Launonen V - Search Results

1

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: launonen v. Eur J Hum Genet. 2000 Oct;8(10):757-63. doi: 10.1038/sj.ejhg.5200529. Eur J Hum Genet. 2000. PMID: 11039575

2

No germline FH mutations in familial breast cancer patients.

Kiuru M, Lehtonen R, Eerola H, Aittomäki K, Blomqvist C, Nevanlinna H, Aaltonen LA, Launonen V. Kiuru M, et al. Among authors: launonen v. Eur J Hum Genet. 2005 Apr;13(4):506-9. doi: 10.1038/sj.ejhg.5201326. Eur J Hum Genet. 2005. PMID: 15523491

3

Germ-line TP53 mutations in Finnish cancer families exhibiting features of the Li-Fraumeni syndrome and negative for BRCA1 and BRCA2.

Huusko P, Castrén K, Launonen V, Soini Y, Pääkkönen K, Leisti J, Vähäkangas K, Winqvist R. Huusko P, et al. Among authors: launonen v. Cancer Genet Cytogenet. 1999 Jul 1;112(1):9-14. doi: 10.1016/s0165-4608(98)00258-1. Cancer Genet Cytogenet. 1999. PMID: 10432928

4

Evidence of founder mutations in Finnish BRCA1 and BRCA2 families.

Huusko P, Pääkkönen K, Launonen V, Pöyhönen M, Blanco G, Kauppila A, Puistola U, Kiviniemi H, Kujala M, Leisti J, Winqvist R. Huusko P, et al. Among authors: launonen v. Am J Hum Genet. 1998 Jun;62(6):1544-8. doi: 10.1086/301880. Am J Hum Genet. 1998. PMID: 9585608 Free PMC article. No abstract available.

5

Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414del4 found in male breast cancer.

Balci A, Huusko P, Pääkkönen K, Launonen V, Uner A, Ekmekçi A, Winqvist R. Balci A, et al. Among authors: launonen v. Eur J Cancer. 1999 May;35(5):707-10. doi: 10.1016/s0959-8049(99)00014-3. Eur J Cancer. 1999. PMID: 10505028

6

Mutation analysis of the CHK2 gene in families with hereditary breast cancer.

Allinen M, Huusko P, Mäntyniemi S, Launonen V, Winqvist R. Allinen M, et al. Among authors: launonen v. Br J Cancer. 2001 Jul 20;85(2):209-12. doi: 10.1054/bjoc.2001.1858. Br J Cancer. 2001. PMID: 11461078 Free PMC article.

7

Germline fumarate hydratase mutations in patients with ovarian mucinous cystadenoma.

Ylisaukko-oja SK, Cybulski C, Lehtonen R, Kiuru M, Matyjasik J, Szymañska A, Szymañska-Pasternak J, Dyrskjot L, Butzow R, Orntoft TF, Launonen V, Lubiñski J, Aaltonen LA. Ylisaukko-oja SK, et al. Among authors: launonen v. Eur J Hum Genet. 2006 Jul;14(7):880-3. doi: 10.1038/sj.ejhg.5201630. Epub 2006 Apr 26. Eur J Hum Genet. 2006. PMID: 16639410

8

Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer: correlation to clinicopathological variables.

Launonen V, Mannermaa A, Stenbäck F, Kosma VM, Puistola U, Huusko P, Anttila M, Bloigu R, Saarikoski S, Kauppila A, Winqvist R. Launonen V, et al. Cancer Genet Cytogenet. 2000 Oct 1;122(1):49-54. doi: 10.1016/s0165-4608(00)00279-x. Cancer Genet Cytogenet. 2000. PMID: 11104033

9

Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers.

Georgitsi M, Karhu A, Winqvist R, Visakorpi T, Waltering K, Vahteristo P, Launonen V, Aaltonen LA. Georgitsi M, et al. Among authors: launonen v. Br J Cancer. 2007 Jan 29;96(2):352-6. doi: 10.1038/sj.bjc.6603573. Br J Cancer. 2007. PMID: 17242703 Free PMC article.

10

Chromosome 11q22.3-q25 LOH in ovarian cancer: association with a more aggressive disease course and involved subregions.

Launonen V, Stenbäck F, Puistola U, Bloigu R, Huusko P, Kytölä S, Kauppila A, Winqvist R. Launonen V, et al. Gynecol Oncol. 1998 Nov;71(2):299-304. doi: 10.1006/gyno.1998.5186. Gynecol Oncol. 1998. PMID: 9826475

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