Olaug K. Rødningen

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

Asbjørg Stray‐Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon et al. · Journal of Allergy and Clinical Immunology · 2016 · 269 citations · Full text

Primary Immunodeficiency, Mendelian Disorder, Autoimmune Disease +9

PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia

Asbjørg Stray‐Pedersen, Paul Hoff Backe, Hanne Sørmo Sorte et al. · The American Journal of Human Genetics · 2014 · 176 citations · Full text

Mendelian Disorder, Autoimmune Disease, Pgm3 Mutations Cause +13

Microarray analysis of the transcriptional responseto single or multiple doses of ionizing radiation in human subcutaneous fibroblasts

Olaug K. Rødningen, Jens Overgaard, Jan Alsner et al. · Radiotherapy and Oncology · 2005 · 91 citations

Radiation Oncology, Radiobiology, Radiation Therapy +13

15q11.2 microdeletion – Seven new patients with delayed development and/or behavioural problems

Charlotte von der Lippe, Cecilie F. Rustad, Ketil Heimdal et al. · European Journal of Medical Genetics · 2010 · 86 citations

Psychiatry, Pediatrics, Abnormal Development +2

Radiation-induced gene expression in human subcutaneous fibroblasts is predictive of radiation-induced fibrosis

Olaug K. Rødningen, Anne‐Lise Børresen‐Dale, Jan Alsner et al. · Radiotherapy and Oncology · 2007 · 85 citations

Fibrosis, Radiation Medicine, Radiation-induced Fibrosis +10