Evolution of language: Lessons from the genome

por Fisher, Simon E.
Publicado 2016

Neurogenomics of speech and language disorders: the road ahead

por Deriziotis, Pelagia, Fisher, Simon E
Publicado 2013

Foxp2 Mutations Impair Auditory-Motor Association Learning

por Kurt, Simone, Fisher, Simon E., Ehret, Günter
Publicado 2012

Molecular networks of the FOXP2 transcription factor in the brain

por den Hoed, Joery, Devaraju, Karthikeyan, Fisher, Simon E
Publicado 2021

Recent advances in the genetics of language impairment

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

Genetic architecture of the white matter connectome of the human brain

por Sha, Zhiqiang, Schijven, Dick, Fisher, Simon E., Francks, Clyde
Publicado 2023

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 2015

Mapping of Human FOXP2 Enhancers Reveals Complex Regulation

por Becker, Martin, Devanna, Paolo, Fisher, Simon E., Vernes, Sonja C.
Publicado 2018

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 2016

Effects of Cortical FoxP1 Knockdowns on Learned Song Preference in Female Zebra Finches

por Heim, Fabian, Fisher, Simon E., Scharff, Constance, ten Cate, Carel, Riebel, Katharina
Publicado 2023

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

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

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

por de Kovel, Carolien G. F., Lisgo, Steven N., Fisher, Simon E., Francks, Clyde
Publicado 2018

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

por van Rhijn, Jon-Ruben, Fisher, Simon E., Vernes, Sonja C., Nadif Kasri, Nael
Publicado 2018

The genetics of situs inversus without primary ciliary dyskinesia

por Postema, Merel C., Carrion-Castillo, Amaia, Fisher, Simon E., Vingerhoets, Guy, Francks, Clyde
Publicado 2020

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

por Urbanus, Bastiaan H. A., Peter, Saša, Fisher, Simon E., De Zeeuw, Chris I.
Publicado 2020

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

por Verhoef, Ellen, Shapland, Chin Yang, Fisher, Simon E., Dale, Philip S., St Pourcain, Beate
Publicado 2021

Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23

por Smeets, Cleo J.L.M., Ma, Kai Yu, Fisher, Simon E., Verbeek, Dineke S.
Publicado 2020

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 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 2016

Relations between hemispheric asymmetries of grey matter and auditory processing of spoken syllables in 281 healthy adults

por Guadalupe, Tulio, Kong, Xiang-Zhen, Akkermans, Sophie E. A., Fisher, Simon E., Francks, Clyde
Publicado 2021