Lista de obras - Kieran Murphy - Dominio Público Uruguay

A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

article

A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome

artículo científico publicado en 2008

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A cross-sectional study of the prevalence of psychopathology in adults with congenital heart disease

scientific article published on 01 February 2002

A genomewide linkage study of age at onset in schizophrenia

article

A neuropsychological investigation of male premutation carriers of fragile X syndrome

artículo científico publicado en 2004

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

artículo científico publicado en 2003

Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype

artículo científico publicado en 2001

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study

artículo científico publicado en 2019

Alzheimer's disease and Down's syndrome: an in vivo MRI study

artículo científico publicado en 2008

An event related functional magnetic resonance imaging study of facial emotion processing in Asperger syndrome

artículo científico publicado en 2007

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

artículo científico publicado en 2014

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility

artículo científico publicado en 2006

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Anti-NMDA receptor encephalitis: an important differential diagnosis in psychosis

artículo científico publicado en 2011

Association between PRODH and schizophrenia is not confirmed

artículo científico publicado en 2003

Brain anatomy and ageing in non-demented adults with Down's syndrome: an in vivo MRI study

artículo científico publicado en 2009

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study

artículo científico publicado en 2004

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study

artículo científico publicado en 2006

CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia

article

COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome

artículo científico publicado en 2011

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

artículo científico publicado en 2008

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

article

Clinical symptomatology and the psychosis risk gene ZNF804A.

artículo científico publicado en 2010

Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome

artículo científico publicado en 2004

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis

artículo científico publicado en 2015

Discriminating power of localized three-dimensional facial morphology

artículo científico publicado en 2005

Down syndrome with and without dementia: an in vivo proton Magnetic Resonance Spectroscopy study with implications for Alzheimer's disease

artículo científico publicado en 2011

Executive functions and memory abilities in children with 22q11.2 deletion syndrome

artículo científico publicado en 2010

Factor analysis of schizophrenic symptoms using the OPCRIT checklist

scientific article published on 01 December 1996

Failure to confirm association betweenPIK4CAand psychosis in 22q11.2 deletion syndrome

artículo científico publicado en 2010

Fragile X syndrome: a pilot proton magnetic resonance spectroscopy study in premutation carriers

artículo científico publicado en 2012

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.

artículo científico publicado en 2014

Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes

artículo científico publicado en 2005

High rates of schizophrenia in adults with velo-cardio-facial syndrome

artículo científico publicado en 1999

Hippocampal glutamate-glutamine (Glx) in adults with Down syndrome: a preliminary study using in vivo proton magnetic resonance spectroscopy ((1)H MRS).

artículo científico publicado en 2014

Hippocampal myo-inositol and cognitive ability in adults with Down syndrome: an in vivo proton magnetic resonance spectroscopy study

artículo científico publicado en 2005

In vivo 1H-magnetic resonance spectroscopy study of amygdala-hippocampal and parietal regions in autism

artículo científico publicado en 2006

In vivo brain anatomy of adult males with Fragile X syndrome: an MRI study

artículo científico publicado en 2010

Increased use of security personnel in Irish psychiatric hospitals: 2008-2012

artículo científico publicado en 2015

Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

artículo científico publicado en 2011

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

artículo científico publicado en 2018

Linkage study of chromosome 6p in sib-pairs with schizophrenia

artículo científico publicado en 1997

Maturation of limbic regions in Asperger syndrome: a preliminary study using proton magnetic resonance spectroscopy and structural magnetic resonance imaging

artículo científico publicado en 2010

Migraine and depersonalization disorder

artículo científico publicado en 2004

Migraine: another headache for psychiatrists?

artículo científico publicado en 2004

Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137.

artículo científico publicado en 2012

No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples

artículo científico publicado en 2005

No evidence for allelic association between schizophrenia and a functional variant of the human dopamine ?-hydroxylase gene (DBH)

article

Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia

artículo científico publicado en 2011

Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging

artículo científico publicado en 2006

Psychiatric and neuropsychological profiles of people with psychogenic nonepileptic seizures

artículo científico publicado en 2014

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

artículo científico publicado en 2014

Psychosis and autism: magnetic resonance imaging study of brain anatomy

artículo científico publicado en 2009

Quality of Life and Functioning One Year After Experiencing Accumulated Coercive Events During Psychiatric Admission

artículo científico publicado en 2015

Relationship between reaction time, fine motor control, and visual-spatial perception on vigilance and visual-motor tasks in 22q11.2 Deletion Syndrome

article

Schizophrenia and velo-cardio-facial syndrome.

artículo científico publicado en 2002

Schizophrenia two-hit hypothesis in velo-cardio facial syndrome

artículo científico publicado en 2013

Sibling pairs with schizophrenia or schizoaffective disorder: associations of subtypes, symptoms and demographic variables

artículo científico publicado en 1998

Strong evidence that GNB1L is associated with schizophrenia

artículo científico publicado en 2007

Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology

artículo científico publicado en 2012

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

artículo científico publicado en 2006

The Letter-Number Sequencing Test and its association with potential to work among people with psychotic illness

artículo científico publicado en 2009

The behavioural phenotype in velo-cardio-facial syndrome.

artículo científico publicado en 2004

The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy

artículo científico publicado en 2004

The kings schizotypy questionnaire as a quantitative measure of schizophrenia liability

artículo científico publicado en 2000

The molecular genetics of schizophrenia

artículo científico publicado en 1996

The new genetics of schizophrenia.

artículo científico publicado en 2003

Treatment of refractory chronic daily headache with the atypical antipsychotic ziprasidone--a case series

artículo científico publicado en 2005

Trial of risperidone in India--concerns

Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia ⬇️

artículo científico publicado el 1 de noviembre de 2001

Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study

artículo científico

White matter integrity in Asperger syndrome: a preliminary diffusion tensor magnetic resonance imaging study in adults

artículo científico publicado en 2010

White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents

artículo científico publicado en 2010

Lista de obras de Kieran Murphy

A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A cross-sectional study of the prevalence of psychopathology in adults with congenital heart disease

A genomewide linkage study of age at onset in schizophrenia

A neuropsychological investigation of male premutation carriers of fragile X syndrome

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study

Alzheimer's disease and Down's syndrome: an in vivo MRI study

An event related functional magnetic resonance imaging study of facial emotion processing in Asperger syndrome

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility

Analysis of shared heritability in common disorders of the brain

Anti-NMDA receptor encephalitis: an important differential diagnosis in psychosis

Association between PRODH and schizophrenia is not confirmed

Brain anatomy and ageing in non-demented adults with Down's syndrome: an in vivo MRI study

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study

CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia

COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

Clinical symptomatology and the psychosis risk gene ZNF804A.

Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis

Discriminating power of localized three-dimensional facial morphology

Down syndrome with and without dementia: an in vivo proton Magnetic Resonance Spectroscopy study with implications for Alzheimer's disease

Executive functions and memory abilities in children with 22q11.2 deletion syndrome

Factor analysis of schizophrenic symptoms using the OPCRIT checklist

Failure to confirm association betweenPIK4CAand psychosis in 22q11.2 deletion syndrome

Fragile X syndrome: a pilot proton magnetic resonance spectroscopy study in premutation carriers

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.

Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes

High rates of schizophrenia in adults with velo-cardio-facial syndrome

Hippocampal glutamate-glutamine (Glx) in adults with Down syndrome: a preliminary study using in vivo proton magnetic resonance spectroscopy ((1)H MRS).

Hippocampal myo-inositol and cognitive ability in adults with Down syndrome: an in vivo proton magnetic resonance spectroscopy study

In vivo 1H-magnetic resonance spectroscopy study of amygdala-hippocampal and parietal regions in autism

In vivo brain anatomy of adult males with Fragile X syndrome: an MRI study

Increased use of security personnel in Irish psychiatric hospitals: 2008-2012

Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

Linkage study of chromosome 6p in sib-pairs with schizophrenia

Maturation of limbic regions in Asperger syndrome: a preliminary study using proton magnetic resonance spectroscopy and structural magnetic resonance imaging

Migraine and depersonalization disorder

Migraine: another headache for psychiatrists?

Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137.

No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples

No evidence for allelic association between schizophrenia and a functional variant of the human dopamine ?-hydroxylase gene (DBH)

Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia

Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging

Psychiatric and neuropsychological profiles of people with psychogenic nonepileptic seizures

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

Psychosis and autism: magnetic resonance imaging study of brain anatomy

Quality of Life and Functioning One Year After Experiencing Accumulated Coercive Events During Psychiatric Admission

Relationship between reaction time, fine motor control, and visual-spatial perception on vigilance and visual-motor tasks in 22q11.2 Deletion Syndrome

Schizophrenia and velo-cardio-facial syndrome.

Schizophrenia two-hit hypothesis in velo-cardio facial syndrome

Sibling pairs with schizophrenia or schizoaffective disorder: associations of subtypes, symptoms and demographic variables

Strong evidence that GNB1L is associated with schizophrenia

Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

The Letter-Number Sequencing Test and its association with potential to work among people with psychotic illness

The behavioural phenotype in velo-cardio-facial syndrome.

The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy

The kings schizotypy questionnaire as a quantitative measure of schizophrenia liability

The molecular genetics of schizophrenia

The new genetics of schizophrenia.

Treatment of refractory chronic daily headache with the atypical antipsychotic ziprasidone--a case series

Trial of risperidone in India--concerns

Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia ⬇️

Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study

White matter integrity in Asperger syndrome: a preliminary diffusion tensor magnetic resonance imaging study in adults

White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents