Colleen A Morris

Colleen A Morris

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Colleen A Morris

Colleen A Morris

Publications by authors named "Colleen A Morris"

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Williams-Beuren syndrome in diverse populations.

Am J Med Genet A 2018 05;176(5):1128-1136

Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland.

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http://doi.wiley.com/10.1002/ajmg.a.38672
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http://dx.doi.org/10.1002/ajmg.a.38672DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007881PMC
May 2018

7q11.23 Duplication syndrome: Physical characteristics and natural history.

Am J Med Genet A 2015 Dec 3;167A(12):2916-35. Epub 2015 Sep 3.

Departments of Medicine and Molecular Genetics and Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.37340DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005957PMC
December 2015

Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23.

Am J Hum Genet 2015 Aug 9;97(2):216-27. Epub 2015 Jul 9.

Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada; Department of Medicine, University of Toronto, ON M5G 2C4, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.05.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573259PMC
August 2015

Children with 7q11.23 duplication syndrome: psychological characteristics.

Am J Med Genet A 2015 Jul 21;167(7):1436-50. Epub 2015 Apr 21.

Departments of Medicine and Molecular Genetics and Institute of Medical Science, University of Toronto, Toronto, ON, Canada.

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http://dx.doi.org/10.1002/ajmg.a.37071DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545595PMC
July 2015

The Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function.

Proc Natl Acad Sci U S A 2012 Apr 12;109(14):E860-6. Epub 2012 Mar 12.

Section on Integrative Neuroimaging, National Institute of Mental Health, Intramural Research Program, National Institutes of Health, Bethesda, MD 20892, USA.

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http://www.pnas.org/cgi/doi/10.1073/pnas.1114774109
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http://dx.doi.org/10.1073/pnas.1114774109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325656PMC
April 2012

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

Authors:
Colleen A Morris

Am J Med Genet C Semin Med Genet 2010 Nov;154C(4):427-31

Genetics Division of the Department of Pediatrics at the University of Nevada School of Medicine, USA.

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http://doi.wiley.com/10.1002/ajmg.c.30286
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http://dx.doi.org/10.1002/ajmg.c.30286DOI Listing
November 2010

Introduction: Williams syndrome.

Authors:
Colleen A Morris

Am J Med Genet C Semin Med Genet 2010 May;154C(2):203-8

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http://dx.doi.org/10.1002/ajmg.c.30266DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946897PMC
May 2010

Genetic counseling of adults with Williams syndrome: a first study.

Am J Med Genet C Semin Med Genet 2010 May;154C(2):307-15

Department of Pediatrics, University of Nevada School of Medicine, NV, USA.

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http://dx.doi.org/10.1002/ajmg.c.30264DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953462PMC
May 2010

Retinotopically defined primary visual cortex in Williams syndrome.

Brain 2009 Mar 2;132(Pt 3):635-44. Epub 2009 Mar 2.

Section on Integrative Neuroimaging, Clinical Brain Disorders Branch, National Institute of Mental Health, NIH, DHHS, Bethesda, MD 20892-1365, USA.

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http://dx.doi.org/10.1093/brain/awn362DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724925PMC
March 2009

A genetic model for understanding higher order visual processing: functional interactions of the ventral visual stream in Williams syndrome.

Cereb Cortex 2008 Oct 27;18(10):2402-9. Epub 2008 Feb 27.

Section on Integrative Neuroimaging, Clinical Brain Disorders Branch, Genes, Cognition and Psychosis Program, National Institute of Mental Health, NIH, DHHS, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1093/cercor/bhn004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2733313PMC
October 2008

Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome.

Proc Natl Acad Sci U S A 2007 Sep 7;104(38):15117-22. Epub 2007 Sep 7.

Clinical Brain Disorders Branch, Genes Cognition and Psychosis Program, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1073/pnas.0704311104DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1986622PMC
September 2007

Diagnosis and management of medical problems in adults with Williams-Beuren syndrome.

Am J Med Genet C Semin Med Genet 2007 Aug;145C(3):280-90

Harvard Medical School, Boston, USA.

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http://dx.doi.org/10.1002/ajmg.c.30139DOI Listing
August 2007

BAC-FISH refutes report of an 8p22-8p23.1 inversion or duplication in 8 patients with Kabuki syndrome.

BMC Med Genet 2006 May 18;7:46. Epub 2006 May 18.

Department of Pediatrics/Division of Genetics, University of Nevada School of Medicine, Las Vegas, NV, USA.

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http://dx.doi.org/10.1186/1471-2350-7-46DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513556PMC
May 2006

Bilateral semilunar valve disease in a child with partial deletion of the Williams-Beuren syndrome region is associated with elastin haploinsufficiency.

J Heart Valve Dis 2006 May;15(3):352-5

Division of Cardiology, Cincinnati Children's Hospital, Cincinnati, Ohio 45229-3039, USA.

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May 2006

Neural correlates of genetically abnormal social cognition in Williams syndrome.

Nat Neurosci 2005 Aug 10;8(8):991-3. Epub 2005 Jul 10.

Section on Integrative Neuroimaging, National Institute of Mental Health, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1038/nn1494DOI Listing
August 2005

Genetic contributions to human gyrification: sulcal morphometry in Williams syndrome.

J Neurosci 2005 Aug;25(34):7840-6

National Institute of Mental Health, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1523/JNEUROSCI.1722-05.2005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6725255PMC
August 2005

Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome.

J Clin Invest 2005 Jul 9;115(7):1888-95. Epub 2005 Jun 9.

Genes, Cognition, and Psychosis Program, National Institute of Mental Health, NIH, Department of Health and Human Services, Bethesda, MD 20892-1365, USA.

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http://dx.doi.org/10.1172/JCI24892DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1143592PMC
July 2005

Intellectual abilities and adaptive behavior of children and adolescents with Kabuki syndrome: a preliminary study.

Am J Med Genet A 2005 Jan;132A(3):248-55

Department of Psychological and Brain Sciences, University of Louisville, Louisville, Kentucky 40292, USA.

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http://dx.doi.org/10.1002/ajmg.a.30334DOI Listing
January 2005

Neural basis of genetically determined visuospatial construction deficit in Williams syndrome.

Neuron 2004 Sep;43(5):623-31

Unit on Integrative Neuroimaging, Clinical Brain Disorders Branch, National Institute of Mental Health, National Institutes of Health, Department of Health and Human Services, 10-4C101, 9000 Rockville Pike, Bethesda, MD 20892, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S089662730400521
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http://dx.doi.org/10.1016/j.neuron.2004.08.014DOI Listing
September 2004

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

Dev Neuropsychol 2003 ;23(1-2):243-68

Department of Psychological and Brain Sciences, University of Louisville, KY 40292, USA.

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http://dx.doi.org/10.1080/87565641.2003.9651894DOI Listing
July 2003

Heat shock protein 27 gene: chromosomal and molecular location and relationship to Williams syndrome.

Am J Med Genet A 2003 Jul;120A(3):320-5

Department of Pediatrics, Division of Genetics, Laboratory of Molecular Cytogenetics, University of Nevada School of Medicine, Las Vegas 89102, USA.

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http://dx.doi.org/10.1002/ajmg.a.20055DOI Listing
July 2003

Behavioral phenotypes in genetic syndromes: genetic clues to human behavior.

Adv Pediatr 2002 ;49:59-86

Department of Pediatrics, University of California, Irvine, USA.

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January 2003

New perspectives on the face in fetal alcohol syndrome: what anthropometry tells us.

Am J Med Genet 2002 May;109(4):249-60

St. Vincent Hospitals and Health Services, 2001 West 86th Street, PO Box 40970, Indianapolis, IN 46240, USA.

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http://dx.doi.org/10.1002/ajmg.10197DOI Listing
May 2002