Stephan CF Neuhauss, PhD

Affiliations: 
Institute of Molecular Life Sciences Universität Zürich, Zürich, ZH, Switzerland 
Area:
Visual System, Zebrafish, Retina, Eye Movements
Website:
http://www.imls.uzh.ch/research/Neuhauss.html
Google:
"Stephan Neuhauss"
Bio:

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)
 
SNBCP
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Publications

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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
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