Publications 2018

  • Beck SC, Karlstetter M, Garcia Garrido M, Feng Y, Dannhausen K, Mühlfriedel R, Sothilingam V, Seebauer B, Berger W, Hammes HP, Seeliger MW, Langmann T (2018) Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina. Sci Rep 8:5970
  • Gerth-Kahlert C, Koller S (2018) Ciliopathies. Klin Monbl Augenheilkd 235:264-272
  • Gerth-Kahlert C, Maggi J,Toteberg-Harms M, Tiwari A, Budde B, Nürnberg P, Koller S, Berger W (2018) Absence of goniodysgenesis in patients with chromosome 13q microdeletion-related microcoria. Ophthalmol Glaucoma 1:145-147
  • Gerth-Kahlert C, Tiwari A, Hauri-Hohl MM, Hanson JVM, Bahr A, Palmowski-Wolfe A, Güngör T, Berger W (2018) Unusual retinopathy in a child with severe combined immune deficiency. Ophthalmic Genet 39:92-94
  • Neubauer J, Lecca MR, Russo G, Bartsch C, Medeiros-Domingo A, Berger W, Haas C (2018) Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes. Int J Legal Med 132:1057-1065
  • Valomon A, Holst SC, Borrello A, Weigend S, Müller T, Berger W, Sommerauer M, Baumann CR, Landolt HP (2018) Effects of COMT genotype and tolcapone on lapses of sustained attention after sleep deprivation in healthy young men. Neuropsychopharmacology 43:1599-1607