Evolution of language: Lessons from the genome

von Fisher, Simon E.
Veröffentlicht in Psychon Bull Rev (2016)

Neurogenomics of speech and language disorders: the road ahead

von Deriziotis, Pelagia, Fisher, Simon E
Veröffentlicht 2013

Bridging senses: novel insights from synaesthesia

von Fisher, Simon E., Tilot, Amanda K.
Veröffentlicht in Philos Trans R Soc Lond B Biol Sci (2019)

Foxp2 Mutations Impair Auditory-Motor Association Learning

von Kurt, Simone, Fisher, Simon E., Ehret, Günter
Veröffentlicht 2012

Recent advances in the genetics of language impairment

von Newbury, Dianne F, Fisher, Simon E, Monaco, Anthony P
Veröffentlicht 2010

Persistence and transmission of recessive deafness and sign language: new insights from village sign languages

von Gialluisi, Alessandro, Dediu, Dan, Francks, Clyde, Fisher, Simon E
Veröffentlicht 2013

A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer

von Becker, Martin, Devanna, Paolo, Fisher, Simon E., Vernes, Sonja C.
Veröffentlicht in Mol Cytogenet (2015)

Mapping of Human FOXP2 Enhancers Reveals Complex Regulation

von Becker, Martin, Devanna, Paolo, Fisher, Simon E., Vernes, Sonja C.
Veröffentlicht in Front Mol Neurosci (2018)

Investigating Protein-protein Interactions in Live Cells Using Bioluminescence Resonance Energy Transfer

von Deriziotis, Pelagia, Graham, Sarah A., Estruch, Sara B., Fisher, Simon E.
Veröffentlicht 2014

The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers

von Estruch, Sara B., Graham, Sarah A., Deriziotis, Pelagia, Fisher, Simon E.
Veröffentlicht in Sci Rep (2016)

A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment

von Lozano, Reymundo, Vino, Arianna, Lozano, Cristina, Fisher, Simon E, Deriziotis, Pelagia
Veröffentlicht in Eur J Hum Genet (2015)

Defining the biological bases of individual differences in musicality

von Gingras, Bruno, Honing, Henkjan, Peretz, Isabelle, Trainor, Laurel J., Fisher, Simon E.
Veröffentlicht in Philos Trans R Soc Lond B Biol Sci (2015)

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

von Vernes, Sonja C, MacDermot, Kay D, Monaco, Anthony P, Fisher, Simon E
Veröffentlicht 2009

Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains

von de Kovel, Carolien G. F., Lisgo, Steven N., Fisher, Simon E., Francks, Clyde
Veröffentlicht in Sci Rep (2018)

Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release

von van Rhijn, Jon-Ruben, Fisher, Simon E., Vernes, Sonja C., Nadif Kasri, Nael
Veröffentlicht in Brain Struct Funct (2018)

The genetics of situs inversus without primary ciliary dyskinesia

von Postema, Merel C., Carrion-Castillo, Amaia, Fisher, Simon E., Vingerhoets, Guy, Francks, Clyde
Veröffentlicht in Sci Rep (2020)

Region-specific Foxp2 deletions in cortex, striatum or cerebellum cannot explain vocalization deficits observed in spontaneous global knockouts

von Urbanus, Bastiaan H. A., Peter, Saša, Fisher, Simon E., De Zeeuw, Chris I.
Veröffentlicht in Sci Rep (2020)

The developmental genetic architecture of vocabulary skills during the first three years of life: Capturing emerging associations with later-life reading and cognition

von Verhoef, Ellen, Shapland, Chin Yang, Fisher, Simon E., Dale, Philip S., St Pourcain, Beate
Veröffentlicht in PLoS Genet (2021)

Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23

von Smeets, Cleo J.L.M., Ma, Kai Yu, Fisher, Simon E., Verbeek, Dineke S.
Veröffentlicht in Brain Pathol (2020)

Singing Mice, Songbirds, and More: Models for FOXP2 Function and Dysfunction in Human Speech and Language

von White, Stephanie A., Fisher, Simon E., Geschwind, Daniel H., Scharff, Constance, Holy, Timothy E.
Veröffentlicht 2006