Ariansen S - Search Results

1

[Mutation testing for non-small-cell lung cancer].

Brustugun OT, Helland Å, Fjellbirkeland L, Kleinberg L, Ariansen S, Jebsen P, Scott H, Dønnem T, Bremnes R, Berg T, Grønberg BH, Dai HY, Wahl SG, Mangseth K, Helgeland L. Brustugun OT, et al. Among authors: ariansen s. Tidsskr Nor Laegeforen. 2012 Apr 30;132(8):952-5. doi: 10.4045/tidsskr.11.1017. Tidsskr Nor Laegeforen. 2012. PMID: 22562326 Free article. Norwegian.

2

EGFR gene alterations in a Norwegian cohort of lung cancer patients selected for surgery.

Helland Å, Skaug HM, Kleinberg L, Iversen ML, Rud AK, Fleischer T, Sagerup C, Solberg S, Jørgensen L, Ariansen S, Brustugun OT. Helland Å, et al. Among authors: ariansen s. J Thorac Oncol. 2011 May;6(5):947-50. doi: 10.1097/JTO.0b013e31820db209. J Thorac Oncol. 2011. PMID: 21623266 Free article.

3

Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers.

Grindedal EM, Heramb C, Karsrud I, Ariansen SL, Mæhle L, Undlien DE, Norum J, Schlichting E. Grindedal EM, et al. Among authors: ariansen sl. BMC Cancer. 2017 Jun 21;17(1):438. doi: 10.1186/s12885-017-3422-2. BMC Cancer. 2017. PMID: 28637432 Free PMC article.

4

BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.

Heramb C, Wangensteen T, Grindedal EM, Ariansen SL, Lothe S, Heimdal KR, Mæhle L. Heramb C, et al. Among authors: ariansen sl. Hered Cancer Clin Pract. 2018 Jan 10;16:3. doi: 10.1186/s13053-017-0085-6. eCollection 2018. Hered Cancer Clin Pract. 2018. PMID: 29339979 Free PMC article.

5

BRCA mutation carrier detection. A model-based cost-effectiveness analysis comparing the traditional family history approach and the testing of all patients with breast cancer.

Norum J, Grindedal EM, Heramb C, Karsrud I, Ariansen SL, Undlien DE, Schlichting E, Mæhle L. Norum J, et al. Among authors: ariansen sl. ESMO Open. 2018 Apr 13;3(3):e000328. doi: 10.1136/esmoopen-2018-000328. eCollection 2018. ESMO Open. 2018. PMID: 29682331 Free PMC article.

6

Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas.

Helsing P, Nymoen DA, Ariansen S, Steine SJ, Maehle L, Aamdal S, Langmark F, Loeb M, Akslen LA, Molven A, Andresen PA. Helsing P, et al. Among authors: ariansen s. Genes Chromosomes Cancer. 2008 Feb;47(2):175-84. doi: 10.1002/gcc.20518. Genes Chromosomes Cancer. 2008. PMID: 18023021

7

Chromosomal 20q gain in the DNA diploid component of aneuploid colorectal carcinomas.

De Angelis PM, Stokke T, Beigi M, Flatberg G, Enger M, Haug K, Aass HC, Schjølberg A, Andresen PA, Ariansen S, Bø AS, Mjåland O, Clausen OP. De Angelis PM, et al. Among authors: ariansen s. Int J Cancer. 2007 Jun 15;120(12):2734-8. doi: 10.1002/ijc.22537. Int J Cancer. 2007. PMID: 17354231 Free article.

8

APC mutation spectrum of Norwegian familial adenomatous polyposis families: high ratio of novel mutations.

Andresen PA, Heimdal K, Aaberg K, Eklo K, Ariansen S, Silye A, Fausa O, Aabakken L, Aretz S, Eide TJ, Gedde-Dahl T Jr. Andresen PA, et al. Among authors: ariansen s. J Cancer Res Clin Oncol. 2009 Oct;135(10):1463-70. doi: 10.1007/s00432-009-0594-4. Epub 2009 May 15. J Cancer Res Clin Oncol. 2009. PMID: 19444466

9

Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.

Sjursen W, Haukanes BI, Grindedal EM, Aarset H, Stormorken A, Engebretsen LF, Jonsrud C, Bjørnevoll I, Andresen PA, Ariansen S, Lavik LA, Gilde B, Bowitz-Lothe IM, Maehle L, Møller P. Sjursen W, et al. Among authors: ariansen s. J Med Genet. 2010 Sep;47(9):579-85. doi: 10.1136/jmg.2010.077677. Epub 2010 Jun 28. J Med Genet. 2010. PMID: 20587412 Free PMC article.

10

Diagnostic mRNA splicing assay for variants in BRCA1 and BRCA2 identified two novel pathogenic splicing aberrations.

Wangensteen T, Felde CN, Ahmed D, Mæhle L, Ariansen SL. Wangensteen T, et al. Among authors: ariansen sl. Hered Cancer Clin Pract. 2019 May 22;17:14. doi: 10.1186/s13053-019-0113-9. eCollection 2019. Hered Cancer Clin Pract. 2019. PMID: 31143303 Free PMC article.

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