Barbara Pasini

15.5k citations
135 papers · 12.4k · 6 hit papers · h-index 51

Impact in

Papers in

    • BRCA gene mutations in cancer 33
    • Genomic variations and chromosomal abnormalities 9
    • Cutaneous Melanoma Detection and Management 8

Barbara Pasini

132 papers receiving 11.8k citations

Barbara Pasini's Hit Papers

Association of Type and Location ofBRCA1andBRCA2Mutations With Risk of Breast and Ovarian Cancer 2015 · 397 citations
3970+10+21Years since publication50010001.5k2.0k2.5k

Peers

Barbara Pasini
Comparison fields: 5 of 127
  • Genetics 5.0k
  • Reproductive Medicine 1.2k
  • Cancer Research 2.0k
  • Gastroenterology 547
  • Endocrinology, Diabetes and Metabolism 1.4k
Replace Paul J. Goodfellow with:
Paul J. Goodfellow United States
Patricia L. M. Dahia United States
Charles H.C.M. Buys Netherlands
Emma Roisin Woodward United Kingdom
Kennichi Kakudo Japan
Catherine Bonaïti‐Pellié France
Rosemarie Davidson United Kingdom
Shirley Victoria Hodgson United Kingdom
Barbara Jarząb Poland
Juul Wijnen Netherlands
Barbara Pasini relative to Paul J. Goodfellow United States Paul J. Goodfellow's profile →
Citations per field
00.5×5×10×14.0×
Paul J. Goodfellow · 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 135 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies
Hit paper breakdown →
20032866
2
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
Hit paper breakdown →
1994989
3
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease
Hit paper breakdown →
1994622
4
Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1 / 2 (CIMBA)
Hit paper breakdown →
2012529
5 2000439
6
Association of Type and Location ofBRCA1andBRCA2Mutations With Risk of Breast and Ovarian Cancer
Hit paper breakdown →
2015397
7
Recurrent SomaticDICER1Mutations in Nonepithelial Ovarian Cancers
Hit paper breakdown →
2011390
8 2007376
9 2018242
10 2009213
11 1995196
12 2007186
13 2009173
14 2011167
15 1996165
16 1996146
17 2005143
18 2011130
19 2006127
20 1997121

About Barbara Pasini

Barbara Pasini is a scholar working on Genetics, Oncology, Endocrinology, Diabetes and Metabolism, Cancer Research and Molecular Biology, having authored 135 papers that have together received 12.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (33 papers), Adrenal and Paraganglionic Tumors (11 papers), DNA Repair Mechanisms (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Cutaneous Melanoma Detection and Management (8 papers), Ovarian cancer diagnosis and treatment (8 papers), Congenital gastrointestinal and neural anomalies (8 papers) and Hormonal Regulation and Hypertension (7 papers). The work is most often cited by research in Genetics (5.0k citations), Reproductive Medicine (1.2k citations), Cancer Research (2.0k citations), Gastroenterology (547 citations) and Endocrinology, Diabetes and Metabolism (1.4k citations). Barbara Pasini has collaborated with scholars based in Italy, United States and Canada. Frequent co-authors include Isabella Ceccherini, Constantine A. Stratakis, Giovanni Romeo, Yin Luo, 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, Human Mutation, Breast Cancer Research, European Journal of Human Genetics and The Journal of Clinical Endocrinology & Metabolism.

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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