V. Multi-level analysis of cortical neuroanatomy in Williams syndrome

Journal of Cognitive Neuroscience

Volumn 12, Issue SUPPL. 1, 2000, Pages 74-88

  Galaburda, Albert M ^a   Bellugi, Ursula ^b  

^a BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

^b Beth Israel Deaconess Medical Center ^*

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN ASYMMETRY; BRAIN CORTEX; BRAIN SIZE; GENE DELETION; HUMAN; IMMUNOCYTOCHEMISTRY; NEUROANATOMY; OCCIPITAL LOBE; PARIETAL LOBE; PRIORITY JOURNAL; WILLIAMS BEUREN SYNDROME;

EID: 0034124109     PISSN: 0898929X     EISSN: None     Source Type: Journal    
DOI: 10.1162/089892900561995     Document Type: Article

References (39)

1. Atkinson, J., King, J., Braddick, O., Nokes, L., Anker, S., & Braddick, F. (1997). A specific deficit of dorsal stream function in Williams syndrome. NeuroReport, 8, 1919-1922.
2. Bellugi, U., Adolphs, R., Cassady, C., & Chiles, M. (1999a). An experimental investigation of hypersociability in Williams syndrome. NeuroReport, 10, 1-5.
3. Bellugi, U., Hickok, G., Lai, Z. C., & Jernigan, T. (1997). Links between brain & behavior: Clues to the neurobiology of Williams syndrome. International behavioral Neuroscience Society Abstracts, 6, 57.
4. Bellugi, U., Klima, E. S., & Wang, P. P. (1996). Cognitive and neural development: Clues from genetically based syndromes. In D. Magnussen (Ed.), The life-span development of individuals: Behavioral, neurobiological, and phsychosocial perpectives (pp. 223-243). The Nobel Symposium. New York: Cambridge University Press.
5. Bellugi, U., Lai, Z. C., & Korenberg, J. (In Press). Genes, brains and behavior: What genetic disorders reveal about behavior. In E. Bizzi, P. Calissano, & V. Volterra (Eds.), Frontiers of Biology Vol 4: The Brain of Homo Sapiens. Rome, Italy: Istituto della Enciclopedia Italiana.
6. Bellugi, U., Lichtenberger, L., Jones, W., Lai, Z., & St. George, M. (this volume). The neurocognitive profile of Williams syndrome: A complex pattern of strengths and weaknesses.
7. Bellugi, U., Lichtenberger, L., Mills, D., Galaburda, A., & Korenberg, J.R. (1999b). Bridging cognition, the brain and molecular genetics: Evidence from Williams syndrome. Trends in Neurosciences, 5, 197-207.
8. Bellugi, U., Mills, D., Jernigan, T., Hickok, G., & Galaburda, A. (1999c). Linking cognition, brain structure and brain function in Williams syndrome. In H. Tager-Flusberg (Ed.), Neurodevelopmental disorders: Contributions to a new framework from the cognitive neurosciences (pp. 111-139). Cambridge, MA: MIT Press.
9. Courchesne, E., Bellugi, U., & Singer, N. (1995). Infantile autism and Williams syndrome: Social and neural worlds apart. Special Issue, Genetic Counseling, 6, 144-145.
10. Courchesne, E., Yeung-Courchesne, R., Press, G. A., Hesselink, J. R., Jernigan, T. L. (1988). Hypoplasia of cerebellar vermal lobules VI and VII in autism. New England Journal of Medicine, 318, 1349-1354.
11. Damasio, A. R. (1994). Descartes' error: Emotion, reason, and the human brain. New York: G.P. Putnam's Sons.
12. Deacon, T. W. (1990). Rethinking mammalian brain evolution. American Zoology, 30, 629-705.
13. Ewart, A. K., Morris, C. A. Atkinson, D., Jin, W., Sternes, K., Spallone, P., Stock, A. D. Leppert, M., & Keating, M. T. (1993). Hemizygosity at the elastin locus in the developmental disorder, Williams syndrome. Nature Genetics, 5, 11-18.
14. Frank, R. J., Damasio, H., & Grabowski, T. J. (1997). Brainvox: An interactive, multimodal visualization and analysis system for neuroanatomical imaging. Neuroimage, 5, 13-30.
15. Galaburda, A., Wang, P. P., Bellugi, U., & Rossen, M. (1994). Cytoarchitectonic anomalies in a genetically based disorder: Williams syndrome. NeuroReport, 5, 757-758.
16. Hickok, G., Neville, H., Mills, D., Jones, W., Rossen, M., & Bellugi, U. (1995). Electrophysiological and quantitative MR analysis of the cortical auditory system in Williams syndrome. Cognitive Neuroscience Society Abstracts, 2, 66.
17. Jernigan, T. L., & Bellugi, U. (1990). Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome. Archives of Neurology, 47, 529-533.
18. Jernigan, T. L., & Bellugi, U. (1994). Neuroanatomical distinctions between Williams and Down syndromes. In S. Broman & J. Grafman (Eds.), Atypical cognitive deficits in developmental disorders: Implications for brain function (pp. 57-66). Hillsdale, NJ: Erlbaum.
19. Jernigan, T. L., Wang, P. P., & Bellugi, U. (1995). Neuromorphological characteristics of Williams syndrome. Special Issue, Genetic Counseling, 6, 145-146.
20. Jones, W., Bellugi, U., Lai, Z., Chiles, M., Reilly, J., Lincoln, A., & Adolphs, R. (this volume). Hypersociability in Williams syndrome.
21. Jones, W., Lai, Z. L., & Bellugi, U. (February, 1999). Relations between cerebellar vermal areas and neuropsychological performance in Williams syndrome. Journal of the International Neuropsychological Society, 5, 152.
22. Korenberg, J., Chen, X. -N., Hirota, H., Lai, Z., Bellugi, U., Burian, D., Roe, B., & Matsoka, R. (this volume). Genome structure and cognitive map of Williams syndrome.
23. Korenberg, J. R., Chen, X. -N., Lai, Z., Yimlamai, D., Bisighini, R., & Bellugi, U. (1997a). Williams syndrome: The search for the genetic origins of cognition. American Journal Human Genetics, 61, 103.
24. Korenberg, J. R., Chen, X. -N., Mitchell, S., & Sun, Z. -G. (1997b). The genomic organization of Williams syndrome. International Behavioral Neuroscience Society Abstracts, 6, 59.
25. Korenberg, J. R., Chen, X. -N., Mitchell, S., Sun, Z. -G., Hubert, R., Vataru, E. S., & Bellugi, U. (1996). The genomic organization of Williams syndrome. American Society for Human Genetics Supplement, 59, A304.
26. Korenberg, J. R., Hirota, H., Chen, X. -N., Lai, Z., Yimlamai, D., Matsuoka, R., & Bellugi, U. (1998). The molecular genetic basis of Williams syndrome. Presentation in symposium, Bridging cognition, brain and gene: Evidence from Williams syndrome. Abstract, Cognitive Neuroscience Society 1998 Annual Meeting Abstract Program, 11.
27. Lenhoff, H. M., Wang, P. P., Greenberg, F., & Bellugi, U. (1997). Williams syndrome and the brain. Scientific American, 277, 68-73.
28. Lowery, M., Morris, C., Ewart, A., Brothman, L., Zhu, X., Leonard, C., Carey, J., Keating, M., & Rothman, A. (1995). Strong correlations of elastin deletions, detected by FISH, with Williams syndrome: Evaluation of 235 patients. American Journal of Human Genetics, 57, 49-53.
29. Mills, D. L. (1998). Electrophysiological markers for Williams syndrome. Presentation in symposium, Bridging cognition, brain and gene: Evidence from Williams syndrome. Abstract, Cognitive Neuroscience Society 1998 Annual Meeting Abstract Program, 10.
30. Mills, D., Alvarez, T., St. George, M., Applebaum, L., Bellugi, U., & Neville, H. (this volume). Electrophysiological studies of face processing in Williams syndrome.
31. Mills, D., Neville, H., Appelbaum, G., Prat, C., & Bellugi, U. (1997). Electrophysiological markers of Williams syndrome. International Behavioral Neuroscience Society Abstracts, 6, 59.
32. Neville, H., Mills, D., & Bellugi, U. (1995). Functional brain organization in Williams syndrome. Abstract, Special Issue, Genetic Counseling, 6, 141-142.
33. Osborne, L. R., Herbrick, J., Greavette, T., Heng, H. H. Q., Tsui, L. -C., & Scherer, S. (1997a). PM52-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. Genomics, 45, 402-406.
34. Osborne, L. R., Sodar, S., Shi, X. -M., Pober, B., Costa, T., Scherer, S. W., & Tsui, L. -C. (1997b). Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome. American Journal of Human Genetics, 61, 449-452.
35. Perez-Jurado, L. A., Wang, Y. K., Peoples, R., Coloma, A., Cruces, J., & Francke, U. (1998). A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK. Human Molecular Genetics, 7, 325-334.
36. Reiss, A., Eliez, S., Schmitt, J. E., Strous, E., Lai, Z., Jones, W., & Bellugi, U. (this volume). Neuroanatomy of Williams syndrome: A high-resolution MRI study.
37. Sawchenko, P., Dargusch, R., Arias, C., & Bellugi, U. (1997). Evidence for elastin expression in cerebellar Purkinje cells: Implications for Williams syndrome. International Behavioral Neuroscience Society Abstracts, 6, 59.
38. Wang, P. P., Doherty, S. D., Hesselink, J. R., & Bellugi, U. (1992). Callosal morphology concurs with neurobehavioral and neuropathological findings in two neurodevelopmental disorders. Archives of Neurology, 49, 407-411.
39. Wang, Y. K., Samos, C. H., Peoples, R., Perez-Jurado, L. A., Nusse, R., & Francke, U. (1997) A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23. Human Molecular Genetics, 6, 465-472.