Elisa Cattaneo

1.2k total citations
30 papers, 658 citations indexed

About

Elisa Cattaneo is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Elisa Cattaneo has authored 30 papers receiving a total of 658 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Elisa Cattaneo's work include Genetic factors in colorectal cancer (7 papers), Dermatological and Skeletal Disorders (3 papers) and Peptidase Inhibition and Analysis (3 papers). Elisa Cattaneo is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Dermatological and Skeletal Disorders (3 papers) and Peptidase Inhibition and Analysis (3 papers). Elisa Cattaneo collaborates with scholars based in Italy, Switzerland and United Kingdom. Elisa Cattaneo's co-authors include Giancarlo Marra, Josef Jiricny, Mirco Menigatti, Jacob Sabates–Bellver, Endre Laczkó, Hans Clevers, Teresa Valentina Ranalli, Janusz M. Bujnicki, Mariagrazia de Palo and Michal A. Kurowski and has published in prestigious journals such as PLoS ONE, Molecular Cancer and International Journal of Environmental Research and Public Health.

In The Last Decade

Elisa Cattaneo

26 papers receiving 649 citations

Peers

Elisa Cattaneo

ONCOL

PFM

GENET

Carrie R. Graveel United States

Il-Jin Kim South Korea

Nagendra K. Chaturvedi United States

Jung Hun Song South Korea

Ralitsa R. Madsen United Kingdom

Kathryn M. Kinross Australia

Anja Kafka Croatia

Rumana Rafiq United Kingdom

Yusuke Nakamura Japan

Alfa Bai Hong Kong

Carrie R. Graveel United States

Elisa Cattaneo

419 ×1.0

201 ×1.2

ONCOL

110 ×0.8

51 ×0.4

PFM

53 ×0.7

GENET

Citations per year, relative to Elisa Cattaneo Elisa Cattaneo (= 1×) peers Carrie R. Graveel

Countries citing papers authored by Elisa Cattaneo

Since Specialization

Citations

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

Fields of papers citing papers by Elisa Cattaneo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Cattaneo

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

All Works

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20 of 20 papers shown

Faiola, S., A. Barreca, Arianna Laoreti, et al.. (2025). Congenital Vascular Anomalies: Prenatal Diagnosis, Perinatal Outcome and Postnatal Follow up. Prenatal Diagnosis. 45(12). 1590–1603.

Laoreti, Arianna, et al.. (2025). TNNC1 Gene Mutation in Ebstein’s Anomaly and Left Ventricular Hypertrabeculation: A Case Report of a New Causative Mutation?. Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano). 15(3). 24–24.

Cattaneo, Elisa, Luigina Spaccini, Maria Iascone, et al.. (2024). Novel Genetic Variant in HUWE1. Neurology Genetics. 10(4). e200169–e200169. 1 indexed citations

Cattaneo, Elisa, et al.. (2024). Giant congenital fibroblastic connective tissue nevus associated with vascular anomalies. Journal of Cutaneous Pathology. 51(7). 485–489.

Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2023). Comparison of first‐tier whole‐exome sequencing with a multi‐step traditional approach for diagnosing paediatric outpatients: An Italian prospective study. Molecular Genetics & Genomic Medicine. 12(1). e2316–e2316. 4 indexed citations

Moneghini, Laura, Delfina Tosi, Daniela Graziani, et al.. (2020). CD10 and CD34 as markers in vascular malformations with PIK3CA and TEK mutations. Human Pathology. 99. 98–106. 4 indexed citations

Mameli, Chiara, Siham Chafai Elalaoui, Elisa Cattaneo, et al.. (2020). Natural history of non-lethal Raine syndrome during childhood. Orphanet Journal of Rare Diseases. 15(1). 93–93. 15 indexed citations

Stasi, Martina Di, Elisa Cattaneo, Chiara Doneda, et al.. (2020). Cerebellar dysplasia related to PIK3CA mutation: a three-case series. Neurogenetics. 22(1). 27–32. 1 indexed citations

Paccagnini, S., Elena Pozzi, Luigina Spaccini, et al.. (2018). Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 59–59. 1 indexed citations

10.

Picciolini, Odoardo, Matteo Porro, Elisa Cattaneo, et al.. (2016). Moebius syndrome: clinical features, diagnosis, management and early intervention. The Italian Journal of Pediatrics/Italian journal of pediatrics. 42(1). 56–56. 67 indexed citations

11.

Silipigni, Rosamaria, Elisa Cattaneo, Marco Baccarin, Monica Fumagalli, & Maria Francesca Bedeschi. (2015). Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical features. European Journal of Medical Genetics. 59(1). 39–42. 2 indexed citations

12.

Okoniewski, Michał, Mirco Menigatti, Elisa Cattaneo, et al.. (2014). A comprehensive look at transcription factor gene expression changes in colorectal adenomas. BMC Cancer. 14(1). 46–46. 18 indexed citations

13.

Cattaneo, Elisa, et al.. (2013). First Evidence of Vertical Paternal Transmission of Osteopatia Striata With Cranial Sclerosis. American Journal of Medical Genetics Part A. 161(5). 1173–1176. 5 indexed citations

14.

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

15.

Maglietta, Rosalia, Vania Liuzzi, Elisa Cattaneo, et al.. (2012). Molecular pathways undergoing dramatic transcriptomic changes during tumor development in the human colon. BMC Cancer. 12(1). 608–608. 15 indexed citations

16.

Cattaneo, Elisa, Endre Laczkó, Federico Buffoli, et al.. (2011). Preinvasive colorectal lesion transcriptomes correlate with endoscopic morphology (polypoid vs. nonpolypoid). EMBO Molecular Medicine. 3(6). 334–347. 34 indexed citations

17.

Menigatti, Mirco, Elisa Cattaneo, Jacob Sabates–Bellver, et al.. (2009). The protein tyrosine phosphatase receptor type R gene is an early and frequent target of silencing in human colorectal tumorigenesis. Molecular Cancer. 8(1). 124–124. 30 indexed citations

18.

Fiorito, Chiara, Ilaria Lucca, Marco Oderda, et al.. (2008). Neuroendocrine bladder cancer: oncological emergency?. Urologia Journal. 75(1). 57–61. 1 indexed citations

19.

Sabates–Bellver, Jacob, Laurens G. van der Flier, Mariagrazia de Palo, et al.. (2007). Transcriptome Profile of Human Colorectal Adenomas. Molecular Cancer Research. 5(12). 1263–1275. 406 indexed citations

20.

Butler, P. D., Elisa Cattaneo, & D. G. Wild. (1985). Interactions between Mutations Affecting Ribosome Synthesis in Escherichia coli. Microbiology. 131(4). 945–949. 2 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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