Johannsson O - Search Results

1

BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease.

Haraldsson K, Loman N, Zhang QX, Johannsson O, Olsson H, Borg A. Haraldsson K, et al. Among authors: johannsson o. Cancer Res. 1998 Apr 1;58(7):1367-71. Cancer Res. 1998. PMID: 9537231

2

High frequency of allelic imbalance at the BRCA1 region on chromosome 17q in both familial and sporadic ductal breast carcinomas.

Borg A, Zhang QX, Johannsson O, Olsson H. Borg A, et al. Among authors: johannsson o. J Natl Cancer Inst. 1994 May 18;86(10):792-4. doi: 10.1093/jnci/86.10.792. J Natl Cancer Inst. 1994. PMID: 8169978 No abstract available.

3

Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden.

Johannsson O, Ostermeyer EA, Håkansson S, Friedman LS, Johansson U, Sellberg G, Brøndum-Nielsen K, Sele V, Olsson H, King MC, Borg A. Johannsson O, et al. Am J Hum Genet. 1996 Mar;58(3):441-50. Am J Hum Genet. 1996. PMID: 8644702 Free PMC article.

4

Infrequent occurrence of microsatellite instability in sporadic and familial breast cancer.

Jönsson M, Johannsson O, Borg A. Jönsson M, et al. Among authors: johannsson o. Eur J Cancer. 1995 Dec;31A(13-14):2330-4. doi: 10.1016/0959-8049(95)00447-5. Eur J Cancer. 1995. PMID: 8652265

5

Novel germline p16 mutation in familial malignant melanoma in southern Sweden.

Borg A, Johannsson U, Johannsson O, Häkansson S, Westerdahl J, Mäsbäck A, Olsson H, Ingvar C. Borg A, et al. Among authors: johannsson u, johannsson o. Cancer Res. 1996 Jun 1;56(11):2497-500. Cancer Res. 1996. PMID: 8653684

6

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: johannsson ot. Cancer Res. 1996 Aug 15;56(16):3663-5. Cancer Res. 1996. PMID: 8706004

7

A novel p53 germline alteration identified in a late onset breast cancer kindred.

Sun XF, Johannsson O, Håkansson S, Sellberg G, Nordenskjöld B, Olsson H, Borg A. Sun XF, et al. Among authors: johannsson o. Oncogene. 1996 Jul 18;13(2):407-11. Oncogene. 1996. PMID: 8710380

8

Allelic loss at chromosome 13q12-q13 is associated with poor prognosis in familial and sporadic breast cancer.

van den Berg J, Johannsson O, Håkansson S, Olsson H, Borg A. van den Berg J, et al. Among authors: johannsson o. Br J Cancer. 1996 Nov;74(10):1615-9. doi: 10.1038/bjc.1996.597. Br J Cancer. 1996. PMID: 8932343 Free PMC article.

9

Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations.

Tirkkonen M, Johannsson O, Agnarsson BA, Olsson H, Ingvarsson S, Karhu R, Tanner M, Isola J, Barkardottir RB, Borg A, Kallioniemi OP. Tirkkonen M, et al. Among authors: johannsson o. Cancer Res. 1997 Apr 1;57(7):1222-7. Cancer Res. 1997. PMID: 9102202

10

BRCA1 mutations and survival in women with ovarian cancer.

Johannsson O, Ranstam J, Borg A, Olsson H. Johannsson O, et al. N Engl J Med. 1997 Apr 24;336(17):1255-6; author reply 1256-7. N Engl J Med. 1997. PMID: 9121523 No abstract available.

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