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Journal Abstract Search
199 related items for PubMed ID: 37633900
1. Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome. Kippenhan JS, Gregory MD, Nash T, Kohn P, Mervis CB, Eisenberg DP, Garvey MH, Roe K, Morris CA, Kolachana B, Pani AM, Sorcher L, Berman KF. J Neurodev Disord; 2023 Aug 26; 15(1):29. PubMed ID: 37633900 [Abstract] [Full Text] [Related]
4. In-depth analysis of spatial cognition in Williams syndrome: A critical assessment of the role of the LIMK1 gene. Gray V, Karmiloff-Smith A, Funnell E, Tassabehji M. Neuropsychologia; 2006 Aug 26; 44(5):679-85. PubMed ID: 16216290 [Abstract] [Full Text] [Related]
5. From genes to brain development to phenotypic behavior: "dorsal-stream vulnerability" in relation to spatial cognition, attention, and planning of actions in Williams syndrome (WS) and other developmental disorders. Atkinson J, Braddick O. Prog Brain Res; 2011 Aug 26; 189():261-83. PubMed ID: 21489394 [Abstract] [Full Text] [Related]
6. Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome. Marenco S, Siuta MA, Kippenhan JS, Grodofsky S, Chang WL, Kohn P, Mervis CB, Morris CA, Weinberger DR, Meyer-Lindenberg A, Pierpaoli C, Berman KF. Proc Natl Acad Sci U S A; 2007 Sep 18; 104(38):15117-22. PubMed ID: 17827280 [Abstract] [Full Text] [Related]
7. A genetic model for understanding higher order visual processing: functional interactions of the ventral visual stream in Williams syndrome. Sarpal D, Buchsbaum BR, Kohn PD, Kippenhan JS, Mervis CB, Morris CA, Meyer-Lindenberg A, Berman KF. Cereb Cortex; 2008 Oct 18; 18(10):2402-9. PubMed ID: 18308711 [Abstract] [Full Text] [Related]
8. Inefficient search of large-scale space in Williams syndrome: further insights on the role of LIMK1 deletion in deficits of spatial cognition. Smith AD, Gilchrist ID, Hood B, Tassabehji M, Karmiloff-Smith A. Perception; 2009 Oct 18; 38(5):694-701. PubMed ID: 19662944 [Abstract] [Full Text] [Related]
10. Neurobiological models of visuospatial cognition in children with Williams syndrome: measures of dorsal-stream and frontal function. Atkinson J, Braddick O, Anker S, Curran W, Andrew R, Wattam-Bell J, Braddick F. Dev Neuropsychol; 2003 Oct 18; 23(1-2):139-72. PubMed ID: 12730023 [Abstract] [Full Text] [Related]
11. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region. Morris CA, Mervis CB, Hobart HH, Gregg RG, Bertrand J, Ensing GJ, Sommer A, Moore CA, Hopkin RJ, Spallone PA, Keating MT, Osborne L, Kimberley KW, Stock AD. Am J Med Genet A; 2003 Nov 15; 123A(1):45-59. PubMed ID: 14556246 [Abstract] [Full Text] [Related]
12. Contrasting neurofunctional correlates of face- and visuospatial-processing in children and adolescents with Williams syndrome: convergent results from four fMRI paradigms. Garvey MH, Nash T, Kippenhan JS, Kohn P, Mervis CB, Eisenberg DP, Ye J, Gregory MD, Berman KF. Sci Rep; 2024 May 05; 14(1):10304. PubMed ID: 38705917 [Abstract] [Full Text] [Related]
14. The behavioral phenotype of Williams syndrome: A recognizable pattern of neurodevelopment. Morris CA. Am J Med Genet C Semin Med Genet; 2010 Nov 15; 154C(4):427-31. PubMed ID: 20981771 [Abstract] [Full Text] [Related]