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
Citation sources
Countries
Institutions
- Inserm1.1%
- Harvard University0.7%
- Memorial Sloan Kettering Cancer Center0.7%
- University of Cambridge0.6%
- University of Toronto0.6%
- Dana-Farber Cancer Institute0.6%
- Other95.7%
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
- Olga M. Sinilnikova20
- Lesley McGuffog16
- Marc‐Henri Stern15
- Claude Houdayer14
- Lisa Golmard14
- David E. Goldgar13
- Marion Gauthier‐Villars13
- Susan L. Neuhausen13
- Antonis C. Antoniou12
- Catherine Dubois d’Enghien12
- Daniel Barrowdale12
- Sue Healey11
- Anne Vincent‐Salomon10
- Fergus J. Couch10
- Irene L. Andrulis10
- Nadine Andrieu10
- Virginie Caux‐Moncoutier10
- Brigitte Bressac–de Paillerets9
- Chrystelle Colas9
- Olivier Delattre9
- Valérie Bonadona9
- Alain Fourquet8
- Catherine Dehainault8
- Olivier Caron8
All papers
- Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
Authors: Karoline Kuchenbaecker, John L. Hopper, Daniel R. Barnes, Kelly‐Anne Phillips, Thea M. Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E. van Leeuwen, Roger L. Milne, Nadine Andrieu, David E. Goldgar, Mary Beth Terry, Matti A. Rookus, Douglas F. Easton, Antonis C. Antoniou, Lesley McGuffog, D. Gareth Evans, Daniel Barrowdale, Debra Frost, Julian Adlard, Kai-Ren Ong, Louise Izatt, Marc Tischkowitz, Rosalind A. Eeles, Rosemarie Davidson, Shirley Hodgson, Steve Ellis, Catherine Noguès, Christine Lasset, Dominique Stoppa‐Lyonnet, 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
- LMO2 -Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1
Authors: S. Hacein-Bey-Abina, Christof von Kalle, Manfred Schmidt, Matthew P. McCormack, N. M. Wulffraat, Philippe Leboulch, Apiradee Lim, Cameron S. Osborne, Robert Pawliuk, Estelle Morillon, Ricardo U. Sorensen, A. Förster, Peter Fraser, J. I. Cohen, Geneviève de Saint Basile, Ian E. Alexander, Uwe Wintergerst, Thierry Frébourg, Alain Aurias, Dominique Stoppa‐Lyonnet, Serge Romana, I Radford-Weiss, Fabian Gross, F Valensi, Éric Delabesse, Elizabeth Macintyre, F Sigaux, Jean Soulier, Lily E. Leiva, Manuela Wissler, Claudia Prinz, Terence H. Rabbitts, Françoise Le Deist, Alain Fischer, Marina Cavazzana - Science 2003 cited by 3,561
- Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers
Authors: Gaëlle Bougeard, Mariette Renaux‐Petel, Jean‐Michel Flaman, Camille Charbonnier, Pierre Fermey, 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 - Journal of Clinical Oncology 2015 cited by 753
- The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity
Authors: Markus G. Seidel, Gerhard Kindle, Benjamin Gathmann, Isabella Quinti, Matthew Buckland, Joris van Montfrans, Raphael Scheible, Stephan Rusch, Lukas Gasteiger, Bodo Grimbacher, Nizar Mahlaoui, Stephan Ehl, Mario Abinun, Michael H. Albert, Sarah Beaussant-Cohen, Jacinta Bustamante, Andrew J. Cant, Jean‐Laurent Casanova, Helen Chapel, Geneviève de Saint Basile, Esther de Vries, Inderjeet Dokal, Jean Donadieu, Anne Durandy, David Edgar, Teresa Español, Amos Etzioni, Alain Fischer, Bobby Gaspar, Richard A. Gatti, 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
- Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants
Authors: Shuai Li, Valentina Silvestri, Goska Leslie, Timothy R. Rebbeck, Susan L. Neuhausen, John L. Hopper, Henriette Roed Nielsen, Andrew Lee, Xin Yang, Lesley McGuffog, Michael T. Parsons, Irene L. Andrulis, Norbert Arnold, Muriel Belotti, Åke Borg, Bruno Buecher, Saundra S. Buys, Sandrine M. Caputo, Wendy K. Chung, Chrystelle Colas, Sarah V. Colonna, Jackie Cook, Mary B. Daly, Miguel de la Hoya, Antoine de Pauw, Hélène Delhomelle, Jacqueline Eason, Christoph Engel, D. Gareth Evans, Ulrike Faust, 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
- Ploidy and Large-Scale Genomic Instability Consistently Identify Basal-like Breast Carcinomas with BRCA1/2 Inactivation
Authors: Tatiana Popova, Élodie Manié, Guillaume Rieunier, Virginie Caux‐Moncoutier, Carole Tirapo, Thierry Dubois, Olivier Delattre, Brigitte Sigal‐Zafrani, Marc A. Bollet, Michel Longy, Claude Houdayer, Xavier Sastre‐Garau, Anne Vincent‐Salomon, Dominique Stoppa‐Lyonnet, Marc‐Henri Stern - Cancer Research 2012 cited by 681
- 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: Nasim Mavaddat, Daniel Barrowdale, Irene L. Andrulis, Susan M. Domchek, Diana Eccles, Heli Nevanlinna, Susan J. Ramus, Amanda B. Spurdle, Mark E. Robson, Mark E. Sherman, Anna Marie Mulligan, Fergus J. Couch, Christoph Engel, Lesley McGuffog, Sue Healey, Olga M. Sinilnikova, Melissa C. Southey, Mary Beth Terry, David E. Goldgar, Frances P. O’Malley, Esther M. John, Ramūnas Janavičius, Laima Tihomirova, Thomas van Overeem Hansen, Finn C. Nielsen, Ana Osório, Alexandra Stavropoulou, Javier Benı́tez, Siranoush Manoukian, Bernard Peissel, 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
- Deep learning identifies morphological patterns of homologous recombination deficiency in luminal breast cancers from whole slide images
Authors: Tristan Lazard, Guillaume Bataillon, Peter Naylor, Tatiana Popova, François‐Clément Bidard, Dominique Stoppa‐Lyonnet, Marc‐Henri Stern, Étienne Decencière, Thomas Walter, Anne Vincent‐Salomon - Cell Reports Medicine 2022 cited by 75
- Comprehensive Study of the Clinical Phenotype of GermlineBAP1Variant-Carrying Families Worldwide
Authors: Sebastian Walpole, Antonia L. Pritchard, Colleen M. Cebulla, Robert Pilarski, Meredith Stautberg, Frederick H. Davidorf, Arnaud de la Fouchardière, Odile Cabaret, Lisa Golmard, Dominique Stoppa‐Lyonnet, Erin M. Garfield, Ching-Ni Jenny Njauw, Mitchell Cheung, Joni A. Turunen, Pauliina Repo, Reetta-Stiina Järvinen, Remco van Doorn, Martine J. Jager, Gregorius P. M. Luyten, Marina Marinkovic, Cindy Chau, Míriam Potrony, Veronica Höiom, Hildur Helgadóttir, Lorenza Pastorino, William Bruno, Virginia Andreotti, Bruna Dalmasso, Giulia Ciccarese, Paola Queirolo, 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
- Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families
Authors: Deborah Ford, Douglas F. Easton, Michael R. Stratton, Steven A. Narod, David E. Goldgar, Peter Devilee, D. Timothy Bishop, Barbara Weber, Gilbert Lenoir, Jenny Chang‐Claude, Hagay Sobol, M. Dawn Teare, Jeffery P. Struewing, Aðalgeir Arason, Siegfried Scherneck, Julian Peto, Timothy R. Rebbeck, Patricia N. Tonin, Susan L. Neuhausen, Rósa B. Barkardóttir, Jórunn E. Eyfjörd, H. Lynch, Bruce A.J. Ponder, Simon A. Gayther, J.M. Birch, Annika Lindblom, Dominique Stoppa‐Lyonnet, Y.-J. Bignon, Åke Borg, Ute Hamann, 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
- Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia
Authors: Marie Sébert, Stéphanie Gachet, Thierry Leblanc, Alix Rousseau, Olivier Bluteau, Rathana Kim, Raouf Ben Abdelali, Flore Sicre de Fontbrune, Loïc Maillard, Carèle Fédronie, Valentine Murigneux, Léa Bellenger, Naïra Naouar, Samuel Quentin, Lucie Hernandez, Nadia Vasquez, Mélanie Da Costa, Pedro Henrique Prata, Lise Larcher, Marie de Tersant, Matthieu Duchmann, Anna Raimbault, Franck Trimoreau, Odile Fenneteau, Wendy Cuccuini, Nathalie Gachard, Nathalie Auger, Giulia Tueur, Maud Blanluet, Claude Gazin, 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
- A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma
Authors: Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub, Mahaut de Lichy, Karine Bille, Philippe Dessen, Benoit d’Hayer, Hamida Mohamdi, Audrey Remenieras, E. Maubec, Arnaud de la Fouchardière, Vincent Molinié, P. Vabres, Stéphane Dalle, Nicolas Poulalhon, Tanguy Martin‐Denavit, L. Thomas, Pascale Andry-Benzaquen, N. Dupin, F. Boitier, Annick Rossi, Jean‐Luc Perrot, B. Labeille, Caroline Robert, Bernard Escudier, Olivier Caron, Laurence Brugières, Simon Saule, Betty Gardie, 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
- A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression
Authors: Jing Liu, Daniela Ottaviani, Meriem Sefta, Céline Desbrousses, Elodie Chapeaublanc, Rosario Aschero, Nanor Sirab, Fabiana Lubieniecki, Gabriela Lamas, Laurie Tonon, Catherine Dehainault, Clément Hua, Paul Fréneaux, Sacha Reichman, Narjesse Karboul, Anne Biton, Liliana Mirabal-Ortega, Magalie Larcher, Céline Brulard, Sandrine Arrufat, Nicolás André, Nabila Elarouci, Tatiana Popova, Fariba Némati, Didier Decaudin, David Gentien, Sylvain Baulande, Odette Mariani, Florent Dufour, Sylvain Guibert, 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
- ShallowHRD: detection of homologous recombination deficiency from shallow whole genome sequencing
Authors: Alexandre Eeckhoutte, Alexandre Houy, Elodie Manié, Manon Reverdy, Ivan Bièche, Elisabetta Marangoni, Oumou Goundiam, Anne Vincent-Salomon, Dominique Stoppa-Lyonnet, François-Clément Bidard, Marc-Henri Stern, Tatiana G. Popova - Bioinformatics, Bioinform. 2020 cited by 73
- Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
Authors: Daniel R. Barnes, Matti A. Rookus, Lesley McGuffog, Goska Leslie, Thea M. Mooij, Joe Dennis, Nasim Mavaddat, Julian Adlard, Munaza Ahmed, Kristiina Aittomäki, Nadine Andrieu, Irene L. Andrulis, Norbert Arnold, Banu Arun, Jacopo Azzollini, Judith Balmañà, Rósa B. Barkardóttir, Daniel Barrowdale, Javier Benı́tez, Pascaline Berthet, Katarzyna Białkowska, Amie Blanco, Marinus J. Blok, Bernardo Bonanni, Susanne E. Boonen, Åke Borg, Anikó Bozsik, Angela R. Bradbury, Paul Brennan, Carole Brewer, 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
- BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2
Authors: Melissa Cline, Rachel G. Liao, Michael T. Parsons, Benedict Paten, Faisal Alquaddoomi, Antonis C. Antoniou, Samantha Baxter, Larry Brody, Robert Cook‐Deegan, Amy Coffin, Fergus J. Couch, Brian Craft, Robert Currie, Chloe C. Dlott, Lena Dolman, Johan T. den Dunnen, Stephanie O. M. Dyke, Susan M. Domchek, Douglas F. Easton, Zachary Fischmann, William D. Foulkes, Judy E. Garber, David E. Goldgar, Mary J. Goldman, Peter Goodhand, Steven M. Harrison, David Haussler, Kazuto Kato, Bartha Maria Knoppers, Charles Markello, 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
- Shallow whole genome sequencing approach to detect Homologous Recombination Deficiency in the PAOLA-1/ENGOT-OV25 phase-III trial
Authors: Céline Callens, Manuel Rodrigues, Adrien Briaux, Éléonore Frouin, Alexandre Eeckhoutte, Éric Pujade-Lauraine, Victor Renault, Dominique Stoppa‐Lyonnet, Ivan Bièche, Guillaume Bataillon, Lucie Karayan‐Tapon, Tristan Rochelle, Florian Heitz, Sabrina Chiara Cecere, M.J. Rubio Pérez, Christoph Grimm, Trine Jakobi Nøttrup, Nicoletta Colombo, Ignace Vergote, Kan Yonemori, Isabelle Ray‐Coquard, Marc‐Henri Stern, Tatiana Popova - Oncogene 2023 cited by 31
- Sensitivity and predictive value of criteria for p53germline mutation screening
Authors: Agnès Chompret, Anne S. Abel, Dominique Stoppa‐Lyonnet, Laurence Brugières, Sabine Pagès, Jean Feunteun, Catherine Bonaïti‐Pellié - Journal of Medical Genetics 2001 cited by 342
- Incidence, Presentation, and Prognosis of Malignancies in Ataxia-Telangiectasia: A Report From the French National Registry of Primary Immune Deficiencies
Authors: Felipe Suárez, Nizar Mahlaoui, Danielle Canioni, Chantal Andriamanga, Catherine Dubois d’Enghien, Nicole Brousse, Jean‐Philippe Jaïs, Alain Fischer, Olivier Hermine, Dominique Stoppa‐Lyonnet - Journal of Clinical Oncology 2014 cited by 251
- Molecular basis of the Li–Fraumeni syndrome: an update from the French LFS families
Authors: Gaëlle Bougeard, Richard Sesboüé, Stéphanie Baert‐Desurmont, Stéphanie Vasseur, Cosette Martin, Julie Tinat, Laurence Brugières, Agnès Chompret, Brigitte Bressac–de Paillerets, Dominique Stoppa‐Lyonnet, Catherine Bonaïti‐Pellié, Thierry Frébourg - Journal of Medical Genetics 2008 cited by 226
- Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia
Authors: Massimo Bogliolo, Dominique Bluteau, James Lespinasse, Roser Pujol, Nadia Vasquez, Catherine Dubois d’Enghien, Dominique Stoppa‐Lyonnet, Thierry Leblanc, Jean Soulier, Jordi Surrallés - Genetics in Medicine 2017 cited by 80
- The biological effects and clinical implications of BRCA mutations: where do we go from here?
Authors: Dominique Stoppa‐Lyonnet - European Journal of Human Genetics 2016 cited by 115
- Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Authors: EMBRACE, Karoline Kuchenbaecker, GEMO Study Collaborators, Breast Cancer Family Registry, HEBON, KConFab Investigators, Australian Cancer Study (Ovarian Cancer Investigators), Australian Ovarian Cancer Study Group, Susan J. Ramus, Jonathan P. Tyrer, Andrew Lee, Howard C. Shen, Jonathan Beesley, Kate Lawrenson, Lesley McGuffog, Sue Healey, Janet M. Lee, Tassja J. Spindler, Yvonne G. Lin, Tanja Pejović, Yukie T. Bean, Qiyuan Li, Simon G. Coetzee, Dennis J. Hazelett, Alexander Miron, Melissa C. Southey, Mary Beth Terry, David E. Goldgar, Saundra S. Buys, Ramūnas Janavičius, 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
- Adaptive nanopore sequencing to determine pathogenicity ofBRCA1exonic duplication
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