Dominique Stoppa‐Lyonnet

Active 1987–2025

Also published as
Dominique Stoppa-Lyonnet · Dominique Stoppa Lyonnet
128
Papers
28,599
Citations
81
h-index
125
i10-index

Citations

Citations per year for Dominique Stoppa‐Lyonnet1945: 1 citations1988: 3 citations1989: 1 citations1990: 4 citations1991: 14 citations1992: 6 citations1993: 7 citations1994: 4 citations1995: 2 citations1996: 29 citations1997: 66 citations1998: 59 citations1999: 70 citations2000: 100 citations2001: 120 citations2002: 135 citations2003: 98 citations2004: 174 citations2005: 228 citations2006: 198 citations2007: 195 citations2008: 188 citations2009: 178 citations2010: 216 citations2011: 208 citations2012: 169 citations2013: 216 citations2014: 226 citations2015: 198 citations2016: 238 citations2017: 225 citations2018: 214 citations2019: 782 citations2020: 862 citations2021: 781 citations2022: 581 citations2023: 354 citations2024: 725 citations2025: 279 citations2026: 6 citations1946–1987: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,206 citing papers, 23.1% of this breakdownUnited Kingdom: 1,194 citing papers, 8.6% of this breakdownFrance: 864 citing papers, 6.2% of this breakdownGermany: 798 citing papers, 5.7% of this breakdownCanada: 661 citing papers, 4.8% of this breakdownItaly: 623 citing papers, 4.5% of this breakdownAustralia: 563 citing papers, 4% of this breakdownNetherlands: 502 citing papers, 3.6% of this breakdownChina: 478 citing papers, 3.4% of this breakdownSpain: 426 citing papers, 3.1% of this breakdownSweden: 299 citing papers, 2.2% of this breakdownJapan: 282 citing papers, 2% of this breakdown
0%23.1%Other 28.8%

Fields

  • Biochemistry, Genetics and Molecular Biology59.1%
  • Medicine33.4%
  • Immunology and Microbiology4.3%
  • Neuroscience1%
  • Computer Science0.7%
  • Agricultural and Biological Sciences0.5%
  • Other1%

Topics

  • BRCA gene mutations in cancer10.6%
  • DNA Repair Mechanisms5%
  • Cancer Genomics and Diagnostics4%
  • CRISPR and Genetic Engineering4%
  • PARP inhibition in cancer therapy3.6%
  • Genetic factors in colorectal cancer3%
  • Other69.8%

Coauthors

All papers

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  1. Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jean‐Pierre Fricker, Laurence Faivre, Pascaline Berthet, Maartje J. Hooning, Lizet E. van der Kolk, Carolien M. Kets, Muriel A. Adank, Esther M. John, Wendy K. Chung, Irene L. Andrulis, Melissa C. Southey, Mary B. Daly, Saundra S. Buys, Ana Osório, Christoph Engel, Karin Kast, Rita K. Schmutzler, Trinidad Caldés, Anna Jakubowska, Jacques Simard, Michael Friedländer, Sue‐Anne McLachlan, Eva Macháčková, Lenka Foretová, Yen Y. Tan, Christian F. Singer, Edith Oláh, Anne‐Marie Gerdes, Brita Arver, Håkan Olsson - JAMA 2017 cited by 2,863

  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. Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers

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

  4. The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrew R. Gennery, Sofia Grigoriadou, Steven M. Holland, Gritta Janka, Maria Kanariou, Christoph Klein, Helen J. Lachmann, Desa Lilić, Ania Manson, N. Pascual Martínez, Isabelle Meyts, Nicolette Moes, Despina Moshous, Bénédicte Neven, Hans D. Ochs, Capucine Pïcard, Ellen D. Renner, Frédéric Rieux‐Laucat, Reinhard Seger, Annarosa Soresina, Dominique Stoppa‐Lyonnet, Vojtěch Thon, Adrian J. Thrasher, Frank L. van de Veerdonk, Anna Villa, Corry M.R. Weemaes, Klaus Warnatz, Beata M. Wolska, Shen-Yin Zhang - The Journal of Allergy and Clinical Immunology In Practice 2019 cited by 621

  5. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tanja N. Fehm, Florentia Fostira, George Fountzilas, Megan Frone, Vanesa Garcia-Barberan, Pilar Garre, Marion Gauthier-Villars, Andrea Gehrig, Gord Glendon, David E. Goldgar, Lisa Golmard, Mark H. Greene, Eric Hahnen, Ute Hamann, Helen Hanson, Tiara Hassan, Julia Hentschel, Judit Horvath, Louise Izatt, Ramunas Janavicius, Yue Jiao, Esther M. John, Beth Y. Karlan, Sung-Won Kim, Irene Konstantopoulou, Ava Kwong, Anthony Laugé, Jong Won Lee, Fabienne Lesueur, Noura Mebirouk, Alfons Meindl, Emmanuelle Mouret-Fourme, Hannah Musgrave, Joanne Ngeow Yuen Yie, Dieter Niederacher, Sue K. Park, Inge Sokilde Pedersen, Juliane Ramser, Susan J. Ramus, Johanna Rantala, Muhammad U. Rashid, Florian Reichl, Julia Ritter, Andreas Rump, Marta Santamariña, Claire Saule, Gunnar Schmidt, Rita K. Schmutzler, Leigha Senter, Saba Shariff, Christian F. Singer, Melissa C. Southey, Dominique Stoppa-Lyonnet, Christian Sutter, Yen Tan, Soo Hwang Teo, Mary Beth Terry, Mads Thomassen, Marc Tischkowitz, Amanda E. Toland, Diana Torres, Ana Vega, Sebastian A. Wagner, Shan Wang-Gohrke, Barbara Wappenschmidt, Bernhard H. F. Weber, Drakoulis Yannoukakos, Amanda B. Spurdle, Douglas F. Easton, Georgia Chenevix-Trench and 2 more - Journal of Clinical Oncology 2022 cited by 275

  6. Ploidy and Large-Scale Genomic Instability Consistently Identify Basal-like Breast Carcinomas with BRCA1/2 Inactivation

    Authors: , , , , , , , , , , , , , , - Cancer Research 2012 cited by 681

  7. Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1 / 2 (CIMBA)

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Monica Barile, Sara Volorio, Barbara Pasini, Riccardo Dolcetti, Anna Laura Putignano, Laura Ottini, Paolo Radice, Ute Hamann, Muhammad Usman Rashid, Frans B.L. Hogervorst, Mieke Kriege, Rob B. van der Luijt, Susan Peock, Debra Frost, D. Gareth Evans, Carole Brewer, Lisa Walker, Mark T. Rogers, Lucy Side, Catherine Houghton, JoEllen Weaver, Andrew K. Godwin, Rita K. Schmutzler, Barbara Wappenschmidt, Alfons Meindl, Karin Kast, Norbert Arnold, Dieter Niederacher, Christian Sutter, Helmut Deißler, Doroteha Gadzicki, Sabine Preisler‐Adams, Raymonda Varon-Mateeva, Ines Schönbuchner, Heidrun Gevensleben, Dominique Stoppa‐Lyonnet, Muriel Belotti, Laure Barjhoux, Claudine Isaacs, Beth N. Peshkin, Trinidad Caldés, Miguel de la Hoya, Carmen Cañadas, Tuomas Heikkinen, Päivi Heikkilä, Kristiina Aittomäki, Ignacio Blanco, Conxi Lázaro, Joan Brunet, Bjarni A. Agnarsson, Aðalgeir Arason, Rósa B. Barkardóttir, Martine Dumont, Jacques Simard, Marco Montagna, Simona Agata, Emma D’Andrea, Max Yan, Stephen B. Fox, Timothy R. Rebbeck, Wendy S. Rubinstein, Nadine Tung, Judy E. Garber, Xianshu Wang, Zachary Fredericksen, V. Shane Pankratz, Noralane M. Lindor, Csilla I. Szabo, Kenneth Offit, Rita A. Sakr and 33 more - Cancer Epidemiology Biomarkers & Prevention 2012 cited by 668

  8. Deep learning identifies morphological patterns of homologous recombination deficiency in luminal breast cancers from whole slide images

    Authors: , , , , , , , , , - Cell Reports Medicine 2022 cited by 75

  9. Comprehensive Study of the Clinical Phenotype of GermlineBAP1Variant-Carrying Families Worldwide

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Luca Mastracci, Karin Wadt, Jens Folke Kiilgaard, Michael R. Speicher, Natasha M. van Poppelen, Emine Kılıç, Rana’a T. Al‐Jamal, Irma Dianzani, Marta Betti, Carsten Bergmann, Sandro Santagata, Sonika Dahiya, Saleem Taibjee, Jo Burke, Nicola Poplawski, Sally J. O’Shea, Julia Newton‐Bishop, Julian Adlard, David J. Adams, Anne-Marie Lane, Ivana K. Kim, Sonja Klebe, Hilary Racher, J. William Harbour, Michael L. Nickerson, Rajmohan Murali, Jane M. Palmer, Madeleine Howlie, Judith Symmons, Hayley R. Hamilton, Sunil Warrier, William Glasson, Peter A. Johansson, Carla Daniela Robles‐Espinoza, Raúl Ossio, Annelies de Klein, Susana Puig, Paola Ghiorzo, Maartje Nielsen, Tero Kivelä, Hensin Tsao, Joseph R. Testa, Pedram Gerami, Marc‐Henri Stern, Brigitte Bressac–de Paillerets, Mohamed H. Abdel‐Rahman, Nicholas K. Hayward - JNCI Journal of the National Cancer Institute 2018 cited by 241

  10. Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , N E Haites, Rodney J. Scott, C.M. Maugard, Hans F. A. Vasen, Susanne Seitz, Lisa Cannon‐Albright, Andrew Craig Schofield, M Zelada-Hedman - The American Journal of Human Genetics 1998 cited by 3,047

  11. Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michèle Souyri, Francina Langa Vives, Aarón Méndez-Bermúdez, Hélène Lapillonne, Étienne Lengliné, Emmanuel Raffoux, Pierre Fenaux, Lionel Adès, Édouard Forcade, Charlotte Jubert, Carine Domenech, Marion Strullu, Bénedicte Bruno, Nimrod Buchbinder, Caroline Thomas, Arnaud Petit, Guy Leverger, Gérard Michel, Marina Cavazzana, Éliane Gluckman, Yves Bertrand, Nicolas Boissel, André Baruchel, Jean‐Hugues Dalle, Emmanuelle Clappier, Éric Gilson, Ludovic Deriano, Sylvie Chevret, François Sigaux, Gèrard Socié, Dominique Stoppa‐Lyonnet, Hugues de Thé, Christophe Antoniewski, Dominique Bluteau, Régis Peffault de Latour, Jean Soulier - Cell stem cell 2023 cited by 75

  12. A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sophie Gad, Stéphane Richard, Jérôme Couturier, Bin Tean Teh, Paola Ghiorzo, Lorenza Pastorino, Susana Puig, Célia Bádenas, Håkan Olsson, Christian Ingvar, Etienne Rouleau, Rosette Lidereau, Philippe Bahadoran, Philippe Vielh, Eve Corda, Hélène Blanché, Diana Zélénika, Pilar Galán, The French Familial Melanoma Study Group, F. Aubin, Bertrand Bachollet, Céline Becuwe, Pascaline Berthet, Yves Jean Bignon, Valérie Bonadona, Jean‐Louis Bonafé, Marie‐Noëlle Bonnet‐Dupeyron, F. Cambazard, J. Chevrant‐Breton, Isabelle Coupier, S. Dalac, Liliane Demange, M. D’Incan, Catherine Dugast, Laurence Faivre, Lynda Vincent-Fétita, Marion Gauthier-Villars, Brigitte Gilbert, Florent Grange, Jean‐Jacques Grob, Philippe Humbert, Nicolas Janin, Pascal Joly, Delphine Kérob, Christine Lasset, Dominique Leroux, J. Levang, Jean‐Marc Limacher, C. Bulaï Livideanu, Michel Longy, Alain Lortholary, Dominique Stoppa-Lyonnet, Sandrine Mansard, L Mansuy, Karine Marrou, Christine Matéus, Christine Maugard, Nicolás Meyer, Catherine Noguès, P Souteyrand, Laurence Venat‐Bouvet, Hélène Zattara, Valérie Chaudru, Gilbert Lenoir, Mark Lathrop, Irwin Davidson, Marie-Françoise Avril, Florence Démenais, Robert Ballotti, Brigitte Bressac–de Paillerets - Nature 2011 cited by 522

  13. A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Céline Vallot, Livia Lumbroso-Le Rouïc, Alexandre Matet, Laurence Desjardins, Guillem Pascual‐Pasto, Mariona Suñol, Jaume Mora, Genoveva Correa Llano, Jérôme Couturier, Emmanuel Barillot, Paula Schaiquevich, Marion Gauthier‐Villars, Dominique Stoppa‐Lyonnet, Lisa Golmard, Claude Houdayer, Hervé J. Brisse, Isabelle Bernard‐Pierrot, Éric Letouzé, Alain Viari, Simon Saule, Xavier Sastre‐Garau, François Doz, Ángel M. Carcaboso, Nathalie Cassoux, Célio Pouponnot, Olivier Goureau, Guillermo Chantada, Aurélien de Reyniès, Isabelle Aerts, François Radvanyi - Nature Communications 2021 cited by 106

  14. ShallowHRD: detection of homologous recombination deficiency from shallow whole genome sequencing

    Authors: , , , , , , , , , , , - Bioinformatics, Bioinform. 2020 cited by 73

  15. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joan Brunet, Saundra S. Buys, Trinidad Caldés, Maria A. Caligo, Ian Campbell, Lise Lotte Christensen, Wendy K. Chung, Kathleen Claes, Chrystelle Colas, Pascaline Berthet, Chrystelle Colas, Marie‐Agnès Collonge‐Rame, Capucine Delnatte, Laurence Faivre, Sophie Giraud, Christine Lasset, Véronique Mari, Noura Mebirouk, Emmanuelle Mouret‐Fourme, Hélène Schuster, Dominique Stoppa‐Lyonnet, Julian Adlard, Munaza Ahmed, Antonis C. Antoniou, Daniel Barrowdale, Paul Brennan, Carole Brewer, Jackie Cook, Rosemarie Davidson, Douglas F. Easton, Rosalind A. Eeles, D. Gareth Evans, Debra Frost, Helen Hanson, Louise Izatt, Kai-Ren Ong, Lucy Side, Aoife O’Shaughnessy-Kirwan, Marc Tischkowitz, Lisa Walker, Marie‐Agnès Collonge‐Rame, Jackie Cook, Mary B. Daly, Rosemarie Davidson, Miguel de la Hoya, Robin De Putter, Capucine Delnatte, Peter Devilee, Orland Dı́ez, Yuan Chun Ding, Susan M. Domchek, Cecilia M. Dorfling, Martine Dumont, Rosalind A. Eeles, Bent Ejlertsen, Christoph Engel, D. Gareth Evans, Laurence Faivre, Lenka Foretová, Florentia Fostira, Michael Friedländer, Eitan Friedman, Debra Frost, Patricia A. Ganz, Judy E. Garber, Andrea Gehrig, Anne‐Marie Gerdes, Paul Gesta, Sophie Giraud, Gord Glendon and 139 more - Genetics in Medicine 2020 cited by 145

  16. BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Robert L. Nussbaum, Kenneth Offit, Sharon E. Plon, Jem Rashbass, Heidi L. Rehm, Mark E. Robson, Wendy S. Rubinstein, Dominique Stoppa‐Lyonnet, Sean V. Tavtigian, Adrian Thorogood, Can Zhang, Marc Zimmermann, BRCA Challenge Authors, John Burn, Stephen J. Chanock, Gunnar Rätsch, Amanda B. Spurdle - PLoS Genetics 2018 cited by 210

  17. Shallow whole genome sequencing approach to detect Homologous Recombination Deficiency in the PAOLA-1/ENGOT-OV25 phase-III trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Oncogene 2023 cited by 31

  18. Sensitivity and predictive value of criteria for p53germline mutation screening

    Authors: , , , , , , - Journal of Medical Genetics 2001 cited by 342

  19. Incidence, Presentation, and Prognosis of Malignancies in Ataxia-Telangiectasia: A Report From the French National Registry of Primary Immune Deficiencies

    Authors: , , , , , , , , , - Journal of Clinical Oncology 2014 cited by 251

  20. Molecular basis of the Li–Fraumeni syndrome: an update from the French LFS families

    Authors: , , , , , , , , , , , - Journal of Medical Genetics 2008 cited by 226

  21. Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia

    Authors: , , , , , , , , , - Genetics in Medicine 2017 cited by 80

  22. The biological effects and clinical implications of BRCA mutations: where do we go from here?

    Authors: - European Journal of Human Genetics 2016 cited by 115

  23. Identification of six new susceptibility loci for invasive epithelial ovarian cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Cecilia M. Dorfling, Elizabeth J. van Rensburg, Susan L. Neuhausen, Yuan Chun Ding, Thomas van Overeem Hansen, Lars Jønson, Anne‐Marie Gerdes, Bent Ejlertsen, Daniel Barrowdale, Joe Dennis, Javier Benı́tez, Ana Osório, María J. García, Ian K. Komenaka, Jeffrey N. Weitzel, Pamela Ganschow, Paolo Peterlongo, Loris Bernard, Alessandra Viel, Bernardo Bonanni, Bernard Peissel, Siranoush Manoukian, Paolo Radice, Laura Papi, Laura Ottini, Florentia Fostira, Irene Konstantopoulou, Judy E. Garber, Debra Frost, Jo Perkins, Radka Platte, Steve Ellis, Andrew K. Godwin, Rita K. Schmutzler, Alfons Meindl, Christoph Engel, Christian Sutter, Olga M. Sinilnikova, Francesca Damiola, Sylvie Mazoyer, Dominique Stoppa‐Lyonnet, Kathleen Claes, Kim De Leeneer, Judy Kirk, Gustavo C. Rodriguez, Marion Piedmonte, David M. O’Malley, Miguel de la Hoya, Trinidad Caldés, Kristiina Aittomäki, Heli Nevanlinna, Margriet Collée, Matti A. Rookus, Jan C. Oosterwijk, Laima Tihomirova, Nadine Tung, Ute Hamann, Claudine Isaccs, Marc Tischkowitz, Evgeny N. Imyanitov, Maria A. Caligo, Ian Campbell, Frans B.L. Hogervorst, Edith Oláh, Orland Dı́ez, Ignacio Blanco, Joan Brunet, Conxi Lázaro, Miquel Angel Pujana, Anna Jakubowska and 196 more - Nature Genetics 2015 cited by 262

  24. Adaptive nanopore sequencing to determine pathogenicity ofBRCA1exonic duplication

    Authors: , , , , , , , , , , , , , , , , - Journal of Medical Genetics 2023 cited by 23