Thierry Frébourg

Active 1986–2024

134
Papers
28,401
Citations
90
h-index
134
i10-index

Citations

Citations per year for Thierry Frébourg1972: 1 citations1988: 1 citations1989: 1 citations1990: 4 citations1991: 3 citations1992: 2 citations1993: 3 citations1994: 5 citations1995: 12 citations1996: 30 citations1997: 33 citations1998: 37 citations1999: 58 citations2000: 69 citations2001: 54 citations2002: 82 citations2003: 72 citations2004: 117 citations2005: 154 citations2006: 167 citations2007: 162 citations2008: 189 citations2009: 221 citations2010: 269 citations2011: 254 citations2012: 226 citations2013: 211 citations2014: 202 citations2015: 236 citations2016: 262 citations2017: 315 citations2018: 267 citations2019: 774 citations2020: 820 citations2021: 820 citations2022: 602 citations2023: 479 citations2024: 855 citations2025: 340 citations2026: 7 citations1973–1987: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,275 citing papers, 25.2% of this breakdownUnited Kingdom: 979 citing papers, 7.5% of this breakdownFrance: 968 citing papers, 7.5% of this breakdownGermany: 833 citing papers, 6.4% of this breakdownChina: 704 citing papers, 5.4% of this breakdownItaly: 690 citing papers, 5.3% of this breakdownCanada: 500 citing papers, 3.9% of this breakdownNetherlands: 488 citing papers, 3.8% of this breakdownAustralia: 402 citing papers, 3.1% of this breakdownSpain: 384 citing papers, 3% of this breakdownJapan: 362 citing papers, 2.8% of this breakdownBelgium: 298 citing papers, 2.3% of this breakdown
0%25.2%Other 23.8%

Fields

  • Medicine58.7%
  • Biochemistry, Genetics and Molecular Biology32.4%
  • Neuroscience4%
  • Immunology and Microbiology2.9%
  • Computer Science0.4%
  • Engineering0.4%
  • Other1.2%

Topics

  • Alzheimer's disease research and treatments5.1%
  • Genetic factors in colorectal cancer3.4%
  • Cancer Genomics and Diagnostics3.2%
  • Virus-based gene therapy research2.8%
  • Cancer Immunotherapy and Biomarkers2.4%
  • CRISPR and Genetic Engineering2.3%
  • Other80.8%

Coauthors

All papers

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  1. Soft tissue and visceral sarcomas: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up☆

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Rick L. Haas, A.B. Hassan, Stefanie Hecker‐Nolting, Nadia Hindi, Peter Hohenberger, Heikki Joensuu, Robin L. Jones, Christiane Jungels, Paul C. Jutte, Leo Kager, Bernd Kasper, Akira Kawai, Kateřina Kopečková, Dagmar Adámková Krákorová, Axel Le Cesne, Franel Le Grange, Eric Legius, Andreas Leithner, Antonio López–Pousa, Javier Martín‐Broto, Ofer Merimsky, Christina Messiou, Olivier Mir, Michael Montemurro, Bruce Morland, Carlo Morosi, Emanuela Palmerini, Maria A. Pantaleo, Raimondo Piana, Sophie Piperno‐Neumann, Peter Reichardt, Piotr Rutkowski, Akmal Safwat, Claudia Sangalli, Marta Sbaraglia, Susanne Scheipl, Patrick Schöffski, Stefan Sleijfer, D. Strauß, Sandra J. Strauss, Kirsten Sundby Hall, Annalisa Trama, Mojca Unk, Michiel A. J. van de Sande, Winette T.A. van der Graaf, Winan J. van Houdt, Thierry Frébourg, Paolo G. Casali, Silvia Stacchiotti - Annals of Oncology 2021 cited by 989

  2. LMO2 -Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Claudia Prinz, Terence H. Rabbitts, Françoise Le Deist, Alain Fischer, Marina Cavazzana - Science 2003 cited by 3,561

  3. Integrative Analyses of Colorectal Cancer Show Immunoscore Is a Stronger Predictor of Patient Survival Than Microsatellite Instability

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jean‐Baptiste Latouche, Jérôme Galon - Immunity 2016 cited by 1,068

  4. Bone sarcomas: ESMO–EURACAN–GENTURIS–ERN PaedCan Clinical Practice Guideline for diagnosis, treatment and follow-up

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alessandro Gronchi, Rick L. Haas, A.B. Hassan, Stefanie Hecker‐Nolting, Nadia Hindi, Peter Hohenberger, Heikki Joensuu, Robin L. Jones, Christiane Jungels, Paul C. Jutte, Leo Kager, Bernd Kasper, Akira Kawai, Kateřina Kopečková, Dagmar Adámková Krákorová, Axel Le Cesne, Franel Le Grange, Eric Legius, Andreas Leithner, A. López Pousa, Javier Martín‐Broto, Ofer Merimsky, Christina Messiou, Aisha Miah, Olivier Mir, Michael Montemurro, Bruce Morland, Carlo Morosi, Emanuela Palmerini, Maria A. Pantaleo, Raimondo Piana, Sophie Piperno‐Neumann, Peter Reichardt, Piotr Rutkowski, Akmal Safwat, Claudia Sangalli, Marta Sbaraglia, Susanne Scheipl, Patrick Schöffski, Stefan Sleijfer, D. Strauß, Kirsten Sundby Hall, Annalisa Trama, Mojca Unk, Michiel A. J. van de Sande, Winette T.A. van der Graaf, Winan J. van Houdt, Thierry Frébourg, Ruth Ladenstein, Paolo G. Casali, Silvia Stacchiotti - Annals of Oncology 2021 cited by 455

  5. Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vanessa L. Merker, Miriam J. Smith, David A. Stevenson, Monique Anten, Arthur S. Aylsworth, Diana Baralle, S. Barbarot, Fred G. Barker, Shay Ben‐Shachar, Amanda L. Bergner, D. Bessis, Ignacio Blanco, Cathérine Cassiman, Patricia Ciavarelli, Maurizio Clementi, Thierry Frébourg, Marco Giovannini, Dorothy Halliday, Chris Hammond, C. Oliver Hanemann, Helen Hanson, Arvid Heiberg, K.H. Ly, Michel Kalamarides, Matthias A. Karajannis, Daniela Kroshinsky, Margarita Larralde, Conxi Lázaro, Lu Q. Le, Michael P. Link, Robert Listernick, Mia MacCollin, Conor Mallucci, Christopher L. Moertel, Amy Mueller, Joanne Ngeow, Rianne Oostenbrink, Roger J. Packer, Laura Papi, Allyson Parry, Juha Peltonen, Dominique C. Pichard, Bruce Poppe, Nilton Alves de Rezende, Luiz Oswaldo Carneiro Rodrigues, Tena Rosser, Martino Ruggieri, Eduard Serra, Verena Steinke‐Lange, Stavros Stivaros, Amy Taylor, Jaan Toelen, James H. Tonsgard, Eva Trevisson, Meena Upadhyaya, Ali Varan, Meredith Wilson, Hao Wu, Gelareh Zadeh, Susan Huson, D. Gareth Evans, Scott R. Plotkin - Genetics in Medicine 2021 cited by 771

  6. Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers

    Authors: , , , , , , , , , , , , , , , , , - Journal of Clinical Oncology 2015 cited by 753

  7. Gastrointestinal stromal tumours: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Heikki Joensuu, Robin L. Jones, Christiane Jungels, Paul C. Jutte, Bernd Kasper, Akira Kawai, Kateřina Kopečková, Dagmar Adámková Krákorová, Axel Le Cesne, Franel Le Grange, Eric Legius, Andreas Leithner, Antonio López–Pousa, Javier Martín‐Broto, Ofer Merimsky, Christina Messiou, Aisha Miah, Olivier Mir, Michael Montemurro, Carlo Morosi, Emanuela Palmerini, Maria A. Pantaleo, Raimondo Piana, Sophie Piperno‐Neumann, Peter Reichardt, Piotr Rutkowski, Akmal Safwat, Claudia Sangalli, Marta Sbaraglia, S. Scheipl, Patrick Schöffski, Stefan Sleijfer, D. Strauß, Sandra J. Strauss, Kirsten Sundby Hall, Annalisa Trama, Mojca Unk, Michiel A. J. van de Sande, Winette T.A. van der Graaf, Winan J. van Houdt, Thierry Frébourg, Alessandro Gronchi, Silvia Stacchiotti - Annals of Oncology 2021 cited by 563

  8. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

    Authors: , , , , , , , , , , , , - Nature Genetics 2005 cited by 1,253

  9. Guidelines for the Li–Fraumeni and heritable TP53-related cancer syndromes

    Authors: , , , , , - European Journal of Human Genetics 2020 cited by 329

  10. Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , - Clinical Cancer Research 2017 cited by 521

  11. Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Arthur S. Aylsworth, Diana Baralle, S. Barbarot, Fred G. Barker, Shay Ben‐Shachar, Amanda L. Bergner, D. Bessis, Ignacio Blanco, Cathérine Cassiman, Patricia Ciavarelli, Maurizio Clementi, Thierry Frébourg, Alicia Gomes, Dorothy Halliday, Chris Hammond Helen Hanson Arvid Heiberg, K.H. Ly, Justin T. Jordan, Matthias A. Karajannis, Daniela Kroshinsky, Margarita Larralde, Conxi Lázaro, Lu Q. Le, Michael P. Link, Robert Listernick, Conor Mallucci, Vanessa L. Merker, Christopher L. Moertel, Amy Mueller, Joanne Ngeow, Rianne Oostenbrink, Roger J. Packer, Allyson Parry, Juha Peltonen, Dominique C. Pichard, Bruce Poppe, Nilton Alves de Rezende, Luiz Oswaldo Carneiro Rodrigues, Tena Rosser, Martino Ruggieri, Eduard Serra, Verena Steinke‐Lange, Stavros Stivaros, Amy Taylor, Jaan Toelen, James H. Tonsgard, Eva Trevisson, Meena Upadhyaya, Ali Varan, Meredith Wilson, Hao Wu, Gelareh Zadeh, Susan Huson, P. Wolkenstein, D. Gareth Evans - Genetics in Medicine 2022 cited by 276

  12. Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

    Authors: , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 1999 cited by 788

  13. Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood

    Authors: , , , , , , - Clinical Cancer Research 2017 cited by 221

  14. High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2012 cited by 318

  15. Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Raj Ramesar, Lene Juel Rasmussen, Brigitte Royer‐Pokora, Rodney J. Scott, Rolf H. Sijmons, Sean V. Tavtigian, Carli M.J. Tops, Thomas Weber, Juul Wijnen, Michael O. Woods, Finlay Macrae, Maurizio Genuardi - Nature Genetics 2013 cited by 476

  16. Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification

    Authors: , , , , , , , , , , , , , , , , , , , , , - Neurology 2012 cited by 277

  17. Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma

    Authors: , , , , , , , , , , , , , , , - Nature 2008 cited by 898

  18. Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dominique Campion, Didier Hannequin, the French IBGC study group, Patrick Ahtoy, Mathieu Anheim, Jérôme Augustin, Xavier Ayrignac, Françoise Billé-Turc, Dominique Campion, Boris Chaumette, Michel Clanet, Luc Defebvre, Gilles Defer, Nathalie Derache, Mira Didic, Franck Durif, Emmanuel Flamand‐Roze, Guillaume Fromager, Maurice Giroud, Alice Goldenberg, Olivier Guillin, Lucie Guyant‐Maréchal, Didier Hannequin, Cécile Hubsch, Snejana Jurici, Pierre Krystkowiak, Pierre Labauge, Antoine Layet, Isabelle Le Ber, Thibaud Lebouvier, Romain Lefaucheur, David Maltête, Olivier Martinaud Donald Morcamp, Gaël Nicolas, Özlem Özkul, Jérémie Pariente, Cyril Pottier, Philippe Rondepierre, Olivier Rouaud, B Salle, Mathilde Sauvée, S. Schaeffer, Christel Thauvin-Robinet, Catherine Thomas-Antérion, Christine Tranchant, Aude Triquenot, Yvan Vaschalde, Marc Vérin, Christophe Verny, Marie Vidailhet, David Wallon - Brain 2013 cited by 233

  19. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Didier Hannequin, Dominique Campion, David Wallon, Olivier Martinaud, Aline Zaréa, Gaël Nicolas, Adeline Rollin‐Sillaire, Stéphanie Bombois, Marie‐Anne Mackowiak, Vincent Deramecourt, Florence Pasquier, Agnès Michon, Isabelle Le Ber, Bruno Dubois, Olivier Godefroy, Frédérique Etcharry‐Bouyx, Valérie Chauviré, Ludivine Chamard, Eric Berger, Éloi Magnin, Jean‐François Dartigues, Sophie Auriacombe, François Tison, Vincent de la Sayette, Dominique Castan, Elsa Dionet, François Sellal, Olivier Rouaud, Christel Thauvin, Olivier Moreaud, Mathilde Sauvée, Maïté Formaglio, Hélène Mollion, Isabelle Roullet‐Solignac, Alain Vighetto, Bernard Croisile, Mira Didic, Olivier Félician, Lejla Koric, Mathieu Ceccaldi, Audrey Gabelle, Cécilia Marelli, Pierre Labauge, Thérèse Jonveaux, Martine Vercelletto, Claire Boutoleau‐Bretonnière, Giovanni Castelnovo, Claire Paquet, Julien Dumurgier, Jacques Hugon, Foucauld De Boisgueheneuc, Serge Belliard, Serge Bakchine, Marie Sarazin, Marie‐Odile Barrellon, Bernard Laurent, Frédéric Blanc, Jérémie Pariente, Snejana Jurici - Neurobiology of Aging 2017 cited by 170

  20. Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emma R. Woodward, Marc Tischkowitz, Eamonn R. Maher, Rosalie E. Ferner, Stefan Aretz, Isabel Spier, Verena Steinke‐Lange, Elke Holinski‐Feder, Evelin Schröck, Thierry Frébourg, Claude Houdayer, Chrystelle Colas, P. Wolkenstein, Vincent Bours, Eric Legius, Bruce Poppe, Kathleen Claes, Robin De Putter, Ignacio Blanco Guillermo, Gabriel Capellá, Joan Brunet Vidal, Conxi Lázaro, Judith Balmañà, Hector Salvador Hernandez, Carla Oliveíra, Manuel R. Teixeira, Svetlana Bajalica‐Lagercrantz, Emma Tham, Jan Lubiński, Karolina Ertmańska, Béla Melegh, Mateja Krajc, Ana Blatnik, Sirkku Peltonen, Marja Hietala - European Journal of Human Genetics 2020 cited by 135

  21. Diagnostic value of CA19.9, circulating tumour DNA and circulating tumour cells in patients with solid pancreatic tumours

    Authors: , , , , , , , , , , , , , , , , , , , , , - British Journal of Cancer 2017 cited by 121

  22. Contribution of de novo and mosaic TP53 mutations to Li-Fraumeni syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Journal of Medical Genetics 2017 cited by 118

  23. Correlation between Density of CD8+ T-cell Infiltrate in Microsatellite Unstable Colorectal Cancers and Frameshift Mutations: A Rationale for Personalized Immunotherapy

    Authors: , , , , , , , , , , , , , , , , , , , , , - Cancer Research 2015 cited by 243

  24. SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dominique Campion, David Wallon, Olivier Martinaud, Gaël Nicolas, Olivier Godefroy, Frédérique Etcharry-Bouyx, Valérie Chauviré, Ludivine Chamard, Eric Berger, Eloi Magnin, Jean-Francois Dartigues, Sophie Auriacombe, Vincent de la Sayette, Fausto Viader, Dominique Castan, Elsa Dionet, Francois Sellal, Olivier Rouaud, Christel Thauvin, Olivier Moreaud, Mathilde Sauvée, Adeline Rollin-Sillaire, Stéphanie Bombois, Marie-Anne Mackowiak, Vincent Deramecourt, Florence Pasquier, Maïté Formaglio, Hélène Mollion, Isabelle Roullet-Solignac, Alain Vighetto, Bernard Croisile, Mira Didic, Olivier Félician, Lejla Koric, Mathieu Ceccaldi, Audrey Gabelle, Cecilia Marelli, Jacques Touchon, Pierre Labauge, Thérèse Jonveaux, Martine Vercelletto, Claire Boutoleau-Bretonnière, Giovanni Castelnovo, David Renaud, Philippe Robert, Claire Paquet, Julien Dumurgier, Jacques Hugon, Agnès Michon, Isabelle Le Ber, Bruno Dubois, Charles Duyckaerts, Foucauld De Boisgueheneuc, Serge Belliard, Serge Bakchine, Marie-Odile Barrellon, Bernard Laurent, Frédéric Blanc, Christine Tranchant, Jérémie Pariente, Michèle Puel, Caroline Hommet, Karl Mondon - Molecular Psychiatry 2015 cited by 134