Patrick R. Benusiglio

3.5k total citations · 1 hit paper
38 papers, 1.3k citations indexed

About

Patrick R. Benusiglio is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Patrick R. Benusiglio has authored 38 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 17 papers in Genetics and 14 papers in Oncology. Recurrent topics in Patrick R. Benusiglio's work include BRCA gene mutations in cancer (11 papers), Cancer-related Molecular Pathways (8 papers) and Genetic factors in colorectal cancer (8 papers). Patrick R. Benusiglio is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Cancer-related Molecular Pathways (8 papers) and Genetic factors in colorectal cancer (8 papers). Patrick R. Benusiglio collaborates with scholars based in France, United Kingdom and Germany. Patrick R. Benusiglio's co-authors include Laure Dossus, Olivier Caron, Brigitte Bressac–de Paillerets, Laurence Brugières, Thierry Frébourg, Émilie Consolino, Dominique Stoppa‐Lyonnet, Julie Tinat, Gaëlle Bougeard and Mariette Renaux‐Petel and has published in prestigious journals such as Journal of Clinical Oncology, Blood and British Journal of Cancer.

In The Last Decade

Patrick R. Benusiglio

36 papers receiving 1.3k 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.

Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers

2015 467 citations Gaëlle Bougeard, Mariette Renaux‐Petel et al. Journal of Clinical Oncology profile →

Peers

Countries citing papers authored by Patrick R. Benusiglio

Since Specialization

Citations

This map shows the geographic impact of Patrick R. Benusiglio'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 Patrick R. Benusiglio with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick R. Benusiglio more than expected).

Fields of papers citing papers by Patrick R. Benusiglio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick R. Benusiglio. 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 Patrick R. Benusiglio. The network helps show where Patrick R. Benusiglio may publish in the future.

Co-authorship network of co-authors of Patrick R. Benusiglio

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick R. Benusiglio. A scholar is included among the top collaborators of Patrick R. Benusiglio 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 Patrick R. Benusiglio. Patrick R. Benusiglio 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

#	Work	Indexed citations
1	A Specific Methylation Class Identifies BAP1‐Deficient Meningiomas, Including Meningeal Tumours With Poorly Differentiated Nonrhabdoid Histology 2025 ·Neuropathology and Applied Neurobiology ·(unknown), Mehdi Touat, Patrick R. Benusiglio, Philipp Euskirchen, Florence Coulet, (unknown), Arnaud de la Fouchardière, Vincent de Montpréville, (unknown), Danièle Bernardeschi, Pierre Laurent‐Puig, Marc Sanson, Michel Kalamarides, Franck Bielle	1
2	Pathogenic germline variants in patients with early-onset colorectal cancer according to phenotype 2025 ·European Journal of Human Genetics ·(unknown), Marion Dhooge, (unknown), (unknown), (unknown), (unknown), (unknown), Florence Coulet, Patrick R. Benusiglio	0
3	Preimplantation genetic testing in patients with genetic susceptibility to cancer 2022 ·Familial Cancer ·(unknown), Nelly Frydman, Céline Moutou, (unknown), (unknown), (unknown), Julie Steffann, (unknown), Nathalie Chabbert‐Buffet, (unknown), Richard J. Kahnoski, Patrick R. Benusiglio	3
4	Response to systemic therapy in fumarate hydratase–deficient renal cell carcinoma 2021 ·European Journal of Cancer ·Lucía Carril-Ajuria, Émeline Colomba, Luigi Cerbone, Carmen Romero, Laurence Crouzet, Brigitte Laguerre, Constance Thibault, Cécile Vicier, Guillermo de Velasco, Aude Fléchon, (unknown), Patrick R. Benusiglio, Brigitte Bressac–de Paillerets, Marine Guillaud-Bataille, Pauline Gaignard, Jean‐Yves Scoazec, Richard J. Kahnoski, Olivier Caron, Bernard Escudier, Laurence Albigès	24
5	Lung cancer is also a hereditary disease 2021 ·European Respiratory Review ·Patrick R. Benusiglio, Vincent Fallet, (unknown), Florence Coulet, J. Cadranel	54
6	Cancer predisposition and germline CTNNA1 variants 2021 ·European Journal of Medical Genetics ·(unknown), Patrick R. Benusiglio, Florence Coulet, Lise Boussemart, Lisa Golmard, Isabel Spier, Robert Hüneburg, Stefan Aretz, Chrystelle Colas, Carla Oliveíra	26
7	Consultation personnalisée d’évaluation du risque de cancer du sein : premiers résultats 2020 ·Bulletin du Cancer ·Catherine Uzan, (unknown), (unknown), (unknown), (unknown), Geoffroy Canlorbe, Henri Azaïs, C. Gonthier, J. Belghiti, Patrick R. Benusiglio, Brigitte Séroussi, Joseph Gligorov, Serge Uzan	2
8	Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019 2020 ·Familial Cancer ·Manon Suerink, Katharina Wimmer, Laurence Brugières, Chrystelle Colas, Richard Gallon, Tim Ripperger, Patrick R. Benusiglio, (unknown), (unknown), Yael Goldberg, James C.H. Hardwick, Matthias Kloor, (unknown), Martine Muleris, Marta Pineda, Clara Ruíz-Ponte, Hans F. A. Vasen	12
9	Utility of a mainstreamed genetic testing pathway in breast and ovarian cancer patients during the COVID-19 pandemic 2020 ·European Journal of Medical Genetics ·Patrick R. Benusiglio, Clément Korenbaum, (unknown), (unknown), (unknown), (unknown), Sandrine Richard, (unknown), Manon Lejeune, Erell Guillerm, (unknown), Jean-Pierre Lotz, Nathalie Chabbert‐Buffet, Joseph Gligorov, Florence Coulet	9
10	Pattern multiplicity and fumarate hydratase (FH)/S-(2-succino)-cysteine (2SC) staining but not eosinophilic nucleoli with perinucleolar halos differentiate hereditary leiomyomatosis and renal cell carcinoma-associated renal cell carcinomas from kidney tumors without FH gene alteration 2018 ·Modern Pathology ·Marie Müller, Marine Guillaud-Bataille, Julia Salleron, Catherine Genestie, Sophie Deveaux, Abdelhamid Slama, Brigitte Bressac–de Paillerets, Richard J. Kahnoski, Patrick R. Benusiglio, Sophie Ferlicot	72
11	Clinical implications of CTNNA1 germline mutations in asymptomatic carriers 2018 ·Gastric Cancer ·Patrick R. Benusiglio, Chrystelle Colas, Erell Guillerm, (unknown), (unknown), Mathilde Warcoin, J Bellanger, Mélanie Eyries, (unknown), (unknown), Florent Soubrier, Yann Parc, Anne Mourrégot, (unknown), Véronica Cusin, Jérôme Alexandre Denis, Isabelle Coupier, Magali Svrcek, Florence Coulet	26
12	Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers 2017 ·Clinical Genetics ·Marie Müller, Sophie Ferlicot, Marine Guillaud‐Bataille, Gwénaël Le Teuff, Catherine Genestie, Scott DeVeaux, Abdelhamid Slama, Nicolas Poulalhon, (unknown), Laurence Albigès, Nadem Soufir, Avril Mf, Betty Gardie, (unknown), Yves Allory, Anne‐Paule Gimenez‐Roqueplo, Brigitte Bressac–de Paillerets, Richard J. Kahnoski, Patrick R. Benusiglio	93
13	Lung Adenocarcinoma as Part of the Li-Fraumeni Syndrome Spectrum 2017 ·JAMA Oncology ·Olivier Caron, Thierry Frébourg, Patrick R. Benusiglio, Stéphanie Foulon, Laurence Brugières	26
14	Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counselling 2016 ·Familial Cancer ·Patrick R. Benusiglio, (unknown), Leila Dorling, Anne Jouinot, (unknown), (unknown), (unknown), (unknown), (unknown), Olivier Caron	18
15	Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers breakdown → 2015 ·Journal of Clinical Oncology ·Gaëlle Bougeard, Mariette Renaux‐Petel, Jean‐Michel Flaman, Camille Charbonnier, (unknown), Muriel Belotti, Marion Gauthier‐Villars, Dominique Stoppa‐Lyonnet, Émilie Consolino, Laurence Brugières, Olivier Caron, Patrick R. Benusiglio, Brigitte Bressac–de Paillerets, Valérie Bonadona, Catherine Bonaïti‐Pellié, Julie Tinat, Stéphanie Baert‐Desurmont, Thierry Frébourg	467
16	Cleft lip, cleft palate, hereditary diffuse gastric cancer and germline mutations in CDH1 2012 ·International Journal of Cancer ·Patrick R. Benusiglio, Olivier Caron, Émilie Consolino, Pierre Duvillard, Florence Coulet, Martine Blayau, David Malka	26
17	Gastrointestinal relapse of multiple myeloma and sustained response to lenalidomide: a case report 2011 ·Journal of Medical Case Reports ·Patrick R. Benusiglio, Thomas McKee, Xavier Montet, Jean‐Marc Dumonceau, (unknown), (unknown), Pierre‐Yves Dietrich	2
18	Focus on ERBB2 2008 ·Pharmacogenomics ·Patrick R. Benusiglio	3
19	Anticoagulation orale et pharmacogénétique: perspectives pour la pratique clinique 2007 ·Revue Médicale Suisse ·Patrick R. Benusiglio, Jules Desmeules, Pierre Dayer	1
20	HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer 2006 ·British Journal of Cancer ·Patrick R. Benusiglio, Paul D.P. Pharoah, Paula Smith, Fabienne Lesueur, Don Conroy, Robert Luben, (unknown), (unknown), Alison M. Dunning, Douglas F. Easton, B. A. J. Ponder	34

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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