Vitenskapelig artikkel

• Berger, Amund Holte; Oftedal, Bergithe Eikeland; Wolff, Anette Susanne Bøe et al. (2025). High-resolution transcriptional impact of AIRE: effects of pathogenic variants p.Arg257Ter, p.Cys311Tyr, and polygenic risk variant p.Arg471Cys. (ekstern lenke)
• Houge, Gunnar Douzgos; Bratland, Eirik; Aukrust, Ingvild et al. (2024). Comparison of the ABC and ACMG systems for variant classification. (ekstern lenke)
• Vogt, Elinor Margrethe; Bratland, Eirik; Berland, Siren et al. (2024). Improving diagnostic precision in primary ovarian insufficiency using comprehensive genetic and autoantibody testing. (ekstern lenke)
• Artaza, Haydee; Eriksson, Daniel; Lavrichenko, Ksenia et al. (2024). Rare copy number variation in autoimmune Addison’s disease. (ekstern lenke)
• Aslaksen, Sigrid; Aukrust, Ingvild; Molday, Laurie et al. (2024). Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies. (ekstern lenke)
• Hoem, Gry; Pastore, Arianna; Bratland, Eirik et al. (2024). Severe isolated exudative vitreoretinopathy caused by biallelic FZD4 variants. (ekstern lenke)
• Kentistou, Katherine A.; Kaisinger, Lena R.; Stankovic, Stasa et al. (2024). Understanding the genetic complexity of puberty timing across the allele frequency spectrum. (ekstern lenke)
• Tkemaladze, Tinatin; Bratland, Eirik; Bregvadze, Kakha et al. (2023). MSMO1 deficiency: a potentially partially treatable, ultrarare neurodevelopmental disorder with psoriasiform dermatitis, alopecia and polydactyly. (ekstern lenke)
• Oftedal, Bergithe Eikeland; Berger, Amund Holte; Bruserud, Øyvind et al. (2023). A partial form of AIRE deficiency underlies a mild form of autoimmune polyendocrine syndrome type 1. (ekstern lenke)
• Sjøgren, Thea; Bratland, Eirik; Røyrvik, Ellen Christine et al. (2022). Screening patients with autoimmune endocrine disorders for cytokine autoantibodies reveals monogenic immune deficiencies. (ekstern lenke)
• Cappuccio, Gerarda; Berti, Camilla Ceccatelli; Baruffini, Enrico et al. (2021). Bi-allelic KARS1 pathogenic variants affecting functions of cytosolic and mitochondrial isoforms are associated with a progressive and multisystem disease. (ekstern lenke)
• Wolff, Anette Susanne Bøe; Breivik, Lars Ertesvåg; Hufthammer, Karl Ove et al. (2021). The natural history of 21-hydroxylase autoantibodies in autoimmune Addison’s disease. (ekstern lenke)
• Sævik, Åse Bjorvatn; Wolff, Anette Susanne Bøe; Björnsdottir, Sigridur et al. (2021). Potential Transcriptional Biomarkers to Guide Glucocorticoid Replacement in Autoimmune Addison's Disease. (ekstern lenke)
• Eriksson, Daniel; Røyrvik, Ellen Christine; Aranda-Guillen, Maribel et al. (2021). GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility. (ekstern lenke)
• Corder, Megan L.; Berland, Siren; Førsvoll, Jostein Andersen et al. (2021). Truncating and zinc-finger variants in GLI2 are associated with hypopituitarism. (ekstern lenke)
• Hellesen, Alexander; Aslaksen, Sigrid; Breivik, Lars Ertesvåg et al. (2021). 21-Hydroxylase-Specific CD8+ T Cells in Autoimmune Addison’s Disease Are Restricted by HLA-A2 and HLA-C7 Molecules. (ekstern lenke)
• Taule-Sivertsen, Peter; Bruland, Ove; Håvik, Aril Løge et al. (2021). The SH3PXD2A-HTRA1 fusion transcript is extremely rare in Norwegian sporadic vestibular schwannoma patients. (ekstern lenke)
• Berger, Amund Holte; Bratland, Eirik; Sjøgren, Thea et al. (2021). Transcriptional changes in regulatory T cells from patients with autoimmune polyendocrine syndrome type 1 suggest functional impairment of lipid metabolism and gut homing. (ekstern lenke)
• Goldfarb, Yael; Givony, Tal; Kadouri, Noam et al. (2021). Mechanistic dissection of dominant AIRE mutations in mouse models reveals AIRE autoregulation. (ekstern lenke)
• Rahman, Mohummad Aminur; Brekke, Jorunn; Arnesen, Victoria Smith et al. (2020). Sequential bortezomib and temozolomide treatment promotes immunological responses in glioblastoma patients with positive clinical outcomes: A phase 1B study. (ekstern lenke)
• Aslaksen, Sigrid; Wolff, Anette Susanne Bøe; Vigeland, Magnus Dehli et al. (2019). Identification and characterization of rare Toll-like receptor 3 variants in patients with autoimmune Addison’s disease. (ekstern lenke)
• Aslaksen, Sigrid; Methlie, Paal; Vigeland, Magnus Dehli et al. (2019). Coexistence of congenital adrenal hyperplasia and autoimmune Addison's disease. (ekstern lenke)
• Hjøllo, Torunn; Bratland, Eirik; Steinsland, Hans et al. (2018). Longitudinal cohort study of serum antibody responses towards Giardia lamblia variant-specific surface proteins in a non-endemic area. (ekstern lenke)
• Hellesen, Alexander; Bratland, Eirik; Husebye, Eystein Sverre (2018). Autoimmune Addison's disease – An update on pathogenesis. (ekstern lenke)
• Hellesen, Alexander; Bratland, Eirik (2018). The potential role for infections in the pathogenesis of autoimmune Addison?s disease. (ekstern lenke)
• Bruserud, Øyvind; Bratland, Eirik; Hellesen, Alexander et al. (2017). Altered immune activation and IL-23 signaling in response to Candida albicans in autoimmune polyendocrine syndrome type 1. (ekstern lenke)
• Bahador, Marzieh; Navarro, Andrea Gras; Rahman, Mohummad Aminur et al. (2017). Increased infiltration and tolerised antigen-specific CD8+ TEM cells in tumor but not peripheral blood have no impact on survival of HCMV+ glioblastoma patients. (ekstern lenke)
• Edvardsen, Kine Susann Waade; Hellesen, Alexander; Husebye, Eystein Sverre et al. (2016). Analysis of cellular and humoral immune responses against cytomegalovirus in patients with autoimmune Addison's disease. (ekstern lenke)
• Hetemäki, Iivo; Jarva, Hanna; Kluger, Nicolas et al. (2016). Anticommensal responses are associated with regulatory T cell defect in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients. (ekstern lenke)
• Bruserud, Øyvind; Oftedal, Bergithe Eikeland; Landegren, Nils et al. (2016). A longitudinal follow-up of autoimmune polyendocrine syndrome type 1. (ekstern lenke)
• Astor, Marianne; Løvås, Kristian; Wolff, Anette Susanne Bøe et al. (2015). Hypomagnesemia and functional hypoparathyroidism due to novel mutations in the Mg-channel TRPM6. (ekstern lenke)
• Oftedal, Bergithe Eikeland; Hellesen, Alexander; Erichsen, Martina Moter et al. (2015). Dominant mutations in the autoimmune regulator AIRE are associated with common organ-specific autoimmune diseases. (ekstern lenke)
• Edvardsen, Kine Susann Waade; Bjånesøy, Trine Elholm; Hellesen, Alexander et al. (2015). Peripheral blood cells from patients with autoimmune Addison's disease poorly respond to interferons in vitro, despite elevated serum levels of interferon-inducible chemokines. (ekstern lenke)
• Fichna, Marta; Zurawek, Magdalena; Bratland, Eirik et al. (2015). Interleukin-2 and subunit alpha of its soluble receptor in autoimmune Addison's disease - An association study and expression analysis. (ekstern lenke)
• Brønstad, Ingeborg; Breivik, Lars Ertesvåg; Methlie, Paal et al. (2014). Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasia. (ekstern lenke)
• Brønstad, Ingeborg; Skinningsrud, Beate; Bratland, Eirik et al. (2014). CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles. (ekstern lenke)
• Breivik, Lars Ertesvåg; Oftedal, Bergithe Eikeland; Wolff, Anette Susanne Bøe et al. (2014). A novel cell-based assay for measuring neutralizing autoantibodies against type I interferons in patients with autoimmune polyendocrine syndrome type 1. (ekstern lenke)
• Bjånesøy, Trine Elholm; Kulle, Bettina; Bratland, Eirik et al. (2014). Altered DNA methylation profile in Norwegian patients with Autoimmune Addison's Disease. (ekstern lenke)
• Dawoodji, Amina; Chen, Ji-Li; Shepherd, Dawn et al. (2014). High frequency of cytolytic 21-hydroxylase-specific CD8+ T cells in autoimmune Addison's disease patients. (ekstern lenke)
• Hellesen, Richard Alexander; Edvardsen, Kine Susann Waade; Breivik, Lars Ertesvåg et al. (2014). The effect of types I and III interferons on adrenocortical cells and its possible implications for autoimmune Addison's disease. (ekstern lenke)
• Bratland, Eirik; Hellesen, Alexander; Husebye, Eystein Sverre (2013). Induction of CXCL10 chemokine in adrenocortical cells by stimulation through toll-like receptor 3. (ekstern lenke)
• Bratland, Eirik; Magitta, Ng'weina Francis; Wolff, Anette Susanne Bøe et al. (2013). 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 activity. (ekstern lenke)
• Bratland, Eirik; Husebye, Eystein Sverre (2011). Cellular immunity and immunopathology in autoimmune Addison’s disease. (ekstern lenke)
• Bratland, Eirik; Skinningsrud, B; Undlien, Dag Erik et al. (2009). T Cell Responses to Steroid Cytochrome P450 21-Hydroxylase in Patients with Autoimmune Primary Adrenal Insufficiency. (ekstern lenke)
• Bratland, Eirik; Bredholt, Geir; Mellgren, Gunnar et al. (2009). The purification and application of biologically active recombinant steroid cytochrome P450 21-hydroxylase: The major autoantigen in autoimmune Addison's disease. (ekstern lenke)
• Oftedal, Bergithe Eikeland; Wolff, Anette Susanne Bøe; Bratland, Eirik et al. (2008). Radioimmunoassay for autoantibodies against interferon omega; its use in the diagnosis of autoimmune polyendocrine syndrome type I. (ekstern lenke)
• Bratland, Eirik; Wolff, Anette Susanne Bøe; Haavik, Jan et al. (2007). Epitope mapping of human aromatic L-amino acid decarboxylase. (ekstern lenke)
• Husebye, Eystein S.Junior; Bratland, Eirik; Bredholt, Geir et al. (2006). The substrate-binding domain of 21-hydroxylase, the main autoantigen in autoimmune Addison's disease, is an immunodominant T cell epitope. (ekstern lenke)

Errata

• Kentistou, Katherine A.; Kaisinger, Lena R.; Stankovic, Stasa et al. (2024). Correction to: Understanding the genetic complexity of puberty timing across the allele frequency spectrum (Nature Genetics, (2024), 56, 7, (1397-1411), 10.1038/s41588-024-01798-4). (ekstern lenke)

Doktorgradsavhandling

• Hellesen, Alexander; Bratland, Eirik (2016). Immuno-endocrine interactions in autoimmune Addison's disease. (ekstern lenke)
• Edvardsen, Kine Susann Waade; Bratland, Eirik (2015). Autoimmunity and viral immunity in Addison’s disease. (ekstern lenke)
• Bratland, Eirik (2009). Cellular immunity in autoimmune Addison's disease : T cell responses to steroid cytochrome P450 21-hydroxylase. (ekstern lenke)

Poster

• Breivik, Lars Ertesvåg; Oftedal, Bergithe Eikeland; Bratland, Eirik et al. (2013). A novel cell-based assay for measuring neutralizing autoantibodies against type I interferons in patients with APS-1. (ekstern lenke)

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