Clark N - Search Results

1

High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers.

Grindedal EM, Blanco I, Stormorken A, Maehle L, Clark N, González S, Capella G, Vasen H, Burn J, Møller P. Grindedal EM, et al. Among authors: clark n. Fam Cancer. 2009;8(2):145-51. doi: 10.1007/s10689-008-9219-3. Epub 2008 Oct 8. Fam Cancer. 2009. PMID: 18841495

2

Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancer.

Stormorken AT, Clark N, Grindedal E, Maehle L, Møller P. Stormorken AT, et al. Among authors: clark n. Scand J Gastroenterol. 2007 May;42(5):611-7. doi: 10.1080/00365520601010230. Scand J Gastroenterol. 2007. PMID: 17454882

3

High risk for ovarian cancer in a prospective series is restricted to BRCA1/2 mutation carriers.

Maehle L, Apold J, Paulsen T, Hagen B, Løvslett K, Fiane B, Van Ghelue M, Clark N, Møller P. Maehle L, et al. Among authors: clark n. Clin Cancer Res. 2008 Nov 15;14(22):7569-73. doi: 10.1158/1078-0432.CCR-08-0112. Clin Cancer Res. 2008. PMID: 19010876

4

Germ-line mutations in mismatch repair genes associated with prostate cancer.

Grindedal EM, Møller P, Eeles R, Stormorken AT, Bowitz-Lothe IM, Landrø SM, Clark N, Kvåle R, Shanley S, Maehle L. Grindedal EM, et al. Among authors: clark n. Cancer Epidemiol Biomarkers Prev. 2009 Sep;18(9):2460-7. doi: 10.1158/1055-9965.EPI-09-0058. Epub 2009 Sep 1. Cancer Epidemiol Biomarkers Prev. 2009. PMID: 19723918 Free article.

5

Age-specific incidence rates for breast cancer in carriers of BRCA1 mutations from Norway.

Møller P, Maehle L, Vabø A, Clark N, Sun P, Narod SA. Møller P, et al. Among authors: clark n. Clin Genet. 2013 Jan;83(1):88-91. doi: 10.1111/j.1399-0004.2012.01855.x. Epub 2012 Mar 1. Clin Genet. 2013. PMID: 22320316

6

Surveillance for familial breast cancer: Differences in outcome according to BRCA mutation status.

Moller P, Evans DG, Reis MM, Gregory H, Anderson E, Maehle L, Lalloo F, Howell A, Apold J, Clark N, Lucassen A, Steel CM. Moller P, et al. Among authors: clark n. Int J Cancer. 2007 Sep 1;121(5):1017-20. doi: 10.1002/ijc.22789. Int J Cancer. 2007. PMID: 17471561

7

Genetic epidemiology of BRCA mutations--family history detects less than 50% of the mutation carriers.

Møller P, Hagen AI, Apold J, Maehle L, Clark N, Fiane B, Løvslett K, Hovig E, Vabø A. Møller P, et al. Among authors: clark n. Eur J Cancer. 2007 Jul;43(11):1713-7. doi: 10.1016/j.ejca.2007.04.023. Epub 2007 Jun 15. Eur J Cancer. 2007. PMID: 17574839

8

No sib pair concordance for breast or ovarian cancer in BRCA1 mutation carriers.

Møller P, Maehle L, Clark N, Apold J. Møller P, et al. Among authors: clark n. Hered Cancer Clin Pract. 2007 Jun 15;5(2):67-71. doi: 10.1186/1897-4287-5-2-67. Hered Cancer Clin Pract. 2007. PMID: 19725986 Free PMC article.

9

A SImplified method for Segregation Analysis (SISA) to determine penetrance and expression of a genetic variant in a family.

Møller P, Clark N, Mæhle L. Møller P, et al. Among authors: clark n. Hum Mutat. 2011 May;32(5):568-71. doi: 10.1002/humu.21441. Epub 2011 Feb 22. Hum Mutat. 2011. PMID: 21309035

10

Survival of patients with BRCA1-associated breast cancer diagnosed in an MRI-based surveillance program.

Møller P, Stormorken A, Jonsrud C, Holmen MM, Hagen AI, Clark N, Vabø A, Sun P, Narod SA, Mæhle L. Møller P, et al. Among authors: clark n. Breast Cancer Res Treat. 2013 May;139(1):155-61. doi: 10.1007/s10549-013-2540-z. Epub 2013 Apr 25. Breast Cancer Res Treat. 2013. PMID: 23615785

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