Morris, Colleen A.

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

Williams Syndrome ResearchConnective tissue disorders research

Cited by 1,138

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

Krantz, I. D., McCallum, J., DeScipio, C., Kaur, M., Gillis, L. A., Yaeger, D., Jukofsky, L., Wasserman, N., Bottani, A., Morris, C. A., et al. (2004) · Nature Genetics

Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders

Cited by 713

Neural correlates of genetically abnormal social cognition in Williams syndrome

Meyer-Lindenberg, A., Hariri, A. R., Munoz, K. E., Mervis, C. B., Mattay, V. S., Morris, C. A., & Berman, K. F. (2005) · Nature Neuroscience

Williams Syndrome ResearchFace Recognition and Perception

Cited by 357

Attentional characteristics of infants and toddlers with Williams syndrome during triadic interactions

Mervis, C. B., Morris, C. A., Klein-Tasman, B. P., Bertrand, J., Kwitny, S., Appelbaum, L. G., & Rice, C. E. (2003) · Developmental Neuropsychology

Williams Syndrome ResearchAutism Spectrum Disorder Research

Cited by 170

Symmetrical dose-dependent dna-methylation profiles in children with deletion or duplication of 7q11.23

Strong, E., Butcher, D. T., Singhania, R., Mervis, C. B., Morris, C. A., De Carvalho, D., Weksberg, R., & Osborne, L. R. (2015) · The American Journal of Human Genetics

Williams Syndrome ResearchEpigenetics and DNA Methylation

Cited by 71