Review

Nature Reviews Neuroscience 7, 380-393 (May 2006) | doi:10.1038/nrn1906

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour

Andreas Meyer-Lindenberg1,2,3, Carolyn B. Mervis4 & Karen Faith Berman3,5  About the authors

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Williams syndrome, a rare disorder caused by hemizygous microdeletion of about 28 genes on chromosome 7q11.23, has long intrigued neuroscientists with its unique combination of striking behavioural abnormalities, such as hypersociability, and characteristic neurocognitive profile. Williams syndrome, therefore, raises fundamental questions about the neural mechanisms of social behaviour, the modularity of mind and brain development, and provides a privileged setting to understand genetic influences on complex brain functions in a 'bottom-up' way. We review recent advances in uncovering the functional and structural neural substrates of Williams syndrome that provide an emerging understanding of how these are related to dissociable genetic contributions characterized both in special participant populations and animal models.

Author affiliations

  1. Unit for Systems Neuroscience in Psychiatry, National Institute of Mental Health, NIH, DHHS, 9000 Rockville Pike, Bethesda, Maryland 20892-1365, USA.
  2. Neuroimaging Core Facility, National Institute of Mental Health, NIH, DHHS, 9000 Rockville Pike, Bethesda, Maryland 20892-1365, USA.
  3. Genes, Cognition and Psychosis Program, National Institute of Mental Health, NIH, DHHS, 9000 Rockville Pike, Bethesda, Maryland 20892-1365, USA.
  4. Neurodevelopmental Sciences Laboratory, Department of Psychological and Brain Sciences, University of Louisville, Louisville, Kentucky 40292, USA.
  5. Section on Integrative Neuroimaging, National Institute of Mental Health, NIH, DHHS, 9000 Rockville Pike, Bethesda, Maryland 20892-1365, USA.

Correspondence to: Andreas Meyer-Lindenberg1,2,3 Email: andreasml@nih.gov

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