Exome sequencing of 85 Williams–Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior

Keyphrases

• Exome Sequencing 100%
• Major Contributor 100%
• Autism Spectrum Disorder 100%
• Social Behavior 100%
• Williams Syndrome 100%
• Behavioral Symptoms 66%
• Social Motivation 66%
• Social Phenotype 66%
• Whole Exome Sequencing 33%
• Non-coding Variants 33%
• Penetrant 33%
• Social Responsiveness Scale 33%
• New Patients 33%
• Exome 33%
• Relevant Genes 33%
• Targeted Analysis 33%
• Social Phobia 33%
• Duplication 33%
• Discovery-based 33%
• Patient Cohort 33%
• BAZ1B 33%
• Rare Variation 33%
• Common Variation 33%
• Social Cognition 33%
• Multigenic 33%
• Significant SNPs 33%
• Cognitive Phenotype 33%
• Physical Symptoms 33%
• Wide Scanning 33%
• GTF2IRD1 33%
• Social Cognitive 33%
• Social Communication 33%
• 7q11.23 33%
• New Allele 33%
• Cognitive Profile 33%

Neuroscience

• Exome Sequencing 100%
• Social Behavior 100%
• Williams Syndrome 100%
• Autism Spectrum Disorder 100%
• Behavior (Neuroscience) 33%
• Social Anxiety Disorder 33%
• Social Cognition 33%

Biochemistry, Genetics and Molecular Biology

• Exome Sequencing 100%
• Williams Syndrome 100%
• Exome 33%
• Allele 33%
• Single Nucleotide Polymorphism 33%
• Social Adaptation 33%
• Social Cognition 33%