List of works - Colleen A. Morris

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

scientific article published on September 1, 1993

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

scientific article

Natural history of Williams syndrome: physical characteristics

scientific article

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

scientific article

Neural correlates of genetically abnormal social cognition in Williams syndrome

scientific article published on 10 July 2005

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

scientific article

Severe expressive-language delay related to duplication of the Williams-Beuren locus

scientific article

Neural basis of genetically determined visuospatial construction deficit in Williams syndrome

scientific article published in September 2004

Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis

scientific article published on July 1, 1997

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region

scientific article published in November 2003

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

scientific article

Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome

scientific article

Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene

scientific article

Williams Syndrome and Related Disorders

scientific article published on January 1, 2000

A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

scientific article

Attentional Characteristics of Infants and Toddlers With Williams Syndrome During Triadic Interactions

scientific article published on January 1, 2003

A novel human gene, WSTF, is deleted in Williams syndrome

scientific article

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

scientific article published on 19 June 2008

Sudden death in Williams syndrome: report of ten cases

scientific article published on December 1996

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

scholarly article

A novel human gene FKBP6 is deleted in Williams syndrome

scientific journal article

Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients

scientific article published on July 1, 1995

Duplication of GTF2I results in separation anxiety in mice and humans

scientific article

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.

scientific article published in June 1994

Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management

scientific article published on July 2008

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

scientific article published on August 2007

Beare-Stevenson cutis gyrata syndrome

scientific article published on September 1, 1992

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

scientific article published on 12 March 2012

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

scientific article published on November 15, 2010

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

scientific article published on September 3, 2015

Familial antiphospholipid antibody syndrome: Criteria for disease and evidence for autosomal dominant inheritance

article

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

scientific article

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome

scientific article

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

scientific article published on 27 February 2008

Introduction: Williams syndrome

scientific article

Hypothesis for development of a behavioral phenotype in Williams syndrome

scientific article published on January 1990

Supravalvular aortic stenosis cosegregates with a familial 6; 7 translocation which disrupts the elastin gene

scientific article published on 01 July 1993

Longitudinal Assessment of Intellectual Abilities of Children With Williams Syndrome: Multilevel Modeling of Performance on the Kaufman Brief Intelligence Test—Second Edition

scientific article published on March 1, 2012

Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content

scientific article

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

scientific article

Children with 7q11.23 duplication syndrome: Psychological characteristics

scientific article published on April 21, 2015

The subtle facial signs of prenatal exposure to alcohol: an anthropometric approach

scientific article published in August 2001

Genetic aspects of supravalvular aortic stenosis

scientific article published on May 1, 1998

The common inversion of the Williams-Beuren syndrome region at 7q11.23 does not cause clinical symptoms

scientific article published in July 2008

Prenatal diagnosis of distal arthrogryposis

scientific article published on March 1988

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

scientific article published on 01 July 2003

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

scientific article published in January 2005

18p- syndrome and hypopituitarism

scientific article published on September 1, 1992

Williams–Beuren syndrome in diverse populations

scientific article published in May 2018

Retinotopically defined primary visual cortex in Williams syndrome

scientific article

List of works by Colleen A. Morris

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

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

Natural history of Williams syndrome: physical characteristics

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

Neural correlates of genetically abnormal social cognition in Williams syndrome

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

Severe expressive-language delay related to duplication of the Williams-Beuren locus

Neural basis of genetically determined visuospatial construction deficit in Williams syndrome

Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region

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

Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome

Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene

Williams Syndrome and Related Disorders

A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

Attentional Characteristics of Infants and Toddlers With Williams Syndrome During Triadic Interactions

A novel human gene, WSTF, is deleted in Williams syndrome

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

Sudden death in Williams syndrome: report of ten cases

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

A novel human gene FKBP6 is deleted in Williams syndrome

Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients

Duplication of GTF2I results in separation anxiety in mice and humans

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.

Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management

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

Beare-Stevenson cutis gyrata syndrome

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

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

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

Familial antiphospholipid antibody syndrome: Criteria for disease and evidence for autosomal dominant inheritance

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

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome

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

Introduction: Williams syndrome

Hypothesis for development of a behavioral phenotype in Williams syndrome

Supravalvular aortic stenosis cosegregates with a familial 6; 7 translocation which disrupts the elastin gene

Longitudinal Assessment of Intellectual Abilities of Children With Williams Syndrome: Multilevel Modeling of Performance on the Kaufman Brief Intelligence Test—Second Edition

Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content

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

Children with 7q11.23 duplication syndrome: Psychological characteristics

The subtle facial signs of prenatal exposure to alcohol: an anthropometric approach

Genetic aspects of supravalvular aortic stenosis

The common inversion of the Williams-Beuren syndrome region at 7q11.23 does not cause clinical symptoms

Prenatal diagnosis of distal arthrogryposis

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

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

18p- syndrome and hypopituitarism

Williams–Beuren syndrome in diverse populations

Retinotopically defined primary visual cortex in Williams syndrome