Hoogerbrugge N - Search Results

1

A patient decision aid for risk-reducing surgery in premenopausal BRCA1/2 mutation carriers: Development process and pilot testing.

Harmsen MG, Steenbeek MP, Hoogerbrugge N, van Doorn HC, Gaarenstroom KN, Vos MC, Massuger LFAG, de Hullu JA, Hermens RPMG. Harmsen MG, et al. Among authors: hoogerbrugge n. Health Expect. 2018 Jun;21(3):659-667. doi: 10.1111/hex.12661. Epub 2017 Dec 27. Health Expect. 2018. PMID: 29281161 Free PMC article.

2

Decision analysis of prophylactic surgery or screening for BRCA1 mutation carriers: a more prominent role for oophorectomy.

van Roosmalen MS, Verhoef LC, Stalmeier PF, Hoogerbrugge N, van Daal WA. van Roosmalen MS, et al. Among authors: hoogerbrugge n. J Clin Oncol. 2002 Apr 15;20(8):2092-100. doi: 10.1200/jco.2002.08.035. J Clin Oncol. 2002. PMID: 11956270

3

High prevalence of premalignant lesions in prophylactically removed breasts from women at hereditary risk for breast cancer.

Hoogerbrugge N, Bult P, de Widt-Levert LM, Beex LV, Kiemeney LA, Ligtenberg MJ, Massuger LF, Boetes C, Manders P, Brunner HG. Hoogerbrugge N, et al. J Clin Oncol. 2003 Jan 1;21(1):41-5. doi: 10.1200/JCO.2003.02.137. J Clin Oncol. 2003. PMID: 12506168 Free article.

4

The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families.

Oldenburg RA, Kroeze-Jansema K, Kraan J, Morreau H, Klijn JG, Hoogerbrugge N, Ligtenberg MJ, van Asperen CJ, Vasen HF, Meijers C, Meijers-Heijboer H, de Bock TH, Cornelisse CJ, Devilee P. Oldenburg RA, et al. Among authors: hoogerbrugge n. Cancer Res. 2003 Dec 1;63(23):8153-7. Cancer Res. 2003. PMID: 14678969

5

Randomised trial of a decision aid and its timing for women being tested for a BRCA1/2 mutation.

van Roosmalen MS, Stalmeier PF, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Hoogerbrugge N, Moog U, van Daal WA. van Roosmalen MS, et al. Among authors: hoogerbrugge n. Br J Cancer. 2004 Jan 26;90(2):333-42. doi: 10.1038/sj.bjc.6601525. Br J Cancer. 2004. PMID: 14735173 Free PMC article. Clinical Trial.

6

[In cases of familial ovarian cancer, always consider the risk of breast cancer].

Kets CM, Niermeijer MF, Massuger LF, Hoogerbrugge N. Kets CM, et al. Among authors: hoogerbrugge n. Ned Tijdschr Geneeskd. 2004 Aug 28;148(35):1709-11. Ned Tijdschr Geneeskd. 2004. PMID: 15468897 Dutch.

7

Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations.

Leegte B, van der Hout AH, Deffenbaugh AM, Bakker MK, Mulder IM, ten Berge A, Leenders EP, Wesseling J, de Hullu J, Hoogerbrugge N, Ligtenberg MJ, Ardern-Jones A, Bancroft E, Salmon A, Barwell J, Eeles R, Oosterwijk JC. Leegte B, et al. Among authors: hoogerbrugge n. J Med Genet. 2005 Mar;42(3):e20. doi: 10.1136/jmg.2004.027243. J Med Genet. 2005. PMID: 15744030 Free PMC article. Review. No abstract available.

8

Surveillance of women at high risk for hereditary ovarian cancer is inefficient.

Oei AL, Massuger LF, Bulten J, Ligtenberg MJ, Hoogerbrugge N, de Hullu JA. Oei AL, et al. Among authors: hoogerbrugge n. Br J Cancer. 2006 Mar 27;94(6):814-9. doi: 10.1038/sj.bjc.6603015. Br J Cancer. 2006. PMID: 16495917 Free PMC article.

9

Numerous high-risk epithelial lesions in familial breast cancer.

Hoogerbrugge N, Bult P, Bonenkamp JJ, Ligtenberg MJ, Kiemeney LA, de Hullu JA, Boetes C, Niermeijer MF, Brunner HG. Hoogerbrugge N, et al. Eur J Cancer. 2006 Oct;42(15):2492-8. doi: 10.1016/j.ejca.2006.05.027. Eur J Cancer. 2006. PMID: 16908132

10

Optimal selection for BRCA1 and BRCA2 mutation testing using a combination of 'easy to apply' probability models.

Bodmer D, Ligtenberg MJ, van der Hout AH, Gloudemans S, Ansink K, Oosterwijk JC, Hoogerbrugge N. Bodmer D, et al. Among authors: hoogerbrugge n. Br J Cancer. 2006 Sep 18;95(6):757-62. doi: 10.1038/sj.bjc.6603306. Epub 2006 Aug 15. Br J Cancer. 2006. PMID: 16909138 Free PMC article.

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