The research group of Vessela N. Kristensen
Cancer Genome Variation
![]() | ”If it were not for the great variability among individuals medicine might as well be science and not an art” Sir William Osler, 1892 |
The tumor initiation, progression and clinical presentation are directly dependent on its genetic and biochemical environment – the entire body. Our group is working on different projects related to how genetic variation affects occurrence of somatic alterations, gene expression patterns and genome wide copy number alterations in human breast and ovarian tumors. Understanding inherited genetic variability and how it affects crucial biological pathways is likely to lead to new successful prevention and treatment strategies.
The research in the group is focusing on constitutive variation such as single nucleotide polymorphisms (SNPs) and copy number variations (CNVs) in relation to:
- Susceptibility
- Clinical presentation
- Treatment response and adverse side effects of treatment
- Gene regulation and proximal phenotypes (RNA expression and metabolic profiles)
The group:
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From left to right: Jo Anders Rønneberg, Hege Edvardsen, Espen Enerly, Miriam Ragle Aure, Peter van Loo (guest scientist), Phuong Vu (adjunct engineer), Grethe I. Grenaker Alnæs, Fatemeh Kaveh, Margarethe Biong and Silje Nordgard.
Grethe I. Grenaker Alnæs
Jo Anders Rønneberg
Hege Edvardsen
Silje Nordgard
Margarethe Biong
Espen Enerly
Miriam Ragle Aure
Fatemeh Kaveh
Christine Haugen
Group contact information:
Professor Vessela N. Kristensen, Email: Vessela.N.Kristensen@rr-research.no
Department of Genetics, Institute for Cancer Research,
Oslo University Hospital Radiumhospitalet, N-0310 Oslo, Norway
Phone: +47 22 78 13 75, Fax: +47 22 78 13 95, Switchboard: +47 22 93 40 00
Department of Genetics, Institute for Cancer Research,
Oslo University Hospital Radiumhospitalet, N-0310 Oslo, Norway
Phone: +47 22 78 13 75, Fax: +47 22 78 13 95, Switchboard: +47 22 93 40 00
News & events
More news
Latest publications
Vessela N. Kristensen
SNPs in genes coding for ROS metabolism and signalling in association with docetaxel clearance
Pharmacogenomics J (in press)
PubMed 20157331
Glycan gene expression signatures in normal and malignant breast tissue; possible role in diagnosis and progression
Mol Oncol (in press)
PubMed 20060370
Frequent aberrant DNA methylation of ABCB1, FOXC1, PPP2R2B and PTEN in ductal carcinoma in situ and early invasive breast cancer
Breast Cancer Res, 12 (1), R3 (in press)
PubMed 20056007





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