Rosalba Carrozzo

8.4k citations

143 papers · 5.3k indexed · h-index 38

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders 49
Molecular Biology top 1%
- Mitochondrial Function and Pathology 86
- ATP Synthase and ATPases Research 50
- RNA modifications and cancer 9
- Coenzyme Q10 studies and effects 7
Biochemistry top 1%
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 11
Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
Renewable Energy, Sustainability and the Environment
- Metalloenzymes and iron-sulfur proteins 7

Co-authors: Filippo M. Santorelli Enrico Bertini Carlo Dionisi‐Vici Fiorella Piemonte Hermann Schägger Teresa Rizza Ilka Wittig Massimo Zeviani
Cited by: Clinical Biochemistry Molecular Biology Biochemistry
Journals: Proceedings of the National Academy of Sciences (2 papers)Journal of Biological Chemistry (2 papers)Circulation (1 paper)
Partner nations: Italy United States United Kingdom

In The Last Decade

Rosalba Carrozzo

140 papers receiving 5.2k citations

Peers

Countries citing papers authored by Rosalba Carrozzo

Since Specialization

Citations

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

Fields of papers citing papers by Rosalba Carrozzo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Rosalba Carrozzo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rosalba Carrozzo Line = papers co-authored together Rosalba Carrozzo links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Imaging-Based Molecular Interaction Between Src and Lamin A/C Mechanosensitive Proteins in the Nucleus of Laminopathic Cells International Journal of Molecular Sciences ·Stefania Petrini,Giulia Bagnato,Michela Piccione,Valentina Doria,Valentina Apollonio,Marco Cappa,Claudia Castiglioni,Filippo M. Santorelli,Teresa Rizza,Rosalba Carrozzo,Enrico Bertini,Barbara Peruzzi	2024	0
2	De Novo DNM1L Mutation in a Patient with Encephalopathy, Cardiomyopathy and Fatal Non-Epileptic Paroxysmal Refractory Vomiting International Journal of Molecular Sciences ·Beatrice Berti,Daniela Verrigni,Alessia Nasca,Michela Di Nottia,Daniela Leone,Alessandra Torraco,Teresa Rizza,Emanuele Bellacchio,Andrea Legati,Concetta Palermo,Silvia Marchet,Costanza Lamperti,Antonio Novelli,Eugenio Mercuri,Enrico Bertini,Marika Pane,Daniele Ghezzi,Rosalba Carrozzo	2024	2
3	Case report: A safeguard in the sea of variants of uncertain significance: a case study on child with high risk neuroblastoma and acute myeloid leukemia Frontiers in Oncology ·Francesco Fabozzi,Rosalba Carrozzo,Mariachiara Lodi,Angela Di Giannatale,Selene Cipri,Chiara Rosignoli,Isabella Giovannoni,Alessandra Stracuzzi,Teresa Rizza,Claudio Montante,Emanuele Agolini,Michela Di Nottia,Federica Galaverna,Giada Del Baldo,Francesco Del Bufalo,Angela Mastronuzzi,Maria Antonietta De Ioris	2024	2
4	TERT Extra-Telomeric Roles: Antioxidant Activity and Mitochondrial Protection International Journal of Molecular Sciences ·Jessica Marinaccio,Emanuela Micheli,Ion Udroiu,Michela Di Nottia,Rosalba Carrozzo,Nicoló Baranzini,Annalisa Grimaldi,Stefano Leone,Sandra Moreno,Maurizio Muzzi,Antonella Sgura	2023	20
5	SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction Clinical Genetics ·Manuela Priolo,Valentina Palermo,Francesca Antonella Aiello,Andrea Ciolfi,Luca Pannone,Valentina Muto,Marialetizia Motta,Cecilia Mancini,Francesca Clementina Radio,Marcello Niceta,Chiara Leoni,Letizia Pintomalli,Rosalba Carrozzo,Giuseppe Rajola,Corrado Mammì,Giuseppe Zampino,Simone Martinelli,Bruno Dallapiccola,Pietro Pichierri,Marco Tartaglia	2022	2
6	Novel Dilated Cardiomyopathy Associated to Calreticulin and Myo7A Gene Mutation in Usher Syndrome ESC Heart Failure ·Andrea Frustaci,Alessandro De Luca,Nicola Galea,Romina Verardo,Valentina Guida,Rosalba Carrozzo,Cristina Chimenti,Emanuela Frustaci,Luigi Sansone,Matteo Antonio Russo	2021	4
7	Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review Parkinsonism & Related Disorders ·Serena Galosi,Emanuele Barca,Rosalba Carrozzo,Tommaso Schirinzi,Catarina M. Quinzii,Maria Lieto,Gessica Vasco,Ginevra Zanni,Michela Di Nottia,Daniele Galatolo,Alessandro Filla,Enrico Bertini,Filippo M. Santorelli,Vincenzo Leuzzi,Richard Haas,Michio Hirano,Jennifer Friedman	2019	18
8	Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy Amyloid ·Marco Luigetti,Guido Primiano,Giulia Bisogni,Cristina Cuccagna,Rosalba Carrozzo,Laura Obici,Daniela Bernardo,Cristina Sancricca,Serenella Servidei	2018	3
9	APOPT 1/ COA 8 assists COX assembly and is oppositely regulated by UPS and ROS EMBO Molecular Medicine ·Alba Signes,Raffaele Cerutti,Anna S. Dickson,Cristiane Benincá,Elizabeth C. Hinchy,Daniele Ghezzi,Rosalba Carrozzo,Enrico Bertini,Michael P. Murphy,James A. Nathan,Carlo Viscomi,Erika Fernández‐Vizarra,Massimo Zeviani	2018	25
10	Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translation Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Michela Di Nottia,Arianna Montanari,Daniela Verrigni,Romina Oliva,Alessandra Torraco,Erika Fernández‐Vizarra,Daria Diodato,Teresa Rizza,Marzia Bianchi,Michela Catteruccia,Massimo Zeviani,Carlo Dionisi‐Vici,Silvia Francisci,Enrico Bertini,Rosalba Carrozzo	2017	18
11	Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1 Neurogenetics ·Mariana Ferreira,Alessandra Torraco,Teresa Rizza,Fabiana Fattori,Maria Chiara Meschini,Cinzia Castana,Nancy E. Go,Frank E. Nargang,Margarida Duarte,Fiorella Piemonte,Carlo Dionisi‐Vici,Arnaldo Videira,Laura Vilarinho,Filippo M. Santorelli,Rosalba Carrozzo,Enrico Bertini	2011	39
12	Clinical and audiological follow up of a family with the 8363G > A mutation in the mitochondrial DNA Neuromuscular Disorders ·Roberto DiFabio,Filippo M. Santorelli,Giuseppe Nola,F. Cricchi,Roberto De Masi,Angelo Ingrosso,Fabiana Fattori,Rosalba Carrozzo,Nicola Vanacore,Francesco Pierelli,Giovanni Ralli,Carlo Casali	2009	2
13	Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutations Journal of Medical Genetics ·Helen Tuppen,Fabiana Fattori,Rosalba Carrozzo,Massimo Zeviani,S. DiMauro,Sara Seneca,Joanne Martindale,S E Olpin,Eileen P. Treacy,Robert McFarland,Filippo M. Santorelli,Rachael W. Taylor	2008	12
14	Supercomplexes and subcomplexes of mitochondrial oxidative phosphorylation Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Ilka Wittig,Rosalba Carrozzo,Filippo M. Santorelli,Hermann Schägger	2006	177
15	A mitochondrial ATPase 6 mutation is associated with Leigh syndrome in a family and affects proton flow and adenosine triphosphate output when modeled in Escherichia coli Acta Paediatrica ·Rosalba Carrozzo,Teresa Rizza,S. Lucioli,Roberta Pierini,Enrico Bertini,Filippo M. Santorelli	2004	2
16	The T9176G mutation of human mtDNA gives a fully assembled but inactive ATP synthase when modeled in Escherichia coli FEBS Letters ·Rosalba Carrozzo,James Murray,Filippo M. Santorelli,Roderick Capaldi	2000	28
17	Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes Cytogenetic and Genome Research ·Antonella Fogli,Sabrina Giglio,Giulia Arrigo,Cristiana Lo Nigro,Massimo Zollo,Luigi Viggiano,Mariano Rocchi,Nicoletta Archidiacono,Orsetta Zuffardi,Rosalba Carrozzo	1999	6
18	Point Mutations and an Intragenic Deletion in LIS1, the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome Human Molecular Genetics ·Cristiana Lo Nigro,Samuel S. Chong,Ann C. M. Smith,William B. Dobyns,Rosalba Carrozzo,David H. Ledbetter	1997	256
19	X/Y translocation in a family with X‐linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene Clinical Genetics ·Andrea Ballabio,Giancarlo Parenti,Rosalba Carrozzo,Giovanni V. Coppa,L. Felici,Valeria Migliori,Margherita Silengo,P Franceschini,Generoso Andria	1988	47
20	Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis. Proceedings of the National Academy of Sciences ·Andrea Ballabio,Giancarlo Parenti,Rosalba Carrozzo,Gianfranco Sebastio,Generoso Andria,Veronica J. Buckle,Niall J. Fraser,Ian Craig,Mariano Rocchi,G. Cara Romeo	1987	115

About Rosalba Carrozzo

Rosalba Carrozzo is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry, having authored 143 papers that have together received 5.3k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (86 papers), ATP Synthase and ATPases Research (50 papers), Metabolism and Genetic Disorders (49 papers), Genetic Neurodegenerative Diseases (11 papers), RNA modifications and cancer (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Coenzyme Q10 studies and effects (7 papers) and Metalloenzymes and iron-sulfur proteins (7 papers). The work is most often cited by research in Clinical Biochemistry (1.5k citations), Molecular Biology (4.0k citations) and Biochemistry (297 citations). Rosalba Carrozzo has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Filippo M. Santorelli, Enrico Bertini, Carlo Dionisi‐Vici, Fiorella Piemonte, Hermann Schägger, Teresa Rizza, Ilka Wittig, Massimo Zeviani, David H. Ledbetter and Samuel S. Chong. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

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