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Concurrent predictors of mathematics achievement for 9-year-old children with Williams syndrome

Scientific reports, 2024-01, Vol.14 (1), p.2454-16, Article 2454

2024

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Contrasting neurofunctional correlates of face- and visuospatial-processing in children and adolescents with Williams syndrome: convergent results from four fMRI paradigms

Scientific reports, 2024-05, Vol.14 (1), p.10304-10304, Article 10304

2024

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Age at Onset of Declarative Gestures and 24-Month Expressive Vocabulary Predict Later Language and Intellectual Abilities in Young Children With Williams Syndrome

Frontiers in psychology, 2019-12, Vol.10, p.2648-2648

2019

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Neural Basis of Genetically Determined Visuospatial Construction Deficit in Williams Syndrome

Neuron (Cambridge, Mass.), 2004-09, Vol.43 (5), p.623-631

2004

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Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23

American journal of human genetics, 2015-08, Vol.97 (2), p.216-227

2015

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

Nature reviews. Neuroscience, 2006-05, Vol.7 (5), p.380-393

2006

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Neurobehavioral implications of habitual snoring in children

Pediatrics (Evanston), 2004-07, Vol.114 (1), p.44-49

2004

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Executive function as measured by the Behavior Rating Inventory of Executive Function‐2: children and adolescents with Williams syndrome

Journal of intellectual disability research, 2022-01, Vol.66 (1-2), p.94-107

2022

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Neural correlates of genetically abnormal social cognition in Williams syndrome

Nature neuroscience, 2005-08, Vol.8 (8), p.991-993

2005

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Duplication of GTF2I Results in Separation Anxiety in Mice and Humans

American journal of human genetics, 2012-06, Vol.90 (6), p.1064-1070

2012

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Neuropsychological components of intellectual disability: the contributions of immediate, working, and associative memory

Journal of intellectual disability research, 2010-05, Vol.54 (5), p.406-417

2010

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Neurobehavioral correlates of sleep‐disordered breathing in children

Journal of sleep research, 2004-06, Vol.13 (2), p.165-172

2004

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Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype

Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.6-11, Article 6

2021

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Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function

Proceedings of the National Academy of Sciences - PNAS, 2012-04, Vol.109 (14), p.E860-E866

2012

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Sleep characteristics and problems of 2-year-olds with Williams syndrome: relations with language and behavior

Journal of neurodevelopmental disorders, 2020-12, Vol.12 (1), p.32-32, Article 32

2020

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Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome

Journal of neurodevelopmental disorders, 2023-08, Vol.15 (1), p.1-29, Article 29

2023

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The Williams Syndrome Cognitive Profile

Brain and cognition, 2000-12, Vol.44 (3), p.604-628

2000

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Patterns and predictors of adaptive skills in 2- to 7-year-old children with Down syndrome

Journal of neurodevelopmental disorders, 2022-03, Vol.14 (1), p.18-18, Article 18

2022

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Genetic Contributions to Human Gyrification: Sulcal Morphometry in Williams Syndrome

The Journal of neuroscience, 2005-08, Vol.25 (34), p.7840-7846

2005

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7q11.23 deletion and duplication

Current opinion in genetics & development, 2021-06, Vol.68, p.41-48

2021

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Effects of Varying Levels of Expertise on the Basic Level of Categorization

Journal of experimental psychology. General, 1997-09, Vol.126 (3), p.248-277

1997

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Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome

Journal of the American Heart Association, 2024-02, Vol.13 (3), p.e031377-e031377

2024

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DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number

Npj genomic medicine, 2023-09, Vol.8 (1), p.25-11, Article 25

2023

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WILLIAMS SYNDROME AND RELATED DISORDERS

Annual review of genomics and human genetics, 2000-01, Vol.1 (1), p.461-484

2000

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Methodological issues in group-matching designs: alpha levels for control variable comparisons and measurement characteristics of control and target variables

Journal of autism and developmental disorders, 2004-02, Vol.34 (1), p.7-17

2004

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Concurrent predictors of mathematics achievement for 9-year-old children with Williams syndrome

Contrasting neurofunctional correlates of face- and visuospatial-processing in children and adolescents with Williams syndrome: convergent results from four fMRI paradigms

Age at Onset of Declarative Gestures and 24-Month Expressive Vocabulary Predict Later Language and Intellectual Abilities in Young Children With Williams Syndrome

Neural Basis of Genetically Determined Visuospatial Construction Deficit in Williams Syndrome

Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23

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

Neurobehavioral implications of habitual snoring in children

Executive function as measured by the Behavior Rating Inventory of Executive Function‐2: children and adolescents with Williams syndrome

Neural correlates of genetically abnormal social cognition in Williams syndrome

Duplication of GTF2I Results in Separation Anxiety in Mice and Humans

Neuropsychological components of intellectual disability: the contributions of immediate, working, and associative memory

Neurobehavioral correlates of sleep‐disordered breathing in children

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype

Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function

Sleep characteristics and problems of 2-year-olds with Williams syndrome: relations with language and behavior

Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome

The Williams Syndrome Cognitive Profile

Patterns and predictors of adaptive skills in 2- to 7-year-old children with Down syndrome

Genetic Contributions to Human Gyrification: Sulcal Morphometry in Williams Syndrome

7q11.23 deletion and duplication

Effects of Varying Levels of Expertise on the Basic Level of Categorization

Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome

DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number

WILLIAMS SYNDROME AND RELATED DISORDERS

Methodological issues in group-matching designs: alpha levels for control variable comparisons and measurement characteristics of control and target variables

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