Gerdes AM - 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: gerdes am. 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

BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer.

Thomassen M, Hansen TV, Borg A, Lianee HT, Wikman F, Pedersen IS, Bisgaard ML, Nielsen FC, Kruse TA, Gerdes AM. Thomassen M, et al. Among authors: gerdes am. Acta Oncol. 2008;47(4):772-7. doi: 10.1080/02841860802004974. Acta Oncol. 2008. PMID: 18465347

3

Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population.

Nilbert M, Wikman FP, Hansen TV, Krarup HB, Orntoft TF, Nielsen FC, Sunde L, Gerdes AM, Cruger D, Timshel S, Bisgaard ML, Bernstein I, Okkels H. Nilbert M, et al. Among authors: gerdes am. Fam Cancer. 2009;8(1):75-83. doi: 10.1007/s10689-008-9199-3. Epub 2008 Jun 20. Fam Cancer. 2009. PMID: 18566915

4

Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients.

Christensen LL, Kariola R, Korhonen MK, Wikman FP, Sunde L, Gerdes AM, Okkels H, Brandt CA, Bernstein I, Hansen TV, Hagemann-Madsen R, Andersen CL, Nyström M, Ørntoft TF. Christensen LL, et al. Among authors: gerdes am. Fam Cancer. 2009;8(4):489-500. doi: 10.1007/s10689-009-9274-4. Epub 2009 Aug 21. Fam Cancer. 2009. PMID: 19697156

5

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. Among authors: gerdes am. Fam Cancer. 2010 Sep;9(3):283-7. doi: 10.1007/s10689-010-9345-6. Fam Cancer. 2010. PMID: 20455026 Free PMC article.

6

A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing.

Thomassen M, Pedersen IS, Vogel I, Hansen TV, Brasch-Andersen C, Brasen CL, Crüger D, Sunde L, Nielsen FC, Jensen UB, Bisgaard ML, Borg A, Gerdes AM, Kruse TA. Thomassen M, et al. Among authors: gerdes am. Breast Cancer Res Treat. 2011 Jul;128(1):179-85. doi: 10.1007/s10549-010-1272-6. Epub 2010 Dec 24. Breast Cancer Res Treat. 2011. PMID: 21184276

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. Among authors: gerdes am. Fam Cancer. 2011 Jun;10(2):207-12. doi: 10.1007/s10689-011-9422-5. Fam Cancer. 2011. PMID: 21318380

8

A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one.

Kantelinen J, Hansen TV, Kansikas M, Krogh LN, Korhonen MK, Ollila S, Nyström M, Gerdes AM, Kariola R. Kantelinen J, et al. Among authors: gerdes am. Fam Cancer. 2011 Sep;10(3):515-20. doi: 10.1007/s10689-011-9436-z. Fam Cancer. 2011. PMID: 21431882

9

[A new genetic diagnosis of familiar gastrointestinal stromal tumour].

Wadt K, Andersen MK, Hansen TV, Gerdes AM. Wadt K, et al. Among authors: gerdes am. Ugeskr Laeger. 2012 May 21;174(21):1462-4. Ugeskr Laeger. 2012. PMID: 22640790 Danish.

10

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. Among authors: gerdes am. Fam Cancer. 2012 Sep;11(3):535-7. doi: 10.1007/s10689-012-9542-6. Fam Cancer. 2012. PMID: 22717761

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