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2,508 results
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Assessing the risk of breast cancer.
Armstrong K, Eisen A, Weber B. Armstrong K, et al. Among authors: weber b. N Engl J Med. 2000 Feb 24;342(8):564-71. doi: 10.1056/NEJM200002243420807. N Engl J Med. 2000. PMID: 10684916 Review. No abstract available.
Factors associated with decisions about clinical BRCA1/2 testing.
Armstrong K, Calzone K, Stopfer J, Fitzgerald G, Coyne J, Weber B. Armstrong K, et al. Among authors: weber b. Cancer Epidemiol Biomarkers Prev. 2000 Nov;9(11):1251-4. Cancer Epidemiol Biomarkers Prev. 2000. PMID: 11097234
Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study. Hereditary Breast Cancer Clinical Study Group.
Narod SA, Brunet JS, Ghadirian P, Robson M, Heimdal K, Neuhausen SL, Stoppa-Lyonnet D, Lerman C, Pasini B, de los Rios P, Weber B, Lynch H; Hereditary Breast Cancer Clinical Study Group. Narod SA, et al. Among authors: weber b. Lancet. 2000 Dec 2;356(9245):1876-81. doi: 10.1016/s0140-6736(00)03258-x. Lancet. 2000. PMID: 11130383
SNPs in ultraconserved elements and familial breast cancer risk.
Yang R, Frank B, Hemminki K, Bartram CR, Wappenschmidt B, Sutter C, Kiechle M, Bugert P, Schmutzler RK, Arnold N, Weber BH, Niederacher D, Meindl A, Burwinkel B. Yang R, et al. Among authors: weber bh. Carcinogenesis. 2008 Feb;29(2):351-5. doi: 10.1093/carcin/bgm290. Epub 2008 Jan 3. Carcinogenesis. 2008. PMID: 18174240
Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity.
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 LZ, Jerry DJ, Bugert P, Weber BH, Niederacher D, Arnold N, Varon-Mateeva R, Wappenschmidt B, Schmutzler RK, Engel C, Meindl A, Bartram CR, Mollenhauer J, Burwinkel B. Tchatchou S, et al. Among authors: weber bh. Hum Mutat. 2010 Jan;31(1):60-6. doi: 10.1002/humu.21134. Hum Mutat. 2010. PMID: 19830809
A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk.
Yang R, Schlehe B, Hemminki K, Sutter C, Bugert P, Wappenschmidt B, Volkmann J, Varon R, Weber BH, Niederacher D, Arnold N, Meindl A, Bartram CR, Schmutzler RK, Burwinkel B. Yang R, et al. Among authors: weber bh. Breast Cancer Res Treat. 2010 Jun;121(3):693-702. doi: 10.1007/s10549-009-0633-5. Epub 2009 Nov 18. Breast Cancer Res Treat. 2010. PMID: 19921425
Breast cancer susceptibility genes: current challenges and future promises.
Weber B. Weber B. Ann Intern Med. 1996 Jun 15;124(12):1088-90. doi: 10.7326/0003-4819-124-12-199606150-00012. Ann Intern Med. 1996. PMID: 8633825 No abstract available.
Tubal ligation and risk of ovarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study.
Narod SA, Sun P, Ghadirian P, Lynch H, Isaacs C, Garber J, Weber B, Karlan B, Fishman D, Rosen B, Tung N, Neuhausen SL. Narod SA, et al. Among authors: weber b. Lancet. 2001 May 12;357(9267):1467-70. doi: 10.1016/s0140-6736(00)04642-0. Lancet. 2001. PMID: 11377596
A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women.
Tchatchou S, Jung A, Hemminki K, Sutter C, Wappenschmidt B, Bugert P, Weber BH, Niederacher D, Arnold N, Varon-Mateeva R, Ditsch N, Meindl A, Schmutzler RK, Bartram CR, Burwinkel B. Tchatchou S, et al. Among authors: weber bh. Carcinogenesis. 2009 Jan;30(1):59-64. doi: 10.1093/carcin/bgn253. Epub 2008 Nov 20. Carcinogenesis. 2009. PMID: 19028706
Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk.
Yang R, Chen B, Hemminki K, Wappenschmidt B, Engel C, Sutter C, Ditsch N, Weber BH, Niederacher D, Arnold N, Meindl A, Bartram CR, Schmutzler RK, Burwinkel B. Yang R, et al. Among authors: weber bh. Breast Cancer Res Treat. 2009 Nov;118(2):407-13. doi: 10.1007/s10549-009-0348-7. Epub 2009 Feb 20. Breast Cancer Res Treat. 2009. PMID: 19229607
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