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Microduplications of 16p11.2 are associated with schizophrenia.
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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
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The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
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Strong association of de novo copy number mutations with autism.
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KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
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Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling.
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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
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Functional impact of global rare copy number variation in autism spectrum disorders.
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Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
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Autism spectrum disorder susceptibility gene TAOK2 affects basal dendrite formation in the neocortex.
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The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
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Kctd13 deletion reduces synaptic transmission via increased RhoA.
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