2021

• Fjær, Roar; Marciniak, Katarzyna; Sundnes, Olav; Hjorthaug, Hanne; Sheng, Ying; Hammarström, Clara Louise. (2021) A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndrome. Human Molecular Genetics
  Academic article

2017

• BJØRGO, KATHRINE; Fjær, Roar; Mørk, Hanne Håberg; Ferdinandusse, Sacha; Falkenberg, KD; Waterham, Hans R.. (2017) Biochemical and genetic characterization of an unusual mild PEX3-related Zellweger spectrum disorder. Molecular Genetics and Metabolism
  Academic article

2016

• Stamberger, Hannah; Nikanorova, Marina; Willemsen, Marjolein H.; Accorsi, Patrizia; Angriman, Marco; Baier, Hartmut. (2016) STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy. Neurology
  Academic literature review
• Moen, Marivi Nabong; Fjær, Roar; Hamdani, El Hassan; Lærdahl, Jon Kristen; Menchini, Robin Johansen; Vigeland, Magnus Dehli. (2016) Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport. Brain
  Academic article

2015

• Magnussen, Gry Irene; Emilsen, Elisabeth; Fleten, Karianne Giller; Engesæter, Birgit Øvstebø; Nähse, Viola; Fjær, Roar. (2015) Combined inhibition of the cell cycle related proteins Wee1 and Chk1/2 induces synergistic anti-cancer effect in melanoma. BMC Cancer
  Academic article
• Fjær, Roar; Brodtkorb, Eylert; Øye, Ane-Marte; Sheng, Ying; Vigeland, Magnus Dehli; Kvistad, Kjell Arne. (2015) Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2. European Journal of Medical Genetics
  Academic article