Gerdes AM - Search Results

1

Prophylactic total gastrectomy in hereditary diffuse gastric cancer: identification of two novel CDH1 gene mutations-a clinical observational study.

Bardram L, Hansen TV, Gerdes AM, Timshel S, Friis-Hansen L, Federspiel B. Bardram L, et al. Among authors: gerdes am. Fam Cancer. 2014 Jun;13(2):231-42. doi: 10.1007/s10689-013-9698-8. Fam Cancer. 2014. PMID: 24389957

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

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.

Antoniou AC, Beesley J, McGuffog L, Sinilnikova OM, Healey S, Neuhausen SL, Ding YC, Rebbeck TR, Weitzel JN, Lynch HT, Isaacs C, Ganz PA, Tomlinson G, Olopade OI, Couch FJ, Wang X, Lindor NM, Pankratz VS, Radice P, Manoukian S, Peissel B, Zaffaroni D, Barile M, Viel A, Allavena A, Dall'Olio V, Peterlongo P, Szabo CI, Zikan M, Claes K, Poppe B, Foretova L, Mai PL, Greene MH, Rennert G, Lejbkowicz F, Glendon G, Ozcelik H, Andrulis IL; Ontario Cancer Genetics Network; Thomassen M, Gerdes AM, Sunde L, Cruger D, Birk Jensen U, Caligo M, Friedman E, Kaufman B, Laitman Y, Milgrom R, Dubrovsky M, Cohen S, Borg A, Jernström H, Lindblom A, Rantala J, Stenmark-Askmalm M, Melin B; SWE-BRCA; Nathanson K, Domchek S, Jakubowska A, Lubinski J, Huzarski T, Osorio A, Lasa A, Durán M, Tejada MI, Godino J, Benitez J, Hamann U, Kriege M, Hoogerbrugge N, van der Luijt RB, van Asperen CJ, Devilee P, Meijers-Heijboer EJ, Blok MJ, Aalfs CM, Hogervorst F, Rookus M; HEBON; Cook M, Oliver C, Frost D, Conroy D, Evans DG, Lalloo F, Pichert G, Davidson R, Cole T, Cook J, Paterson J, Hodgson S, Morrison PJ, Porteous ME, Walker L, Kennedy MJ, Dorkins H, Peock S; EMBRACE; Godwin AK, Stoppa-Lyonnet D, de Pau… See abstract for full author list ➔ Antoniou AC, et al. Among authors: gerdes am. Cancer Res. 2010 Dec 1;70(23):9742-54. doi: 10.1158/0008-5472.CAN-10-1907. Epub 2010 Nov 30. Cancer Res. 2010. PMID: 21118973 Free PMC article.

7

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

8

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

9

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

10

Biomedical informatics as support to individual healthcare in hereditary colon cancer: the Danish HNPCC system.

Bernstein IT, Lindorff-Larsen K, Timshel S, Brandt CA, Dinesen B, Fenger M, Gerdes AM, Iversen LH, Madsen MR, Okkels H, Sunde L, Rahr HB, Wikman FP, Rossing N. Bernstein IT, et al. Among authors: gerdes am. Hum Mutat. 2011 May;32(5):551-6. doi: 10.1002/humu.21435. Epub 2011 Feb 22. Hum Mutat. 2011. PMID: 21520332

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