“Everybody in the world is my friend” hypersociability in young children with Williams syndrome

Doyle, Teresa F., Bellugi, Ursula, Korenberg, Julie R., Graham, John·2004·American Journal of Medical Genetics Part A

Cited by (298)

Items 101–200 of 298

  1. Mother–Child Interaction as a Window to a Unique Social Phenotype in 22q11.2 Deletion Syndrome and in Williams Syndrome
    Omri Weisman, Ruth Feldman, Merav Burg-Malki, Miri Keren, Ronny Geva, Gil Diesendruck, Doron Gothelf · 2015 · Journal of Autism and Developmental Disorders
  2. The other side of the coin: Hypersociability
    Miklós Tóth · 2018 · Genes Brain & Behavior
  3. Siblings of children with Williams syndrome: Correlates of psychosocial adjustment and sibling relationship quality
    Katie R. Cebula, Amanda E. Gillooly, Laura Coulthard, Deborah Michelle Riby, Richard Patrick Hastings · 2019 · Research in Developmental Disabilities
  4. What does Williams syndrome reveal about the determinants of social behavior?
    Anna Järvinen, Ursula Bellugi · 2013 · Frontiers in Human Neuroscience
  5. Using novel control groups to dissect the amygdala's role in Williams syndrome
    Tricia A. Thornton‐Wells, Suzanne N. Avery, Jennifer Urbano Blackford · 2011 · Developmental Cognitive Neuroscience
  6. Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
    Yael Schönherz-Pine, Maayan Davidov, Ariel Knafo‐Noam, Hadas Zilkha, Gal Shoval, Gil Zalsman, Amos Frisch, Abraham Weizman, Doron Gothelf · 2014 · Journal of Neurodevelopmental Disorders
  7. Association between cerebral shape and social use of language in Williams syndrome
    Doron Gothelf, Yvonne M. Searcy, Judy Snitzer Reilly, Philip To Lai, Tope Lanre-Amos, Debra L. Mills, Julie R. Korenberg, Albert M. Galaburda, Ursula Bellugi, Allan L. Reiss · 2008 · American Journal of Medical Genetics Part A
  8. Performance on verbal and low-verbal false belief tasks: Evidence from children with Williams syndrome
    Jo Van Herwegen, Dagmara Dimitriou, Gabriella Rundblad · 2013 · Journal of Communication Disorders
  9. Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA
    Rachel Sayuri Honjo, Roberta Lelis Dutra, Érika Arai Furusawa, Évelin Aline Zanardo, Larissa Sampaio de Athayde, Leslie Domenici Kulikowski, Débora Romeo Bertola, Chong Ae Kim · 2015 · BioMed Research International
  10. The evolutionary social brain: From genes to psychiatric conditions
    Bernard J. Crespi, Christopher R. Badcock · 2008 · Behavioral and Brain Sciences
  11. The contribution of GTF2I haploinsufficiency to Williams syndrome
    Thanathom Chailangkarn, Chalongrat Noree, Alysson Renato Muotri · 2018 · Molecular and Cellular Probes
  12. An Examination of Social Skills, Friendship Quality, and Loneliness for Adults with Williams Syndrome
    Marisa H. Fisher, Cynde Katherine Josol, Carolyn M. Shivers · 2020 · Journal of Autism and Developmental Disorders
  13. Preliminary evidence of abnormal white matter related to the fusiform gyrus in Williams syndrome: a diffusion tensor imaging tractography study
    Brian W. Haas, Fumiko Hoeft, Naama Barnea‐Goraly, Golijeh Golarai, Ursula Bellugi, Allan L. Reiss · 2011 · Genes Brain & Behavior
  14. Idiom comprehension in French-speaking children and adolescents with Williams’ syndrome
    Agnès Lacroix, Marc Aguert, Virginie Dardier, Vesna Stojanovik, Virginie Laval · 2010 · Research in Developmental Disabilities
  15. Parent-Reported Communication Abilities of Children with Sotos Syndrome: Evidence from the Children’s Communication Checklist-2
    Chloe Lane, Jo Van Herwegen, Megan Freeth · 2018 · Journal of Autism and Developmental Disorders
  16. Musicality Correlates With Sociability and Emotionality in Williams Syndrome
    Rowena Ng, Philip To Lai, Daniel J. Levitin, Ursula Bellugi · 2013 · Journal of Mental Health Research in Intellectual Disabilities
  17. Typical visual search performance and atypical gaze behaviors in response to faces in Williams syndrome
    Masahiro Hirai, Yukako Muramatsu, Seiji Mizuno, Naoko Kurahashi, Hirokazu Kurahashi, Miho Nakamura · 2016 · Journal of Neurodevelopmental Disorders
  18. Consistent hypersocial behavior in mice carrying a deletion of Gtf2i but no evidence of hyposocial behavior with Gtf2i duplication: Implications for Williams–Beuren syndrome and autism spectrum disorder
    Loren A. Martin, Erica Iceberg, Gabriel Allaf · 2017 · Brain and Behavior
  19. Parent report of antidepressant, anxiolytic, and antipsychotic medication use in individuals with Williams syndrome: Effectiveness and adverse effects
    Marilee A. Martens, Daisha L. Seyfer, Rebecca Andridge, Jessica E.A. Foster, Monali Chowdhury, Kelsey E. McClure, Daniel Lee Coury · 2012 · Research in Developmental Disabilities
  20. Induced Chromosome Deletion in a Williams-Beuren Syndrome Mouse Model Causes Cardiovascular Abnormalities
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  21. Abnormalities in early visual processes are linked to hypersociability and atypical evaluation of facial trustworthiness: An ERP study with Williams syndrome
    Danielle M. Shore, Rowena Ng, Ursula Bellugi, Debra L. Mills · 2017 · Cognitive Affective & Behavioral Neuroscience
  22. Neuron density is decreased in the prefrontal cortex in Williams syndrome
    Lew, Caroline Horton, Brown, Chelsea, Bellugi, Ursula, Semendeferi, Katerina · 2017 · Autism Research
  23. Autism and Williams syndrome: truly mirror conditions in the socio-cognitive domain?
    Amy Niego, Antonio Benítez‐Burraco · 2020 · International Journal of Developmental Disabilities
  24. Featural versus configural face processing in a rare genetic disorder: Williams syndrome
    Linda Isaac, A. J. Lincoln · 2011 · Journal of Intellectual Disability Research
  25. The Association of Intelligence, Visual-Motor Functioning, and Personality Characteristics With Adaptive Behavior in Individuals With Williams Syndrome
    Trista Juhsin Fu, Alan J. Lincoln, Ursula Bellugi, Yvonne M. Searcy · 2015 · American Journal on Intellectual and Developmental Disabilities
  26. Face repetition detection and social interest: An ERP study in adults with and without Williams syndrome
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  27. Empathic responsiveness and helping behaviours in young children with Williams syndrome
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  28. Joint Attention and Early Social Developmental Cascades in Neurogenetic Disorders
    Laura J. Hahn · 2016 · International review of research in developmental disabilities
  29. Characterizing associations and dissociations between anxiety, social, and cognitive phenotypes of Williams syndrome
    Rowena Ng, Anna M. Järvinen, Ursula Bellugi · 2014 · Research in Developmental Disabilities
  30. Regionally specific increased volume of the amygdala in Williams syndrome: Evidence from surface‐based modeling
    Brian W. Haas, Kristen E. Sheau, Ryan G. Kelley, Paul M. Thompson, Allan L. Reiss · 2012 · Human Brain Mapping
  31. Autonomic response to approachability characteristics, approach behavior, and social functioning in Williams syndrome
    Anna M. Järvinen, Rowena Ng, Ursula Bellugi · 2015 · Neuropsychologia
  32. Parent insights into atypicalities of social approach behaviour in Williams syndrome
    Emma Lough, Jacqui Rodgers, E. Janes, Katie Little, Deborah Michelle Riby · 2016 · Journal of Intellectual Disability Research
  33. Language and emotional abilities in children with Williams syndrome and children with autism spectrum disorder: similarities and differences
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  34. A comparison between linguistic skills and socio‐communicative abilities in Williams syndrome
    Paolo Alfieri, Deny Menghini, Luigi Marotta, Lavinia De Peppo, Lucilla Ravà, Fortunata Salvaguardia, Cristiana Varuzza, Stefano Vicari · 2017 · Journal of Intellectual Disability Research
  35. A cross-syndrome approach to the social phenotype of neurodevelopmental disorders: Focusing on social vulnerability and social interaction style
    Ellen Ridley, Deborah Michelle Riby, Susan Leekam · 2020 · Research in Developmental Disabilities
  36. Do you have a question for me? How children with Williams syndrome respond to ambiguous referential communication during a joint activity
    Daniela Plesa Skwerer, Emily Ammerman, Helen B. Tager-Flusberg · 2012 · Journal of Child Language
  37. Online and Face-to-Face Performance on Two Cognitive Tasks in Children With Williams Syndrome
    Maria Ashworth, Olympia Palikara, Elizabeth Burchell, Harry Robert McSweeney Purser, Dritan Nikolla, Jo Van Herwegen · 2021 · Frontiers in Psychology
  38. Hypersociability associated with developmental delay, macrocephaly and facial dysmorphism points to CHD3 mutations
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  39. Co-Treatment With Verapamil and Curcumin Attenuates the Behavioral Alterations Observed in Williams–Beuren Syndrome Mice by Regulation of MAPK Pathway and Microglia Overexpression
    Paula Ortiz‐Romero, Alejandro González-Simón, Gustavo Egea, Luis Alberto Pérez Jurado, Victoria Campuzano · 2021 · Frontiers in Pharmacology
  40. Prosodic abilities of Spanish-speaking adolescents and adults with Williams syndrome
    Pastora Martínez‐Castilla, María Sotillo, Ruth Campos · 2010 · Language and Cognitive Processes
  41. Problem behaviour and psychosocial functioning in young children with Williams syndrome: parent and teacher perspectives
    Bonnie Klein-Tasman, Ki-hak Lee · 2017 · Journal of Intellectual Disability Research
  42. Genetics of Domesticated Behavior in Dogs and Foxes
    Anna V. Kukekova, Lyudmila N. Trut, Gregory M. Acland · 2013 · Elsevier eBooks
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  44. Exome sequencing of 85 Williams–Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior
    Nathan Kopp, Phoebe C. R. Parrish, Michael Lugo, Joseph D. Dougherty, Beth A. Kozel · 2018 · Molecular Genetics & Genomic Medicine
  45. Altered White Matter and microRNA Expression in a Murine Model Related to Williams Syndrome Suggests That miR-34b/c Affects Brain Development via Ptpru and Dcx Modulation
    Meitar Grad, Ariel Nir, Gilad Levy, Sari Schokoroy Trangle, Guy Shapira, Noam Shomron, Yaniv Assaf, Boaz Barak · 2022 · Cells
  46. What We Do and Don’t Know About Joint Attention
    Henrike Moll · 2023 · Topoi
  47. Mental Illness, Behavior Problems, and Social Behavior in Adults With Down Syndrome
    Claudio Straccia, Stéphanie Baggio, Koviljka Barisnikov · 2013 · Journal of Mental Health Research in Intellectual Disabilities
  48. There's that scary picture: Attention bias to threatening scenes in Williams syndrome
    Helen Frances Dodd, Melanie A. Porter · 2010 · Neuropsychologia
  49. A Dual Comparative Approach: Integrating Lines of Evidence from Human Evolutionary Neuroanatomy and Neurodevelopmental Disorders
    Kari L. Hanson, Branka Hrvoj-Mihić, Katerina Semendeferi · 2014 · Brain Behavior and Evolution
  50. Social adaptive skills and psychopathology in adults with intellectual disabilities of non-specific origin and those with Down syndrome
    Koviljka Barisnikov, Claudio Straccia · 2019 · Research in Developmental Disabilities
  51. Williams Syndrome
    Deborah Michelle Riby, Melanie A. Porter · 2010 · Advances in child development and behavior
  52. Autism and Williams syndrome: Dissimilar socio-cognitive profiles with similar patterns of abnormal gene expression in the blood
    Amy Niego, Antonio Benítez‐Burraco · 2020 · Autism
  53. Cognitive and social profiles in two patients with cobalamin C disease
    Miriam H. Beauchamp, V. Anderson, Avihu Boneh · 2009 · Journal of Inherited Metabolic Disease
  54. Attention allocation to facial expressions of emotion among persons with Williams and Down syndromes
    Karen J. Goldman, Cory Shulman, Yair Bar‐Haim, Rany Abend, Jacob A. Burack · 2016 · Development and Psychopathology
  55. Increased glia density in the caudate nucleus in williams syndrome: Implications for frontostriatal dysfunction in autism
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  56. Mental health problems in children and adolescents with intellectual disability
    Kylie M. Gray, Caroline Mohr · 2004 · Current Opinion in Psychiatry
  57. Parent-child interaction as a dynamic contributor to learning and cognitive development in typical and atypical development / Influencia dinámica entre la interacción padre/madre-hijo y el aprendizaje y el desarrollo cognitivo en el desarrollo típico y atípico
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  58. The use of emotions in narratives in Williams syndrome
    Jo Van Herwegen, Ana Aznar, Harriet R. Tenenbaum · 2014 · Journal of Communication Disorders
  59. Preserved search asymmetry in the detection of fearful faces among neutral faces in individuals with Williams syndrome revealed by measurement of both manual responses and eye tracking
    Masahiro Hirai, Yukako Muramatsu, Seiji Mizuno, Naoko Kurahashi, Hirokazu Kurahashi, Miho Nakamura · 2017 · Journal of Neurodevelopmental Disorders
  60. A Distance-Delivered Social Skills Program for Young Adults with Williams Syndrome: Evaluating Feasibility and Preliminary Efficacy
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  61. Behavioural features of Italian infants and young adults with Williams–Beuren syndrome
    Chiara Gagliardi, S. Martelli, Alessandro Tavano, Renato Borgatti · 2011 · Journal of Intellectual Disability Research
  62. Cortisol Reactivity and Performance Abilities in Social Situations in Adults with Williams Syndrome
    Miriam Diane Lense, Elisabeth M. Dykens · 2013 · American Journal on Intellectual and Developmental Disabilities
  63. Sudden unexpected death in a toddler with Williams syndrome
    Henry F. Krous, Carter E. Wahl, Amy E. Chadwick · 2008 · Forensic Science Medicine and Pathology
  64. The Central Role of Etiology in Science and Practice in Intellectual Disability
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  65. Extensive characterization of a Williams syndrome murine model shows Gtf2ird1‐mediated rescue of select sensorimotor tasks, but no effect on enhanced social behavior
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  66. Decreased Neuron Density and Increased Glia Density in the Ventromedial Prefrontal Cortex (Brodmann Area 25) in Williams Syndrome
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  67. Reasoning About Trust Among Individuals With Williams Syndrome
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  68. Differential Relationships of Anxiety and Autism Symptoms on Social Skills in Young Boys With Fragile X Syndrome
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  69. Attribution of negative intention in Williams syndrome
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  70. Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I
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