Evolution of language: Lessons from the genome

Por Fisher, Simon E.
Publicado no Psychon Bull Rev (2016)

Neurogenomics of speech and language disorders: the road ahead

Por Deriziotis, Pelagia, Fisher, Simon E
Publicado em 2013

Foxp2 Mutations Impair Auditory-Motor Association Learning

Por Kurt, Simone, Fisher, Simon E., Ehret, Günter
Publicado em 2012

Recent advances in the genetics of language impairment

Por Newbury, Dianne F, Fisher, Simon E, Monaco, Anthony P
Publicado em 2010

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

Por Gialluisi, Alessandro, Dediu, Dan, Francks, Clyde, Fisher, Simon E
Publicado em 2013

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

Por Becker, Martin, Devanna, Paolo, Fisher, Simon E., Vernes, Sonja C.
Publicado no Mol Cytogenet (2015)

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

Por Deriziotis, Pelagia, Graham, Sarah A., Estruch, Sara B., Fisher, Simon E.
Publicado em 2014

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

Por Estruch, Sara B., Graham, Sarah A., Deriziotis, Pelagia, Fisher, Simon E.
Publicado no Sci Rep (2016)

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

Por Lozano, Reymundo, Vino, Arianna, Lozano, Cristina, Fisher, Simon E, Deriziotis, Pelagia
Publicado no Eur J Hum Genet (2015)

Defining the biological bases of individual differences in musicality

Por Gingras, Bruno, Honing, Henkjan, Peretz, Isabelle, Trainor, Laurel J., Fisher, Simon E.
Publicado no Philos Trans R Soc Lond B Biol Sci (2015)

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

Por Vernes, Sonja C, MacDermot, Kay D, Monaco, Anthony P, Fisher, Simon E
Publicado em 2009

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

Por White, Stephanie A., Fisher, Simon E., Geschwind, Daniel H., Scharff, Constance, Holy, Timothy E.
Publicado em 2006

Assessing the effects of common variation in the FOXP2 gene on human brain structure

Por Hoogman, Martine, Guadalupe, Tulio, Zwiers, Marcel P., Klarenbeek, Patricia, Francks, Clyde, Fisher, Simon E.
Publicado em 2014

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder

Por Estruch, Sara B., Graham, Sarah A., Chinnappa, Swathi M., Deriziotis, Pelagia, Fisher, Simon E.
Publicado no J Neurodev Disord (2016)

Generation of mice with a conditional Foxp2 null allele

Por French, Catherine A, Groszer, Matthias, Preece, Christopher, Coupe, Anne-Marie, Rajewsky, Klaus, Fisher, Simon E
Publicado em 2007

Is synaesthesia more common in autism?

Por Baron-Cohen, Simon, Johnson, Donielle, Asher, Julian, Wheelwright, Sally, Fisher, Simon E, Gregersen, Peter K, Allison, Carrie
Publicado em 2013

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2

Por Fedorenko, Evelina, Morgan, Angela, Murray, Elizabeth, Cardinaux, Annie, Mei, Cristina, Tager-Flusberg, Helen, Fisher, Simon E, Kanwisher, Nancy
Publicado no Eur J Hum Genet (2016)

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2

Por Fedorenko, Evelina, Morgan, Angela, Murray, Elizabeth, Cardinaux, Annie, Mei, Cristina, Tager-Flusberg, Helen, Fisher, Simon E, Kanwisher, Nancy
Publicado no Eur J Hum Genet (2016)

A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice

Por Chabout, Jonathan, Sarkar, Abhra, Patel, Sheel R., Radden, Taylor, Dunson, David B., Fisher, Simon E., Jarvis, Erich D.
Publicado no Front Behav Neurosci (2016)

FOXP2 Targets Show Evidence of Positive Selection in European Populations

Por Ayub, Qasim, Yngvadottir, Bryndis, Chen, Yuan, Xue, Yali, Hu, Min, Vernes, Sonja C., Fisher, Simon E., Tyler-Smith, Chris
Publicado em 2013