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.
- A genetic epidemiological study of hereditary prostate cancer (HPC) in Finland: Frequent HPCX linkage in families with late-onset disease (2000)
- Clinical Cancer Research
(A1 Refereed original research article in a scientific journal) - Combined analysis of hereditary prostate cancer linkage to 1q24-25: results from 772 hereditary prostate cancer families from the International Consortium for Prostate Cancer Genetics (2000)
- American Journal of Human Genetics
(A1 Refereed original research article in a scientific journal) - Nationwide cancer family ascertainment using Finnish Cancer Registry data on family names and places of birth for 35,761 prostate cancer patients (2000)
- International Journal of Cancer
(A1 Refereed original research article in a scientific journal) - Nationwide cancer family ascertainment using Finnish Cancer Registry data on family names and places of birth for 35,761 prostate cancer patients (2000)
- International Journal of Cancer
(A1 Refereed original research article in a scientific journal) - Two percent of Finnish prostate cancer patients have a germ-line mutation in the hormone-binding domain of the androgen receptor gene (2000)
- Cancer Research
(A1 Refereed original research article in a scientific journal) - Androgen receptor gene alterations and chromosomal gains and losses in prostate carcinomas appearing during finasteride treatment for benign prostatic hyperplasia (1999)
- Clinical Cancer Research
(A1 Refereed original research article in a scientific journal) - Androgen receptor gene mutations in hormone-refractory prostate cancer (1999)
- Journal of Pathology
(A1 Refereed original research article in a scientific journal) - Evidence for a prostate cancer susceptibility locus on the X chromosome (1998)
- Nature Genetics
(A1 Refereed original research article in a scientific journal) - Molecular genetics of human prostate cancer (1997)
- Current Opinion in Urology
(A1 Refereed original research article in a scientific journal) - A physical map of the 6q14-q15 region harboring the locus for the lysosomal membrane sialic acid transport defect (1996)
- Genomics
(A1 Refereed original research article in a scientific journal) - Haplotype analysis in prenatal diagnosis and carrier identification of Salla disease (1996)
- Journal of Medical Genetics
(A1 Refereed original research article in a scientific journal) - LINKAGE DISEQUILIBRIUM UTILIZED TO ESTABLISH A REFINED GENETIC POSITION OF THE SALLA DISEASE LOCUS ON 6Q14-Q15 (1995)
- Genomics
(A1 Refereed original research article in a scientific journal) - THE GENETIC-LOCUS FOR FREE SIALIC-ACID STORAGE DISEASE MAPS TO THE LONG ARM OF CHROMOSOME-6 (1994)
- American Journal of Human Genetics
(A1 Refereed original research article in a scientific journal)