Simon E. Fisher

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 231 publications

Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

Journal: European journal of human genetics : EJHG

Published: February 16, 2026

Evaluating the effects of archaic protein-altering variants in living human adults.

Evaluating the effects of archaic protein-altering variants in living human adults.

Journal: Science advances

Published: December 10, 2025

Structural and functional brain asymmetry in relation to heterogeneous causes of situs inversus totalis.

Structural and functional brain asymmetry in relation to heterogeneous causes of situs inversus totalis.

Journal: Brain structure & function

Published: November 25, 2025

What enables human language? A biocultural framework.

What enables human language? A biocultural framework.

Journal: Science (New York, N.Y.)

Published: November 20, 2025

Genomic Investigations of Spoken and Written Language Abilities: A Guide to Advances in Approaches, Technologies, and Discovery.

Genomic Investigations of Spoken and Written Language Abilities: A Guide to Advances in Approaches, Technologies, and Discovery.

Journal: Journal of speech, language, and hearing research : JSLHR

Published: October 29, 2025

Developing language in a developing body: genetic associations of infant gross motor behaviour and self-care/symbolic actions with emerging language abilities.

Developing language in a developing body: genetic associations of infant gross motor behaviour and self-care/symbolic actions with emerging language abilities.

Journal: Journal of child psychology and psychiatry, and allied disciplines

Published: June 13, 2025

Functional characterization of pathogenic SATB2 missense variants identifies distinct effects on chromatin binding and transcriptional activity.

Functional characterization of pathogenic SATB2 missense variants identifies distinct effects on chromatin binding and transcriptional activity.

Journal: HGG advances

Published: May 29, 2025

The NuRD component CHD3 promotes BMP signalling during cranial neural crest cell specification.

The NuRD component CHD3 promotes BMP signalling during cranial neural crest cell specification.

Journal: EMBO reports

Published: May 06, 2025

Genetic underpinnings of chills from art and music.

Genetic underpinnings of chills from art and music.

Journal: PLoS genetics

Published: April 15, 2025

Conserved sleep disturbances in FOXP1 syndrome originate from developmental dysregulation of peptidergic signaling.

Conserved sleep disturbances in FOXP1 syndrome originate from developmental dysregulation of peptidergic signaling.

Journal: The Journal of clinical investigation

Published: March 17, 2025

Dyslexia Polygenic Index and Socio-Economic Status Interaction Effects on Reading Skills in Australia and the United Kingdom.

Dyslexia Polygenic Index and Socio-Economic Status Interaction Effects on Reading Skills in Australia and the United Kingdom.

Journal: Behavior genetics

Published: March 17, 2025

Patterns of language and visuospatial lateralisation in three-year-old children.

Patterns of language and visuospatial lateralisation in three-year-old children.

Journal: Neuropsychologia

Published: February 19, 2025

Showing 1-12 of 231

Last Updated: 09/26/2026