Hoogerbrugge N - Search Results

1

A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.

van der Hout AH, van den Ouweland AM, van der Luijt RB, Gille HJ, Bodmer D, Brüggenwirth H, Mulder IM, van der Vlies P, Elfferich P, Huisman MT, ten Berge AM, Kromosoeto J, Jansen RP, van Zon PH, Vriesman T, Arts N, Lange MB, Oosterwijk JC, Meijers-Heijboer H, Ausems MG, Hoogerbrugge N, Verhoef S, Halley DJ, Vos YJ, Hogervorst F, Ligtenberg M, Hofstra RM. van der Hout AH, et al. Among authors: hoogerbrugge n. Hum Mutat. 2006 Jul;27(7):654-66. doi: 10.1002/humu.20340. Hum Mutat. 2006. PMID: 16683254

2

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.

3

Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCC.

Hoogerbrugge N, Willems R, Van Krieken HJ, Kiemeney LA, Weijmans M, Nagengast FM, Arts N, Brunner HG, Ligtenberg MJ. Hoogerbrugge N, et al. Clin Genet. 2003 Jan;63(1):64-70. doi: 10.1034/j.1399-0004.2003.630110.x. Clin Genet. 2003. PMID: 12519374

4

Chromosome 3 translocations and the risk to develop renal cell cancer: a Dutch intergroup study.

Van Erp F, Van Ravenswaaij C, Bodmer D, Eleveld M, Hoogerbrugge N, Mulders P, Geurts van Kessel A. Van Erp F, et al. Among authors: hoogerbrugge n. Genet Couns. 2003;14(2):149-54. Genet Couns. 2003. PMID: 12872808 Review.

5

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

6

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.

7

Impact of BRCA1/2 testing and disclosure of a positive test result on women affected and unaffected with breast or ovarian cancer.

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. Am J Med Genet A. 2004 Feb 1;124A(4):346-55. doi: 10.1002/ajmg.a.20374. Am J Med Genet A. 2004. PMID: 14735581 Free article.

8

Current clinical selection strategies for identification of hereditary non-polyposis colorectal cancer families are inadequate: a meta-analysis.

Kievit W, de Bruin JH, Adang EM, Ligtenberg MJ, Nagengast FM, van Krieken JH, Hoogerbrugge N. Kievit W, et al. Among authors: hoogerbrugge n. Clin Genet. 2004 Apr;65(4):308-16. doi: 10.1111/j.1399-0004.2004.00220.x. Clin Genet. 2004. PMID: 15025724

9

Randomized trial of a shared decision-making intervention consisting of trade-offs and individualized treatment information for BRCA1/2 mutation carriers.

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. J Clin Oncol. 2004 Aug 15;22(16):3293-301. doi: 10.1200/JCO.2004.05.066. J Clin Oncol. 2004. PMID: 15310772 Free article. Clinical Trial.

10

[Recognising hereditary non-polyposis colorectal cancer without a clear family history].

de Bruin JH, Nagengast FM, Ligtenberg MJ, van Krieken JH, Niermeijer MF, Hoogerbrugge N. de Bruin JH, et al. Among authors: hoogerbrugge n. Ned Tijdschr Geneeskd. 2004 Oct 16;148(42):2053-7. Ned Tijdschr Geneeskd. 2004. PMID: 15532325 Dutch.

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