The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.
Distinctive Personality Characteristics of 8-, 9-, and 10-Year-Olds With Williams Syndrome
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
“is a neurodevelopmental condition caused by a hemizygous microdeletion on chromosome 7q11.23, and is characterized by hypersociality and being overly empathic [684,685].”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [685]
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 [685]
Citations
Cites
Measuring the Accuracy of Diagnostic Systems
Swets, J. A. (1988) · Science · doi:10.1126/science.3287615 · Cited by 10,058
Personality Structure: Emergence Of The 5-Factor Model
Digman, J. M. (1990) · Annual Review of Psychology · doi:10.1146/annurev.ps.41.020190.002221 · Cited by 6,731
The structure of phenotypic personality traits.
Goldberg, L. R. (1993) · American Psychologist · doi:10.1037/0003-066x.48.1.26 · Cited by 4,816
(1985) · Cited by 1,630
Personality similarity in twins reared apart and together.
Tellegen, A., Lykken, D. T., Bouchard, T. J., Wilcox, K. J., Segal, N. L., & Rich, S. (1988) · Journal of Personality and Social Psychology · doi:10.1037//0022-3514.54.6.1031 · Cited by 1,547
The Role of Ego-Control and Ego-Resiliency in the Organization of Behavior
BLOCK, J. H., & Block, J. (1980) · doi:10.4324/9781315803029-7 · Cited by 1,525
Measurement of Temperament in Infancy
Rothbart, M. K. (1981) · Child Development · doi:10.2307/1129176 · Cited by 1,325
Development of individual differences in temperament
Rothbart, M. K., & Derryberry, D. (1981) · Cited by 1,164
Reactive and effortful processes in the organization of temperament
Derryberry, D., & Rothbart, M. K. (1997) · Development and Psychopathology · doi:10.1017/s0954579497001375 · Cited by 858
Temperament and the development of personality.
Rothbart, M. K., & Ahadi, S. A. (1994) · Journal of Abnormal Psychology · doi:10.1037//0021-843x.103.1.55 · Cited by 669
Flagged first, then by citations
Research works printed but not linked: 13
- Benjamin J., 1997, Israel Journal of Psychiatry and Related Sciences, 34, 270
- Dilts C. V., 1990, American Journal of Medical Genetics Supplement, 6, 126
- 10.1037//0003-066X.48.1.26 · DOI · Paper page
- Gosch A., 1996, Forum Kinderarzt, 9, 8
- Gosch A., 1997, Developmental Medicine and Child Neurology, 39, 327
- 10.1037//0021-843X.105.3.299 · DOI · Paper page
- Levine, G. & Parkinson, S. (1994). Detection, discrimination, and the theory of signal detection. In G. Levine & S. Parkinson (Eds.), Experimental methods in psychology (pp. 204-233). Hillsdale, NJ: Lawrence Erlbaum Associates, Inc.
- Nilsson, D. E. & Bradford, L. W. (1999). Neurofibromatosis. In S. Goldstein & C. R. Reynolds (Eds.), Handbook of neurodevelopmental and genetic disorders in children (pp. 350-367). New York: Guilford.
- 10.1037//1040-3590.10.2.97 · DOI
- Rothbart, M. K. (1994). Broad dimensions of temperament and personality. In P. Ekman & R. J. Davidson (Eds.), The nature of emotion: Fundamental questions (pp. 337-341). New York: Oxford University Press.
- Rothbart M. K., 1994, Merrill-Palmer Quarterly, 40, 21
- Udwin, O. & Dennis, J. (1995). Psychological and behavioral phenotypes in genetically determined syndromes: A review of research findings. In G. O'Brien & W. Yule (Eds.), Behavioural phenotypes (pp. 90-208). London: MacKeith.
- 10.1017/S002196309800256X · DOI
Cited by
Sorted by citations
Items 101–152 of 152
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
Genetic syndromes associated with intellectual disability
Klein-Tasman, B., Phillips, K. D., & Kelderman, J. K. (2001) · Cambridge University Press eBooks · doi:10.1017/cbo9780511545894.011 · Cited by 7
Self-citationThe Innate Endowment for Language
Baker, M. C. (2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195179675.003.0010 · 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-citationWhat Developmental Biology Can Tell Us about Innateness
Marcus, G. (2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195179675.003.0002 · Cited by 6
Genetic Syndromes Associated with Intellectual Disabilities
Abbeduto, L., Thurman, A. J., Bullard, L., Potter, S. N., & McDuffie, A. S. (2019) · Springer eBooks · doi:10.1007/978-3-030-14895-9_13 · Cited by 6
Autobiographical Narratives in Williams Syndrome: Structural, Process and Content Dimensions
Gonçalves, Ó. F., Pinheiro, A. P., Sampaio, A., Sousa, N., Fernández‐Prieto, M., & Henriques, M. I. R. S. (2011) · Journal of Developmental and Physical Disabilities · doi:10.1007/s10882-011-9228-2 · Cited by 5
Meyer‐Lindenberg, A. (2009) · EMBO Molecular Medicine · doi:10.1002/emmm.200900007 · Cited by 4
It Helps to Know Genetic Basis: Williams Syndrome as an Example of Cognitive Disability
Klein-Tasman, B., Gallo, F. J., Phillips, K. D., & Fine, K. M. (2008) · Springer eBooks · doi:10.1007/978-0-387-78965-1_25 · Cited by 4
Self-citationSpeech articulation in children with Williams syndrome or 7q11.23 duplication syndrome.
Huffman, M. J. (2019) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/3242 · Cited by 4
The 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
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
Challenging behavior: Behavioral phenotypes of some genetic syndromes
Buha, N. S., Gligorović, M., & Maksić, J. (2014) · Srpski arhiv za celokupno lekarstvo · doi:10.2298/sarh1410621b · Cited by 3
Two Insights about Naming in the Preschool Child
Gelman, S. A. (2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195179675.003.0012 · Cited by 3
Niccols, A., Thomas, K. E., & Schmidt, L. A. (2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195305012.013.0017 · Cited by 3
Empathy in Williams Syndrome: Clues from Typical and Atypical Deletion of 7q11.23
Ng, R., Fillet, P., & Bellugi, U. (2019) · Advances in Neurodevelopmental Disorders · doi:10.1007/s41252-019-00128-8 · Cited by 2
Understanding Decision Making and Intellectual and Developmental Disabilities
Khemka, I. (2021) · Springer eBooks · doi:10.1007/978-3-030-74675-9_11 · Cited by 2
Early Communicative Development in Williams Syndrome: A Longitudinal Case Study
Itza, E. D., Llona, F., & Martínez, V. (2023) · Children · doi:10.3390/children10121900 · Cited by 2
Iskustva majki djece s dijagnozom Williamsovog sindroma
Babić, M. M., Jović, K., & Napan, K. (2017) · Hrvatska revija za rehabilitacijska istraživanja · doi:10.31299/hrri.53.1.9 · Cited by 2
Neuroimaging of Williams–Beuren syndrome
Santos, A., & Meyer‐Lindenberg, A. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511782091.038 · Cited by 1
Social Information Processing in Williams Syndrome
Key, A. P. F., & Katzenstein, A. (2018) · International review of research in developmental disabilities · doi:10.1016/bs.irrdd.2018.08.002 · Cited by 1
We Are Social – Therefore We Are: The Interplay of Mind, Culture, and Genetics in Williams Syndrome
Zitzer‐Comfort, C., Reilly, J. S., Korenberg, J. R., & Bellugi, U. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511711879.010 · Cited by 1
Williams–Beuren-szindróma (Williams-szindróma)
Miklós, G., Fekete, G., Haltrich, I., Tóth, M., & Reismann, P. (2017) · Orvosi Hetilap · doi:10.1556/650.2017.30905 · Cited by 1
Patterns of early lexical and gestural development in children with Williams syndrome.
Becerra, A. M. (2016) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/2407 · Cited by 1
John, A. (2011) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/694
Social dysfunction and mental retardation
Pietropaolo, S., Sluyter, F., & Crusio, W. E. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9781107360556.010
Neuronale Mechanismen sozialer Kognition unter genetischem Einfluss
Meyer‐Lindenberg, A. (2012) · Springer eBooks · doi:10.1007/978-3-642-24916-7_7
Osborne, L. R., & Jia, Z. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9781107360556.020 · Cited by 1
Strong versus Weak Adaptationism in Cognition and Language
Atran, S. (2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195179675.003.0009
Disturbance of face memories in a case with Williams syndrome
Nakamichi, K., & Hosokawa, T. (2016) · Higher Brain Function Research · doi:10.2496/hbfr.36.440
GENETIC SYNDROMES AND DYSMORPHOLOGY
Proud, V. K., & Elias, E. R. (2009) · Elsevier eBooks · doi:10.1016/b978-1-4160-3370-7.00026-2
Asif, S. (2021) · Pakistan Social Sciences Review · doi:10.35484/pssr.2021(5-i)82
Klein-Tasman, B., & van der Fluit, F. (2010) · Springer eBooks · doi:10.1007/978-0-387-79948-3_1609
Self-citationSkwerer, D. P. (2021) · Springer eBooks · doi:10.1007/978-3-030-74985-9_6
Understanding Children's Private Speech and Self-Regulation Learning in Web 2.0
Agina, A. M., Tennyson, R. D., & Kommers, P. (2015) · IGI Global eBooks · doi:10.4018/978-1-4666-8111-8.ch069
Neuronale Mechanismen sozialer Kognition unter genetischem Einfluss
Meyer‐Lindenberg, A. (2007) · Springer eBooks · doi:10.1007/978-3-540-27241-0_6
Reilly, J. S., & Lai, P. T. (2010) · doi:10.1093/oso/9780195342680.003.0031
van der Fluit, F., Brei, N. G., & Klein-Tasman, B. (2018) · Springer eBooks · doi:10.1007/978-3-319-57111-9_1609
Self-citation(2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195179675.002.0001
(2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195179675.001.0001.002.003
(2005) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195179675.001.0001.002.005
Sensory Patterns of Children with Williams Syndrome
Huri̇, M., Kars, S., Şahın, S., Pekçetin, S., & Kashefimehr, B. (2024) · Paediatria Croatica · doi:10.13112/pc.2023.8
Foti, F., Costanzo, F., Fabrizio, C., Termine, A., Menghini, D., Iaquinta, T., Vicari, S., Petrosini, L., & Blake, P. R. (2024) · Figshare · doi:10.6084/m9.figshare.26944596
Foti, F., Costanzo, F., Fabrizio, C., Termine, A., Menghini, D., Iaquinta, T., Vicari, S., Petrosini, L., & Blake, P. R. (2024) · Figshare · doi:10.6084/m9.figshare.26944608
Foti, F., Costanzo, F., Fabrizio, C., Termine, A., Menghini, D., Iaquinta, T., Vicari, S., Petrosini, L., & Blake, P. R. (2024) · Figshare · doi:10.6084/m9.figshare.26944602
Foti, F., Costanzo, F., Fabrizio, C., Termine, A., Menghini, D., Iaquinta, T., Vicari, S., Petrosini, L., & Blake, P. R. (2024) · Figshare · doi:10.6084/m9.figshare.26944599
Foti, F., Costanzo, F., Fabrizio, C., Termine, A., Menghini, D., Iaquinta, T., Vicari, S., Petrosini, L., & Blake, P. R. (2024) · Figshare · doi:10.6084/m9.figshare.26944605
Melogno, S., & Pinto, M. A. (2025) · Springer eBooks · doi:10.1007/978-3-032-03024-5_3
Begam, M. (2026) · Bengal Journal of Psychiatry · doi:10.25259/bjpsy_21_2025
Neurodevelopmental Disorders in Common Syndromes
Toriello, H. V. (2011) · Springer eBooks · doi:10.1007/978-94-007-0627-9_6
Metadata
- Authors
- Klein-Tasman, B., & Mervis, C.
- ORCID
- Mervis, Carolyn
- Venue
- Developmental Neuropsychology
- Publisher
- Informa UK Limited
- Published
- 2003-02-01
- Volume
- 23
- Issue
- 1
- Pages
- 269-290
- ISSN
- 1532-6942 (ISSN-L)
- 8756-5641
- OpenAlex
- W4252392275
- Cited by
- 148
- References
- 28
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 1 · 2021: 5 · 2020: 3 · 2019: 4 · 2018: 8 · 2017: 6 · 2016: 7 · 2015: 5 · 2014: 4 · 2013: 5 · 2012: 13
- FWCI
- 2.51
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Developmental Neuropsychology (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Williams Syndrome Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Social Sciences › Psychology › Clinical Psychology › Personality Traits and Psychology
- Keywords
- Williams syndrome, personality traits, children, genetic syndromes, child development
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