Francesca Cavalcanti

5.1k total citations
43 papers, 1.3k citations indexed

About

Francesca Cavalcanti is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Francesca Cavalcanti has authored 43 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Cellular and Molecular Neuroscience, 27 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Francesca Cavalcanti's work include Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (18 papers) and Hereditary Neurological Disorders (9 papers). Francesca Cavalcanti is often cited by papers focused on Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (18 papers) and Hereditary Neurological Disorders (9 papers). Francesca Cavalcanti collaborates with scholars based in Italy, United Kingdom and United States. Francesca Cavalcanti's co-authors include Alessandro Filla, Antonella Monticelli, Giuseppe De Michele, Luigi Pianese, Sergio Cocozza, G Campanella, Lucio Santoro, Sebastiano Cavallaro, A. Perretti and Valentina La Cognata and has published in prestigious journals such as Neurology, Annals of Neurology and International Journal of Molecular Sciences.

In The Last Decade

Francesca Cavalcanti

41 papers receiving 1.2k citations

Peers

Countries citing papers authored by Francesca Cavalcanti

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Cavalcanti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Cavalcanti

This figure shows the co-authorship network connecting the top 25 collaborators of Francesca Cavalcanti. A scholar is included among the top collaborators of Francesca Cavalcanti 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 Francesca Cavalcanti. Francesca Cavalcanti 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:

20 of 20 papers shown

#	Work	Indexed citations
1	The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions 2024 ·International Journal of Molecular Sciences ·(unknown), Luigi Citrigno, Béatrice Gréco, (unknown), Giuseppe Passarino, Raffaele Maletta, (unknown), Alberto Montesanto, Patrizia Spadafora, Francesca Cavalcanti	6
2	Unusual Age‐Dependent Behavior of Leukocytes Telomere Length in Friedreich's Ataxia 2024 ·Movement Disorders ·Daniela Scarabino, Liana Veneziano, Suran Nethisinghe, Elide Mantuano, Alessia Fiore, (unknown), Nita Solanky, Ginevra Zanni, Francesca Cavalcanti, Rosa Maria Corbo, Paola Giunti	2
3	Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 2022 ·Pediatric Neurology ·(unknown), (unknown), Chiara Veredice, Ilaria Contaldo, Michela Quintiliani, Martina Ricci, (unknown), Luigi Citrigno, (unknown), Patrizia Spadafora, Francesca Cavalcanti, Domenica Battaglia	5
4	Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report 2019 ·BMC Medical Genetics ·T. Sprovieri, C Ungaro, Serena Sivo, Michela Quintiliani, Ilaria Contaldo, Chiara Veredice, Luigi Citrigno, M. Muglia, Francesca Cavalcanti, Sebastiano Cavallaro, Eugenio Mercuri, Domenica Battaglia	7
5	Parkin Alternative Splicing: Not only Parkinsonism 2016 ·Valentina La Cognata, Velia D’Agata, Francesca Cavalcanti, Sebastiano Cavallaro, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1
6	A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson’s disease 2016 ·Neurogenetics ·Valentina La Cognata, Giovanna Morello, (unknown), Velia D’Agata, Chiara Criscuolo, Francesca Cavalcanti, Sebastiano Cavallaro	9
7	Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP 2013 ·Epilepsy Research ·Angelo Labate, Patrizia Tarantino, (unknown), Monica Gagliardi, Francesca Cavalcanti, Edoardo Ferlazzo, (unknown), Gemma Incorpora, Grazia Annesi, Umberto Aguglia, Antonio Gambardella	23
8	An Axon Regeneration Signature in a Charcot-Marie-Tooth Disease Type 2 Patient 2009 ·Journal of Neurogenetics ·Francesca Cavalcanti, Thomas Kidd, (unknown), A. Patitucci, Paola Valentino, Francesco Bono, Rita Nisticò, Aldo Quattrone	5
9	Accuracy of clinical diagnostic criteria for Friedreich's ataxia 2000 ·Movement Disorders ·Alessandro Filla, Giuseppe De Michele, Giovanni Coppola, Antonio Federico, Giuseppe Vita, António Toscano, Antonino Uncini, (unknown), Paolo Barone, Valentina Scarano, A. Perretti, Lucio Santoro, Antonella Monticelli, Francesca Cavalcanti, Giuseppe Caruso, Sergio Cocozza	35
10	Why do some Friedreich's ataxia patients retain tendon reflexes? 1999 ·Journal of Neurology ·Giovanni Coppola, Giuseppe De Michele, Francesca Cavalcanti, Luigi Pianese, A. Perretti, Lucio Santoro, Giuseppe Vita, António Toscano, Marianna Amboni, G. Grimaldi, Elena Salvatore, Giuseppe Caruso, Alessandro Filla	24
11	Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich's ataxia 1999 ·Journal of Neurology Neurosurgery & Psychiatry ·Lucio Santoro, Giuseppe De Michele, A. Perretti, C. Crisci, Sergio Cocozza, Francesca Cavalcanti, M. Ragno, Antonella Monticelli, Alessandro Filla, Giuseppe Caruso	42
12	Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's Ataxia 1998 ·Human Molecular Genetics ·Giovanna De Michele, Francesca Cavalcanti, Chiara Criscuolo, Luigi Pianese, Antonella Monticelli, Alessandro Filla, Sirio Cocozza	59
13	A New Locus for Autosomal Recessive Hereditary Spastic Paraplegia Maps to Chromosome 16q24.3 1998 ·The American Journal of Human Genetics ·Giuseppe De Michele, Maurizio De Fusco, Francesca Cavalcanti, Alessandro Filla, R. Marconi, Giampiero Volpe, Antonella Monticelli, Andrea Ballabio, Giorgio Casari, Sergio Cocozza	93
14	Childhood Onset of Friedreich Ataxia: A Clinical and Genetic Study of 36 Cases 1996 ·Neuropediatrics ·Giuseppe De Michele, Luigi Di Maio, Alessandro Filla, (unknown), Sergio Cocozza, Francesca Cavalcanti, (unknown), G Campanella	22
15	Isolation of a New Gene in the Friedreich Ataxia Candidate Region on Human Chromosome 9 by cDNA Direct Selection 1994 ·Biochemical Medicine and Metabolic Biology ·Massimo Pandolfo, Antonio Pizzuti, (unknown), M. Munaro, (unknown), Francesca Cavalcanti, Alessandro Filla, Antonella Monticelli, Luigi Pianese, Sirio Cocozza	6
16	Evidence of a genetic marker associated with early onset in Friedreich's ataxia 1993 ·Journal of Neurology ·Sergio Cocozza, A. Antonelli, G Campanella, Francesca Cavalcanti, Giuseppe De Michele, Stefano Di Donato, Alessandro Filla, Antonella Monticelli, Luigi Pianese, Anna Lisa Piccinelli, Antonio Porcellini, (unknown), S Varrone, Massimo Pandolfo	2
17	A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1 1993 ·Human Molecular Genetics ·Massimo Pandolfo, M. Munaro, (unknown), (unknown), Luigi Pianese, Francesca Cavalcanti, Antonella Monticelli, Stefano Di Donato	9
18	Linkage Disequilibrium Analysis of Friedreich's Ataxia in 140 Caucasian Families: Positioning of the Disease Locus and Evaluation of Allelic Heterogeneity 1993 ·European Journal of Human Genetics ·Giorgio Sirugo, Sirio Cocozza, Alexis Brice, Francesca Cavalcanti, Giuseppe De Michele, Ivano Dones, Alessandro Filla, Michel Kœnig, Diego Lorenzetti, Antonella Monticelli, Luigi Pianese, (unknown), François Rousseau, Jean‐Louis Mandel, S. Di Donato, (unknown)	13
19	Intrafamilial phenotype variation in Friedreich's disease: possible exceptions to diagnostic criteria 1991 ·Journal of Neurology ·Alessandro Filla, Giuseppe De Michele, Francesca Cavalcanti, Filippo M. Santorelli, Lucio Santoro, G Campanella	13
20	Effects of 1-methyl-4-phenylpiridinium ion on mitochondrial metabolism in frog brain 1990 ·Medical science research ·(unknown), G. De Michele, Filippo M. Santorelli, (unknown), (unknown), Francesca Cavalcanti, G Campanella	1

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