Stephan CF Neuhauss, PhD

Institute of Molecular Life Sciences Universität Zürich, Zürich, ZH, Switzerland 
Visual System, Zebrafish, Retina, Eye Movements
"Stephan Neuhauss"

1967 born in Ulm (Germany)
1987-1990 Biology at University Tübingen
1990-1992Biology at University of Oregon, Group of Monte WesterfieldMSc
1992-1996 PhD at Massachussetts General Hospital; Group of Wolfgang Driever
1996-2000 Postdoctoral stay at MPI Tübingen (Prof. Friedrich Bonhoeffer)
2000-2002 Oberassitant, Brain Research Institute Zürich, ETH Zürich
2002-2005 Assistent Professor ETH Zürich
2005- Associated Professor University of Zürich

Mean distance: 16.02 (cluster 11)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Dona M, Slijkerman R, Lerner K, et al. (2018) Usherin defects lead to early-onset retinal dysfunction in zebrafish. Experimental Eye Research
Gopal SR, Chen DH, Chou SW, et al. (2015) Zebrafish Models for the Mechanosensory Hair Cell Dysfunction in Usher Syndrome 3 Reveal That Clarin-1 Is an Essential Hair Bundle Protein. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 10188-201
Carmean V, Yonkers MA, Tellez MB, et al. (2015) pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability. Journal of Neurophysiology. 114: 1146-57
Hodel C, Niklaus S, Heidemann M, et al. (2014) Myosin VIIA is a marker for the cone accessory outer segment in zebrafish. Anatomical Record (Hoboken, N.J. : 2007). 297: 1777-84
Sirisi S, Folgueira M, López-Hernández T, et al. (2014) Megalencephalic leukoencephalopathy with subcortical cysts protein 1 regulates glial surface localization of GLIALCAM from fish to humans. Human Molecular Genetics. 23: 5069-86
Tuz K, Bachmann-Gagescu R, O'Day DR, et al. (2014) Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy. American Journal of Human Genetics. 94: 62-72
Dooley CM, Schwarz H, Mueller KP, et al. (2013) Slc45a2 and V-ATPase are regulators of melanosomal pH homeostasis in zebrafish, providing a mechanism for human pigment evolution and disease. Pigment Cell & Melanoma Research. 26: 205-17
Glover G, Mueller KP, Söllner C, et al. (2012) The Usher gene cadherin 23 is expressed in the zebrafish brain and a subset of retinal amacrine cells. Molecular Vision. 18: 2309-22
Tschopp M, Takamiya M, Cerveny KL, et al. (2010) Funduscopy in adult zebrafish and its application to isolate mutant strains with ocular defects. Plos One. 5: e15427
Haug MF, Biehlmaier O, Mueller KP, et al. (2010) Visual acuity in larval zebrafish: behavior and histology. Frontiers in Zoology. 7: 8
See more...