Nevanlinna H - Search Results

1

ATM variants and cancer risk in breast cancer patients from Southern Finland.

Tommiska J, Jansen L, Kilpivaara O, Edvardsen H, Kristensen V, Tamminen A, Aittomäki K, Blomqvist C, Børresen-Dale AL, Nevanlinna H. Tommiska J, et al. Among authors: nevanlinna h. BMC Cancer. 2006 Aug 16;6:209. doi: 10.1186/1471-2407-6-209. BMC Cancer. 2006. PMID: 16914028 Free PMC article.

2

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.

3

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

4

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.

5

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.

6

Familial breast cancer in southern Finland: how prevalent are breast cancer families and can we trust the family history reported by patients?

Eerola H, Blomqvist C, Pukkala E, Pyrhönen S, Nevanlinna H. Eerola H, et al. Among authors: nevanlinna h. Eur J Cancer. 2000 Jun;36(9):1143-8. doi: 10.1016/s0959-8049(00)00093-9. Eur J Cancer. 2000. PMID: 10854948

7

Population-based study of BRCA1 and BRCA2 mutations in 1035 unselected Finnish breast cancer patients.

Syrjäkoski K, Vahteristo P, Eerola H, Tamminen A, Kivinummi K, Sarantaus L, Holli K, Blomqvist C, Kallioniemi OP, Kainu T, Nevanlinna H. Syrjäkoski K, et al. Among authors: nevanlinna h. J Natl Cancer Inst. 2000 Sep 20;92(18):1529-31. doi: 10.1093/jnci/92.18.1529. J Natl Cancer Inst. 2000. PMID: 10995809 No abstract available.

8

Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.

Sarantaus L, Huusko P, Eerola H, Launonen V, Vehmanen P, Rapakko K, Gillanders E, Syrjäkoski K, Kainu T, Vahteristo P, Krahe R, Pääkkönen K, Hartikainen J, Blomqvist C, Löppönen T, Holli K, Ryynänen M, Bützow R, Borg A, Wasteson Arver B, Holmberg E, Mannermaa A, Kere J, Kallioniemi OP, Winqvist R, Nevanlinna H. Sarantaus L, et al. Among authors: nevanlinna h. Eur J Hum Genet. 2000 Oct;8(10):757-63. doi: 10.1038/sj.ejhg.5200529. Eur J Hum Genet. 2000. PMID: 11039575

9

Germline TP53 alterations in Finnish breast cancer families are rare and occur at conserved mutation-prone sites.

Rapakko K, Allinen M, Syrjäkoski K, Vahteristo P, Huusko P, Vähäkangas K, Eerola H, Kainu T, Kallioniemi OP, Nevanlinna H, Winqvist R. Rapakko K, et al. Among authors: nevanlinna h. Br J Cancer. 2001 Jan 5;84(1):116-9. doi: 10.1054/bjoc.2000.1530. Br J Cancer. 2001. PMID: 11139324 Free PMC article.

10

Involvement of BRCA1 and BRCA2 in breast cancer in a western Finnish sub-population.

Pääkkönen K, Sauramo S, Sarantaus L, Vahteristo P, Hartikainen A, Vehmanen P, Ignatius J, Ollikainen V, Kääriäinen H, Vauramo E, Nevanlinna H, Krahe R, Holli K, Kere J. Pääkkönen K, et al. Among authors: nevanlinna h. Genet Epidemiol. 2001 Feb;20(2):239-46. doi: 10.1002/1098-2272(200102)20:2<239::AID-GEPI6>3.0.CO;2-Y. Genet Epidemiol. 2001. PMID: 11180449

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