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Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 22, 2007
Differential gene expression before and after ionizing radiation of subcutaneous fibroblasts identifies breast cancer patients resistant to radiation-induced fibrosisJan Alsner, Olaug K Rødningen, Jens Overgaard
European Journal of Medical Genetics|September 15, 2012
A de novo 163 kb interstitial 1q44 microdeletion in a boy with thin corpus callosum, psychomotor delay and seizuresKaja K Selmer, Einar Bryne, Olaug K Rødningen, et al.
European Journal of Medical Genetics|August 30, 2008
1.4Mb recurrent 22q11.2 distal deletion syndrome, two new cases expand the phenotypeOlaug K Rødningen, Trine Prescott, Ann-Sofie Eriksson, et al.
European Journal of Medical Genetics|November 4, 2010
Exon trapping analysis of c.301-19G > A in intron 1 of the SHH gene in a patient with a microform of holoprosencephalyMari Ann Kulseth, Robert Lyle, Olaug K Rødningen, et al.
Clinical Dysmorphology|December 6, 2008
Two brothers with a microduplication including the MECP2 gene: rapid head growth in infancy and resolution of susceptibility to infectionTrine E Prescott, Olaug K Rødningen, Alf Bjørnstad, et al.
Psychiatric Genetics|January 2, 2013
Copy number variation findings among 50 children and adolescents with autism spectrum disorderHanne S Sorte, Elen Gjevik, Eili Sponheim, et al.
American Journal of Medical Genetics. Part A|May 3, 2013
De novo 19p13.2 microdeletion encompassing the insulin receptor and resistin genes in a patient with obesity and learning disabilityTeresia Wangensteen, Lars Retterstøl, Olaug K Rødningen, et al.
European Journal of Medical Genetics|June 10, 2014
Haploinsufficiency of XPO1 and USP34 by a de novo 230 kb deletion in 2p15, in a patient with mild intellectual disability and cranio-facial dysmorphismsMadeleine Fannemel, Tuva Barøy, Asbjørn Holmgren, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|November 21, 2008
ABCB4 sequence variations in young adults with cholesterol gallstone diseaseKarl Esten Nakken, Knut Jørgen Labori, Olaug K Rødningen, et al.
Molecular Genetics & Genomic Medicine|November 30, 2016
A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunctionHanne S Sorte, Liv T Osnes, Børre Fevang, et al.
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