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

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

Ewart, A. K., Morris, C. A., Atkinson, D., Jin, W., Sternes, K., Spallone, P., Stock, A. D., Leppert, M., & Keating, M. T. (1993) · Nature Genetics · doi:10.1038/ng0993-11 · Cited by 1,138 · see citing works

I. The Neurocognitive Profile of Williams Syndrome: A Complex Pattern of Strengths and Weaknesses

Bellugi, U., Lichtenberger, L., Jones, W., Lai, Z. C., & George, M. S. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900561959 · Cited by 706 · see citing works

LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition

Frangiskakis, J. M., Ewart, A. K., Morris, C. A., Mervis, C. Β., Bertrand, J., Robinson, B. F., Klein, B. P., Ensing, G. J., Everett, L. A., Green, E. D., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)80077-x · Cited by 555 · see citing works

II. Hypersociability in Williams Syndrome

Jones, W., Bellugi, U., Lai, Z., Chiles, M., Reilly, J., Lincoln, A., & Adolphs, R. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900561968 · Cited by 503 · see citing works

Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome

Bellugi, U., Lichtenberger, L., Mills, D. L., Galaburda, A. M., & Korenberg, J. R. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01397-1 · Cited by 351 · see citing works

Anxiety, Fears, and Phobias in Persons With Williams Syndrome

Dykens, E. M. (2003) · Developmental Neuropsychology · doi:10.1080/87565641.2003.9651896 · Cited by 289 · see citing works

VI. Genome structure and cognitive map of Williams syndrome

Korenberg, J. R., Chen, X.-N., Hirota, H., Lai, Z., Bellugi, U., Burian, D., Roe, B., & Matsuoka, R. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900562002 · Cited by 285 · see citing works

Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis

Li, D. (1997) · Human Molecular Genetics · doi:10.1093/hmg/6.7.1021 · Cited by 284 · see citing works

Williams Syndrome and Related Disorders

Morris, C. A., & Mervis, C. Β. (2000) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.1.1.461 · Cited by 247 · see citing works

COGNITIVE ABILITIES AND BEHAVIOURAL CHARACTERISTICS OF CHILDREN WITH IDIOPATHIC INFANTILE HYPERCALCAEMIA

Udwin, O., Yule, W., & Martin, N. (1987) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.1987.tb00212.x · Cited by 235 · see citing works

Towards the neural basis for hypersociability in a genetic syndrome

Bellugi, U., Adolphs, R., Cassady, C., & Chiles, M. (1999) · NeuroReport · doi:10.1097/00001756-199906030-00006 · Cited by 207 · see citing works

Chromosome 22q11 deletion syndrome: Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications

Swillen, A., Vogels, A., Devriendt, K., & Fryns, J. P. (2000) · American Journal of Medical Genetics · doi:10.1002/1096-8628(200022)97:2 · Cited by 188 · see citing works

Personality characteristics and behaviour problems in individuals of different ages with Williams syndrome

Gosch, A., & Pankau, R. (1997) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.1997.tb07481.x · Cited by 185 · see citing works

Anxiety, Fears, and Phobias in Persons With Williams Syndrome

Dykens, E. M. (2003) · Developmental Neuropsychology · doi:10.1207/s15326942dn231&2_13 · Cited by 148 · see citing works

Social‐emotional and behavioral adjustment in children with Williams‐Beuren syndrome

Gosch, A., & Pankau, R. (1994) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320530406 · Cited by 141 · see citing works

Temperament in Williams syndrome

Tomc, S. A., Williamson, N. K., & Pauli, R. M. (1990) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320360321 · Cited by 100 · see citing works

Mental Retardation Related to Hypercalcaemia

von Arnim, G., & Engel, P. (1964) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.1964.tb08138.x · Cited by 88 · see citing works

Williams syndrome: an exploration of neurocognitive and genetic features

Bellugi, U., Korenberg, J. R., & Klima, E. S. (2001) · Clinical Neuroscience Research · doi:10.1016/s1566-2772(01)00008-1 · Cited by 47 · see citing works

Preface

Bellugi, U., & George, M. S. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900561940 · Cited by 15 · see citing works

BAC Resource for Molecular Cytogenetics

Chen, X., & Korenberg, J. R. (2003) · Molecular Cytogenetics · doi:10.1385/1-59259-300-3:391 · Cited by 5 · see citing works

Untitled work

(2000) · doi:10.1002/1098-2779(2000)6:2

Can we safely target the WNT pathway?

Kahn, M. (2014) · Nature Reviews Drug Discovery · doi:10.1038/nrd4233 · Cited by 1,039 · see citing works

Automated apparatus for quantitation of social approach behaviors in mice

Nadler, J. J., Moy, S. S., Dold, G., Trang, D., Simmons, N., Perez, A., Young, N. B., Barbaro, R. P., Piven, J., Magnuson, T. R., et al. (2004) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2004.00071.x · Cited by 775 · see citing works

Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype

Martens, M. A., Wilson, S. J., & Reutens, D. C. (2008) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2008.01887.x · Cited by 479 · see citing works

Language abilities in Williams syndrome: A critical review

Brock, J. (2007) · Development and Psychopathology · doi:10.1017/s095457940707006x · Cited by 323 · see citing works

Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings

Dichter, G. S., Damiano, C. A., & Allen, J. A. (2012) · Journal of Neurodevelopmental Disorders · doi:10.1186/1866-1955-4-19 · Cited by 299 · see citing works

Do Faces Capture the Attention of Individuals with Williams Syndrome or Autism? Evidence from Tracking Eye Movements

Riby, D. M., & Hancock, P. J. B. (2009) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-008-0641-z · Cited by 259 · see citing works

Wnt/β-catenin signaling plays an ever-expanding role in stem cell self-renewal, tumorigenesis and cancer chemoresistance

Mohammed, M. K., Shao, C. C., Wang, J., Wei, Q., Wang, X. W., Collier, Z. J., Tang, S., Liu, H., Zhang, F., Huang, J., et al. (2016) · Genes & Diseases · doi:10.1016/j.gendis.2015.12.004 · Cited by 260 · see citing works

Looking at movies and cartoons: eye‐tracking evidence from Williams syndrome and autism

Riby, D. M., & Hancock, P. (2008) · Journal of Intellectual Disability Research · doi:10.1111/j.1365-2788.2008.01142.x · Cited by 224 · see citing works

Neurobiology of social behavior abnormalities in autism and Williams syndrome

Barak, B., & Feng, G. (2016) · Nature Neuroscience · doi:10.1038/nn.4276 · Cited by 224 · see citing works

Wnt signaling in development and disease

Freese, J. L., Pino, D., & Pleasure, S. J. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.09.003 · Cited by 219 · see citing works

A human neurodevelopmental model for Williams syndrome

Chailangkarn, T., Trujillo, C. A., Freitas, B. C., Hrvoj-Mihic, B., Herai, R. H., Yu, D. X., Brown, T. T., Marchetto, M. C., Bardy, C., McHenry, L., et al. (2016) · Nature · doi:10.1038/nature19067 · Cited by 195 · see citing works

Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders

Schumann, C. M., Bauman, M. D., & Amaral, D. G. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.09.028 · Cited by 178 · see citing works

Structural variants in genes associated with human Williams-Beuren syndrome underlie stereotypical hypersociability in domestic dogs

vonHoldt, B. M., Shuldiner, E., Koch, I. J., Kartzinel, R. Y., Hogan, A., Brubaker, L., Wanser, S., Stahler, D., Wynne, C. D. L., Ostrander, E. A., et al. (2017) · Science Advances · doi:10.1126/sciadv.1700398 · Cited by 186 · see citing works

Symmetry of Cortical Folding Abnormalities in Williams Syndrome Revealed by Surface-Based Analyses

Essen, D. C. V., Dierker, D. L., Snyder, A. Z., Raichle, M. E., Reiss, A. L., & Korenberg, J. R. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4154-05.2006 · Cited by 183 · see citing works

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior

Järvinen-Pasley, A., Bellugi, U., Reilly, J., MILLS, D. L., Galaburda, A., Reiss, A. L., & Korenberg, J. R. (2008) · Development and Psychopathology · doi:10.1017/s0954579408000011 · Cited by 177 · see citing works

Is everybody always my friend? Perception of approachability in Williams syndrome

Frigerio, E., Burt, D. M., Gagliardi, C., Cioffi, G., Martelli, S., Perrett, D. I., & Borgatti, R. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2005.05.008 · Cited by 165 · see citing works

The social phenotype of Williams syndrome

Järvinen, A., Korenberg, J. R., & Bellugi, U. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.12.006 · Cited by 161 · see citing works

Aversion, awareness, and attraction: investigating claims of hyperacusis in the Williams syndrome phenotype

Levitin, D. J., Cole, K., Lincoln, A. J., & Bellugi, U. (2005) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2004.00376.x · Cited by 141 · see citing works

Hyperacusis in Williams syndrome

Gothelf, D., Farber, N., Raveh, E., Apter, A., & Attias, J. (2006) · Neurology · doi:10.1212/01.wnl.0000196643.35395.5f · Cited by 141 · see citing works

Perceiving facial and vocal expressions of emotion in individuals with Williams syndrome

Plesa-Skwerer, D., Faja, S., Schofield, C., Verbalis, A., & Tager-Flusberg, H. (2006) · American Journal on Mental Retardation · doi:10.1352/0895-8017(2006)111[15:pfaveo]2.0.co;2 · Cited by 136 · see citing works

Genetic Influences on Sociability: Heightened Amygdala Reactivity and Event-Related Responses to Positive Social Stimuli in Williams Syndrome

Haas, B. W., Mills, D. L., Yam, A., Hoeft, F., Bellugi, U., & Reiss, A. L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5324-08.2009 · Cited by 136 · see citing works

Characterizing the Musical Phenotype in Individuals With Williams Syndrome

Levitin, D. J., Cole, K., Chiles, M., Lai, Z. C., Lincoln, A. J., & Bellugi, U. (2004) · Child Neuropsychology · doi:10.1080/09297040490909288 · Cited by 124 · see citing works

Socio-Communicative Deficits in Young Children with Williams Syndrome: Performance on the Autism Diagnostic Observation Schedule

Klein-Tasman, B., Mervis, C. Β., Lord, C., & Phillips, K. D. (2006) · Child Neuropsychology · doi:10.1080/09297040601033680 · Cited by 129 · see citing works

Approachability and the amygdala: Insights from Williams syndrome

Martens, M. A., Wilson, S. J., Dudgeon, P., & Reutens, D. C. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.04.017 · Cited by 121 · see citing works

Age‐related differences in neural correlates of face recognition during the toddler and preschool years

Carver, L. J., Dawson, G., Panagiotides, H., Meltzoff, A. N., McPartland, J. C., Gray, J., & MUNSON, J. A. (2003) · Developmental Psychobiology · doi:10.1002/dev.10078 · Cited by 111 · see citing works

Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1‐targeted mice

Young, E. J., Lipina, T. V., Tam, E., Mandel, A., Clapcote, S. J., Bechard, A. R., Chambers, J., Mount, H. T. J., Fletcher, P. J., Roder, J., et al. (2007) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2007.00343.x · Cited by 109 · see citing works

Is it Williams syndrome?GTF2IRD1implicated in visual–spatial construction andGTF2Iin sociability revealed by high resolution arrays

Dai, L., Bellugi, U., Chen, X. ‐., Pulst‐Korenberg, A. M., Järvinen‐Pasley, A., Tirosh‐Wagner, T., Eis, P. S., Graham, J. M., Mills, D. L., Searcy, Y. M., et al. (2009) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.32652 · Cited by 107 · see citing works

Induced chromosome deletions cause hypersociability and other features of Williams–Beuren syndrome in mice

Li, H. H., Roy, M., Kusçuoglu, U., Spencer, C. M., Halm, B., Harrison, K. C., Bayle, J. H., Splendore, A., Ding, F., Meltzer, L. A., et al. (2009) · EMBO Molecular Medicine · doi:10.1002/emmm.200900003 · Cited by 104 · see citing works

Social Interaction Behaviors Discriminate Young Children With Autism and Williams Syndrome

Lincoln, A. J., Searcy, Y. M., JONES, W., & Lord, C. (2007) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/chi.0b013e31802b9522 · Cited by 94 · see citing works

Honing in on the Social Phenotype in Williams Syndrome Using Multiple Measures and Multiple Raters

Klein-Tasman, B., Li-Barber, K. T., & Magargee, E. T. (2010) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-010-1060-5 · Cited by 90 · see citing works

What gene–environment interactions can tell us about social competence in typical and atypical populations

Iarocci, G., Yager, J., & Elfers, T. (2007) · Brain and Cognition · doi:10.1016/j.bandc.2007.01.008 · Cited by 87 · see citing works

Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome

van Hagen, J. M., van der Geest, J. N., van der Giessen, R. S., Haselen, G. C. L.-V., Eussen, H. J., Gille, J. J. P., Govaerts, L. C. P., Wouters, C. H., de Coo, I. F. M., Hoogenraad, C. C., et al. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.12.009 · Cited by 84 · see citing works

Behavioral phenotypes of genetic syndromes with intellectual disability: Comparison of adaptive profiles

Nuovo, S. D., & Buono, S. (2011) · Psychiatry Research · doi:10.1016/j.psychres.2011.03.015 · Cited by 82 · see citing works

Auditory Attraction: Activation of Visual Cortex by Music and Sound in Williams Syndrome

Thornton‐Wells, T. A., Cannistraci, C. J., Anderson, A. W., Kim, C.-Y., Eapen, M., Gore, J. C., Blake, R., & Dykens, E. M. (2010) · American Journal on Intellectual and Developmental Disabilities · doi:10.1352/1944-7588-115.172 · Cited by 74 · see citing works

To modulate or not to modulate: Differing results in uniquely shaped Williams syndrome brains

Eckert, M. A., Tenforde, A. S., Galaburda, A. M., Bellugi, U., Korenberg, J. R., Mills, D. L., & Reiss, A. L. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.05.014 · Cited by 74 · see citing works

Theory of Mind in Williams Syndrome Assessed Using a Nonverbal Task

Porter, M. A., Coltheart, M., & Langdon, R. A. (2007) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-007-0447-4 · Cited by 70 · see citing works

Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder

Puimedon, M. S., Sahún, I., Velot, É., Dubus, P. R., Borralleras, C., Rodrigues, A. J., Valero, M. C., Valverde, O., Sousa, N., Hérault, Y., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu368 · Cited by 69 · see citing works

Regional Brain Differences in Cortical Thickness, Surface Area and Subcortical Volume in Individuals with Williams Syndrome

Meda, S. A., Pryweller, J. R., & Thornton‐Wells, T. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031913 · Cited by 66 · see citing works

Gaze aversion as a cognitive load management strategy in autism spectrum disorder and Williams syndrome

Doherty‐Sneddon, G., Riby, D. M., & Whittle, L. (2011) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2011.02481.x · Cited by 66 · see citing works

Affiliative behavior in Williams syndrome: social perception and real-life social behavior

Järvinen-Pasley, A., Adolphs, R., Yam, A., Hill, K. J., Grichanik, M., Reilly, J., Mills, D., Reiss, A. L., Korenberg, J. R., & Bellugi, U. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.03.032 · Cited by 63 · see citing works

Social Phenotypes in Neurogenetic Syndromes

Feinstein, C., & Singh, S. (2007) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2007.03.006 · Cited by 62 · see citing works

Attention to Faces in Williams Syndrome

Riby, D. M., Jones, N., Brown, P. H., Robinson, L. J., Langton, S., Bruce, V., & Riby, L. M. (2010) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-010-1141-5 · Cited by 61 · see citing works

Heterogeneity of social approach behaviour in Williams syndrome: The role of response inhibition

Little, K., Riby, D. M., Janes, E., Clark, F., Fleck, R., & Rodgers, J. (2013) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2012.11.020 · Cited by 58 · see citing works

Individual differences in social behavior predict amygdala response to fearful facial expressions in Williams syndrome

Haas, B. W., Hoeft, F., Searcy, Y. M., Mills, D., Bellugi, U., & Reiss, A. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.12.030 · Cited by 56 · see citing works

Nature and nurture: Williams syndrome across cultures

Zitzer‐Comfort, C., Doyle, T. F., Masataka, N., Korenberg, J. R., & Bellugi, U. (2007) · Developmental Science · doi:10.1111/j.1467-7687.2007.00626.x · Cited by 55 · see citing works

I see happy people: Attention bias towards happy but not angry facial expressions in Williams syndrome

Dodd, H. F., & Porter, M. A. (2010) · Cognitive Neuropsychiatry · doi:10.1080/13546801003737157 · Cited by 54 · see citing works

Narrative language in Williams Syndrome and its neuropsychological correlates

Marini, A., Martelli, S., Gagliardi, C., Fabbro, F., & Borgatti, R. (2009) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2009.10.002 · Cited by 54 · see citing works

Stranger danger awareness in W illiams syndrome

Riby, D. M., Kirk, H., Hanley, M., & Riby, L. M. (2013) · Journal of Intellectual Disability Research · doi:10.1111/jir.12055 · Cited by 53 · see citing works

Cell Competition During Growth and Regeneration

Gogna, R., Shee, K., & Moreno, E. (2015) · Annual Review of Genetics · doi:10.1146/annurev-genet-112414-055214 · Cited by 50 · see citing works

Williams Syndrome and Music: A Systematic Integrative Review

Thakur, D., Martens, M. A., Smith, D. S., & Roth, E. A. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02203 · Cited by 49 · see citing works

Brain trust

Damásio, A. R. (2005) · Nature · doi:10.1038/435571a · Cited by 49 · see citing works

Stuck on you: Face-to-face arousal and gaze aversion in Williams syndrome

Doherty‐Sneddon, G., Riby, D. M., Calderwood, L., & Ainsworth, L. (2009) · Cognitive Neuropsychiatry · doi:10.1080/13546800903043336 · Cited by 48 · see citing works

Behavioural profile and maternal stress in Greek young children with Williams syndrome

Papaeliou, C. F., Polemikos, N., Fryssira, E., Kodakos, A., Kaila, M., Yiota, X., Benaveli, E., Michaelides, C., Stroggilos, V., & Vrettopoulou, M. (2011) · Child Care Health and Development · doi:10.1111/j.1365-2214.2011.01306.x

Common and distinct neural correlates of facial emotion processing in social anxiety disorder and Williams syndrome: A systematic review and voxel-based meta-analysis of functional resonance imaging studies

Binelli, C., Subirà, S., Batalla, A., Muñiz, A., Sugranyes, G., Crippa, J. A. S., Farré, M., Pérez‐Jurado, L. A., & Martín‐Santos, R. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.08.027 · Cited by 46 · see citing works

Contrasting patterns of language-associated brain activity in autism and Williams syndrome

Fishman, I., Yam, A., Bellugi, U., Lincoln, A. J., & Mills, D. L. (2010) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq075 · Cited by 46 · see citing works

Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams–Beuren Syndrome

Borralleras, C., Sahún, I., Jurado, L. A. P., & Campuzano, V. (2015) · Molecular Therapy · doi:10.1038/mt.2015.130 · Cited by 45 · see citing works

Who reports it best? A comparison between parent-report, self-report, and the real life social behaviors of adults with Williams syndrome

Fisher, M. H., Mello, M. P., & Dykens, E. M. (2014) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2014.08.011 · Cited by 44 · see citing works

Affect, Social Behavior, and the Brain in Williams Syndrome

Bellugi, U., Järvinen‐Pasley, A., Doyle, T. F., Reilly, J. S., Reiss, A. L., & Korenberg, J. R. (2007) · Current Directions in Psychological Science · doi:10.1111/j.1467-8721.2007.00484.x · Cited by 44 · see citing works

Cerebral Lateralization of Pro- and Anti-Social Tendencies

Hecht, D. (2014) · Experimental Neurobiology · doi:10.5607/en.2014.23.1.1 · Cited by 43 · see citing works

Morphological differences in the mirror neuron system in Williams syndrome

Ng, R., Brown, T. T., Erhart, M. J., Järvinen, A. M., Korenberg, J. R., Bellugi, U., & Halgren, E. (2015) · Social Neuroscience · doi:10.1080/17470919.2015.1070746 · Cited by 42 · see citing works

Phenotypic psychiatric characterization of children with Williams syndrome and response of those with ADHD to methylphenidate treatment

Green, T., Avda, S., Dotan, I., Zarchi, O., Basel‐Vanagaite, L., Zalsman, G., Weizman, A., & Gothelf, D. (2011) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31247 · Cited by 40 · see citing works

A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome

Mimura, M., Hoeft, F., Kato, M., Kobayashi, N., Sheau, K., Piggot, J., Mills, D., Galaburda, A., Korenberg, J. R., Bellugi, U., et al. (2010) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-009-9041-8 · Cited by 38 · see citing works

Developmental and cognitive troubles in Williams syndrome

Martens, M. A. (2013) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52891-9.00033-6 · Cited by 38 · see citing works

Genetics of behavior in the silver fox

Kukekova, A. V., Temnykh, S. V., Johnson, J. L., Trut, L. N., & Acland, G. M. (2011) · Mammalian Genome · doi:10.1007/s00335-011-9373-z · Cited by 40 · see citing works

Williams Syndrome, Human Self-Domestication, and Language Evolution

Niego, A., & Benítez‐Burraco, A. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.00521 · Cited by 35 · see citing works

Social Brain Development in Williams Syndrome: The Current Status and Directions for Future Research

Haas, B. W., & Reiss, A. L. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00186 · Cited by 37 · see citing works

The neurobiology of Williams syndrome: Cascading influences of visual system impairment?

Eckert, M. A., Galaburda, A. M., Mills, D. L., Bellugi, U., Korenberg, J. R., & Reiss, A. L. (2006) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-005-5553-x · Cited by 35 · see citing works

Enhanced prefrontal serotonin 5-HT1A currents in a mouse model of Williams-Beuren syndrome with low innate anxiety

Proulx, É., Young, E. J., Osborne, L. R., & Lambe, E. K. (2010) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-010-9044-5 · Cited by 35 · see citing works

Mutation of Gtf2ird1 from the Williams–Beuren syndrome critical region results in facial dysplasia, motor dysfunction, and altered vocalisations

Howard, M. L., Palmer, S. J., Taylor, K. M., Arthurson, G. J., Spitzer, M. W., Du, X., Pang, T. Y., Renoir, T., Hardeman, E. C., & Hannan, A. J. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.12.010 · Cited by 35 · see citing works

ORIGINAL ARTICLE: Genomic sister‐disorders of neurodevelopment: an evolutionary approach

Crespi, B. J., Summers, K., & Dorus, S. (2009) · Evolutionary Applications · doi:10.1111/j.1752-4571.2008.00056.x · Cited by 35 · see citing works

Social approach in pre‐school children with Williams syndrome: the role of the face

Dodd, H. F., Porter, M. A., Peters, G. L., & Rapee, R. M. (2010) · Journal of Intellectual Disability Research · doi:10.1111/j.1365-2788.2009.01241.x · Cited by 33 · see citing works

Altered Microstructure Within Social-Cognitive Brain Networks During Childhood in Williams Syndrome

Haas, B. W., Barnea‐Goraly, N., Sheau, K. E., Yamagata, B., Ullas, S., & Reiss, A. L. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht135 · Cited by 33 · see citing works

Narration and collaborative conversation in French-speaking children with Williams syndrome

Lacroix, A., Bernicot, J., & Reilly, J. S. (2007) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2007.03.004 · Cited by 33 · see citing works

Facial emotion processing in patients with social anxiety disorder and Williams–Beuren syndrome: an fMRI study

Binelli, C., Muñiz, A., Subirà, S., Navinés, R., Blanco‐Hinojo, L., Pérez-García, D., Crippa, J. A. S., Farré, M., Jurado, L. A. P., Pujol, J., et al. (2016) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.140384 · Cited by 29 · see citing works

Epigallocatechin-3-gallate improves cardiac hypertrophy and short-term memory deficits in a Williams-Beuren syndrome mouse model

Ortiz‐Romero, P., Borralleras, C., Bosch-Morató, M., Guivernau, B., Albericio, G., Muñoz, F. J., Jurado, L. A. P., & Campuzano, V. (2018) · PLoS ONE · doi:10.1371/journal.pone.0194476 · Cited by 32 · see citing works

Evaluation of a stranger safety training programme for adults with W illiams syndrome

Fisher, M. H. (2013) · Journal of Intellectual Disability Research · doi:10.1111/jir.12108 · Cited by 32 · see citing works

Face‐to‐face interference in typical and atypical development

Riby, D. M., Doherty‐Sneddon, G., & Whittle, L. (2011) · Developmental Science · doi:10.1111/j.1467-7687.2011.01125.x · Cited by 32 · see citing works

A Common Polymorphism in a Williams Syndrome Gene Predicts Amygdala Reactivity and Extraversion in Healthy Adults

Swartz, J. R., Waller, R. E., Bogdan, R., Knodt, A. R., Sabhlok, A., Hyde, L. W., & Hariri, A. R. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.12.007 · Cited by 31 · see citing works

White matter integrity deficits in prefrontal–amygdala pathways in Williams syndrome

Avery, S. N., Thornton‐Wells, T. A., Anderson, A. W., & Blackford, J. U. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.065 · Cited by 30 · see citing works

Discrimination training reduces high rate social approach behaviors in Angelman syndrome: Proof of principle

Heald, M., Allen, D., Villa, D., & Oliver, C. (2013) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2013.02.012 · Cited by 31 · see citing works

Atypical unfamiliar face processing in Williams syndrome: What can it tell us about typical familiarity effects?

Riby, D. M., Doherty‐Sneddon, G., & Bruce, V. (2007) · Cognitive Neuropsychiatry · doi:10.1080/13546800701779206 · Cited by 31 · see citing works

What and Why Understanding in Autism Spectrum Disorders and W illiams Syndrome: Similarities and Differences

Sparaci, L., Stefanini, S., D’Elia, L., Vicari, S., & Rizzolatti, G. (2014) · Autism Research · doi:10.1002/aur.1370 · Cited by 30 · see citing works

Gaze aversion during social style interactions in autism spectrum disorder and Williams syndrome

Doherty‐Sneddon, G., Whittle, L., & Riby, D. M. (2012) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2012.09.022 · Cited by 30 · see citing works

Toward a deeper characterization of the social phenotype of Williams syndrome: The association between personality and social drive

Ng, R., Järvinen, A. M., & Bellugi, U. (2014) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2014.04.015 · Cited by 29 · see citing works

Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models

Kopp, N., McCullough, K. B., Maloney, S. E., & Dougherty, J. D. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz176 · Cited by 29 · see citing works

Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome

Järvinen‐Pasley, A., Vines, B. W., Hill, K. J., Yam, A., Grichanik, M., Mills, D. L., Reiss, A. L., Korenberg, J. R., & Bellugi, U. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.10.003 · Cited by 30 · see citing works

Differences in Social Motivation in Children with Smith–Magenis Syndrome and Down Syndrome

Wilde, L., Mitchell, A., & Oliver, C. (2016) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-016-2743-3 · Cited by 29 · see citing works

Acquired Extroversion Associated With Bitemporal Variant of Frontotemporal Dementia

Mendez, M. F., Chen, A. K., Shapira, J. S., Lu, P.-H., & Miller, B. L. (2006) · Journal of Neuropsychiatry · doi:10.1176/jnp.18.1.100 · Cited by 29 · see citing works

The Williams Syndrome Social Phenotype

Thurman, A. J., & Fisher, M. H. (2015) · International review of research in developmental disabilities · doi:10.1016/bs.irrdd.2015.06.002 · Cited by 29 · see citing works

Understanding motor acts and motor intentions in Williams syndrome

Sparaci, L., Stefanini, S., Marotta, L., Vicari, S., & Rizzolatti, G. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.03.019 · Cited by 28 · see citing works

Williams syndrome-specific neuroanatomical profile and its associations with behavioral features

Fan, C. C., Brown, T. T., Bartsch, H., Kuperman, J. M., Hagler, D. J., Schork, A. J., Searcy, Y. M., Bellugi, U., Halgren, E., & Dale, A. M. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.05.011 · Cited by 28 · see citing works

Hyperactive Auditory Efferent System and Lack of Acoustic Reflexes in Williams Syndrome

Attias, J., Raveh, E., Ben-Naftali, N. F., Zarchi, O., & Gothelf, D. (2008) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp.2008.19.3-4.193 · Cited by 28 · see citing works

Receptive prosody in adolescents and adults with Williams syndrome

Skwerer, D. P., Schofield, C. A., Verbalis, A. D., Faja, S., & Tager-Flusberg, H. B. (2006) · Language and Cognitive Processes · doi:10.1080/01690960600632671 · Cited by 28 · see citing works

The Relationship between Anxiety and the Social Judgements of Approachability And Trustworthiness

Willis, M. L., Dodd, H. F., & Palermo, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076825 · Cited by 27 · see citing works

A multimeasure approach to investigating affective appraisal of social information in Williams syndrome

Skwerer, D. P., Ammerman, E., André, M., Ciciolla, L. M., Fine, A. B., & Tager-Flusberg, H. B. (2011) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-011-9100-9 · Cited by 27 · see citing works

Beyond Behaviour: Is Social Anxiety Low in Williams Syndrome?

Dodd, H. F., Schniering, C. A., & Porter, M. A. (2009) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-009-0806-4 · Cited by 27 · see citing works

Narratives in Children with Williams Syndrome: A Cross Linguistic Perspective

Reilly, J. S., Bernicot, J., Vicari, S., Lacroix, A., & Bellugi, U. (2006) · Springer eBooks · doi:10.1007/1-4020-7911-7_22 · Cited by 27 · see citing works

Language and sociability: insights from Williams syndrome

Fishman, I., Yam, A., Bellugi, U., & Mills, D. L. (2011) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-011-9086-3 · Cited by 25 · see citing works

Le syndrome de Williams-Beuren : une approche pluridisciplinaire

Lacroix, A., Pezet, M., Capel, A. V., Bonnet, D., Hennèquin, M., Jacob, M., Bricca, G., Couet, D., Faury, G., Bernicot, J., et al. (2008) · Archives de Pédiatrie · doi:10.1016/j.arcped.2008.11.011 · Cited by 26 · see citing works

The Psychology of Decision Making

Hickson, L., & Khemka, I. (2014) · International review of research in developmental disabilities · doi:10.1016/b978-0-12-800278-0.00006-3 · Cited by 25 · see citing works

With Williams Syndrome

Children, H. I. Y., Doyle, T. F., Bellugi, U., Korenberg, J. R. ;. R., & Graham, J. M. (2015)

Hypersociability in Williams Syndrome

Jones, W., Bellugi, U., Lai, Z. C., Chiles, M., Reilly, J. S., Lincoln, A., & Adolphs, R. (2000) · CaltechAUTHORS (California Institute of Technology) · Cited by 18 · see citing works

Williams Syndrome: A Genetic Deletion Disorder Presenting Clues to the Biology of Sociability and Clinical Challenges of Hypersociability

Deutsch, S. I., Rosse, R. B., & Schwartz, B. L. (2007) · CNS Spectrums · doi:10.1017/s1092852900015686 · Cited by 14 · see citing works

II. Hypersociability in Williams Syndrome

Jones, W., Bellugi, U., Lai, Z., Chiles, M., Reilly, J., Lincoln, A., & Adolphs, R. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900561968 · Cited by 503 · see citing works

Towards the neural basis for hypersociability in a genetic syndrome

Bellugi, U., Adolphs, R., Cassady, C., & Chiles, M. (1999) · NeuroReport · doi:10.1097/00001756-199906030-00006 · Cited by 207 · see citing works