# Williams Syndrome Research

**Type:** Topics  
**Canonical URL:** https://scholariq.org/topics/williams-syndrome-research/

## Facts

| Field | Value |
| --- | --- |
| Description | This cluster of papers explores the genetic, neurodevelopmental, cognitive, and behavioral aspects of Williams Syndrome. It covers topics such as the cognitive profile, social cognition, visuospatial processing, neuroanatomy, cardiovascular abnormalities, hypersociability, and language abilities associated with Williams Syndrome. |
| Domain | Life Sciences |
| Field | Neuroscience |
| OpenAlex ID | t13258 |
| Works | 42 |

## Topic papers all

Showing 15 of 42.

- [Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism](https://scholariq.org/papers/multiple-recurrent-de-novo-cnvs-including-duplications-of-the-7q11-23-williams/)
- [Mapping brain maturation](https://scholariq.org/papers/mapping-brain-maturation/)
- [Language acquisition in autism spectrum disorders: A developmental review](https://scholariq.org/papers/language-acquisition-in-autism-spectrum-disorders-a-developmental-review/)
- [A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke](https://scholariq.org/papers/a-sequence-variant-in-zfhx3-on-16q22-associates-with-atrial-fibrillation-and/)
- [Beyond Pragmatics: Morphosyntactic Development in Autism](https://scholariq.org/papers/beyond-pragmatics-morphosyntactic-development-in-autism/)
- [Mutations in Cardiac T-Box Factor Gene TBX20 are associated with Diverse Cardiac Pathologies, Including Defects of Septation and Valvulogenesis and Cardiomyopathy](https://scholariq.org/papers/mutations-in-cardiac-t-box-factor-gene-tbx20-are-associated-with-diverse-cardiac/)
- [More Is Not Always Better: Increased Fractional Anisotropy of Superior Longitudinal Fasciculus Associated with Poor Visuospatial Abilities in Williams Syndrome](https://scholariq.org/papers/more-is-not-always-better-increased-fractional-anisotropy-of-superior/)
- [Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome](https://scholariq.org/papers/cognitive-decline-preceding-the-onset-of-psychosis-in-patients-with-22q11-2/)
- [Motor Development and Neuropsychological Patterns in Persons with Down Syndrome](https://scholariq.org/papers/motor-development-and-neuropsychological-patterns-in-persons-with-down-syndrome/)
- [Linguistic Abilities in Italian Children With Williams Syndrome](https://scholariq.org/papers/linguistic-abilities-in-italian-children-with-williams-syndrome/)
- [Hypertrophic Cardiomyopathy: The Future of Treatment](https://scholariq.org/papers/hypertrophic-cardiomyopathy-the-future-of-treatment/)
- [How should children with West syndrome be efficiently and accurately investigated? Results from the National Infantile Spasms Consortium](https://scholariq.org/papers/how-should-children-with-west-syndrome-be-efficiently-and-accurately/)
- [Genetic and environmental contributions to abdominal aortic aneurysm development in a twin population](https://scholariq.org/papers/genetic-and-environmental-contributions-to-abdominal-aortic-aneurysm-development/)
- [Autistic Sociality](https://scholariq.org/papers/autistic-sociality/)
- [On Mosaics and Melting Pots: Conceptual Considerations of Comparison and Matching Strategies](https://scholariq.org/papers/on-mosaics-and-melting-pots-conceptual-considerations-of-comparison-and-matching/)

## Topic primary papers

- [Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism](https://scholariq.org/papers/multiple-recurrent-de-novo-cnvs-including-duplications-of-the-7q11-23-williams/)
- [Mapping brain maturation](https://scholariq.org/papers/mapping-brain-maturation/)
- [More Is Not Always Better: Increased Fractional Anisotropy of Superior Longitudinal Fasciculus Associated with Poor Visuospatial Abilities in Williams Syndrome](https://scholariq.org/papers/more-is-not-always-better-increased-fractional-anisotropy-of-superior/)
- [Linguistic Abilities in Italian Children With Williams Syndrome](https://scholariq.org/papers/linguistic-abilities-in-italian-children-with-williams-syndrome/)
- [Periventricular nodular heterotopia and Williams syndrome](https://scholariq.org/papers/periventricular-nodular-heterotopia-and-williams-syndrome/)
- [The developmental trajectory of disruptive behavior in Down syndrome, fragile X syndrome, Prader–Willi syndrome and Williams syndrome](https://scholariq.org/papers/the-developmental-trajectory-of-disruptive-behavior-in-down-syndrome-fragile-x/)
- [Voiding Dysfunction and the Williams-Beuren Syndrome: A Clinical and Urodynamic Investigation](https://scholariq.org/papers/voiding-dysfunction-and-the-williams-beuren-syndrome-a-clinical-and-urodynamic/)
- [Williams syndrome hemideletion and LIMK1 variation both affect dorsal stream functional connectivity](https://scholariq.org/papers/williams-syndrome-hemideletion-and-limk1-variation-both-affect-dorsal-stream/)
- [Gene of the month: <i>GTF2I</i>](https://scholariq.org/papers/gene-of-the-month-i-gtf2i-i/)
- [Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study](https://scholariq.org/papers/underrepresentation-of-phenotypic-variability-of-16p13-11-microduplication/)
- [Idiopathic infantile hypercalcaemia in 5-month old girl.](https://scholariq.org/papers/idiopathic-infantile-hypercalcaemia-in-5-month-old-girl/)
- [Imaging Genetics of Williams Syndrome](https://scholariq.org/papers/imaging-genetics-of-williams-syndrome/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.