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Publications by Arnold, N

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Number of items: 8.

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, (GC-HBOC) (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.

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.

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.

This list was generated on Tue Jun 2 00:47:53 2020 CEST.
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