Dr. Simon E. Fisher
Biography | Publications | Talks | Complete CV
1994-1997 | 1998-2001 | 2002-2004 | 2005-2007 | 2008-present
2010
Marcus GF, Fisher SE (2010) Genes and language. In: Cambridge Encyclopedia of the Language Sciences (ed. Hogan PC) 341-344 (Cambridge University Press, New York, USA)
Vernes SC, Fisher SE (2010) Functional genomic dissection of speech and language disorders. In: Genomics, Proteomics, and the Nervous System (ed. Clelland JD) in press (Springer)
Roll P, Vernes SC, Bruneau N, Cillario J, Ponsole-Lenfant M, Massacrier A, Rudolf G, Khalife M, Hirsch E, Fisher SE, Szepetowski P (2010) Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Hum. Mol. Genet. 2010 Sep 21. [Epub ahead of print]
Gaub S, Groszer M, Fisher SE, Ehret G (2010) The structure of innate vocalizations in Foxp2-deficient mouse pups. Genes Brain. Behav. 9: 390-401
Fisher SE (2010) Genetic susceptibility to stuttering. N. Engl. J. Med. 362: 750-2
Newbury DF, Fisher SE, Monaco AP (2010) Recent advances in the genetics of language impairment. Genome Med. 2: 6
2009
Vernes SC, Fisher SE (2009) Unravelling neurogenetic networks implicated in developmental language disorders. Biochem. Soc. Trans. 37: 1263-9
Kurt S, Groszer M, Fisher SE, Ehret G (2009) Modified sound-evoked brainstem potentials in Foxp2 mutant mice. Brain Res. 1289: 30-6 [abstract] [pdf]
Ramus F, Fisher SE (2009) Genetics of language. In: The Cognitive Neurosciences 4th Edition (ed. Gazzaniga MS) 855-71 (MIT Press, Cambridge, MA, USA)
Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, O'Hare A, Shaw D, Simkin Z, Simonoff E, Slonims V, Watson J, Ragoussis J, Fisher SE, Seckl JR, Helms PJ, Bolton PF, Pickles A, Conti-Ramsden G, Baird G, Bishop DV, Monaco AP (2009) CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment. Am. J. Hum. Genet. 85: 264-72 [abstract] [free pdf] [supplemental data]
Enard W, Gehre S, Hammerschmidt K, Hölter SM, Blass T, Somel M, Brückner MK, Schreiweis C, Winter C, Sohr R, Becker L, Wiebe V, Nickel B, Giger T, Müller U, Groszer M, Adler T, Aguilar A, Bolle I, Calzada-Wack J, Dalke C, Ehrhardt N, Favor J, Fuchs H, Gailus-Durner V, Hans W, Hölzlwimmer G, Javaheri A, Kalaydjiev S, Kallnik M, Kling E, Kunder S, Mossbrugger I, Naton B, Racz I, Rathkolb B, Rozman J, Schrewe A, Busch DH, Graw J, Ivandic B, Klingenspor M, Klopstock T, Ollert M, Quintanilla-Martinez L, Schulz H, Wolf E, Wurst W, Zimmer A, Fisher SE, Morgenstern R, Arendt T, de Angelis MH, Fischer J, Schwarz J, Pääbo S (2009) A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell 137: 961-71 [abstract] [pdf] [supplemental data]
Vernes SC, MacDermot KD, Monaco AP, Fisher SE (2009) Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. Eur. J. Hum. Genet. 17: 1354-8 [abstract] [free pdf] [supplementary data]
Fisher SE, Scharff C (2009) FOXP2 as a molecular window into speech and language. Trends Genet. 25: 166-77 (refereed review article) [abstract] [article]
2008
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: 2337-45 [abstract] [free pdf] [supplementary appendix]
Groszer M, Keays DA, Deacon RMJ, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SDM, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JNP, Fisher SE (2008) Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr. Biol. 18: 354-62 [abstract] [free pdf] [supplemental data]
Falcaro M, Pickles A, Newbury DF, Addis L, Banfield E, Fisher SE, Monaco AP, Simkin Z, Conti-Ramsden G; The SLI Consortium (2008) Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment. Genes Brain Behav. 7: 393-402 [abstract] [pdf]