Bergthorsson JT - Search Results

1

Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus.

Kainu T, Juo SH, Desper R, Schaffer AA, Gillanders E, Rozenblum E, Freas-Lutz D, Weaver D, Stephan D, Bailey-Wilson J, Kallioniemi OP, Tirkkonen M, Syrjäkoski K, Kuukasjärvi T, Koivisto P, Karhu R, Holli K, Arason A, Johannesdottir G, Bergthorsson JT, Johannsdottir H, Egilsson V, Barkardottir RB, Johannsson O, Haraldsson K, Sandberg T, Holmberg E, Grönberg H, Olsson H, Borg A, Vehmanen P, Eerola H, Heikkila P, Pyrhönen S, Nevanlinna H. Kainu T, et al. Among authors: bergthorsson jt. Proc Natl Acad Sci U S A. 2000 Aug 15;97(17):9603-8. doi: 10.1073/pnas.97.17.9603. Proc Natl Acad Sci U S A. 2000. PMID: 10944226 Free PMC article.

2

Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13.

Gudmundsson J, Johannesdottir G, Bergthorsson JT, Arason A, Ingvarsson S, Egilsson V, Barkardottir RB. Gudmundsson J, et al. Among authors: bergthorsson jt. Cancer Res. 1995 Nov 1;55(21):4830-2. Cancer Res. 1995. PMID: 7585515

3

Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype.

Gudmundsson J, Johannesdottir G, Arason A, Bergthorsson JT, Ingvarsson S, Egilsson V, Barkardottir RB. Gudmundsson J, et al. Among authors: bergthorsson jt. Am J Hum Genet. 1996 Apr;58(4):749-56. Am J Hum Genet. 1996. PMID: 8644738 Free PMC article.

4

High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients.

Johannesdottir G, Gudmundsson J, Bergthorsson JT, Arason A, Agnarsson BA, Eiriksdottir G, Johannsson OT, Borg A, Ingvarsson S, Easton DF, Egilsson V, Barkardottir RB. Johannesdottir G, et al. Among authors: bergthorsson jt. Cancer Res. 1996 Aug 15;56(16):3663-5. Cancer Res. 1996. PMID: 8706004

5

Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer.

Bergthorsson JT, Johannesdottir G, Arason A, Benediktsdottir KR, Agnarsson BA, Bailey-Wilson JE, Gillanders E, Smith J, Trent J, Barkardottir RB. Bergthorsson JT, et al. Hum Genet. 2000 Oct;107(4):372-5. doi: 10.1007/s004390000384. Hum Genet. 2000. PMID: 11129338

6

Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3.

Bergthorsson JT, Eiriksdottir G, Barkardottir RB, Egilsson V, Arason A, Ingvarsson S. Bergthorsson JT, et al. Hum Genet. 1995 Oct;96(4):437-43. doi: 10.1007/BF00191803. Hum Genet. 1995. PMID: 7557967

7

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. Eur J Cancer. 1998 Jan;34(1):142-7. doi: 10.1016/s0959-8049(97)00339-0. Eur J Cancer. 1998. PMID: 9624249

8

A population study of mutations and LOH at breast cancer gene loci in tumours from sister pairs: two recurrent mutations seem to account for all BRCA1/BRCA2 linked breast cancer in Iceland.

Arason A, Jonasdottir A, Barkardottir RB, Bergthorsson JT, Teare MD, Easton DF, Egilsson V. Arason A, et al. Among authors: bergthorsson jt. J Med Genet. 1998 Jun;35(6):446-9. doi: 10.1136/jmg.35.6.446. J Med Genet. 1998. PMID: 9643283 Free PMC article.

9

BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.

Bergthorsson JT, Ejlertsen B, Olsen JH, Borg A, Nielsen KV, Barkardottir RB, Klausen S, Mouridsen HT, Winther K, Fenger K, Niebuhr A, Harboe TL, Niebuhr E. Bergthorsson JT, et al. J Med Genet. 2001 Jun;38(6):361-8. doi: 10.1136/jmg.38.6.361. J Med Genet. 2001. PMID: 11389159 Free PMC article.

10

Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non-polyposis colon cancer trait.

Bergthorsson JT, Egilsson V, Gudmundsson J, Arason A, Ingvarsson S. Bergthorsson JT, et al. Clin Genet. 1995 Jun;47(6):305-10. doi: 10.1111/j.1399-0004.1995.tb03970.x. Clin Genet. 1995. PMID: 7554364

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