Pelagia Deriziotis

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 20 publications

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

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Journal: Nature communications
Published: May 03, 2019

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Journal: Nature communications
Published: February 17, 2019

De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder.

De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder.

Journal: American journal of human genetics
Published: February 10, 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

Functional characterization of TBR1 variants in neurodevelopmental disorder.

Functional characterization of TBR1 variants in neurodevelopmental disorder.

Journal: Scientific reports
Published: May 14, 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

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Journal: Nature communications
Published: November 09, 2017

Speech and Language: Translating the Genome.

Speech and Language: Translating the Genome.

Journal: Trends in genetics : TIG
Published: May 13, 2017

Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.

Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.

Journal: Human mutation
Published: February 09, 2017

Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.

Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.

Journal: PLoS genetics
Published: September 17, 2016

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

Journal: Journal of neurodevelopmental disorders
Published: June 29, 2016
Showing 1-12 of 20

Last Updated: 09/26/2026