About: Kieran Murphy

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher (ORCID 0000-0003-2930-4465)

Attributes	Values
rdf:type	Item
description	연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl) researcher (ORCID 0000-0003-2930-4465) (en)
rdfs:label	Kieran Murphy (en) Kieran Murphy (es) Kieran Murphy (nl) Kieran Murphy (ast) Kieran Murphy (fr) Kieran Murphy (nb) Kieran Murphy (sl)
skos:prefLabel	Kieran Murphy (en) Kieran Murphy (es) Kieran Murphy (nl) Kieran Murphy (ast) Kieran Murphy (fr) Kieran Murphy (nb) Kieran Murphy (sl)
name	Kieran Murphy (en) Kieran Murphy (es) Kieran Murphy (nl) Kieran Murphy (ast) Kieran Murphy (fr) Kieran Murphy (nb) Kieran Murphy (sl)
Scopus author ID	wds:Q40487258-47F5F996-0302-486A-AA5D-069DA2DF5811
Scopus author ID	7402863717
given name	wds:Q40487258-9e91eabf-4202-9c36-705f-8fa155e2b785
given name	Kieran
instance of	wds:Q40487258-C403E782-D504-4740-9331-A1D8FEE9A926
instance of	Homo sapiens
skos:altLabel	Kieran C Murphy (en)
occupation	wds:Q40487258-8FEBF22F-82EF-46AD-899B-53982BB914A3
sex or gender	wds:Q40487258-29DB3D96-7CA6-4C24-9223-4F81B2F6BE29
ISNI	wds:Q40487258-EDEAFE62-AE41-44F4-897F-115186452F2C
VIAF ID	wds:Q40487258-882F7498-CAEC-4EEC-B891-DB357B399D5C
Library of Congress authority ID	wds:Q40487258-75106029-0CC4-4F02-974A-9F42B78ED208
family name	wds:Q40487258-C1735CAC-D664-4131-92D6-B10318C381EE
WorldCat Identities ID (superseded)	wds:Q40487258-B328ADF5-422A-40E0-9B6C-AD83E9E76C5F
VIAF ID	http://viaf.org/viaf/274859098
Library of Congress authority ID	http://id.loc.gov/authorities/names/nb2005007653
occupation	researcher
sex or gender	male
ISNI	0000000384281171
VIAF ID	274859098
Library of Congress authority ID	nb2005007653
family name	Murphy
WorldCat Identities ID (superseded)	lccn-nb2005007653
ORCID iD	wds:Q40487258-6E75F737-A3CC-4C23-AFD9-6325D89D243F
ORCID iD	https://orcid.org/0000-0003-2930-4465
ORCID iD	0000-0003-2930-4465
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q40487258
is author of	White matter integrity in Asperger syndrome: a preliminary diffusion tensor magnetic resonance imaging study in adults. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome 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 Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome Executive functions and memory abilities in children with 22q11.2 deletion syndrome A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs In vivo brain anatomy of adult males with Fragile X syndrome: an MRI study. Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy. A systematic genomewide linkage study in 353 sib pairs with schizophrenia Association between PRODH and schizophrenia is not confirmed Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects Schizophrenia and velo-cardio-facial syndrome. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Brain anatomy and ageing in non-demented adults with Down's syndrome: an in vivo MRI study. CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia Psychosis and autism: magnetic resonance imaging study of brain anatomy. A neuropsychological investigation of male premutation carriers of fragile X syndrome. No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples Factor analysis of schizophrenic symptoms using the OPCRIT checklist Discriminating power of localized three-dimensional facial morphology The molecular genetics of schizophrenia Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome. Anti-NMDA receptor encephalitis: an important differential diagnosis in psychosis. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents Clinical symptomatology and the psychosis risk gene ZNF804A. Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging. Strong evidence that GNB1L is associated with schizophrenia Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome. Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. An event related functional magnetic resonance imaging study of facial emotion processing in Asperger syndrome. The new genetics of schizophrenia. A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome. Hippocampal myo-inositol and cognitive ability in adults with Down syndrome: an in vivo proton magnetic resonance spectroscopy study Down syndrome with and without dementia: an in vivo proton Magnetic Resonance Spectroscopy study with implications for Alzheimer's disease. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

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