Eiriksdottir G - Search Results

1

Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival.

Ragnarsson G, Eiriksdottir G, Johannsdottir JT, Jonasson JG, Egilsson V, Ingvarsson S. Ragnarsson G, et al. Among authors: eiriksdottir g. Br J Cancer. 1999 Mar;79(9-10):1468-74. doi: 10.1038/sj.bjc.6690234. Br J Cancer. 1999. PMID: 10188892 Free PMC article.

2

High frequency of allelic imbalance at chromosome region 16q22-23 in human breast cancer: correlation with high PgR and low S phase.

Skirnisdottir S, Eiriksdottir G, Baldursson T, Barkardottir RB, Egilsson V, Ingvarrson S. Skirnisdottir S, et al. Among authors: eiriksdottir g. Int J Cancer. 1995 Apr 21;64(2):112-6. doi: 10.1002/ijc.2910640207. Int J Cancer. 1995. PMID: 7615353

3

Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations.

Gudmundsson J, Barkardottir RB, Eiriksdottir G, Baldursson T, Arason A, Egilsson V, Ingvarsson S. Gudmundsson J, et al. Among authors: eiriksdottir g. Br J Cancer. 1995 Sep;72(3):696-701. doi: 10.1038/bjc.1995.396. Br J Cancer. 1995. PMID: 7669583 Free PMC article.

4

Loss of heterozygosity on chromosome 9 in human breast cancer: association with clinical variables and genetic changes at other chromosome regions.

Eiriksdottir G, Sigurdsson A, Jonasson JG, Agnarsson BA, Sigurdsson H, Gudmundsson J, Bergthorsson JT, Barkardottir RB, Egilsson V, Ingvarsson S. Eiriksdottir G, et al. Int J Cancer. 1995 Dec 20;64(6):378-82. doi: 10.1002/ijc.2910640605. Int J Cancer. 1995. PMID: 8550238

5

Loss of heterozygosity at chromosome 7q in human breast cancer: association with clinical variables.

Kristjansson AK, Eiriksdottir G, Ragnarsson G, Sigurdsson A, Gudmundsson J, Barkardottir RB, Jonasson JG, Egilsson V, Ingvarsson S. Kristjansson AK, et al. Among authors: eiriksdottir g. Anticancer Res. 1997 Jan-Feb;17(1A):93-8. Anticancer Res. 1997. PMID: 9066635

6

High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriers.

Eiriksdottir G, Barkardottir RB, Agnarsson BA, Johannesdottir G, Olafsdottir K, Egilsson V, Ingvarsson S. Eiriksdottir G, et al. Oncogene. 1998 Jan 8;16(1):21-6. doi: 10.1038/sj.onc.1201509. Oncogene. 1998. PMID: 9467939

7

High frequency of LOH at chromosome 18q in human breast cancer: association with high S-phase fraction and low progesterone receptor content.

Huiping C, Eiriksdottir G, Sigurdsson A, Sigurgeirsdottir JR, Barkardottir RB, Egilsson V, Ingvarsson S. Huiping C, et al. Among authors: eiriksdottir g. Anticancer Res. 1998 Mar-Apr;18(2A):1031-6. Anticancer Res. 1998. PMID: 9615760

8

Chromosome imbalance at the 3p14 region in human breast tumours: high frequency in patients with inherited predisposition due to BRCA2.

Bergthorsson JT, Johannsdottir J, Jonasdottir A, Eiriksdottir G, Egilsson V, Ingvarsson S, Barkardottir RB, Arason A. Bergthorsson JT, et al. Among authors: eiriksdottir g. Eur J Cancer. 1998 Jan;34(1):142-7. doi: 10.1016/s0959-8049(97)00339-0. Eur J Cancer. 1998. PMID: 9624249

9

High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutation.

Ingvarsson S, Geirsdottir EK, Johannesdottir G, Sigbjörnsdóttir BI, Eiriksdottir G, Ragnarsson G, Agnarsson BA, Gudmundsson J, Jonasson JG, Sigurdsson A, Egilsson V, Barkardottir RB. Ingvarsson S, et al. Among authors: eiriksdottir g. Cancer Res. 1998 Oct 1;58(19):4421-5. Cancer Res. 1998. PMID: 9766673

10

Replication error in human breast cancer: comparison with clinical variables and family history of cancer.

Huiping C, Johannsdottir JT, Arason A, Olafsdottir GH, Eiriksdottir G, Egilsson V, Ingvarsson S. Huiping C, et al. Among authors: eiriksdottir g. Oncol Rep. 1999 Jan-Feb;6(1):117-22. Oncol Rep. 1999. PMID: 9864413

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