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Page 1
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes.
Rozenblum E, Vahteristo P, Sandberg T, Bergthorsson JT, Syrjakoski K, Weaver D, Haraldsson K, Johannsdottir HK, Vehmanen P, Nigam S, Golberger N, Robbins C, Pak E, Dutra A, Gillander E, Stephan DA, Bailey-Wilson J, Juo SH, Kainu T, Arason A, Barkardottir RB, Nevanlinna H, Borg A, Kallioniemi OP. Rozenblum E, et al. Among authors: kainu t. Hum Genet. 2002 Feb;110(2):111-21. doi: 10.1007/s00439-001-0646-6. Epub 2001 Dec 14. Hum Genet. 2002. PMID: 11935316
Genome-wide scanning for linkage in Finnish breast cancer families.
Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, Leisti J, Blanco G, Puistola U, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi OP. Huusko P, et al. Among authors: kainu t. Eur J Hum Genet. 2004 Feb;12(2):98-104. doi: 10.1038/sj.ejhg.5201091. Eur J Hum Genet. 2004. PMID: 14560309
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. 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.
BRCA2 mutations in 154 finnish male breast cancer patients.
Syrjäkoski K, Kuukasjärvi T, Waltering K, Haraldsson K, Auvinen A, Borg A, Kainu T, Kallioniemi OP, Koivisto PA. Syrjäkoski K, et al. Among authors: kainu t. Neoplasia. 2004 Sep-Oct;6(5):541-5. doi: 10.1593/neo.04193. Neoplasia. 2004. PMID: 15548363 Free PMC article.
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region.
Baffoe-Bonnie AB, Smith JR, Stephan DA, Schleutker J, Carpten JD, Kainu T, Gillanders EM, Matikainen M, Teslovich TM, Tammela T, Sood R, Balshem AM, Scarborough SD, Xu J, Isaacs WB, Trent JM, Kallioniemi OP, Bailey-Wilson JE. Baffoe-Bonnie AB, et al. Among authors: kainu t. Hum Genet. 2005 Aug;117(4):307-16. doi: 10.1007/s00439-005-1306-z. Epub 2005 May 20. Hum Genet. 2005. PMID: 15906096
Somatic genetic alterations in BRCA2-associated and sporadic male breast cancer.
Tirkkonen M, Kainu T, Loman N, Jóhannsson OT, Olsson H, Barkardóttir RB, Kallioniemi OP, Borg A. Tirkkonen M, et al. Among authors: kainu t. Genes Chromosomes Cancer. 1999 Jan;24(1):56-61. doi: 10.1002/(sici)1098-2264(199901)24:1<56::aid-gcc8>3.0.co;2-x. Genes Chromosomes Cancer. 1999. PMID: 9892109
Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families.
Barkardottir RB, Sarantaus L, Arason A, Vehmanen P, Bendahl PO, Kainu T, Syrjäkoski K, Krahe R, Huusko P, Pyrhönen S, Holli K, Kallioniemi OP, Egilsson V, Kere J, Nevanlinna H. Barkardottir RB, et al. Among authors: kainu t. Eur J Hum Genet. 2001 Oct;9(10):773-9. doi: 10.1038/sj.ejhg.5200717. Eur J Hum Genet. 2001. PMID: 11781689
Androgen receptor gene alterations in Finnish male breast cancer.
Syrjäkoski K, Hyytinen ER, Kuukasjärvi T, Auvinen A, Kallioniemi OP, Kainu T, Koivisto PA. Syrjäkoski K, et al. Among authors: kainu t. Breast Cancer Res Treat. 2003 Jan;77(2):167-70. doi: 10.1023/a:1021369508561. Breast Cancer Res Treat. 2003. PMID: 12602915
27 results