The behavioral phenotype of Williams syndrome: A recognizable pattern of neurodevelopment by Morris, Colleen A.

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Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23 by Strong, Emma, Butcher, Darci T., Singhania, Rajat, Mervis, Carolyn B., Morris, Colleen A., De Carvalho, Daniel, Weksberg, Rosanna, Osborne, Lucy R.

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Health Care Supervision for Children With Williams Syndrome by Morris, Colleen A, Braddock, Stephen R

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Introduction: Williams syndrome by Morris, Colleen A.

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Duplication of GTF2I Results in Separation Anxiety in Mice and Humans by Mervis, Carolyn B., Dida, Joana, Lam, Emily, Crawford-Zelli, Nicole A., Young, Edwin J., Henderson, Danielle R., Onay, Tuncer, Morris, Colleen A., Woodruff-Borden, Janet, Yeomans, John, Osborne, Lucy R.

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Florilegium, Sydney's Painted Garden by Morris, Colleen

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Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype by Qaiser, Farah, Yin, Yue, Mervis, Carolyn B, Morris, Colleen A, Klein-Tasman, Bonita P, Tam, Elaine, Osborne, Lucy R, Yuen, Ryan K C

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7q11.23 Duplication syndrome: Physical characteristics and natural history by Morris, Colleen A., Mervis, Carolyn B., Paciorkowski, Alex P., Abdul-Rahman, Omar, Dugan, Sarah L., Rope, Alan F., Bader, Patricia, Hendon, Laura G., Velleman, Shelley L., Klein-Tasman, Bonita P., Osborne, Lucy R.

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Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function by Jabbi, Mbemba, Kippenhan, J. Shane, Kohn, Philip, Marenco, Stefano, Mervis, Carolyn B, Morris, Colleen A, Meyer-Lindenberg, Andreas, Berman, Karen Faith

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Neural Basis of Genetically Determined Visuospatial Construction Deficit in Williams Syndrome by Meyer-Lindenberg, Andreas, Kohn, Philip, Mervis, Carolyn B., Kippenhan, J.Shane, Olsen, Rosanna K., Morris, Colleen A., Berman, Karen Faith

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Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome by Kippenhan, J. Shane, Gregory, Michael D, Nash, Tiffany, Kohn, Philip, Mervis, Carolyn B, Eisenberg, Daniel P, Garvey, Madeline H, Roe, Katherine, Morris, Colleen A, Kolachana, Bhaskar, Pani, Ariel M, Sorcher, Leah, Berman, Karen F

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Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome by Liu, Delong, Billington, Jr, Charles J, Raja, Neelam, Wong, Zoe C, Levin, Mark D, Resch, Wulfgang, Alba, Camille, Hupalo, Daniel N, Biamino, Elisa, Bedeschi, Maria Francesca, Digilio, Maria Cristina, Squeo, Gabriella Maria, Villa, Roberta, Parrish, Pheobe C R, Knutsen, Russell H, Osgood, Sharon, Freeman, Joy A, Dalgard, Clifton L, Merla, Giuseppe, Pober, Barbara R, Mervis, Carolyn B, Roberts, Amy E, Morris, Colleen A, Osborne, Lucy R, Kozel, Beth A

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Montague Island vegetable garden restoration project by Morris, Colleen

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DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number by Strong, Emma, Mervis, Carolyn B., Tam, Elaine, Morris, Colleen A., Klein-Tasman, Bonita P., Velleman, Shelley L., Osborne, Lucy R.

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Neighborhood disinvestment and severe maternal morbidity in the state of California by Mujahid, Mahasin S., Wall-Wieler, Elizabeth, Hailu, Elleni M., Berkowitz, Rachel L., Gao, Xing, Morris, Colleen M., Abrams, Barbara, Lyndon, Audrey, Carmichael, Suzan L.

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Children with 7q11.23 duplication syndrome: Psychological characteristics by Mervis, Carolyn B., Klein-Tasman, Bonita P., Huffman, Myra J., Velleman, Shelley L., Pitts, C. Holley, Henderson, Danielle R., Woodruff-Borden, Janet, Morris, Colleen A., Osborne, Lucy R.

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Modernist design and the Australian garden by Morris, Colleen

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Genetic Contributions to Human Gyrification: Sulcal Morphometry in Williams Syndrome by Kippenhan, J. Shane, Olsen, Rosanna K, Mervis, Carolyn B, Morris, Colleen A, Kohn, Philip, Meyer-Lindenberg, Andreas, Berman, Karen Faith

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Diagnosis and management of medical problems in adults with Williams-Beuren syndrome by Pober, Barbara R., Morris, Colleen A.

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Infantile Spasms Is Associated with Deletion of the MAGI2 Gene on Chromosome 7q11.23-q21.11 by Marshall, Christian R., Young, Edwin J., Pani, Ariel M., Freckmann, Mary-Louise, Lacassie, Yves, Howald, Cédric, Fitzgerald, Kristi K., Peippo, Maarit, Morris, Colleen A., Shane, Kate, Priolo, Manuela, Morimoto, Masafumi, Kondo, Ikuko, Manguoglu, Esra, Berker-Karauzum, Sibel, Edery, Patrick, Hobart, Holly H., Mervis, Carolyn B., Zuffardi, Orsetta, Reymond, Alexandre, Kaplan, Paige, Tassabehji, May, Gregg, Ronald G., Scherer, Stephen W., Osborne, Lucy R.

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