Johanna Schleutker
PhD, Professor of Medical Genetics
Cancer, Infections and Immunity johanna.schleutker@utu.fi +358 29 450 2726 +358 50 443 7237 Kiinamyllynkatu 10 Turku ORCID identifier: https://orcid.org/0000-0002-1863-0305 |
Cancer genetics; hereditary cancer; genomics; human genetics
Johanna Schleutker got her PhD in 1995 in University of Turku, Faculty of Medicine.The topic of her doctoral thesis was "Linkage disequilibrium is Salla disease; positioning of the sialic acid transport defect". She then moved to University of Tampere, and did her post doc in 1996-1998 in the Cancer Genetics research group of Professor Olli Kallioniemi. Her career continued in the US where she spent the years of 1999-2000 working as a research associate at the National Human Genome Research Institute, National Institutes of Health, Bethesda, MD. During the NIH years, she studied genetics of familial prostate cancer in the group of Dr. Jeffrey M.Trent. After her return to Finland, Schleutker started her own research group in 2001 at the Insitute of Medical Technology, University of Tampere, and has ever since focused her studies on genetics and genetic susceptibility of prostate and breast cancer. Schleutker got a professorship in University of Tampere in 2008. In 2011 she started as a professor of medical genetics in University of Turku.
The Schleutker group "Genetic Predisposition to Cancer" is studying both breast and prostate cancer genetics, the main emphasis being on prostate cancer. Of all cancers, prostate cancer (PrCa) has been reported as one of the most heritable diseases: genetic factors have been estimated to account for 57% of the risk. The goal is to identify and characterize predisposing genes and variants, especially those affecting aggressive outcome, including treatment responses to therapies. Further, the aim is to develop tools for prognostic purposes, i.e. prognostic biomarkers. The group has identified many significant genomic risk regions, candidate genes and variants, which have been then further profiled and characterized by functional studies. The group has produced (by 2021) 12 PhD degrees and published over 190 original, peer-reviewed articles in international journals.
Genetics, cancer genetics, hereditary cancer, genomics, molecular biology.
- Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPXG) families (2012)
- BMC Medical Genetics
(A1 Refereed original research article in a scientific journal) - Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG (2012)
- Prostate
(A1 Refereed original research article in a scientific journal) - Clinical and histopathological characteristics of familial prostate cancer in Finland (2012)
- BJU International
(A1 Refereed original research article in a scientific journal) - Exclusion of the 750-kb genetically unstable region at Xq27 as a candidate locus for protate malignancy in HPCX1-linked families (2012)
- Genes, Chromosomes and Cancer
(A1 Refereed original research article in a scientific journal) - Polymorphisms in androgen signaling pathway predisposing to prostate cancer (2012)
- Molecular and Cellular Endocrinology
(A2 Refereed review article in a scientific journal ) - Screening of Finnish RAD51C founder mutations in prostate and colorectal cancer patients (2012)
- BMC Cancer
(A1 Refereed original research article in a scientific journal) - Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the Interntional Consortium for Prostate Cancer Genetics (ICPCG) (2012)
- Human Genetics
(A1 Refereed original research article in a scientific journal) - Contribution of ARLTS1 Cys 148Arg (T442C) Variant with Prostate Cancer Risk and ARLTS1 Function in Prostate Cancer Cells (2011)
- PLoS ONE
(A1 Refereed original research article in a scientific journal) - Contribution of ARLTS1 Cys148Arg (T442C) Variant with Prostate Cancer Risk and ARLTS1 Function in Prostate Cancer Cells (2011) Siltanen S, Wahlfors T, Schindler M, Saramaki OR, Mpindi JP, Latonen L, Vessella RL, Tammela TLJ, Kallioniemi O, Visakorpi T, Schleutker J
(A1 Refereed original research article in a scientific journal) - Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22 (2011)
- International Journal of Cancer
(A1 Refereed original research article in a scientific journal) - Identification of an aggressive prostate cancer predisposing variant at 11q13 (2011)
- International Journal of Cancer
(A1 Refereed original research article in a scientific journal) - RAD51C is a susceptibility gene for ovarian cancer (2011)
- Human Molecular Genetics
(A1 Refereed original research article in a scientific journal) - Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals (2011)
- Breast Cancer Research
(A1 Refereed original research article in a scientific journal) - Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study (2011)
- Nature Genetics
(A1 Refereed original research article in a scientific journal) - Genome-Wide Linkage Analysis of 1,233 Prostate Cancer Pedigrees From the International Consortium for Prostate Cancer Genetics Using Novel sum LINK and sum LOD Analyses (2010)
- Prostate
(A1 Refereed original research article in a scientific journal) - C-reactive protein haplotype is associated with high PSA as a marker of metastatic prostate cancer but not with overall cancer risk (2009)
- British Journal of Cancer
(A1 Refereed original research article in a scientific journal) - Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility (2009)
- Nature Genetics
(A1 Refereed original research article in a scientific journal) - Incidence of cancer in finnish families with clinically aggressive and nonaggressive prostate cancer (2009)
- Cancer Epidemiology, Biomarkers and Prevention
(A1 Refereed original research article in a scientific journal) - PALB2 variants in hereditary and unselected Finnish Prostate cancer cases (2009)
- Journal of Negative Results in BioMedicine
(A1 Refereed original research article in a scientific journal) - Polymorphisms in Genes Involved in Androgen Pathways as Risk Factors for Prostate Cancer (2009)
- Journal of Urology
(A2 Refereed review article in a scientific journal )