(Q34530657)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

review article

1 reference

title

Schizophrenia and velo-cardio-facial syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

author name string

Kieran C Murphy

series ordinal

1

1 reference

2 August 2017

language of work or name

English

0 references

publication date

1 February 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

volume

359

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

issue

9304

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

page(s)

426-430

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

A single dominant gene still cannot account for the transmission of schizophrenia

7 December 2019

cites work

1 reference

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7 January 2021

Genetic basis of schizophrenia.

1 reference

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7 January 2021

Dissecting the genetic complexity of schizophrenia

1 reference

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7 January 2021

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

1 reference

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7 January 2021

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

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7 January 2021

Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

1 reference

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7 January 2021

Epidemiology of Schizophrenia

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7 January 2021

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

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7 January 2021

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

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7 January 2021

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

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7 January 2021

Velocardiofacial syndrome in childhood-onset schizophrenia.

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7 January 2021

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

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7 January 2021

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

1 reference

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7 January 2021

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

1 reference

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7 January 2021

Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3

1 reference

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7 January 2021

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

1 reference

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7 January 2021

A genome-wide search for schizophrenia susceptibility genes

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Implications of normal brain development for the pathogenesis of schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Is schizophrenia a neurodevelopmental disorder?

1 reference

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7 January 2021

Deletions of human chromosome 22 and associated birth defects.

1 reference

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7 January 2021

Information processing and attention dysfunctions in schizophrenia

1 reference

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7 January 2021

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

1 reference

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7 January 2021

Clinical correlates of septum pellucidum cavities: an unusual association with psychosis

1 reference

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7 January 2021

Cerebellum and schizophrenia: a selective review.

1 reference

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7 January 2021

Meta-analysis of brain and cranial size in schizophrenia

1 reference

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7 January 2021

Brain anomalies in velo-cardio-facial syndrome.

1 reference

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7 January 2021

Cerebellar atrophy in a patient with velocardiofacial syndrome

1 reference

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7 January 2021

Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia

1 reference

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7 January 2021

Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.

1 reference

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7 January 2021

Midline brain anomalies and schizophrenia in people with CATCH 22 syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Meta-analysis of regional brain volumes in schizophrenia

1 reference

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7 January 2021

Reduction of the parahippocampal gyrus and the hippocampus in patients with chronic schizophrenia

1 reference

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7 January 2021

Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

A novel 22q11.2 microdeletion in DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Possible role for COMT in psychosis associated with velo-cardio-facial syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

From neuropathology to neurodevelopment

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2907604-3

7 January 2021

10.1016/S0140-6736(02)07604-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11844533%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference