Kruse TA - Search Results

1

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: kruse ta. Acta Oncol. 2008;47(4):772-7. doi: 10.1080/02841860802004974. Acta Oncol. 2008. PMID: 18465347

2

Multipoint linkage analysis in Menkes disease.

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

3

Mutations in the ALK-1 gene and the phenotype of hereditary hemorrhagic telangiectasia in two large Danish families.

Kjeldsen AD, Brusgaard K, Poulsen L, Kruse T, Rasmussen K, Green A, Vase P. Kjeldsen AD, et al. Am J Med Genet. 2001 Feb 1;98(4):298-302. doi: 10.1002/1096-8628(20010201)98:4<298::aid-ajmg1093>3.0.co;2-k. Am J Med Genet. 2001. PMID: 11170071

4

Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia.

Brusgaard K, Kjeldsen AD, Poulsen L, Moss H, Vase P, Rasmussen K, Kruse TA, Hørder M. Brusgaard K, et al. Among authors: kruse ta. Clin Genet. 2004 Dec;66(6):556-61. doi: 10.1111/j.1399-0004.2004.00341.x. Clin Genet. 2004. PMID: 15521985

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: kruse ta. 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

A genome-wide search for risk genes using homozygosity mapping and microarrays with 1,494 single-nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder.

Ewald H, Wikman FP, Teruel BM, Buttenschön HN, Torralba M, Als TD, El Daoud A, Flint TJ, Jorgensen TH, Blanco L, Kruse TA, Orntoft TF, Mors O. Ewald H, et al. Among authors: kruse ta. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):25-30. doi: 10.1002/ajmg.b.30106. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15558715

7

'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: kruse ta. Clin Genet. 2005 Sep;68(3):228-33. doi: 10.1111/j.1399-0004.2005.00484.x. Clin Genet. 2005. PMID: 16098011

8

Evaluation of two different models to predict BRCA1 and BRCA2 mutations in a cohort of Danish hereditary breast and/or ovarian cancer families.

Gerdes AM, Cruger DG, Thomassen M, Kruse TA. Gerdes AM, et al. Among authors: kruse ta. Clin Genet. 2006 Feb;69(2):171-8. doi: 10.1111/j.1399-0004.2006.00568.x. Clin Genet. 2006. PMID: 16433698

9

Spotting and validation of a genome wide oligonucleotide chip with duplicate measurement of each gene.

Thomassen M, Skov V, Eiriksdottir F, Tan Q, Jochumsen K, Fritzner N, Brusgaard K, Dahlgaard J, Kruse TA. Thomassen M, et al. Among authors: kruse ta. Biochem Biophys Res Commun. 2006 Jun 16;344(4):1111-20. doi: 10.1016/j.bbrc.2006.03.227. Epub 2006 Apr 19. Biochem Biophys Res Commun. 2006. PMID: 16647037

10

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: kruse ta. Genet Test. 2006 Summer;10(2):116-20. doi: 10.1089/gte.2006.10.116. Genet Test. 2006. PMID: 16792514

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