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, 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.
, Weber, Bernhard H. F.
, Niederacher, D., Arnold, N.
, Meindl, A., Bartram, C. R., Schmutzler, R. K., Müller, H., Arndt, V.
, Brenner, H.
, Sohn, C. und 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), S. 549-554.
Volltext nicht vorhanden.
, Niederacher, D., Arnold, N.
, Meindl, A., Bartram, C., Schmutzler, R. K. und 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), S. 693-702.
Volltext nicht vorhanden.
, Schlehe, B., Hemminki, K., Sutter, C., Ditsch, N., Blackburn, A.
, Hill, L. Z., Jerry, D. J., Bugert, P., Weber, Bernhard H. F.
, et, al., make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference
, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference
(2010)
Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity.
Human Mutation 31 (1), S. 60-66.
Volltext nicht vorhanden.
, Niederacher, D., Arnold, N.
, Varon-Mateeva, R., Ditsch, N., Meindl, A., Schmutzler, R. K., Bartram, C. R. und 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), S. 59-64.
Volltext nicht vorhanden.
, 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. und Oesterreich, S.
(2009)
Nuclear receptor coregulator SNP discovery and impact on breast cancer risk.
BMC Cancer 9, S. 438.
Volltext nicht vorhanden.
, Sutter, C., Ditsch, N., Weber, Bernhard H. F.
, Niederacher, D., Arnold, N.
, Meindl, A., Bartram, C., Schmutzler, R. und 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), S. 407-413.
Volltext nicht vorhanden.
, Weber, Bernhard H. F.
, Niederacher, D., Meindl, A. und Burwinkel, B.
(2008)
SNPs in ultraconserved elements and familial breast Cancer Risk.
Carcinogenesis 29 (2), S. 351-355.
Volltext nicht vorhanden.
, Weber, Bernhard H. F.
, Niederacher, D., Burwinkel, B., Bartram, C. R., Hemminki, K. und 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), S. 267-277.
Volltext nicht vorhanden.
, Weber, Bernhard H. F.
, Niederacher, D., Bartram, C. R. und 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), S. 423-426.
Volltext nicht vorhanden.
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