Francesca Boaretto

1.6k total citations
26 papers, 811 citations indexed

About

Francesca Boaretto is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Surgery. According to data from OpenAlex, Francesca Boaretto has authored 26 papers receiving a total of 811 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Surgery. Recurrent topics in Francesca Boaretto's work include Hereditary Neurological Disorders (5 papers), Cancer, Hypoxia, and Metabolism (5 papers) and Neurological diseases and metabolism (4 papers). Francesca Boaretto is often cited by papers focused on Hereditary Neurological Disorders (5 papers), Cancer, Hypoxia, and Metabolism (5 papers) and Neurological diseases and metabolism (4 papers). Francesca Boaretto collaborates with scholars based in Italy, United States and United Kingdom. Francesca Boaretto's co-authors include Giuseppe Opocher, Giovanni Vazza, Maria Luisa Mostacciuolo, Francesca Schiavi, Elizabeth E. King, Charles D. Stiles, James D. Lechleiter, Yuejuan Qin, Kalyan Buddavarapu and E. Sandra Chocrón and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Francesca Boaretto

25 papers receiving 802 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Francesca Boaretto Italy 12 269 252 244 230 171 26 811
Graeme R. Clark United Kingdom 12 140 0.5× 367 1.5× 156 0.6× 75 0.3× 102 0.6× 19 815
Stephan Niemann Germany 18 565 2.1× 668 2.7× 639 2.6× 422 1.8× 232 1.4× 26 1.6k
Lesley Tannahill United Kingdom 18 95 0.4× 339 1.3× 195 0.8× 623 2.7× 71 0.4× 24 1.1k
Claudimara Ferini Pacicco Lotfi Brazil 16 247 0.9× 284 1.1× 259 1.1× 259 1.1× 39 0.2× 48 783
Carole Auger France 15 207 0.8× 205 0.8× 83 0.3× 369 1.6× 113 0.7× 31 753
S Staddon United Kingdom 10 99 0.4× 293 1.2× 96 0.4× 120 0.5× 92 0.5× 14 770
Mabrouka Doghman France 17 409 1.5× 603 2.4× 473 1.9× 239 1.0× 31 0.2× 31 1.2k
Phuong T. Hoang United States 8 138 0.5× 511 2.0× 127 0.5× 37 0.2× 57 0.3× 11 783
John Bicknell United Kingdom 15 116 0.4× 320 1.3× 129 0.5× 463 2.0× 98 0.6× 18 853
R.R. Frants Netherlands 19 109 0.4× 396 1.6× 229 0.9× 30 0.1× 118 0.7× 33 1.1k

Countries citing papers authored by Francesca Boaretto

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Boaretto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Boaretto

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

All Works

20 of 20 papers shown
1.
Colciago, Alessandra, Alessandra Fasciani, Raffaele De Francesco, et al.. (2024). Typical NF2 and LTZR1 mutations are retained in an immortalized human schwann cell model of schwannomatosis. Heliyon. 10(19). e38957–e38957. 1 indexed citations
2.
Fortugno, Paola, Valeria Cinquina, Chiara Rigon, et al.. (2023). Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome. European Journal of Human Genetics. 31(5). 596–601. 2 indexed citations
3.
Piccolo, C., Chiara Rigon, Eva Trevisson, et al.. (2021). DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature. SHILAP Revista de lepidopterología. 11(4). 582–593. 8 indexed citations
4.
Pallafacchina, Giorgia, Sofia Zanin, V. Crippa, et al.. (2016). Loss-of-function mutations in theSIGMAR1gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+signalling. Human Molecular Genetics. 25(17). 3741–3753. 78 indexed citations
5.
Feletti, Alberto, Mariagiulia Anglani, Bruno Scarpa, et al.. (2016). Von Hippel-Lindau disease: an evaluation of natural history and functional disability. Neuro-Oncology. 18(7). 1011–1020. 33 indexed citations
6.
Ferrara, Alfonso Massimiliano, Monica Sciacco, Stefania Zovato, et al.. (2016). Coexistence of VHL Disease and CPT2 Deficiency: A Case Report. Cancer Research and Treatment. 48(4). 1438–1442. 6 indexed citations
7.
Boaretto, Francesca, Deborah Snijders, Maria Luisa Mostacciuolo, et al.. (2016). Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel. Journal of Molecular Diagnostics. 18(6). 912–922. 32 indexed citations
8.
Manno, Nicola, Francesca Boaretto, Salvatore Musumeci, et al.. (2014). High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites. Carbohydrate Polymers. 113. 607–614. 10 indexed citations
9.
Boaretto, Francesca, Chiara Briani, Elena Pegoraro, et al.. (2014). Mutation Analysis of MFN2, GJB1, MPZ and PMP22 in Italian Patients with Axonal Charcot–Marie–Tooth Disease. NeuroMolecular Medicine. 16(3). 540–550. 23 indexed citations
10.
Occhi, Gianluca, Daniela Regazzo, Giampaolo Trivellin, et al.. (2013). A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype. PLoS Genetics. 9(3). e1003350–e1003350. 111 indexed citations
11.
Bertolin, Cinzia, Carla D’Ascenzo, Giorgia Querin, et al.. (2013). Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants. Neurobiology of Aging. 35(5). 1212.e7–1212.e10. 8 indexed citations
12.
Bertolin, Cinzia, Francesca Boaretto, Giovanni Barbon, et al.. (2010). Novel mutations in the L1CAM gene support the complexity of L1 syndrome. Journal of the Neurological Sciences. 294(1-2). 124–126. 6 indexed citations
13.
Qin, Yuejuan, Elizabeth E. King, Kalyan Buddavarapu, et al.. (2010). Germline mutations in TMEM127 confer susceptibility to pheochromocytoma. Nature Genetics. 42(3). 229–233. 266 indexed citations
14.
Striano, Pasquale, Antonio Gambardella, Antonietta Coppola, et al.. (2007). Familial mesial temporal lobe epilepsy (FMTLE). Journal of Neurology. 255(1). 16–23. 44 indexed citations
15.
Vazza, Giovanni, Cinzia Bertolin, Andrea Vettori, et al.. (2006). Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26. Molecular Psychiatry. 12(1). 87–93. 38 indexed citations
16.
Simonati, Alessandro, et al.. (2006). A novel missense mutation in the L1CAM gene in a boy with L1 disease. Neurological Sciences. 27(2). 114–117. 6 indexed citations
17.
Boaretto, Francesca, et al.. (2004). Distal hereditary motor neuropathy (DHMN): a new locus for an autosomal recessive form. Journal of the Peripheral Nervous System. 9(2). 122–123. 1 indexed citations
18.
Pennesi, Marco, Federico Marchetti, Sérgio Crovella, et al.. (2004). A new mutation in two siblings with cystinosis presenting with Bartter syndrome. Pediatric Nephrology. 20(2). 217–219. 10 indexed citations
19.
Crovella, Sérgio, Doroti Pirulli, Francesco De Seta, et al.. (2002). Quantitative in situ detection of high-risk human papillomavirus in cytological specimens by SYBR Green I fluorescent labeling.. Clinical and Experimental Medicine. 2(1). 1–6. 1 indexed citations
20.
Vazza, Giovanni, et al.. (2000). A New Locus for Autosomal Recessive Spastic Paraplegia Associated with Mental Retardation and Distal Motor Neuropathy, SPG14, Maps to Chromosome 3q27-q28. The American Journal of Human Genetics. 67(2). 504–509. 48 indexed citations

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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