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.
- ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer (2008)
- European Journal of Human Genetics
(A1 Refereed original research article in a scientific journal) - Multiple novel prostate cancer predisposition loci confirmed by an international study: The PRACTICAL consortium (2008)
- Cancer Epidemiology, Biomarkers and Prevention
(A1 Refereed original research article in a scientific journal) - The interaction of CYP3A5 polymorphisms along the androgen metabolism pathway in prostate cancer (2008)
- International Journal of Cancer
(A1 Refereed original research article in a scientific journal) - A recurrent mutation in PALB2 in Finnish cancer families (2007)
- Nature
(A1 Refereed original research article in a scientific journal) - Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics (2007)
- Human Molecular Genetics
(A1 Refereed original research article in a scientific journal) - KLF6 IVS1 -27G > A variant and the risk of prostate cancer in Finland (2007)
- European Urology
(A1 Refereed original research article in a scientific journal) - Lactase persistence, dietary intake of milk, and the risk for prostate cancer in Sweden and Finland (2007)
- Cancer Epidemiology, Biomarkers and Prevention
(A1 Refereed original research article in a scientific journal) - Mutational analysis of SPANXGenes in families with X-linked prostate cancer (2007)
- Prostate
(A1 Refereed original research article in a scientific journal) - Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance (2007)
- Human Genetics
(A1 Refereed original research article in a scientific journal) - EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis (2006)
- BMC Cancer
(A1 Refereed original research article in a scientific journal) - Identification of germline MLH1 alterations in familial prostate cancer (2006)
- European Journal of Cancer
(A1 Refereed original research article in a scientific journal) - Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies (2006)
- Journal of Medical Genetics
(A1 Refereed original research article in a scientific journal) - Profiling genetic variation along the androgen biosynthesis and metabolism pathways implicates several single nucleotide polymorphisms and their combinations as prostate cancer risk factors (2006)
- Cancer Research
(A1 Refereed original research article in a scientific journal) - Role of the Nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancer (2006)
- Cancer Epidemiology, Biomarkers and Prevention
(A1 Refereed original research article in a scientific journal) - Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect (2006)
- Human Genetics
(A1 Refereed original research article in a scientific journal) - A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics (2005)
- American Journal of Human Genetics
(A1 Refereed original research article in a scientific journal) - A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region (2005)
- Human Genetics
(A1 Refereed original research article in a scientific journal) - CHEK2 mutations in primary glioblastomas (2005) Sallinen SL, Ikonen T, Haapasalo H, Schleutker J
(Other publication) - Dynamic structure of the SPANX gene cluster mapped to the prostate cancer susceptibility locus HPCX at Xq27 (2005)
- Genome Research
(A1 Refereed original research article in a scientific journal) - Dynamic structure of the SPANX gene cluster mapped to the prostate cancer susceptibility locus HPCX at Xq27 (2005)
- Genome Research
(A1 Refereed original research article in a scientific journal)