Laura Papi

11.4k total citations · 1 hit paper
68 papers, 3.2k citations indexed

About

Laura Papi is a scholar working on Molecular Biology, Neurology and Pathology and Forensic Medicine. According to data from OpenAlex, Laura Papi has authored 68 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 27 papers in Neurology and 20 papers in Pathology and Forensic Medicine. Recurrent topics in Laura Papi's work include Neurofibromatosis and Schwannoma Cases (25 papers), Genetic factors in colorectal cancer (16 papers) and Meningioma and schwannoma management (14 papers). Laura Papi is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (25 papers), Genetic factors in colorectal cancer (16 papers) and Meningioma and schwannoma management (14 papers). Laura Papi collaborates with scholars based in Italy, United States and United Kingdom. Laura Papi's co-authors include Alan Tunnacliffe, Julia K. Moore, Emily Gardner, Sara Mole, Bruce A.J. Ponder, Håkan Telenius, Donald R. Love, Lois M. Mulligan, Margaret A. Ponder and Charis Eng and has published in prestigious journals such as Nature, Nucleic Acids Research and PLoS ONE.

In The Last Decade

Laura Papi

68 papers receiving 3.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

1993 1.4k citations Emily Gardner, Sara Mole et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Laura Papi Italy	25	1.2k	892	859	791	766	68	3.2k
Margaret A. Ponder United Kingdom	22	1.3k 1.1×	1.2k 1.4×	1.2k 1.4×	1.7k 2.1×	1.0k 1.3×	25	4.2k
Emily Gardner United Kingdom	14	1.0k 0.9×	794 0.9×	360 0.4×	1.3k 1.6×	812 1.1×	30	2.8k
Marco Gessi Italy	31	1.1k 1.0×	434 0.5×	702 0.8×	229 0.3×	416 0.5×	138	3.2k
Rudy M. Landsvater Netherlands	12	780 0.7×	499 0.6×	218 0.3×	778 1.0×	574 0.7×	15	1.9k
Katrin M. Carlson United States	10	716 0.6×	541 0.6×	244 0.3×	813 1.0×	497 0.6×	13	1.9k
George Kontogeorgos Greece	28	540 0.5×	877 1.0×	436 0.5×	1.9k 2.3×	416 0.5×	124	3.5k
Anne Barlier France	38	1.1k 1.0×	1.2k 1.4×	726 0.8×	2.4k 3.1×	469 0.6×	165	4.4k
Koji Toshima Japan	9	631 0.5×	616 0.7×	227 0.3×	1.2k 1.5×	517 0.7×	13	2.0k
Renato Spaziante Italy	28	668 0.6×	646 0.7×	508 0.6×	737 0.9×	1.0k 1.3×	115	3.2k
Rein P. Stulp Netherlands	14	767 0.7×	284 0.3×	235 0.3×	501 0.6×	312 0.4×	20	1.8k

Countries citing papers authored by Laura Papi

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Laura Papi

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Papi. A scholar is included among the top collaborators of Laura Papi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Laura Papi. Laura Papi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

1.

Papi, Laura, Paolo Caravelli, Anna Sonia Petronio, et al.. (2024). Do We Need Fasting Prior to Coronary Angiography? The CORO-NF Randomized Pragmatic Study. The American Journal of Medicine. 137(7). 666–672. 5 indexed citations

2.

Colciago, Alessandra, Alessandra Fasciani, Raffaele De Francesco, et al.. (2024). Typical NF2 and LTZR1 mutations are retained in an immortalized human schwann cell model of schwannomatosis. Heliyon. 10(19). e38957–e38957. 1 indexed citations

3.

Palone, Francesco, et al.. (2023). Loadability curves for the new Terna's “5F” high capacity overhead lines. IRIS Research product catalog (Sapienza University of Rome). 1–6. 5 indexed citations

4.

Evans, D. Gareth, David Pang, Nicolas Champollion, et al.. (2022). ERN GENTURIS clinical practice guidelines for the diagnosis, treatment, management and surveillance of people with schwannomatosis. European Journal of Human Genetics. 30(7). 812–817. 16 indexed citations

5.

Ko, Aram, Mohammad Hasanain, Young Taek Oh, et al.. (2022). LZTR1 Mutation Mediates Oncogenesis through Stabilization of EGFR and AXL. Cancer Discovery. 13(3). 702–723. 13 indexed citations

6.

Contini, Elisa, Irene Paganini, Roberta Sestini, et al.. (2015). A Systematic Assessment of Accuracy in Detecting Somatic Mosaic Variants by Deep Amplicon Sequencing: Application to NF2 Gene. PLoS ONE. 10(6). e0129099–e0129099. 15 indexed citations

7.

Paganini, Irene, Roberta Sestini, Matilde Cacciatore, et al.. (2015). Broadening the spectrum of SMARCB1-associated malignant tumors: a case of uterine leiomyosarcoma in a patient with schwannomatosis. Human Pathology. 46(8). 1226–1231. 9 indexed citations

8.

DiFrancesco, Jacopo C., Roberta Sestini, Federica Cossu, et al.. (2014). Novel neurofibromatosis type 2 mutation presenting with status epilepticus. Epileptic Disorders. 16(1). 132–137. 9 indexed citations

9.

Pin, Elisa, Chiara Pastrello, Rossella Tricarico, et al.. (2012). MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH‐Associated Polyposis. International Journal of Cancer. 132(5). 1060–1069. 11 indexed citations

10.

Vignoli, Marina, Stefania Nobili, Cristina Napoli, et al.. (2011). Thymidylate synthase expression and genotype have no major impact on the clinical outcome of colorectal cancer patients treated with 5-fluorouracil. Pharmacological Research. 64(3). 242–248. 18 indexed citations

11.

Papi, Laura, Anna Laura Putignano, Irene Piaceri, et al.. (2009). A PALB2 germline mutation associated with hereditary breast cancer in Italy. Familial Cancer. 9(2). 181–185. 33 indexed citations

12.

Sestini, Roberta, et al.. (2008). NF2 Mutation Screening by Denaturing High-Performance Liquid Chromatography and High-Resolution Melting Analysis. Genetic Testing. 12(2). 311–318. 13 indexed citations

13.

Sestini, Roberta, Anna Laura Putignano, Franco Ammannati, & Laura Papi. (2005). Detection of Rearrangements in the NF2 Gene Using Semi-Quantitative Multiplex Fluorescent PCR. Genetic Testing. 9(1). 14–19. 1 indexed citations

14.

Sestini, Roberta, et al.. (2004). Genetic insights into familial tumors of the nervous system. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 129C(1). 74–84. 40 indexed citations

15.

Bagnoli, Siro, Anna Laura Putignano, Silvana Baglioni, et al.. (2004). Susceptibility to Refractory Ulcerative Colitis Is Associated with Polymorphism in the hMLH1 Mismatch Repair Gene. Inflammatory Bowel Diseases. 10(6). 705–708. 19 indexed citations

16.

Tedde, Andrea, Francesca Vitelli, Franco Ammannati, et al.. (1996). Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin. Human Genetics. 97(5). 638–641. 19 indexed citations

17.

Tedde, Andrea, Francesca Vitelli, Franco Ammannati, et al.. (1996). Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas. Human Genetics. 97(5). 632–637. 1 indexed citations

18.

Tedde, Andrea, Francesca Vitelli, Franco Ammannati, et al.. (1996). Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas. Human Genetics. 97(5). 632–637. 62 indexed citations

19.

Gardner, Emily, et al.. (1991). EXTENDING THE GENETIC-MAP OF THE PERICENTROMERIC REGION OF CHROMOSOME-10. UCL Discovery (University College London). 1 indexed citations

20.

Gardner, Emily, et al.. (1991). IS THE RET PROTOONCOGENE A CANDIDATE FOR THE MEN2 GENE. UCL Discovery (University College London). 6 indexed citations

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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