutomu Suzuki, Massimo Zeviani	18
4	Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA) 2009 ·BMJ Case Reports ·Erika Fernández‐Vizarra, Angela Berardinelli, Lucia Valente, Valeria Tiranti, Massimo Zeviani	47
5	Identification of novel mutations in five patients with mitochondrial encephalomyopathy 2008 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Lucia Valente, Daniela Piga, Eleonora Lamantea, Franco Carrara, Graziella Uziel, Paola Cudia, (unknown), Laura Farina, Lucía Morandi, Marina Mora, Antonella Spinazzola, Massimo Zeviani, Valeria Tiranti	78
6	Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants 2007 ·Brain ·Lodovica Vergani, Adriana Malena, Patrizia Sabatelli, Emanuele Loro, (unknown), Paula Magalhães, Lucia Valente, (unknown), F. Carrara, Bertrand Léger, Joanna Poulton, Aaron P. Russell, Ian Holt	13
7	Infantile Encephalopathy and Defective Mitochondrial DNA Translation in Patients with Mutations of Mitochondrial Elongation Factors EFG1 and EFTu 2006 ·The American Journal of Human Genetics ·Lucia Valente, Valeria Tiranti, Renè Massimiliano Marsano, Edoardo Malfatti, Erika Fernández‐Vizarra, Claudia Donnini, Paolo Mereghetti, Luca De Gioia, Alberto Burlina, Claudio Castellan, Giacomo P. Comi, Salvatore Savasta, Iliana Ferrero, Massimo Zeviani	157
8	Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA) 2006 ·Journal of Medical Genetics ·Erika Fernández‐Vizarra, Angela Berardinelli, Lucia Valente, Valeria Tiranti, Massimo Zeviani	107
9	Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy 2005 ·FEBS Journal ·Maura Floreani, Eleonora Napoli, Andrea Martinuzzi, Giorgia Pantano, Valentina Riva, (unknown), Elena Bisetto, Lucia Valente, Valério Carelli, Federica Dabbeni‐Sala	85
10	Antioxidant defences and homeostasis of reactive oxygen species in different human mitochondrial DNA‐depleted cell lines 2004 ·European Journal of Biochemistry ·Lodovica Vergani, Maura Floreani, Aaron P. Russell, (unknown), Eleonora Napoli, Anna Cabrelle, Lucia Valente, (unknown), Bertrand Léger, Federica Dabbeni‐Sala	44
11	Phenotype modulators in myophosphorylase deficiency 2003 ·Annals of Neurology ·Andrea Martinuzzi, Elena Sartori, Francesco Mari, (unknown), Lucia Valente, C. Angelini, Gabriele Siciliano, Tiziana Mongini, Paola Tonin, Giuliano Tomelleri, António Toscano, Luciano Merlini, Laurence A. Bindoff, (unknown)	77

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.

Explore authors with similar magnitude of impact