Entries of Niederacher, D. on the publication server

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. and 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), pp. 465-471. Fulltext not available.

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. and 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), pp. 105-116. Fulltext not available.

Yang, R., Dick, M., Marme, F., Schneeweiss, A., Langheinz, A., Hemminki, K., Sutter, C., Bugert, P., Wappenschmidt, B., Varon, R., Schott, S. , Weber, Bernhard H. F. , Niederacher, D., Arnold, N. , Meindl, A., Bartram, C. R., Schmutzler, R. K., Müller, H., Arndt, V. , Brenner, H. , Sohn, C. and Burwinkel, B. (2011) Genetic variants within miR-126 and miR-335 are not associated with breast cancer risk. Breast Cancer Research and Treatment 127 (2), pp. 549-554. Fulltext not available.

Yang, R., Schlehe, B., Hemminki, K., Sutter, C., Bugert, P., Wappenschmidt, B., Volkmann, J., Varon, R., Weber, Bernhard H. F. , Niederacher, D., Arnold, N. , Meindl, A., Bartram, C., Schmutzler, R. K. and Burwinkel, B. (2010) A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk. Breast Cancer Research and Treatment 121 (3), pp. 693-702. Fulltext not available.

Tchatchou, S., Jung, A., Hemminki, K., Sutter, C., Wappenschmidt, B., Bugert, P., Weber, Bernhard H. F. , Niederacher, D., Arnold, N. , Varon-Mateeva, R., Ditsch, N., Meindl, A., Schmutzler, R. K., Bartram, C. R. and Burwinkel, B. (2009) A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women. Carcinogenesis 30 (1), pp. 59-64. Fulltext not available.

Osorio, A. , Milne, R. L., Pita, G., Peterlongo, P. , Heikkinen, T. , Simard, J., Chenevix-Trench, G., Spurdle, A. B. , Beesley, J. , Chen, X., Healey, S., Neuhausen, S. L., Ding, Y. C., Couch, F. J., Wang, X., Lindor, N., Manoukian, S., Barile, M., Viel, A. , Tizzoni, L., Szabo, C. I., Foretova, L., Zikan, M. , Claes, K. , Greene, M. H., Mai, P., Rennert, G., Lejbkowicz, F., Barnett-Griness, O., Andrulis, I. L., Ozcelik, H., Weerasooriya, N., Gerdes, A.-M. , Thomassen, M., Cruger, D. G., Caligo, M. A. , Friedman, E., Kaufman, B., Laitman, Y., Cohen, S., Kontorovich, T., Gershoni-Baruch, R., Dagan, E., Jernström, H., Askmalm, M. S., Arver, B., Malmer, B., Domchek, S. M., Nathanson, K. L. , Brunet, J. , Ramón y Cajal, T., Yannoukakos, D. , Hamann, U., Hogervorst, F. B. L., Verhoef, S., García, E.B. Gómez, Wijnen, J. T., van den Ouweland, A., Easton, D. F., Peock, S., Cook, M., Oliver, C. T., Frost, D., Luccarini, C., Evans, D. G. , Lalloo, F., Eeles, R. , Pichert, G., Cook, J., Hodgson, S., Morrison, P. J., Douglas, F., Godwin, A. K., Sinilnikova, O. M., Barjhoux, L., Stoppa-Lyonnet, D., Moncoutier, V., Giraud, S., Cassini, C., Olivier-Faivre, L., Révillion, F., Peyrat, J.-P., Muller, D., Fricker, J.-P., Lynch, H. T., John, E. M., Buys, S. M., Daly, M., Hopper, J. L., Terry, M. B., Miron, A., Yassin, Y., Goldgar, D., Singer, C. F., Gschwantler-Kaulich, D., Pfeiler, G., Spiess, A.-C., Hansen, Thomas v. O., Johannsson, O. T., Kirchhoff, T. , Offit, K., Kosarin, K., Piedmonte, M., Rodriguez, G. C., Wakeley, K., Boggess, J. F., Basil, J., Schwartz, P. E., Blank, S. V., Toland, A. E., Montagna, M., Casella, C., Imyanitov, E. N., Allavena, A., Schmutzler, R. K., Versmold, B., Engel, C. , Meindl, A., Ditsch, N., Arnold, N. , Niederacher, D., Deißler, H., Fiebig, B., Varon-Mateeva, R., Schaefer, D., Froster, U. G., Caldes, T., de la Hoya, M., McGuffog, L., Antoniou, A. C., Nevanlinna, H. , Radice, P. and Benítez, J. (2009) Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). British Journal of Cancer 101 (12), pp. 2048-2054. Fulltext not available.

Hartmaier, R. J. , Tchatchou, S., Richter, A. S., Wang, J., McGuire, S. E., Skaar, T. C., Rae, J. M., Hemminki, K., Sutter, C., Ditsch, N., Bugert, P., Weber, Bernhard H. F. , Niederacher, D., Arnold, N. , Varon-Mateeva, R., Wappenschmidt, B., Schmutzler, R. K., Meindl, A., Bartram, C. R., Burwinkel, B. and Oesterreich, S. (2009) Nuclear receptor coregulator SNP discovery and impact on breast cancer risk. BMC Cancer 9, p. 438. Fulltext not available.

Yang, R., Chen, B., Hemminki, K., Wappenschmidt, B., Engel, C. , Sutter, C., Ditsch, N., Weber, Bernhard H. F. , Niederacher, D., Arnold, N. , Meindl, A., Bartram, C., Schmutzler, R. and Burwinkel, B. (2009) Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk. Breast Cancer Research and Treatment 118 (2), pp. 407-413. Fulltext not available.

Yang, R., Frank, B., Hemminki, K., Bartram, C. R., Wappenschmidt, B., Sutter, C., Kiechle, M., Bugert, P., Schmutzler, R. K., Arnold, N. , Weber, Bernhard H. F. , Niederacher, D., Meindl, A. and Burwinkel, B. (2008) SNPs in ultraconserved elements and familial breast Cancer Risk. Carcinogenesis 29 (2), pp. 351-355. Fulltext not available.

Vaclavicek, A., Bermejo, J. L., Schmutzler, R. K., Sutter, C., Wappenschmidt, B., Meindl, A., Kiechle, M., Arnold, N. , Weber, Bernhard H. F. , Niederacher, D., Burwinkel, B., Bartram, C. R., Hemminki, K. and Försti, A. (2007) Polymorphisms in the Janus kinase 2 (JAK)/signal transducer and activator of transcription (STAT) genes: putative association of the STAT gene region with familial breast cancer. Endocrine related cancer 14 (2), pp. 267-277. Fulltext not available.

Wirtenberger, M., Schmutzhard, J., Hemminki, K., Meindl, A., Sutter, C., Schmutzler, R. K., Wappenschmidt, B., Kiechle, M., Arnold, A. , Weber, Bernhard H. F. , Niederacher, D., Bartram, C. R. and Burwinkel, B. (2007) The functional genetic variant Ile646Val located in the kinase binding domain of the A kinase anchoring protein 10 is associated with familial breast cancer. Carcinogenesis 28 (2), pp. 423-426. Fulltext not available.