C. Phillip Morris

Interaction between DRD2 C957T polymorphism and an acute psychosocial stressor on reward-related behavioral impulsivity (2009)

White, Melanie J., Lawford, Bruce R., Morris, C. Phillip, Young, Ross McD.

The dopamine D2 receptor (DRD2) C957T polymorphism CC genotype is associated with decreased striatal binding of DRD2 and executive function and working memory impairments in healthy adults. We...

Interaction between DRD2 C957T polymorphism and an acute psychosocial stressor on reward-related behavioral impulsivity (2009)

White, Melanie J., Lawford, Bruce R., Morris, C. Phillip, Young, Ross McD.

The dopamine D2 receptor (DRD2) C957T polymorphism CC genotype is associated with decreased striatal binding of DRD2 and executive function and working memory impairments in healthy adults. We...

Interaction between DRD2 C957T polymorphism and an acute psychosocial stressor on reward-related behavioral impulsivity (2009)

White, Melanie J., Lawford, Bruce R., Morris, C. Phillip, Young, Ross McD.

The dopamine D2 receptor (DRD2) C957T polymorphism CC genotype is associated with decreased striatal binding of DRD2 and executive function and working memory impairments in healthy adults. We...

Interaction between DRD2 C957T polymorphism and an acute psychosocial stressor on reward-related behavioral impulsivity (2009)

White, Melanie J., Lawford, Bruce R., Morris, C. Phillip, Young, Ross McD.

The dopamine D2 receptor (DRD2) C957T polymorphism CC genotype is associated with decreased striatal binding of DRD2 and executive function and working memory impairments in healthy adults. We...

Interaction between DRD2 C957T polymorphism and an acute psychosocial stressor on reward-related behavioral impulsivity (2009)

White, Melanie J., Lawford, Bruce R., Morris, C. Phillip, Young, Ross McD.

The dopamine D2 receptor (DRD2) C957T polymorphism CC genotype is associated with decreased striatal binding of DRD2 and executive function and working memory impairments in healthy adults. We...

Behavioral phenotypes of impulsivity related to the ANKK1gene are independent of an acute stressor (2008)

White, Melanie J, Morris, C Phillip, Lawford, Bruce R, Young, Ross

Abstract Background The A1 allele of the ANKK1 Taq IA polymorphism (previously reported as located in the D2 dopamine receptor (DRD2) gene) is associated with reduced DRD2 density in the striatum and...

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans (2008)

Voisey, Joanne, Swagell, Christopher D., Hughes, Ian P., Morris, C. Phillip, Van Daal, Angela, Noble, Earnest P., ...

Background: Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic...

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans (2008)

Voisey, Joanne, Swagell, Christopher D., Hughes, Ian P., Morris, C. Phillip, Van Daal, Angela, Noble, Earnest P., ...

Background: Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic...

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans (2008)

Voisey, Joanne, Swagell, Christopher D., Hughes, Ian P., Morris, C. Phillip, Van Daal, Angela, Noble, Earnest P., ...

Background: Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic...

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans (2008)

Voisey, Joanne, Swagell, Christopher D., Hughes, Ian P., Morris, C. Phillip, Van Daal, Angela, Noble, Earnest P., ...

Background: Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic...

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans (2008)

Voisey, Joanne, Swagell, Christopher D., Hughes, Ian P., Morris, C. Phillip, Van Daal, Angela, Noble, Earnest P., ...

Background: Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic...

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans (2008)

Voisey, Joanne, Swagell, Christopher D., Hughes, Ian P., Morris, C. Phillip, Van Daal, Angela, Noble, Earnest P., ...

Background: Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic...

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans (2008)

Voisey, Joanne, Swagell, Christopher D., Hughes, Ian P., Morris, C. Phillip, Van Daal, Angela M., Noble, Earnest P., ...

Background: Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic...

The DRD2 gene 957C>T polymorphism is associated with posttraumatic stress disorder in war veterans (2008)

Voisey, Joanne, Swagell, Christopher D., Hughes, Ian P., Morris, C. Phillip, Van Daal, Angela M., Noble, Earnest P., ...

Background: Variations in genes related to the dopaminergic pathway have been implicated in neuropsychiatric disorders such as schizophrenia, substance misuse, Alzheimer's disease and Post Traumatic...

Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis (2007)

Coussens, Anna K, Wilkinson, Christopher R, Hughes, Ian P, Morris, C Phillip, Van Daal, Angela, Anderson, Peter J, ...

Abstract Background Craniosynostosis, the premature fusion of calvarial sutures, is a common craniofacial abnormality. Causative mutations in more than 10 genes have been identified, involving...

PSA/KLK3 AREI promoter polymorphism alters androgen receptor binding and is associated with prostate cancer susceptibility (2007)

Lai, John, Kedda, Mary-Anne, Hinze, Kimberly, Smith, Robert L.G., Yaxley, John, Spurdle, Amanda B., ...

The proximal promoter of the kallikrein-related peptidase 3 gene (KLK3/PSA) contains a single-nucleotide polymorphism (G-158A) located within the second canonical half-site for the prostate-specific...

PSA/KLK3 AREI promoter polymorphism alters androgen receptor binding and is associated with prostate cancer susceptibility (2006)

Lai, John, Kedda, Mary-Anne, Hinze, Kimberly, Smith, Robert LG, Yaxley, John, Spurdle, Amanda B, ...

The proximal promoter of the kallikrein-related peptidase 3 gene (KLK3/PSA) contains a single nucleotide polymorphism (G-158A) located within the second canonical half-site for the PSA androgen...

PSA/KLK3 AREI promoter polymorphism alters androgen receptor binding and is associated with prostate cancer susceptibility (2006)

Lai, John, Kedda, Mary-Anne, Hinze, Kimberly, Smith, Robert L. G., Yaxley, John, Spurdle, Amanda B., ...

The proximal promoter of the kallikrein-related peptidase 3 gene (KLK3/PSA) contains a single nucleotide polymorphism (G-158A) located within the second canonical half-site for the PSA androgen...

The C/C genotype of the C957T polymorphism of the dopamine D2 receptor (DRD2) is associated with schizophrenia (2005)

Lawford, Bruce R, Young, Ross McD, Swagell, Christopher D, Barnes, Mark, Burton, Simon C, Ward, Warren K, ...

The T allele of the human dopamine D2 receptor (DRD2) gene C957T polymorphism is associated with reduced mRNA translation and stability. This results in decreased dopamine induced DRD2 upregulation...

The C/C genotype of the C957T polymorphism of the dopamine D2 receptor (DRD2) is associated with schizophrenia (2005)

Lawford, Bruce R, Young, Ross McD, Swagell, Christopher D, Barnes, Mark, Burton, Simon C, Ward, Warren K, ...

The T allele of the human dopamine D2 receptor (DRD2) gene C957T polymorphism is associated with reduced mRNA translation and stability. This results in decreased dopamine induced DRD2 upregulation...

The C/C genotype of the C957T polymorphism of the dopamine D2 receptor (DRD2) is associated with schizophrenia (2005)

Lawford, Bruce R, Young, Ross McD, Swagell, Christopher D, Barnes, Mark, Burton, Simon C, Ward, Warren K, ...

The T allele of the human dopamine D2 receptor (DRD2) gene C957T polymorphism is associated with reduced mRNA translation and stability. This results in decreased dopamine induced DRD2 upregulation...

The C/C genotype of the C957T polymorphism of the dopamine D2 receptor (DRD2) is associated with schizophrenia (2005)

Lawford, Bruce R, Young, Ross McD, Swagell, Christopher D, Barnes, Mark, Burton, Simon C, Ward, Warren K, ...

The T allele of the human dopamine D2 receptor (DRD2) gene C957T polymorphism is associated with reduced mRNA translation and stability. This results in decreased dopamine induced DRD2 upregulation...

Solid-phase Amplification and Detection: A Single-tube Diagnostic Assay for Infectious Agents (2001)

Harris, R, Morris, C Phillip, Somodevilla-Torres, M, Timms, Peter, Van Daal, Angela

The Factor V HR2 Haplotype: Prevalence and Association of the A4070G and A6755G Polymorphisms (2001)

Marsh, Neville, Morris, C Phillip, Walsh, Terence

Solid-phase Amplification and Detection: A Single-tube Diagnostic Assay for Infectious Agents (2001)

Harris, R, Morris, C Phillip, Somodevilla-Torres, M, Timms, Peter, Van Daal, Angela

The Factor V HR2 Haplotype: Prevalence and Association of the A4070G and A6755G Polymorphisms (2001)

Marsh, Neville, Morris, C Phillip, Walsh, Terence

Solid-phase Amplification and Detection: A Single-tube Diagnostic Assay for Infectious Agents (2001)

Harris, R, Morris, C Phillip, Somodevilla-Torres, M, Timms, Peter, Van Daal, Angela

The Factor V HR2 Haplotype: Prevalence and Association of the A4070G and A6755G Polymorphisms (2001)

Marsh, Neville, Morris, C Phillip, Walsh, Terence

Solid-phase Amplification and Detection: A Single-tube Diagnostic Assay for Infectious Agents (2001)

Harris, R, Morris, C Phillip, Somodevilla-Torres, M, Timms, Peter, Van Daal, Angela

The Factor V HR2 Haplotype: Prevalence and Association of the A4070G and A6755G Polymorphisms (2001)

Marsh, Neville, Morris, C Phillip, Walsh, Terence

Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein (1995)

Brooks, Douglas Alexander, Robertson, Daniel A, Bindloss, Colleen, Litjens, Tom, Anson, Donald S, Peters, Christoph, ...

Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein (1995)

Brooks, Douglas Alexander, Robertson, Daniel A, Bindloss, Colleen, Litjens, Tom, Anson, Donald S, Peters, Christoph, ...

Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein (1995)

Brooks, Douglas Alexander, Robertson, Daniel A, Bindloss, Colleen, Litjens, Tom, Anson, Donald S, Peters, Christoph, ...

Metachromatic leukodystrophy: a nonsense mutation (Q486X) in the arylsulphatase A (ARSA) gene (1994)

Harvey, John S., Carey, William F., Nelson, Paul V., Morris, C. Phillip

A nonsense mutation (R220X) in the {alpha}-galactosidase A gene detected in a female carrier of Fabry disease (1994)

Meaney, Cathy, Blanch, Lianne C., Morris, C.Phillip

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 (1994)

Bunge, Susanna, Kleijer, Wim J., Steglich, Cordula, Beck, Michael, Zuther, Cornelia, Morris, C.Phillip, ...

A group of 46 European patients with mucopoly-saccharidosis type I (MPS I) was screened for mutations of the α-L-iduronidase gene. The 2 common nonsense mutations, W402X and Q70X, were identified...

Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes (1993)

Scott, Hamish S, Litjens, Tom, Nelson, Paul V, Thompson, Phillip R, Brooks, Douglas Alexander, Hopwood, John J, ...

Long-term clinical-progress in bone-marrow transplanted mucopolysaccharidosis type-I patients with a defined genotype (1993)

Hopwood, John J, Vellodi, A, Scott, Hamish S, Morris, C Phillip, Litjens, Tom, Clements, Peter R, ...

Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes (1993)

Scott, Hamish S, Litjens, Tom, Nelson, Paul V, Thompson, Phillip R, Brooks, Douglas Alexander, Hopwood, John J, ...

Long-term clinical-progress in bone-marrow transplanted mucopolysaccharidosis type-I patients with a defined genotype (1993)

Hopwood, John J, Vellodi, A, Scott, Hamish S, Morris, C Phillip, Litjens, Tom, Clements, Peter R, ...

Multiple polymorphisms within the {alpha}-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotype (1993)

S.Scott, Hamish, V.Nelson, Paul, Litjens, Tom, J.Hopwood, John, Morris, C.Phillip

Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome) (1993)

Bunge, Susanna, Steglich, Cordula, Zuther, Cornelia, Beck, Michael, Morris, C. Phillip, Schwinger, Eberhard, ...

Mutations of the iduronate-2-sulfatase gene were identified in 16 patients with mucopolysaccharidosis type II (Hunter syndrome). Together with another 10 cases reported by us earlier it emerges that...

Long-term clinical-progress in bone-marrow transplanted mucopolysaccharidosis type-I patients with a defined genotype (1993)

Hopwood, John J, Vellodi, A, Scott, Hamish S, Morris, C Phillip, Litjens, Tom, Clements, Peter R, ...

Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes (1993)

Scott, Hamish S, Litjens, Tom, Nelson, Paul V, Thompson, Phillip R, Brooks, Douglas Alexander, Hopwood, John J, ...

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

Coussens, Anna K, Wilkinson, Christopher R, Hughes, Ian P, Morris, C Phillip, Van Daal, Angela, Anderson, Peter J, ...

Behavioral phenotypes of impulsivity related to the ANKK1 gene are independent of an acute stressor

White, Melanie J, Morris, C Phillip, Lawford, Bruce R, Young, Ross McD

An arylsulphatase A (ARSA) frameshift mutation (289insG) in metachromatic leukodystrophy (MLD)

Perkins, Kelly J, Carey, William F, Morris, C Phillip