Laura Papi
Impact in
- Neurology top 1%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
-
- Thyroid Cancer Diagnosis and Treatment
Papers in
- Neurology 26
- Neurofibromatosis and Schwannoma Cases 24
- Neuroblastoma Research and Treatments 6
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- Chromatin Remodeling and Cancer 10
- Co-authors
- Alan Tunnacliffe (4 shared papers)Sara Mole (4 shared papers)Emily Gardner (5 shared papers)Julia K. Moore (2 shared papers)Margaret A. Ponder (2 shared papers)Bruce A.J. Ponder (2 shared papers)Håkan Telenius (2 shared papers)Lois M. Mulligan (3 shared papers)
- Journals
- Human Genetics (6 papers)European Journal of Human Genetics (4 papers)Clinical Genetics (3 papers)Human Molecular Genetics (3 papers)Familial Cancer (3 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Laura Papi
68 papers receiving 3.3k citations
Laura Papi's Hit Papers
Peers
Comparison fields: 5 of 90
- Neurology 880
- Endocrinology, Diabetes and Metabolism 835
- Pathology and Forensic Medicine 591
- Oncology 663
- Epidemiology 807
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 68 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 | 1590 |
| 2 | 2007 | 134 | |
| 3 | 1994 | 132 | |
| 4 | 2013 | 130 | |
| 5 | 1997 | 81 | |
| 6 | 1993 | 80 | |
| 7 | 2009 | 80 | |
| 8 | 1996 | 66 | |
| 9 | 2005 | 64 | |
| 10 | 1993 | 61 | |
| 11 | 1999 | 60 | |
| 12 | 1995 | 59 | |
| 13 | 2014 | 58 | |
| 14 | 2004 | 53 | |
| 15 | 2003 | 47 | |
| 16 | 2008 | 44 | |
| 17 | 2005 | 43 | |
| 18 | 2017 | 41 | |
| 19 | 2013 | 41 | |
| 20 | 2017 | 39 |
About Laura Papi
Laura Papi is a scholar working on Neurology, Molecular Biology, Pathology and Forensic Medicine, Epidemiology and Genetics, having authored 68 papers that have together received 3.5k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (24 papers), Genetic factors in colorectal cancer (15 papers), Meningioma and schwannoma management (13 papers), Chromatin Remodeling and Cancer (10 papers), Neuroblastoma Research and Treatments (6 papers), Sarcoma Diagnosis and Treatment (6 papers), Cancer Genomics and Diagnostics (6 papers) and BRCA gene mutations in cancer (6 papers). The work is most often cited by research in Neurology (880 citations), Endocrinology, Diabetes and Metabolism (835 citations), Pathology and Forensic Medicine (591 citations), Oncology (663 citations) and Epidemiology (807 citations). Laura Papi has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Alan Tunnacliffe, Sara Mole, Emily Gardner, Julia K. Moore, Margaret A. Ponder, Bruce A.J. Ponder, Håkan Telenius, Lois M. Mulligan, Donald R. Love and Charis Eng. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, Clinical Genetics, Human Molecular Genetics and Familial Cancer.
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.