Simon Fisher

Last updated

Simon Fisher
Simon Fisher (British Geneticist).jpg
Fisher in 2010
Born
Simon E. Fisher

(1970-08-19) 19 August 1970 (age 51) [1]
Alma mater
Awards Crick Lecture (2008)
Scientific career
Fields
Thesis Positional cloning of the gene responsible for dent's disease  (1995)
Doctoral advisor Ian W. Craig [3]
Other academic advisors Anthony Monaco
Doctoral students Sonja Vernes [4]
Website www.mpi.nl/people/fisher-simon

Simon E. Fisher (born 1970) is a British geneticist and neuroscientist who has pioneered research into the genetic basis of human speech and language. [2] [5] [6] He is a director of the Max Planck Institute for Psycholinguistics and Professor of language and genetics at the Donders Institute for Brain, Cognition and Behaviour in Nijmegen, The Netherlands. [1] [7]

Contents

Education

Fisher was an undergraduate student at Trinity Hall, Cambridge where he read Natural Sciences. He was a postgraduate student at St. Catherine's College, Oxford [3] where he was awarded a Doctor of Philosophy degree from the University of Oxford in 1995 for research on positional cloning of the gene responsible for Dent's disease supervised by Ian W. Craig  [ Wikidata ]. [3]

Career and research

Following his DPhil, he was a postdoctoral researcher in Anthony Monaco's laboratory at the Wellcome Trust Centre for Human Genetics in Oxford.

Fisher is the co-discoverer of FOXP2, the first gene to be implicated in a human speech and language disorder. [8] [9] [10] His subsequent research has used FOXP2 and other language-related genes [11] as molecular windows into neural pathways critical for language. [12]

Awards and honours

Awards and prizes in recognition of his work include the Francis Crick Lecture in 2008 [13] and the inaugural Eric Kandel Young Neuroscientists Prize in 2009. [14] [15]

Related Research Articles

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FOXP2 Transcription factor gene of the forkhead box family

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Kathryn Emma Watkins is an experimental psychologist in the Wellcome Trust centre for integrative neuroimaging at the University of Oxford and a tutorial fellow at St Anne's College, Oxford. Her research investigates the brain processes that underlie speech, language and development.

Sonja Catherine Vernes is a Dutch neuroscientist and Head of the Neurogenetics of Vocal Communication Research Group at the University of St Andrews. She holds a UK Research and Innovation (UKRI) future leaders fellowship. Her research investigates vocal communication between mammals. She was a laureate for the 2022 Blavatnik Awards for Young Scientists.

References

  1. 1 2 "Dr. Simon E. Fisher". mpg.de. Nijmegen, Netherlands: Max Planck Institute for Psycholinguistics. Archived from the original on 3 January 2016. Retrieved 23 October 2012.
  2. 1 2 Simon Fisher publications indexed by Google Scholar OOjs UI icon edit-ltr-progressive.svg
  3. 1 2 3 Fisher, Simon E. (1995). Positional cloning of the gene responsible for Dent's disease. ox.ac.uk (DPhil thesis). University of Oxford. OCLC   557355457. EThOS   uk.bl.ethos.307141. Open Access logo PLoS transparent.svg
  4. Vernes, Sonja (2007). Investigation of the role of FOXP transcription factors in neurodevelopment. ox.ac.uk (DPhil thesis). University of Oxford. OCLC   317354555. EThOS   uk.bl.ethos.497468.
  5. Simon Fisher publications from Europe PubMed Central
  6. Zimmer, Carl (17 October 2011). "The Language Fossils Buried in Every Cell of Your Body | Human Evolution". discovermagazine.com. Retrieved 23 October 2012.
  7. "Brief Biography — Simon E. Fisher — Max Planck Institute for Psycholinguistics". Mpi.nl. 28 September 2012. Retrieved 23 October 2012.
  8. Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME (1998). "Localisation of a gene implicated in a severe speech and language disorder". Nature Genetics. 18 (2): 168–70. doi:10.1038/ng0298-168. hdl: 11858/00-001M-0000-0012-CBD9-5 . PMID   9462748. S2CID   3190318.
  9. Lai CSL, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (2001). "A forkhead-domain gene is mutated in a severe speech and language disorder". Nature. 413 (6855): 519–23. Bibcode:2001Natur.413..519L. doi:10.1038/35097076. PMID   11586359. S2CID   4421562.
  10. MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE (2005). "Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits". Am. J. Hum. Genet. 76 (6): 1074–80. doi:10.1086/430841. PMC   1196445 . PMID   15877281.
  11. Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE (2008). "A functional genetic link between distinct developmental language disorders". N. Engl. J. Med. 359 (22): 2337–45. doi:10.1056/NEJMoa0802828. PMC   2756409 . PMID   18987363.
  12. Fisher SE, Scharff C (2009). "FOXP2 as a molecular window into speech and language". Trends Genet. 25 (4): 166–77. doi:10.1016/j.tig.2009.03.002. hdl: 11858/00-001M-0000-0012-CA31-7 . PMID   19304338.
  13. "rewards excellence in science - News". Royal Society. 10 July 2008. Archived from the original on 20 October 2012. Retrieved 23 October 2012.
  14. "Simon Fisher wins young neuroscientist prize". ox.ac.uk. University of Oxford. Archived from the original on 20 October 2012. Retrieved 23 October 2012.
  15. Fisher, S. E.; Ridley, M. (2013). "Culture, Genes, and the Human Revolution". Science. 340 (6135): 929–930. Bibcode:2013Sci...340..929F. doi:10.1126/science.1236171. PMID   23704558. S2CID   39849683.