The DOI matches its Crossref record; 53 of the 53 references it cites were found in a registry or an index.
Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome
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Citations
Cites
On The Language Instinct: (412952005-009)
Pinker, S., & American Psychological Association (1994) · PsycEXTRA Dataset · doi:10.1037/e412952005-009 · Cited by 5,646
(1996) · Cited by 3,692
Development itself is the key to understanding developmental disorders
Karmiloff-Smith, A. (1998) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(98)01230-3 · Cited by 1,299
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
LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition
Frangiskakis, J. M., Ewart, A. K., Morris, C. A., Mervis, C. B., 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 558
Karmiloff-Smith, A., Klima, E., Bellugi, U., Grant, J., & Baron-Cohen, S. (1995) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1995.7.2.196 · Cited by 372
Self-citationWang, P. P., & Bellugi, U. (1994) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/01688639408402641 · Cited by 327
Self-citationA specific deficit of dorsal stream function in Williamsʼ syndrome
Atkinson, J., King, J., Braddick, O., Nokes, L., Anker, S., & Braddick, F. (1997) · NeuroReport · doi:10.1097/00001756-199705260-00025 · Cited by 308
Lowery, M. C., Morris, C. A., Ewart, A. K., Brothman, L. J., Zhu, X., Leonard, C. O., Carey, J. C., Keating, M. T., & Brothman, A. R. (1995) · PubMed Central · Cited by 307
Cerebral Morphologic Distinctions Between Williams and Down Syndromes
Jernigan, T. L., Bellugi, U., Sowell, E., Doherty, S., & Hesselink, J. R. (1993) · Archives of Neurology · doi:10.1001/archneur.1993.00540020062019 · Cited by 293
Self-citation
Cited by
Neural reuse: A fundamental organizational principle of the brain
Anderson, M. L. (2010) · Behavioral and Brain Sciences · doi:10.1017/s0140525x10000853 · Cited by 1,212
Dendritic Anomalies in Disorders Associated with Mental Retardation
Kaufmann, W. E. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.981 · Cited by 731
Abnormal Spine Morphology and Enhanced LTP in LIMK-1 Knockout Mice
Meng, Y., Zhang, Y., Tregoubov, V., Janus, C., Cruz, L., Jackson, M., Lu, W.-Y., MacDonald, J. F., Wang, J. Y., Falls, D. L., et al. (2002) · Neuron · doi:10.1016/s0896-6273(02)00758-4 · Cited by 688
A componential view of theory of mind: evidence from Williams syndrome
Tager-Flusberg, H. (2000) · Cognition · doi:10.1016/s0010-0277(00)00069-x · Cited by 567
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
Self-citation
Metadata
- Authors
- Bellugi, U., Lichtenberger, L., Mills, D., Galaburda, A., & Korenberg, J. R.
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 1999-05
- Volume
- 22
- Issue
- 5
- Pages
- 197-207
- ISSN
- 0166-2236 (ISSN-L)
- OpenAlex
- W2152924070
- Cited by
- 353
- References
- 53
- FWCI
- 0.96
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome. https://app.cochat.ai/papers/10.1016/s0166-2236(99)01397-1
- The paper
- Bellugi, U., Lichtenberger, L., Mills, D., Galaburda, A., & Korenberg, J. R. (1999). Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome. Trends in Neurosciences. https://doi.org/10.1016/s0166-2236(99)01397-1
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
