CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 (Q24603800)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1	scientific article

Statements

instance of

scholarly article

0 references

title

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

0 references

main subject

schizophrenia

0 references

author

Elliott Rees

series ordinal

1

0 references

George Kirov

series ordinal

30

0 references

Michael Gill

series ordinal

18

0 references

Michael C O'Donovan

series ordinal

28

0 references

Sophie E Legge

object named as

Sophie E Legge

series ordinal

9

0 references

Jennifer L. Moran

object named as

Jennifer L Moran

series ordinal

10

0 references

Derek W. Morris

object named as

Derek W Morris

series ordinal

13

0 references

Aiden Corvin

object named as

Aiden Corvin

series ordinal

19

0 references

Christina M. Hultman

series ordinal

22

object named as

Christina Hultman

0 references

Kenneth Kendler

series ordinal

15

object named as

Kenneth S Kendler

0 references

Patrick F. Sullivan

series ordinal

25

object named as

Patrick F Sullivan

0 references

Pamela Sklar

series ordinal

21

object named as

Pamela Sklar

0 references

Michele T Pato

series ordinal

24

object named as

Michele Pato

0 references

James Walters

series ordinal

2

object named as

James T R Walters

0 references

Jin P Szatkiewicz

series ordinal

5

object named as

Jin Szatkiewicz

0 references

Douglas F Levinson

series ordinal

12

object named as

Douglas Levinson

0 references

Francis A O'Neill

series ordinal

16

object named as

Francis A O'Neill

0 references

Steven A McCarroll

series ordinal

27

object named as

Steven A McCarroll

0 references

Colm O'Dushlaine

series ordinal

4

object named as

Colm O'Dushlaine

0 references

Kimberly Chambert

series ordinal

3

object named as

Kimberly D Chambert

0 references

Giulio Genovese

series ordinal

11

object named as

Giulio Genovese

0 references

Paul Cormican

series ordinal

14

object named as

Paul Cormican

0 references

Brien P. Riley

series ordinal

17

object named as

Brien Riley

0 references

Pablo V Gejman

series ordinal

26

object named as

Pablo V Gejman

0 references

author name string

Alexander L Richards

series ordinal

6

0 references

Lyudmila Georgieva

series ordinal

7

0 references

Gerwyn Mahoney-Davies

series ordinal

8

0 references

Carlos Pato

series ordinal

23

0 references

Michael J Owen

series ordinal

29

0 references

language of work or name

English

0 references

publication date

15 March 2014

0 references

published in

Human Molecular Genetics

0 references

volume

23

0 references

issue

6

0 references

page(s)

1669-76

0 references

cites work

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

Neurexin 1 (NRXN1) deletions in schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

Disruption of the neurexin 1 gene is associated with schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

Large recurrent microdeletions associated with schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

Paracingulin regulates the activity of Rac1 and RhoA GTPases by recruiting Tiam1 and GEF-H1 to epithelial junctions

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

CNVs: harbingers of a rare variant revolution in psychiatric genetics

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

A copy number variation morbidity map of developmental delay

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Copy number variants in German patients with schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

The genomic psychiatry cohort: partners in discovery

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

The SLC1 high-affinity glutamate and neutral amino acid transporter family.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Cingulin, paracingulin, and PLEKHA7: signaling and cytoskeletal adaptors at the apical junctional complex

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

De novo rates and selection of schizophrenia-associated copy number variants

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

De novo rates and selection of large copy number variation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Phenotypic variability and genetic susceptibility to genomic disorders

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Microdeletions of 3q29 confer high risk for schizophrenia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Monosomy 1p36 deletion syndrome.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Glutamate and schizophrenia: beyond the dopamine hypothesis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

The human gamma-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

SCAN. Schedules for Clinical Assessment in Neuropsychiatry

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

27 September 2017

Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3929090

retrieved

30 May 2018

Identifiers

DOI

10.1093/HMG/DDT540

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2096036

OpenCitations bibliographic resource ID

2096036

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2096036

PMC publication ID

3929090

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2096036

PubMed publication ID

24163246

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2096036

ResearchGate publication ID

273199669

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24603800&oldid=1746320407"