Publications by authors named "Colleen Morris"

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Case report of paroxysmal dystonia in a child with KBG syndrome: Expansion of the phenotype and utility of whole exome sequencing.
Christina R Dantam, Elizabeth Wilkes, Holly N Summers, Colleen A Morris, Rooman F Ahad

Medicine (Baltimore)· August 2025

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Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome.
Delong Liu, Charles J Billington, Neelam Raja, Zoe C Wong, Mark D Levin, Colleen A Morris

J Am Heart Assoc· February 2024

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

NPJ Genom Med· September 2023

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Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome.
J Shane Kippenhan, Michael D Gregory, Tiffany Nash, Philip Kohn, Carolyn B Mervis, Colleen A Morris

J Neurodev Disord· August 2023

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

Am J Obstet Gynecol MFM· June 2023

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Reply to Gomby: The utility of HOLC maps to capture historical housing discrimination.
Mahasin S Mujahid, Xing Gao, Loni P Tabb, Colleen Morris, Tené T Lewis

Proc Natl Acad Sci U S A· April 2022

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Historical redlining and cardiovascular health: The Multi-Ethnic Study of Atherosclerosis.
Mahasin S Mujahid, Xing Gao, Loni P Tabb, Colleen Morris, Tené T Lewis

Proc Natl Acad Sci U S A· December 2021

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Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.
Farah Qaiser, Yue Yin, Carolyn B Mervis, Colleen A Morris, Bonita P Klein-Tasman

Orphanet J Rare Dis· January 2021

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

Pediatrics· February 2020

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Williams-Beuren syndrome in diverse populations.
Paul Kruszka, Antonio R Porras, Deise Helena de Souza, Angélica Moresco, Victoria Huckstadt, Colleen A Morris

Am J Med Genet A· May 2018

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Digital Breast Tomosynthesis: Cost-Effectiveness of Using Private and Medicare Insurance in Community-Based Health Care Facilities.
Sara A Hunter, Colleen Morris, Karl Nelson, Brandon J Snyder, Thomas B Poulton

AJR Am J Roentgenol· May 2017

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Nine year old boy with chromosome 1q23.3-q25.1 deletion.
Felicia Lam, Colleen Morris

Am J Med Genet A· November 2016

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7q11.23 Duplication syndrome: Physical characteristics and natural history.
Colleen A Morris, Carolyn B Mervis, Alex P Paciorkowski, Omar Abdul-Rahman, Sarah L Dugan

Am J Med Genet A· December 2015

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Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23.
Emma Strong, Darci T Butcher, Rajat Singhania, Carolyn B Mervis, Colleen A Morris

Am J Hum Genet· August 2015

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Children with 7q11.23 duplication syndrome: psychological characteristics.
Carolyn B Mervis, Bonita P Klein-Tasman, Myra J Huffman, Shelley L Velleman, C Holley Pitts, Colleen A Morris

Am J Med Genet A· July 2015

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Duplication of GTF2I results in separation anxiety in mice and humans.
Carolyn B Mervis, Joana Dida, Emily Lam, Nicole A Crawford-Zelli, Edwin J Young, Colleen A Morris

Am J Hum Genet· June 2012

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The Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function.
Mbemba Jabbi, J Shane Kippenhan, Philip Kohn, Stefano Marenco, Carolyn B Mervis, Colleen A Morris

Proc Natl Acad Sci U S A· April 2012

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Longitudinal assessment of intellectual abilities of children with Williams syndrome: multilevel modeling of performance on the Kaufman Brief Intelligence Test-Second Edition.
Carolyn B Mervis, Doris J Kistler, Angela E John, Colleen A Morris

Am J Intellect Dev Disabil· March 2012

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Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome.
Mark C Hannibal, Kati J Buckingham, Sarah B Ng, Jeffrey E Ming, Anita E Beck, Colleen A Morris

Am J Med Genet A· July 2011

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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.
Colleen A Morris, Carolyn B Mervis, Lucy R Osborne

Mol Cytogenet· February 2011

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

Am J Med Genet C Semin Med Genet· November 2010

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Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.
Ariel M Pani, Holly H Hobart, Colleen A Morris, Carolyn B Mervis, Patricia Bray-Ward

PLoS One· August 2010

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Genetic counseling of adults with Williams syndrome: a first study.
Katrina Farwig, Amanda G Harmon, Kristina M Fontana, Carolyn B Mervis, Colleen A Morris

Am J Med Genet C Semin Med Genet· May 2010

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