Francesca Pantaleoni

3.9k total citations
29 papers, 1.3k citations indexed

About

Francesca Pantaleoni is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Francesca Pantaleoni has authored 29 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 14 papers in Immunology and 8 papers in Genetics. Recurrent topics in Francesca Pantaleoni's work include Protein Tyrosine Phosphatases (16 papers), Galectins and Cancer Biology (10 papers) and RNA modifications and cancer (5 papers). Francesca Pantaleoni is often cited by papers focused on Protein Tyrosine Phosphatases (16 papers), Galectins and Cancer Biology (10 papers) and RNA modifications and cancer (5 papers). Francesca Pantaleoni collaborates with scholars based in Italy, United States and Germany. Francesca Pantaleoni's co-authors include Marco Tartaglia, Mario Boccadoro, Massimo Massaia, Giuseppe Zampino, Marta Coscia, Bruno Dallapiccola, Barbara Castella, Myriam Foglietta, Chiara Riganti and Amalia Bosìa and has published in prestigious journals such as Blood, The Journal of Immunology and The American Journal of Human Genetics.

In The Last Decade

Francesca Pantaleoni

29 papers receiving 1.3k citations

Peers

Francesca Pantaleoni
Lauren Shea United States
Steffen Aulwurm Germany
Ching Ching Leow United States
K Wright Australia
Abhik Ray Chaudhury United States
Chrystelle Lamagna United States
Po Y. Ho United States
Valentina Ciccarone United States
Mélanie Tichet France
Michael Kluge Germany
Lauren Shea United States
Francesca Pantaleoni
Citations per year, relative to Francesca Pantaleoni Francesca Pantaleoni (= 1×) peers Lauren Shea

Countries citing papers authored by Francesca Pantaleoni

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Pantaleoni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Pantaleoni

This figure shows the co-authorship network connecting the top 25 collaborators of Francesca Pantaleoni. A scholar is included among the top collaborators of Francesca Pantaleoni 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 Pantaleoni. Francesca Pantaleoni 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.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants. European Journal of Human Genetics. 31(7). 805–814. 4 indexed citations
2.
Leoni, Chiara, Nazario Foschi, Francesco Pierconti, et al.. (2022). Prevalence of bladder cancer in Costello syndrome: New insights to drive clinical decision‐making. Clinical Genetics. 101(4). 454–458. 5 indexed citations
3.
Leoni, Chiara, Francesca Clementina Radio, Giovanni Chillemi, et al.. (2021). Broadening the phenotypic spectrum of Beta3GalT6 ‐associated phenotypes. American Journal of Medical Genetics Part A. 185(10). 3153–3160. 4 indexed citations
4.
Martinelli, Simone, Luca Pannone, Christina Lißewski, et al.. (2020). Pathogenic PTPN11 variants involving the poly‐glutamine Gln 255 ‐Gln 256 ‐Gln 257 stretch highlight the relevance of helix B in SHP2's functional regulation. Human Mutation. 41(6). 1171–1182. 1 indexed citations
5.
Motta, Marialetizia, Lena Sagi‐Dain, Oliver H.F. Krumbach, et al.. (2019). Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy. Human Molecular Genetics. 29(11). 1772–1783. 24 indexed citations
6.
Niceta, Marcello, Sabina Barresi, Francesca Pantaleoni, et al.. (2018). TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerations. European Journal of Medical Genetics. 62(6). 103534–103534. 16 indexed citations
7.
Pantaleoni, Francesca, Dorit Lev, Ion Cristian Cirstea, et al.. (2017). AberrantHRAStranscript processing underlies a distinctive phenotype within the RASopathy clinical spectrum. Human Mutation. 38(7). 798–804. 13 indexed citations
8.
Tafazoli, Alireza, Francesca Pantaleoni, Rahim Vakili, et al.. (2017). Novel mutations and their genotype-phenotype correlations in patients with Noonan syndrome, using next-generation sequencing. Advances in Medical Sciences. 63(1). 87–93. 13 indexed citations
9.
Leoni, Chiara, David A. Stevenson, Roberto De Sanctis, et al.. (2013). Decreased bone mineral density in Costello syndrome. Molecular Genetics and Metabolism. 111(1). 41–45. 19 indexed citations
10.
Alfieri, Paolo, Laura Cesarini, Maria Mallardi, et al.. (2011). Long Term Memory Profile of Disorders Associated with Dysregulation of the RAS-MAPK Signaling Cascade. Behavior Genetics. 41(3). 423–429. 23 indexed citations
11.
Coscia, Marta, Francesca Pantaleoni, Chiara Riganti, et al.. (2011). IGHV unmutated CLL B cells are more prone to spontaneous apoptosis and subject to environmental prosurvival signals than mutated CLL B cells. Leukemia. 25(5). 828–837. 56 indexed citations
12.
Coscia, Marta, Elena Quaglino, Manuela Iezzi, et al.. (2009). Zoledronic acid repolarizes tumour‐associated macrophages and inhibits mammary carcinogenesis by targeting the mevalonate pathway. Journal of Cellular and Molecular Medicine. 14(12). 2803–2815. 220 indexed citations
13.
Kratz, Christian P., Giuseppe Zampino, Marjolein Kriek, et al.. (2009). Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations. American Journal of Medical Genetics Part A. 149A(5). 1036–1040. 45 indexed citations
14.
Dentici, Maria Lisa, Anna Sárközy, Francesca Pantaleoni, et al.. (2009). Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype–phenotype correlations. European Journal of Human Genetics. 17(6). 733–740. 56 indexed citations
15.
Cesarini, Laura, Paolo Alfieri, Francesca Pantaleoni, et al.. (2009). Cognitive profile of disorders associated with dysregulation of the RAS/MAPK signaling cascade. American Journal of Medical Genetics Part A. 149A(2). 140–146. 73 indexed citations
16.
Alfieri, Paolo, Laura Cesarini, Giuseppe Zampino, et al.. (2008). Visual Function in Noonan and LEOPARD Syndrome. Neuropediatrics. 39(6). 335–340. 21 indexed citations
17.
Carta, Claudio, Francesca Pantaleoni, Gianfranco Bocchinfuso, et al.. (2006). Germline Missense Mutations Affecting KRAS Isoform B Are Associated with a Severe Noonan Syndrome Phenotype. The American Journal of Human Genetics. 79(1). 129–135. 161 indexed citations
18.
Zampino, Giuseppe, Francesca Pantaleoni, Claudio Carta, et al.. (2006). Diversity, parental germline origin, and phenotypic spectrum of de novoHRASmissense changes in Costello syndrome. Human Mutation. 28(3). 265–272. 99 indexed citations
19.
Bocchinfuso, Gianfranco, Lorenzo Stella, Simone Martinelli, et al.. (2006). Structural and functional effects of disease‐causing amino acid substitutions affecting residues Ala72 and Glu76 of the protein tyrosine phosphatase SHP‐2. Proteins Structure Function and Bioinformatics. 66(4). 963–974. 22 indexed citations
20.
Mariani, Sara, Michela Muraro, Francesca Pantaleoni, et al.. (2005). Effector γδ T cells and tumor cells as immune targets of zoledronic acid in multiple myeloma. Leukemia. 19(4). 664–670. 109 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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