Steve D. M. Brown
Mary Lyon Centre at MRC Harwell(GB)Medical Research Council(GB)University of Sheffield(GB)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Ear Surgery and Otitis Media, Animal Genetics and Reproduction, CRISPR and Genetic Engineering, Bioinformatics and Genomic Networks
Most-Cited Works
- → High-throughput discovery of novel developmental phenotypes(2016)1,278 cited
- → Defective myosin VIIA gene responsible for Usher syndrome type IB(1995)1,065 cited
- → α-Synuclein impairs macroautophagy: implications for Parkinson’s disease(2010)817 cited
- → Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment(1997)797 cited
- → A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse(2000)656 cited
- → Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse(2003)621 cited