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Acta Neurochirurgica|November 24, 2021
Genetic alterations associated with malignant transformation of sporadic vestibular schwannomaAril Løge Håvik, Ove Bruland, Hrvoje Miletic, et al.
Investigative Ophthalmology & Visual Science|June 2, 2015
Development of congenital stromal corneal dystrophy is dependent on export and extracellular deposition of truncated decorinAnne Elisabeth Christensen Mellgren, Ove Bruland, Anni Vedeler, et al.
Investigative Ophthalmology & Visual Science|July 8, 2026
Loss of ATRAID in Late-Onset, Non-Syndromic Retinitis PigmentosaRoya Mehrasa, Ragnhild Wivestad Jansson, Hanah Kurosawa, et al.
Frontiers in Immunology|May 7, 2025
High-resolution transcriptional impact of AIRE: effects of pathogenic variants p.Arg257Ter, p.Cys311Tyr, and polygenic risk variant p.Arg471CysAmund Holte Berger, Bergithe Eikeland Oftedal, Anette Susanne Bøe Wolff, et al.
The Journal of General Virology|June 20, 2001
Cloning and identification of the infectious salmon anaemia virus haemagglutininBjørn Krossøy, Magnus Devold, Lisette Sanders, et al.
European Journal of Pediatrics|August 4, 2004
Chronic mucocutaneous candidiasis and primary hypothyroidism in two familiesAnne Grethe Myhre, Asbjørg Stray-Pedersen, Steinar Spangen, et al.
Orphanet Journal of Rare Diseases|January 5, 2013
MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencingKristoffer Haugarvoll, Stefan Johansson, Charalampos Tzoulis, et al.
Immunobiology|November 28, 2012
Autoantibodies against aromatic amino acid hydroxylases in patients with autoimmune polyendocrine syndrome type 1 target multiple antigenic determinants and reveal regulatory regions crucial for enzymatic activityEirik Bratland, Ng'weina Francis Magitta, Anette Susanne Bøe Wolff, et al.
Orphanet Journal of Rare Diseases|September 5, 2015
Friedreich ataxia in Norway - an epidemiological, molecular and clinical studyIselin Marie Wedding, Mette Kroken, Sandra Pilar Henriksen, et al.
FEBS Open Bio|March 29, 2025
On subcellular distribution of the zinc finger 469 protein (ZNF469) and observed discrepancy in the localization of endogenous and overexpressed ZNF469Anne Elisabeth Christensen Mellgren, Ileana Cristea, Thomas Stevenson, et al.
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