(Q43742579)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24115684%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

title

A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability (English)

1 reference

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27 February 2020

0 references

1 reference

6

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27 February 2020

Andrew G. McKechanie

8

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27 February 2020

Allan F McRae

9

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27 February 2020

Jennifer L. Moran

10

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27 February 2020

Benjamin S Pickard

11

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27 February 2020

Naomi R. Wray

15

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27 February 2020

Peter M. Visscher

16

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27 February 2020

Eske M Derks

1

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27 February 2020

Jurgen Del Favero

4

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27 February 2020

Mandy Johnstone

5

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27 February 2020

13

Pamela Sklar

1 reference

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27 February 2020

17

Douglas H R Blackwood

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27 February 2020

12

Shaun Purcell

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27 February 2020

author name string

Muhammad Ayub

2

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27 February 2020

Kimberly Chambert

3

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27 February 2020

Alan Maclean

7

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27 February 2020

David M StClair

14

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27 February 2020

publication date

25 September 2013

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

27 February 2020

number of pages

8

1 reference

based on heuristic

inferred from page(s)

published in

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27 February 2020

volume

162B

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27 February 2020

issue

8

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27 February 2020

page(s)

847-854

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The genetic association database

27 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Pre-frontal lobe gyrification index in schizophrenia, mental retardation and comorbid groups: an automated study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Psychosis and adults with intellectual disabilities. Prevalence, incidence, and related factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

‘Pfropfschizophrenie’ revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Copy number variations in neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Genomic microarrays in mental retardation: a practical workflow for diagnostic applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

The role of primary cilia in neuronal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Neuroanatomy of comorbid schizophrenia and learning disability: a controlled study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32189

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.32189

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24115684%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

1 reference