(Q34555512)

3 August 2017

title

De novo CNVs in bipolar affective disorder and schizophrenia (English)

1 reference

3 August 2017

0 references

13

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3 August 2017

Elliott Rees

2

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Jennifer L. Moran

Jennifer L Moran

3

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Peter Holmans

Peter Holmans

10

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Michael C O'Donovan

Michael C O'Donovan

11

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Steven A McCarroll

9

Steven McCarroll

1 reference

3 August 2017

8

Pamela Sklar

1 reference

3 August 2017

7

Shaun Purcell

1 reference

3 August 2017

4

Kimberly D Chambert

1 reference

3 August 2017

6

Nicholas Craddock

1 reference

3 August 2017

5

Vihra Milanova

1 reference

3 August 2017

Lyudmila Georgieva

1

1 reference

3 August 2017

Michael J Owen

12

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3 August 2017

publication date

23 July 2014

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3 August 2017

published in

Human Molecular Genetics

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3 August 2017

volume

23

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3 August 2017

issue

24

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3 August 2017

page(s)

6677-6683

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

3 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Implication of a rare deletion at distal 16p11.2 in schizophrenia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Genetic analysis for two italian siblings with usher syndrome and schizophrenia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

CNVs: harbingers of a rare variant revolution in psychiatric genetics

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Comorbid bipolar disorder and Usher syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Microduplications of 16p11.2 are associated with schizophrenia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Singleton deletions throughout the genome increase risk of bipolar disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Strong association of de novo copy number mutations with sporadic schizophrenia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

The bipolar disorder phenome database: a resource for genetic studies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Family, twin, and adoption studies of bipolar disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

The Heritability of Bipolar Affective Disorder and the Genetic Relationship to Unipolar Depression

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Genetics of bipolar disorder.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

SCAN. Schedules for Clinical Assessment in Neuropsychiatry

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4240207

Association at SYNE1 in both bipolar disorder and recurrent major depression

7 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU379

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU379

Reduced burden of very large and rare CNVs in bipolar affective disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU379

Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU379

De novo copy number variants associated with intellectual disability have a paternal origin and age bias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU379

21 January 2018

Identifiers

DOI

10.1093/HMG/DDU379

1 reference

3 August 2017

1 reference

3 August 2017

1 reference