Stephen D. M. Brown

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Steve Brown
File:Professor Steve David Macleod Brown FRS.jpg
Steve Brown in 2015, portrait from the Royal Society
Born Stephen David Macleod Brown
(1955-05-03) 3 May 1955 (age 68)[1]
Dumfries, Scotland[1]
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Institutions <templatestyles src="Plainlist/styles.css"/>
Alma mater University of Cambridge (BA, PhD)
Thesis The molecular organisation and evolution of rodent genomes (1981)
Doctoral advisor Gabriel Dover[5][6][7]
Doctoral students <templatestyles src="Plainlist/styles.css"/>
  • Mahmood Bhutta[8]
  • Leanne Carrott[9]
  • Michael Crompton[10] 
Notable awards <templatestyles src="Plainlist/styles.css"/>
Website
www.har.mrc.ac.uk/research/lifetime-studies/genetics-and-pathobiology-deafness

Steve David Macleod Brown FRS[11] FMedSci[2] is director of the Medical Research Council (MRC) Mammalian Genetics Unit, MRC Harwell at Harwell Science and Innovation Campus, Oxfordshire,[11][12][13][14][15] a research centre on mouse genetics. In addition, he is the head of the Genetics and Pathobiology of Deafness research group there.[16]

Education

Brown was educated at Belfast Royal Academy[1] and St Catharine's College, Cambridge where he was awarded a Bachelor of Arts degree in 1977[1] followed by a PhD in 1981 for research on the molecular organisation and evolution of rodent genomes[17] supervised by Gabriel Dover.[5]

Research

Brown conducts research in mouse genetics and genomics. He has studied repeated sequences in the DNA of mice and produced molecular maps of mouse chromosomes, which were used to sequence the mouse genome.[5][11][18] He subsequently pioneered efforts to functionally annotate the mouse genome and identify and generate novel disease models through mutagenesis and phenotyping. In particular, he has identified key proteins involved in hearing, contributing to the understanding of the genetics of deafness.[11] For example, research in Brown's laboratory has shown that a mutation in the Evi1 gene increases susceptibility to inflammation of the middle ear (otitis media) in mice, leading to hearing loss.[19]

A particular focus has been the use of mouse models to elucidate the molecular basis of genetic deafness. With Karen Steel, he discovered myosin VIIA as the gene underlying the shaker-1 mutant — one of the first deafness genes to be identified.[20]

Career

Prior to being appointed director of Harwell in 1998, Brown was a professor at Imperial College London.[21] He is chair of the International Mouse Phenotyping Consortium steering committee and joint editor-in-chief of the journal Mammalian Genome.[22][23]

Awards and honours

Brown was awarded The Genetics Society Medal in 2009,[citation needed] elected a Fellow of the Academy of Medical Sciences in 2001.,[2] and elected a Fellow of the Royal Society (FRS) in 2015.[11][20] His certificate of election reads: <templatestyles src="Template:Blockquote/styles.css" />

Stephen Brown is distinguished for his research in mouse genetics and genomics. He pioneered studies of repeated sequences in the mouse genome and the use of novel approaches to generate molecular maps of mouse chromosomes, work that underpinned the sequencing of the mouse genome. He has been at the forefront of new approaches in mutagenesis and phenotyping for the functional annotation of the mouse genome and the identification and characterisation of disease models. Notably, in collaboration he has utilised the mouse to study the genetics of deafness, identifying key proteins involved in auditory transduction, which has transformed our understanding in this field.[11]

References

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    “All text published under the heading 'Biography' on Fellow profile pages is available under Creative Commons Attribution 4.0 International License.” --Royal Society Terms, conditions and policies at the Wayback Machine (archived September 25, 2015)

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