Møller P - Search Results

1

Germline PTEN mutations are rare and highly penetrant.

Rustad CF, Bjørnslett M, Heimdal KR, Mæhle L, Apold J, Møller P. Rustad CF, et al. Among authors: moller p. Hered Cancer Clin Pract. 2006 Dec 15;4(4):177-85. doi: 10.1186/1897-4287-4-4-177. Hered Cancer Clin Pract. 2006. PMID: 20223021 Free PMC article.

2

Oral contraceptives and risk of familial breast cancer.

Heimdal K, Skovlund E, Møller P. Heimdal K, et al. Among authors: moller p. Cancer Detect Prev. 2002;26(1):23-7. doi: 10.1016/s0361-090x(02)00004-1. Cancer Detect Prev. 2002. PMID: 12088199

3

Survival in prospectively ascertained familial breast cancer: analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy.

Møller P, Borg A, Evans DG, Haites N, Reis MM, Vasen H, Anderson E, Steel CM, Apold J, Goudie D, Howell A, Lalloo F, Maehle L, Gregory H, Heimdal K. Møller P, et al. Int J Cancer. 2002 Oct 20;101(6):555-9. doi: 10.1002/ijc.10641. Int J Cancer. 2002. PMID: 12237897

4

The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours.

Stormorken AT, Müller W, Lindblom A, Heimdal K, Aase S, Lothe IM, Norèn T, Wijnen JT, Möslein G, Møller P. Stormorken AT, et al. Among authors: moller p. Fam Cancer. 2003;2(1):9-13. doi: 10.1023/a:1023362205205. Fam Cancer. 2003. PMID: 14574162

5

Uptake of BRCA1 genetic testing in adult sisters and daughters of known mutation carriers in Norway.

Bodd TL, Reichelt J, Heimdal K, Moller P. Bodd TL, et al. Among authors: moller p. J Genet Couns. 2003 Oct;12(5):405-17. doi: 10.1023/a:1025864703405. J Genet Couns. 2003. PMID: 14758817

6

[Retinoblastoma--hereditary eye cancer in children?].

Møller P, Apold J. Møller P, et al. Tidsskr Nor Laegeforen. 2004 Mar 18;124(6):830; author reply 830. Tidsskr Nor Laegeforen. 2004. PMID: 15039827 Free article. Norwegian. No abstract available.

7

BRCA1 testing with definitive results: a prospective study of psychological distress in a large clinic-based sample.

Reichelt JG, Heimdal K, Møller P, Dahl AA. Reichelt JG, et al. Among authors: moller p. Fam Cancer. 2004;3(1):21-8. doi: 10.1023/B:FAME.0000026820.32469.4a. Fam Cancer. 2004. PMID: 15131402

8

Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancer.

Hope Q, Bullock S, Evans C, Meitz J, Hamel N, Edwards SM, Severi G, Dearnaley D, Jhavar S, Southgate C, Falconer A, Dowe A, Muir K, Houlston RS, Engert JC, Roquis D, Sinnett D, Simard J, Heimdal K, Møller P, Maehle L, Badzioch M, Eeles RA, Easton DF, English DR, Southey MC, Hopper JL, Foulkes WD, Giles GG; Cancer Research UK/British Association of Urological Surgeons' Section of Oncology Collaborators. Hope Q, et al. Among authors: moller p. Cancer Epidemiol Biomarkers Prev. 2005 Feb;14(2):397-402. doi: 10.1158/1055-9965.EPI-04-0202. Cancer Epidemiol Biomarkers Prev. 2005. PMID: 15734964 Free article.

9

Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations.

Geirdal AØ, Reichelt JG, Dahl AA, Heimdal K, Maehle L, Stormorken A, Møller P. Geirdal AØ, et al. Among authors: moller p. Fam Cancer. 2005;4(2):121-6. doi: 10.1007/s10689-004-7995-y. Fam Cancer. 2005. PMID: 15951962

10

Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer.

Stormorken AT, Bowitz-Lothe IM, Norèn T, Kure E, Aase S, Wijnen J, Apold J, Heimdal K, Møller P. Stormorken AT, et al. Among authors: moller p. J Clin Oncol. 2005 Jul 20;23(21):4705-12. doi: 10.1200/JCO.2005.05.180. J Clin Oncol. 2005. PMID: 16034045

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