Thierry Frébourg

34.5k citations

276 papers · 14.1k indexed · 5 hit papers · h-index 60

Impact in

Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
Oncology top 0.5%
- Cancer-related Molecular Pathways
- Colorectal Cancer Treatments and Studies

Papers in

Oncology 93
- Cancer-related Molecular Pathways 48
- Colorectal Cancer Treatments and Studies 21
Pathology and Forensic Medicine 59
- Genetic factors in colorectal cancer 52

Co-authors: Dominique Campion Didier Hannequin Alexis Brice Cosette Martin Grégory Raux Jean‐Michel Flaman Cécile Dumanchin Anne Rovelet‐Lecrux
Journals: European Journal of Human Genetics (19 papers)Human Mutation (15 papers)Journal of Clinical Oncology (13 papers)Journal of Medical Genetics (10 papers)International Journal of Cancer (7 papers)
Partner nations: France United States Italy

In The Last Decade

Thierry Frébourg

271 papers receiving 13.7k citations

Hit Papers

5 papers align trajectories log scale

Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers 2015 · 467 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.

2015 Journal of Clinical Oncology
2008 Nature
2007 British Journal of Cancer
2005 Nature Genetics
1999 The American Journal of Human Genetics

Peers

Countries citing papers authored by Thierry Frébourg

Since Specialization

Citations

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

Fields of papers citing papers by Thierry Frébourg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Thierry Frébourg, 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 Thierry Frébourg Line = papers co-authored together Thierry Frébourg links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings American Journal of Medical Genetics Part A ·Maud Blanluet, Sandra Chantot‐Bastaraud, Pascal Chambon, Kévin Cassinari, Gabriella Vera, Alice Goldenberg, Boris Keren, Nathalie Le Meur, Didier Hannequin, Bertrand Macé, Jean‐Pierre Siffroi, Thierry Frébourg, Gaël Nicolas, Géraldine Joly‐Hélas	2021	1
2	Assessment of Multiplex Digital Droplet RT-PCR as a Diagnostic Tool for SARS-CoV-2 Detection in Nasopharyngeal Swabs and Saliva Samples Clinical Chemistry ·Kévin Cassinari, Élodie Alessandri-Gradt, Pascal Chambon, Françoise Charbonnier, Shoji KODAMA, Ludivine Beaussire, Kévin Alexandre, Nasrin Sarafan‐Vasseur, Claude Houdayer, Manuel Etienne, François Caron, Jean‐Christophe Plantier, Thierry Frébourg	2020	30
3	Blood functional assay for rapid clinical interpretation of germline TP53 variants Journal of Medical Genetics ·二郎川妻, Sandra A. Frederixon, Sophie Coutant, Céline Derambure, Carmencita M. David-Padilla, Françoise Charbonnier, Jacqueline Bou, Emilie Bouvignies, Татьяна Юрьевна Разсадкина, Stéphanie Vasseur, Michael Farrell, Olivier Ingster, Alfred E. Seyler, 諒俊今泉, Gaëlle Bougeard, Thierry Frébourg, Isabelle Tournier	2020	11
4	Rhabdomyosarcoma associated with germline TP53 alteration in children and adolescents: The French experience Pediatric Blood & Cancer ·E. P. Wildner, Gaëlle Bougeard, Marie Karanian, Giselle Hoosgood, Cécile Boulanger, Hélène Boutroux, Claire Briandet, Christine Chevreau, Nadège Corradini, Carole Coze, Anne Sophie Defachelles, Lela Dwi Rahmawati, Daniel Orbach, Christophe Piguet, Jean‐Yves Scoazec, Cécile Verite, Marjolaine Willems, Thierry Frébourg, Véronique Minard‐Colin, Laurence Brugières	2020	18
5	Familial solitary chondrosarcoma resulting from germline EXT2 mutation Genes Chromosomes and Cancer ·Yunlin Zhu, Henn Julian, Sophie Coutant, Émilie Angot, Jean‐Christophe Sabourin, Paul Michelin, Sh.D. Miniskul, Françoise Charbonnier, Myriam Vézain, Gaëlle Bougeard, Stéphanie Baert‐Desurmont, Thierry Frébourg, Isabelle Tournier	2016	5
6	BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer Familial Cancer ·Rizki Alfiansyah, Tebiary Lepinus, Audrey Emmanuelle Dugué, Angélina Legros, Alexandra Leconte, Bénédicte Clarisse, Л. И. Медведева, Fei Li, Catherine Dugast, Caroline Abadie, Thierry Frébourg, Julie Tinat, Isabelle Tennevet, Valérie Layet, Florence Joly, Laurent Castéra, Pascaline Berthet, Dominique Vaur, Sophie Krieger	2016	0
7	Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers Journal of Clinical Oncology ·Gaëlle Bougeard, Mariette Renaux‐Petel, Jean‐Michel Flaman, Camille Charbonnier, Henn Julian, 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 Hit paper breakdown →	2015	467
8	A new genotoxicity assay based on p53 target gene induction Mutation Research/Genetic Toxicology and Environmental Mutagenesis ·Sandro P. Berni Brum, 諒俊今泉, Rodrigo de Freitas Amorim, Sahil Adriouch, Gaëlle Bougeard, Thierry Frébourg, Jean‐Michel Flaman	2015	17
9	The first mutations in the MYH gene reported in Moroccan colon cancer patients Gene ·Н. С. Сергеева, Imane Cherkaoui Jaouad, Stéphanie Baert‐Desurmont, Karim Ouldim, Emmanuel So, Hakimova Durdona Tilloyevna, Thierry Frébourg, A. Sefiani	2012	5
10	Development of a Nonfluorescent Multiplex Semiquantitative Polymerase Chain Reaction to Confirm Rearrangements Detected by Array-Comparative Genomic Hybridization Genetic Testing and Molecular Biomarkers ·Vincent Huin, Nathalie Drouot, Pascal Chambon, Nathalie Le Meur, Thierry Frébourg, Mario Tosi, Pascale Saugier-Véber	2011	1
11	Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation European Journal of Human Genetics ·Pascale Saugier-Véber, Alice Goldenberg, Valérie Drouin‐Garraud, S.W. Song, Valérie Layet, Nathalie Drouot, Nathalie Le Meur, Brigitte Gilbert‐Dussardier, Géraldine Joly‐Hélas, Hélène Moirot, Annick Rossi, Mario Tosi, Thierry Frébourg	2006	27
12	CORRECTION Journal of Medical Genetics ·洋一髙山, F. Charbonnier, Cosette Martin, Steve Marshall, Thierry Frébourg, Yahia Al Arabi, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2004	0
13	Inactivation of the RRB1-Pescadillo pathway involved in ribosome biogenesis induces chromosomal instability Oncogene ·Audrey Killian, Nathalie Le Meur, Richard Sesboüé, Jeannette Bourguignon, Gaëlle Bougeard, Julien Gautherot, Christian Bastard, Thierry Frébourg, Jean‐Michel Flaman	2004	58
14	Severe myoclonus‐dystonia syndrome associated with a novel epsilon‐sarcoglycan gene truncating mutation American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·孝治吉沢, Grégory Raux, Cécile Dumanchin, Guillaume Lefebvre, G Zorn, Alexis P. Rondon, Dominique Campion, D. Parain, Thierry Frébourg, Didier Hannequin	2003	32
15	TP63 gene mutation in ADULT syndrome European Journal of Human Genetics ·Jeanne Amiel, Gaëlle Bougeard, Christine Francannet, Valérie Raclin, Arnold Münnich, Stanislas Lyonnet, Thierry Frébourg	2001	69
16	A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease Human Mutation ·Grégory Raux, René Gantier, Cosette Martin, D. Onose, Alexis Brice, Thierry Frébourg, Dominique Campion	2000	17
17	No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients Schizophrenia Research ·Florence Thibaut, Margarida de Freitas Soares Pinto, Didier Hannequin, T R Nuriev, Cosette Martin, Sonia Dollfus, Dominique Campion, Thierry Frébourg, Michel Petit	1998	22
18	Formes autosomiques dominantes Thierry Frébourg, Cécile Dumanchin, Dominique Campion	1997	1
19	An Sp1 Binding Site and the Minimal Promoter Contribute to Overexpression of the Cytokeratin 18 Gene in Tumorigenic Clones Relative to That in Nontumorigenic Clones of a Human Carcinoma Cell Line Molecular and Cellular Biology ·Yanti Sibarani, Thierry Frébourg, Rahiska Tisa Agustin, Славов.В., Г. М. Магомедова, Christian Lavialle, Olivier Brison	1995	30
20	The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease Genomics ·Dominique Campion, Cosette Martin, Roland Heilig, Françoise Charbonnier, Viviane Moreau, Jean‐Michel Flaman, Jean‐Louis Petit, Didier Hannequin, Alexis Brice, Thierry Frébourg	1995	79

About Thierry Frébourg

Thierry Frébourg is a scholar working on Oncology, Pathology and Forensic Medicine, Cancer Research, Genetics and Molecular Biology, having authored 276 papers that have together received 14.1k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (52 papers), Cancer-related Molecular Pathways (48 papers), Alzheimer's disease research and treatments (42 papers), Cancer Genomics and Diagnostics (37 papers), Genomic variations and chromosomal abnormalities (30 papers), Colorectal Cancer Treatments and Studies (21 papers), RNA Research and Splicing (17 papers) and Epigenetics and DNA Methylation (16 papers). The work is most often cited by research in Cancer Research (2.5k citations), Oncology (4.5k citations), Pathology and Forensic Medicine (2.2k citations), Neurology (1.7k citations) and Physiology (2.5k citations). Thierry Frébourg has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Dominique Campion, Didier Hannequin, Alexis Brice, Cosette Martin, Grégory Raux, Jean‐Michel Flaman, Cécile Dumanchin, Anne Rovelet‐Lecrux, F. Charbonnier and Laurence Brugières. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, Journal of Clinical Oncology, Journal of Medical Genetics and International Journal of 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.

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