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Hanne Meijers-Heijboer

PROF.DR., (Principal Investigator)

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

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  • 2023

    PRDM10 directs FLCN expression in a novel disorder overlapping with Birt-Hogg-Dubé syndrome and familial lipomatosis

    van de Beek, I., Glykofridis, I. E., Oosterwijk, J. C., Akker, P. C., Diercks, G. F. H., Bolling, M. C., Waisfisz, Q., Mensenkamp, A. R., Balk, J. A., Zwart, R., Postma, A. V., Meijers-Heijboer, H. E. J., Moorselaar, R. J. A., Wolthuis, R. M. F. & Houweling, A. C., 1 Apr 2023, In: Human Molecular Genetics. 32, 7, p. 1223-1235 13 p.

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

    Open Access
    4 Citations (Scopus)
  • 2022

    Combined germline pathogenic variants in FLCN and TP53 are associated with early onset renal cell carcinoma and brain tumors

    van de Beek, I., Glykofridis, I. E., Wagner, A., den Toom, D. T., Bongers, E. M. H. F., van Leenders, G. J. L. H., Johannesma, P. C., Meijers-Heijboer, H. E. J., Wolthuis, R. M. F., van Steensel, M. A. M., Dubbink, H. J. & Houweling, A. C., 2022, (E-pub ahead of print) In: Molecular genetics and genomic medicine.

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

    Open Access
    2 Citations (Scopus)

  • Detection and localization of early- and late-stage cancers using platelet RNA

    In 't Veld, S. G. J. G., Arkani, M., Post, E., Antunes-Ferreira, M., D'Ambrosi, S., Vessies, D. C. L., Vermunt, L., Vancura, A., Muller, M., Niemeijer, A-L. N., Tannous, J., Meijer, L. L., Le Large, T. Y. S., Mantini, G., Wondergem, N. E., Heinhuis, K. M., van Wilpe, S., Smits, A. J., Drees, E. E. E., Roos, E., & 96 othersLeurs, C. E., Tjon Kon Fat, L-A., van der Lelij, E. J., Dwarshuis, G., Kamphuis, M. J., Visser, L. E., Harting, R., Gregory, A., Schweiger, M. W., Wedekind, L. E., Ramaker, J., Zwaan, K., Verschueren, H., Bahce, I., de Langen, A. J., Smit, E. F., van den Heuvel, M. M., Hartemink, K. J., Kuijpers, M. J. E., Oude Egbrink, M. G. A., Griffioen, A. W., Rossel, R., Hiltermann, T. J. N., Lee-Lewandrowski, E., Lewandrowski, K. B., De Witt Hamer, P. C., Kouwenhoven, M., Reijneveld, J. C., Leenders, W. P. J., Hoeben, A., Verdonck-de Leeuw, I. M., Leemans, C. R., Baatenburg de Jong, R. J., Terhaard, C. H. J., Takes, R. P., Langendijk, J. A., de Jager, S. C., Kraaijeveld, A. O., Pasterkamp, G., Smits, M., Schalken, J. A., Łapińska-Szumczyk, S., Łojkowska, A., Żaczek, A. J., Lokhorst, H., van de Donk, N. W. C. J., Nijhof, I., Prins, H-J., Zijlstra, J. M., Idema, S., Baayen, J. C., Teunissen, C. E., Killestein, J., Besselink, M. G., Brammen, L., Bachleitner-Hofmann, T., Mateen, F., Plukker, J. T. M., Heger, M., de Mast, Q., Lisman, T., Pegtel, D. M., Bogaard, H-J., Jassem, J., Supernat, A., Mehra, N., Gerritsen, W., de Kroon, C. D., Lok, C. A. R., Piek, J. M. J., Steeghs, N., van Houdt, W. J., Brakenhoff, R. H., Sonke, G. S., Verheul, H. M., Giovannetti, E., Kazemier, G., Sabrkhany, S., Schuuring, E., Sistermans, E. A., Wolthuis, R., Meijers-Heijboer, H., Dorsman, J., Oudejans, C., Ylstra, B., Westerman, B. A., van den Broek, D., Koppers-Lalic, D., Wesseling, P., Nilsson, R. J. A., Vandertop, W. P., Noske, D. P., Tannous, B. A., Sol, N., Best, M. G. & Wurdinger, T., 12 Sept 2022, In: Cancer cell. 40, 9, p. 999-1009.e6 18 p.

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

    Open Access
    32 Citations (Scopus)

  • Long-Term Weight Outcome After Bariatric Surgery in Patients with Melanocortin-4 Receptor Gene Variants: a Case–Control Study of 105 Patients

    Cooiman, M. I., Alsters, S. I. M., Duquesnoy, M., Hazebroek, E. J., Meijers-Heijboer, H. J., Chahal, H., le Beyec-le Bihan, J., Clément, K., Soula, H., Blakemore, A. I., Poitou, C. & van Haelst, M. M., 1 Mar 2022, In: Obesity Surgery. 32, 3, p. 837-844 8 p.

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

    15 Citations (Scopus)
  • 2021

    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)

  • 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.

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

    18 Citations (Scopus)

  • Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms

    van Walree, E. S., Dombrowsky, G., Jansen, I. E., Mirkov, M. U., Zwart, R., Ilgun, A., Guo, D., Clur, S. A. B., Amin, A. S., Savage, J. E., van der Wal, A. C., Waisfisz, Q., Maugeri, A., Wilsdon, A., Bu’Lock, F. A., Hurles, M. E., Dittrich, S., Berger, F., Audain Martinez, E., Christoffels, V. M., & 6 othersHitz, M. P., Milewicz, D. M., Posthuma, D., Meijers-Heijboer, H., Postma, A. V. & Mathijssen, I. B., Jan 2021, In: Genetics in medicine. 23, 1, p. 103-110 8 p.

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

    Open Access
    5 Citations (Scopus)

  • Isolated Increased Nuchal Translucency in First Trimester Ultrasound Scan: Diagnostic Yield of Prenatal Microarray and Outcome of Pregnancy

    Stuurman, K. E., van der Mespel-Brouwer, M. H., Engels, M. A. J., Elting, M. W., Bhola, S. L. & Meijers-Heijboer, H., 18 Oct 2021, In: Frontiers in Medicine. 8, 737936.

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

    Open Access
    10 Citations (Scopus)

  • Loss of FLCN-FNIP1/2 induces a non-canonical interferon response in human renal tubular epithelial cells

    Glykofridis, I. E., Knol, J. C., Balk, J. A., Westland, D., Pham, T. V., Piersma, S. R., Lougheed, S. M., Derakhshan, S., Veen, P., Rooimans, M. A., van Mil, S. E., Böttger, F., Poddighe, P. J., van de Beek, I., Drost, J., Zwartkruis, F. J. T., de Menezes, R. X., Meijers-Heijboer, H. E. J., Houweling, A. C., Jimenez, C. R., & 1 othersWolthuis, R. M. F., 1 Jan 2021, In: eLife. 10, p. 1-71 71 p., e61630.

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

    Open Access
    13 Citations (Scopus)

  • The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

    OCGN Investigators, HEBON Investigators, KConFab Investigators, GEMO Study Collaborators & EMBRACE Collaborators, 1 Sept 2021, In: Genetics in medicine. 23, 9, p. 1726-1737 12 p.

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

    Open Access
    15 Citations (Scopus)
  • 2020

    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)

  • 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)

  • Clonality, antigen recognition, and suppression of CD8+ T cells differentially affect prognosis of breast cancer subtypes

    Hammerl, D., Massink, M. P. G., Smid, M., van Deurzen, C. H. M., Meijers-Heijboer, H. E. J., Waisfisz, Q., Debets, R. & Martens, J. W. M., 15 Jan 2020, In: Clinical Cancer Research. 26, 2, p. 505-517 13 p.

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

    Open Access
    26 Citations (Scopus)

  • Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

    GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators & ABCTB Investigators, 1 Jan 2020, In: Nature Genetics. 52, 1, p. 56-73 18 p.

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

    92 Citations (Scopus)

  • Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients With Morbid Obesity

    Cooiman, MI., Kleinendorst, L., Aarts, E. O., Janssen, I. M. C., Ploos van Amstel, H. K., Blakemore, A. I., Hazebroek, E. J., Meijers-Heijboer, EJ., van der Zwaag, B., Berends, F. J. & van Haelst, MM., 1 Feb 2020, In: Obesity Surgery. 30, 2, p. 470-477 8 p., 10.1007/s11695-019-04184-w.

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

    40 Citations (Scopus)

  • Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2

    van Dijk, F. S., Semler, O., Etich, J., Köhler, A., Jimenez-Estrada, J. A., Bravenboer, N., Claeys, L., Riesebos, E., Gegic, S., Piersma, S. R., Jimenez, C. R., Waisfisz, Q., Flores, C. L., Nevado, J., Harsevoort, A. J., Janus, G. J. M., Franken, A. A. M., van der Sar, A. M., Meijers-Heijboer, H., Heath, K. E., & 18 othersLapunzina, P., Nikkels, P. G. J., Santen, G. W. E., Nüchel, J., Plomann, M., Wagener, R., Rehberg, M., Hoyer-Kuhn, H., Eekhoff, E. M. W., Pals, G., Mörgelin, M., Newstead, S., Wilson, B. T., Ruiz-Perez, V. L., Maugeri, A., Netzer, C., Zaucke, F. & Micha, D., 5 Nov 2020, In: American journal of human genetics. 107, 5, p. 989 - 999 11 p.

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

    35 Citations (Scopus)

  • No evidence for increased prevalence of colorectal carcinoma in 399 Dutch patients with Birt-Hogg-Dubé syndrome

    van de Beek, I., Glykofridis, I. E., Wolthuis, R. M. F., Gille, H. J. J. P., Johannesma, P. C., Meijers-Heijboer, H. E. J., Moorselaar, R. J. A. V., Houweling, A. C. & van Moorselaar, J. R. A., 18 Feb 2020, In: British journal of cancer. 122, 4, p. 590-594 5 p.

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

    Open Access
    8 Citations (Scopus)

  • Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

    GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2, 1 Oct 2020, In: Genetics in medicine. 22, 10, p. 1653-1666 14 p.

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

    Open Access
    80 Citations (Scopus)

  • Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers: An international prospective cohort of BRCA1 and BRCA2 mutation carriers

    GENEPSO, EMBRACE, HEBON, KConFab Investigators, IBCCS, kConFab & BCFR, 16 Jan 2020, In: Breast Cancer Research. 22, 1, p. 8 1 p., 8.

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

    Open Access
    35 Citations (Scopus)
  • 2019

    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

    30 Citations (Scopus)

  • Centenarian controls increase variant effect sizes by an average twofold in an extreme case–extreme control analysis of Alzheimer’s disease

    Tesi, N., van der Lee, S. J., Hulsman, M., Jansen, I. E., Stringa, N., van Schoor, N., Meijers-Heijboer, H., Huisman, M., Scheltens, P., Reinders, M. J. T., van der Flier, W. M. & Holstege, H., 1 Feb 2019, In: European journal of human genetics. 27, 2, p. 244-253 10 p.

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

    Open Access
    38 Citations (Scopus)

  • Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation

    Holtkamp, K. C. A., Henneman, L., Gille, J. J. P., Meijers-Heijboer, H., Cornel, M. C. & Lakeman, P., 4 Apr 2019, In: Journal of Community Genetics. 10, 2, p. 249-257

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

    Open Access
    4 Citations (Scopus)

  • Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

    HEBON, EMBRACE & GEMO Study Collaborators, 1 Jan 2019, In: Journal of the National Cancer Institute. 111, 4, p. 350-364 15 p.

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

    25 Citations (Scopus)

  • Leptin receptor deficiency: A systematic literature review and prevalence estimation based on population genetics

    Kleinendorst, L., Abawi, O., van der Kamp, H. J., Alders, M., Meijers-Heijboer, H. E. J., van Rossum, E. F. C., van den Akker, E. L. T. & van Haelst, M. M., 1 Jan 2019, In: European journal of endocrinology. 182, 1, p. 47-56 10 p.

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

    44 Citations (Scopus)

  • Loss-of-function variants in myocardin cause congenital megabladder in humans and mice

    Houweling, A. C., Beaman, G. M., Postma, A. V., Blair Gainous, T., Lichtenbelt, K. D., Brancati, F., Lopes, F. M., van der Made, I., Polstra, A. M., Robinson, M. L., Wright, K. D., Ellingford, J. M., Jackson, A. R., Overwater, E., Genesio, R., Romano, S., Camerota, L., D'Angelo, E., Meijers-Heijboer, E. J., Christoffels, V. M., & 5 othersMcHugh, K. M., Black, B. L., Newman, W. G., Woolf, A. S. & Creemers, E. E., 2 Dec 2019, In: Journal of clinical investigation. 129, 12, p. 5374-5380 7 p.

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

    Open Access
    21 Citations (Scopus)

  • Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

    EMBRACE Collaborators, KConFab Investigators, GEMO Study Collaborators & HEBON Investigators, 16 Jul 2019, In: British journal of cancer. 121, 2, p. 180-192 13 p.

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

    15 Citations (Scopus)

  • Polygenetische risicopredictie van veelvoorkomende ziekten

    Jansen, P. R., Broeders, M. J. M., Cornel, M. C. & Meijers-Heijboer, H., 2019, In: Nederlands Tijdschrift voor Geneeskunde. 163

    Research output: Contribution to journal › Article › Professional

  • Polygenetische risicopredictie van veelvoorkomende ziekten: Van epidemiologie naar klinische toepassing

    Translated title of the contribution: Polygenic risk prediction of common diseases: from epidemiology to clinical applicationJansen, P. R., Broeders, M. J. M., Cornel, M. C. & Meijers-Heijboer, H., 1 Jan 2019, In: Nederlands Tijdschrift voor Geneeskunde. 163, 40, 7 p., D3870.

    Research output: Contribution to journal › Article › Professional

    Open Access

  • Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: Update on genetic testing in the NGS era

    Stuurman, K. E., Joosten, M., van der Burgt, I., Elting, M., Yntema, H. G., Meijers-Heijboer, H. & Rinne, T., 1 Oct 2019, In: Journal of medical genetics. 56, 10, p. 654-661

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

    39 Citations (Scopus)

  • Renal imaging in 199 Dutch patients with Birt-Hogg-Dubé syndrome: Screening compliance and outcome

    Johannesma, P. C., van de Beek, I., van der Wel, T. J. W. T., Reinhard, R., Rozendaal, L., Starink, T. M., van Waesberghe, J. H. T. M., Horenblas, S., Gille, H. J. J. P., Jonker, M. A., Meijers-Heijboer, H. E. J., Postmus, P. E., Houweling, A. C. & van Moorselaar, J. R. A., 1 Mar 2019, In: PLOS ONE. 14, 3, e0212952.

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

    Open Access
    16 Citations (Scopus)

  • Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers

    Heemskerk-Gerritsen, B. A. M., Jager, A., Koppert, L. B., Obdeijn, A. I-M., Collée, M., Meijers-Heijboer, H. E. J., Jenner, D. J., Oldenburg, H. S. A., van Engelen, K., de Vries, J., van Asperen, C. J., Devilee, P., Blok, M. J., Kets, C. M., Ausems, M. G. E. M., Seynaeve, C., Rookus, M. A. & Hooning, M. J., 1 Oct 2019, In: Breast cancer research and treatment. 177, 3, p. 723-733 11 p.

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

    Open Access
    107 Citations (Scopus)
  • 2018

    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-+

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

    Open Access
    137 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.

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

    25 Citations (Scopus)

  • Genetic obesity: Next-generation sequencing results of 1230 patients with obesity: next-generation sequencing results of 1230 patients with obesity

    Kleinendorst, L., Massink, M. P. G., Cooiman, M. I., Savas, M., van der Baan-Slootweg, O. H., Roelants, R. J., Janssen, I. C. M., Meijers-Heijboer, H. J., Knoers, N. V. A. M., Ploos van Amstel, H. K., van Rossum, E. F. C., van den Akker, E. L. T., van Haaften, G., van der Zwaag, B. & van Haelst, M. M., Sept 2018, In: Journal of medical genetics. 55, 9, p. 578-586 9 p.

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

    55 Citations (Scopus)

  • Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

    CREAM Consortium & CREAM, Jun 2018, In: Nature Genetics. 50, 6, p. 834-848 15 p.

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

    Open Access
    207 Citations (Scopus)

  • Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

    EMBRACE, Bradbury, A. R., Brewer, C., Buecher, B., Buys, S. S., Caldes, T., Caliebe, A., Caligo, M. A., Campbell, I., Caputo, S., Chiquette, J., Chung, W. K., Claes, K. B. M., Cook, J., Davidson, R., de la Hoya, M., de Leeneer, K., de Pauw, A., Delnatte, C., Diez, O., & 173 othersDing, Y. C., Ditsch, N., Domchek, S. M., Dorfling, C. M., Velazquez, C., Dworniczak, B., Eason, J., Easton, D. F., Eeles, R., Ehrencrona, H., Ejlertsen, B., Engel, C., Engert, S., Evans, D. G., Faivre, L., Feliubadaló, L., Ferrer, S. F., Foretova, L., Fowler, J., Frost, D., Galvão, H. C. R., Ganz, P. A., Garber, J., Gauthier-Villars, M., Gehrig, A., Gerdes, A-M., Gesta, P., Giannini, G., Giraud, S., Glendon, G., Godwin, A. K., Greene, M. H., Gronwald, J., Gutierrez-Barrera, A., Hahnen, E., Hauke, J., Henderson, A., Hentschel, J., Hogervorst, F. B. L., Honisch, E., Imyanitov, E. N., Isaacs, C., Izatt, L., Izquierdo, A., Jakubowska, A., James, P., Janavicius, R., Jensen, U. B., John, E. M., Joseph, V., Kaczmarek, K., Karlan, B. Y., Kast, K., Investigators, KC., Kim, S-W., Konstantopoulou, I., Korach, J., Laitman, Y., Lasa, A., Lasset, C., Lázaro, C., Lee, A., Lee, M. H., Lester, J., Lesueur, F., Liljegren, A., Lindor, N. M., Longy, M., Loud, J. T., Lu, K. H., Lubinski, J., Machackova, E., Manoukian, S., Mari, V., Martínez-Bouzas, C., Matrai, Z., Mebirouk, N., Meindl, A., Mensenkamp, A. R., Mickys, U., Miller, A., Montagna, M., Moysich, K. B., Mulligan, A. M., Musinsky, J., Neuhausen, S. L., Nevanlinna, H., Ngeow, J., Nguyen, H. P., Niederacher, D., Nielsen, H. R., Nielsen, F. C., Nussbaum, R. L., Offit, K., Öfverholm, A., Ong, K-R., Osorio, A., Papi, L., Papp, J., Pasini, B., Pedersen, I. S., MSc, A. P., MSc, N. P., Peterlongo, P., Pohl, E., Ba, N. P., Prajzendanc, K., Prieur, F., Pujol, P., Radice, P., Ramus, S. J., Rantala, J., Rashid, M. U., Rhiem, K., Robson, M., Rodriguez, G. C., Rogers, M. T., Rudaitis, V., Schmidt, A. Y., Schmutzler, R. K., Senter, L., Shah, P. D., Sharma, P., Side, L. E., Simard, J., Singer, C. F., Skytte, A-B., Slavin, T. P., Snape, K., Sobol, H., Southey, M., Steele, L., Steinemann, D., Sukiennicki, G., Sutter, C., Szabo, C. I., Tan, Y. Y., Teixeira, M. R., Terry, M. B., Teulé, A., Thomas, A., Thull, D. L., Tischkowitz, M., Tognazzo, S., Toland, A. E., Topka, S., Trainer, A. H., Tung, N., van Asperen, C. J., van der Hout, A. H., van der Kolk, L. E., van der Luijt, R. B., van Heetvelde, M., Varesco, L., Varon-Mateeva, R., Vega, A., Villarreal-Garza, C., von Wachenfeldt, A., Walker, L., Wang-Gohrke, S., Wappenschmidt, B., Weber, B. H. F., Yannoukakos, D., Yoon, S-Y., Zanzottera, C., Zidan, J., Zorn, K. K., Selkirk, C. G. H., Hulick, P. J., Chenevix-Trench, G., Spurdle, A. B., Antoniou, A. C. & Nathanson, K. L., May 2018, In: Human mutation. 39, 5, p. 593-620 28 p.

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

    Open Access
    199 Citations (Scopus)

  • Preconception carrier screening for multiple disorders: evaluation of a screening offer in a Dutch founder population

    Mathijssen, I. B., Holtkamp, K. C. A., Ottenheim, C. P. E., van Eeten-Nijman, J. M. C., Lakeman, P., Meijers-Heijboer, H., van Maarle, M. C. & Henneman, L., Feb 2018, In: European journal of human genetics. 26, 2, p. 166-175

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

    19 Citations (Scopus)

  • Recontacting in light of new genetic diagnostic techniques for patients with intellectual disability: Feasibility and parental perspectives: Feasibility and parental perspectives

    Beunders, G., Dekker, M., Haver, O., Meijers-Heijboer, H. J. & Henneman, L., Apr 2018, In: European journal of medical genetics. 61, 4, p. 213-218

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

    13 Citations (Scopus)

  • The 100-plus Study of cognitively healthy centenarians: rationale, design and cohort description

    Holstege, H., Beker, N., Dijkstra, T., Pieterse, K., Wemmenhove, E., Schouten, K., Thiessens, L., Horsten, D., Rechtuijt, S., Sikkes, S., van Poppel, F. W. A., Meijers-Heijboer, H., Hulsman, M. & Scheltens, P., Dec 2018, In: European Journal of Epidemiology. 33, 12, p. 1229-1249

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

    37 Citations (Scopus)

  • The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?

    HEBON, Jun 2018, In: European journal of human genetics. 26, 6, p. 848-857 10 p.

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

    5 Citations (Scopus)

  • The Effect of Predictive Testing in Adult-Onset Neurodegenerative Diseases on Social and Personal Life

    Cohn-Hokke, P. E., van Swieten, J. C., Pijnenburg, Y. A. L., Tibben, A., Meijers-Heijboer, H. & Kievit, A., 1 Aug 2018, In: Journal of genetic counseling. 27, 4, p. 947-954 8 p.

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

    9 Citations (Scopus)

  • Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates

    Henneman, P., Bouman, A., Mul, A., Knegt, L., van der Kevie-Kersemaekers, A-M., Zwaveling-Soonawala, N., Meijers-Heijboer, H. E. J., Paul van Trotsenburg, A. S. & Mannens, M. M., 2018, In: PLOS ONE. 13, 3, p. e0194938 e0194938.

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

    Open Access
    19 Citations (Scopus)
  • 2017

    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.

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

    Open Access
    5 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.

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

    836 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.

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

    19 Citations (Scopus)

  • Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: A clinical interpretation strategy

    Holstege, H., Van Der Lee, S. J., Hulsman, M., Wong, T. H., Van Rooij, J. G. J., Weiss, M., Louwersheimer, E., Wolters, F. J., Amin, N., Uitterlinden, A. G., Hofman, A., Ikram, M. A., Van Swieten, J. C., Meijers-Heijboer, H., Van Der Flier, W. M., Reinders, M. J. T., Van Duijn, C. M. & Scheltens, P., 1 Aug 2017, In: European journal of human genetics. 25, 8, p. 973-981 9 p.

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

    78 Citations (Scopus)

  • DNA-diagnostiek bij dementie

    Translated title of the contribution: DNA diagnostics in dementiaAalfs, C. M., Vervenne-van Spaendonk, R., Pijnenburg, Y. A. L., Cohn-Hokke, P. E., Meijers, H. J. & Scheltens, P., 2017, In: Nederlands Tijdschrift voor Geneeskunde. 161, 38-39, p. D1774 d1774.

    Research output: Contribution to journal › Article › Professional

  • Genomic landscape of retinoblastoma in Rb−/−p130−/− mice resembles human retinoblastoma

    Kooi, I. E., van Mil, S. E., MacPherson, D., Mol, B. M., Moll, A. C., Meijers-Heijboer, H., Kaspers, G. J. L., Cloos, J., te Riele, H. & Dorsman, J. C., 1 Mar 2017, In: Genes Chromosomes and Cancer. 56, 3, p. 231-242 12 p.

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

    5 Citations (Scopus)

  • Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

    HEBON Study, AOCS study group, EMBRACE Study, OPAL study group, KConFab Investigators, GEMO Study Collaborators, Blok, M. J., Bodelon, C., Bogdanova, N., Bojesen, A., Bonanni, B., Borg, Å., Bradbury, A. R., Brenton, J. D., Brewer, C., Brinton, L., Broberg, P., Brooks-Wilson, A., Bruinsma, F., Brunet, J., & 350 othersBuecher, B., Butzow, R., Buys, S. S., Caldes, T., Caligo, M. A., Campbell, I., Cannioto, R., Carney, M. E., Cescon, T., Chan, S. B., Chang-Claude, J., Chanock, S., Chen, X. Q., Chiew, Y-E., Chiquette, J., Chung, W. K., Claes, K. B. M., Conner, T., Cook, L. S., Cook, J., Cramer, D. W., Cunningham, J. M., D'Aloisio, A. A., Daly, M. B., Damiola, F., Damirovna, S. D., Dansonka-Mieszkowska, A., Dao, F., Davidson, R., Defazio, A., Delnatte, C., Doheny, K. F., Diez, O., Ding, Y. C., Doherty, J. A., Domchek, S. M., Dorfling, C. M., Dörk, T., Dossus, L., Duran, M., Dürst, M., Dworniczak, B., Eccles, D., Edwards, T., Eeles, R., Eilber, U., Ejlertsen, B., Ekici, A. B., Ellis, S., Elvira, M., Eng, K. H., Engel, C., Evans, D. G., Fasching, P. A., Ferguson, S., Ferrer, S. F., Flanagan, J. M., Fogarty, Z. C., Fortner, R. T., Fostira, F., Foulkes, W. D., Fountzilas, G., Fridley, B. L., Friebel, T. M., Friedman, E., Frost, D., Ganz, P. A., Garber, J., García, M. J., Garcia-Barberan, V., Gehrig, A., Gentry-Maharaj, A., Gerdes, A-M., Giles, G. G., Glasspool, R., Glendon, G., Godwin, A. K., Goldgar, D. E., Goranova, T., Gore, M., Greene, M. H., Gronwald, J., Gruber, S., Hahnen, E., Haiman, C. A., Håkansson, N., Hamann, U., Hansen, T. V. O., Harrington, P. A., Harris, H. R., Hauke, J., Hein, A., Henderson, A., Hildebrandt, M. A. T., Hillemanns, P., Hodgson, S., Høgdall, C. K., Høgdall, E., Hogervorst, F. B. L., Holland, H., Hosking, K., Huang, R-Y., Hulick, P. J., Hung, J., Hunter, D. J., Huntsman, D. G., Huzarski, T., Imyanitov, E. N., Isaacs, C., Iversen, E. 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    Research output: Contribution to journal › Article › Academic › peer-review

    268 Citations (Scopus)

  • Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

    Milne, R. L., Kuchenbaecker, K. B., Michailidou, K., Beesley, J., Kar, S., Lindstrom, S., Hui, S., Lemaçon, A., Soucy, P., Dennis, J., Jiang, X., Rostamianfar, A., Finucane, H., Bolla, M. K., McGuffog, L., Wang, Q., Aalfs, C. M., Abctctb, I., Adams, M., Adlard, J., & 711 othersAgata, S., Ahmed, S., Ahsan, H., Aittom, K. Ä., Fares, A. E., Allen, J., Ambrosone, C. B., Amos, C. I., Andrulis, I. L., Anton-Culver, H., Antonenkova, N. N., Arndt, V., Arnold, N., Aronson, K. J., Auber, B., Auer, P. L., Ausems, M. G. M., Azzollini, J., François, B., Balma, J. N., Barile, M., Barjhoux, L., Barkardottir, R. B., Barrdahl, M., Barnes, D., Barrowdale, D., Baynes, C., Beckmann, M. W., Benitez, J., Bermisheva, M., Bernstein, L., Bignon, Y. J., Blazer, K. R., Blok, M. J., Blomqvist, C., Blot, W., Bobolis, K., Boeckx, B., Bogdanova, N. V., Bojesen, A., Bojesen, S. E., Bonanni, B., Anne-Lise, B. D., Bozsik, A., Bradbury, A. R., Brand, J. S., Brauch, H., Brenner, H., Brigitte, B. D. 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L., Hu, C., Huang, G., Hulick, P. J., Humphreys, K., Hunter, D. J., Imyanitov, E. N., Isaacs, C., Iwasaki, M., Izatt, L., Jakubowska, A., James, P., Janavicius, R., Janni, W., Jensen, U. B., John, E. M., Johnson, N., Jones, K., Jones, M., Jukkola-Vuorinen, A., Kaaks, R., Kabisch, M., Kaczmarek, K., Kang, D., Kast, K., Keeman, R., Kerin, M. J., Kets, C. M., Keupers, M. H., Khan, S., Khusnutdinova, E., Kiiski, J. I., Kim, S. W., Knight, J. A., Konstantopoulou, I., Kosma, V. M., Kristensen, V. N., Kruse, T. A., Kwong, A., Lænkholm, A. V., Laitman, Y., Lalloo, F., Lambrechts, D., Landsman, K., Lasset, C., Lazaro, C., Marchand, L. L., Milne, R. L., Kuchenbaecker, K. B., Michailidou, K., Beesley, J., Kar, S., Lindström, S., Hui, S., Lemaçon, A., Soucy, P., Dennis, J., Jiang, X., Rostamianfar, A., Finucane, H., Bolla, M. K., McGuffog, L., Wang, Q., Aalfs, C. M., Adams, M., Adlard, J., Agata, S., Ahmed, S., Ahsan, H., Aittom, K. Ä., Al-Ejeh, F., Allen, J., Ambrosone, C. B., Amos, C. 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B., Clarke, C. L., Conner, T., Conroy, D. M., Cook, J., Cordina-Duverger, E., Cornelissen, S., Coupier, I., Cox, A., Cox, D. G., Cross, S. S., Cuk, K., Cunningham, J. M., Czene, K., Daly, M. B., Damiola, F., Darabi, H., Davidson, R., Leeneer, K. D., Devilee, P., Dicks, E., Diez, O., Ding, Y. C., Ditsch, N., Doheny, K. F., Domchek, S. M., Dorfling, C. M., Dörk, T., Dos-Santos-Silva, I., Dubois, S., Dugué, P. A., Dumont, M., Dunning, A. M., Durcan, L., Dwek, M., Dworniczak, B., Eccles, D., Eeles, R., Ehrencrona, H., Eilber, U., Ejlertsen, B., Ekici, A. B., Eliassen, A. H., Engel, C., Eriksson, M., Fachal, L., Faivre, L., Fasching, P. A., Faust, U., Figueroa, J., Dieter, F. J., Fletcher, O., Flyger, H., Foulkes, W. D., Friedman, E., Fritschi, L., Frost, D., Gabrielson, M., Gaddam, P., Gammon, M. D., Ganz, P. A., Gapstur, S. M., Garber, J., Garcia-Barberan, V., Garciá-Saénz, J. A., Gaudet, M. M., Gauthier-Villars, M., Gehrig, A., Georgoulias, V., Gerdes, A. M., Giles, G. G., Glendon, G., Godwin, A. K., Goldberg, M. S., Goldgar, D. E., González-Neira, A., Goodfellow, P., Greene, M. H., Grenaker, G. A. I., Grip, M., Gronwald, J., Grundy, A., Gschwantler-Kaulich, D., Guénel, P., Guo, Q., Haeberle, L., Hahnen, E., Haiman, C. A., Håkansson, N., Hallberg, E., Hamann, U., Hamel, N., Hankinson, S., Hansen, T. V., Harrington, P., Hart, S. N., Hartikainen, J. M., Healey, C. S., Hein, A., Helbig, S., Henderson, A., Heyworth, J., Hicks, B., Hillemanns, P., Hodgson, S., Hogervorst, F. B., Hollestelle, A., Hooning, M. J., Hoover, B., Hopper, J. L., Hu, C., Huang, G., Hulick, P. J., Humphreys, K., Hunter, D. J., Imyanitov, E. N., Isaacs, C., Iwasaki, M., Izatt, L., Jakubowska, A., James, P., Janavicius, R., Janni, W., Jensen, U. B., John, E. M., Johnson, N., Jones, K., Jones, M., Jukkola-Vuorinen, A., Kaaks, R., Kabisch, M., Kaczmarek, K., Kang, D., Kast, K., Keeman, R., Kerin, M. J., Kets, C. M., Keupers, M., Khan, S., Khusnutdinova, E., Kiiski, J. I., Kim, S. W., Knight, J. A., Konstantopoulou, I., Kosma, V. M., Kristensen, V. N., Kruse, T. A., Kwong, A., Lænkholm, A. V., Laitman, Y., Lalloo, F., Lambrechts, D., Landsman, K., Lasset, C., Lazaro, C., Marchand, L. L., Lecarpentier, J., Lee, A., Lee, E., Won, J. L., Lee, M. H., Lejbkowicz, F., Lesueur, F., Li, J., Lilyquist, J., Lincoln, A., Lindblom, A., Lissowska, J., Lo, W. Y., Loibl, S., Long, J., Loud, J. T., Lubinski, J., Luccarini, C., Lush, M., MacInnis, R. J., Maishman, T., Makalic, E., Kostovska, I. M., Malone, K. E., Siranoush, M., Manson, J. E., Margolin, S., Martens, J. W., Martinez, M. E., Matsuo, K., Mavroudis, D., Mazoyer, S., McLean, C., Meijers-Heijboer, H., Menéndez, P., Meyer, J., Miao, H., Miller, A., Miller, N., Mitchell, G., Montagna, M., Muir, K., Mulligan, A. M., Mulot, C., Nadesan, S., Nathanson, K. L., Neuhausen, S. L., Nevanlinna, H., Nevelsteen, I., Niederacher, D., Nielsen, S. F., Nordestgaard, B. G., Norman, A., Nussbaum, R. L., Olah, E., Olopade, O. 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F., Sohn, C., Southey, M. C., Spinelli, J. J., Spurdle, A. B., Stegmaier, C., Stoppa-Lyonnet, D., Sukiennicki, G., Surowy, H., Sutter, C., Swerdlow, A., Szabo, C. I., Tamimi, R. M., Tan, Y. Y., Taylor, J. A., Tejada, M. I., Tengström, M., Teo, S. H., Terry, M. B., Tessier, D. C., Teul, A. E., Thöne, K., Thull, D. L., Tibiletti, M. G., Tihomirova, L., Tischkowitz, M., Toland, A. E., Tollenaar, R. A. M., Tomlinson, I., Tong, L., Torres, D., Tranchant, M., Truong, T., Tucker, K., Tung, N., Tyrer, J., Ulmer, H. U., Vachon, C., Christi, V. A. J., Den Berg, D. V., Ouweland, A. M. V., Rensburg, E. J., Varesco, L., Varon-Mateeva, R., Vega, A., Viel, A., Vijai, J., Vincent, D., Vollenweider, J., Walker, L., Wang, Z., Wang-Gohrke, S., Wappenschmidt, B., Weinberg, C. R., Weitzel, J. N., Wendt, C., Wesseling, J., Whittemore, A. S., Wijnen, J. T., Willett, W., Winqvist, R., Wolk, A., Wu, A. H., Xia, L., Yang, X. R., Yannoukakos, D., Zaffaroni, D., Zheng, W., Zhu, B., Ziogas, A., Ziv, E., Zorn, K. 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    Research output: Contribution to journal › Article › Academic › peer-review

    223 Citations (Scopus)