Cited by 357Williams Syndrome ResearchFace Recognition and PerceptionGenetics and Neurodevelopmental Disorders

Neural correlates of genetically abnormal social cognition in Williams syndrome

Meyer-Lindenberg, Andreas, Hariri, Ahmad R, Munoz, Karen E, Mervis, Carolyn B, Mattay, Venkata S, Morris, Colleen A, Berman, Karen Faith·2005·Nature Neuroscience

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.

Integrity signals

Registry

Crossref · 10.1038/nn1494

Cites

17 of 17 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Cites

Flagged first, then by citations

Cited by

Sorted by citations

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
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 ›

Are you an author, or do you see a problem with this page? Request a review