Entries of Ditsch, N. 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.

Tchatchou, S., Riedel, A., Lyer, S., Schmutzhard, J., Strobel-Freidekind, O., Gronert-Sum, S., Mietag, C., D'Amato, M., Schlehe, B., Hemminki, K., Sutter, C., Ditsch, N., Blackburn, A., Hill, L. Z., Jerry, D. J., Bugert, P., Weber, Bernhard H. F. and et, al. (2010) Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity. Human Mutation 31 (1), pp. 60-66. 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.

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.