Sara B. Estruch
Nijmegen, GE, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions.
Journal: Human molecular genetics
Published: July 12, 2022
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family.
Journal: Human genetics
Published: November 16, 2020
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.
Journal: Scientific reports
Published: May 14, 2018
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.
Journal: Human molecular genetics
Published: November 28, 2017
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.
Journal: Journal of neurodevelopmental disorders
Published: June 29, 2016
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
Journal: American journal of human genetics
Published: March 29, 2016
Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer.
Journal: Journal of visualized experiments : JoVE
Published: June 05, 2014
De novo TBR1 mutations in sporadic autism disrupt protein functions.
Journal: Nature communications
Published: March 13, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026