Ileana Ferrero

2.4k total citations
19 papers, 1.1k citations indexed

About

Ileana Ferrero is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Ileana Ferrero has authored 19 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 2 papers in Surgery. Recurrent topics in Ileana Ferrero's work include Mitochondrial Function and Pathology (11 papers), RNA modifications and cancer (6 papers) and Metabolism and Genetic Disorders (4 papers). Ileana Ferrero is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), RNA modifications and cancer (6 papers) and Metabolism and Genetic Disorders (4 papers). Ileana Ferrero collaborates with scholars based in Italy, United Kingdom and Germany. Ileana Ferrero's co-authors include Massimo Zeviani, P Goffrini, Tiziana Lodi, Federica Invernizzi, Daniele Ghezzi, Tim M. Strom, Holger Prokisch, Pio D’Adamo, Paolo Gasparini and Cristina Dallabona and has published in prestigious journals such as Nature Genetics, Journal of Bacteriology and The American Journal of Human Genetics.

In The Last Decade

Ileana Ferrero

18 papers receiving 1.1k citations

Peers

Countries citing papers authored by Ileana Ferrero

Since Specialization

Citations

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

Fields of papers citing papers by Ileana Ferrero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ileana Ferrero

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 2017 ·Human Molecular Genetics ·Caterina Garone, Aaron R. D’Souza, Cristina Dallabona, Tiziana Lodi, Pedro Rebelo‐Guiomar, Joanna Rorbach, Maria Alice Donati, Elena Procopio, Martino Montomoli, Renzo Guerrini, Massimo Zeviani, Sarah E. Calvo, Vamsi K. Mootha, Salvatore DiMauro, Ileana Ferrero, Michal Minczuk	51
2	Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 2017 ·Apollo (University of Cambridge) ·Caterina Garone, Aaron R. D’Souza, Cristina Dallabona, Tiziana Lodi, Pedro Rebelo‐Guiomar, Joanna Rorbach, Maria Alice Donati, Elena Procopio, Martino Montomoli, Renzo Guerrini, Massimo Zeviani, Sarah E. Calvo, Vamsi K. Mootha, Salvatore DiMauro, Ileana Ferrero, Michal Minczuk	2
3	Defective i6A37 Modification of Mitochondrial and Cytosolic tRNAs Results from Pathogenic Mutations in TRIT1 and Its Substrate tRNA 2014 ·PLoS Genetics ·John W. Yarham, Tek N. Lamichhane, Angela Pyle, Sandy Mattijssen, Enrico Baruffini, Francesco Bruni, Claudia Donnini, Alex Vassilev, Langping He, Emma L. Blakely, Helen Griffin, Mauro Santibanez‐Koref, Laurence A. Bindoff, Ileana Ferrero, Patrick F. Chinnery, Robert McFarland, Richard J Maraia, Robert W. Taylor	102
4	ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy 2013 ·The American Journal of Human Genetics ·Tobias B. Haack, Robert Kopajtich, Peter Freisinger, Thomas Wieland, Joanna Rorbach, Thomas J. Nicholls, Enrico Baruffini, (unknown), Katharina Danhauser, Franz Zimmermann, Ralf A. Husain, (unknown), Helen Mundy, Ileana Ferrero, Tim M. Strom, Thomas Meitinger, Robert W. Taylor, Michal Minczuk, Johannes A. Mayr, Holger Prokisch	97
5	A Homozygous Mutation inLYRM7/MZM1LAssociated with Early Onset Encephalopathy, Lactic Acidosis, and Severe Reduction of Mitochondrial ComplexIIIActivity 2013 ·Human Mutation ·Federica Invernizzi, Marco Tigano, Cristina Dallabona, Claudia Donnini, Ileana Ferrero, (unknown), Daniele Ghezzi, Costanza Lamperti, Massimo Zeviani	57
6	Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome 2012 ·Human Molecular Genetics ·Elena Panizza, Tonino Ercolino, Luigi Mori, Elena Rapizzi, Maurizio Castellano, Giuseppe Opocher, Ileana Ferrero, H. P. H. Neumann, Massimo Mannelli, P Goffrini	25
7	The impairment of HCCS leads to MLS syndrome by activating a non‐canonical cell death pathway in the brain and eyes 2012 ·EMBO Molecular Medicine ·Alessia Indrieri, Iván Conte, Giancarlo Chesi, Alessia Romano, (unknown), Rosarita Tatè, Daniele Ghezzi, Massimo Zeviani, P Goffrini, Ileana Ferrero, Paola Bovolenta, Brunella Franco	32
8	Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis 2012 ·The American Journal of Human Genetics ·Daniele Ghezzi, Enrico Baruffini, Tobias B. Haack, Federica Invernizzi, Laura Melchionda, Cristina Dallabona, Tim M. Strom, Rossella Parini, Alberto Burlina, Thomas Meitinger, Holger Prokisch, Ileana Ferrero, Massimo Zeviani	136
9	Extension of Chronological Lifespan by Hexokinase Mutation inKluyveromyces lactisInvolves Increased Level of the Mitochondrial Chaperonin Hsp60 2012 ·Journal of Aging Research ·Lisa Rizzetto, Elena Zanni, Daniela Uccelletti, Ileana Ferrero, P Goffrini	3
10	Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency 2012 ·Journal of Medical Genetics ·Charlotte L. Alston, James Davison, Francesca Meloni, Francois H. van der Westhuizen, (unknown), Hue‐Tran Hornig‐Do, Andrew C. Peet, Paul Gissen, P Goffrini, Ileana Ferrero, Evangeline Wassmer, Robert McFarland, Robert W. Taylor	89
11	Mitochondrial diseases and the role of the yeast models 2010 ·FEMS Yeast Research ·Teresa Rinaldi, Cristina Dallabona, Ileana Ferrero, Laura Frontali, Monique Bolotin‐Fukuhara	32
12	Functional study in a yeast model of a novel succinate dehydrogenase subunit B gene germline missense mutation (C191Y) diagnosed in a patient affected by a glomus tumor 2009 ·Human Molecular Genetics ·P Goffrini, Tonino Ercolino, Elena Panizza, Valentino Giaché, Leonardo Cavone, Alberto Chiarugi, (unknown), Ileana Ferrero, Massimo Mannelli	56
13	SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy 2009 ·Nature Genetics ·Daniele Ghezzi, P Goffrini, Graziella Uziel, Rita Horváth, Thomas Klopstock, Hanns Lochmüller, Pio D’Adamo, Paolo Gasparini, Tim M. Strom, Holger Prokisch, Federica Invernizzi, Ileana Ferrero, Massimo Zeviani	190
14	Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathy 2008 ·Neuromuscular Disorders ·Giuliana Galassi, Eleonora Lamantea, Federica Invernizzi, (unknown), Isabella Pisano, Ileana Ferrero, Luigi Palmieri, Massimo Zeviani	29
15	Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase 2008 ·The American Journal of Human Genetics ·(unknown), Erika Fernández‐Vizarra, Saad AlShahwan, Eman Bakhsh, P Goffrini, Ileana Ferrero, Paolo Mereghetti, Pio D’Adamo, Paolo Gasparini, Massimo Zeviani	143
16	[The pro-apoptotic factors Fas Ligand and Trail. Molecular mechanisms, physiopathological role and therapeutic potential]. 2001 ·PubMed ·(unknown), Carlo Smirne, Ileana Ferrero, (unknown), (unknown), Graziella Bellone, G Emanuelli	1
17	Isolation of the DLD gene of Saccharomyces cerevisiae encoding the mitochondrial enzyme D-lactate ferricytochrome c oxidoreductase 1993 ·Molecular and General Genetics MGG ·Tiziana Lodi, Ileana Ferrero	74
18	Allelism of IMP1 and GAL2 genes of Saccharomyces cerevisiae 1992 ·Journal of Bacteriology ·Claudia Donnini, Tiziana Lodi, Ileana Ferrero, (unknown), P. P. Puglisi	16
19	Mitochondrial NAD, L-lactate dehydrogenase and NAD, D-lactate dehydrogenase in the yeast Saccharomyces cerevisiae. 1983 ·PubMed ·(unknown), Francesca Tassi, Tiziana Lodi, Ileana Ferrero	12

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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