Barbara Pasini
Impact in
-
- Thyroid Cancer Diagnosis and Treatment
- Gastroenterology top 1%
Papers in
- Surgery 23
- Adrenal and Paraganglionic Tumors 10
- Congenital gastrointestinal and neural anomalies 8
- Congenital Diaphragmatic Hernia Studies 6
- Co-authors
- Isabella Ceccherini (11 shared papers)Giovanni Romeo (7 shared papers)Yin Luo (4 shared papers)Constantine A. Stratakis (5 shared papers)Renata Bocciardi (8 shared papers)Robert M.W. Hofstra (4 shared papers)Rein P. Stulp (2 shared papers)Tineke Stelwagen (3 shared papers)
- Journals
- Oncogene (5 papers)European Journal of Human Genetics (3 papers)Human Mutation (3 papers)European Journal of Endocrinology (3 papers)European Journal of Medical Genetics (2 papers)
- Partner nations
- ItalyUnited StatesFrance
In The Last Decade
Barbara Pasini
89 papers receiving 5.3k citations
Barbara Pasini's Hit Papers
Peers
Comparison fields: 5 of 101
- Endocrinology, Diabetes and Metabolism 1.2k
- Gastroenterology 325
- Cancer Research 714
- Genetics 1.2k
- Surgery 1.6k
Countries citing papers authored by Barbara Pasini
This map shows the geographic impact of Barbara Pasini'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 Barbara Pasini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara Pasini more than expected).
Fields of papers citing papers by Barbara Pasini
This network shows the impact of papers produced by Barbara Pasini. 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 Barbara Pasini. The network helps show where Barbara Pasini may publish in the future.
Co-authors
The 25 scholars most cited alongside Barbara Pasini, 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 92 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma Hit paper breakdown → | 1994 | 876 |
| 2 | Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease Hit paper breakdown → | 1994 | 532 |
| 3 | 2000 | 388 | |
| 4 | 2007 | 327 | |
| 5 | 2009 | 193 | |
| 6 | 1996 | 161 | |
| 7 | 1995 | 159 | |
| 8 | 2009 | 156 | |
| 9 | 2011 | 143 | |
| 10 | 1996 | 135 | |
| 11 | 2006 | 117 | |
| 12 | 2011 | 113 | |
| 13 | RET activation by germline MEN2A and MEN2B mutations. | 1995 | 107 |
| 14 | 1997 | 104 | |
| 15 | 1997 | 104 | |
| 16 | 2003 | 97 | |
| 17 | 2001 | 96 | |
| 18 | 2006 | 88 | |
| 19 | 2020 | 86 | |
| 20 | 2008 | 77 |
About Barbara Pasini
Barbara Pasini is a scholar working on Molecular Biology, Surgery, Genetics, Oncology and Endocrinology, Diabetes and Metabolism, having authored 92 papers that have together received 5.4k indexed citations. Recurring topics across this work include Adrenal and Paraganglionic Tumors (10 papers), BRCA gene mutations in cancer (10 papers), Congenital gastrointestinal and neural anomalies (8 papers), Cutaneous Melanoma Detection and Management (7 papers), Genetic factors in colorectal cancer (7 papers), Cancer, Hypoxia, and Metabolism (7 papers), Hormonal Regulation and Hypertension (6 papers) and Congenital Diaphragmatic Hernia Studies (6 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.2k citations), Gastroenterology (325 citations), Cancer Research (714 citations), Genetics (1.2k citations) and Surgery (1.6k citations). Barbara Pasini has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Isabella Ceccherini, Giovanni Romeo, Yin Luo, Constantine A. Stratakis, Renata Bocciardi, Robert M.W. Hofstra, Rein P. Stulp, Tineke Stelwagen, Rudy M. Landsvater and Jo W.M. Höppener. Their work appears in journals such as Oncogene, European Journal of Human Genetics, Human Mutation, European Journal of Endocrinology and European Journal of Medical 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.