Arianna Vino

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 17 publications

De novo protein-coding gene variants in developmental stuttering.

De novo protein-coding gene variants in developmental stuttering.

Journal: Molecular psychiatry

Published: November 22, 2024

Genome Sequencing of Idiopathic Speech Delay.

Genome Sequencing of Idiopathic Speech Delay.

Journal: Human mutation

Published: September 18, 2023

SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder.

SETBP1 variants outside the degron disrupt DNA-binding, transcription and neuronal differentiation capacity to cause a heterogeneous neurodevelopmental disorder.

Journal: Nature communications

Published: January 25, 2023

Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions.

Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions.

Journal: Human molecular genetics

Published: July 12, 2022

Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities.

Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 29, 2020

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.

Journal: American journal of human genetics

Published: April 02, 2020

Correction to 'Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits'.

Correction to 'Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits'.

Journal: Philosophical transactions of the Royal Society of London. Series B, Biological sciences

Published: February 21, 2020

Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits.

Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits.

Journal: Philosophical transactions of the Royal Society of London. Series B, Biological sciences

Published: October 22, 2019

Toward Robust Functional Neuroimaging Genetics of Cognition.

Toward Robust Functional Neuroimaging Genetics of Cognition.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: April 19, 2019

Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.

Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.

Journal: Human molecular genetics

Published: June 28, 2018

Rare variants in axonogenesis genes connect three families with sound-color synesthesia.

Rare variants in axonogenesis genes connect three families with sound-color synesthesia.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: March 07, 2018

Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.

Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.

Journal: Human molecular genetics

Published: November 28, 2017

Showing 1-12 of 17

Last Updated: 09/26/2026