Hansen TVO - Search Results

1

A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families.

Djursby M, Wadt K, Frederiksen JH, Madsen MB, Berchtold LA, Hasselby JP, Willemoe GL, Hansen TVO, Gerdes AM. Djursby M, et al. Among authors: hansen tvo. Hered Cancer Clin Pract. 2020 Apr 7;18:8. doi: 10.1186/s13053-020-00140-3. eCollection 2020. Hered Cancer Clin Pract. 2020. PMID: 32292534 Free PMC article.

2

Identification of six pathogenic RAD51C mutations via mutational screening of 1228 Danish individuals with increased risk of hereditary breast and/or ovarian cancer.

Jønson L, Ahlborn LB, Steffensen AY, Djursby M, Ejlertsen B, Timshel S, Nielsen FC, Gerdes AM, Hansen TV. Jønson L, et al. Breast Cancer Res Treat. 2016 Jan;155(2):215-22. doi: 10.1007/s10549-015-3674-y. Epub 2016 Jan 6. Breast Cancer Res Treat. 2016. PMID: 26740214

3

Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.

Bennedbæk M, Rossing M, Rasmussen ÅK, Gerdes AM, Skytte AB, Jensen UB, Nielsen FC, Hansen TVO. Bennedbæk M, et al. Among authors: hansen tvo. Hered Cancer Clin Pract. 2016 Jun 8;14:13. doi: 10.1186/s13053-016-0053-6. eCollection 2016. Hered Cancer Clin Pract. 2016. PMID: 27279923 Free PMC article.

4

Classification of the spliceogenic BRCA1 c.4096+3A>G variant as likely benign based on cosegregation data and identification of a healthy homozygous carrier.

Byrjalsen A, Steffensen AY, Hansen TVO, Wadt K, Gerdes AM. Byrjalsen A, et al. Among authors: hansen tvo. Clin Case Rep. 2017 Apr 22;5(6):876-879. doi: 10.1002/ccr3.944. eCollection 2017 Jun. Clin Case Rep. 2017. PMID: 28588830 Free PMC article.

5

Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations.

Ahlborn LB, Steffensen AY, Jønson L, Djursby M, Nielsen FC, Gerdes AM, Hansen TV. Ahlborn LB, et al. Fam Cancer. 2015 Mar;14(1):129-33. doi: 10.1007/s10689-014-9747-y. Fam Cancer. 2015. PMID: 25154786

6

Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations.

Steffensen AY, Jønson L, Ejlertsen B, Gerdes AM, Nielsen FC, Hansen TV. Steffensen AY, et al. Fam Cancer. 2010 Sep;9(3):283-7. doi: 10.1007/s10689-010-9345-6. Fam Cancer. 2010. PMID: 20455026 Free PMC article.

7

Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutations.

Hansen TV, Jønson L, Steffensen AY, Andersen MK, Kjaergaard S, Gerdes AM, Ejlertsen B, Nielsen FC. Hansen TV, et al. Fam Cancer. 2011 Jun;10(2):207-12. doi: 10.1007/s10689-011-9422-5. Fam Cancer. 2011. PMID: 21318380

8

Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma.

Wadt KA, Gerdes AM, Hansen TV, Toft BG, Friis-Hansen L, Andersen MK. Wadt KA, et al. Fam Cancer. 2012 Sep;11(3):535-7. doi: 10.1007/s10689-012-9542-6. Fam Cancer. 2012. PMID: 22717761

9

Germline RAD51B truncating mutation in a family with cutaneous melanoma.

Wadt KA, Aoude LG, Golmard L, Hansen TV, Sastre-Garau X, Hayward NK, Gerdes AM. Wadt KA, et al. Fam Cancer. 2015 Jun;14(2):337-40. doi: 10.1007/s10689-015-9781-4. Fam Cancer. 2015. PMID: 25600502

10

Classification of MSH6 Variants of Uncertain Significance Using Functional Assays.

Frederiksen JH, Jensen SB, Tümer Z, Hansen TVO. Frederiksen JH, et al. Among authors: hansen tvo. Int J Mol Sci. 2021 Aug 11;22(16):8627. doi: 10.3390/ijms22168627. Int J Mol Sci. 2021. PMID: 34445333 Free PMC article. Review.

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