Nevanlinna H - Search Results

1

Risk of cancer in BRCA1 and BRCA2 mutation-positive and -negative breast cancer families (Finland).

Eerola H, Pukkala E, Pyrhönen S, Blomqvist C, Sankila R, Nevanlinna H. Eerola H, et al. Among authors: nevanlinna h. Cancer Causes Control. 2001 Oct;12(8):739-46. doi: 10.1023/a:1011272919982. Cancer Causes Control. 2001. PMID: 11562114

2

Amplification of fgfr4 gene in human breast and gynecological cancers.

Jaakkola S, Salmikangas P, Nylund S, Partanen J, Armstrong E, Pyrhönen S, Lehtovirta P, Nevanlinna H. Jaakkola S, et al. Among authors: nevanlinna h. Int J Cancer. 1993 May 28;54(3):378-82. doi: 10.1002/ijc.2910540305. Int J Cancer. 1993. PMID: 8099571

3

Evidence for involvement of BRCA1 in sporadic breast carcinomas.

Cropp CS, Nevanlinna HA, Pyrhönen S, Stenman UH, Salmikangas P, Albertsen H, White R, Callahan R. Cropp CS, et al. Among authors: nevanlinna ha. Cancer Res. 1994 May 15;54(10):2548-51. Cancer Res. 1994. PMID: 8168077

4

A low proportion of BRCA2 mutations in Finnish breast cancer families.

Vehmanen P, Friedman LS, Eerola H, Sarantaus L, Pyrhönen S, Ponder BA, Muhonen T, Nevanlinna H. Vehmanen P, et al. Among authors: nevanlinna h. Am J Hum Genet. 1997 May;60(5):1050-8. Am J Hum Genet. 1997. PMID: 9150152 Free PMC article.

5

Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes.

Vehmanen P, Friedman LS, Eerola H, McClure M, Ward B, Sarantaus L, Kainu T, Syrjäkoski K, Pyrhönen S, Kallioniemi OP, Muhonen T, Luce M, Frank TS, Nevanlinna H. Vehmanen P, et al. Among authors: nevanlinna h. Hum Mol Genet. 1997 Dec;6(13):2309-15. doi: 10.1093/hmg/6.13.2309. Hum Mol Genet. 1997. PMID: 9361038

6

Breast cancer risk estimation in families with history of breast cancer.

Muhonen T, Eerola H, Vehmanen P, Nevanlinna H, Aktan K, Blomqvist C, Kääriäinen H, Pyrhönen S. Muhonen T, et al. Among authors: nevanlinna h. Br J Cancer. 1997;76(9):1228-31. doi: 10.1038/bjc.1997.538. Br J Cancer. 1997. PMID: 9365174 Free PMC article.

7

A missense mutation in the BRCA2 gene in three siblings with ovarian cancer.

Roth S, Kristo P, Auranen A, Shayehgi M, Seal S, Collins N, Barfoot R, Rahman N, Klemi PJ, Grénman S, Sarantaus L, Nevanlinna H, Butzow R, Ashworth A, Stratton MR, Aaltonen LA. Roth S, et al. Among authors: nevanlinna h. Br J Cancer. 1998 Apr;77(8):1199-202. doi: 10.1038/bjc.1998.202. Br J Cancer. 1998. PMID: 9579822 Free PMC article.

8

Genetic changes in inherited and sporadic ovarian carcinomas by comparative genomic hybridization: extensive similarity except for a difference at chromosome 2q24-q32.

Tapper J, Sarantaus L, Vahteristo P, Nevanlinna H, Hemmer S, Seppälä M, Knuutila S, Butzow R. Tapper J, et al. Among authors: nevanlinna h. Cancer Res. 1998 Jul 1;58(13):2715-9. Cancer Res. 1998. PMID: 9661879

9

Tenascin-C expression in invasion border of early breast cancer: a predictor of local and distant recurrence.

Jahkola T, Toivonen T, Virtanen I, von Smitten K, Nordling S, von Boguslawski K, Haglund C, Nevanlinna H, Blomqvist C. Jahkola T, et al. Among authors: nevanlinna h. Br J Cancer. 1998 Dec;78(11):1507-13. doi: 10.1038/bjc.1998.714. Br J Cancer. 1998. PMID: 9836485 Free PMC article.

10

Cancer risks in BRCA2 mutation carriers.

Breast Cancer Linkage Consortium. Breast Cancer Linkage Consortium. J Natl Cancer Inst. 1999 Aug 4;91(15):1310-6. doi: 10.1093/jnci/91.15.1310. J Natl Cancer Inst. 1999. PMID: 10433620

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