Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Caroline Kientz"'
Autor:
Caroline Kientz, Marie-Odile Joly, Laurence Faivre, Alix Clemenson, Sophie Dalac, Côme Lepage, Caroline Chapusot, Caroline Jacquot, Renaud Schiappa, Marine Lebrun
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-4 (2017)
Abstract Background The tumor spectrum in the Lynch syndrome is well defined, comprising an increased risk of developing colonic and extracolonic malignancies. Muir-Torre syndrome is a variant with a higher risk of skin disease. Patients have been de
Externí odkaz:
https://doaj.org/article/7d02ade405f34cb29ce637ad88e533e9
Autor:
Clémentine Legrand, Marine Lebrun, Pierre Naïbo, Magalie Peysselon, Fabienne Prieur, Caroline Kientz, Françoise Desseigne, Sandrine Handallou, Jean-Marc Rey, Sophie Nambot, Vincent Goussot, Nadim Hamzaoui, Qing Wang
Publikováno v:
European Journal of Medical Genetics. 65:104409
The POLD1 gene is involved in DNA proofreading to ensure accurate DNA replication. Some germline alterations in its exonuclease domain are associated with predisposition to cancers and colonic polyps. Only a few pathogenic variants have been clearly
Autor:
Sophie Dalac, Laurence Faivre, Renaud Schiappa, Alix Clemenson, Marie-Odile Joly, Côme Lepage, Marine Lebrun, Caroline Kientz, Caroline Chapusot, Caroline Jacquot
Publikováno v:
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice, BioMed Central, 2017, 15 (1), pp.6. ⟨10.1186/s13053-017-0066-9⟩
Hereditary Cancer in Clinical Practice, BioMed Central, 2017, 15 (1), pp.6. 〈https://hccpjournal.biomedcentral.com/articles/10.1186/s13053-017-0066-9〉. 〈10.1186/s13053-017-0066-9〉
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-4 (2017)
Hereditary Cancer in Clinical Practice, BioMed Central, 2017, 15 (1), pp.6. ⟨10.1186/s13053-017-0066-9⟩
Hereditary Cancer in Clinical Practice, BioMed Central, 2017, 15 (1), pp.6. 〈https://hccpjournal.biomedcentral.com/articles/10.1186/s13053-017-0066-9〉. 〈10.1186/s13053-017-0066-9〉
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-4 (2017)
IF 1.590; International audience; Background: The tumor spectrum in the Lynch syndrome is well defined, comprising an increased risk of developing colonic and extracolonic malignancies. Muir-Torre syndrome is a variant with a higher risk of skin dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ca8f11ddad5673a992a7190e085bef4
https://hal.archives-ouvertes.fr/hal-01541073
https://hal.archives-ouvertes.fr/hal-01541073
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.
Autor:
Hakkaart, Christopher1 (AUTHOR), Pearson, John F.1 (AUTHOR), Marquart, Louise2,3 (AUTHOR), Dennis, Joe4 (AUTHOR), Wiggins, George A. R.1 (AUTHOR), Barnes, Daniel R.4 (AUTHOR), Robinson, Bridget A.5,6 (AUTHOR), Mace, Peter D.7 (AUTHOR), Aittomäki, Kristiina8 (AUTHOR), Andrulis, Irene L.9,10 (AUTHOR), Arun, Banu K.11 (AUTHOR), Azzollini, Jacopo12 (AUTHOR), Balmaña, Judith13,14 (AUTHOR), Barkardottir, Rosa B.15,16 (AUTHOR), Belhadj, Sami17 (AUTHOR), Berger, Lieke18 (AUTHOR), Blok, Marinus J.19 (AUTHOR), Boonen, Susanne E.20 (AUTHOR), Borde, Julika21,22,23 (AUTHOR), Bradbury, Angela R.24 (AUTHOR)
Publikováno v:
Communications Biology. 10/6/2022, Vol. 5 Issue 1, p1-15. 15p.
Autor:
Jiao, Yue1,2,3 (AUTHOR), Lesueur, Fabienne2,3 (AUTHOR), Azencott, Chloé-Agathe2,4 (AUTHOR), Laurent, Maïté1 (AUTHOR), Mebirouk, Noura2,3 (AUTHOR), Laborde, Lilian5 (AUTHOR), Beauvallet, Juana2,3 (AUTHOR), Dondon, Marie-Gabrielle2,3 (AUTHOR), Eon-Marchais, Séverine2,3 (AUTHOR), Laugé, Anthony1 (AUTHOR), GEMO Study Collaborators (AUTHOR), Boutry-Kryza, Nadia (AUTHOR), Calender, Alain (AUTHOR), Giraud, Sophie (AUTHOR), Léone, Mélanie (AUTHOR), Bressac-de-Paillerets, Brigitte (AUTHOR), Caron, Olivier (AUTHOR), Guillaud-Bataille, Marine (AUTHOR), Bignon, Yves-Jean (AUTHOR), Uhrhammer, Nancy (AUTHOR)
Publikováno v:
BMC Medical Research Methodology. 7/29/2021, Vol. 21 Issue 1, p1-11. 11p.
Autor:
Osorio, Ana1,2, Milne, Roger L.3, Kuchenbaecker, Karoline4, Vaclová, Tereza1, Pita, Guillermo5, Alonso, Rosario5 aosorio@cnio.es, Peterlongo, Paolo6, Blanco, Ignacio7, de la Hoya, Miguel8, Duran, Mercedes9, Díez, Orland10, Ramón y Cajal, Teresa11, Konstantopoulou, Irene12, Martínez-Bouzas, Cristina13, Andrés Conejero, Raquel14, Soucy, Penny15, McGuffog, Lesley4, Barrowdale, Daniel4, Lee, Andrew4, SWE-BRCA16
Publikováno v:
PLoS Genetics. Apr2014, Vol. 10 Issue 4, p1-12. 12p.
Autor:
Couch, Fergus J.1 couch.fergus@mayo.edu, Xianshu Wang2, McGuffog, Lesley3, Lee, Andrew3, Olswold, Curtis4, Kuchenbaecker, Karoline B.3, Soucy, Penny5, Fredericksen, Zachary4, Barrowdale, Daniel3, Dennis, Joe3, Gaudet, Mia M.6, Dicks, Ed3, Kosel, Matthew4, Healey, Sue7, Sinilnikova, Olga M.8,9, Lee, Adam10, Bacot, François11, Vincent, Daniel11, Hogervorst, Frans B. L.12, Peock, Susan3
Publikováno v:
PLoS Genetics. Mar2013, Vol. 9 Issue 3, Special section p1-21. 21p. 2 Diagrams, 4 Charts, 1 Graph.
Autor:
Gaudet, Mia M.1, Kuchenbaecker, Karoline B.2, Vijai, Joseph3, Klein, Robert J.4, Kirchhoff, Tomas5, McGuffog, Lesley2, Barrowdale, Daniel2, Dunning, Alison M.6, Lee, Andrew2, Dennis, Joe2, Healey, Sue7, Dicks, Ed2, Soucy, Penny8, Sinilnikova, Olga M.9,10, Pankratz, Vernon S.11, Xianshu Wang12, Eldridge, Ronald C.13, Tessier, Daniel C.14, Vincent, Daniel14, Bacot, Francois14
Publikováno v:
PLoS Genetics. Mar2013, Vol. 9 Issue 3, p1-15. 15p. 2 Charts, 2 Graphs.
Autor:
Kientz, Caroline, Prieur, Fabienne, Clemenson, Alix, Joly, Marie-Odile, Stachowicz, Marie-Laure, Auclair, Jessie, Attignon, Valéry, Schiappa, Renaud, Wang, Qing
Publikováno v:
Familial Cancer; Jan2020, Vol. 19 Issue 1, p11-14, 4p
Autor:
Jakubowska, A1, Rozkrut, D2, Antoniou, A3, Hamann, U4, Scott, R J5, McGuffog, L6, Healy, S7, Sinilnikova, O M8, Rennert, G9, Lejbkowicz, F9, Flugelman, A9, Andrulis, I L10, Glendon, G11, Ozcelik, H12, Thomassen, M13, Paligo, M14, Aretini, P14, Kantala, J15, Aroer, B16, von Wachenfeldt, A16
Publikováno v:
British Journal of Cancer. 6/5/2012, Vol. 106 Issue 12, p2016-2024. 9p. 4 Charts.