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The Journal of Clinical Investigation|June 14, 2005
Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndromeAndreas Meyer-Lindenberg, Carolyn B Mervis, Deepak Sarpal, et al.Proceedings of the National Academy of Sciences of the United States of America|September 11, 2007
Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndromeStefano Marenco, Michael A Siuta, J Shane Kippenhan, et al.American Journal of Medical Genetics. Part A|September 4, 2015
7q11.23 Duplication syndrome: Physical characteristics and natural historyColleen A Morris, Carolyn B Mervis, Alex P Paciorkowski, et al.Plos One|September 9, 2010
Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndromeAriel M Pani, Holly H Hobart, Colleen A Morris, et al.Journal of Neurodevelopmental Disorders|August 26, 2023
Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndromeJ Shane Kippenhan, Michael D Gregory, Tiffany Nash, et al.The New England Journal of Medicine|October 21, 2005
Severe expressive-language delay related to duplication of the Williams-Beuren locusMartin J Somerville, Carolyn B Mervis, Edwin J Young, et al.American Journal of Medical Genetics. Part A|October 14, 2003
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome regionColleen A Morris, Carolyn B Mervis, Holly H Hobart, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and managementAngela E Lin, Craig T Basson, Elizabeth Goldmuntz, et al.Biorxiv : the Preprint Server for Biology|January 16, 2026
Pannexin-1 channel activity regulates neurogenesis and cell survival in the developing cortexNorma K Hylton, David J Kang, Steven C Decker, et al.Birth Defects Research|August 27, 2024
Paternal Valproate Treatment and Risk of Childhood Neurodevelopmental Disorders: Precautionary Regulatory Measures Are Insufficiently SubstantiatedJoan D Garey, Per Damkier, Anthony R Scialli, et al.Pageof 10