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List of works by Charles Phillip Morris

A DRD2 and ANKK1 haplotype is associated with nicotine dependence

scientific article published on 29 February 2012

A cDNA clone for human glucosamine-6-sulphatase reveals differences between arylsulphatases and non-arylsulphatases

scientific article published on December 1, 1992

A common mutation for mucopolysaccharidosis type I associated with a severe Hurler syndrome phenotype

scientific article published in January 1992

A nonsense mutation (R220X) in the alpha-galactosidase A gene detected in a female carrier of Fabry disease

scientific article published on 01 June 1994

A novel DRD2 single-nucleotide polymorphism associated with schizophrenia predicts age of onset: HapMap tag-single-nucleotide polymorphism analysis

scientific article published on 23 August 2011

A novel SNP in COMT is associated with alcohol dependence but not opiate or nicotine dependence: a case control study

scientific article published on December 31, 2011

A sensitive mutation screening strategy for Fabry disease: detection of nine mutations in the alpha-galactosidase A gene

scientific article published on 01 January 1996

A splicing mutation (1898 + 1G-->T) in the CFTR gene causing cystic fibrosis.

scientific article published in January 1995

Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome

scientific article

Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering on.

scientific article published in February 2018

An 86-bp VNTR within IDUA is the basis of the D4S111 polymorphic locus

scientific article published on 01 December 1992

An N-acetylgalactosamine-4-sulfatase mutation (delta G238) results in a severe Maroteaux-Lamy phenotype

scientific article published on 01 January 1992

An arylsulfatase A (ARSA) missense mutation (T274M) causing late-infantile metachromatic leukodystrophy.

scientific article

Analysis of HapMap tag-SNPs in dysbindin (DTNBP1) reveals evidence of consistent association with schizophrenia.

scientific article published on 7 July 2010

Association of NOS1AP variants and depression phenotypes in schizophrenia

scientific article published on 8 September 2015

BDNF SNPs are implicated in comorbid alcohol dependence in schizophrenia but not in alcohol-dependent patients without schizophrenia

scientific article published on 3 July 2014

Brain-derived neurotrophic factor ( BDNF) gene: no major impact on antidepressant treatment response

scientific article published on 23 February 2009

Cannabinoid receptor 1 (CNR1) gene: impact on antidepressant treatment response and emotion processing in major depression.

scientific article published on 24 June 2008

Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase

article

Cigarette smoking in young adults: the influence of the HTR2A T102C polymorphism and punishment sensitivity.

scientific article

Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndrome

scientific article

Correction of alpha-L-fucosidase deficiency in fucosidosis fibroblasts by retroviral vector-mediated gene transfer

scientific article published on August 1, 1992

Cystic fibrosis prenatal diagnosis: confirmation of an equivocal microvillar enzyme result by direct analysis of the common gene mutation

scientific article published on 01 September 1990

DRD2 C957T and TaqIA Genotyping Reveals Gender Effects and Unique Low-Risk and High-Risk Genotypes in Alcohol Dependence

scientific article published on 11 May 2012

DRD2/ANKK1 Taq1A (rs 1800497 C>T) genotypes are associated with susceptibility to second generation antipsychotic-induced akathisia.

scientific article published on 31 October 2012

Dopamine D₃ receptor gene variation: impact on electroconvulsive therapy response and ventral striatum responsiveness in depression.

scientific article

Dysbindin (DTNBP1) variants are associated with hallucinations in schizophrenia.

scientific article published on 16 February 2015

Dysbindin (DTNBP1)--a role in psychotic depression?

scientific article

Effect of fatty acids, glucose, and insulin on hepatic glucose uptake and glycolysis

scientific article published on 01 June 2006

Epigenetic analysis confirms no accelerated brain aging in schizophrenia

scientific article published on 4 September 2017

Expression analysis of a human hepatic cell line in response to palmitate.

scientific article published on March 2005

Gene amplification directly from Guthrie blood spots

scientific article published on 01 December 1990

Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probe

scientific article published on 01 January 1992

Genetic mapping of new RFLPs at Xq27–q28

scientific article published on 01 January 1991

Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromes

scientific article published on 01 April 1992

Genome-wide DNA methylation analysis of human brain tissue from schizophrenia patients.

scientific article published on 07 January 2014

Haemochromatosis and HLA-H.

scientific article

HapMap tag-SNP analysis confirms a role for COMT in schizophrenia risk and reveals a novel association

scientific article published on 08 October 2010

Human N-acetylgalactosamine-4-sulphatase: protein maturation and isolation of genomic clones.

scientific article published on May 1991

Human alpha-L-iduronidase: cDNA isolation and expression

scientific journal article

Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase gene.

scientific article published on July 1991

Identification of genes differentially expressed by prematurely fused human sutures using a novel in vivo - in vitro approach

scientific article published on 17 December 2007

Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome)

scientific article published on 01 November 1993

Importance of the glycosylation and polyadenylation variants in metachromatic leukodystrophy pseudodeficiency phenotype.

scientific article published in August 1998

In vitro differentiation of human calvarial suture derived cells with and without dexamethasone does not induce in vivo-like expression

scientific article

Interaction between DRD2 C957T polymorphism and an acute psychosocial stressor on reward-related behavioral impulsivity.

scientific article

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

scientific article published on 08 October 2019

Interrogation of multimeric DNA amplification products by competitive primer extension using bst DNA polymerase (large fragment)

scientific article published on 01 November 2001

Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes.

scientific article published in January 1992

Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotype

scientific article published on 01 January 1993

Metachromatic leukodystrophy: a nonsense mutation (Q486X) in the arylsulphatase A (ARSA) gene

scientific article published on 01 January 1994

Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene

scientific article published on 01 June 1992

Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene

scientific article

Molecular genetics of metachromatic leukodystrophy

scientific article

Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications.

scientific article published on January 1995

Morquio A syndrome: cloning, sequence, and structure of the human N-acetylgalactosamine 6-sulfatase (GALNS) gene

scientific article (publication date: August 1994)

Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major allele

scientific article published on 01 March 1992

Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patients

scientific article published in June 1994

Multiple polymorphisms within the alpha-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotype

scientific article

Mutation analysis of 19 North American mucopolysaccharidosis type I patients: identification of two additional frequent mutations

scientific article published on 01 January 1994

Mutation analysis of 28 Gaucher disease patients: the Australasian experience

scientific article published on 01 January 1994

Mutation analysis of Australasian Gaucher disease patients

scientific article published on 01 September 1995

NOS1AP is associated with increased severity of PTSD and depression in untreated combat veterans

scientific article published on 9 November 2012

Neonatal screening for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis: four years' experience.

scientific article published on June 1994

Neural regulation of muscarinic receptors in chick expansor secundariorum muscle

scientific article published in Nature

PCR detection of two RFLPs in exon I of the alpha-L-iduronidase (IDUA) gene

scientific article (publication date: November 1992)

PCR of a VNTR linked to mucopolysaccharidosis type I and Huntington disease

scientific article published on November 25, 1991

PSA/KLK3 AREI promoter polymorphism alters androgen receptor binding and is associated with prostate cancer susceptibility

scientific article published on 6 December 2006

Persons with age-related maculopathy risk genotypes and clinically normal eyes have reduced mesopic vision

scientific article

Population frequency of the arylsulphatase A pseudo-deficiency allele

scientific article (publication date: May 1991)

Progress towards understanding the genetics of posttraumatic stress disorder

scientific article

Pyruvate carboxylase in the yeast pyc mutant

scientific article published on 01 October 1987

Regulation of human hepatocyte gene expression by fatty acids.

scientific article published on 13 August 2007

Relationship Among CFH and ARMS2 Genotypes, Macular Pigment Optical Density, and Neuroretinal Function in Persons Without Age-Related Macular Degeneration

scientific article published in November 2012

Reply to Migeon.

scientific article

SNP technologies for drug discovery: a current review.

scientific article published on September 2008

Sequence and domain structure of yeast pyruvate carboxylase

scientific article published in August 1988

Solid-phase amplification and detection: a single-tube diagnostic assay for infectious agents.

scientific article published on June 2001

Structure and sequence of the human alpha-L-iduronidase gene

scientific article published on August 1, 1992

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans

scientific article published in January 2009

The Effect of BCMO1 Gene Variants on Macular Pigment Optical Density in Young Healthy Caucasians.

scientific article published on 4 December 2014

The challenge of predicting macular degeneration

scientific article published on 22 July 2011

The factor V HR2 haplotype: prevalence and association of the A4070G and A6755G polymorphisms.

scientific article published in April 2001

The frequency of the common (delta F508) cystic fibrosis mutation in the Australian population

scientific article published on 01 March 1990

The iduronate sulfatase gene: Isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome

article

The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3

scientific article

The mucopolysaccharidoses. Diagnosis, molecular genetics and treatment.

scientific article published on October 1990

The relationship between BCMO1 gene variants and macular pigment optical density in persons with and without age-related macular degeneration

scientific article

The terminal structures of feather keratin mRNA

scientific article published on 01 August 1979

Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein

scientific article

Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis

scientific article

Visual function and risk genotypes in maternally inherited diabetes and deafness.

scientific article published in October 2013

Yeast pyruvate carboxylase: gene isolation

scientific article published in May 1987

alpha-L-iduronidase mutations (Q70X and P533R) associate with a severe Hurler phenotype

scientific article published in January 1992