Stephan CF Neuhauss, PhD
Affiliations: | Institute of Molecular Life Sciences | Universität Zürich, Zürich, ZH, Switzerland |
Area:
Visual System, Zebrafish, Retina, Eye MovementsWebsite:
http://www.imls.uzh.ch/research/Neuhauss.htmlGoogle:
"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) | S | N | B | C | P |
Cross-listing: danioTree
Parents
Sign in to add mentor| Monte Westerfield | research assistant | 1990-1992 | Universität Zürich | |
| (MSc) | ||||
| Wolfgang Driever | grad student | 1992-1996 | MGH | |
| Friedrich Bonhoeffer | post-doc | Max Planck Institute for Developmental Biology, Tübingen | ||
Children
Sign in to add trainee| Sara A Haddad | post-doc | University of Zurich (UZH) | |
| Oliver Biehlmaier | post-doc | 2005-2009 | Universität Zürich |
| Lucia Cadetti | research scientist | Universität Zürich |
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Publications
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| Schlegel DK, Ramkumar S, von Lintig J, et al. (2021) Disturbed retinoid metabolism upon loss of impairs cone function and leads to subretinal lipid deposits and photoreceptor degeneration in the zebrafish retina. Elife. 10 |
| Bachmann-Gagescu R, Neuhauss SC. (2019) The photoreceptor cilium and its diseases. Current Opinion in Genetics & Development. 56: 22-33 |
| 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 |