Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23
Strong, Emma, Butcher, Darci T., Singhania, Rajat, Mervis, Carolyn B., Morris, Colleen A., De Carvalho, Daniel, Weksberg, Rosanna, Osborne, Lucy R.
Published in American journal of human genetics (06.08.2015)
Published in American journal of human genetics (06.08.2015)
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Journal Article
Duplication of GTF2I Results in Separation Anxiety in Mice and Humans
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.
Published in American journal of human genetics (08.06.2012)
Published in American journal of human genetics (08.06.2012)
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Journal Article
Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype
Qaiser, Farah, Yin, Yue, Mervis, Carolyn B, Morris, Colleen A, Klein-Tasman, Bonita P, Tam, Elaine, Osborne, Lucy R, Yuen, Ryan K C
Published in Orphanet journal of rare diseases (06.01.2021)
Published in Orphanet journal of rare diseases (06.01.2021)
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Journal Article
Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function
Jabbi, Mbemba, Kippenhan, J. Shane, Kohn, Philip, Marenco, Stefano, Mervis, Carolyn B, Morris, Colleen A, Meyer-Lindenberg, Andreas, Berman, Karen Faith
Published in Proceedings of the National Academy of Sciences - PNAS (03.04.2012)
Published in Proceedings of the National Academy of Sciences - PNAS (03.04.2012)
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Journal Article
Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome
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
Published in Journal of neurodevelopmental disorders (26.08.2023)
Published in Journal of neurodevelopmental disorders (26.08.2023)
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Journal Article
Neural Basis of Genetically Determined Visuospatial Construction Deficit in Williams Syndrome
Meyer-Lindenberg, Andreas, Kohn, Philip, Mervis, Carolyn B., Kippenhan, J.Shane, Olsen, Rosanna K., Morris, Colleen A., Berman, Karen Faith
Published in Neuron (Cambridge, Mass.) (02.09.2004)
Published in Neuron (Cambridge, Mass.) (02.09.2004)
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Journal Article
DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number
Strong, Emma, Mervis, Carolyn B, Tam, Elaine, Morris, Colleen A, Klein-Tasman, Bonita P, Velleman, Shelley L, Osborne, Lucy R
Published in Npj genomic medicine (14.09.2023)
Published in Npj genomic medicine (14.09.2023)
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Journal Article
Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome
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
Published in Journal of the American Heart Association (06.02.2024)
Published in Journal of the American Heart Association (06.02.2024)
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Journal Article
Genetic Contributions to Human Gyrification: Sulcal Morphometry in Williams Syndrome
Kippenhan, J. Shane, Olsen, Rosanna K, Mervis, Carolyn B, Morris, Colleen A, Kohn, Philip, Meyer-Lindenberg, Andreas, Berman, Karen Faith
Published in The Journal of neuroscience (24.08.2005)
Published in The Journal of neuroscience (24.08.2005)
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Journal Article
Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome
Marenco, Stefano, Siuta, Michael A, Kippenhan, J. Shane, Grodofsky, Samuel, Chang, Wei-li, Kohn, Philip, Mervis, Carolyn B, Morris, Colleen A, Weinberger, Daniel R, Meyer-Lindenberg, Andreas, Pierpaoli, Carlo, Berman, Karen Faith
Published in Proceedings of the National Academy of Sciences - PNAS (18.09.2007)
Published in Proceedings of the National Academy of Sciences - PNAS (18.09.2007)
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Journal Article
Introduction: Williams syndrome
Morris, Colleen A.
Published in American journal of medical genetics. Part C, Seminars in medical genetics (15.05.2010)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (15.05.2010)
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Journal Article
Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome
Pani, Ariel M, Hobart, Holly H, Morris, Colleen A, Mervis, Carolyn B, Bray-Ward, Patricia, Kimberley, Kendra W, Rios, Cecilia M, Clark, Robin C, Gulbronson, Maricela D, Gowans, Gordon C, Gregg, Ronald G
Published in PloS one (31.08.2010)
Published in PloS one (31.08.2010)
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Journal Article
Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
Ewart, Amanda K, Morris, Colleen A, Atkinson, Donald, Jin, Weishan, Sternes, Keith, Spallone, Patricia, Stock, A. Dean, Leppert, Mark, Keating, Mark T
Published in Nature genetics (01.09.1993)
Published in Nature genetics (01.09.1993)
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Journal Article
LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition
Frangiskakis, J.Michael, Ewart, Amanda K, Morris, Colleen A, Mervis, Carolyn B, Bertrand, Jacquelyn, Robinson, Byron F, Klein, Bonita P, Ensing, Gregory J, Everett, Lorraine A, Green, Eric D, Pröschel, Christoph, Gutowski, Nick J, Noble, Mark, Atkinson, Donald L, Odelberg, Shannon J, Keating, Mark T
Published in Cell (12.07.1996)
Published in Cell (12.07.1996)
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Journal Article
7q11.23 Duplication syndrome: Physical characteristics and natural history
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.
Published in American journal of medical genetics. Part A (01.12.2015)
Published in American journal of medical genetics. Part A (01.12.2015)
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Journal Article
Frequency of the 7q11.23 inversion polymorphism in transmitting parents of children with Williams syndrome and in the general population does not differ between North America and Europe
Morris, Colleen A, Mervis, Carolyn B, Osborne, Lucy R
Published in Molecular cytogenetics (28.02.2011)
Published in Molecular cytogenetics (28.02.2011)
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Journal Article