Møller P - Search Results

1

Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry.

Stormorken AT, Müller W, Lemkemeyer B, Apold J, Wijnen JT, Fodde R, Möslein G, Møller P. Stormorken AT, et al. Among authors: moller p. Fam Cancer. 2001;1(3-4):169-73. doi: 10.1023/a:1021151227983. Fam Cancer. 2001. PMID: 14574174

2

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

Vasen HF, Stormorken A, Menko FH, Nagengast FM, Kleibeuker JH, Griffioen G, Taal BG, Moller P, Wijnen JT. Vasen HF, et al. Among authors: moller p. J Clin Oncol. 2001 Oct 15;19(20):4074-80. doi: 10.1200/JCO.2001.19.20.4074. J Clin Oncol. 2001. PMID: 11600610

3

Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.

Vasen HF, Möslein G, Alonso A, Aretz S, Bernstein I, Bertario L, Blanco I, Bulow S, Burn J, Capella G, Colas C, Engel C, Frayling I, Rahner N, Hes FJ, Hodgson S, Mecklin JP, Møller P, Myrhøj T, Nagengast FM, Parc Y, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen J, Lubinski J, Järvinen H, Claes E, Heinimann K, Karagiannis JA, Lindblom A, Dove-Edwin I, Müller H. Vasen HF, et al. Among authors: moller p. Fam Cancer. 2010 Jun;9(2):109-15. doi: 10.1007/s10689-009-9291-3. Epub 2009 Sep 18. Fam Cancer. 2010. PMID: 19763885

4

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.

Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, Bakker B, Losekoot M, Møller P, Fodde R. Wijnen J, et al. Among authors: moller p. Am J Hum Genet. 1997 Aug;61(2):329-35. doi: 10.1086/514847. Am J Hum Genet. 1997. PMID: 9311737 Free PMC article.

5

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

Wijnen JT, Vasen HF, Khan PM, Zwinderman AH, van der Klift H, Mulder A, Tops C, Møller P, Fodde R. Wijnen JT, et al. Among authors: moller p. N Engl J Med. 1998 Aug 20;339(8):511-8. doi: 10.1056/NEJM199808203390804. N Engl J Med. 1998. PMID: 9709044 Free article.

6

Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients.

de Leeuw WJ, Dierssen J, Vasen HF, Wijnen JT, Kenter GG, Meijers-Heijboer H, Brocker-Vriends A, Stormorken A, Moller P, Menko F, Cornelisse CJ, Morreau H. de Leeuw WJ, et al. Among authors: moller p. J Pathol. 2000 Nov;192(3):328-35. doi: 10.1002/1096-9896(2000)9999:9999<::AID-PATH701>3.0.CO;2-2. J Pathol. 2000. PMID: 11054716

7

[Hereditary colorectal cancer].

Stormorken AT, Apold J, Heimdal K, Møller P. Stormorken AT, et al. Among authors: moller p. Tidsskr Nor Laegeforen. 1999 Oct 30;119(26):3933-6. Tidsskr Nor Laegeforen. 1999. PMID: 10592756 Review. Norwegian.

8

The BRCA1 syndrome and other inherited breast or breast-ovarian cancers in a Norwegian prospective series.

Møller P, Borg A, Heimdal K, Apold J, Vallon-Christersson J, Hovig E, Maehle L; Norwegian Inherited Breast Cancer Group; Norwegian Inherited Ovarian Cancer Group. Møller P, et al. Eur J Cancer. 2001 May;37(8):1027-32. doi: 10.1016/s0959-8049(01)00075-2. Eur J Cancer. 2001. PMID: 11334729

9

The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer.

Heimdal K, Maehle L, Apold J, Pedersen JC, Møller P. Heimdal K, et al. Among authors: moller p. Eur J Cancer. 2003 Oct;39(15):2205-13. doi: 10.1016/s0959-8049(03)00548-3. Eur J Cancer. 2003. PMID: 14522380

10

Genetic epidemiology of BRCA1 mutations in Norway.

Møller P, Heimdal K, Apold J, Fredriksen A, Borg A, Hovig E, Hagen A, Hagen B, Pedersen JC, Maehle L; Norwegian Inherited Breast Cancer Group; Norwegian Inherited Ovarian Cancer Group. Møller P, et al. Eur J Cancer. 2001 Dec;37(18):2428-34. doi: 10.1016/s0959-8049(01)00299-4. Eur J Cancer. 2001. PMID: 11720839

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