Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 105

1.

The Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function.

Jabbi M, Kippenhan JS, Kohn P, Marenco S, Mervis CB, Morris CA, Meyer-Lindenberg A, Berman KF.

Proc Natl Acad Sci U S A. 2012 Apr 3;109(14):E860-6. doi: 10.1073/pnas.1114774109. Epub 2012 Mar 12.

PMID:
22411788
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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. Epub 2007 Sep 7.

PMID:
17827280
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Genetic contributions to human gyrification: sulcal morphometry in Williams syndrome.

Kippenhan JS, Olsen RK, Mervis CB, Morris CA, Kohn P, Meyer-Lindenberg A, Berman KF.

J Neurosci. 2005 Aug 24;25(34):7840-6.

PMID:
16120786
[PubMed - indexed for MEDLINE]
Free Article
4.

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(10):2402-9. doi: 10.1093/cercor/bhn004. Epub 2008 Feb 27.

PMID:
18308711
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.

Järvinen-Pasley A, Bellugi U, Reilly J, Mills DL, Galaburda A, Reiss AL, Korenberg JR.

Dev Psychopathol. 2008 Winter;20(1):1-35. doi: 10.1017/S0954579408000011. Review.

PMID:
18211726
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome.

Meyer-Lindenberg A, Mervis CB, Sarpal D, Koch P, Steele S, Kohn P, Marenco S, Morris CA, Das S, Kippenhan S, Mattay VS, Weinberger DR, Berman KF.

J Clin Invest. 2005 Jul;115(7):1888-95. Epub 2005 Jun 9.

PMID:
15951840
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

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. doi: 10.1002/ajmg.c.30286. Review.

PMID:
20981771
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
14556246
[PubMed - indexed for MEDLINE]
9.

Neural basis of genetically determined visuospatial construction deficit in Williams syndrome.

Meyer-Lindenberg A, Kohn P, Mervis CB, Kippenhan JS, Olsen RK, Morris CA, Berman KF.

Neuron. 2004 Sep 2;43(5):623-31.

PMID:
15339645
[PubMed - indexed for MEDLINE]
10.

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;38(5):694-701.

PMID:
19662944
[PubMed - indexed for MEDLINE]
11.

"Everybody in the world is my friend" hypersociability in young children with Williams syndrome.

Doyle TF, Bellugi U, Korenberg JR, Graham J.

Am J Med Genet A. 2004 Jan 30;124A(3):263-73.

PMID:
14708099
[PubMed - indexed for MEDLINE]
12.

Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior.

Dai L, Carter CS, Ying J, Bellugi U, Pournajafi-Nazarloo H, Korenberg JR.

PLoS One. 2012;7(6):e38513. doi: 10.1371/journal.pone.0038513. Epub 2012 Jun 12.

PMID:
22719898
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The social phenotype of Williams syndrome.

Järvinen A, Korenberg JR, Bellugi U.

Curr Opin Neurobiol. 2013 Jun;23(3):414-22. doi: 10.1016/j.conb.2012.12.006. Epub 2013 Jan 15. Review.

PMID:
23332975
[PubMed - indexed for MEDLINE]
14.

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes.

Meng X, Lu X, Li Z, Green ED, Massa H, Trask BJ, Morris CA, Keating MT.

Hum Genet. 1998 Nov;103(5):590-9.

PMID:
9860302
[PubMed - indexed for MEDLINE]
15.

Association between cerebral shape and social use of language in Williams syndrome.

Gothelf D, Searcy YM, Reilly J, Lai PT, Lanre-Amos T, Mills D, Korenberg JR, Galaburda A, Bellugi U, Reiss AL.

Am J Med Genet A. 2008 Nov 1;146A(21):2753-61. doi: 10.1002/ajmg.a.32507.

PMID:
18924169
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

LIMK1 and CLIP-115: linking cytoskeletal defects to Williams syndrome.

Hoogenraad CC, Akhmanova A, Galjart N, De Zeeuw CI.

Bioessays. 2004 Feb;26(2):141-50. Review.

PMID:
14745832
[PubMed - indexed for MEDLINE]
17.

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.

Sakurai T, Dorr NP, Takahashi N, McInnes LA, Elder GA, Buxbaum JD.

Autism Res. 2011 Feb;4(1):28-39. doi: 10.1002/aur.169. Epub 2010 Dec 3.

PMID:
21328569
[PubMed - indexed for MEDLINE]
18.

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;44(5):679-85. Epub 2005 Oct 10.

PMID:
16216290
[PubMed - indexed for MEDLINE]
19.

Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content.

Muñoz KE, Meyer-Lindenberg A, Hariri AR, Mervis CB, Mattay VS, Morris CA, Berman KF.

Neuroimage. 2010 Mar;50(1):340-6. doi: 10.1016/j.neuroimage.2009.11.069. Epub 2009 Dec 11.

PMID:
20004252
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Comparative genomic sequence analysis of the Williams syndrome region (LIMK1-RFC2) of human chromosome 7q11.23.

Martindale DW, Wilson MD, Wang D, Burke RD, Chen X, Duronio V, Koop BF.

Mamm Genome. 2000 Oct;11(10):890-8.

PMID:
11003705
[PubMed - indexed for MEDLINE]
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk