Barbara Pasini

15.4k citations
93 papers · 5.9k · 2 hit papers · h-index 34

Impact in

Papers in

    • Adrenal and Paraganglionic Tumors 10
    • Congenital gastrointestinal and neural anomalies 8
    • Congenital Diaphragmatic Hernia Studies 6

Barbara Pasini

90 papers receiving 5.6k citations

Barbara Pasini's Hit Papers

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease 1994 · 593 citations
5930+10+21Years since publication250500750

Peers

Barbara Pasini
Comparison fields: 5 of 105
  • Endocrinology, Diabetes and Metabolism 1.3k
  • Gastroenterology 347
  • Cancer Research 781
  • Genetics 1.3k
  • Surgery 1.8k
Replace Lois M. Mulligan with:
Lois M. Mulligan Canada
Kennichi Kakudo Japan
Lawrence S. Kirschner United States
Maya Lodish United States
Klaus Kaserer Austria
Bharati Bapat Canada
Laura Papi Italy
Oliver Gimm Germany
Anthony P. Heaney United States
Jan Zedenius Sweden
Barbara Pasini relative to Lois M. Mulligan Canada Lois M. Mulligan's profile →
Citations per field
00.5×2.8×
Lois M. Mulligan · 1×
Citations per year

Countries citing papers authored by Barbara Pasini

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Barbara Pasini Line = papers co-authored together Barbara Pasini links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 93 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 →
1994965
2
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease
Hit paper breakdown →
1994593
3 2000422
4 2007361
5 2009207
6 1995194
7 1996167
8 2009162
9 2011156
10 1996148
11 2006125
12 2011123
13
RET activation by germline MEN2A and MEN2B mutations.
1995115
14 1997111
15 1997106
16 2001105
17 2003105
18 2006101
19 202089
20
The physical map of the human RET proto-oncogene.
199582

About Barbara Pasini

Barbara Pasini is a scholar working on Molecular Biology, Surgery, Genetics, Oncology and Endocrinology, Diabetes and Metabolism, having authored 93 papers that have together received 5.9k 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), Hormonal Regulation and Hypertension (7 papers), Genetic factors in colorectal cancer (7 papers), Cancer, Hypoxia, and Metabolism (7 papers) and Congenital Diaphragmatic Hernia Studies (6 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.3k citations), Gastroenterology (347 citations), Cancer Research (781 citations), Genetics (1.3k citations) and Surgery (1.8k 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, Rudy M. Landsvater, Tineke Stelwagen and Virginia Barone. Their work appears in journals such as Oncogene, European Journal of Human Genetics, European Journal of Endocrinology, Human Mutation and Surgery.

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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