❭ Research by medical division ❭ Clinical Neuroscience ❭ Department of Neurology ❭ Movement, neuromuscular disease and ALS [Toft] ❭ Scientists

Scientists

NameUnit(s)
Berge, Victoria-SeidlMolecular studies of Parkinson's disease [Toft]
Bjerknes, Silje KristinInger Marie Skogseid’s Project Group [Skogseid] ; Molecular studies of Parkinson's disease
Dietrichs, EspenClinical Studies of Movement Disorders
Elsais, AhmedClinical Studies of Movement Disorders
Frich, Jan ChristianClinical Studies of Movement Disorders
Gundersen, VidarClinical Studies of Movement Disorders
Iqbal, ZafarMolecular studies of Parkinson's disease [Toft]
Kerty, EmiliaClinical Studies of Movement Disorders
Kvernmo, Nadja Anette MyrvikInger Marie Skogseid’s Project Group [Skogseid]
Maniaol, Angelina HatløMyasthenia gravis and amyotrophic lateral sclerosis [Maniaol]
Popperud, Trine HaugClinical Studies of Movement Disorders
Siewers, VibekeInger Marie Skogseid’s Project Group [Skogseid]
Skogseid, Inger MarieInger Marie Skogseid’s Project Group [Skogseid]
Toft, MathiasMolecular studies of Parkinson's disease [Toft]
Wedding, Iselin MarieInger Marie Skogseid’s Project Group [Skogseid]
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Home Department of Neurology Movement, neuromuscular disease and ALS [Toft]

  • Molecular studies of Parkinson's disease
  • Clinical Studies of Movement Disorders
  • Inger Marie Skogseid's project group
  • Myasthenia and amyotrophic lateral sclerosis
  • Scientists
  • Publications

Recent publications

Tsukada K, Lototska L, Tsukada A, Sarusie MVK, Gönenç II, Sherlaw-Sturrock C, Kanade M, Palek M, Oliver AW, Jones SE, Jhujh SS, Bannister J, Ali A, Raza M, Toft M, Iqbal Z, Fatima A, Miller TCR, Larsen LA, Stewart GS, Ochs F, Blackford AN (2026)
DDIAS shields single-stranded DNA in mitosis and promotes vertebrate brain development
Cell (in press)
DOI 10.1016/j.cell.2026.07.041, PubMed 42636811

Wang Q, Sobering AK, Tirrito C, Haghshenas S, Hjortshøj TD, Platzer K, Redler S, March ME, Matsuoka LS, Xi H, Zoodsma J, Chen Y, Mori M, Leung ML, Couque N, Verloes A, Pouzet A, Giesbertz NA, Simon ME, Yearwood AK, Assing DL, Hsieh TC, Li JM, Levy MA, Kerkhof J, McConkey H, Rzasa J, Lauzon-Young C, Sulaiman RA, Abdulwahab F et al. (2026)
Biallelic inactivating variants in the chromatin remodeler DMAP1 cause a syndromic neurodevelopmental disorder
J Clin Invest, 136 (15)
DOI 10.1172/JCI198229, PubMed 42275155

Hermansen MV, Ørstavik K, Steen U, Toft M, Brunborg C, Wekre LL (2026)
The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway - A Description of Demographic, Medical, and Neurological Findings
Am J Med Genet C Semin Med Genet (in press)
DOI 10.1002/ajmg.c.70017, PubMed 42271604

More publications

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