Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia (Q39414858)

11 September 2017

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia (English)

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disability affecting intellectual abilities

11 September 2017

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intellectual disability

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inferred from title

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13

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27602560%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Elliott Rees

1

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31 May 2020

Kimberley Kendall

2

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31 May 2020

Antonio F Pardiñas

3

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31 May 2020

Sophie E Legge

4

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31 May 2020

Andrew Pocklington

5

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31 May 2020

Valentina Escott-Price

6

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31 May 2020

James H. MacCabe

7

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31 May 2020

David Collier

8

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31 May 2020

Michael C O'Donovan

10

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31 May 2020

James Walters

12

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31 May 2020

author name string

Peter Holmans

9

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31 May 2020

Michael J Owen

11

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31 May 2020

language of work or name

English

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publication date

1 September 2016

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11 September 2017

7

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inferred from page(s)

published in

JAMA Psychiatry

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31 May 2020

volume

73

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31 May 2020

issue

9

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31 May 2020

page(s)

963-969

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Gender differences in CNV burden do not confound schizophrenia CNV associations.

31 May 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Refining analyses of copy number variation identifies specific genes associated with developmental delay

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Biological insights from 108 schizophrenia-associated genetic loci

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Analysis of copy number variations at 15 schizophrenia-associated loci.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Evidence that duplications of 22q11.2 protect against schizophrenia

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

The penetrance of copy number variations for schizophrenia and developmental delay.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Genetic architectures of psychiatric disorders: the emerging picture and its implications

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

CNVs: harbingers of a rare variant revolution in psychiatric genetics

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

A copy number variation morbidity map of developmental delay

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Rare chromosomal deletions and duplications increase risk of schizophrenia

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

PLINK: a tool set for whole-genome association and population-based linkage analyses

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Increased female autosomal burden of rare copy number variants in human populations and in autism families.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5014093

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

17 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27602560

inferred from PubMed ID database lookup

12 December 2020

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Identifiers

DOI

10.1001/JAMAPSYCHIATRY.2016.1831

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27602560%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

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31 May 2020

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