Laura Papi
Impact in
Papers in
- Co-authors
- Alan Tunnacliffe (4 shared papers)Emily Gardner (5 shared papers)Sara Mole (4 shared papers)Lois M. Mulligan (3 shared papers)Margaret A. Ponder (2 shared papers)Håkan Telenius (2 shared papers)Donald R. Love (2 shared papers)Bruce A.J. Ponder (2 shared papers)
- Journals
- Breast Cancer Research (7 papers)Nature Genetics (6 papers)Human Mutation (5 papers)Neurology (5 papers)European Journal of Human Genetics (5 papers)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Laura Papi
104 papers receiving 8.6k citations
Laura Papi's Hit Papers
Peers
Comparison fields: 5 of 129
- Genetics 3.4k
- Neurology 1.4k
- Endocrinology, Diabetes and Metabolism 989
- Reproductive Medicine 361
- Pathology and Forensic Medicine 561
Countries citing papers authored by Laura Papi
This map shows the geographic impact of Laura Papi'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 Laura Papi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura Papi more than expected).
Fields of papers citing papers by Laura Papi
This network shows the impact of papers produced by Laura Papi. 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 Laura Papi. The network helps show where Laura Papi may publish in the future.
Co-authors
The 25 scholars most cited alongside Laura Papi, 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 106 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A Hit paper breakdown → | 1993 | 1624 |
| 2 | Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 Hit paper breakdown → | 2011 | 1146 |
| 3 | Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation Hit paper breakdown → | 2021 | 469 |
| 4 | Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer Hit paper breakdown → | 2017 | 368 |
| 5 | 2013 | 331 | |
| 6 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses Hit paper breakdown → | 2020 | 321 |
| 7 | Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer Hit paper breakdown → | 2017 | 306 |
| 8 | 2018 | 245 | |
| 9 | 2015 | 198 | |
| 10 | Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation Hit paper breakdown → | 2022 | 168 |
| 11 | 2007 | 146 | |
| 12 | 2013 | 143 | |
| 13 | 1994 | 131 | |
| 14 | 2016 | 125 | |
| 15 | 2019 | 121 | |
| 16 | 2014 | 106 | |
| 17 | 2011 | 105 | |
| 18 | 2014 | 102 | |
| 19 | 2020 | 95 | |
| 20 | 2005 | 90 |
About Laura Papi
Laura Papi is a scholar working on Neurology, Genetics, Pathology and Forensic Medicine, Endocrinology, Diabetes and Metabolism and Epidemiology, having authored 106 papers that have together received 8.9k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (35 papers), Neurofibromatosis and Schwannoma Cases (34 papers), Genetic factors in colorectal cancer (13 papers), Genetic Associations and Epidemiology (10 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Thyroid Cancer Diagnosis and Treatment (4 papers) and Meningioma and schwannoma management (3 papers). The work is most often cited by research in Genetics (3.4k citations), Neurology (1.4k citations), Endocrinology, Diabetes and Metabolism (989 citations), Reproductive Medicine (361 citations) and Pathology and Forensic Medicine (561 citations). Laura Papi has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Alan Tunnacliffe, Emily Gardner, Sara Mole, Lois M. Mulligan, Margaret A. Ponder, Håkan Telenius, Donald R. Love, Bruce A.J. Ponder, John B. Kwok and Charis Eng. Their work appears in journals such as Breast Cancer Research, Nature Genetics, Human Mutation, Neurology 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.