Winqvist R - Search Results

1

No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer families.

Karppinen SM, Vuosku J, Heikkinen K, Allinen M, Winqvist R. Karppinen SM, et al. Among authors: winqvist r. Eur J Cancer. 2003 Feb;39(3):366-71. doi: 10.1016/s0959-8049(02)00498-7. Eur J Cancer. 2003. PMID: 12565990

2

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: winqvist r. Cancer Genet Cytogenet. 1999 Jul 1;112(1):9-14. doi: 10.1016/s0165-4608(98)00258-1. Cancer Genet Cytogenet. 1999. PMID: 10432928

3

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: winqvist r. Eur J Cancer. 1999 May;35(5):707-10. doi: 10.1016/s0959-8049(99)00014-3. Eur J Cancer. 1999. PMID: 10505028

4

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: winqvist r. 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.

5

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: winqvist r. 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.

6

Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families.

Lahti-Domenici J, Rapakko K, Pääkkönen K, Allinen M, Nevanlinna H, Kujala M, Huusko P, Winqvist R. Lahti-Domenici J, et al. Among authors: winqvist r. Cancer Genet Cytogenet. 2001 Sep;129(2):120-3. doi: 10.1016/s0165-4608(01)00437-x. Cancer Genet Cytogenet. 2001. PMID: 11566341

7

ATM mutations in Finnish breast cancer patients.

Allinen M, Launonen V, Laake K, Jansen L, Huusko P, Kääriäinen H, Børresen-Dale AL, Winqvist R. Allinen M, et al. Among authors: winqvist r. J Med Genet. 2002 Mar;39(3):192-6. doi: 10.1136/jmg.39.3.192. J Med Genet. 2002. PMID: 11897822 Free PMC article. No abstract available.

8

Analysis of 11q21-24 loss of heterozygosity candidate target genes in breast cancer: indications of TSLC1 promoter hypermethylation.

Allinen M, Peri L, Kujala S, Lahti-Domenici J, Outila K, Karppinen SM, Launonen V, Winqvist R. Allinen M, et al. Among authors: winqvist r. Genes Chromosomes Cancer. 2002 Aug;34(4):384-9. doi: 10.1002/gcc.10079. Genes Chromosomes Cancer. 2002. PMID: 12112527

9

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: winqvist r. Eur J Hum Genet. 2004 Feb;12(2):98-104. doi: 10.1038/sj.ejhg.5201091. Eur J Hum Genet. 2004. PMID: 14560309

10

Mutation screening of Mre11 complex genes: indication of RAD50 involvement in breast and ovarian cancer susceptibility.

Heikkinen K, Karppinen SM, Soini Y, Mäkinen M, Winqvist R. Heikkinen K, et al. Among authors: winqvist r. J Med Genet. 2003 Dec;40(12):e131. doi: 10.1136/jmg.40.12.e131. J Med Genet. 2003. PMID: 14684699 Free PMC article. No abstract available.

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