(Q50568018)

15 March 2018

title

Chromosomal microarray analysis-a routine clinical genetic test for patients with schizophrenia. (English)

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15 March 2018

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Kate Baker

1

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author name string

Gregory Costain

series ordinal

2

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15 March 2018

Wai Lun Alan Fung

series ordinal

3

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15 March 2018

Anne S Bassett

series ordinal

4

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15 March 2018

publication date

5 September 2014

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15 March 2018

published in

The Lancet Psychiatry

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15 March 2018

volume

1

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15 March 2018

issue

5

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15 March 2018

page(s)

329-331

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15 March 2018

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

cites work

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Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research

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Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

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De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

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7 January 2021

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7 January 2021

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays

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7 January 2021

Practical guidelines for managing patients with 22q11.2 deletion syndrome

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1q21.1 Microduplication expression in adults

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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

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Evaluating genetic counseling for individuals with schizophrenia in the molecular age

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Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome

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The NIMH Research Domain Criteria (RDoC) Project: precision medicine for psychiatry

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Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?

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De novo mutations in schizophrenia implicate synaptic networks

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Identifiers

DOI

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15 March 2018

PubMed ID

26360988

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15 March 2018