A. Rökman

发表

ELAC2/HPC2 involvement in hereditary and sporadic prostate cancer.

J. Schleutker, T. Tammela, O. Kallioniemi, 2001, Cancer research.

Combined genome-wide scan for prostate cancer susceptibility genes.

J. Carpten, E. Gillanders, J. Trent, 2004, Journal of the National Cancer Institute.

Germ-line alterations in MSR1 gene and prostate cancer risk.

J. Schleutker, T. Tammela, A. Rökman, 2003, Clinical cancer research : an official journal of the American Association for Cancer Research.

CHEK2 variants associate with hereditary prostate cancer

J. Schleutker, T. Tammela, A. Rökman, 2003, British Journal of Cancer.

In Search of High-Penetrant Hereditary Prostate Cancer Susceptibility Genes

A. Rökman, 2004 .

BRCA1 and BRCA2 mutations have no major role in predisposition to prostate cancer in Finland

J. Schleutker, T. Tammela, O. Kallioniemi, 2003, Journal of medical genetics.

Genetic changes in familial prostate cancer by comparative genomic hybridization

J. Schleutker, O. Kallioniemi, A. Rökman, 2001, The Prostate.

No fumarate hydratase (FH) mutations in hereditary prostate cancer

D. Schaid, L. Aaltonen, J. Schleutker, 2003, Journal of medical genetics.

Preservation of nucleic acids and tissue morphology in paraffin-embedded clinical samples: comparison of five molecular fixatives

Jorma Isola, J. Isola, A. Rökman, 2013, Journal of Clinical Pathology.

Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer.

J. Carpten, J. Trent, J. Schleutker, 2002, American journal of human genetics.

of ELAC2 in prostate cancer, suggest moderate familial risk, and estimate that risk genotypes in ELAC2 may cause 2% of prostate cancer in the general population.

N. Camp, J. Schleutker, A. Rökman, 2002 .

Androgen receptor CAG polymorphism and prostate cancer risk

J. Schleutker, T. Tammela, O. Kallioniemi, 2002, Human Genetics.

Chromosomal changes in locally recurrent, hormone-refractory prostate carcinomas by karyotyping and comparative genomic hybridization.

T. Tammela, A. Rökman, P. Koivisto, 2001, Cancer genetics and cytogenetics.

Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus

E. Gillanders, J. Trent, Kenneth D. Gibbs, 2004, Human Genetics.

Genetic changes in familial prostate cancer by comparative genomic hybridization

J. Schleutker, O. Kallioniemi, A. Rökman, 2001, The Prostate.

Combined genome-wide scan for prostate cancer susceptibility genes.

J. Carpten, E. Gillanders, J. Trent, 2004, Journal of the National Cancer Institute.