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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: vehmanen p. Eur J Hum Genet. 2004 Feb;12(2):98-104. doi: 10.1038/sj.ejhg.5201091. Eur J Hum Genet. 2004. PMID: 14560309
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: vehmanen p. Br J Cancer. 1997;76(9):1228-31. doi: 10.1038/bjc.1997.538. Br J Cancer. 1997. PMID: 9365174 Free PMC article.
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: vehmanen p. Eur J Hum Genet. 2000 Oct;8(10):757-63. doi: 10.1038/sj.ejhg.5200529. Eur J Hum Genet. 2000. PMID: 11039575
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: vehmanen p. 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
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: vehmanen p. Eur J Hum Genet. 2001 Oct;9(10):773-9. doi: 10.1038/sj.ejhg.5200717. Eur J Hum Genet. 2001. PMID: 11781689
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. Among authors: vehmanen p. 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.
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: vehmanen p. Hum Genet. 2002 Feb;110(2):111-21. doi: 10.1007/s00439-001-0646-6. Epub 2001 Dec 14. Hum Genet. 2002. PMID: 11935316
12 results