Nevanlinna H - Search Results

1

Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.

Rafiq S, Tapper W, Collins A, Khan S, Politopoulos I, Gerty S, Blomqvist C, Couch FJ, Nevanlinna H, Liu J, Eccles D. Rafiq S, et al. Among authors: nevanlinna h. Cancer Res. 2013 Mar 15;73(6):1883-91. doi: 10.1158/0008-5472.CAN-12-3377. Epub 2013 Jan 14. Cancer Res. 2013. PMID: 23319801 Free PMC article.

2

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.

3

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.

4

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

5

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.

6

A probability model for predicting BRCA1 and BRCA2 mutations in breast and breast-ovarian cancer families.

Vahteristo P, Eerola H, Tamminen A, Blomqvist C, Nevanlinna H. Vahteristo P, et al. Among authors: nevanlinna h. Br J Cancer. 2001 Mar 2;84(5):704-8. doi: 10.1054/bjoc.2000.1626. Br J Cancer. 2001. PMID: 11237395 Free PMC article.

7

Survival of breast cancer patients in BRCA1, BRCA2, and non-BRCA1/2 breast cancer families: a relative survival analysis from Finland.

Eerola H, Vahteristo P, Sarantaus L, Kyyrönen P, Pyrhönen S, Blomqvist C, Pukkala E, Nevanlinna H, Sankila R. Eerola H, et al. Among authors: nevanlinna h. Int J Cancer. 2001 Aug 1;93(3):368-72. doi: 10.1002/ijc.1341. Int J Cancer. 2001. PMID: 11433401

8

p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predisposition.

Vahteristo P, Tamminen A, Karvinen P, Eerola H, Eklund C, Aaltonen LA, Blomqvist C, Aittomäki K, Nevanlinna H. Vahteristo P, et al. Among authors: nevanlinna h. Cancer Res. 2001 Aug 1;61(15):5718-22. Cancer Res. 2001. PMID: 11479205

9

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

10

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.

Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, Loman N, Olsson H, Johannsson O, Borg A, Pasini B, Radice P, Manoukian S, Eccles DM, Tang N, Olah E, Anton-Culver H, Warner E, Lubinski J, Gronwald J, Gorski B, Tulinius H, Thorlacius S, Eerola H, Nevanlinna H, Syrjäkoski K, Kallioniemi OP, Thompson D, Evans C, Peto J, Lalloo F, Evans DG, Easton DF. Antoniou A, et al. Among authors: nevanlinna h. Am J Hum Genet. 2003 May;72(5):1117-30. doi: 10.1086/375033. Epub 2003 Apr 3. Am J Hum Genet. 2003. PMID: 12677558 Free PMC article.

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