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C

Chrystelle Colas

Institut Curie
H指数:41
被引数:6,586

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Correction: follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: data from the PRED-IdF network

更正：随访、癌症风险和Peutz-Jeghers综合征的死亡率：来自PRED-IdF网络的数据

European Journal of Human Genetics
IF4.6
2026-07-030
OA
Maxime 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
Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network

Peutz-Jeghers综合征的随访、癌症风险和死亡率：PRED-IdF网络的数据

European Journal of Human Genetics
IF4.6
2026-05-130
OAAI
Maxime 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
Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study

优先考虑欧洲策略，以可持续方式获取癌症领域的高质量遗传咨询：一项德尔菲研究

European Journal of Human Genetics
IF4.6
2026-02-130
OAAI
J. 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
Genetic background predicts uveal melanoma patients’ outcomes

遗传背景预测葡萄膜黑色素瘤患者的预后

Ophthalmology Science
IF4.6
2025-10-100
OAAI
Thibault 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
Myeloid neoplasms risks for germline DDX41 pathogenic variants carriers

携带胚系DDX41致病性变异的髓系肿瘤风险

European Journal of Human Genetics
IF4.6
2025-10-030
PRE
Marie-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
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)

PTEN错构瘤综合征（PHTS）中第二原发癌的风险

Genetics in Medicine
IF6.2
2025-05-240
OAAI
Linda 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
Clinico-pathological Characteristics of Breast Invasive Lobular Carcinoma in non-CDH1 genetic predisposition. Experience from the Institut Curie
LABORATORY INVESTIGATION
IF4.2
2025-03-010
PRE
Djerroudi, 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
Features of colorectal adenomas among young patients with Lynch syndrome according to path_MMR: Results from the PRED-IdF registry
DIGESTIVE AND LIVER DISEASE
IF3.8
2024-04-011
PRE
Alric, 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
Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction

在基于canrik的乳腺癌风险预测中纳入遗传和非遗传危险因素的临床意义

BREAST
IF7.9
2024-02-014
OAAI
Tuechler, 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
Male breast cancer: No evidence for mosaic BRCA1 promoter methylation involvement
BREAST
IF7.9
2024-02-010
OAAI
Schwartz, 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
Familial uveal melanoma and other tumors in 25 families with monoallelic germline MBD4 variants
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
IF7.2
2023-12-070
PRE
Villy, 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
Impact of molecular profiling and ESCAT classification on patient outcome: The experience of Institut Curie Molecular Tumor Board
MOLECULAR CANCER THERAPEUTICS
IF5.5
2023-12-010
PRE
Kamal, 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
Mosaic BRCA1 promoter methylation contribution in hereditary breast/ovarian cancer pedigrees
JOURNAL OF MEDICAL GENETICS
IF3.7
2023-09-253
PRE
Schwartz, 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

研究方向

暂未获取到该数据
D
Dominique Stoppa‐Lyonnet
H 指数:83论文数:659被引数:3.3万
B
Bruno Buecher
H 指数:36论文数:231被引数:7,727
L
Lisa Golmard
H 指数:29论文数:139被引数:3,055
F
Florence Coulet
H 指数:44论文数:255被引数:7,538
M
Martine Muleris
H 指数:39论文数:138被引数:4,794
P
Patrick R. Benusiglio
H 指数:24论文数:110被引数:3,489
L
Laurence Brugières
H 指数:75论文数:472被引数:2.1万
E
Emmanuelle Mouret‐Fourme
H 指数:25论文数:119被引数:1,747
A
Antoine De Pauw
H 指数:26论文数:126被引数:3,302
A
Alex Duval
H 指数:52论文数:184被引数:1.0万