Einträge von Kast, K. auf dem Publikationsserver

Ortmann, Olaf , Schüler-Toprak, S., Kast, K., Fehm, T., Hahne, A., Huber, D., Kühnle, E., Mohr, K., Rhiem, K., Seitz, S. und Speiser, D. (2024) The risk of endocrine interventions in carriers of a genetic predisposition for breast and gynecologic cancers: recommendations of the German Consortium for Hereditary Breast and Ovarian Cancer. Journal of Cancer Research and Clinical Oncology 150 (9).

Huber, D., Seitz, S., Kast, K., Emons, G. und Ortmann, Olaf (2021) Hormone replacement therapy in BRCA mutation carriers and risk of ovarian, endometrial, and breast cancer: a systematic review. Journal of Cancer Research and Clinical Oncology 147, S. 2035-2045.

Ortmann, Olaf, Huber, D., Seitz, S., Kast, K. und Emons, G. (2020) Use of fertility treatments in BRCA1/2 mutation carriers and risk for ovarian and breast cancer: a systematic review. Archives of Gynecology and Obstetrics 302, S. 715-720.

Huber, D., Seitz, S., Kast, K., Emons, G. und Ortmann, Olaf (2020) Use of oral contraceptives in BRCA mutation carriers and risk for ovarian and breast cancer: a systematic review. Archives of Gynecology and Obstetrics 301, S. 875-884. Volltext nicht vorhanden.

Kast, K., Rhiem, K., Wappenschmidt, B., Hahnen, E., Hauke, J., Bluemcke, B., Zarghooni, V., Herold, N., Ditsch, N., Kiechle, M., Braun, M., Fischer, C., Dikow, N., Schott, S. , Rahner, N., Niederacher, D., Fehm, T., Gehrig, A., Mueller-Reible, C., Arnold, N. , Maass, N., Borck, G., de Gregorio, N., Scholz, C., Auber, B., Varon-Manteeva, R., Speiser, D., Horvath, J., Lichey, N., Wimberger, P., Stark, S., Faust, U., Weber, Bernhard H. F. , Emons, G., Zachariae, S., Meindl, A., Schmutzler, R. K., Engel, C. und German Consortium for Hereditary Breast and Ovarian Cancer, . (2016) Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer. Journal of Medical Genetics 53 (7), S. 465-471. Volltext nicht vorhanden.

Ramus, S. J. , Kartsonaki, C., Gayther, S. A., Pharoah, P. D. P., Sinilnikova, O. M., Beesley, J. , Chen, X., McGuffog, L., Healey, S., Couch, F. J., Wang, X., Fredericksen, Z., Peterlongo, P. , Manoukian, S., Peissel, B. , Zaffaroni, D. , Roversi, G., Barile, M., Viel, A. , Allavena, A., Ottini, L., Papi, L. , Gismondi, V., Capra, F., Radice, P. , Greene, M. H., Mai, P. L., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Gerdes, A.-M. , Kruse, T. A., Cruger, D., Jensen, U. B. , Caligo, M. A. , Olsson, H. , Kristoffersson, U., Lindblom, A., Arver, B., Karlsson, P., Stenmark Askmalm, M., Borg, A., Neuhausen, S. L., Ding, Y. C., Nathanson, K. L. , Domchek, S. M., Jakubowska, A. , Lubinski, J., Huzarski, T., Byrski, T., Gronwald, J. , Gorski, B., Cybulski, C., Debniak, T., Osorio, A. , Duran, M., Tejada, M.-I., Benitez, J., Hamann, U., Rookus, M. A., Verhoef, S., Tilanus-Linthorst, M. A., Vreeswijk, M. P., Bodmer, D., Ausems, M. G. E. M., van Os, T. A., Asperen, C. J., Blok, M. J., Meijers-Heijboer, H. E. J., Peock, S., Cook, M., Oliver, C., Frost, D., Dunning, A. M. , Evans, D. G. , Eeles, R. , Pichert, G., Cole, T., Hodgson, S., Brewer, C., Morrison, P. J., Porteous, M., Kennedy, M. J., Rogers, M. T., Side, L. E., Donaldson, A., Gregory, H., Godwin, A., Stoppa-Lyonnet, D., Moncoutier, V., Castera, L., Mazoyer, S. , Barjhoux, L., Bonadona, V., Leroux, D., Faivre, L., Lidereau, R., Nogues, C., Bignon, Y.-J., Prieur, F., Collonge-Rame, M.-A., Venat-Bouvet, L., Fert-Ferrer, S., Miron, A., Buys, S. S., Hopper, J. L., Daly, M. B., John, E. M., Terry, M. B., Goldgar, D., Hansen, T. v. O., Jonson, L., Ejlertsen, B., Agnarsson, B. A., Offit, K., Kirchhoff, T. , Vijai, J., Dutra-Clarke, A. V. C., Przybylo, J. A., Montagna, M., Casella, C., Imyanitov, E. N., Janavicius, R. , Blanco, I. , Lazaro, C., Moysich, K. B., Karlan, B. Y., Gross, J., Beattie, M. S., Schmutzler, R., Wappenschmidt, B., Meindl, A., Ruehl, I., Fiebig, B., Sutter, C., Arnold, N. , Deissler, H., Varon-Mateeva, R., Kast, K., Niederacher, D., Gadzicki, D., Caldes, T., de la Hoya, M. , Nevanlinna, H. , Aittomaki, K., Simard, J., Soucy, P., Spurdle, A. B. , Holland, H., Chenevix-Trench, G., Easton, D. F. und Antoniou, A. C. (2011) Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers. JNCI Journal of the National Cancer Institute 103 (2), S. 105-116. Volltext nicht vorhanden.