Rare Mutations in XRCC2 Increase the Risk of Breast Cancer
Park, D.J., Lesueur, F., Nguyen-Dumont, T., Pertesi, M., Odefrey, F., Hammet, F., Neuhausen, S.L., John, E.M., Andrulis, I.L., Terry, M.B., Daly, M., Buys, S., Le Calvez-Kelm, F., Lonie, A., Pope, B.J., Tsimiklis, H., Voegele, C., Hilbers, F.M., Hoogerbrugge, N., Barroso, A., Osorio, A., Giles, G.G., Devilee, P., Benitez, J., Hopper, J.L., Tavtigian, S.V., Goldgar, D.E., Southey, M.C.
Published in American journal of human genetics (06.04.2012)
Published in American journal of human genetics (06.04.2012)
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Genetic modifiers of CHEK21100delC-associated breast cancer risk
Muranen, Taru A, Greco, Dario, Blomqvist, Carl, Aittomäki, Kristiina, Khan, Sofia, Hogervorst, Frans, Verhoef, Senno, Pharoah, Paul D P, Dunning, Alison M, Shah, Mitul, Luben, Robert, Bojesen, Stig E, Nordestgaard, Børge G, Schoemaker, Minouk, Swerdlow, Anthony, García-Closas, Montserrat, Figueroa, Jonine, Dörk, Thilo, Bogdanova, Natalia V, Hall, Per, Li, Jingmei, Khusnutdinova, Elza, Bermisheva, Marina, Kristensen, Vessela, Borresen-Dale, Anne-Lise, Peto, Julian, Dos Santos Silva, Isabel, Couch, Fergus J, Olson, Janet E, Hillemans, Peter, Park-Simon, Tjoung-Won, Brauch, Hiltrud, Hamann, Ute, Burwinkel, Barbara, Marme, Frederik, Meindl, Alfons, Schmutzler, Rita K, Cox, Angela, Cross, Simon S, Sawyer, Elinor J, Tomlinson, Ian, Lambrechts, Diether, Moisse, Matthieu, Lindblom, Annika, Margolin, Sara, Hollestelle, Antoinette, Martens, John W M, Fasching, Peter A, Beckmann, Matthias W, Andrulis, Irene L, Knight, Julia A, Anton-Culver, Hoda, Ziogas, Argyrios, Giles, Graham G, Milne, Roger L, Brenner, Hermann, Arndt, Volker, Mannermaa, Arto, Kosma, Veli-Matti, Chang-Claude, Jenny, Rudolph, Anja, Devilee, Peter, Seynaeve, Caroline, Hopper, John L, Southey, Melissa C, John, Esther M, Whittemore, Alice S, Bolla, Manjeet K, Wang, Qin, Michailidou, Kyriaki, Dennis, Joe, Easton, Douglas F, Schmidt, Marjanka K, Nevanlinna, Heli
Published in Genetics in medicine (01.05.2017)
Published in Genetics in medicine (01.05.2017)
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Survival and contralateral breast cancer in CHEK2 1100delC breast cancer patients: impact of adjuvant chemotherapy
KRIEGE, M, HOLLESTELLE, A, MARTENS, J. W. M, SEYNAEVE, C, JAGER, A, HUIJTS, P. E. A, BERNS, E. M, SIEUWERTS, A. M, MEIJER-VAN GELDER, M. E, COLLEE, J. M, DEVILEE, P, HOONING, M. J
Published in British journal of cancer (26.08.2014)
Published in British journal of cancer (26.08.2014)
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Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families
Ford, D., Easton, D.F., Stratton, M., Narod, S., Goldgar, D., Devilee, P., Bishop, D.T., Weber, B., Lenoir, G., Chang-Claude, J., Sobol, H., Teare, M.D., Struewing, J., Arason, A., Scherneck, S., Peto, J., Rebbeck, T.R., Tonin, P., Neuhausen, S., Barkardottir, R., Eyfjord, J., Lynch, H., Ponder, B.A.J., Gayther, S.A., Birch, J.M., Lindblom, A., Stoppa-Lyonnet, D., Bignon, Y., Borg, A., Hamann, U., Haites, N., Scott, R.J., Maugard, C.M., Vasen, H., Seitz, S., Cannon-Albright, L.A., Schofield, A., Zelada-Hedman, M.
Published in American journal of human genetics (01.03.1998)
Published in American journal of human genetics (01.03.1998)
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Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD‐related paraganglioma
Hoekstra, A.S., Ende, B., Julià, X.P., Breemen, L., Scheurwater, K., Tops, C.M., Malinoc, A., Devilee, P., Neumann, H.P.H., Bayley, J.‐P.
Published in Clinical genetics (01.04.2017)
Published in Clinical genetics (01.04.2017)
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Genetic susceptibility for breast cancer: How many more genes to be found?
Oldenburg, R.A, Meijers-Heijboer, H, Cornelisse, C.J, Devilee, P
Published in Critical reviews in oncology/hematology (01.08.2007)
Published in Critical reviews in oncology/hematology (01.08.2007)
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Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients
Hensen, E. F., Siemers, M. D., Jansen, J. C., Corssmit, E. P. M., Romijn, J. A., Tops, C. M. J., van der Mey, A. G. L., Devilee, P., Cornelisse, C. J., Bayley, J. P., Vriends, A. H. J. T.
Published in Clinical endocrinology (Oxford) (01.11.2011)
Published in Clinical endocrinology (Oxford) (01.11.2011)
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A new conditional Apc-mutant mouse model for colorectal cancer
Robanus-Maandag, Els C., Koelink, Pim J., Breukel, Cor, Salvatori, Daniela C.F., Jagmohan-Changur, Shantie C., Bosch, Cathy A.J., Verspaget, Hein W., Devilee, Peter, Fodde, Riccardo, Smits, Ron
Published in Carcinogenesis (New York) (01.05.2010)
Published in Carcinogenesis (New York) (01.05.2010)
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High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands
Hensen, EF, van Duinen, N, Jansen, JC, Corssmit, EPM, Tops, CMJ, Romijn, JA, Vriends, AHJT, van der Mey, AGL, Cornelisse, CJ, Devilee, P, Bayley, JP
Published in Clinical genetics (01.03.2012)
Published in Clinical genetics (01.03.2012)
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Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation
Meijers-Heijboer, EJ, Verhoog, LC, Brekelmans, CTM, Seynaeve, C, Tilanus-Linthorst, MMA, Wagner, A, Dukel, L, Devilee, P, van den Ouweland, AMW, van Geel, AN, Klijn, JGM
Published in The Lancet (British edition) (10.06.2000)
Published in The Lancet (British edition) (10.06.2000)
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COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer
TOMLINSON, Ipm, DUNLOP, M, AALTONEN, L. A, HEMMINKI, K, LINDBLOM, A, FÖRSTI, A, SIEBER, O, LITON, L, VAN WEZEL, T, MORREAU, H, WIJNEN, J. T, DEVILEE, P, CAMPBELL, H, MATSUDA, K, NAKAMURA, Y, CASTELLVI-BEL, S, RUIZ-PONTE, C, CASTELLS, A, CARRACEDO, A, HO, Jwc, SHAM, P, HOFSTRA, Rmw, VODICKA, P, ZANKE, B, BRENNER, H, HAMPE, J, SCHAFMAYER, C, TEPEL, J, SCHREIBER, S, VÖLZKE, H, LERCH, M. M, SCHMIDT, C. A, BUCH, S, MORENO, V, GALLINGER, S, VILLANUEVA, C. M, PETERLONGO, P, RADICE, P, ECHEVERRY, M. M, VELEZ, A, CARVAJAL-CARMONA, L, SCOTT, R, PENEGAR, S, BRODERICK, P, TENESA, A, HUDSON, T, HOULSTON, R. S, KOESSLER, T, PHAROAH, P. D, NIITTYMÄKIX, I, TUUPANENX, S
Published in British journal of cancer (19.01.2010)
Published in British journal of cancer (19.01.2010)
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Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1
Verhoog, LC, Brekelmans, CTM, Seynaeve, C, van den Bosch, LMC, Dahmen, G, van Geel, AN, Tilanus-Linthorst, MMA, Bartels, CCM, Wagner, A, van den Ouweland, A, Devilee, P, Meijers-Heijboer, EJ, Klijn, JGM
Published in The Lancet (British edition) (31.01.1998)
Published in The Lancet (British edition) (31.01.1998)
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Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK21100delC variant
de Bock, G H, Schutte, M, Krol-Warmerdam, E M M, Seynaeve, C, Blom, J, Brekelmans, C T M, Meijers-Heijboer, H, van Asperen, C J, Cornelisse, C J, Devilee, P, Tollenaar, R A E M, Klijn, J G M
Published in Journal of medical genetics (01.10.2004)
Published in Journal of medical genetics (01.10.2004)
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Survival in Hereditary Breast Cancer Associated With Germline Mutations of BRCA2
VERHOOG, L. C, BREKELMANS, C. T. M, VAN DEN OUWELAND, A. M. W, MEIJERS-HEIJBOER, E. J, KLIJN, J. G. M, SEYNAEVE, C, DAHMEN, G, VAN GEEL, A. N, BARTELS, C. C. M, TILANUS-LINTHORST, M. M. A, WAGNER, A, DEVILEE, P, HALLEY, D. J. J
Published in Journal of clinical oncology (01.11.1999)
Published in Journal of clinical oncology (01.11.1999)
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A non-BRCA1/2 hereditary breast cancer sub-group defined by aCGH profiling of genetically related patients
Didraga, M. A., van Beers, E. H., Joosse, S. A., Brandwijk, K. I. M., Oldenburg, R. A., Wessels, L. F. A., Hogervorst, F. B. L., Ligtenberg, M. J., Hoogerbrugge, N., Verhoef, S., Devilee, P., Nederlof, P. M.
Published in Breast cancer research and treatment (01.11.2011)
Published in Breast cancer research and treatment (01.11.2011)
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Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1
ENG, Charis, BRODY, Lawrence C, WAGNER, Teresa M. U, DEVILEE, Peter, VIJG, Jan, SZABO, Csilla, TAVTIGIAN, Sean V, NATHANSON, Katharine L, OSTRANDER, Elaine, FRANK, Thomas S
Published in Journal of medical genetics (01.12.2001)
Published in Journal of medical genetics (01.12.2001)
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Instability of short tandem repeats (microsatellites) in human cancers
Wooster, R, Cleton-Jansen, A.-M, Collins, N, Mangion, J, Cornelis, R.S, Cooper, C.S, Gusterson, B.A, Ponder, B.A.J, von Deimling, A, Wiestler, O.D, Cornelisse, C.J, Devilee, P, Stratton, M.R
Published in Nature genetics (01.02.1994)
Published in Nature genetics (01.02.1994)
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A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families
PEELEN, T, VAN VLIET, M, VAN DER LUIJT, R, VAN DER HOUT, A. H, GILLE, J. J. P, PALS, G, JEDEMA, I, OLMER, R, VAN LEEUWEN, I, NEWMAN, B, PLANDSOEN, M, VAN DER EST, M, PETRIJ-BOSCH, A, BRINK, G, HAGEMAN, S, ARTS, P. J. W, BAKKER, M. M, WILLEMS, H. W, VAN DER LOOIJ, E, NEYNS, B, BONDUELLE, M, JANSEN, R, OOSDERWIJK, J. C, MIEREMET, R, SIJMONS, R, SMEETS, H. J. M, VAN ASPEREN, C. J, MEIJERS-HEIJBOER, H, KLIJN, J. G. M, DE GREVE, J, KING, M.-C, MENKO, F. H, BRUNNER, H. G, HALLEY, D, SZABO, C, VAN OMMEN, G.-J. B, VASEN, H. F. A, CORNELISSE, C. J, VAN'VEER, L. J, DE KNIJFF, P, BAKKER, E, DEVILEE, P, VAN DEN OUWELAND, A. M. W, HOGERVORST, F, BROHET, R, LIGTENBERG, M. J. L, TEUGELS, E
Published in American journal of human genetics (01.05.1997)
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Published in American journal of human genetics (01.05.1997)
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