Ove Bruland

Haukeland University Hospital — Norway

Medicine · Health Sciences

26h-index2.3kcitations74works1.82yr avg
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Research Topics

Fibromyalgia and Chronic Fatigue Syndrome Research(7), S100 Proteins and Annexins(6), Genetic Neurodegenerative Diseases(5), Neurofibromatosis and Schwannoma Cases(5), Meningioma and schwannoma management(5)

Publications74 total

Recurrent platelet-derived growth factor receptor beta gene mutations in Kosaki overgrowth syndrome: a molecular and clinical overview
Clinical Dysmorphology·2025
Variable response of germline activating PDGFRB variants to receptor tyrosine kinase inhibitors: implications for treatment
European Journal of Human Genetics·2025· 1 cited
Plasma cell targeting with the anti-CD38 antibody daratumumab in myalgic encephalomyelitis/chronic fatigue syndrome—a clinical pilot study
Frontiers in Medicine·2025· 1 citedOpen Access
Temperature as a Key Modulator: Investigating Phosphorylation Patterns of p.Asn666 <i>PDGFRB</i> Variants and Their Role in Downstream Signaling
Human Mutation·2025Open Access
Elevated cholesterol in <i>ATAD3</i> mutants is a compensatory mechanism that leads to membrane cholesterol aggregation
Brain·2024· 7 citedOpen Access
Corneal Vascularization Associated With a Novel <i>PDGFRB</i> Variant
Investigative Ophthalmology & Visual Science·2023· 5 citedOpen Access
Xeno-free generation of human induced pluripotent stem cells from donor-matched fibroblasts isolated from dermal and oral tissues
Stem Cell Research & Therapy·2023· 5 citedOpen Access
Functional characterization of all‐trans retinoic acid‐induced differentiation factor (ATRAID)
FEBS Open Bio·2023· 3 citedOpen Access
Author response for "Functional characterization of all‐trans retinoic acid‐induced differentiation factor (&lt;scp&gt;ATRAID&lt;/scp&gt;)"
2023
Xeno-free generation of human induced pluripotent stem cells from donor-matched fibroblasts isolated from dermal and oral tissues
Research Square (Research Square)·2023Open Access
A Pellino‐2 variant is associated with constitutive <scp>NLRP3</scp> inflammasome activation in a family with ocular pterygium–digital keloid dysplasia
FEBS Letters·2023· 2 citedOpen Access
Additional file 2 of Xeno-free generation of human induced pluripotent stem cells from donor-matched fibroblasts isolated from dermal and oral tissues
Figshare·2023Open Access
Corneal neovascularization associated with a novel <scp>PDGFRB</scp> gene variant: Implications for precision medicine treatment
Acta Ophthalmologica·2022
Activity monitoring and patient-reported outcome measures in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients
PLoS ONE·2022· 12 citedOpen Access
Genetic alterations associated with malignant transformation of sporadic vestibular schwannoma
Acta Neurochirurgica·2021· 7 citedOpen Access
Pellino‐2 in nonimmune cells: novel interaction partners and intracellular localization
FEBS Letters·2021· 4 citedOpen Access
K<sup>+</sup> regulates relocation of Pellino‐2 to the site of NLRP3 inflammasome activation in macrophages
FEBS Letters·2021· 7 citedOpen Access
The SH3PXD2A-HTRA1 fusion transcript is extremely rare in Norwegian sporadic vestibular schwannoma patients
Journal of Neuro-Oncology·2021· 12 citedOpen Access
Temperature-dependent autoactivation associated with clinical variability of <i>PDGFRB</i> Asn666 substitutions
Human Molecular Genetics·2021· 14 citedOpen Access
Clinical features and molecular genetics of patients with ABCA4‐retinal dystrophies
Acta Ophthalmologica·2020· 16 citedOpen Access
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Frequent Co-authors

Øystein Fluge(15), Olav Dahl(12), Dipak Sapkota(11), Per M. Knappskog(11), Olav Mella(8), Cecilie Bredrup(8), Eyvind Rødahl(7), Kristin Risa(6), Gunnar Houge(6), Morten Lund‐Johansen(5), Kine Alme(4), Ingrid G. Rekeland(4), Kari Sørland(4), Lars A. Akslen(4), Johan R. Lillehaug(4), Daniela Elena Costea(4), Endre N. Vasstrand(4), Salah O. Ibrahim(4), Ileana Cristea(4), Erling Dahl Borkamo(4)