Copy number variation in schizophrenia in Sweden (Q34742638)

24776740

4 August 2017

title

Copy number variation in schizophrenia in Sweden (English)

1 reference

4 August 2017

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16

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1 June 2020

Michael C O'Donovan

17

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Guanhua Chen

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Jennifer L. Moran

5

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Douglas M. Ruderfer

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Sarah E Bergen

10

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Patrik K E Magnusson

12

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James J. Crowley

14

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Elliott Rees

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James Walters

19

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1 June 2020

author name string

J P Szatkiewicz

1

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C O'Dushlaine

2

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K Chambert

4

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B M Neale

6

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M Fromer

7

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S Akterin

9

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A Kähler

11

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Y Kim

13

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M J Owen

18

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E Scolnick

20

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P Sklar

21

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S Purcell

22

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S A McCarroll

24

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P F Sullivan

25

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C M Hultman

23

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1 June 2020

language of work or name

English

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publication date

29 April 2014

1 reference

4 August 2017

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1 June 2020

volume

19

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1 June 2020

issue

7

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1 June 2020

page(s)

762-773

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24776740 AND SRC:MED&resulttype=core&format=json

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

1 June 2020

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Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.

7 July 2018

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7 July 2018

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Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder

7 July 2018

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7 July 2018

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7 July 2018

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CNVs: harbingers of a rare variant revolution in psychiatric genetics

7 July 2018

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High frequencies of de novo CNVs in bipolar disorder and schizophrenia

7 July 2018

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

7 July 2018

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Genome-wide association study identifies five new schizophrenia loci

7 July 2018

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7 July 2018

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FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

7 July 2018

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

7 July 2018

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Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients

7 July 2018

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7 July 2018

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

7 July 2018

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7 July 2018

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Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Investigating the association between cigarette smoking and schizophrenia in a cohort study

7 July 2018

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7 July 2018

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7 July 2018

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Prenatal and perinatal risk factors for schizophrenia, affective psychosis, and reactive psychosis of early onset: case-control study

7 July 2018

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7 July 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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26 October 2018

1 reference

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Participation in population studies

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24776740

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/MP.2014.40

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24776740 AND SRC:MED&resulttype=core&format=json

Dimensions Publication ID

1 June 2020

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1 June 2020

24776740

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