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Chrystelle Colas

Institut Curie

41H-index
194Paper Count
6.6KCitation Count
Published Papers 75
Publication Date
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Correction: follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: data from the PRED-IdF network
errEuropean Journal of Human Genetics
IF4.6
err2026-07-03
err0
errOAAI
errMaxime Rémond; Youenn Drouet; Antoine Dardenne; Guillaume Perrod; Jeanne Netter; Yann Parc; Christophe Cellier; Romain Coriat; Solenne Farelly; Fanny Maksimovic; Diane Molière; Julie Metras; Patrick Benusiglio; Olivier Caron; Catherine Genestie; Christine Lasset; Chrystelle Colas; Bruno Buecher; Emmanuelle Fourme; Anne-Sophie Bats; Florence Coulet; Albain Chansavang; Nadim Hamzaoui; Marion Dhooge
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Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network
errEuropean Journal of Human Genetics
IF4.6
err2026-05-13
err0
errOAAI
errMaxime Rémond; Youenn Drouet; Antoine Dardenne; Guillaume Perrod; Jeanne Netter; Yann Parc; Christophe Cellier; Romain Coriat; Solenne Farelly; Fanny Maksimovic; Diane Molière; Julie Metras; Patrick Benusiglio; Olivier Caron; Catherine Genestie; Christine Lasset; Chrystelle Colas; Bruno Buecher; Emmanuelle Fourme; Anne-Sophie Bats; Florence Coulet; Albain Chansavang; Nadim Hamzaoui; Marion Dhooge
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Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study
errEuropean Journal of Human Genetics
IF4.6
err2026-02-13
err0
errOAAI
errJ. Matt McCrary; Els Van Valckenborgh; Denis Horgan; Evgenia Aleksandrova; Ralf Bargou; Regina Lohajova Behulova; Ivica Belina; Ann Liza Egesberg Bøhme; Joan Brunet; Florin Burada; Adela Chirita-Emandi; Andrada Ciuca; Chrystelle Colas; Anastasia Constantinidou; Razvan-Ovidiu Curca; Viorica Cursaru; Miriam Dalmas; Zanda Daneberga; Evandro de Azambuja; Antoine De Pauw; Robin De Putter; Turem Delikurt-Tuncalp; Deirdre Donnelly; Hans Ehrencrona; Lenka Foretova; Fabrizia Galli; Maurizio Genuardi; Rachel Giles; Claire Grima; Ramūnas Janavičius; Helena Kääriäinen; Barbara Klink; Mateja Krajc; Joanna Kufel-Grabowska; Baiba Lace; Liis Leitsalu; Christophe Le Tourneau; Marianne Lodahl; Francesca Mari; Erika Matos; Luca Mazzarella; Tamara Hussong Milagre; Martin Mistrik; Barbara Moss; Amy Nolan; Rosie O’Shea; Milena Paneque; Attila Patócs; Rebecka Pestoff; Hélène A. Poirel; Martine Risch; Manuel Rodrigues; Katharina M. Roetzer; Andrea Ros; Evelin Schröck; Gunda Schwaninger; Lucie Slámová; Kostas Stamatopoulos; Sonja Strang-Karlsson; Krzysztof Szczałuba; Virginie Szymczak; Philippe Theis; Jacqueline Turner; Olga Valcina; Christopher Vella; Wendy A. G. van Zelst-Stams; Karin A. W. Wadt; Johannes Zschocke; Joelle Ronez; Tim Ripperger; Marc Van Den Bulcke; Anke Katharina Bergmann
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Results of a multigene panel testing approach targeting patients with suspected genetic predisposition to pancreatic ductal adenocarcinoma
errEuropean Journal of Human Genetics
IF4.6
err2026-01-29
err0
PREAI
errBruno Buecher; Mathilde Warcoin; Emilie Rolland; Rukhshona Abdullazoda; Aurélia Le Guillevic; Chrystelle Colas; Lisa Golmard
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Genetic predisposition to breast cancer
errANNALES DE CHIRURGIE PLASTIQUE ESTHETIQUE
IF0.5
err2025-11-01
err0
PREAI
errStoppa-Lyonnet, D.; Colas, C.
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errSave
Genetic background predicts uveal melanoma patients’ outcomes
errOphthalmology Science
IF4.6
err2025-10-10
err0
errOAAI
errThibault Verrier; Anaïs Le Ven; Alexandre Houy; Erwin Brosens; Emine Kilic; Wishal D. Ramdas; Tolga Bicer; Agathe Garcia; Anne-Charlotte Lefranc; Sandra Vanhuele; Amanda F. Kahn; Gaelle Pierron; Alexandre Matet; Nathalie Cassoux; Chrystelle Colas; Manuel Rodrigues; Josselin Noirel; Marc-Henri Stern
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Myeloid neoplasms risks for germline DDX41 pathogenic variants carriers
errEuropean Journal of Human Genetics
IF4.6
err2025-10-03
err0
PREAI
errMarie-Charlotte Villy; Youenn Drouet; Lise Larcher; Yoann Vial; Benjamin Dauriat; Léa Veyrune; Laurène Fenwarth; Marie-Mathilde Auboiroux; Lucie Freiman; Sophie Nambot; Léa Patay; Marjolaine Willems; Emma Lachaier; Bénédicte Bonte; Delphine Lebon; Mathis Lepage; Olivier Ingster; Nathalie Gachard; Thomas Cluzeau; Michael Loschi; Jean Soulier; Pascale Flandrin-Gresta; Pascal Turlure; Nicolas Duployez; Emmanuelle Clappier; Dominique Stoppa-Lyonnet; Christine Lasset; Chrystelle Colas; Marie Sebert
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The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)
errGenetics in Medicine
IF6.2
err2025-05-24
err0
errOAAI
errLinda A.J. Hendricks; Katja C.J. Verbeek; Janneke H.M. Schuurs-Hoeijmakers; Mirjam M. de Jong; Thera P. Links; Hilde Brems; Mio Aerden; Joan Brunet; Roser Lleuger-Pujol; Robert Hüneburg; Stefan Aretz; Chrystelle Colas; Marie-Charlotte Villy; Emma R. Woodward; D. Gareth Evans; Daniëlle G.M. Bosch; Stephany H. Donze; Lenka Foretová; Ana Blatnik; Edward M. Leter; Marc Tischkowitz; Arne Jahn; Robin de Putter; Juliette Dupont; Siri Briskemyr; Verena Steinke-Lange; Margherita Baldassarri; Violetta C. Anastasiadou; Arvīds Irmejs; Carla Oliveira; Rachel S. van der Post; Arjen R. Mensenkamp; Bianca Tesi; Ninni Mu; Patrick R. Benusiglio; Anna Gerasimenko; Giovanni Innella; Daniela Turchetti; Claude Houdayer; Maud Branchaud; Hildegunn Høberg Vetti; Marianne Tveit Haavind; Judith Balmaña; Maite Torres; Maurizio Genuardi; Arianna Panfili; Kjersti Jørgensen; Lovise Mæhle; Nicoline Hoogerbrugge; Janet R. Vos
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Clinico-pathological Characteristics of Breast Invasive Lobular Carcinoma in non-CDH1 genetic predisposition. Experience from the Institut Curie
errLABORATORY INVESTIGATION
IF4.2
err2025-03-01
err0
PREAI
errDjerroudi, Lounes; Brahimaj, Rigleta; Colas, Chrystelle; Montecalvo, Victoire; Golmard, Lisa; Saule, Claire; Buecher, Bruno; Delhomelle, Helene; Le Gall, Jessica; Warcoin, Mathilde; Pages, Melanie; Pouget, Nicolas; Reyal, Fabien; Kirova, Youlia; Malhaire, Caroline; Stoppa-Lyonnet, Dominique; Mouret-Fourme, Emmanuelle; Vincent-Salomon, Anne
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ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-10-17
err3
errOAAI
errColas, Chrystelle; Guerrini-Rousseau, Lea; Suerink, Manon; Gallon, Richard; Kratz, Christian P.; Ayuso, Eloise; Brugieres, Laurence; Wimmer, Katharina
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ORIC-114, a highly selective, brain penetrant EGFR and HER2 inhibitor, demonstrates best-in-class properties against Exon 20 insertions and other atypical EGFR mutations
errEUROPEAN JOURNAL OF CANCER
IF7.1
err2024-10-01
err0
PREAI
errJunttila, M.; Repellin, C. E.; Warne, R.; Long, J. E.; Sambucetti, L.; Ashley, P.; Andreatta, G.; Baik, J.; Salaniwal, S.; Colas, C.; Romero, A.; Soroceanu, L.; Patel, R.; Maneval, E. Chow; Multani, P. S.; Daemen, A.; Friedman, L.
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Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants
errNPJ PRECISION ONCOLOGY
IF8
err2024-05-24
err3
errOAAI
errGallon, Richard; Brekelmans, Carlijn; Martin, Marie; Bours, Vincent; Schamschula, Esther; Amberger, Albert; Muleris, Martine; Colas, Chrystelle; Dekervel, Jeroen; De Hertogh, Gert; Coupier, Jerome; Colleye, Orphal; Sepulchre, Edith; Burn, John; Brems, Hilde; Legius, Eric; Wimmer, Katharina
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Features of colorectal adenomas among young patients with Lynch syndrome according to path_MMR: Results from the PRED-IdF registry
errDIGESTIVE AND LIVER DISEASE
IF3.8
err2024-04-01
err1
PREAI
errAlric, Hadrien; Coffin, Elise; Lekhal, Celine; Benusiglio, Patrick R.; Dhooge, Marion; Colas, Chrystelle; Caron, Olivier; Cusin, Veronica; Becq, Aymeric; Robles, Enrique Perez Cuadrado; Leenhardt, Romain; Perkins, Geraldine; Buecher, Bruno; Bellanger, Jerome; Rahmi, Gabriel; Malka, David; Laurent-Puig, Pierre; Chaussade, Stanislas; Benamouzig, Robert; Parc, Yann; Cellier, Christophe; Perrod, Guillaume
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Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction
errBREAST
IF7.9
err2024-02-01
err4
errOAAI
errTuechler, Anja; De Pauw, Antoine; Ernst, Corinna; Anota, Amelie; Lakeman, Inge M. M.; Dick, Julia; van der Stoep, Nienke; van Asperen, Christi J.; Maringa, Monika; Herold, Natalie; Bluemcke, Britta; Remy, Robert; Westerhoff, Anke; Stommel-Jenner, Denise J.; Frouin, Eleonore; Richters, Lisa; Golmard, Lisa; Kuetting, Nadine; Colas, Chrystelle; Wappenschmidt, Barbara; Rhiem, Kerstin; Devilee, Peter; Stoppa-Lyonnet, Dominique; Schmutzler, Rita K.; Hahnen, Eric
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Male breast cancer: No evidence for mosaic BRCA1 promoter methylation involvement
errBREAST
IF7.9
err2024-02-01
err0
errOAAI
errSchwartz, Mathias; Ibadioune, Sabrina; Vacher, Sophie; Villy, Marie-Charlotte; Trabelsi-Grati, Olfa; Le Gall, Jessica; Caputo, Sandrine M.; Delhomelle, Helene; Warcoin, Mathilde; Moncoutier, Virginie; Bourneix, Christine; Boutry-Kryza, Nadia; De Pauw, Antoine; Stern, Marc-Henri; Buecher, Bruno; Mouret-Fourme, Emmanuelle; Colas, Chrystelle; Stoppa-Lyonnet, Dominique; Masliah-Planchon, Julien; Golmard, Lisa; Bieche, Ivan
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Familial uveal melanoma and other tumors in 25 families with monoallelic germline MBD4 variants
errJNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
IF7.2
err2023-12-07
err0
PREAI
errVilly, Marie-Charlotte; Le Ven, Anais; Le Mentec, Marine; Masliah-Planchon, Julien; Houy, Alexandre; Bieche, Ivan; Vacher, Sophie; Vincent-Salomon, Anne; Dubois d'Enghien, Catherine; Schwartz, Mathias; Piperno-Neumann, Sophie; Matet, Alexandre; Malaise, Denis; Bubien, Virginie; Lortholary, Alain; Ait Omar, Amal; Cavaille, Mathias; Stoppa-Lyonnet, Dominique; Cassoux, Nathalie; Stern, Marc-Henri; Rodrigues, Manuel; Golmard, Lisa; Colas, Chrystelle
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Impact of molecular profiling and ESCAT classification on patient outcome: The experience of Institut Curie Molecular Tumor Board
errMOLECULAR CANCER THERAPEUTICS
IF5.5
err2023-12-01
err0
PREAI
errKamal, Maud; Abadi, Kimya Rahmani Narj; Sanchez, Raphael; Dupain, Celia; Guillou, Isabelle; Marret, Gregoire; Ajgal, Zahra Castel; Sablin, Marie Paule; Neuzillet, Cindy; Lecerf, Amani Asnacios; Borcoman, Edith; Hescot, Segolene; Coussy, Florence; Rodrigues, Manuel; Girard, Nicolas; Watson, Sarah; Planchon, Julien Masliah; Wong, Jennifer; Hamza, Abderaouf; Callens, Celine; Grati, Olfa Trabelsi; Melaabi, Samia; Driouch, Keltouma; Mouret-Fourme, Emmanuelle; Colas, Chrystelle; Antonio, Samantha; Mariani, Odette; Nijnikoff, Michele; Vincent-Salomon, Anne; Allory, Yves; Bieche, Ivan; Le Tourneau, Christophe
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Real-world gastric cancer (GC) in Latin America (LATAM) and Europe (EU)
errANNALS OF ONCOLOGY
IF65.4
err2023-10-01
err1
PREAI
errFreile, B.; Derks, S.; van Schooten, T.; Carneiro, F.; Barros, R.; Caballero, C.; Colas, C. V. Gauna; Riquelme, A.; Pizarro, G.; Garrido, M.; Ruiz, E.; Fernandez-Figueroa, E.; Takahashi, A. M. Leon; Mariani, J.; Luca, M. R.; O'Connor, J. M. R.; Esteso, F.; Cervantes, A.; Fleitas, T. C.
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Neurofibromatosis type 1 mosaicism in patients with constitutional mismatch repair deficiency
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2023-09-29
err6
errOAAI
errGuerrini-Rousseau, Lea; Pasmant, Eric; Muleris, Martine; Abbou, Samuel; Adam-De-Beaumais, Tiphaine; Brugieres, Laurence; Cabaret, Odile; Colas, Chrystelle; Cotteret, Sophie; Decq, Philippe; Dufour, Christelle; Guillerm, Erell; Rouleau, Etienne; Varlet, Pascale; Zili, Saima; Vidaud, Dominique; Grill, Jacques
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Mosaic BRCA1 promoter methylation contribution in hereditary breast/ovarian cancer pedigrees
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2023-09-25
err3
PREAI
errSchwartz, Mathias; Ibadioune, Sabrina; Chansavang, Albain; Vacher, Sophie; Caputo, Sandrine M.; Delhomelle, Helene; Wong, Jennifer; Abidallah, Khadija; Moncoutier, Virginie; Becette, Veronique; Popova, Tatiana; Suybeng, Voreak; De Pauw, Antoine; Stern, Marc-Henri; Colas, Chrystelle; Mouret-Fourme, Emmanuelle; Stoppa-Lyonnet, Dominique; Golmard, Lisa; Bieche, Ivan; Masliah-Planchon, Julien
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