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Tiwari, Amit; Bahr, Angela; Bähr, Luzy; Fleischhauer, Johannes; Zinkernagel, Martin; Winkler, Niklas; Barthelmes, Daniel; Berger, Lieselotte Erika; Gerth-Kahlert, Christina; Neidhardt, John; Berger, Wolfgang (2016). Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies. Scientific Reports, 6(28755), p. 28755. Nature Publishing Group 10.1038/srep28755
Schindera, Christina; Wingeier, Kevin; Goeggel Simonetti, Barbara; Diepold, Miriam; Nauer, Claude B; Fleischhauer, Johannes; Steinlin, Maja (2011). Macrocephaly in neurofibromatosis type 1: a sign post for optic pathway gliomas? Child's nervous system, 27(12), pp. 2107-11. Heidelberg: Springer-Verlag 10.1007/s00381-011-1554-2
Abegg, Mathias; Tappeiner, Christoph; Wolf-Schnurrbusch, Ute; Barthelmes, Daniel; Wolf, Sebastian; Fleischhauer, Johannes (2008). Treatment of branch retinal vein occlusion induced macular edema with bevacizumab. BMC ophthalmology, 8(18), p. 18. London: BioMed Central 10.1186/1471-2415-8-18
Neidhardt, John; Glaus, Esther; Lorenz, Birgit; Netzer, Christian; Li, Yün; Schambeck, Maria; Wittmer, Mariana; Feil, Silke; Kirschner-Schwabe, Renate; Rosenberg, Thomas; Cremers, Frans P M; Bergen, Arthur A B; Barthelmes, Daniel; Baraki, Husnia; Schmid, Fabian; Tanner, Gaby; Fleischhauer, Johannes; Orth, Ulrike; Becker, Christian; Wegscheider, Erika; ... (2008). Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing. Molecular vision, 14, pp. 1081-1093. Atlanta, Ga.: Emory University
Fischer, M Dominik; Fleischhauer, Johannes; Keusch, Gérald; Abegg, Mathias (2007). Rise in intraocular pressure during haemodialysis in a patient with reduced outflow facility. British journal of ophthalmology, 91(8), pp. 1091-3. London: BMJ Publishing Group 10.1136/bjo.2006.110072
Neidhardt, John; Glaus, Esther; Barthelmes, Daniel; Zeitz, Christina; Fleischhauer, Johannes; Berger, Wolfgang (2007). Identification and characterization of a novel RPGR isoform in human retina. Human mutation, 28(8), pp. 797-807. Hoboken, N.J.: Wiley-Blackwell 10.1002/humu.20521
