Antonio Percesepe

5.9k total citations · 1 hit paper
121 papers, 3.5k citations indexed

About

Antonio Percesepe is a scholar working on Pathology and Forensic Medicine, Genetics and Oncology. According to data from OpenAlex, Antonio Percesepe has authored 121 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Pathology and Forensic Medicine, 39 papers in Genetics and 38 papers in Oncology. Recurrent topics in Antonio Percesepe's work include Genetic factors in colorectal cancer (47 papers), Colorectal Cancer Screening and Detection (30 papers) and Colorectal Cancer Treatments and Studies (19 papers). Antonio Percesepe is often cited by papers focused on Genetic factors in colorectal cancer (47 papers), Colorectal Cancer Screening and Detection (30 papers) and Colorectal Cancer Treatments and Studies (19 papers). Antonio Percesepe collaborates with scholars based in Italy, United States and United Kingdom. Antonio Percesepe's co-authors include Maurizio Ponz de Leòn, M. Anti, Piero Benatti, Païvi Peltomäki, Luca Roncucci, Franco Armelao, Lauri A. Aaltonen, Albert de la Chapelle, Paula Kristo and Giancarlo Marra and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Oncology and Gastroenterology.

In The Last Decade

Antonio Percesepe

114 papers receiving 3.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

1998 856 citations Lauri A. Aaltonen, Reijo Salovaara et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Antonio Percesepe Italy	31	2.0k	1.7k	840	829	679	121	3.5k
Yoko Yamamoto Japan	24	825 0.4×	1.0k 0.6×	391 0.5×	1.4k 1.7×	593 0.9×	49	3.0k
Harald Jüppner United States	28	730 0.4×	1.6k 1.0×	219 0.3×	3.5k 4.2×	2.4k 3.5×	65	6.4k
Saira Ahmed United States	23	364 0.2×	454 0.3×	453 0.5×	2.0k 2.5×	348 0.5×	36	3.2k
Nobuaki Sasano Japan	31	498 0.3×	682 0.4×	692 0.8×	629 0.8×	396 0.6×	141	3.4k
Michael Zimmer United States	24	690 0.4×	711 0.4×	817 1.0×	1.6k 2.0×	463 0.7×	52	3.1k
S Saez France	27	472 0.2×	710 0.4×	414 0.5×	697 0.8×	796 1.2×	80	2.3k
Ann Randolph United States	21	488 0.2×	555 0.3×	337 0.4×	799 1.0×	291 0.4×	32	2.1k
Lucie Canaff Canada	35	458 0.2×	783 0.5×	128 0.2×	1.6k 2.0×	491 0.7×	69	3.4k
Vorasuk Shotelersuk Thailand	29	740 0.4×	182 0.1×	154 0.2×	1.6k 1.9×	1.1k 1.6×	230	4.3k
S. Baba Japan	27	618 0.3×	705 0.4×	264 0.3×	739 0.9×	180 0.3×	149	2.8k

Countries citing papers authored by Antonio Percesepe

Since Specialization

Citations

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

Fields of papers citing papers by Antonio Percesepe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonio Percesepe

This figure shows the co-authorship network connecting the top 25 collaborators of Antonio Percesepe. A scholar is included among the top collaborators of Antonio Percesepe 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 Antonio Percesepe. Antonio Percesepe 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

1.

Azzoni, Cinzia, Lorena Bottarelli, Domenico Corradi, et al.. (2025). The Pathogenesis of the Neurofibroma-to-Sarcoma Transition in Neurofibromatosis Type I: From Molecular Profiles to Diagnostic Applications. Cancers. 17(24). 3955–3955.

2.

Gemignani, Franco, et al.. (2024). Charcot–Marie–Tooth Disease with Myelin Protein Zero Mutation Presenting as Painful, Predominant Small-Fiber Neuropathy. International Journal of Molecular Sciences. 25(3). 1654–1654. 1 indexed citations

3.

Uliana, Vera, Anna Negrotti, Walter Serra, et al.. (2024). Phenotypic Expansion of Autosomal Dominant LZTR1-Related Disorders with Special Emphasis on Adult-Onset Features. Genes. 15(7). 916–916. 1 indexed citations

4.

Barili, Valeria, Vera Uliana, Melissa Bellini, et al.. (2023). Success and Pitfalls of Genetic Testing in Undiagnosed Diseases: Whole Exome Sequencing and Beyond. Genes. 14(6). 1241–1241. 1 indexed citations

5.

Riccardi, Federica, Antonio Coppola, Gianna Franca Rivolta, et al.. (2022). The effect of carriers’ reproductive choices and pregnancy history on sporadic severe haemophilia: A 20‐year retrospective study through a regional registry. Haemophilia. 28(2). 308–315. 1 indexed citations

6.

Ponti, Giovanni, Giovanni Pellacani, Aldo Tomasi, et al.. (2014). Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report. Journal of Medical Case Reports. 8(1). 333–333. 5 indexed citations

7.

Stanghellini, Ilaria, et al.. (2014). Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis. The Italian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 39–39. 12 indexed citations

8.

Forabosco, Antonino, et al.. (2009). Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses. European Journal of Human Genetics. 17(7). 897–903. 87 indexed citations

9.

Bertucci, Emma, et al.. (2007). Age‐specific risk of fetal loss post second trimester amniocentesis: analysis of 5043 cases. Prenatal Diagnosis. 27(2). 180–183. 21 indexed citations

10.

Leòn, Maurizio Ponz de, Piero Benatti, Monica Pedroni, et al.. (2000). Problems in the identification of hereditary nonpolyposis colorectal cancer in two families with late development of full-blown clinical spectrum. The American Journal of Gastroenterology. 95(8). 2110–2115. 2 indexed citations

11.

Pedroni, Monica, Maria Grazia Tamassia, Antonio Percesepe, et al.. (1999). Microsatellite instability in multiple colorectal tumors. International Journal of Cancer. 81(1). 1–5. 6 indexed citations

12.

Pedroni, Monica, Maria Grazia Tamassia, Antonio Percesepe, et al.. (1999). Microsatellite instability in multiple colorectal tumors. International Journal of Cancer. 81(1). 1–5. 74 indexed citations

13.

Aaltonen, Lauri A., Reijo Salovaara, Paula Kristo, et al.. (1998). Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease. New England Journal of Medicine. 338(21). 1481–1487. 856 indexed citations breakdown →

14.

Percesepe, Antonio, Paula Kristo, Lauri A. Aaltonen, et al.. (1998). Mismatch repair genes and mononucleotide tracts as mutation targets in colorectal tumors with different degrees of microsatellite instability. Oncogene. 17(2). 157–163. 60 indexed citations

15.

Scapoli, Chiara, Andrew Collins, Piero Benatti, et al.. (1997). A two-locus model for hereditary non-polyposis colorectal cancer in Modena, Italy. Annals of Human Genetics. 61(2). 109–119.

16.

Percesepe, Antonio, Piero Benatti, Luca Roncucci, et al.. (1997). Survival analysis in families affected by hereditary non-polyposis colorectal cancer. International Journal of Cancer. 71(3). 373–376. 49 indexed citations

17.

Scapoli, Chiara, Andrew Collins, Piero Benatti, et al.. (1997). A two‐locus model for hereditary non‐polyposis colorectal cancer in Modena, Italy. Annals of Human Genetics. 61(2). 109–119. 2 indexed citations

18.

Fante, Rossella, Luca Roncucci, Carmela Di Gregorio, et al.. (1996). Frequency and clinical features of multiple tumors of the large bowel in the general population and in patients with hereditary colorectal carcinoma. Cancer. 77(10). 2013–2021. 48 indexed citations

19.

Percesepe, Antonio, M. Anti, Luca Roncucci, et al.. (1995). The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer. British Journal of Cancer. 72(5). 1320–1323. 24 indexed citations

20.

Anti, M., Giancarlo Marra, Franco Armelao, et al.. (1993). Rectal epithelial cell proliferation patterns as predictors of adenomatous colorectal polyp recurrence.. Gut. 34(4). 525–530. 61 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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