Paolo Peterlongo

23.9k total citations
31 papers, 1.0k citations indexed

About

Paolo Peterlongo is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Paolo Peterlongo has authored 31 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Oncology. Recurrent topics in Paolo Peterlongo's work include BRCA gene mutations in cancer (10 papers), DNA Repair Mechanisms (7 papers) and Genetic factors in colorectal cancer (7 papers). Paolo Peterlongo is often cited by papers focused on BRCA gene mutations in cancer (10 papers), DNA Repair Mechanisms (7 papers) and Genetic factors in colorectal cancer (7 papers). Paolo Peterlongo collaborates with scholars based in Italy, United States and Australia. Paolo Peterlongo's co-authors include Lidia Larizza, Enrica Morra, Carla B. Ripamonti, Roberto Cairoli, Alessandro Beghini, Cristina Mecucci, Gaia Roversi, Genovefa A. Papanicolaou, Jaya M. Satagopan and Nathan A. Ellis and has published in prestigious journals such as Journal of Clinical Oncology, Blood and PLoS ONE.

In The Last Decade

Paolo Peterlongo

30 papers receiving 993 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paolo Peterlongo Italy 13 450 231 207 206 198 31 1.0k
Kathryn A. Kolquist United States 12 634 1.4× 467 2.0× 92 0.4× 449 2.2× 188 0.9× 20 1.5k
Ester Mejstříková Czechia 25 349 0.8× 192 0.8× 155 0.7× 383 1.9× 807 4.1× 68 1.4k
A Zander Germany 17 317 0.7× 420 1.8× 95 0.5× 273 1.3× 465 2.3× 51 1.1k
Michael A. Linden United States 20 562 1.2× 306 1.3× 147 0.7× 165 0.8× 582 2.9× 88 1.3k
Jeffrey M. Gerold United States 8 320 0.7× 276 1.2× 98 0.5× 215 1.0× 97 0.5× 9 989
Ondřej Hrušák Czechia 23 384 0.9× 190 0.8× 172 0.8× 241 1.2× 847 4.3× 82 1.5k
Rajive Kumar India 19 351 0.8× 146 0.6× 147 0.7× 163 0.8× 328 1.7× 96 973
S A Cannistra United States 15 405 0.9× 324 1.4× 96 0.5× 368 1.8× 141 0.7× 24 1.1k
Ghislaine Bernard France 20 511 1.1× 226 1.0× 278 1.3× 523 2.5× 110 0.6× 28 1.5k
Leo M. Budel Netherlands 13 201 0.4× 332 1.4× 242 1.2× 161 0.8× 107 0.5× 24 780

Countries citing papers authored by Paolo Peterlongo

Since Specialization
Citations

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

Fields of papers citing papers by Paolo Peterlongo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paolo Peterlongo

This figure shows the co-authorship network connecting the top 25 collaborators of Paolo Peterlongo. A scholar is included among the top collaborators of Paolo Peterlongo 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 Paolo Peterlongo. Paolo Peterlongo 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.
Peterlongo, Paolo, Gisella Figlioli, Andrew J. Deans, & Fergus J. Couch. (2021). Protein truncating variants in FANCM and risk for ER-negative/triple negative breast cancer. npj Breast Cancer. 7(1). 130–130. 7 indexed citations
2.
Rizzolo, Piera, Veronica Zelli, Valentina Silvestri, et al.. (2018). Abstract 1236: Insight into genetic susceptibility to BRCA-negative male breast cancer by multigene panel testing: Results from a multicenter study in Italy. Cancer Research. 78(13_Supplement). 1236–1236. 1 indexed citations
3.
Caleca, Laura, Irene Catucci, Gisella Figlioli, et al.. (2018). Two Missense Variants Detected in Breast Cancer Probands Preventing BRCA2-PALB2 Protein Interaction. Frontiers in Oncology. 8. 11 indexed citations
4.
Catucci, Irene, Silvia Casadei, Yuan Chun Ding, et al.. (2016). Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2. Breast Cancer Research and Treatment. 160(1). 121–129. 8 indexed citations
5.
Roversi, Gaia, M. Crippa, Daniela Perotti, et al.. (2015). Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors. Scientific Reports. 5(1). 15454–15454. 7 indexed citations
6.
Bernardi, Daniela, Stefano Ciatto, Marco Pellegrini, et al.. (2012). Prospective study of breast tomosynthesis as a triage to assessment in screening. Breast Cancer Research and Treatment. 133(1). 267–271. 67 indexed citations
7.
Catucci, Irene, Roni Milgrom, Anya Kushnir, et al.. (2012). Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families. Familial Cancer. 11(3). 483–491. 24 indexed citations
8.
Catucci, Irene, Mara Colombo, Paolo Verderio, et al.. (2012). Sequencing Analysis of SLX4/FANCP Gene in Italian Familial Breast Cancer Cases. PLoS ONE. 7(2). e31038–e31038. 10 indexed citations
9.
Donner, Davide, et al.. (2011). Paragangliomas in an endemic area: from genetics to morphofunctional imaging. A pictorial essay. La radiologia medica. 117(3). 471–487. 7 indexed citations
10.
Verderio, Paolo, Sara Pizzamiglio, Melissa C. Southey, et al.. (2010). A BRCA1 promoter variant (rs11655505) and breast cancer risk. Journal of Medical Genetics. 47(4). 268–270. 6 indexed citations
11.
Beesley, Jonathan, Sharon E. Johnatty, Xiaohong Chen, et al.. (2010). No evidence for an association between the earwax-associated polymorphism in ABCC11 and breast cancer risk in Caucasian women. Breast Cancer Research and Treatment. 126(1). 235–239. 9 indexed citations
12.
Catucci, Irene, Paolo Verderio, Sara Pizzamiglio, et al.. (2010). The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers. Breast Cancer Research and Treatment. 125(3). 855–860. 10 indexed citations
13.
Peterlongo, Paolo, et al.. (2009). Toll-Like Receptor 4 Polymorphisms and Risk of Gram-Negative Bacteremia after Allogeneic Stem Cell Transplantation. A Prospective Pilot Study. Biology of Blood and Marrow Transplantation. 15(9). 1130–1133. 12 indexed citations
14.
Peterlongo, Paolo, Nandita Mitra, Miguel de la Hoya, et al.. (2006). Increased frequency of disease-causing MYH mutations in colon cancer families. Carcinogenesis. 27(11). 2243–2249. 39 indexed citations
15.
Mitra, Nandita, Alex Smith, Shaokun Chuai, et al.. (2004). Localization of Cancer Susceptibility Genes by Genome-wide Single-Nucleotide Polymorphism Linkage-Disequilibrium Mapping. Cancer Research. 64(21). 8116–8125. 11 indexed citations
16.
Peterlongo, Paolo, Khédoudja Nafa, Emily Glogowski, et al.. (2003). MSH6 germline mutations are rare in colorectal cancer families. International Journal of Cancer. 107(4). 571–579. 42 indexed citations
17.
Beghini, Alessandro, Paolo Peterlongo, Carla B. Ripamonti, et al.. (2000). C-kit mutations in core binding factor leukemias. Blood. 95(2). 726–728. 240 indexed citations
18.
Beghini, Alessandro, Carla B. Ripamonti, Paolo Peterlongo, et al.. (2000). RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia. Human Molecular Genetics. 9(15). 2297–2304. 135 indexed citations
19.
Sechi, GianPietro, Stefano Sotgiu, Maria Paola Valenti, et al.. (2000). Beneficial Effect of Fluoxetine in a Case of Sporadic Hyperekplexia. Clinical Neuropharmacology. 23(3). 161–163. 13 indexed citations
20.
Bauer, Michael, et al.. (1996). Giant cell tumour of the mandibular condyle. European Radiology. 6(4). 557–560. 6 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kathryn A. Kolquist Breakdown of academic impact, for papers by Ester Mejstříková Breakdown of academic impact, for papers by A Zander Breakdown of academic impact, for papers by Michael A. Linden Breakdown of academic impact, for papers by Jeffrey M. Gerold Breakdown of academic impact, for papers by Ondřej Hrušák Breakdown of academic impact, for papers by Rajive Kumar Breakdown of academic impact, for papers by S A Cannistra Breakdown of academic impact, for papers by Ghislaine Bernard Breakdown of academic impact, for papers by Leo M. Budel
Rankless by CCL
2026