about
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndromeAn inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.Discriminating power of localized three-dimensional facial morphology.The new genetics of schizophrenia.No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples.Schizophrenia and velo-cardio-facial syndrome.Strong evidence that GNB1L is associated with schizophrenia.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.White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents.Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (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).The behavioural phenotype in velo-cardio-facial syndrome.Fragile X syndrome: a pilot proton magnetic resonance spectroscopy study in premutation carriers.Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study.Hippocampal myo-inositol and cognitive ability in adults with Down syndrome: an in vivo proton magnetic resonance spectroscopy study.Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome.Quality of Life and Functioning One Year After Experiencing Accumulated Coercive Events During Psychiatric Admission.Psychiatric and neuropsychological profiles of people with psychogenic nonepileptic seizures.A systematic genomewide linkage study in 353 sib pairs with schizophreniaMaturation of limbic regions in Asperger syndrome: a preliminary study using proton magnetic resonance spectroscopy and structural magnetic resonance imaging.Executive functions and memory abilities in children with 22q11.2 deletion syndrome.Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes.Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137.Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.Migraine: another headache for psychiatrists?Association between PRODH and schizophrenia is not confirmed.COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome.Treatment of refractory chronic daily headache with the atypical antipsychotic ziprasidone--a case series.Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.In vivo brain anatomy of adult males with Fragile X syndrome: an MRI study.White matter integrity in Asperger syndrome: a preliminary diffusion tensor magnetic resonance imaging study in adults.An event related functional magnetic resonance imaging study of facial emotion processing in Asperger syndrome.Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging.Brain anatomy and ageing in non-demented adults with Down's syndrome: an in vivo MRI study.Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.Psychosis and autism: magnetic resonance imaging study of brain anatomy.A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome.Anti-NMDA receptor encephalitis: an important differential diagnosis in psychosis.Alzheimer's disease and Down's syndrome: an in vivo MRI study.
P50
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P50
description
hulumtues
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հետազոտող
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name
Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran C Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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Kieran Murphy
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