Mario Falchetti
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
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- Genetic factors in colorectal cancer
Papers in
- Genetics 15
- BRCA gene mutations in cancer 10
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- RNA Research and Splicing 2
- DNA Repair Mechanisms 2
- Co-authors
- Laura Ottini (22 shared papers)Domenico Palli (14 shared papers)Calogero Saieva (9 shared papers)Giovanna Masala (12 shared papers)Francesco Sera (6 shared papers)Renato Mariani‐Costantini (8 shared papers)Ines Zanna (9 shared papers)Piera Rizzolo (9 shared papers)
- Journals
- Breast Cancer Research and Treatment (6 papers)Human Pathology (2 papers)Clinical Cancer Research (1 paper)Modern Pathology (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- ItalyUnited StatesRussia
In The Last Decade
Mario Falchetti
24 papers receiving 958 citations
Peers
Comparison fields: 5 of 83
- Genetics 388
- Pathology and Forensic Medicine 241
- Cancer Research 176
- Dermatology 94
- Oncology 229
Countries citing papers authored by Mario Falchetti
This map shows the geographic impact of Mario Falchetti'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 Mario Falchetti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mario Falchetti more than expected).
Fields of papers citing papers by Mario Falchetti
This network shows the impact of papers produced by Mario Falchetti. 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 Mario Falchetti. The network helps show where Mario Falchetti may publish in the future.
Co-authors
The 25 scholars most cited alongside Mario Falchetti, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 262 | |
| 2 | 2008 | 101 | |
| 3 | BRCA1 and BRCA2 mutation status and tumor characteristics in male breast cancer: a population-based study in Italy. | 2003 | 90 |
| 4 | Red meat, family history, and increased risk of gastric cancer with microsatellite instability. | 2001 | 82 |
| 5 | 2005 | 60 | |
| 6 | 2008 | 45 | |
| 7 | 2012 | 42 | |
| 8 | 1998 | 36 | |
| 9 | 1994 | 35 | |
| 10 | 2007 | 35 | |
| 11 | 2005 | 33 | |
| 12 | 2008 | 27 | |
| 13 | 2007 | 26 | |
| 14 | 2007 | 21 | |
| 15 | 2010 | 19 | |
| 16 | 2009 | 15 | |
| 17 | 2010 | 13 | |
| 18 | 2010 | 12 | |
| 19 | 2008 | 7 | |
| 20 | 2014 | 6 |
About Mario Falchetti
Mario Falchetti is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Public Health, Environmental and Occupational Health and Oncology, having authored 25 papers that have together received 977 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genetic factors in colorectal cancer (8 papers), Male Breast Health Studies (8 papers), Cancer Genomics and Diagnostics (3 papers), RNA Research and Splicing (2 papers), Ovarian cancer diagnosis and treatment (2 papers), Cholangiocarcinoma and Gallbladder Cancer Studies (2 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Genetics (388 citations), Pathology and Forensic Medicine (241 citations), Cancer Research (176 citations), Dermatology (94 citations) and Oncology (229 citations). Mario Falchetti has collaborated with scholars based in Italy, United States and Russia. Frequent co-authors include Laura Ottini, Domenico Palli, Calogero Saieva, Giovanna Masala, Francesco Sera, Renato Mariani‐Costantini, Ines Zanna, Piera Rizzolo, Emanuele de Rinaldis and Alessandro Giuliani. Their work appears in journals such as Breast Cancer Research and Treatment, Human Pathology, Clinical Cancer Research, Modern Pathology and European Journal of Human Genetics.
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.