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

    Fachal, L., Aschard, H., Beesley, J., Barnes, D. R., Allen, J., Kar, S., Pooley, K. A., Dennis, J., Michailidou, K., Turman, C., Soucy, P., Lemacon, A., Lush, M., Tyrer, J. P., Ghoussaini, M., Marjaneh, M. M., Jiang, X., Agata, S., Aittomaki, K., Rosario Alonso, M. & 38 others, Andrulis, I. L., Anton-Culver, H., Antonenkova, N. N., Arason, A., Arndt, V., Aronson, K. J., Arun, B. K., Auber, B., Auer, P. L., Azzollini, J., Balmana, J., Barkardottir, R. B., Barrowdale, D., Beeghly-Fadiel, A., Benitez, J., Bermisheva, M., Bialkowska, K., Blanco, A. M., Blomqvist, C., Blot, W., Bogdanova, N., Bojesen, S. E., Bolla, M. K., Bonanni, B., Borg, A., Bosse, K., Brauch, H., Brenner, H., de Boer, M., Garcia, E. G., Blok, M., GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, ABCTB Investigators, Dunning, A. M. & Kraft, P., Jan 2020, In: Nature Genetics. 52, 1, p. 56–73 18 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  • An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

    Suerink, M., Rodriguez-Girondo, M., van der Klift, H. M., Colas, C., Brugieres, L., Lavoine, N., Jongmans, M., Capella Munar, G., Evans, D. G., Farrell, M. P., Genuardi, M., Goldberg, Y., Gomez-Garcia, E., Heinimann, K., Hoell, J., Aretz, S., Jasperson, K. W., Kedar, I., Modi, M. B., Nikolaev, S. & 19 others, van Os, T. A. M., Ripperger, T., Rueda, D., Senter, L., Sjursen, W., Sunde, L., Therkildsen, C., Tibiletti, M. G., Trainer, A. H., Vos, Y. J., Wagner, A., Winship, I., Wimmer, K., Zimmermann, S. Y., Vasen, H. F., van Asperen, C. J., Houwing-Duistermaat, J. J., ten Broeke, S. W. & Nielsen, M., Dec 2019, In: Genetics in Medicine. 21, 12, p. 2706-2712 7 p.

    Research output: Contribution to journalArticleAcademicpeer-review

    Open Access
  • Germline BRCA-Associated Endometrial Carcinoma Is a Distinct Clinicopathologic Entity

    de Jonge, M. M., Ritterhouse, L. L., de Kroon, C. D., Vreeswijk, M. P. G., Segal, J. P., Puranik, R., Rookus, M. A., Hogervorst, F. B. L., van Leeuwen, F. E., Adank, M. A., Schmidt, M. K., Jenner, D. J., Collee, J. M., van den Ouweland, A. M. W., Hooning, M. J., Boere, I. A., van Asperen, C. J., Devilee, P., van der Luijt, R. B., van Cronenburg, T. C. T. E. F. & 23 others, Wevers, M. R., Mensenkamp, A. R., Ausems, M. G. E. M., Koudijs, M. J., Meijers-Heijboer, H. E. J., van Os, T. A. M., van Engelen, K., Gille, J. J. P., Gomez-Garcia, E. B., Blok, M. J., de Boer, M., Oosterwijk, J. C., van der Hout, A. H., Mourits, M. J., de Bock, G. H., Siesling, S., Verloop, J., van den Broek, E. C., Hollema, H., Smit, V. T. H. B. M., Howitt, B. E., Bosse, T. & HEBON Group, 15 Dec 2019, In: Clinical Cancer Research. 25, 24, p. 7517-7526 10 p.

    Research output: Contribution to journalArticleAcademicpeer-review

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

    Qian, F., Wang, S., Mitchell, J., McGuffog, L., Barrowdale, D., Leslie, G., Oosterwijk, J. C., Chung, W. K., Evans, D. G., Engel, C., Kast, K., Aalfs, C. M., Adank, M. A., Adlard, J., Agnarsson, B. A., Aittomaki, K., Alducci, E., Andrulis, I. L., Arun, B. K., Ausems, M. G. E. M. & 34 others, Azzollini, J., Barouk-Simonet, E., Barwell, J., Belotti, M., Benitez, J., Berger, A., Borg, A., Bradbury, A. R., Brunet, J., Buys, S. S., Caldes, T., Caligo, M. A., Campbell, I., Caputo, S. M., Chiquette, J., Claes, K. B. M., Collee, J. M., Couch, F. J., Coupier, I., Daly, M. B., Davidson, R., Diez, O., Domchek, S. M., Donaldson, A., Dorfling, C. M., Eeles, R., Feliubadalo, L., Foretova, L., Fowler, J., Gomez Garcia, E. B., GEMO Study Collaborators, HEBON, EMBRACE & Huo, D., Apr 2019, In: Journal of the National Cancer Institute. 111, 4, p. 350-364 15 p., 132.

    Research output: Contribution to journalArticleAcademicpeer-review

  • Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

    Parsons, M. T., Tudini, E., Li, H., Hahnen, E., Wappenschmidt, B., Feliubadalo, L., Aalfs, C. M., Agata, S., Aittomaki, K., Alducci, E., Concepcion Alonso-Cerezo, M., Arnold, N., Auber, B., Austin, R., Azzollini, J., Balmana, J., Barbieri, E., Bartram, C. R., Blanco, A., Bluemcke, B. & 33 others, Bonache, S., Bonanni, B., Borg, A., Bortesi, B., Brunet, J., Bruzzone, C., Bucksch, K., Cagnoli, G., Caldes, T., Caliebe, A., Caligo, M. A., Calvello, M., Capone, G. L., Caputo, S. M., Carnevali, I., Carrasco, E., Caux-Moncoutier, V., Cavalli, P., Cini, G., Clarke, E. M., Concolino, P., Cops, E. J., Cortesi, L., Couch, F. J., Darder, E., de la Hoya, M., Dean, M., Debatin, I., Del Valle, J., Janssen, L. A., Gomez Garcia, E., KConFab Investigators & Spurdle, A. B., Sep 2019, In: Human Mutation. 40, 9, p. 1557-1578 22 p.

    Research output: Contribution to journalArticleAcademicpeer-review

    Open Access