Laura Papi
- Neurology top 1%
- Neurofibromatosis and Schwannoma Cases 25
- Neuroblastoma Research and Treatments 6
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- Genetic factors in colorectal cancer 16
- Oncology top 5%
- Epidemiology top 5%
- Meningioma and schwannoma management 14
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- Chromatin Remodeling and Cancer 10
- DNA Repair Mechanisms 6
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- BRCA gene mutations in cancer 7
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- Cancer Genomics and Diagnostics 6
- Co-authors
- Alan TunnacliffeJulia K. MooreEmily GardnerSara MoleLois M. MulliganBruce A.J. PonderMargaret A. PonderHåkan Telenius
- Journals
- Human Genetics (6 papers)European Journal of Human Genetics (4 papers)Familial Cancer (3 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Laura Papi
68 papers receiving 3.1k citations
Hit Papers
Peers
Comparison fields: 5 of 96
- Neurology 859
- Endocrinology, Diabetes and Metabolism 791
- Pathology and Forensic Medicine 641
- Oncology 766
- Epidemiology 892
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 5 | |
| 2 | 2022 | 16 | |
| 3 | 2022 | 13 | |
| 4 | 2020 | 2 | |
| 5 | 2017 | 9 | |
| 6 | 2017 | 37 | |
| 7 | 2015 | 15 | |
| 8 | 2015 | 9 | |
| 9 | 2014 | 9 | |
| 10 | 2014 | 20 | |
| 11 | 2013 | 36 | |
| 12 | 2013 | 117 | |
| 13 | 2012 | 11 | |
| 14 | 2009 | 33 | |
| 15 | 2008 | 13 | |
| 16 | 2005 | 1 | |
| 17 | 2005 | 62 | |
| 18 | 2004 | 40 | |
| 19 | EXTENDING THE GENETIC-MAP OF THE PERICENTROMERIC REGION OF CHROMOSOME-10 | 1991 | 1 |
| 20 | IS THE RET PROTOONCOGENE A CANDIDATE FOR THE MEN2 GENE | 1991 | 6 |
About Laura Papi
Laura Papi is a scholar working on Neurology, Pathology and Forensic Medicine and Genetics, having authored 68 papers that have together received 3.2k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (25 papers), Genetic factors in colorectal cancer (16 papers), Meningioma and schwannoma management (14 papers), Chromatin Remodeling and Cancer (10 papers), BRCA gene mutations in cancer (7 papers), DNA Repair Mechanisms (6 papers), Cancer Genomics and Diagnostics (6 papers) and Neuroblastoma Research and Treatments (6 papers). The work is most often cited by research in Neurology (859 citations), Endocrinology, Diabetes and Metabolism (791 citations) and Pathology and Forensic Medicine (641 citations). Laura Papi has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Alan Tunnacliffe, Julia K. Moore, Emily Gardner, Sara Mole, Lois M. Mulligan, Bruce A.J. Ponder, Margaret A. Ponder, Håkan Telenius, Donald R. Love and John B. Kwok. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, Familial Cancer, Human Molecular Genetics and Clinical 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.