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Chrystelle Colas

Paris Dauphine University - PSL Research University

SCHOLARLY PAPERS

2

DOWNLOADS

145

TOTAL CITATIONS

0

Scholarly Papers (2)

1.

Lymphomas Associated with Constitutional Mismatch Repair Deficiency: A Joint International Analysis of C4CMMRD, IRRDC and EICNH Intergroups

Number of pages: 15 Posted: 25 Jul 2023
Université Paris Saclay - Department of Children and Adolescents Oncology, University of Toronto - The Hospital for Sick Children - SickKids, University of Toronto - The Hospital for Sick Children - SickKids, Medical University Vienna - St. Anna Children's Hospital, Arthur and Sonia Labatt Brain Tumor Research Centre, NHS Foundation Trust - Department of Paediatric Haematology and Oncology, University Hospital Münster, Paris Dauphine University - PSL Research University, Université Libre de Bruxelles (ULB) - Hemato-Oncology department, Arthur and Sonia Labatt Brain Tumor Research Centre, Tel Aviv University - Department of Pediatric Hematology-Oncology, University Hospital Münster, Tel Aviv University - Rabin Medical Center, Medical University of Innsbruck, Poznan University of Medical Sciences, Motol University Hospital, Hannover Medical School, Princess Maxima Center for Pediatric Oncology, Hospital Universitario Doce de Octubre - Pediatric Oncology Unit, Hospital Duran i Reynals (ICO) - Catalan Institute of Oncology, Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, Hospital Universitario Doce de Octubre - Hereditary Cancer Genetic Diagnostic Laboratory, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER) - Grupo de Medicina Xenómica, Children’s Health Ireland, KU Leuven - Department of Oncology, Medical University of Innsbruck, University Paris-Saclay - Biostatistic and Epidemiology Unit, Gustave Roussy, The Hospital for Sick Children - Division of Haematology / Oncology and Gustave Roussy
Downloads 111 (635,507)

Abstract:

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Lymphoma, CMMRD, Cancer-predisposition

2.

Association and Performance of Polygenic Risk Scores for Breast Cancer Among French Women Presenting or Not a Familial Predisposition to the Disease

Number of pages: 18 Posted: 08 Sep 2022
INSERM, U900, University of Paris-Saclay, INSERM, U900, INSERM, U900, Paris Dauphine University - PSL Research University, INSERM, U900, University of Paris-Saclay, INSERM, U900, INSERM, U900, University of Paris-Saclay, University of Paris-Saclay, University of Paris-Saclay, University of Paris-Saclay, Centre Georges-François Leclerc, CHU de Brest, Centre François Baclesse, Claude Bernard Lyon 1 University, Paris Dauphine University - PSL Research University, Gustave Roussy, Université Clermont Auvergne, University Hospital Caremeau, Paris Dauphine University - PSL Research University, CHU Hôpital Saint-Jacques, CHU de Montpellier - Arnaud de Villeneuve Hospital, Institut de Cancérologie de l'Ouest, Paris Dauphine University - PSL Research University, Grenoble Alpes University Hospital, Centre Hospitalier de Chambéry, Paris Dauphine University - PSL Research University, CH Georges Renon, Hospices Civils de Lyon, Institut Claudius Regaud, Paris Dauphine University - PSL Research University, Claude Bernard Lyon 1 University, University of Lille - CHU Lille, Hospices Civils de Lyon, Université Cote d'Azur - Hôpital Pasteur, Hôpital Privé du Confluent, Hôpital de Mercy, Centre Antoine Lacassagne, University of Strasbourg - Hôpitaux Universitaires de Strasbourg, François Rabelais University - CHU Bretonneau - CHU Hôpitaux De Tours, Paris Dauphine University - PSL Research University, Centre Georges-François Leclerc, Institut Paoli-Calmettes, Institut Paoli-Calmettes, CHU Saint-Etienne, University of Paris-Saclay, Bergonié Institute, Institut Paoli-Calmettes, Institut Claudius Regaud, CHU Clermont-Ferrand, Centre François Baclesse, Hôpital Universitaire Dupuytren, University of Paris-Saclay, University of Paris-Saclay - INSERM, CESP, Centre National de Recherche en Génomique Humaine, Institut Curie, INSERM, U900 and INSERM, U900
Downloads 34 (1,263,436)

Abstract:

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breast cancer, genetic susceptibility, BRCA1, BRCA2, SNP, Polygenic risk score, risk prediction