Polymorphisms in Genes Involved in Androgen Pathways as Risk Factors for Prostate CancerMONONEN, Nina; SCHLEUTKER, Johanna.The Journal of urology. 2009, Vol 181, Num 4, pp 1541-1549, issn 0022-5347, 9 p.Article

CHEK2 mutations in primary glioblastomasSALLINEN, Satu-Leena; IKONEN, Tarja; HAAPASALO, Hannu et al.Journal of neuro-oncology. 2005, Vol 74, Num 1, pp 93-95, issn 0167-594X, 3 p.Article

Nationwide cancer family ascertainment using finnish cancer registry data on family names and places of birth for 35,761 prostate cancer patientsMATIKAINEN, Mika P; SANKILA, Risto; SCHLEUTKER, Johanna et al.International journal of cancer. 2000, Vol 88, Num 2, pp 307-312, issn 0020-7136Article

Fine mapping of 11q13.5 identifies regions associated with prostate cancer and prostate cancer deathNURMINEN, Riikka; LEHTONEN, Rainer; AUVINEN, Anssi et al.European journal of cancer (1990). 2013, Vol 49, Num 15, pp 3335-3343, issn 0959-8049, 9 p.Article

Incidence of Cancer in Finnish Families with Clinically Aggressive and Nonaggressive Prostate CancerPAKKANEN, Sanna; PUKKALA, Eero; KAINULAINEN, Heidi et al.Cancer epidemiology, biomarkers & prevention. 2009, Vol 18, Num 11, pp 3049-3056, issn 1055-9965, 8 p.Article

Profiling genetic variation along the androgen biosynthesis and metabolism pathways implicates several single nucleotide polymorphisms and their combinations as prostate cancer risk factorsMONONEN, Nina; SEPPÄLÄ, Eija H; KALLIONIEMI, Olli et al.Cancer research (Baltimore). 2006, Vol 66, Num 2, pp 743-747, issn 0008-5472, 5 p.Article

A major locus for hereditary prostate cancer in Finland : localization by linkage disequilibrium of a haplotype in the HPCX regionBAFFOE-BONNIE, Agnes B; SMITH, Jeffrey R; SOOD, Raman et al.Human genetics. 2005, Vol 117, Num 4, pp 307-316, issn 0340-6717, 10 p.Article

Genetic changes in familial prostate cancer by comparative genomic hybridizationRÖKMAN, Annika; KOIVISTO, Pasi A; MATIKAINEN, Mika P et al.The Prostate. 2001, Vol 46, Num 3, pp 233-239, issn 0270-4137Article

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association studyKOTE-JARAI, Zsofia; OLAMA, Ali Amin Al; HUNTER, David J et al.Nature genetics. 2011, Vol 43, Num 8, pp 785-791, issn 1061-4036, 7 p.Article

Germline mutation analysis of the androgen receptor gene in Finnish patients with prostate cancerKOIVISTO, Pasi A; HYYTINEN, Eija-R; MATIKAINEN, Mika et al.The Journal of urology. 2004, Vol 171, Num 1, pp 431-433, issn 0022-5347, 3 p.Article

Combined genome-wide scan for prostate cancer susceptibility genesGILLANDERS, Elizabeth M; JIANFENG XU; ALBERTUS, Julie et al.Journal of the National Cancer Institute. 2004, Vol 96, Num 16, pp 1240-1247, issn 0027-8874, 8 p.Article

Genome-wide scan for linkage in Finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26SCHLEUTKER, Johanna; BAFFOE-BONNIE, Agnes B; GIBBS, Kenneth D et al.The Prostate. 2003, Vol 57, Num 4, pp 280-289, issn 0270-4137, 10 p.Article

Androgen receptor CAG polymorphism and prostate cancer riskMONONEN, Nina; IKONEN, Tarja; AUTIO, Ville et al.Human genetics. 2002, Vol 111, Num 2, pp 166-171, issn 0340-6717Article

Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22CROPP, Cheryl D; SIMPSON, Claire L; BAILEY-WILSON, Joan et al.International journal of cancer (Print). 2011, Vol 129, Num 10, pp 2400-2407, issn 0020-7136, 8 p.Article

Genome-Wide Linkage Analysis of I,233 Prostate Cancer Pedigrees From the International Consortium for Prostate Cancer Genetics Using Novel sum LINK and sum LOD AnalysesBRYCE CHRISTENSEN, G; BAFFOE-BONNIE, Agnes B; FOULKES, William D et al.The Prostate. 2010, Vol 70, Num 7, pp 735-744, issn 0270-4137, 10 p.Article

Identification of seven new prostate cancer susceptibility loci through a genome-wide association studyEELES, Rosalind A; KOTE-JARAIL, Zsofia; SCHLEUTKER, Johanna et al.Nature genetics. 2009, Vol 41, Num 10, pp 1116-1121, issn 1061-4036, 6 p.Article

A recurrent mutation in PALB2 in Finnish cancer familiesERKKO, Hannele; BING XIA; MIRON, Alexander et al.Nature (London). 2007, Vol 446, Num 7133, pp 316-319, issn 0028-0836, 4 p.Article

Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritancePAKKANEN, Sanna; BAFFOE-BANNIE, Agnes B; MATIKAINEN, Mika P et al.Human genetics. 2007, Vol 121, Num 2, pp 257-267, issn 0340-6717, 11 p.Article

Role of the nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancerHEBBRING, Scott J; FREDRIKSSON, Henna; AUTIO, Ville et al.Cancer epidemiology, biomarkers & prevention. 2006, Vol 15, Num 5, pp 935-938, issn 1055-9965, 4 p.Article

Association of E-Cadherin germ-line alterations with prostate cancerIKONEN, Tarja; MATIKAINEN, Mika; KOIVISTO, Pasi A et al.Clinical cancer research. 2001, Vol 7, Num 11, pp 3465-3471, issn 1078-0432Article

Clinical and histopathological characteristics of familial prostate cancer in FinlandPAKKANEN, Sanna; KUJALA, Paula M; HA, Nati et al.BJU international (Papier). 2012, Vol 109, Num 4, pp 557-563, issn 1464-4096, 7 p.Article

Compelling evidence for a prostate cancer gene at 22q12.3 by the international Consortium for Prostate Cancer GeneticsCAMP, Nicola J; CANNON-ALBRIGHT, Lisa A; SEVERI, Gianluca et al.Human molecular genetics (Print). 2007, Vol 16, Num 11, pp 1271-1278, issn 0964-6906, 8 p.Article

Hemochromatosis gene mutations among Finnish male breast and prostate cancer patientsSYRJÄKOSKI, Kirsi; FREDRIKSSON, Henna; IKONEN, Tarja et al.International journal of cancer. 2006, Vol 118, Num 2, pp 518-520, issn 0020-7136, 3 p.Article

Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effectCHANG, Bao-Li; LANGE, Ethan M; LANGEFELD, Carl D et al.Human genetics. 2006, Vol 118, Num 6, pp 716-724, issn 0340-6717, 9 p.Article

Kruppel-like factor 6 germ-line mutations are infrequent in finnish hereditary prostate cancerKOIVISTO, Pasi A; HYYTINEN, Eija-R; MATIKAINEN, Mika et al.The Journal of urology. 2004, Vol 172, Num 2, pp 506-507, issn 0022-5347, 2 p.Article