Hovig E - Search Results

1

Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.

Dominguez-Valentin M, Evans DGR, Nakken S, Tubeuf H, Vodak D, Ekstrøm PO, Nissen AM, Morak M, Holinski-Feder E, Martins A, Møller P, Hovig E. Dominguez-Valentin M, et al. Among authors: hovig e. Hered Cancer Clin Pract. 2018 Jan 15;16:4. doi: 10.1186/s13053-018-0086-0. eCollection 2018. Hered Cancer Clin Pract. 2018. PMID: 29371908 Free PMC article.

2

Penetrances of BRCA1 1675delA and 1135insA with respect to breast cancer and ovarian cancer.

Dørum A, Heimdal K, Hovig E, Inganäs M, Møller P. Dørum A, et al. Among authors: hovig e. Am J Hum Genet. 1999 Sep;65(3):671-9. doi: 10.1086/302530. Am J Hum Genet. 1999. PMID: 10441573 Free PMC article.

3

Three per cent of Norwegian ovarian cancers are caused by BRCA1 1675delA or 1135insA.

Dørum A, Hovig E, Tropé C, Inganas M, Møller P. Dørum A, et al. Among authors: hovig e. Eur J Cancer. 1999 May;35(5):779-81. doi: 10.1016/s0959-8049(99)00050-7. Eur J Cancer. 1999. PMID: 10505039

4

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. Among authors: hovig e. Eur J Cancer. 2001 May;37(8):1027-32. doi: 10.1016/s0959-8049(01)00075-2. Eur J Cancer. 2001. PMID: 11334729

5

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. Among authors: hovig e. Eur J Cancer. 2001 Dec;37(18):2428-34. doi: 10.1016/s0959-8049(01)00299-4. Eur J Cancer. 2001. PMID: 11720839

6

Determination of hereditary mutations in the BRCA1 gene using archived serum samples and capillary electrophoresis.

Ekstrøm PO, Bjørge T, Dørum A, Longva AS, Heintz KM, Warren DJ, Hansen S, Gislefoss RE, Hovig E. Ekstrøm PO, et al. Among authors: hovig e. Anal Chem. 2004 Aug 1;76(15):4406-9. doi: 10.1021/ac049788k. Anal Chem. 2004. PMID: 15283579

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: hovig e. 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

Large-scale inference of the point mutational spectrum in human segmental duplications.

Nakken S, Rødland EA, Rognes T, Hovig E. Nakken S, et al. Among authors: hovig e. BMC Genomics. 2009 Jan 22;10:43. doi: 10.1186/1471-2164-10-43. BMC Genomics. 2009. PMID: 19161616 Free PMC article.

9

The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterparts.

Nakken S, Rognes T, Hovig E. Nakken S, et al. Among authors: hovig e. Nucleic Acids Res. 2009 Sep;37(17):5749-56. doi: 10.1093/nar/gkp590. Epub 2009 Jul 17. Nucleic Acids Res. 2009. PMID: 19617376 Free PMC article.

10

MUTYH Mutations Do Not Cause HNPCC or Late Onset Familial Colorectal Cancer.

Stormorken A, Heintz KM, Andresen PA, Hovig E, Møller P. Stormorken A, et al. Among authors: hovig e. Hered Cancer Clin Pract. 2006 May 15;4(2):90-3. doi: 10.1186/1897-4287-4-2-90. Hered Cancer Clin Pract. 2006. PMID: 20223013 Free PMC article.

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