Stephen W. Wilson
Affiliations: | University College London, London, United Kingdom |
Area:
Neural developmentGoogle:
"Stephen Wilson"Mean distance: 14.08 (cluster 57) | S | N | B | C | P |
Cross-listing: danioTree
Parents
Sign in to add mentorNigel Holder | grad student | Kings College London | |
Stephen S. Easter Jr. | post-doc | 1989-1992 | University of Michigan |
Children
Sign in to add traineeWilliam Norton | grad student | UCL (London) | |
Isaac H. Bianco | grad student | 2002-2008 | UCL |
Matthias Carl | post-doc | UCL | |
Corinne Houart | post-doc | ||
Thomas A. Hawkins | post-doc | 2004- | UCL |
Rodrigo M. Young | post-doc | 2006- | UCL |
Máté Varga | post-doc | 2006-2009 | University College London (UCL), England, UK (danioTree) |
Kara Cerveny | post-doc | 2005-2010 | UCL (Chemistry Tree) |
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Publications
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Hernández-Bejarano M, Gestri G, Monfries C, et al. (2022) Foxd1-dependent induction of a temporal retinal character is required for visual function. Development (Cambridge, England). 149 |
Turner KJ, Hawkins TA, Henriques PM, et al. (2022) A Structural Atlas of the Developing Zebrafish Telencephalon Based on Spatially-Restricted Transgene Expression. Frontiers in Neuroanatomy. 16: 840924 |
Tuschl K, White RJ, Trivedi C, et al. (2022) Loss of slc39a14 causes simultaneous manganese hypersensitivity and deficiency in zebrafish. Disease Models & Mechanisms |
Kroll F, Powell GT, Ghosh M, et al. (2021) A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes. Elife. 10 |
Varga M, Csályi K, Bertyák I, et al. (2020) Tissue-Specific Requirement for the GINS Complex During Zebrafish Development. Frontiers in Cell and Developmental Biology. 8: 373 |
Varga M, Csályi K, Bertyák I, et al. (2020) Tissue-Specific Requirement for the GINS Complex During Zebrafish Development Frontiers in Cell and Developmental Biology. 8 |
Young RM, Ewan KB, Ferrer VP, et al. (2019) Developmentally regulated splice variants mediate transcriptional repressor functions during eye formation. Elife. 8 |
Cavodeassi F, Wilson SW. (2019) Looking to the future of zebrafish as a model to understand the genetic basis of eye disease. Human Genetics |
Holt RJ, Young RM, Crespo B, et al. (2019) De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies. American Journal of Human Genetics |
Lekk I, Duboc V, Faro A, et al. (2019) Sox1a mediates the ability of the parapineal to impart habenular left-right asymmetry. Elife. 8 |