Skorpen F - Search Results

1

OP006. A preeclampsia genome-wide linkage scan in norwegian families.

Roten LT, Johnson MP, Thompsen LC, Gundersen AS, Solberg P, Tollaksen K, Lyslo I, Tappert C, Odland ML, Strand KM, Fenstad MH, Drabløs F, Skorpen F, Moses EK, Austgulen R, Bjørge L. Roten LT, et al. Among authors: skorpen f. Pregnancy Hypertens. 2013 Apr;3(2):64. doi: 10.1016/j.preghy.2013.04.022. Epub 2013 Jun 6. Pregnancy Hypertens. 2013. PMID: 26105851

2

A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2).

Roten LT, Fenstad MH, Forsmo S, Johnson MP, Moses EK, Austgulen R, Skorpen F. Roten LT, et al. Among authors: skorpen f. Mol Hum Reprod. 2011 Jul;17(7):439-46. doi: 10.1093/molehr/gar014. Epub 2011 Feb 25. Mol Hum Reprod. 2011. PMID: 21355050 Free PMC article.

3

Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.

Rakvåg TT, Ross JR, Sato H, Skorpen F, Kaasa S, Klepstad P. Rakvåg TT, et al. Among authors: skorpen f. Mol Pain. 2008 Dec 18;4:64. doi: 10.1186/1744-8069-4-64. Mol Pain. 2008. PMID: 19094200 Free PMC article.

4

COMT genotypes and use of antipsychotic medication: linking population-based prescription database to the HUNT study.

Hagen K, Stovner LJ, Skorpen F, Pettersen E, Zwart JA. Hagen K, et al. Among authors: skorpen f. Pharmacoepidemiol Drug Saf. 2008 Apr;17(4):372-7. doi: 10.1002/pds.1567. Pharmacoepidemiol Drug Saf. 2008. PMID: 18302304

5

Variation in the COMT gene: implications for pain perception and pain treatment.

Andersen S, Skorpen F. Andersen S, et al. Among authors: skorpen f. Pharmacogenomics. 2009 Apr;10(4):669-84. doi: 10.2217/pgs.09.13. Pharmacogenomics. 2009. PMID: 19374521 Review.

6

The association between headache and Val158Met polymorphism in the catechol-O-methyltransferase gene: the HUNT Study.

Hagen K, Pettersen E, Stovner LJ, Skorpen F, Zwart JA. Hagen K, et al. Among authors: skorpen f. J Headache Pain. 2006 Apr;7(2):70-4. doi: 10.1007/s10194-006-0281-7. Epub 2006 Apr 26. J Headache Pain. 2006. PMID: 16688411 Free PMC article.

7

High systolic blood pressure is associated with Val/Val genotype in the catechol-o-methyltransferase gene. The Nord-Trøndelag Health Study (HUNT).

Hagen K, Pettersen E, Stovner LJ, Skorpen F, Holmen J, Zwart JA. Hagen K, et al. Among authors: skorpen f. Am J Hypertens. 2007 Jan;20(1):21-6. doi: 10.1016/j.amjhyper.2006.05.023. Am J Hypertens. 2007. PMID: 17198907

8

No large-effect low-frequency coding variation found for myocardial infarction.

Holmen OL, Zhang H, Zhou W, Schmidt E, Hovelson DH, Langhammer A, Løchen ML, Ganesh SK, Mathiesen EB, Vatten L, Platou C, Wilsgaard T, Chen J, Skorpen F, Dalen H, Boehnke M, Abecasis GR, Njølstad I, Hveem K, Willer CJ. Holmen OL, et al. Among authors: skorpen f. Hum Mol Genet. 2014 Sep 1;23(17):4721-8. doi: 10.1093/hmg/ddu175. Epub 2014 Apr 12. Hum Mol Genet. 2014. PMID: 24728188 Free PMC article.

9

The Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene may influence morphine requirements in cancer pain patients.

Rakvåg TT, Klepstad P, Baar C, Kvam TM, Dale O, Kaasa S, Krokan HE, Skorpen F. Rakvåg TT, et al. Among authors: skorpen f. Pain. 2005 Jul;116(1-2):73-8. doi: 10.1016/j.pain.2005.03.032. Pain. 2005. PMID: 15927391

10

No association between chronic musculoskeletal complaints and Val158Met polymorphism in the Catechol-O-methyltransferase gene. The HUNT study.

Hagen K, Pettersen E, Stovner LJ, Skorpen F, Zwart JA. Hagen K, et al. Among authors: skorpen f. BMC Musculoskelet Disord. 2006 May 4;7:40. doi: 10.1186/1471-2474-7-40. BMC Musculoskelet Disord. 2006. PMID: 16674809 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

117 results

Search Page