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De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature
CAUSES Study
Division of Genetics and Genomic Medicine
Center for the Investigation of Membrane Excitability Diseases
Institute of Clinical and Translational Sciences (ICTS)
Research output
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Contribution to journal
›
Article
›
peer-review
24
Scopus citations
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Dive into the research topics of 'De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature'. Together they form a unique fingerprint.
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Keyphrases
Intellectual Disability
100%
Autistic Traits
100%
Neurocognitive
100%
Tbr1
100%
Autism Spectrum Disorder
37%
Structural Brain Abnormalities
25%
Hippocampus
12%
Neocortical
12%
Proband
12%
Cerebral Cortex
12%
Risk Genes
12%
Mutant Mice
12%
Dysgenesis
12%
Clinical Reports
12%
Structural Brain
12%
Geneticists
12%
Neurodevelopmental Disorders
12%
Brain Malformation
12%
FMRI Analysis
12%
International Data Sharing
12%
Facial Features
12%
MRI Images
12%
Anterior Commissure
12%
Human Disease Genes
12%
T-box Transcription Factors
12%
Biochemistry, Genetics and Molecular Biology
Intellectual Disability
100%
TBR1
100%
Magnetic Resonance Imaging
25%
Proband
12%
Candidate Gene
12%
Mouse Mutant
12%
T Box Transcription Factor
12%