Olivier Caron - Concepedia

Author

Olivier Caron

Also Known As

Antoniou, Antonis C, BCFR, Bertrand Cariou, Brigitte Bressac-de Paillerets, Brigitte Bressac-de-Paillerets, Caron, O., Caron, Olivier, Caron, Olivier M.D., Christine Lasset, Claude Desrochers

249

Publications

8.6K

Citations

H-Index

Concepts

All Affiliations

Institut Gustave Roussy Inserm Institut Curie Université Paris Cité Assistance Publique – Hôpitaux de Paris

About

Olivier Caron is an author at Institut Gustave Roussy specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	23	1.8K
2	Health Sciences	3	3	128
3	Public Health	3	3	161
4	Behavioral Sciences	1	1	20
5	Biostatistics	1	1	29

Olivier Caron

Publications

5.2K

Citations

H-Index

Page 1

	Year	Citations
Revisiting Li-Fraumeni Syndrome From <i>TP53</i> Mutation Carriers Gaëlle Bougeard, Mariette Renaux‐Petel, Jean‐Michel Flaman, Journal of Clinical Oncology	2015	719
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Nature Somatic VariantGeneticsMelanomaRenal CarcinomaPathology	2011	513
High cumulative risks of cancer in patients with <i>PTEN</i> hamartoma tumour syndrome Virginie Bubien, Françoise Bonnet, Véronique Brouste, Journal of Medical Genetics	2013	358
Germline BAP1 Mutations Predispose to Renal Cell Carcinomas Tatiana Popova, Lucie Hebert, Virginie Jacquemin, The American Journal of Human Genetics UrologySomatic VariantGenitourinary CancerRenal Cell CarcinomasPathology	2013	272
Radio-induced malignancies after breast cancer postoperative radiotherapy in patients with Li-Fraumeni syndrome S. Heymann, Suzette Delaloge, Arslane Skander Rahal, Radiation Oncology	2010	204
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D) Hans F. A. Vasen, Zeinab Ghorbanoghli, Franck Bourdeaut, Journal of Medical Genetics	2014	199
<i>CDH1</i> germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study Patrick R. Benusiglio, David Malka, Étienne Rouleau, Journal of Medical Genetics	2013	148
Novel <i>FH</i> mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma Betty Gardie, Audrey Remenieras, Darouna Kattygnarath, Journal of Medical Genetics	2011	140
Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotype Valérie Biancalana, Olivier Caron, Sabina Gallati, Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyMedicine	2003	118
High Frequency of Germline <i>SUFU</i> Mutations in Children With Desmoplastic/Nodular Medulloblastoma Younger Than 3 Years of Age Laurence Brugières, Audrey Remenieras, Gaëlle Pierron, Journal of Clinical Oncology	2012	116

Page 1