Associated Papers
Novel TBR1 c.1303C>T Variant Led to Diagnosis of Intellectual Developmental Disorder with Autism and Speech Delay: Application of Comprehensive Family-Based Whole-Genome Analysis.
Ćuk M et al.
Genes, 2025
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions.
Sollis E et al.
Human Molecular Genetics, 2023
A de novo frameshift pathogenic variant in TBR1 identified in autism without intellectual disability.
Sapey-Triomphe LA et al.
Human Genomics, 2020
Functional characterization of TBR1 variants in neurodevelopmental disorder.
den Hoed J et al.
Scientific Reports, 2018
The TBR1-related autistic-spectrum-disorder phenotype and its clinical spectrum.
McDermott JH et al.
European Journal of Medical Genetics, 2018
Brain-specific transcriptional regulator T-brain-1 controls brain wiring and neuronal activity in autism spectrum disorders.
Huang TN et al.
Frontiers in Neuroscience, 2015
De novo TBR1 mutations in sporadic autism disrupt protein functions.
Deriziotis P et al.
Nature Communications, 2014
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