List of works - Colleen A. Morris

18p- syndrome and hypopituitarism ⬇️

scientific article published on September 1, 1992

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

scientific article published on 3 September 2015

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

scientific article published in June 1994

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

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

scientific article

A novel human gene FKBP6 is deleted in Williams syndrome

scientific journal article

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

scientific article

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

scientific article

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

scientific article published on July 2008

Alpha 1 antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndrome

scientific article

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

scientific article published on January 1, 2003

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

scientific article published on 18 May 2006

Beare-Stevenson cutis gyrata syndrome

scientific article published on September 1, 1992

Behavioral phenotypes in genetic syndromes: genetic clues to human behavior

scientific article

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

scientific article

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

scientific article

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

scientific article published on August 2007

Duplication of GTF2I results in separation anxiety in mice and humans

scientific article

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

scientific article published on July 1, 1997

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

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 ⬇️

scientific article published on February 28, 2011

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

scientific article

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

Genetic aspects of supravalvular aortic stenosis

scientific article published on May 1, 1998

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

scholarly article

Genetic counseling of adults with Williams syndrome: a first study

scientific article

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome

scientific article

Health Care Supervision for Children With Williams Syndrome

scientific article published on 21 January 2020

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

scientific article published on 01 July 2003

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

scientific article published on September 1, 1993

Hypothesis for development of a behavioral phenotype in Williams syndrome

scientific article published on January 1990

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

scientific article published on 19 June 2008

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

scientific article published in January 2005

Intracranial arteries in individuals with the elastin gene hemideletion of Williams syndrome

scientific article published on 18 July 2013

Introduction: Williams syndrome

scientific article

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

scientific article

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

scientific article

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

Natural history of Williams syndrome: physical characteristics

scientific article

Neural basis of genetically determined visuospatial construction deficit in Williams syndrome

scientific article published in September 2004

Neural correlates of genetically abnormal social cognition in Williams syndrome

scientific article published on 10 July 2005

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

scientific article

Nine year old boy with chromosome 1q23.3-q25.1 deletion

scientific article published on 15 July 2016

Prenatal diagnosis of distal arthrogryposis

scientific article published on March 1988

Retinotopically defined primary visual cortex in Williams syndrome

scientific article

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

scientific article

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

scientific article

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

scientific article published on July 1, 1995

Sudden death in Williams syndrome: report of ten cases

scientific article published on December 1996

Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene

scientific article

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

scientific article published on 01 July 1993

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

scientific article

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

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

scientific article published in July 2008

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

scientific article

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

scientific article published in August 2001

Three diagnostic signs in Williams syndrome

Williams Syndrome and Related Disorders ⬇️

scientific article published on January 1, 2000

Williams–Beuren syndrome in diverse populations

scientific article published in May 2018

List of works by Colleen A. Morris

18p- syndrome and hypopituitarism ⬇️

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

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

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

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

A novel human gene FKBP6 is deleted in Williams syndrome

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

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

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

Alpha 1 antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndrome

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

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

Beare-Stevenson cutis gyrata syndrome

Behavioral phenotypes in genetic syndromes: genetic clues to human behavior

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

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

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

Duplication of GTF2I results in separation anxiety in mice and humans

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

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

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 ⬇️

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

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

Genetic aspects of supravalvular aortic stenosis

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

Genetic counseling of adults with Williams syndrome: a first study

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome

Health Care Supervision for Children With Williams Syndrome

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

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

Hypothesis for development of a behavioral phenotype in Williams syndrome

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

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

Intracranial arteries in individuals with the elastin gene hemideletion of Williams syndrome

Introduction: Williams syndrome

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

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

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

Natural history of Williams syndrome: physical characteristics

Neural basis of genetically determined visuospatial construction deficit in Williams syndrome

Neural correlates of genetically abnormal social cognition in Williams syndrome

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

Nine year old boy with chromosome 1q23.3-q25.1 deletion

Prenatal diagnosis of distal arthrogryposis

Retinotopically defined primary visual cortex in Williams syndrome

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

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

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

Sudden death in Williams syndrome: report of ten cases

Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene

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

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

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 ⬇️

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

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

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

Three diagnostic signs in Williams syndrome

Williams Syndrome and Related Disorders ⬇️

Williams–Beuren syndrome in diverse populations