Gilbert Lenoir

34.9k citations

254 papers · 15.5k indexed · 4 hit papers · h-index 64

Impact in

Pathology and Forensic Medicine top 0.1%
- Lymphoma Diagnosis and Treatment
Oncology top 0.2%
- Viral-associated cancers and disorders
- Cancer-related Molecular Pathways

Papers in

Pathology and Forensic Medicine 80
- Lymphoma Diagnosis and Treatment 66
Oncology 103
- Viral-associated cancers and disorders 74

Co-authors: Philip Leder Rebecca Taub Jim Battey Christopher Moulding William S. Murphy Huntington Potter Timothy A. Stewart Claude Turc‐Carel
Journals: International Journal of Cancer (24 papers)Oncogene (11 papers)Human Mutation (9 papers)Genes Chromosomes and Cancer (7 papers)Proceedings of the National Academy of Sciences (7 papers)
Partner nations: France United States Canada

In The Last Decade

Gilbert Lenoir

252 papers receiving 14.7k citations

Hit Papers

align trajectories log scale

The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts 1994 · 816 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1994 New England Journal of Medicine
1983 Science
1983 Cell
1982 Proceedings of the National Academy of Sciences

Peers

Countries citing papers authored by Gilbert Lenoir

Since Specialization

Citations

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

Fields of papers citing papers by Gilbert Lenoir

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gilbert Lenoir. 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 Gilbert Lenoir. The network helps show where Gilbert Lenoir may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Gilbert Lenoir, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Gilbert Lenoir Line = papers co-authored together Gilbert Lenoir links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Leviers et freins à la prise de décision partagée en France en 2021 : enquête nationale auprès des patients atteints de cancer Bulletin du Cancer ·Michel Winock, Richard I. Steim, Gilbert Lenoir, Fadila Farsi, Nora Moumjid, François Blot	2023	2
2	Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients. PubMed ·Georges Lucotte, Heiko Steuer, Christine Hubans, Jean‐Pierre Lagarde, Gilbert Lenoir	2009	9
3	Pharmacogenetic study in Hodgkin lymphomas reveals the impact of UGT1A1 polymorphisms on patient prognosis Blood ·Vincent Ribrag, Serge Koscielny, Olivier Casasnovas, Cécile Cazeneuve, Pauline Brice, Franck Morschhauser, Jean Gabarre, Aspasia Stamatoullas, Gilbert Lenoir, Gilles Salles	2008	25
4	Contribution of germline BRCA1 and BRCA2sequence alterations to breast cancer in Northern India BMC Medical Genetics ·Sunita Saxena, Jerin Johnkutty, Mishi Kaushal, T Scovazzi, O. Okeke, R. S. Mohil, علی اصغر باقری, 隆新関, Veena Sharma, Prakash Chand Sharma, Gilbert Lenoir, David E. Goldgar, Csilla I. Szabo	2006	77
5	A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) family. PubMed ·Karine Fontaine, F. Sanaei, Rifki Hermana, Gilbert Lenoir, G Lucotte	2005	8
6	Prédispositions génétiques aux cancers : actualités et perspectives en 2005 médecine/sciences ·Dominique Stoppa‐Lyonnet, Gilbert Lenoir	2005	2
7	Mitotic catastrophe constitutes a special case of apoptosis whose suppression entails aneuploidy Oncogene ·Maria Castedo, Jean‐Luc Perfettini, Thomas Roumier, Alexander Valent, Hana Raslová, Kenichi Yakushijin, David Horne, Jean Feunteun, Gilbert Lenoir, René H. Medema, William Vainchenker, Guido Kroemer	2004	248
8	Distinct BRCA1 Rearrangements Involving the BRCA1 Pseudogene Suggest the Existence of a Recombination Hot Spot The American Journal of Human Genetics ·Nadine Puget, Sophie Gad, S. N. Smith, Olga M. Sinilnikova, Dominique Stoppa‐Lyonnet, Gilbert Lenoir, Sylvie Mazoyer	2002	88
9	BRCA1 andBRCA2 sequence variants in Chinese breast cancer families Human Mutation ·Astrid Senders, Csilla I. Szabo, Qin Fenghu, Nicola M. Suter, James E. Frasher, Elaine A. Ostrander, Olga M. Sinilnikova, Gilbert Lenoir, David E. Goldgar, Manu Rajankutty	2002	34
10	Screening for Genomic Rearrangements in Families with Breast and Ovarian Cancer Identifies BRCA1 Mutations Previously Missed by Conformation-Sensitive Gel Electrophoresis or Sequencing The American Journal of Human Genetics ·A. Mireille Baart, Katherine L. Nathanson, (unknown), Danielle Antin‐Ozerkis, Helen A. Shih, Anne‐Marie Martin, Gilbert Lenoir, Sylvie Mazoyer, Barbara L. Weber	2000	117
11	An Update on DNA-Based BRCA1/BRCA2 Genetic Counseling in Hereditary Breast Cancer Cancer Genetics and Cytogenetics ·Henry T. Lynch, Patrice Watson, Susan Tinley, Carrie Snyder, Carolyn Durham, Jane Lynch, Miliauskas, Olga Serova, Gilbert Lenoir, Caryn Lerman, Steven A. Narod	1999	61
12	Various mechanisms cause RET-mediated signaling defects in Hirschsprung's disease. Journal of Clinical Investigation ·Anna Pelet, Olivier Geneste, Patrick Edery, Andrea Pasini, Brigitte Letellier, C.-I.H. Chen, A Munnich, Gilbert Lenoir, Stanislas Lyonnet, Marc Billaud	1998	83
13	Distinct biological properties of two RET isoforms activated by MEN 2A and MEN 2B mutations Oncogene ·Mireille Rossel, Andrea Pasini, Abdollah Pirouzi, Linxuan Pan, Nghia Thanh Dang, Isabelle Schuffenecker, Jaya S. Anand, Leo A. van Grunsven, José Luis Urdiales, Brian B. Rudkin, Gilbert Lenoir, Marc Billaud	1997	84
14	Mutations clustered in exon 5 of the p⁵³ gene in primary nasopharyngeal carcinomas from Southeastern Asia International Journal of Cancer ·Sandra Indermuhle, Jean‐Pierre Armand, Gilbert Lenoir, Yuriko Tanishima, Jianping Liang, Evelyne May, Pierre May	1995	21
15	Cytogenetic and molecular analysis of 6q deletions in burkitt's lymphoma cell lines Genes Chromosomes and Cancer ·Nasser Z. Parsa, Asit B. Mukherjee, R. S. K. Chaganti, Gianluca Gaïdano, Robert Hauptschein, Riccardo Dalla‐Favera, Gilbert Lenoir	1994	33
16	Neurofibromatosis type 2 appears to be a genetically homogeneous disease. Europe PMC (PubMed Central) ·Steven A. Narod, Dilys M. Parry, Jillian S. Parboosingh, Gilbert Lenoir, Martin Ruttledge, Georges Fischer, Roswell Eldridge, Robert L. Martuza, Marina Frontali, Jonathan L. Haines, James F. Gusella, Guy A. Rouleau	1992	41
17	Are Bilateral Tumours Hereditary? International Journal of Epidemiology ·Steven A. Narod, Gilbert Lenoir	1991	8
18	t(2;8) variant translocation in burkitt's lymphoma: Mapping of chromosomal breakpoints by in situ hybridization International Journal of Cancer ·S. Adolph, H. Hameister, Berthold Henglein, Martin Lipp, P. Hartl, Frank Baas, Gilbert Lenoir, Georg W. Bornkamm	1989	3
19	[Epstein-Barr virus and infectious mononucleosis. A clinical study of Epstein-Barr antibodies (author's transl)]. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Clayton Barcelos Zabeu, М. Н. Селянинов, ゆかり田中, Cynthia Lynn Cormier, Gilbert Lenoir	1978	1
20	In vitro transforming activity of EBV. I-Establishment and properties of two EBV strains (M81 and M72) produced by immortalized Callithrix jacchus lymphocytes. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Claude Des̀granges, Gilbert Lenoir, G de-Thé, J. M. Seigneurin, J. Hilgers, Scott Wilkinson	1976	24

About Gilbert Lenoir

Gilbert Lenoir is a scholar working on Pathology and Forensic Medicine, Oncology, Genetics, Rheumatology and Immunology, having authored 254 papers that have together received 15.5k indexed citations. Recurring topics across this work include Viral-associated cancers and disorders (74 papers), Lymphoma Diagnosis and Treatment (66 papers), BRCA gene mutations in cancer (46 papers), Genomic variations and chromosomal abnormalities (25 papers), Parvovirus B19 Infection Studies (21 papers), Immune Cell Function and Interaction (18 papers), Eosinophilic Disorders and Syndromes (17 papers) and Cytomegalovirus and herpesvirus research (17 papers). The work is most often cited by research in Pathology and Forensic Medicine (3.5k citations), Oncology (5.2k citations), Cancer Research (1.9k citations), Genetics (3.4k citations) and Genetics (1.2k citations). Gilbert Lenoir has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Philip Leder, Rebecca Taub, Jim Battey, Christopher Moulding, William S. Murphy, Huntington Potter, Timothy A. Stewart, Claude Turc‐Carel, Steven R. Tronick and Ilan R. Kirsch. Their work appears in journals such as International Journal of Cancer, Oncogene, Human Mutation, Genes Chromosomes and Cancer and Proceedings of the National Academy of Sciences.

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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