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Hanne Meijers-Heijboer

PROF.DR., (Principal Investigator)

 https://orcid.org/0000-0003-1169-3853
1991 …2023

Research activity per year

Search results

  • A BRCA1/2 mutation, high breast density and prominent pushing margins of a tumor independently contribute to a frequent false-negative mammography

    Tilanus-Linthorst, M., Verhoog, L., Obdeijn, I-M., Bartels, K., Menke-Pluymers, M., Eggermont, A., Klijn, J., Meijers-Heijboer, H., van der Kwast, T. & Brekelmans, C., 2002, In: International journal of cancer. Journal international du cancer. 102, 1, p. 91-95

    Research output: Contribution to journal › Article › Academic › peer-review

    174 Citations (Scopus)

  • A BRCA1/2 mutation, high breast density and prominent pushing margins of a tumor independently contribute to a frequent false-negative mammography (vol 102, pg 91, 2002)

    Tilanus-Linthorst, M., Verhoog, L., Obdeijn, I. M., Bartels, K., Menke-Pluymers, M., Eggermont, A., Klijn, J., Meijers-Heijboer, H., van der Kwast, T. & Brekelmans, C., 2002, In: International journal of cancer. Journal international du cancer. 102, 6, p. 665

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

    2 Citations (Scopus)

  • Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22

    Rahman, N., Teare, M. D., Seal, S., Renard, H., Mangion, J., Cour, C., Thompson, D., Shugart, Y., Eccles, D., Devilee, P., Meijers, H., Nathanson, K. L., Neuhausen, S. L., Weber, B., Chang-Claude, J., Easton, D. F., Goldgar, D. & Stratton, M. R., 2000, In: Oncogene. 19, 36, p. 4170-4173

    Research output: Contribution to journal › Article › Academic › peer-review

    31 Citations (Scopus)

  • A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

    GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators & ABCTB Investigators, 1 Dec 2021, In: Nature communications. 12, 1, 1078.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    17 Citations (Scopus)

  • Accuracy of BRCA1 and BRCA2 founder mutation analysis in formalin-fixed and paraffin-embedded (FFPE) tissue

    Adank, M. A., Brogi, E., Bogomolniy, F., Wadsworth, E. A., Lafaro, K. J., Yee, C. J., Kirchhoff, T., Meijers-Heijboer, E. J., Kauff, N. D., Boyd, J. & Offit, K., 2006, In: Familial Cancer. 5, 4, p. 337-342

    Research output: Contribution to journal › Article › Academic › peer-review

    13 Citations (Scopus)

  • Addition of a 161-SNP polygenic risk score to family history-based risk prediction: Impact on clinical management in non- BRCA1/2 breast cancer families

    Lakeman, I. M. M., Hilbers, F. S., Rodríguez-Girondo, M., Lee, A., Vreeswijk, M. P. G., Hollestelle, A., Seynaeve, C., Meijers-Heijboer, H., Oosterwijk, J. C., Hoogerbrugge, N., Olah, E., Vasen, H. F. A., van Asperen, C. J. & Devilee, P., 1 Sept 2019, In: Journal of medical genetics. 56, 9, p. 581-589 9 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    31 Citations (Scopus)

  • A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype

    Beunders, G., van de Kamp, J., Vasudevan, P., Morton, J., Smets, K., Kleefstra, T., de Munnik, S. A., Schuurs-Hoeijmakers, J., Ceulemans, B., Zollino, M., Hoffjan, S., Wieczorek, S., So, J., Mercer, L., Walker, T., Velsher, L., Parker, M. J., Magee, A. C., Elffers, B., Frank Kooy, R., & 4 othersYntema, H. G., Meijers-Heijboer, E. J., Sistermans, E. A. & The DDD study, DDD. S., 1 Aug 2016, In: Journal of medical genetics. 53, 8, p. 523-532 10 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    37 Citations (Scopus)

  • A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: Application in a Dutch cancer clinic setting

    Van Der Hout, A. H., Van Den Ouweland, A. M. W., Van Der Luijt, R. B., Gille, H. J. P., Bodmer, D., Brüggenwirth, H., Mulder, I. M., Van Der Vlies, P., Elfferich, P., Huisman, M. T., Ten Berge, A. M., Kromosoeto, J., Jansen, R. P. M., Van Zon, P. H. A., Vriesman, T., Arts, N., Boutmy-De Lange, M., Oosterwijk, J. C., Meijers-Heijboer, H., Ausems, M. G. E. M., & 7 othersHoogerbrugge, N., Verhoef, S., Halley, D. J. J., Vos, Y. J., Hogervorst, F., Ligtenberg, M. & Hofstra, R. M. W., Jul 2006, In: Human mutation. 27, 7, p. 654-666 13 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    72 Citations (Scopus)

  • A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites

    de Vries, Y., Lwiwski, N., Levitus, M., Kuyt, B., Israels, S. J., Arwert, F., Zwaan, M., Greenberg, C. R., Alter, B. P., Joenje, H. & Meijers-Heijboer, H., 2012, In: Anemia. 2012, p. 865170 865170.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    14 Citations (Scopus)

  • Age- and Tumor Subtype Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

    Schmidt, M. K., Hogervorst, F., van Hien, R., Cornelissen, S., Broeks, A., Adank, M. A., Meijers, H., Waisfisz, Q., Hollestelle, A., Schutte, M., van den Ouweland, A., Hooning, M., Andrulis, I. L., Anton-Culver, H., Antonenkova, N. N., Antoniou, A. C., Arndt, V., Bermisheva, M., Bogdanova, N. V., Bolla, M. K., & 64 othersBrauch, H., Brenner, H., Bruning, T., Burwinkel, B., Chang-Claude, J., Chenevix-Trench, G., Couch, F. J., Cox, A., Cross, S. S., Czene, K., Dunning, A. M., Fasching, P. A., Figueroa, J., Fletcher, O., Flyger, H., Galle, E., Garcia-Closas, M., Giles, G. G., Haeberle, L., Hall, P., Hillemanns, P., Hopper, J. L., Jakubowska, A., John, E. M., Jones, M., Khusnutdinova, E., Knight, J. A., Kosma, V-M., Kristensen, V., Lee, A., Lindblom, A., Lubinski, J., Mannermaa, A., Margolin, S., Meindl, A., Milne, R. L., Muranen, T. A., Newcomb, P. A., Offit, K., Park-Simon, T-W., Peto, J., Pharoah, P. D. P., Robson, M., Rudolph, A., Sawyer, E. J., Schmutzler, R. K., Seynaeve, C., Soens, J., Southey, M. C., Spurdle, A. B., Surowy, H., Swerdlow, A., Tollenaar, R. A. E. M., Tomlinson, I., Trentham-Dietz, A., Vachon, C., Wang, Q., Whittemore, A. S., Ziogas, A., van der Kolk, L., Nevanlinna, H., Doerk, T., Bojesen, S. & Easton, D. F., 10 Aug 2016, In: Journal of clinical oncology. 34, 23, p. 2750-+

    Research output: Contribution to journal › Article › Academic › peer-review

    135 Citations (Scopus)

  • Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer

    Cornelis, R. S., Vasen, H. F., Meijers-Heijboer, H., Ford, D., van Vliet, M., van Tilborg, A. A., Cleton, F. J., Klijn, J. G., Menko, F. H. & Meera Khan, P., 1995, In: Human genetics. 95, 5, p. 539-544

    Research output: Contribution to journal › Article › Academic › peer-review

    17 Citations (Scopus)

  • A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age

    Ahsan, H., Halpern, J., Kibriya, M. G., Pierce, B. L., Tong, L., Gamazon, E., McGuire, V., Felberg, A., Shi, J., Jasmine, F., Roy, S., Brutus, R., Argos, M., Melkonian, S., Chang-Claude, J., Andrulis, I., Hopper, J. L., John, E. M., Malone, K., Ursin, G., & 57 othersGammon, M. D., Thomas, D. C., Seminara, D., Casey, G., Knight, J. A., Southey, M. C., Giles, G. G., Santella, R. M., Lee, E., Conti, D., Duggan, D., Gallinger, S., Haile, R., Jenkins, M., Lindor, N. M., Newcomb, P., Michailidou, K., Apicella, C., Park, D. J., Peto, J., Fletcher, O., dos Santos Silva, I., Lathrop, M., Hunter, D. J., Chanock, S. J., Meindl, A., Schmutzler, R. K., Müller-Myhsok, B., Lochmann, M., Beckmann, L., Hein, R., Makalic, E., Schmidt, D. F., Bui, Q. M., Stone, J., Flesch-Janys, D., Dahmen, N., Nevanlinna, H., Aittomäki, K., Blomqvist, C., Hall, P., Czene, K., Irwanto, A., Liu, J., Rahman, N., Turnbull, C., Dunning, A. M., Pharoah, P., Waisfisz, Q., Meijers-Heijboer, H., Uitterlinden, A. G., Rivadeneira, F., Nicolae, D., Easton, D. F., Cox, N. J., Whittemore, A. S. & Aittomaki, K., 2014, In: Cancer epidemiology, biomarkers & prevention. 23, 4, p. 658-669

    Research output: Contribution to journal › Article › Academic › peer-review

    77 Citations (Scopus)

  • A genome wide linkage search for breast cancer susceptibility genes

    Smith, P., McGuffog, L., Easton, D. F., Mann, G. J., Pupo, G. M., Newman, B., Chenevix-Trench, G., Szabo, C., Southey, M., Renard, H., Odefrey, F., Lynch, H., Stoppa-Lyonnet, D., Couch, F., Hopper, J. L., Giles, G. G., McCredie, M. R. E., Buys, S., Andrulis, I., Senie, R., & 27 othersGoldgar, D. E., Oldenburg, R., Kroeze-Jansema, K., Kraan, J., Meijers-Heijboer, H., Klijn, J. G. M., van Asperen, C., van Leeuwen, I., Vasen, H. F. A., Cornelisse, C. J., Devilee, P., Baskcomb, L., Seal, S., Barfoot, R., Mangion, J., Hall, A., Edkins, S., Rapley, E., Wooster, R., Chang-Claude, J., Eccles, D., Evans, D. G., Futreal, P. A., Nathanson, K. L., Weber, B. L., Rahman, N. & Stratton, M. R., 2006, In: Genes, chromosomes & cancer. 45, 7, p. 646-655

    Research output: Contribution to journal › Article › Academic › peer-review

    110 Citations (Scopus)

  • 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., Petrij-Bosch, A., Mieremet, R., Szabo, C., van den Ouweland, A. M. W., Hogervorst, F., Brohet, R., Ligtenberg, M. J. L., Teugels, E., 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., & 27 othersBrink, G., Hageman, S., Arts, P. J. W., Bakker, M. M., Willems, H. W., van der Looij, E., Neyns, B., Bonduelle, M., Jansen, R., Oosterwijk, J. C., 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., van Ommen, G. J. B., Vasen, H. F. A., Cornelisse, C. J., van't Veer, L. J., de Knijff, P., Bakker, E. & Devilee, P., May 1997, In: American journal of human genetics. 60, 5, p. 1041-1049 9 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    157 Citations (Scopus)

  • Alcohol Consumption, Cigarette Smoking, and Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Results from The BRCA1 and BRCA2 Cohort Consortium

    GENEPSO study, EMBRACE Study, HEBON Investigators & KConFab Investigators, 1 Feb 2020, In: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 29, 2, p. 368-378 11 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    22 Citations (Scopus)

  • A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

    Antoniou, A. C., Wang, X., Fredericksen, Z. S., McGuffog, L., Tarrell, R., Sinilnikova, O. M., Healey, S., Morrison, J., Kartsonaki, C., Lesnick, T., Ghoussaini, M., Barrowdale, D., Peock, S., Cook, M., Oliver, C., Frost, D., Eccles, D., Evans, D. G., Eeles, R., Izatt, L., & 158 othersChu, C., Douglas, F., Paterson, J., Stoppa-Lyonnet, D., Houdayer, C., Mazoyer, S., Giraud, S., Lasset, C., Remenieras, A., Caron, O., Hardouin, A., Berthet, P., Hogervorst, F. B. L., Rookus, M. A., Jager, A., van den Ouweland, A., Hoogerbrugge, N., van der Luijt, R. B., Meijers-Heijboer, H., Gómez García, E. B., Devilee, P., Vreeswijk, M. P. G., Lubinski, J., Jakubowska, A., Gronwald, J., Huzarski, T., Byrski, T., Górski, B., Cybulski, C., Spurdle, A. B., Holland, H., Goldgar, D. E., John, E. M., Hopper, J. L., Southey, M., Buys, S. S., Daly, M. B., Terry, M-B., Schmutzler, R. K., Wappenschmidt, B., Engel, C., Meindl, A., Preisler-Adams, S., Arnold, N., Niederacher, D., Sutter, C., Domchek, S. M., Nathanson, K. L., Rebbeck, T., Blum, J. L., Piedmonte, M., Rodriguez, G. C., Wakeley, K., Boggess, J. F., Basil, J., Blank, S. V., Friedman, E., Kaufman, B., Laitman, Y., Milgrom, R., Andrulis, I. L., Glendon, G., Ozcelik, H., Kirchhoff, T., Vijai, J., Gaudet, M. M., Altshuler, D., Guiducci, C., Loman, N., Harbst, K., Rantala, J., Ehrencrona, H., Gerdes, A-M., Thomassen, M., Sunde, L., Peterlongo, P., Manoukian, S., Bonanni, B., Viel, A., Radice, P., Caldes, T., de la Hoya, M., Singer, C. F., Fink-Retter, A., Greene, M. H., Mai, P. L., Loud, J. T., Guidugli, L., Lindor, N. M., Hansen, T. V. O., Nielsen, F. C., Blanco, I., Lazaro, C., Garber, J., Ramus, S. J., Gayther, S. A., Phelan, C., Narod, S., Szabo, C. I., Benitez, J., Osorio, A., Nevanlinna, H., Heikkinen, T., Caligo, M. A., Beattie, M. S., Hamann, U., Godwin, A. K., Montagna, M., Casella, C., Neuhausen, S. L., Karlan, B. Y., Tung, N., Toland, A. E., Weitzel, J., Olopade, O., Simard, J., Soucy, P., Rubinstein, W. S., Arason, A., Rennert, G., Martin, N. G., Montgomery, G. W., Chang-Claude, J., Flesch-Janys, D., Brauch, H., Severi, G., Baglietto, L., Cox, A., Cross, S. S., Miron, P., Gerty, S. M., Tapper, W., Yannoukakos, D., Fountzilas, G., Fasching, P. A., Beckmann, M. W., dos Santos Silva, I., Peto, J., Lambrechts, D., Paridaens, R., Rüdiger, T., Försti, A., Winqvist, R., Pylkäs, K., Diasio, R. B., Lee, A. M., Eckel-Passow, J., Vachon, C., Blows, F., Driver, K., Dunning, A., Pharoah, P. P. D., Offit, K., Pankratz, V. S., Hakonarson, H., Chenevix-Trench, G., Easton, D. F. & Couch, F. J., 2010, In: Nature Genetics. 42, 10, p. 885-892

    Research output: Contribution to journal › Article › Academic › peer-review

    269 Citations (Scopus)

  • 'A low risk is still a risk': exploring women's attitudes towards genetic testing for breast cancer susceptibility in order to target disease prevention

    Henneman, L., Timmermans, D. R., Bouwman, C. M., Cornel, M. C. & Meijers-Heijboer, H., 2011, In: Public Health Genomics. 14, 4-5, p. 238-247

    Research output: Contribution to journal › Article › Academic › peer-review

    46 Citations (Scopus)

  • A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11

    Siddiq, A., Couch, F. J., Chen, G. K., Lindström, S., Eccles, D., Millikan, R. C., Michailidou, K., Stram, D. O., Beckmann, L., Rhie, S. K., Ambrosone, C. B., Aittomäki, K., Amiano, P., Apicella, C., Baglietto, L., Bandera, E. V., Beckmann, M. W., Berg, C. D., Bernstein, L., Blomqvist, C., & 123 othersBrauch, H., Brinton, L., Bui, Q. M., Buring, J. E., Buys, S. S., Campa, D., Carpenter, J. E., Chasman, D. I., Chang-Claude, J., Chen, C., Clavel-Chapelon, F., Cox, A., Cross, S. S., Czene, K., Deming, S. L., Diasio, R. B., Diver, W. R., Dunning, A. M., Durcan, L., Ekici, A. B., Fasching, P. A., Feigelson, H. S., Fejerman, L., Figueroa, J. D., Fletcher, O., Flesch-Janys, D., Gaudet, M. M., Gerty, S. M., Rodriguez-Gil, J. L., Giles, G. G., van Gils, C. H., Godwin, A. K., Graham, N., Greco, D., Hall, P., Hankinson, S. E., Hartmann, A., Hein, R., Heinz, J., Hoover, R. N., Hopper, J. L., Hu, J. J., Huntsman, S., Ingles, S. A., Irwanto, A., Isaacs, C., Jacobs, K. B., John, E. M., Justenhoven, C., Kaaks, R., Kolonel, L. N., Coetzee, G. A., Lathrop, M., Le Marchand, L., Lee, A. M., Lee, I. -M., Lesnick, T., Lichtner, P., Liu, J., Lund, E., Makalic, E., Martin, N. G., McLean, C. A., Meijers-Heijboer, H., Meindl, A., Miron, P., Monroe, K. R., Montgomery, G. W., Müller-Myhsok, B., Nickels, S., Nyante, S. J., Olswold, C., Overvad, K., Palli, D., Park, D. J., Palmer, J. R., Pathak, H., Peto, J., Pharoah, P., Rahman, N., Rivadeneira, F., Schmidt, D. F., Schmutzler, R. K., Slager, S., Southey, M. C., Stevens, K. N., Sinn, H-P., Press, M. F., Ross, E., Riboli, E., Ridker, P. M., Schumacher, F. R., Severi, G., dos Santos Silva, I., Stone, J., Sund, M., Tapper, W. J., Thun, M. J., Travis, R. C., Turnbull, C., Uitterlinden, A. G., Waisfisz, Q., Wang, X., Wang, Z., Weaver, J., Schulz-Wendtland, R., Wilkens, L. R., van den Berg, D., Zheng, W., Ziegler, R. G., Ziv, E., Nevanlinna, H., Easton, D. F., Hunter, D. J., Henderson, B. E., Chanock, S. J., Garcia-Closas, M., Kraft, P., Haiman, C. A., Vachon, C. M., Lindstrom, S., Aittomaki, K. & Lee, AM., 2012, In: Human Molecular Genetics. 21, 24, p. 5373-5384

    Research output: Contribution to journal › Article › Academic › peer-review

    146 Citations (Scopus)

  • A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression

    Kooi, I. E., Mol, B. M., Massink, M. P. G., de Jong, M. C., de Graaf, P., van der Valk, P., Meijers-Heijboer, H., Kaspers, G. J. L., Moll, A. C., te Riele, H., Cloos, J. & Dorsman, J. C., 26 Apr 2016, In: PLOS ONE. 11, 4

    Research output: Contribution to journal › Article › Academic › peer-review

    57 Citations (Scopus)

  • A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers

    Thompson, D., Seal, S., Schutte, M., McGuffog, L., Barfoot, R., Renwick, A., Eeles, R., Sodha, N., Houlston, R., Shanley, S., Klijn, J., Wasielewski, M., Chang-Claude, J., Futreal, P. A., Weber, B. L., Nathanson, K. L., Stratton, M., Meijers-Heijboer, H., Rahman, N. & Easton, D. F., 2006, In: Cancer epidemiology, biomarkers & prevention. 15, 12, p. 2542-2545

    Research output: Contribution to journal › Article › Academic › peer-review

    46 Citations (Scopus)

  • Analysis of the Novel Fanconi Anemia Gene SLX4/FANCP in Familial Breast Cancer Cases

    Bakker, J. L., van Mil, S. E., Crossan, G., Sabbaghian, N., de Leeneer, K., Poppe, B., Adank, M., Gille, H., Verheul, H., Meijers-Heijboer, H., de Winter, J. P., Claes, K., Tischkowitz, M., Waisfisz, Q. & Gille, J. J. P., 2013, In: Human mutation. 34, 1, p. 70-73

    Research output: Contribution to journal › Article › Academic › peer-review

    19 Citations (Scopus)

  • Angiotensin II blockade in Marfan's syndrome

    van Dijk, F. S., Meijers-Heijboer, H. & Pals, G., 2008, In: New England journal of medicine. 359, 16, p. 1733; author reply 1733-1733; author reply 1734

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

    2 Citations (Scopus)

  • A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

    Ding, Y. C., McGuffog, L., Healey, S., Friedman, E., Laitman, Y., Paluch-Shimon, S., Kaufman, B., Liljegren, A., Lindblom, A., Olsson, H., Kristoffersson, U., Stenmark-Askmalm, M., Melin, B., Domchek, S. M., Nathanson, K. L., Rebbeck, T. R., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., & 142 othersGronwald, J., Huzarski, T., Cybulski, C., Byrski, T., Osorio, A., Cajal, T. R., Stavropoulou, A. V., Benítez, J., Hamann, U., Rookus, M., Aalfs, C. M., de Lange, J. L., Meijers-Heijboer, H. E. J., Oosterwijk, J. C., van Asperen, C. J., Gómez García, E. B., Hoogerbrugge, N., Jager, A., van der Luijt, R. B., Easton, D. F., Peock, S., Frost, D., Ellis, S. D., Platte, R., Fineberg, E., Evans, D. G., Lalloo, F., Izatt, L., Eeles, R., Adlard, J., Davidson, R., Eccles, D., Cole, T., Cook, J., Brewer, C., Tischkowitz, M., Godwin, A. K., Pathak, H., Stoppa-Lyonnet, D., Sinilnikova, O. M., Mazoyer, S., Barjhoux, L., Léoné, M., Gauthier-Villars, M., Caux-Moncoutier, V., de Pauw, A., Hardouin, A., Berthet, P., Dreyfus, H., Ferrer, S. F., Collonge-Rame, M-A., Sokolowska, J., Buys, S., Daly, M., Miron, A., Terry, M. B., Chung, W., John, E. M., Southey, M., Goldgar, D., Singer, C. F., tea, M-K. M., Gschwantler-Kaulich, D., Fink-Retter, A., Hansen, T. V. O., Ejlertsen, B., Johannsson, O. T., Offit, K., Sarrel, K., Gaudet, M. M., Vijai, J., Robson, M., Piedmonte, M. R., Andrews, L., Cohn, D., DeMars, L. R., DiSilvestro, P., Rodriguez, G., Toland, A. E., Montagna, M., Agata, S., Imyanitov, E., Isaacs, C., Janavicius, R., Lazaro, C., Blanco, I., Ramus, S. J., Sucheston, L., Karlan, B. Y., Gross, J., Ganz, P. A., Beattie, M. S., Schmutzler, R. K., Wappenschmidt, B., Meindl, A., Arnold, N., Niederacher, D., Preisler-Adams, S., Gadzicki, D., Varon-Mateeva, R., Deissler, H., Gehrig, A., Sutter, C., Kast, K., Nevanlinna, H., Aittomäki, K., Simard, J., Spurdle, A. B., Beesley, J., Chen, X., Tomlinson, G. E., Weitzel, J., Garber, J. E., Olopade, O. I., Rubinstein, W. S., Tung, N., Blum, J. L., Narod, S. A., Brummel, S., Gillen, D. L., Lindor, N., Fredericksen, Z., Pankratz, V. S., Couch, F. J., Radice, P., Peterlongo, P., Greene, M. H., Loud, J. T., Mai, P. L., Andrulis, I. L., Glendon, G., Ozcelik, H., Gerdes, A-M., Thomassen, M., Jensen, U. B., Skytte, A-B., Caligo, M. A., Lee, A., Chenevix-Trench, G., Antoniou, A. C., Neuhausen, S. L. & Shani, P. S., 2012, In: Cancer epidemiology, biomarkers & prevention. 21, 8, p. 1362-1370

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    19 Citations (Scopus)

  • An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

    Blein, S., Bardel, C., Danjean, V., McGuffog, L., Healey, S., Barrowdale, D., Lee, A., Dennis, J., Kuchenbaecker, K. B., Soucy, P., Terry, M. B., Chung, W. K., Goldgar, D. E., Buys, S. S., Janavicius, R., Tihomirova, L., Tung, N., Dorfling, C. M., van Rensburg, E. J., Neuhausen, S. L., & 186 othersDing, Y. C., Gerdes, A-M., Ejlertsen, B., Nielsen, F. C., Hansen, T. VO., Osorio, A., Benitez, J., Conejero, R. A., Segota, E., Weitzel, J. N., Thelander, M., Peterlongo, P., Radice, P., Pensotti, V., Dolcetti, R., Bonanni, B., Peissel, B., Zaffaroni, D., Scuvera, G., Manoukian, S., Varesco, L., Capone, G. L., Papi, L., Ottini, L., Yannoukakos, D., Konstantopoulou, I., Garber, J., Hamann, U., Donaldson, A., Brady, A., Brewer, C., Foo, C., Evans, D. G., Frost, D., Eccles, D., Douglas, F., Cook, J., Adlard, J., Barwell, J., Walker, L., Izatt, L., Side, L. E., Kennedy, M. J., Tischkowitz, M., Rogers, M. T., Porteous, M. E., Morrison, P. J., Platte, R., Eeles, R., Davidson, R., Hodgson, S., Cole, T., Godwin, A. K., Isaacs, C., Claes, K., de Leeneer, K., Meindl, A., Gehrig, A., Wappenschmidt, B., Sutter, C., Engel, C., Niederacher, D., Steinemann, D., Plendl, H., Kast, K., Rhiem, K., Ditsch, N., Arnold, N., Varon-Mateeva, R., Schmutzler, R. K., Preisler-Adams, S., Markov, N. B., Wang-Gohrke, S., de Pauw, A., Lefol, C., Lasset, C., Leroux, D., Rouleau, E., Damiola, F., Dreyfus, H., Barjhoux, L., Golmard, L., Uhrhammer, N., Bonadona, V., Sornin, V., Bignon, Y-J., Carter, J., van Le, L., Piedmonte, M., DiSilvestro, P. A., de la Hoya, M., Caldes, T., Nevanlinna, H., Aittomäki, K., Jager, A., van den Ouweland, A. M., Kets, C. M., Aalfs, C. M., van Leeuwen, F. E., Hogervorst, F. B., Meijers-Heijboer, H. E., Oosterwijk, J. C., van Roozendaal, K. E., Rookus, M. A., Devilee, P., van der Luijt, R. B., Olah, E., Diez, O., Teulé, A., Lazaro, C., Blanco, I., del Valle, J., Jakubowska, A., Sukiennicki, G., Gronwald, J., Lubinski, J., Durda, K., Jaworska-Bieniek, K., Agnarsson, B. A., Maugard, C., Amadori, A., Montagna, M., Teixeira, M. R., Spurdle, A. B., Foulkes, W., Olswold, C., Lindor, N. M., Pankratz, V. S., Szabo, C. I., Lincoln, A., Jacobs, L., Corines, M., Robson, M., Vijai, J., Berger, A., Fink-Retter, A., Singer, C. F., Rappaport, C., Kaulich, D. G., Pfeiler, G., tea, M-K., Greene, M. H., Mai, P. L., Rennert, G., Imyanitov, E. N., Mulligan, A. M., Glendon, G., Andrulis, I. L., Tchatchou, S., Toland, A. E., Pedersen, I. S., Thomassen, M., Kruse, T. A., Jensen, U. B., Caligo, M. A., Friedman, E., Zidan, J., Laitman, Y., Lindblom, A., Melin, B., Arver, B., Loman, N., Rosenquist, R., Olopade, O. I., Nussbaum, R. L., Ramus, S. J., Nathanson, K. L., Domchek, S. M., Rebbeck, T. R., Arun, B. K., Mitchell, G., Karlan, B. Y., Lester, J., Orsulic, S., Stoppa-Lyonnet, D., Thomas, G., Simard, J., Couch, F. J., Offit, K., Easton, D. F., Chenevix-Trench, G., Antoniou, A. C., Mazoyer, S., Phelan, C. M., Sinilnikova, O. M. & Cox, D. G., 2015, In: Breast Cancer Research. 17, 1, p. 61 61.

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    30 Citations (Scopus)

  • A novel CCM2 variant in a family with non-progressive cognitive complaints and cerebral microbleeds

    Cohn-Hokke, P. E., Holstege, H., Weiss, M. M., van der Flier, W. M., Barkhof, F., Sistermans, E. A., Pijnenburg, Y. A. L., van Swieten, J. C., Meijers-Heijboer, H. & Scheltens, P., 1 Apr 2017, In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 174, 3, p. 220-226 7 p.

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    Open Access
    5 Citations (Scopus)

  • A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

    Ameziane, N., May, P., Haitjema, A., van de Vrugt, H. J., van Rossum-Fikkert, S. E., Ristic, D., Williams, G. J., Balk, J., Rockx, D., Li, H., Rooimans, M. A., Oostra, A. B., Velleuer, E., Dietrich, R., Bleijerveld, O. B., Maarten Altelaar, A. F., Meijers-Heijboer, H., Joenje, H., Glusman, G., Roach, J., & 9 othersHood, L., Galas, D., Wyman, C., Balling, R., den Dunnen, J., de Winter, J. P., Kanaar, R., Gelinas, R. & Dorsman, J. C., 2015, In: Nature communications. 6, p. 8829 8829.

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    113 Citations (Scopus)

  • A Novel Splice Site Mutation in the Noncoding Region of BRCA2: Implications for Fanconi Anemia and Familial Breast Cancer Diagnostics

    Bakker, J. L., Thirthagiri, E., van Mil, S. E., Adank, M. A., Ikeda, H., Verheul, H. M. W., Meijers-Heijboer, H., de Winter, J. P., Sharan, S. K. & Waisfisz, Q., 2014, In: Human mutation. 35, 4, p. 442-446

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    9 Citations (Scopus)

  • A partial BRCA1 sequence homology mapping to 4q28

    Stec, I., van Vliet, M., van Eijk, R., Meijers, H., Kroeze, K. H., Dauwerse, J. G., van Ommen, G. J., Cornelisse, C. J., den Dunnen, J. T. & Devilee, P., 2001, In: Cytogenetics and Cell Genetics. 94, 1-2, p. 26-29

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    3 Citations (Scopus)

  • A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships

    van Oostrom, I., Meijers-Heijboer, H., Duivenvoorden, H. J., Bröcker-Vriends, A. H. J. T., van Asperen, C. J., Sijmons, R. H., Seynaeve, C., van Gool, A. R., Klijn, J. G. M., Riedijk, S. R., van Dooren, S. & Tibben, A., 2007, In: Psycho-Oncology. 16, 4, p. 320-328

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    45 Citations (Scopus)

  • Are ATM mutations 7271T-->G and IVS10-6T-->G really high-risk breast cancer-susceptibility alleles?

    Szabo, C. I., Schutte, M., Broeks, A., Houwing-Duistermaat, J. J., Thorstenson, Y. R., Durocher, F., Oldenburg, R. A., Wasielewski, M., Odefrey, F., Thompson, D., Floore, A. N., Kraan, J., Klijn, J. G. M., van den Ouweland, A. M. W., Wagner, T. M. U., Devilee, P., Simard, J., van 't Veer, L. J., Goldgar, D. E. & Meijers-Heijboer, H., 2004, In: Cancer research. 64, 3, p. 840-843

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    48 Citations (Scopus)

  • Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

    AUTHOR GROUP, Aittomaki, K., Jonson, L., Ejlertsen, B., de la Hoya, M., Caldees, T., Dunning, A. M., Oliver, C., Fineberg, E., Cook, M., Peock, S., McCann, E., Murray, A., Jacobs, C., Pichert, G., Lalloo, F., Chu, C., Dorkins, H., Paterson, J., Ong, K. R., & 33 othersTeixeira, M. R., Hogervorst, F. B. L., van der Hout, A. H., Seynaeve, C., van der Luijt, R. B., Ligtenberg, M. J. L., Devilee, P., Wijnen, J. T., Rookus, M. A., Blok, M. J., van den Ouweland, A. M. W., Rodriguez, G. C., Phillips, K. A. A., Piedmonte, M., Nerenstone, S. R., Bae-Jump, V. L., O'Malley, D. M., Ratner, E. S., Schmutzler, R. K., Wappenschmidt, B., Rhiem, K., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Plendl, H. J., Niederacher, D., Sutter, C., Wang-Gohrke, S., Steinemann, D., Preisler-Adams, S., Antoniou, A. C. & Pujana, M. A., 2015, In: PLOS ONE. 10, 4, p. e0120020 e0120020.

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    32 Citations (Scopus)

  • Association analysis identifies 65 new breast cancer risk loci

    NBCS Collaborators, ABCTB Investigators, kConFab/AOCS Investigators, Bogdanova, N. V., Bojesen, S. E., Bonanni, B., Børresen-Dale, A-L., Brand, J. S., Brauch, H., Brennan, P., Brenner, H., Brinton, L., Broberg, P., Brock, I. W., Broeks, A., Brooks-Wilson, A., Brucker, S. Y., Brüning, T., Burwinkel, B., Butterbach, K., & 292 othersCai, Q., Cai, H., Caldés, T., Canzian, F., Carracedo, A., Carter, B. D., Castelao, J. E., Chan, T. L., David Cheng, T-Y., Seng Chia, K., Choi, J-Y., Christiansen, H., Clarke, C. L., Collée, M., Conroy, D. M., Cordina-Duverger, E., Cornelissen, S., Cox, D. G., Cox, A., Cross, S. S., Cunningham, J. M., Czene, K., Daly, M. B., Devilee, P., Doheny, K. F., Dörk, T., Dos-Santos-Silva, I., Dumont, M., Durcan, L., Dwek, M., Eccles, D. M., Ekici, A. B., Eliassen, A. H., Ellberg, C., Elvira, M., Engel, C., Eriksson, M., Fasching, P. A., Figueroa, J., Flesch-Janys, D., Fletcher, O., Flyger, H., Fritschi, L., Gaborieau, V., Gabrielson, M., Gago-Dominguez, M., Gao, Y-T., Gapstur, S. M., García-Sáenz, J. A., Gaudet, M. M., Georgoulias, V., Giles, G. G., Glendon, G., Goldberg, M. S., Goldgar, D. E., González-Neira, A., Grenaker Alnæs, G. I., Grip, M., Gronwald, J., Grundy, A., Guénel, P., Haeberle, L., Hahnen, E., Haiman, C. A., Håkansson, N., Hamann, U., Hamel, N., Hankinson, S., Harrington, P., Hart, S. N., Hartikainen, J. M., Hartman, M., Hein, A., Heyworth, J., Hicks, B., Hillemanns, P., Ho, D. N., Hollestelle, A., Hoover, R. N., Hopper, J. L., Hou, M-F., Hsiung, C-N., Huang, G., Humphreys, K., Ishiguro, J., Ito, H., Iwasaki, M., Iwata, H., Jakubowska, A., Janni, W., John, E. M., Johnson, N., Jones, K., Jones, M., Jukkola-Vuorinen, A., Kaaks, R., Kabisch, M., Kaczmarek, K., Kang, D., Kasuga, Y., Kerin, M. J., Khan, S., Khusnutdinova, E., Kiiski, J. I., Kim, S-W., Knight, J. A., Kosma, V-M., Kristensen, V. N., Krüger, U., Kwong, A., Lambrechts, D., Le Marchand, L., Lee, E., Lee, M. H., Lee, J. W., Neng Lee, C., Lejbkowicz, F., Li, J., Lilyquist, J., Lindblom, A., Lissowska, J., Lo, W-Y., Loibl, S., Long, J., Lophatananon, A., Lubinski, J., Luccarini, C., Lux, M. P., Ma, E. S. K., MacInnis, R. J., Maishman, T., Makalic, E., Malone, K. E., Kostovska, I. M., Mannermaa, A., Manoukian, S., Manson, J. E., Margolin, S., Mariapun, S., Martinez, M. E., Matsuo, K., Mavroudis, D., McKay, J., McLean, C., Meindl, A., Menéndez, P., Menon, U., Meyer, J., Miao, H., Miller, N., Taib, N. A. M., Muir, K., Mulligan, A. M., Mulot, C., Neuhausen, S. L., Nevanlinna, H., Neven, P., Nielsen, S. F., Noh, D-Y., Nordestgaard, B. G., Norman, A., Olopade, O. I., Olson, J. E., Olsson, H., Olswold, C., Orr, N., Pankratz, V. S., Park, S. K., Park-Simon, T-W., Lloyd, R., Perez, J. I. A., Peterlongo, P., Peto, J., Phillips, K-A., Pinchev, M., Plaseska-Karanfilska, D., Prentice, R., Presneau, N., Prokofyeva, D., Pugh, E., Pylkäs, K., Rack, B., Radice, P., Rahman, N., Rennert, G., Rennert, H. S., Rhenius, V., Romero, A., Romm, J., Ruddy, K. J., Rüdiger, T., Rudolph, A., Ruebner, M., Rutgers, E. J. T., Saloustros, E., Sandler, D. P., Sangrajrang, S., Sawyer, E. J., Schmidt, D. F., Schmutzler, R. K., Schneeweiss, A., Schoemaker, M. J., Schumacher, F., Schürmann, P., Scott, R. J., Scott, C., Seal, S., Seynaeve, C., Shah, M., Sharma, P., Shen, C-Y., Sheng, G., Sherman, M. E., Shrubsole, M. J., Shu, X-O., Smeets, A., Sohn, C., Southey, M. C., Spinelli, J. J., Stegmaier, C., Stewart-Brown, S., Stone, J., Stram, D. O., Surowy, H., Swerdlow, A., Tamimi, R., Taylor, J. A., Tengström, M., teo, S. H., Beth Terry, M., Tessier, D. C., Thanasitthichai, S., Thöne, K., Tollenaar, R. A. E. M., Tomlinson, I., Tong, L., Torres, D., Truong, T., Tseng, C-C., Tsugane, S., Ulmer, H-U., Ursin, G., Untch, M., Vachon, C., van Asperen, C. J., van den Berg, D., van den Ouweland, A. M. W., van der Kolk, L., van der Luijt, R. B., Vincent, D., Vollenweider, J., Wang-Gohrke, S., Weinberg, C. R., Wendt, C., Whittemore, A. S., Wildiers, H., Willett, W., Winqvist, R., Wolk, A., Wu, A. H., Xia, L., Yamaji, T., Yang, X. R., Har Yip, C., Yoo, K-Y., Yu, J-C., Zheng, W., Zheng, Y., Zhu, B., Ziogas, A., Ziv, E., Lakhani, S. R., Antoniou, A. C., Droit, A., Andrulis, I. L., Amos, C. I., Couch, F. J., Pharoah, P. D. P., Chang-Claude, J., Hall, P., Hunter, D. J., Milne, R. L., García-Closas, M., Schmidt, M. K., Chanock, S. J., Dunning, A. M., Edwards, S. L., Bader, G. D., Chenevix-Trench, G., Simard, J., Kraft, P. & Easton, D. F., 2 Nov 2017, In: NATURE. 551, 7678, p. 92-94 3 p.

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    846 Citations (Scopus)

  • Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses

    Khankari, N. K., Shu, X. O., Wen, W., Kraft, P., Lindström, S., Peters, U., Schildkraut, J., Schumacher, F., Bofetta, P., Risch, A., Bickeböller, H., Amos, C. I., Easton, D., Eeles, R. A., Gruber, S. B., Haiman, C. A., Hunter, D. J., Chanock, S. J., Pierce, B. L., Zheng, W., & 94 othersBlalock, K., Campbell, P. T., Casey, G., Conti, D. V., Edlund, C. K., Figueiredo, J., James Gauderman, W., Gong, J., Green, R. C., Harju, J. F., Harrison, T. A., Jacobs, E. J., Jenkins, M. A., Jiao, S., Li, L., Lin, Y., Manion, F. J., Moreno, V., Mukherjee, B., Raskin, L., Schumacher, F. R., Seminara, D., Severi, G., Stenzel, S. L., Thomas, D. C., Hopper, J. L., Southey, M. C., Makalic, E., Schmidt, D. F., Fletcher, O., Peto, J., Gibson, L., dos Santos Silva, I., Ahsan, H., Whittemore, A., Waisfisz, Q., Meijers-Heijboer, H., Adank, M., van der Luijt, R. B., Uitterlinden, A. G., Hofman, A., Meindl, A., Schmutzler, R. K., Müller-Myhsok, B., Lichtner, P., Nevanlinna, H., Muranen, T. A., Aittomäki, K., Blomqvist, C., Chang-Claude, J., Hein, R., Dahmen, N., Beckman, L., Crisponi, L., Hall, P., Czene, K., Irwanto, A., Liu, J., Easton, D. F., Turnbull, C., Rahman, N., Eeles, R., Kote-Jarai, Z., Muir, K., Giles, G., Neal, D., Donovan, J. L., Hamdy, F. C., Wiklund, F., Gronberg, H., Haiman, C., Schumacher, F., Travis, R., Riboli, E., Hunter, D., Gapstur, S., Berndt, S., Chanock, S., Han, Y., Su, L., Wei, Y., Hung, R. J., Brhane, Y., McLaughlin, J., Brennan, P., McKay, J. D., Rosenberger, A., Houlston, R. S., Caporaso, N., Teresa Landi, M., Heinrich, J., Wu, X., Ye, Y. & Christiani, D. C., 1 Sept 2016, In: PLoS medicine. 13, 9, e1002118.

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    62 Citations (Scopus)

  • Association between the CHEK2*1100delC germ line mutation and estrogen receptor status

    de Bock, G. H., Mourits, M. J. E., 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., 2006, In: International journal of gynecological cancer. 16, Suppl. 2, p. 552-555

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    16 Citations (Scopus)

  • Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

    EMBRACE, GEMO Study Collaborators, HEBON, KConFab Investigators, Foretova, L., Fostira, F., Foulkes, W. D., Fountzilas, G., Friedman, E., Frost, D., Ganschow, P., Ganz, P. A., Garber, J., Gayther, S. A., Gerdes, A-M., Glendon, G., Godwin, A. K., Goldgar, D. E., Greene, M. H., Gronwald, J., & 102 othersHahnen, E., Hamann, U., Hansen, T. V. O., Hart, S., Hays, J. L., Hogervorst, F. B. L., Hulick, P. J., Imyanitov, E. N., Isaacs, C., Izatt, L., Jakubowska, A., James, P., Janavicius, R., Jensen, U. B., John, E. M., Joseph, V., Just, W., Kaczmarek, K., Karlan, B. Y., Kets, C. M., Kirk, J., Kriege, M., Laitman, Y., Laurent, M., Lazaro, C., Leslie, G., Lester, J., Lesueur, F., Liljegren, A., Loman, N., Loud, J. T., Manoukian, S., Mariani, M., Mazoyer, S., McGuffog, L., Meindl, A., Miller, A., Montagna, M., Mulligan, A. M., Nathanson, K. L., Neuhausen, S. L., Nevanlinna, H., Nussbaum, R. L., Olah, E., Olopade, O. I., Ong, K-R., Osorio, A., Papi, L., Park, S. K., Pedersen, I. S., Peissel, B., Segura, P. P., Peterlongo, P., Phelan, C. M., Radice, P., Rantala, J., Rappaport-Fuerhauser, C., Rennert, G., Richardson, A., Robson, M., Rodriguez, G. C., Rookus, M. A., Schmutzler, R. K., Sevenet, N., Shah, P. D., Singer, C. F., Slavin, T. P., Snape, K., Sokolowska, J., Sønderstrup, I. M. H., Southey, M., Spurdle, A. B., Stadler, Z., Stoppa-Lyonnet, D., Sukiennicki, G., Sutter, C., Tan, Y., tea, M-K., Teixeira, M. R., Teulé, A., teo, S-H., Terry, M. B., Thomassen, M., Tihomirova, L., Tischkowitz, M., Tognazzo, S., Toland, A. E., Tung, N., van den Ouweland, A. M. W., van der Luijt, R. B., van Rensburg, E. J., Varon-Mateeva, R., Wappenschmidt, B., Wijnen, J. T., Rebbeck, T., Chenevix-Trench, G., Offit, K., Couch, F. J., Nord, S., Easton, D. F., Antoniou, A. C. & Simard, J., 1 Jan 2017, In: Breast cancer research and treatment. 161, 1, p. 117-134 18 p.

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    19 Citations (Scopus)

  • Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

    Zhao, Z., Wen, W., Michailidou, K., Bolla, M. K., Wang, Q., Zhang, B., Long, J., Shu, X-O., Schmidt, M. K., Milne, R. L., Garcia-Closas, M., Chang-Claude, J., Lindstrom, S., Bojesen, S. E., Ahsan, H., Aittomaki, K., Andrulis, I. L., Anton-Culver, H., Arndt, V., Beckmann, M. W., & 98 othersBeeghly-Fadiel, A., Benitez, J., Blomqvist, C., Bogdanova, N. V., Borresen-Dale, A-L., Brand, J., Brauch, H., Brenner, H., Burwinkel, B., Cai, Q., Casey, G., Chenevix-Trench, G., Couch, F. J., Cox, A., Cross, S. S., Czene, K., Doerk, T., Dumont, M., Fasching, P. A., Figueroa, J., Flesch-Janys, D., Fletcher, O., Flyger, H., Fostira, F., Gammon, M., Giles, G. G., Guenel, P., Haiman, C. A., Hamann, U., Harrington, P., Hartman, M., Hooning, M. J., Hopper, J. L., Jakubowska, A., Jasmine, F., John, E. M., Johnson, N., Kabisch, M., Khan, S., Kibriya, M., Knight, J. A., Kosma, V-M., Kriege, M., Kristensen, V., Le Marchand, L., Lee, E., Li, J., Lindblom, A., Lophatananon, A., Luben, R., Lubinski, J., Malone, K. E., Mannermaa, A., Manoukian, S., Margolin, S., Marme, F., McLean, C., Meijers-Heijboer, H., Meindl, A., Miao, H., Muir, K., Neuhausen, S. L., Nevanlinna, H., Neven, P., Olson, J. E., Perkins, B., Peterlongo, P., Phillips, K-A., Pylkas, K., Rudolph, A., Santella, R., Sawyer, E. J., Schmutzler, R. K., Schoemaker, M., Shah, M., Shrubsole, M., Southey, M. C., Swerdlow, A. J., Toland, A. E., Tomlinson, I., Torres, D., Therese Truong, T., Ursin, G., Van Der Luijt, R. B., Verhoef, S., Wang-Gohrke, S., Whittemore, A. S., Winqvist, R., Zamora, M. P., Zhao, H., Dunning, A. M., Simard, J., Hall, P., Kraft, P., Pharoah, P., Hunter, D., Easton, D. F. & Zheng, W., May 2016, In: CCC. Cancer Causes and Control. 27, 5, p. 679-693

    Research output: Contribution to journal › Article › Academic › peer-review

    20 Citations (Scopus)

  • Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

    Patel, V. L., Busch, E. L., Friebel, T. M., Cronin, A., Leslie, G., McGuffog, L., Adlard, J., Agata, S., Agnarsson, B. A., Ahmed, M., Aittomäki, K., Alducci, E., Andrulis, I. L., Arason, A., Arnold, N., Artioli, G., Arver, B., Auber, B., Azzollini, J., Balmaña, J., & 244 othersBarkardottir, R. B., Barnes, D. R., Barroso, A., Barrowdale, D., Belotti, M., Benitez, J., Bertelsen, B., Blok, M. J., Bodrogi, I., Bonadona, V., Bonanni, B., Bondavalli, D., Boonen, S. E., Borde, J., Borg, A., Bradbury, A. R., Brady, A., Brewer, C., Brunet, J., Buecher, B., Buys, S. S., Cabezas-Camarero, S., Caldés, T., Caliebe, A., Caligo, M. A., Calvello, M., Campbell, I. G., Carnevali, I., Carrasco, E., Chan, T. L., Chu, A. T. W., Chung, W. K., Claes, K. B. M., Collaborators, G. S., Collaborators, E., Cook, J., Cortesi, L., Couch, F. J., Daly, M. B., Damante, G., Darder, E., Davidson, R., de la Hoya, M., Puppa, L. D., Dennis, J., Díez, O., Ding, Y. C., Ditsch, N., Domchek, S. M., Donaldson, A., Dworniczak, B., Easton, D. F., Eccles, D. M., Eeles, R. A., Ehrencrona, H., Ejlertsen, B., Engel, C., Evans, D. G., Faivre, L., Faust, U., Feliubadaló, L., Foretova, L., Fostira, F., Fountzilas, G., Frost, D., García-Barberán, V., Garre, P., Gauthier-Villars, M., Géczi, L., Gehrig, A., Gerdes, A. M., Gesta, P., Giannini, G., Glendon, G., Godwin, A. K., Radice, P., Greene, M. H., Gutierrez-Barrera, A. M., Hahnen, E., Hamann, U., Hauke, J., Herold, N., Hogervorst, F. B. L., Honisch, E., Hopper, J. L., Hulick, P. J., Investigators, KC. F., Investigators, H., Izatt, L., Jager, A., James, P., Janavicius, R., Jensen, U. B., Jensen, T. D., Johannsson, O. T., John, E. M., Joseph, V., Kang, E., Kast, K., Kiiski, J. I., Kim, S. W., Kim, Z., Ko, K. P., Konstantopoulou, I., Kramer, G., Krogh, L., Kruse, T. A., Kwong, A., Larsen, M., Lasset, C., Lautrup, C., Lazaro, C., Lee, J., Lee, J. W., Lee, M. H., Lemke, J., Lesueur, F., Liljegren, A., Lindblom, A., Llovet, P., Lopez-Fernández, A., Lopez-Perolio, I., Lorca, V., Loud, J. T., Ma, E. S. K., Mai, P. L., Manoukian, S., Mari, V., Martin, L., Matricardi, L., Mebirouk, N., Medici, V., Meijers-Heijboer, H. E. J., Meindl, A., Mensenkamp, A. R., Miller, C., Gomes, D. M., Montagna, M., Mooij, T. M., Moserle, L., Mouret-Fourme, E., Mulligan, A. M., Nathanson, K. L., Navratilova, M., Nevanlinna, H., Niederacher, D., Nielsen, F. C. C., Nikitina-Zake, L., Offit, K., Olah, E., Olopade, O. I., Ong, K. R., Osorio, A., Ott, C. E., Palli, D., Park, S. K., Parsons, M. T., Pedersen, I. S., Peissel, B., Peixoto, A., Pérez-Segura, P., Peterlongo, P., Petersen, A. H., Porteous, M. E., Pujana, M. A., Radice, P., Ramser, J., Rantala, J., Rashid, M. U., Rhiem, K., Rizzolo, P., Robson, M. E., Rookus, M. A., Rossing, C. M., Ruddy, K. J., Santos, C., Saule, C., Scarpitta, R., Schmutzler, R. K., Schuster, H., Senter, L., Seynaeve, C. M., Shah, P. D., Sharma, P., Shin, V. Y., Silvestri, V., Simard, J., Singer, C. F., Skytte, A. B., Snape, K., Solano, A. R., Soucy, P., Southey, M. C., Spurdle, A. B., Steele, L., Steinemann, D., Stoppa-Lyonnet, D., Stradella, A., Sunde, L., Sutter, C., Tan, Y. Y., Teixeira, M. R., Teo, S. H., Thomassen, M., Tibiletti, M. G., Tischkowitz, M., Tognazzo, S., Toland, A. E., Tommasi, S., Torres, D., Toss, A., Trainer, A. H., Tung, N., van Asperen, C. J., van der Baan, F. H., van der Kolk, L. E., van der Luijt, R. B., van Hest, L. P., Varesco, L., Varon-Mateeva, R., Viel, A., Vierstrate, J., Villa, R., von Wachenfeldt, A., Wagner, P., Wang-Gohrke, S., Wappenschmidt, B., Weitzel, J. N., Wieme, G., Yadav, S., Yannoukakos, D., Yoon, S. Y., Zanzottera, C., Zorn, K. K., D'Amico, A. V., Freedman, M. L., Pomerantz, M. M., Chenevix-Trench, G., Antoniou, A. C., Neuhausen, S. L., Ottini, L., Nielsen, H. R., Rebbeck, T. R. & Goldgar, D. E., 1 Feb 2020, In: Cancer research. 80, 3, p. 624-638 15 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    36 Citations (Scopus)

  • Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

    AUTHOR GROUP, Nelen, M. R., van den Ouweland, A. M. W., Seynaeve, C., van der Luijt, R. B., Devilee, P., Easton, D. F., Peock, S., Frost, D., Platte, R., Ellis, S. D., Fineberg, E., Evans, D. G., Lalloo, F., Eeles, R., Jacobs, C., Adlard, J., Davidson, R., Eccles, D., Cole, T., & 31 othersCook, J., Godwin, A., Bove, B., Stoppa-Lyonnet, D., Caux-Moncoutier, V., Belotti, M., Tirapo, C., Mazoyer, S., Barjhoux, L., Boutry-Kryza, N., Pujol, P., Coupier, I., Peyrat, J. P., Vennin, P., Muller, D., Fricker, J. P., Venat-Bouvet, L., Johannsson, O., Isaacs, C., Schmutzler, R., Wappenschmidt, B., Meindl, A., Arnold, N., Varon-Mateeva, R., Niederacher, D., Sutter, C., Deissler, H., Preisler-Adams, S., Simard, J., Soucy, P. & Durocher, F., 2012, In: British journal of cancer. 106, 12, p. 2016-2024

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    23 Citations (Scopus)

  • Association of rare MSH6 variants with familial breast cancer

    Wasielewski, M., Riaz, M., Vermeulen, J., van den Ouweland, A., Labrijn-Marks, I., Olmer, R., van der Spaa, L., Klijn, J. G. M., Meijers-Heijboer, H., Dooijes, D. & Schutte, M., 2010, In: Breast cancer research and treatment. 123, 2, p. 315-320

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    Open Access
    11 Citations (Scopus)

  • Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

    AUTHOR GROUP, 2014, In: Breast Cancer Research. 16, 6, p. 3416

    Research output: Contribution to journal › Article › Academic › peer-review

    43 Citations (Scopus)

  • A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

    BCAC, Cornelissen, S., Couch, F. J., Cox, D., Cox, A., Cross, S. S., Cunningham, J. M., Czene, K., Daly, M. B., Devilee, P., Doheny, K. F., Dörk, T., Dos-Santos-Silva, I., Dumont, M., Dwek, M., Eccles, D. M., Eilber, U., Eliassen, A. H., Engel, C., Eriksson, M., & 141 othersFachal, L., Fasching, P. A., Figueroa, J., Flesch-Janys, D., Fletcher, O., Flyger, H., Fritschi, L., Gabrielson, M., Gago-Dominguez, M., Gapstur, S. M., García-Closas, M., Gaudet, M. M., Ghoussaini, M., Giles, G. G., Goldberg, M. S., Goldgar, D. E., González-Neira, A., Guénel, P., Hahnen, E., Haiman, C. A., Håkansson, N., Hall, P., Hallberg, E., Hamann, U., Harrington, P., Hein, A., Hicks, B., Hillemanns, P., Hollestelle, A., Hoover, R. N., Hopper, J. L., Huang, G., Humphreys, K., Hunter, D. J., Jakubowska, A., Janni, W., John, E. M., Johnson, N., Jones, K., Jones, M. E., Jung, A., Kaaks, R., Kerin, M. J., Khusnutdinova, E., Kosma, V-M., Kristensen, V. N., Lambrechts, D., le Marchand, L., Li, J., Lindström, S., Lissowska, J., Lo, W-Y., Loibl, S., Lubinski, J., Luccarini, C., Lux, M. P., MacInnis, R. J., Maishman, T., Kostovska, I. M., Mannermaa, A., Manson, J. E., Margolin, S., Mavroudis, D., Meindl, A., Menon, U., Meyer, J., Mulligan, A. M., Neuhausen, S. L., Nevanlinna, H., Neven, P., Nielsen, S. F., Nordestgaard, B. R. G., Olopade, O. I., Olson, J. E., Olsson, H. K., Peterlongo, P., Peto, J., Plaseska-Karanfilska, D., Prentice, R., Presneau, N., Pylkäs, K., Rack, B., Radice, P., Rahman, N., Rennert, G., Rennert, H. S., Rhenius, V., Romero, A., Romm, J., Rudolph, A., Saloustros, E., Sandler, D. P., Sawyer, E. J., Schmidt, M. K., Schmutzler, R. K., Schneeweiss, A., Scott, R. J., Scott, C. G., Seal, S., Shah, M., Shrubsole, M. J., Smeets, A., Southey, M. C., Spinelli, J. J., Stone, J., Surowy, H., Swerdlow, A. J., Tamimi, R. M., Tapper, W., Taylor, J. A., Terry, M. B., Tessier, D. C., Thomas, A., Thöne, K., Tollenaar, R. A. E. M., Torres, D., Truong, T., Untch, M., Vachon, C., van den Berg, D., Vincent, D., Weinberg, C. R., Wendt, C., Whittemore, A. S., Wildiers, H., Willett, W. C., Winqvist, R., Wolk, A., Xia, L., Yang, X. R., Ziogas, A., Ziv, E., Dunning, A. M., Pharoah, P. D. P., Simard, J., Milne, R. L., Edwards, S. L., Kraft, P., Easton, D. F., Chenevix-Trench, G. & Zheng, W., Jul 2018, In: Nature Genetics. 50, 7, p. 968-+

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    137 Citations (Scopus)

  • Attitudes and distress levels in women at risk to carry a BRCA1/BRCA2 gene mutation who decline genetic testing

    Lodder, L., Frets, P. G., Trijsburg, R. W., Klijn, J. G. M., Seynaeve, C., Tilanus, M. M. A., Bartels, C. C. M., Meijers-Heijboer, E. J., Verhoog, L. C. & Niermeijer, M. F., 2003, In: American journal of medical genetics. Part A. 119A, 3, p. 266-272

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    27 Citations (Scopus)

  • Attitudes towards termination of pregnancy in subjects who underwent presymptomatic testing for the BRCA1/BRCA2 gene mutation in The Netherlands

    Lodder, L. N., Frets, P. G., Trijsburg, R. W., Meijers-Heijboer, E. J., Klijn, J. G. & Niermeijer, M. F., 2000, In: Journal of medical genetics. 37, 11, p. 883-884

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

    23 Citations (Scopus)

  • Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

    Wagner, A., Hendriks, Y., Meijers-Heijboer, E. J., de Leeuw, W. J., Morreau, H., Hofstra, R., Tops, C., Bik, E., Bröcker-Vriends, A. H., van der Meer, C., Lindhout, D., Vasen, H. F., Breuning, M. H., Cornelisse, C. J., van Krimpen, C., Niermeijer, M. F., Zwinderman, A. H., Wijnen, J. & Fodde, R., 2001, In: Journal of medical genetics. 38, 5, p. 318-322

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    132 Citations (Scopus)

  • Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3)

    GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators & ABCTB Investigators, 1 Dec 2021, In: Nature communications. 12, 1, 2986.

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

    Open Access

  • Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan Syndrome

    Franken, R., den Hartog, A. W., Radonic, T., Micha, D., Maugeri, A., van Dijk, F. S., Meijers-Heijboer, H. E., Timmermans, J., Scholte, A. J., van den Berg, M. P., Groenink, M., Mulder, B. J. M., Zwinderman, A. H., de Waard, V. & Pals, G., 2015, In: Circulation. Cardiovascular genetics. 8, 2, p. 383-388

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    132 Citations (Scopus)

  • Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies

    Poley, J-W., Wagner, A., Hoogmans, M. M. C. P., Menko, F. H., Tops, C., Kros, J. M., Reddingius, R. E., Meijers-Heijboer, H., Kuipers, E. J. & Dinjens, W. N. M., 2007, In: Cancer. 109, 11, p. 2349-2356

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    74 Citations (Scopus)

  • Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis

    van Dijk, T., Ferdinandusse, S., Ruiter, J. P. N., Alders, M., Mathijssen, I. B., Parboosingh, J. S., Innes, A. M., Meijers-Heijboer, H., Poll-The, B. T., Bernier, F. P., Wanders, R. J. A., Lamont, R. E. & Baas, F., 1 Dec 2018, In: European journal of human genetics. 26, 12, p. 1752-1758 7 p.

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    25 Citations (Scopus)

  • Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes

    van Walree, E. S., Wyrwoll, M. J., Hamer, G., Rotte, N., Motazacker, M. M., Meijers-Heijboer, H., Alders, M., Meißner, A., Kaminsky, E., Wöste, M., Krallmann, C., Kliesch, S., Hunt, T. J., Clark, A. T., Silber, S., Stallmeyer, B., Friedrich, C., van Pelt, A. M. M., Mathijssen, I. B. & Tüttelmann, F., 27 Dec 2021, In: Human Reproduction. 37, 1, p. 178-189 12 p.

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    18 Citations (Scopus)

  • Body weight and risk of breast cancer in BRCA1/2 mutation carriers

    AUTHOR GROUP, 2011, In: Breast cancer research and treatment. 126, 1, p. 193-202

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    56 Citations (Scopus)