Antoinette Hollestelle

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dr. Antoinette Hollestelle

PhD

 https://orcid.org/0000-0003-1166-1966
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Education/Academic qualification

PhD, A Genetic Basis for Luminal and Basal-Type Breast Cancer, Erasmus University Rotterdam

1 Jan 2005 → 30 Nov 2008

Award Date: 7 Jan 2009

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  • A likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants: Application to BRCA1 and BRCA2

    Zanti, M., O'Mahony, D. G., Parsons, M. T., Li, H., Dennis, J., Aittomäkkiki, K., Andrulis, I. L., Anton-Culver, H., Aronson, K. J., Augustinsson, A., Becher, H., Bojesen, S. E., Bolla, M. K., Brenner, H., Brown, M. A., Buys, S. S., Canzian, F., Caputo, S. M., Castelao, J. E., Chang-Claude, J., & 104 othersCzene, K., Daly, M. B., De Nicolo, A., Devilee, P., Dörk, T., Dunning, A. M., Dwek, M., Eccles, D. M., Engel, C., Gareth Evans, D., Fasching, P. A., Gago-Dominguez, M., García-Closas, M., García-Sáenz, J. A., Gentry-Maharaj, A., Geurts-Giele, W. R. R., Giles, G. G., Glendon, G., Goldberg, M. S., Gómez Garcia, E. B., Göendert, M., Guénel, P., Hahnen, E., Haiman, C. A., Hall, P., Hamann, U., Harkness, E. F., Hogervorst, F. B. L., Hollestelle, A., Hoppe, R., Hopper, J. L., Houdayer, C., Houlston, R. S., Howell, A., Jakimovska, M., Jakubowska, A., Jernström, H., John, E. M., Kaaks, R., Kitahara, C. M., Koutros, S., Kraft, P., Kristensen, V. N., Lacey, J. V., Lambrechts, D., Léoné, M., Lindblom, A., Lubiski, J., Lush, M., Mannermaa, A., Manoochehri, M., Manoukian, S., Margolin, S., Martinez, M. E., Menon, U., Milne, R. L., Monteiro, A. N., Murphy, R. A., Neuhausen, S. L., Nevanlinna, H., Newman, W. G., Offit, K., Park, S. K., James, P., Peterlongo, P., Peto, J., Plaseska-Karanfilska, D., Punie, K., Radice, P., Rashid, M. U., Rennert, G., Romero, A., Rosenberg, E. H., Saloustros, E., Sandler, D. P., Schmidt, M. K., Schmutzler, R. K., Shu, X. O., Simard, J., Southey, M. C., Stone, J., Stoppa-Lyonnet, D., Tamimi, R. M., Tapper, W. J., Taylor, J. A., Teo, S. H., Teras, L. R., Terry, M. B., Thomassen, M., Troester, M. A., Vachon, C. M., Vega, A., Vreeswijk, M. P. G., Wang, Q., Wappenschmidt, B., Weinberg, C. R., Wolk, A., Zheng, W., Feng, B., Couch, F. J., Spurdle, A. B., Easton, D. F., Goldgar, D. E. & Michailidou, K., 2023, In: Human Mutation. 2023, 9961341.

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

    Open Access
    File
    1 Downloads (Pure)

  • Breast cancer genomes from CHEK2 c.1100delC mutation carriers lack somatic TP53 mutations and display a unique structural variant size distribution profile

    Smid, M., Schmidt, M. K., Prager-van der Smissen, W. J. C., Ruigrok-Ritstier, K., Schreurs, M. A. C., Cornelissen, S., Garcia, A. M., Broeks, A., Timmermans, A. M., Trapman-Jansen, A. M. A. C., Collée, J. M., Adank, M. A., Hooning, M. J., Martens, J. W. M. & Hollestelle, A., 9 May 2023, In: Breast Cancer Research. 25, 1, 53.

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

    Open Access
    File
    3 Downloads (Pure)

  • Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases

    Lakeman, I. M. M., Rodriguez-Girondo, M. D. M., Lee, A., Celosse, N., Braspenning, M. E., van Engelen, K., van de Beek, I., van der Hout, A. H., Garcia, E. B. G., Mensenkamp, A. R., Ausems, M. G. E. M., Hooning, M. J., Adank, M. A., Hollestelle, A., Schmidt, M. K., van Asperen, C. J. & Devilee, P., 1 Apr 2023, In: Journal of Medical Genetics. 60, 4, p. 327-336 10 p.

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

    Open Access
    File
    3 Citations (Scopus)
    13 Downloads (Pure)

  • FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

    NBCS Collaborators, Billaud, A., Figlioli, G., Ahearn, T. U., Antonenkova, N. N., Becher, H., Beckmann, M. W., Behrens, S., Benitez, J., Bermisheva, M., Blok, M. J., Bogdanova, N. V., Bonanni, B., Burwinkel, B., Camp, N. J., Campbell, A., Castelao, J. E., Cessna, M. H., Chanock, S. J., Czene, K., & 31 othersDevilee, P., Dörk, T., Engel, C., Eriksson, M., Fasching, P. A., Figueroa, J. D., Gabrielson, M., Gago-Dominguez, M., García-Closas, M., González-Neira, A., Grassmann, F., Guénel, P., Gündert, M., Hadjisavvas, A., Hahnen, E., Hall, P., Hamann, U., Harrington, P. A., He, W., Hillemanns, P., Hollestelle, A., Hooning, M. J., Hoppe, R., Howell, A., Humphreys, K., Jager, A., Jakubowska, A., Khusnutdinova, E. K., Ko, Y-D., Kristensen, V. N. & Lindblom, A., 1 May 2023, In: European Journal of Human Genetics. 31, 5, p. 578-587 10 p.

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

    Open Access
    File
    1 Citation (Scopus)
    1 Downloads (Pure)

  • Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

    NBCS Collaborators & kConFab Investigators, 23 Jun 2023, In: Cancers. 15, 13, 3313.

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

    Open Access
    File
    63 Downloads (Pure)
View all 111 research outputs
  • 1 Editorial work