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Neural correlates of genetically abnormal social cognition in Williams syndrome
Abstract
Williams-Beuren syndrome (WBS), caused by a microdeletion of approximately 21 genes on chromosome 7q11.23, is characterized by unique hypersociability combined with increased non-social anxiety. Using functional neuroimaging, we found reduced amygdala activation in individuals with WBS for threatening faces but increased activation for threatening scenes, relative to matched normal controls. Activation and interactions of prefrontal regions linked to amygdala, especially orbitofrontal cortex, were abnormal, suggesting a genetically controlled neural circuitry for regulating human social behavior.
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“Together, these previous findings suggest that dampened neural response to social threat leads to greater sociability.”
From Effects of MDMA on sociability and neural response to social threat and social reward (2009) · cites this paper as Meyer-Lindenberg et al. 2005
In the citing paper
“patients with Williams-Beuren syndrome, characterized by hypersociability, demonstrate attenuated amygdala responses to social threat (Meyer-Lindenberg et al. 2005).”
From Effects of MDMA on sociability and neural response to social threat and social reward (2009) · cites this paper as Meyer-Lindenberg et al. 2005
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Metadata
- Authors
- Meyer-Lindenberg, A., Hariri, A. R., Munoz, K. E., Mervis, C. B., Mattay, V. S., Morris, C. A., & Berman, K. F.
- Affiliations
- National Institutes of Health (US)
- University of Nevada, Las Vegas (US)
- Venue
- Nature Neuroscience
- Published
- 2005-07-10
- Volume
- 8
- Issue
- 8
- Pages
- 991-993
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W2044271964
- Cited by
- 357
- References
- 17
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 3 · 2023: 5 · 2022: 8 · 2021: 14 · 2020: 12 · 2019: 7 · 2018: 11 · 2017: 20 · 2016: 27 · 2015: 20 · 2014: 25 · 2013: 20 · 2012: 26
- FWCI
- 6.25
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS035102, NS35102)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Williams Syndrome Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- Williams syndrome, social cognition, amygdala, orbitofrontal cortex, threatening faces, hypersociability, chromosome 7q11.23 microdeletion, prefrontal cortex activation
- MeSH terms
- Amygdala, Anxiety, Brain, Brain Mapping, Cognition, Frontal Lobe, Humans, Magnetic Resonance Imaging, Social Behavior, Case-Control Studies, Prefrontal Cortex, Williams Syndrome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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