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Fehr, Alexander G J; Ruetten, Maja; Seth-Smith, Helena M B; Nufer, Lisbeth; Vögtlin, Andrea; Lehner, Angelika; Greub, Gilbert; Crosier, Philip S; Neuhauss, Stephan C F; Vaughan, Lloyd (2016). A Zebrafish Model for Infection with the Obligate Intracellular Pathogen . Frontiers in Microbiology, 7, p. 1829. Frontiers 10.3389/fmicb.2016.01829
Tschopp, Markus; Takamiya, Masanari; Cerveny, Kara L; Gestri, Gaia; Biehlmaier, Oliver; Wilson, Stephen W; Strähle, Uwe; Neuhauss, Stephan C F (2010). Funduscopy in adult zebrafish and its application to isolate mutant strains with ocular defects. PLoS ONE, 5(11), e15427. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0015427
Huang, Ying-Yu; Tschopp, Markus; Straumann, Dominik; Neuhauss, Stephan C F (2010). Vestibular deficits do not underlie looping behavior in achiasmatic fish. Communicative & integrative biology, 3(4), pp. 379-81. Austin, Tex.: Landes Bioscience 10.1007/BF00119911
Kallivretaki, Evangelina; Eggen, Rik I L; Neuhauss, Stephan C F; Kah, Olivier; Segner, Helmut (2007). The zebrafish, brain-specific, aromatase cyp19a2 is neither expressed nor distributed in a sexually dimorphic manner during sexual differentiation. Developmental dynamics, 236(11), pp. 3155-66. New York, N.Y.: John Wiley & Sons 10.1002/dvdy.21344
Konrad, Martin; Schaller, André; Seelow, Dominik; Pandey, Amit Vikram; Waldegger, Siegfried; Lesslauer, Annegret; Vitzthum, Helga; Suzuki, Yoshiro; Luk, John M; Becker, Christian; Schlingmann, Karl P; Schmid, Marcel; Rodriguez-Soriano, Juan; Ariceta, Gema; Cano, Francisco; Enriquez, Ricardo; Juppner, Harald; Bakkaloglu, Sevcan A; Hediger, Matthias A; Gallati, Sabina; ... (2006). Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. American journal of human genetics, 79(5), pp. 949-57. New York, N.Y.: Cell Press 10.1086/508617
Trueb, Beat; Neuhauss, Stephan C F; Baertschi, Stefan; Rieckmann, Thorsten; Schild, Christof; Taeschler, Sara (2005). Fish possess multiple copies of fgfrl1, the gene for a novel FGF receptor. Biochimica et biophysica acta, 1727(1), pp. 65-74. Amsterdam: Elsevier 10.1016/j.bbaexp.2004.12.001
