Genome-wide association analysis of copy number variation in recurrent depressive disorder. (Q37611740)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22042228%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

title

Genome-wide association analysis of copy number variation in recurrent depressive disorder (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22042228%20AND%20SRC:MED&resulttype=core&format=json

genome-wide association study

15 January 2020

main subject

0 references

author

Michael Gill

20

1 reference

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15 January 2020

Ian W. Craig

26

1 reference

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15 January 2020

James Rucker

1

1 reference

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15 January 2020

Gerome Breen

2

1 reference

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15 January 2020

Inti Pedroso

4

1 reference

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15 January 2020

Cathryn Lewis

5

1 reference

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15 January 2020

Sarah Cohen-Woods

6

1 reference

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15 January 2020

Rudolf Uher

7

1 reference

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15 January 2020

Margarita Rivera

9

1 reference

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15 January 2020

Katherine J. Aitchison

10

1 reference

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15 January 2020

Michael R. Barnes

17

1 reference

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15 January 2020

Ole Mors

19

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15 January 2020

Stephen W. Scherer

27

1 reference

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15 January 2020

21

W Maier

1 reference

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15 January 2020

author name string

A Schosser

8

1 reference

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15 January 2020

N Craddock

11

1 reference

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15 January 2020

M J Owen

12

1 reference

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15 January 2020

L Jones

13

1 reference

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15 January 2020

I Jones

14

1 reference

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15 January 2020

A Korszun

15

1 reference

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15 January 2020

P Muglia

16

1 reference

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15 January 2020

M Preisig

18

1 reference

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15 January 2020

J Rice

22

1 reference

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15 January 2020

A E Farmer

25

1 reference

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15 January 2020

P McGuffin

28

1 reference

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15 January 2020

D Pinto

3

1 reference

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15 January 2020

M Rietschel

23

1 reference

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15 January 2020

F Holsboer

24

1 reference

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15 January 2020

language of work or name

English

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publication date

1 November 2011

1 reference

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15 January 2020

1 reference

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15 January 2020

volume

18

1 reference

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15 January 2020

issue

2

1 reference

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15 January 2020

page(s)

183-189

1 reference

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

15 January 2020

cites work

1 reference

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Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder

23 August 2017

1 reference

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23 August 2017

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

23 August 2017

1 reference

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Poor replication of candidate genes for major depressive disorder using genome-wide association data

23 August 2017

1 reference

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The role of copy number variation in schizophrenia

23 August 2017

1 reference

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A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

23 August 2017

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Common disorders are quantitative traits

23 August 2017

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The role of genetic variation in the causation of mental illness: an evolution-informed framework

23 August 2017

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Neurexin 1 (NRXN1) deletions in schizophrenia

23 August 2017

1 reference

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

23 August 2017

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

23 August 2017

1 reference

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Disruption of the neurexin 1 gene is associated with schizophrenia

23 August 2017

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Copy-number variations associated with neuropsychiatric conditions

23 August 2017

1 reference

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Large recurrent microdeletions associated with schizophrenia

23 August 2017

1 reference

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Rare chromosomal deletions and duplications increase risk of schizophrenia

23 August 2017

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Association between microdeletion and microduplication at 16p11.2 and autism

23 August 2017

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

23 August 2017

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Strong association of de novo copy number mutations with autism

23 August 2017

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Structural variation in the human genome

23 August 2017

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Defining the clinical spectrum of deletion 22q11.2

23 August 2017

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The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic study

23 August 2017

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The epidemiology of major depressive disorder: results from the National Comorbidity Survey Replication (NCS-R)

23 August 2017

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23 August 2017

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23 August 2017

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6 September 2017

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28 September 2017

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25 June 2018

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25 June 2018

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1 September 2018

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1 September 2018

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1 September 2018

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Microduplications of 16p11.2 are associated with schizophrenia

1 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FMP.2011.144

Common disorders are quantitative traits

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3939438

Internal consistencies of the original and revised Beck Depression Inventory

3 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22042228

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Excess mortality of mental disorder

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22042228

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/MP.2011.144

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22042228%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22042228%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

PubMed publication ID

22042228

1 reference