Gerdes AM - Search Results

1

Low frequency of large genomic rearrangements of BRCA1 and BRCA2 in western Denmark.

Thomassen M, Gerdes AM, Cruger D, Jensen PK, Kruse TA. Thomassen M, et al. Among authors: gerdes am. Cancer Genet Cytogenet. 2006 Jul 15;168(2):168-71. doi: 10.1016/j.cancergencyto.2005.12.016. Cancer Genet Cytogenet. 2006. PMID: 16843109

2

Multipoint linkage analysis in Menkes disease.

Tønnesen T, Petterson A, Kruse TA, Gerdes AM, Horn N. Tønnesen T, et al. Among authors: gerdes am. Am J Hum Genet. 1992 May;50(5):1012-7. Am J Hum Genet. 1992. PMID: 1570830 Free PMC article.

3

Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer.

Håkansson S, Johannsson O, Johansson U, Sellberg G, Loman N, Gerdes AM, Holmberg E, Dahl N, Pandis N, Kristoffersson U, Olsson H, Borg A. Håkansson S, et al. Among authors: gerdes am. Am J Hum Genet. 1997 May;60(5):1068-78. Am J Hum Genet. 1997. PMID: 9150154 Free PMC article.

4

Fluorescence in situ hybridization of old G-banded and mounted chromosome preparations.

Gerdes AM, Pandis N, Bomme L, Dietrich CU, Teixeira MR, Bardi G, Heim S. Gerdes AM, et al. Cancer Genet Cytogenet. 1997 Oct 1;98(1):9-15. doi: 10.1016/s0165-4608(96)00407-4. Cancer Genet Cytogenet. 1997. PMID: 9309112

5

Loss of heterozygosity at BRCA2 in a ductal carcinoma in situ and three invasive breast carcinomas in a family with a germline BRCA2 mutation.

Thomassen M, Kruse TA, Olsen KE, Borg A, Gerdes AM. Thomassen M, et al. Among authors: gerdes am. Breast Cancer Res Treat. 2004 Oct;87(3):273-6. doi: 10.1007/s10549-004-9503-3. Breast Cancer Res Treat. 2004. PMID: 15528970

6

'Indirect' BRCA1/2 testing: a useful approach in hereditary breast and ovarian cancer families without a living affected relative.

Cruger DG, Kruse TA, Gerdes AM. Cruger DG, et al. Among authors: gerdes am. Clin Genet. 2005 Sep;68(3):228-33. doi: 10.1111/j.1399-0004.2005.00484.x. Clin Genet. 2005. PMID: 16098011

7

A missense mutation in exon 13 in BRCA2, c.7235G>A, results in skipping of exon 13.

Thomassen M, Kruse TA, Jensen PK, Gerdes AM. Thomassen M, et al. Among authors: gerdes am. Genet Test. 2006 Summer;10(2):116-20. doi: 10.1089/gte.2006.10.116. Genet Test. 2006. PMID: 16792514

8

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

9

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

10

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Antoniou AC, Sinilnikova OM, McGuffog L, Healey S, Nevanlinna H, Heikkinen T, Simard J, Spurdle AB, Beesley J, Chen X; Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer; Neuhausen SL, Ding YC, Couch FJ, Wang X, Fredericksen Z, Peterlongo P, Peissel B, Bonanni B, Viel A, Bernard L, Radice P, Szabo CI, Foretova L, Zikan M, Claes K, Greene MH, Mai PL, Rennert G, Lejbkowicz F, Andrulis IL, Ozcelik H, Glendon G; OCGN; Gerdes AM, Thomassen M, Sunde L, Caligo MA, Laitman Y, Kontorovich T, Cohen S, Kaufman B, Dagan E, Baruch RG, Friedman E, Harbst K, Barbany-Bustinza G, Rantala J, Ehrencrona H, Karlsson P, Domchek SM, Nathanson KL, Osorio A, Blanco I, Lasa A, Benítez J, Hamann U, Hogervorst FB, Rookus MA, Collee JM, Devilee P, Ligtenberg MJ, van der Luijt RB, Aalfs CM, Waisfisz Q, Wijnen J, van Roozendaal CE; HEBON; Peock S, Cook M, Frost D, Oliver C, Platte R, Evans DG, Lalloo F, Eeles R, Izatt L, Davidson R, Chu C, Eccles D, Cole T, Hodgson S; EMBRACE; Godwin AK, Stoppa-Lyonnet D, Buecher B, Léoné M, Bressac-de Paillerets B, Remenieras A, Caron O, Lenoir GM, Sevenet N, Longy M, Ferrer SF, Prieur F; GEMO; Goldgar D, Miron A, John EM, Buys SS, Daly M… See abstract for full author list ➔ Antoniou AC, et al. Among authors: gerdes am. Hum Mol Genet. 2009 Nov 15;18(22):4442-56. doi: 10.1093/hmg/ddp372. Epub 2009 Aug 5. Hum Mol Genet. 2009. PMID: 19656774 Free PMC article.

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