The DOI matches its Crossref record; 185 of the 185 references it cites were found in a registry or an index.
Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour
Abstract
Williams syndrome, a rare disorder caused by hemizygous microdeletion of about 28 genes on chromosome 7q11.23, has long intrigued neuroscientists with its unique combination of striking behavioural abnormalities, such as hypersociability, and characteristic neurocognitive profile. Williams syndrome, therefore, raises fundamental questions about the neural mechanisms of social behaviour, the modularity of mind and brain development, and provides a privileged setting to understand genetic influences on complex brain functions in a 'bottom-up' way. We review recent advances in uncovering the functional and structural neural substrates of Williams syndrome that provide an emerging understanding of how these are related to dissociable genetic contributions characterized both in special participant populations and animal models.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“There are currently three models of social function in WS: 1) heightened drive towards non-specific social interaction (for example, social interactions with strangers) [686,687], 2) heightened emotional responsiveness [685], and 3) social fearlessness [688].”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [688]
Citations
Cites
Fodor, J. A. (1983) · doi:10.7551/mitpress/4737.001.0001 · Cited by 7,734
Ingle, D., Goodale, M. A., & Mansfield, R. J. W. (1982) · The MIT Press eBooks · Cited by 4,118
Egan, M. F., Kojima, M., Callicott, J. H., Goldberg, T. E., Kolachana, B. S., Bertolino, A., Zaitsev, E., Gold, B., Goldman, D., Dean, M., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00035-7 · Cited by 3,888
Beyond modularity: a developmental perspective on cognitive science
Karmiloff‐Smith, A. (1993) · Choice Reviews Online · doi:10.5860/choice.30-5872 · Cited by 2,594
Matthei, E. H. (1984) · Language · doi:10.2307/413815 · Cited by 2,189
Karmiloff‐Smith, A. (1992) · The MIT Press eBooks · doi:10.7551/mitpress/1579.001.0001 · Cited by 2,078
KRINGELBACH, M. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.03.006 · Cited by 1,977
The Emotional Brain, Fear, and the Amygdala
LeDoux, J. (2003) · Cellular and Molecular Neurobiology · doi:10.1023/a:1025048802629 · Cited by 1,818
A tension-based theory of morphogenesis and compact wiring in the central nervous system
Essen, D. C. V. (1997) · Nature · doi:10.1038/385313a0 · Cited by 1,668
Cognitive neuroscience of human social behaviour
Adolphs, R. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1056 · Cited by 1,657
Flagged first, then by citations
Research works printed but not linked: 7
- Marenco, S. et al. Preliminary diffusion tensor imaging (DTI) observations in 5 individuals with Williams syndrome (WS). Neuroimage 22 (Suppl. 1), M0363 (2004).
- Olsen, R. K. et al. Retinotopic mapping of early visual areas in Williams syndrome. Presented at the Human Brain Mapping Meeting 2003 (New York, USA). Neuroimage 19 (Suppl. 1), 1550 (2003).
- Nardini, M., Breckenridge, K. E., Eastwood, R. L., Atkinson, J. & Braddick, O. J. Distinct developmental trajectories in three systems for spatial encoding between the ages of 3 and 6 years. Perception S33, 28b (2004).
- Lukács, A., Racsmány, M. & Pléh, C. Vocabulary and morphological patterns in Hungarian children with Williams syndrome: a preliminary report. Acta Linguistica Hungarica 48, 243–269 (2001).
- Mons, A. W., Wilmowski, W. A. & Detweiler, C. Williams Syndrome: a Highly Musical Species (EO Productions International, 1996).
- Gordon, F. E. in Musical Aptitude Profile (Houghton Mifflin, Boston, 1995).
- Gordon, F. E. Primary Measures of Music Audiation (G. I. A. Publications, Chicago, 1980).
Cited by
Sorted by citations
Items 201–300 of 415
Favre, G., Lavenex, P. B., & Lavenex, P. (2012) · Translational Psychiatry · doi:10.1038/tp.2012.105 · Cited by 16
Description of common musculoskeletal findings in Williams Syndrome and implications for therapies
Copes, L. E., Pober, B. R., & Terilli, C. (2016) · Clinical Anatomy · doi:10.1002/ca.22685 · Cited by 15
Brain mechanisms of visuomotor transformation based on deficits in tracing and copying
Ogawa, K., Nagai, C., & Inui, T. (2010) · Japanese Psychological Research · doi:10.1111/j.1468-5884.2010.00427.x · Cited by 14
Green, T., Fierro, K. C., Raman, M. M., Saggar, M., Sheau, K. E., & Reiss, A. L. (2016) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32422 · Cited by 13
Clinical, Research and Treatment Approaches to Affective Disorders
Juruena, M. F. (2012) · InTech eBooks · doi:10.5772/1482 · Cited by 14
Cognitive, Behavioral, and Adaptive Profiles in Williams Syndrome With and Without Loss of GTF2IRD2
Serrano‐Juárez, C. A., Venegas-Vega, C. A., Yáñez-Téllez, M. G., Rodríguez-Camacho, M. A., Silva‐Pereyra, J., Salgado‐Ceballos, H., & Prieto‐Corona, B. (2018) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617718000711 · Cited by 15
Deutsch, S. I., Rosse, R. B., & Schwartz, B. L. (2007) · CNS Spectrums · doi:10.1017/s1092852900015686 · Cited by 14
Chromatin remodeling and SWI/SNF2 factors in human disease
Kokavec, J. (2008) · Frontiers in bioscience · doi:10.2741/3142 · Cited by 14
Bódizs, R., Gombos, F., Gerván, P., Szőcs, K., Réthelyi, J., & Kovács, I. (2014) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2014.07.056 · Cited by 14
Dysfunction of the Hypothalamic-Pituitary-Adrenal axis in STX1A Knockout Mice
Fujiwara, T., Kofuji, T., & Akagawa, K. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02214.x · Cited by 14
Retinotopically defined primary visual cortex in Williams syndrome
Olsen, R. K., Kippenhan, J. S., JAPEE, S. A., Kohn, P. D., Mervis, C. Β., Saad, Z. S., Morris, C. A., Meyer‐Lindenberg, A., & Berman, K. F. (2009) · Brain · doi:10.1093/brain/awn362 · Cited by 14
Self-citationGrad, M., Nir, A., Levy, G., Trangle, S. S., Shapira, G., Shomron, N., Assaf, Y., & Barak, B. (2022) · Cells · doi:10.3390/cells11010158 · Cited by 12
Honjo, R. S., Dutra, R. L., Nunes, M. M., Gomy, I., Kulikowski, L. D., Jehee, F. S., & Kim, C. A. (2012) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2012.07.001 · Cited by 13
Hanson, K. L., Hrvoj-Mihić, B., & Semendeferi, K. (2014) · Brain Behavior and Evolution · doi:10.1159/000365409 · Cited by 13
Dessalegn, B., Landau, B., & Rapp, B. C. (2012) · Neurocase · doi:10.1080/13554794.2012.667127 · Cited by 13
An event related potential study of inhibitory and attentional control in Williams syndrome adults
Greer, J. M. H., Hamilton, C., McMullon, M. E. G., Riby, D. M., & Riby, L. M. (2017) · PLOS ONE · doi:10.1371/journal.pone.0170180 · Cited by 13
Low-Resolution Place and Response Learning Capacities in Down Syndrome
Bostelmann, M., Costanzo, F., Martorana, L., Menghini, D., Vicari, S., Lavenex, P. B., & Lavenex, P. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02049 · Cited by 13
Dolscheid, S., & Penke, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0199743 · Cited by 12
Jasoliya, M., Gu, J., AlOlaby, R. R., Durbin-Johnson, B. P., Chedin, F. L., & Tassone, F. (2022) · Genes · doi:10.3390/genes13101795 · Cited by 12
Prontera, P., Serino, D., Caldini, B., Scarponi, L., Merla, G., Testa, G., Muti, M., Napolioni, V., Mazzotta, G., Piccirilli, M., et al. (2014) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-014-2117-7 · Cited by 13
Hanson, K. L., Lew, C. H., Hrvoj-Mihić, B., Groeniger, K. M., Halgren, E., Bellugi, U., & Semendeferi, K. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22554 · Cited by 15
Triangulating perspectives on functional neuroimaging for disorders of mental health
Anderson, J. A., Mizgalewicz, A., & Illes, J. (2013) · BMC Psychiatry · doi:10.1186/1471-244x-13-208 · Cited by 12
New insights into the role of motion and form vision in neurodevelopmental disorders
JOHNSTON, R. G., Pitchford, N. J., Roach, N. W., & Ledgeway, T. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.09.031 · Cited by 11
Lavenex, P. B., & Lavenex, P. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.669320 · Cited by 11
Autism, language delay and mental retardation in a patient with 7q11 duplication
Depienne, C., Héron, D., Betancur, C., Benyahia, B., Trouillard, O., Bouteiller, D., Verloès, A., Leguern, É., Leboyer, M., & Brice, A. (2009) · BMJ Case Reports · doi:10.1136/bcr.05.2009.1911 · Cited by 11
Hirai, M., Muramatsu, Y., Mizuno, S., Kurahashi, N., Kurahashi, H., & Nakamura, M. (2017) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-017-9190-0 · Cited by 10
Behavioural features of Italian infants and young adults with Williams–Beuren syndrome
Gagliardi, C., Martelli, S., Tavano, A., & Borgatti, R. (2011) · Journal of Intellectual Disability Research · doi:10.1111/j.1365-2788.2010.01376.x · Cited by 11
Williams syndrome and psychosis: a case report
Salgado, H., & Martins-Correia, L. (2014) · Journal of Medical Case Reports · doi:10.1186/1752-1947-8-49 · Cited by 11
The Central Role of Etiology in Science and Practice in Intellectual Disability
(2016) · International review of research in developmental disabilities · doi:10.1016/bs.irrdd.2016.05.005 · Cited by 13
Kamps, F. S., Rennert, R. J., Radwan, S. F., Wahab, S., Pincus, J. E., & Dilks, D. D. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0153-23.2023 · Cited by 9
Intellectual Disabilities and Global Developmental Delay
Pinchefsky, E. F., & Shevell, M. I. (2017) · Springer eBooks · doi:10.1007/978-3-319-57196-6_2 · Cited by 10
The development of visuospatial processing
Stiles, J., Akshoomoff, N. A., & Haist, F. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814411-4.00017-2 · Cited by 13
Genetic and Environmental Influences on Intellectual Disability in Childhood
Carlier, M., & Roubertoux, P. L. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7447-0_3 · Cited by 11
Perceptual Learning in Williams Syndrome: Looking Beyond Averages
Gerván, P., Gombos, F., & Kovács, I. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040282 · Cited by 10
Impaired behavioral and neural representation of scenes in Williams syndrome
Ferrara, K., Landau, B., & Park, S. (2019) · Cortex · doi:10.1016/j.cortex.2019.09.001 · Cited by 10
Järvinen, A. M., Ng, R., Crivelli, D., Arnold, A. J., Woo‐VonHoogenstyn, N., & Bellugi, U. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.04.035 · Cited by 9
Sleep's role in memory consolidation: What can we learn from atypical development?
Luongo, A., Lukowski, A. F., Protho, T., Vorce, H. V., Pisani, L., & Edgin, J. O. (2020) · Advances in child development and behavior · doi:10.1016/bs.acdb.2020.08.001 · Cited by 9
Social feedback enhances learning in Williams syndrome
Kleberg, J. L., Willfors, C., Avdic, H. B., Riby, D. M., Galazka, M. A., Guath, M., Nordgren, A., & Strannegård, C. (2023) · Scientific Reports · doi:10.1038/s41598-022-26055-8 · Cited by 9
Electrophysiological study of face inversion effects in Williams syndrome
Nakamura, M., Watanabe, S., Inagaki, M., Hirai, M., Miki, K., Honda, Y., & Kakigi, R. (2012) · Brain and Development · doi:10.1016/j.braindev.2012.05.010 · Cited by 9
Serrano‐Juárez, C. A., Prieto‐Corona, B., Rodríguez-Camacho, M. A., Venegas-Vega, C. A., Yáñez-Téllez, M. G., Silva‐Pereyra, J., Salgado‐Ceballos, H., Arias‐Trejo, N., & Miranda, M. A. D. L. (2020) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-020-04656-4 · Cited by 9
Tavano, A., Gagliardi, C., Martelli, S., & Borgatti, R. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.07.013 · Cited by 9
Bernardino, I., Rebola, J., Farivar, R., Silva, E., & Castelo-Branco, M. S. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00662 · Cited by 9
Biological first principles for design competence
Dong, A. (2010) · Artificial intelligence for engineering design analysis and manufacturing · doi:10.1017/s0890060410000338 · Cited by 11
Development of Visuospatial Ability and Kanji Copying in Williams Syndrome
Nakamura, M., Mizuno, S., Douyuu, S., Matsumoto, A., Kumagai, T., Watanabe, S., & Kakigi, R. (2009) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2009.02.005 · Cited by 8
Assessment of Intellectual and Visuo-Spatial Abilities in Children and Adults with Williams Syndrome
Mika, M. M., Nunes, M. M., Honjo, R. S., Dutra, R. L., Amaral, V. S. D. S. R., Oh, H. K., Bertola, D. R., Albano, L. M. J., Assumpção, F. B., Teixeira, M. C., et al. (2013) · Universitas Psychologica · doi:10.11144/javeriana.upsy12-2.aiva · Cited by 8
The Organization and Development of Spatial Representation: Insights from Williams Syndrome
Landau, B. (2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195305012.013.0005 · Cited by 8
Trangle, S. S., Rosenberg, T., Parnas, H., Levy, G., Bar, E., Marco, A., & Barak, B. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01921-z · Cited by 8
Fishman, I., Ng, R., & Bellugi, U. (2011) · Social Neuroscience · doi:10.1080/17470919.2011.628759 · Cited by 8
What gestures reveal about cognitive deficits in Williams Syndrome
Mastrogiuseppe, M., & Lee, S. A. (2017) · Developmental Neuropsychology · doi:10.1080/87565641.2017.1393685 · Cited by 8
Oxytocin receptor activation does not mediate associative fear deficits in a Williams Syndrome model
Nygaard, K. R., Swift, R. G., Glick, R. M., Wagner, R. E., Maloney, S. E., Gould, G. G., & Dougherty, J. D. (2021) · Genes Brain & Behavior · doi:10.1111/gbb.12750 · Cited by 7
Hannan, A. J. (2007) · Acta Neuropsychiatrica · doi:10.1111/j.1601-5215.2007.00205.x · Cited by 9
Skuse, D., & Slator, L. (2008) · Psychiatry · doi:10.1016/j.mppsy.2008.05.002 · Cited by 8
Deeper processing is beneficial during episodic memory encoding for adults with Williams syndrome
Greer, J. M. H., Hamiliton, C., Riby, D. M., & Riby, L. M. (2014) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2014.03.004 · Cited by 7
The hyper-IgE syndrome is not caused by a microdeletion syndrome
Pfeifer, D., Woellner, C., Petersen, A. C., Pietrogrande, M. C., Franco, J. L., Yeganeh, M., Ehl, S. R., Matamoros, N., Sprecher, E., Puck, J. M., et al. (2007) · Immunogenetics · doi:10.1007/s00251-007-0257-z · Cited by 7
Integrating Neuropsychology and School Psychology: Potential and Pitfalls
Jantz, P. B., & Plotts, C. A. (2014) · Contemporary School Psychology · doi:10.1007/s40688-013-0006-2 · Cited by 7
Developmental Trajectories in Genetic Disorders
Knowland, V. C. P., & Thomas, M. S. C. (2011) · International review of research in developmental disabilities · doi:10.1016/b978-0-12-374478-4.00003-4 · Cited by 7
Shirai, Y., Li, W., & Suzuki, T. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18020411 · Cited by 7
Greer, J. M. H., Riby, D. M., McMullon, M. E. G., Hamilton, C., & Riby, L. M. (2021) · BMC Psychology · doi:10.1186/s40359-021-00575-w · Cited by 7
Attentional rather than sensory differences characterize auditory processing in Williams syndrome
Jacobs, M., Dykens, E. M., & Key, A. P. F. (2018) · Brain and Cognition · doi:10.1016/j.bandc.2018.01.005 · Cited by 8
Intact point-light walker processing in Williams syndrome: a magnetoencephalography study
Hirai, M., Nakamura, M., Kaneoke, Y., & Kakigi, R. (2009) · Neuroreport · doi:10.1097/wnr.0b013e32832000de · Cited by 7
Social Relevance Boosts Context Processing in Williams Syndrome
Santos, A., Rondan, C., Milne, D., Démonet, J., & Deruelle, C. (2008) · Developmental Neuropsychology · doi:10.1080/87565640802111598 · Cited by 7
Language Development in Williams Syndrome
Mervis, C. Β. (2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195305012.013.0015 · Cited by 6
Self-citationWilliams-Beuren's Syndrome: A Case Report in Prince Sultan Military City, Riyadh, Saudi Arabia 2022
Aodh, A. M., & Almarshadi, A. (2023) · World Journal of Environmental Biosciences · doi:10.51847/dqxngbevlq · Cited by 6
Williams neural stem cells new model for insight into microRNA dysregulation
Palma, I. (2013) · Frontiers in Bioscience-Elite · doi:10.2741/e683 · Cited by 6
Skwerer, D. P. (2017) · International review of research in developmental disabilities · doi:10.1016/bs.irrdd.2017.08.004 · Cited by 9
de Arruda, H. F., Comin, C. H., Miazaki, M., Viana, M. P., & Costa, L. D. F. (2015) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2015.02.019 · Cited by 6
Understanding Strategic Information Use During Emotional Expression Judgments in Williams Syndrome
Ewing, L., Farran, E. K., Karmiloff‐Smith, A., & Smith, M. L. (2017) · Developmental Neuropsychology · doi:10.1080/87565641.2017.1353995 · Cited by 5
Goal-directed behavior: evolution and ontogeny
Ernst, M., & Hardin, M. G. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9780511757402.007 · Cited by 5
Fading-figure tracing in Williams syndrome
Nagai, C., Inui, T., & Iwata, M. (2010) · Brain and Cognition · doi:10.1016/j.bandc.2010.10.007 · Cited by 5
Arastoo, M., Hacker, C., Popovics, P., Lucocq, J. M., & Stewart, A. J. (2015) · Histochemistry and Cell Biology · doi:10.1007/s00418-015-1390-7 · Cited by 5
Fan, C. C., Schork, A. J., Brown, T. T., Spencer, B. E., Akshoomoff, N. A., Chen, C., Kuperman, J. M., Hagler, D. J., Steen, V. M., Hellard, S. L., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0166-y · Cited by 4
Características da avaliação auditiva na síndrome de Williams: revisão sistemática
Silva, L. A. F., Kim, C. A., & Matas, C. G. (2018) · CoDAS · doi:10.1590/2317-1782/20182017267 · Cited by 5
Effects of spatial boundaries on episodic memory development
Rah, Y. J., Kim, J., & Lee, S. A. (2022) · Child Development · doi:10.1111/cdev.13776 · Cited by 5
Shirai, Y., Watanabe, M., Sakagami, H., & Suzuki, T. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13136 · Cited by 5
Benítez‐Burraco, A. (2019) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2019.103828 · Cited by 5
Are feralization and domestication truly mirror processes?
Niego, A., & Benítez‐Burraco, A. (2021) · Ethology Ecology & Evolution · doi:10.1080/03949370.2021.1975314 · Cited by 6
Inui, T. (2013) · Japanese Psychological Research · doi:10.1111/jpr.12004 · Cited by 5
Inattention and Hyperactivity Behavioral Pattern of a Child With Williams Syndrome
Lima, S. D. F. B., Carreiro, L. R. R., Seraceni, M. F. F., Khoury, L. P., Braga, A. C., de Araújo, M. V., & Teixeira, M. C. T. V. (2012) · Clinical Case Studies · doi:10.1177/1534650112457020 · Cited by 5
Hirai, M., Muramatsu, Y., Mizuno, S., Kurahashi, N., Kurahashi, H., & Nakamura, M. (2016) · Journal of Intellectual Disability Research · doi:10.1111/jir.12318 · Cited by 5
Language development in genetic disorders
Richardson, F. M., & Thomas, M. S. C. (2012) · Cambridge University Press eBooks · doi:10.1017/cbo9780511576164.026 · Cited by 5
Neuronal Actin Remodeling and Its Role in Higher Nervous Activity
Zhuravlev, A. V. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262211215 · Cited by 5
Gene mapping methodology powered by induced genome rearrangements
Yone, H., Kono, H., Hirai, H., & Ohta, K. (2022) · Scientific Reports · doi:10.1038/s41598-022-20999-7 · Cited by 4
Garvey, M. H., Nash, T. A., Kippenhan, J. S., Kohn, P. D., Mervis, C. Β., Eisenberg, D. P., Ye, J., Gregory, M. D., & Berman, K. F. (2024) · Scientific Reports · doi:10.1038/s41598-024-60460-5 · Cited by 4
Self-citationSchweiger, J. I., & Meyer‐Lindenberg, A. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.11.008 · Cited by 4
Self-citationGombos, F., Bódizs, R., & Kovács, I. (2017) · Scientific Reports · doi:10.1038/s41598-017-06280-2 · Cited by 4
Jankovic, J. J., Hallett, M., Okun, M. S., Comella, C., Fahn, S., & Goldman, J. G. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-31071-0.00016-0 · Cited by 4
Muramatsu, Y., Tokita, Y., Mizuno, S., & Nakamura, M. (2016) · Brain and Development · doi:10.1016/j.braindev.2016.09.003 · Cited by 4
Sleep-EEG in dizygotic twins discordant for Williams syndrome.
Bódizs, R., Gombos, F., Szőcs, K., Réthelyi, J., Gerván, P., & Kovács, I. (2014) · PubMed · Cited by 4
Genetics, Social Behaviors, Social Environments and Aging
Harris, J. R. (2007) · Twin Research and Human Genetics · doi:10.1375/twin.10.2.235 · Cited by 4
Neuropsychiatric and Behavioral Profiles of 2 Adults With Williams Syndrome
Urgeles, D., Alonso, V., & Ramos‐Moreno, T. (2013) · The Primary Care Companion For CNS Disorders · doi:10.4088/pcc.13m01504 · Cited by 4
Meyer‐Lindenberg, A. (2009) · EMBO Molecular Medicine · doi:10.1002/emmm.200900007 · Cited by 4
Self-citationGregory, M. D., Kolachana, B. S., Shugart, Y. Y., Nash, T. A., Dickinson, D., Eisenberg, D. P., Mervis, C. Β., & Berman, K. F. (2018) · BMC Medical Genetics · doi:10.1186/s12881-018-0563-3 · Cited by 4
Self-citationThe role of social motivation in sharing and fairness: insights from Williams syndrome
Foti, F., Costanzo, F., Fabrizio, C., Termine, A., Menghini, D., Iaquinta, T., Vicari, S., Petrosini, L., & Blake, P. R. (2024) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-024-09568-3 · Cited by 3
Levy, G., Rokach, M., Fischer, I., Kimchi-Feldhorn, O., Shoob, S., Bar, E., Rosenberg, T., Bartman, J., Parnas, H., Grad, M., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-63500-4 · Cited by 4
Psychiatric disorders and the social brain: Distinguishing mentalizing and empathizing
Troisi, A. (2008) · Behavioral and Brain Sciences · doi:10.1017/s0140525x08004408 · Cited by 3
HOW EXPERIENCE INTERACTS WITH BIOLOGICAL DEVELOPMENT
Worthman, C. M., & Plotsky, P. M. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511711879.006 · Cited by 2
Kippenhan, J. S., Gregory, M. D., Nash, T. A., Kohn, P. D., Mervis, C. Β., Eisenberg, D. P., Garvey, M. H., Roe, K. V., Morris, C. A., Kolachana, B. S., et al. (2023) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-023-09493-x · Cited by 3
Self-citationNakajima, M., Nishikawa, C., Miyasaka, Y., Kikkawa, Y., Mori, H., Tsuruta, M., Okuyama, S., & Furukawa, Y. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.02.061 · Cited by 3
Modularity in philosophy, the neurosciences, and psychiatry
Zielasek, J., & Gäebel, W. (2008) · Poiesis & Praxis · doi:10.1007/s10202-008-0065-z · Cited by 3
Severe Eating Disorder in a 28-Year-Old Man With William’s Syndrome
Young, T., Apfeldorf, W. J., Knepper, J. P., & Yager, J. (2009) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2008.08050773 · Cited by 3
Metadata
- Authors
- Meyer-Lindenberg, A., Mervis, C. B., & Faith Berman, K.
- Venue
- Nature Reviews Neuroscience
- Published
- 2006-05
- Volume
- 7
- Issue
- 5
- Pages
- 380-393
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2074408785
- Cited by
- 411
- References
- 184
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 10 · 2023: 11 · 2022: 10 · 2021: 36 · 2020: 11 · 2019: 12 · 2018: 22 · 2017: 22 · 2016: 16 · 2015: 17 · 2014: 21 · 2013: 21 · 2012: 35
- FWCI
- 2.23
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (R01NS035102)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Williams Syndrome Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Keywords
- Williams syndrome, chromosome 7q11.23 microdeletion, neurodevelopmental disorders, hypersociability, social behavior, cognitive profile, neural correlates, brain structure, animal models, modularity of mind, brain development
- MeSH terms
- Animals, Behavior, Brain, Cognition, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Social Behavior, 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