Cecilie Heramb
Oslo, Norway
Last Updated: 09/26/2026
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Found 8 publications
A woman in her 20s with delusions, hallucinations and dystonic eye movements.
Journal: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke
Published: October 26, 2022
"It was an important part of my treatment": a qualitative study of Norwegian breast Cancer patients' experiences with mainstreamed genetic testing.
Journal: Hereditary cancer in clinical practice
Published: August 18, 2021
Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway.
Journal: Familial cancer
Published: February 01, 2020
BRCA mutation carrier detection. A model-based cost-effectiveness analysis comparing the traditional family history approach and the testing of all patients with breast cancer.
Journal: ESMO open
Published: January 19, 2018
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.
Journal: Hereditary cancer in clinical practice
Published: September 20, 2017
Ten modifiers of BRCA1 penetrance validated in a Norwegian series.
Journal: Hereditary cancer in clinical practice
Published: January 23, 2015
The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry.
Journal: Hereditary cancer in clinical practice
Published: January 30, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026