Francesco Baudi

924 total citations
33 papers, 599 citations indexed

About

Francesco Baudi is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Francesco Baudi has authored 33 papers receiving a total of 599 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Genetics and 8 papers in Pathology and Forensic Medicine. Recurrent topics in Francesco Baudi's work include BRCA gene mutations in cancer (10 papers), Genetic factors in colorectal cancer (8 papers) and RNA regulation and disease (4 papers). Francesco Baudi is often cited by papers focused on BRCA gene mutations in cancer (10 papers), Genetic factors in colorectal cancer (8 papers) and RNA regulation and disease (4 papers). Francesco Baudi collaborates with scholars based in Italy and United States. Francesco Baudi's co-authors include Salvatore Venuta, Francesco Costanzo, Barbara Quaresima, Giovanni Cuda, Maria Concetta Faniello, Pierfrancesco Tassone, Francesco Trapasso, Ileana Quinto, Giuseppe Scala and Xueni Chen and has published in prestigious journals such as Journal of Biological Chemistry, Oncogene and Biochemical Journal.

In The Last Decade

Francesco Baudi

32 papers receiving 590 citations

Peers

Francesco Baudi

ONCOL

GENET

IMMUN

Debora Franceschini Italy

Saran Vardhanabhuti United States

Y.F. Wong Hong Kong

Mikael Brink Sweden

Emma D’Andrea Italy

James Fortney United States

S. Markaki Greece

Thomas Boulet France

Manuel Albanese Germany

Adam Asch United States

Debora Franceschini Italy

Francesco Baudi

340 ×1.1

188 ×1.2

ONCOL

324 ×2.8

36 ×0.3

GENET

558 ×6.8

IMMUN

Citations per year, relative to Francesco Baudi Francesco Baudi (= 1×) peers Debora Franceschini

Countries citing papers authored by Francesco Baudi

Since Specialization

Citations

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

Fields of papers citing papers by Francesco Baudi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesco Baudi

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

Lavano, Serena Marianna, Rosario Amato, Lucia D’Antona, et al.. (2024). Germline Variant Spectrum in Southern Italian High-Risk Hereditary Breast Cancer Patients: Insights from Multi-Gene Panel Testing. Current Issues in Molecular Biology. 46(11). 13003–13020.

Vito, Anna Di, Emanuela Chiarella, Ida Perrotta, et al.. (2023). Novel insights into the pharmacological modulation of human periodontal ligament stem cells by the amino-bisphosphonate Alendronate. European Journal of Cell Biology. 102(4). 151354–151354. 4 indexed citations

Paduano, Francesco, Fernanda Fabiani, Lucia D’Antona, et al.. (2022). Germline Testing in a Cohort of Patients at High Risk of Hereditary Cancer Predisposition Syndromes: First Two-Year Results from South Italy. Genes. 13(7). 1286–1286. 6 indexed citations

Paduano, Francesco, Fernanda Fabiani, Francesco Trapasso, et al.. (2021). Case Report: Identification of a Novel Pathogenic Germline TP53 Variant in a Family With Li–Fraumeni Syndrome. Frontiers in Genetics. 12. 734809–734809. 4 indexed citations

Giudice, Amerigo, Alessandro Antonelli, Emanuela Chiarella, et al.. (2020). The Case of Medication-Related Osteonecrosis of the Jaw Addressed from a Pathogenic Point of View. Innovative Therapeutic Strategies: Focus on the Most Recent Discoveries on Oral Mesenchymal Stem Cell-Derived Exosomes. Pharmaceuticals. 13(12). 423–423. 25 indexed citations

Allegra, Eugenia, et al.. (2009). Multiple head and neck tumours and their genetic relationship.. PubMed. 29(5). 237–41. 7 indexed citations

Tagliaferri, Pierosandro, et al.. (2009). BRCA1/2 genetic background-based therapeutic tailoring of human ovarian cancer: hope or reality?. Journal of Ovarian Research. 2(1). 14–14. 22 indexed citations

Quaresima, Barbara, Maria Concetta Faniello, Francesco Baudi, et al.. (2006). In vitro analysis of genomic instability triggered by BRCA1 missense mutations. Human Mutation. 27(7). 715–715. 11 indexed citations

Quaresima, Barbara, Marco Gaspari, Maria Concetta Faniello, et al.. (2006). Specific changes in the proteomic pattern produced by the BRCA1-Ser1841Asn missense mutation. The International Journal of Biochemistry & Cell Biology. 39(1). 220–226. 16 indexed citations

10.

Quaresima, Barbara, Maria Concetta Faniello, Francesco Baudi, et al.. (2006). Missense mutations of BRCA1 gene affect the binding with p53 both in vitro and in vivo. Oncology Reports. 16(4). 811–5. 12 indexed citations

11.

Baudi, Francesco, Anna Maria Lavecchia, Rosa Terracciano, et al.. (2004). A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy. Cancer Letters. 223(2). 285–291. 10 indexed citations

12.

Iuliano, Rodolfo, Ilaria Le Pera, Francesco Baudi, et al.. (2004). The tyrosine phosphatase PTPRJ/DEP-1 genotype affects thyroid carcinogenesis. Oncogene. 23(52). 8432–8438. 47 indexed citations

13.

Puglisi, Fabio, Francesco Baudi, Salvatore Venuta, et al.. (2004). BRCA2 germline mutations in primary cancer of the fallopian tube. Oncology Reports. 12(2). 313–6. 4 indexed citations

14.

Baudi, Francesco, Barbara Quaresima, Maria Concetta Faniello, et al.. (2003). A novel Q3034R BRCA2 germline mutation identified in a fallopian tube cancer patient. Cancer Letters. 191(2). 211–214. 1 indexed citations

15.

Faniello, Maria Concetta, Giuseppa Chirico, Barbara Quaresima, et al.. (2002). An alternative model of H ferritin promoter transactivation by c-Jun. Biochemical Journal. 363(1). 53–53. 23 indexed citations

16.

Baudi, Francesco, Barbara Quaresima, Giovanni Cuda, et al.. (2001). Evidence of a founder mutation of BRCA1 in a highly homogeneous population from southern Italy with breast/ovarian cancer. Human Mutation. 18(2). 163–164. 80 indexed citations

17.

Quaresima, Barbara, Maria Concetta Faniello, Francesco Baudi, et al.. (2001). Transcriptional regulation of the mismatch repair gene hMLH1. Gene. 275(2). 261–265. 19 indexed citations

18.

Quaresima, Barbara, Francesco Baudi, Pierfrancesco Tassone, et al.. (1998). Hereditary nonpolyposis colorectal cancer: Identification of novel germline mutations in two kindreds not fulfilling the Amsterdam criteria. Human Mutation. 12(6). 433–433. 8 indexed citations

19.

Ambrosino, Concetta, Maria Rosaria Ruocco, Xueni Chen, et al.. (1997). HIV-1 Tat Induces the Expression of the Interleukin-6 (IL6) Gene by Binding to the IL6 Leader RNA and by Interacting with CAAT Enhancer-binding Protein β (NF-IL6) Transcription Factors. Journal of Biological Chemistry. 272(23). 14883–14892. 102 indexed citations

20.

Mele, Evelina, Barbara Quaresima, Adriana Zingone, et al.. (1993). Linkage disequilibrium of three polymorphic RFLP markers in the apolipoprotein AI-CIII gene cluster on chromosome 11. Human Genetics. 91(2). 169–74. 14 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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