Genetic copy number variation and general cognitive ability (Q34539953)

2 August 2017

title

Genetic copy number variation and general cognitive ability (English)

1 reference

2 August 2017

Andrew K MacLeod

1

0 references

Lorna M. Lopez

Lorna M Lopez

9

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Antony Payton

Antony Payton

3

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Neil Pendleton

Neil Pendleton

18

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Alan J. Gow

Alan J Gow

10

0 references

David J. Porteous

David J Porteous

20

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Andrew Pickles

Andrew Pickles

14

0 references

Ian Deary

Ian J Deary

21

0 references

Geraldine McNeill

Geraldine McNeill

13

0 references

Dave Liewald

6

David Liewald

1 reference

2 August 2017

19

Pippa A Thomson

1 reference

2 August 2017

17

John M Starr

1 reference

2 August 2017

5

Sarah E Harris

1 reference

2 August 2017

11

Janie Corley

1 reference

2 August 2017

12

Paul Redmond

1 reference

2 August 2017

15

William Ollier

1 reference

2 August 2017

Gail Davies

2

1 reference

2 August 2017

Albert Tenesa

4

1 reference

2 August 2017

Xiayi Ke

7

1 reference

2 August 2017

Michelle Luciano

8

1 reference

2 August 2017

Michael Horan

16

1 reference

2 August 2017

language of work or name

English

0 references

publication date

26 December 2012

1 reference

2 August 2017

1 reference

2 August 2017

volume

7

1 reference

2 August 2017

issue

12

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2 August 2017

page(s)

e37385

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Creative Commons Attribution 4.0 International

2 August 2017

copyright license

start time

26 December 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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

7 July 2018

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7 July 2018

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

7 July 2018

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Common SNPs explain a large proportion of the heritability for human height

7 July 2018

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Functional impact of global rare copy number variation in autism spectrum disorders

7 July 2018

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7 July 2018

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Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients.

7 July 2018

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7 July 2018

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Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

7 July 2018

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Large, rare chromosomal deletions associated with severe early-onset obesity

7 July 2018

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Copy-number variants in neurodevelopmental disorders: promises and challenges

7 July 2018

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Microduplications of 16p11.2 are associated with schizophrenia

7 July 2018

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7 July 2018

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Copy number variations of chromosome 16p13.1 region associated with schizophrenia

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

The impact of genetic research on our understanding of normal cognitive ageing: 1995 to 2009

7 July 2018

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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

7 July 2018

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7 July 2018

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7 July 2018

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

7 July 2018

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Genetic foundations of human intelligence

7 July 2018

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Population analysis of large copy number variants and hotspots of human genetic disease

7 July 2018

1 reference

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Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies

7 July 2018

1 reference

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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

7 July 2018

1 reference

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Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936.

7 July 2018

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Why do intelligent people live longer?

7 July 2018

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Integrated detection and population-genetic analysis of SNPs and copy number variation

7 July 2018

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Large recurrent microdeletions associated with schizophrenia

7 July 2018

1 reference

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Rare chromosomal deletions and duplications increase risk of schizophrenia

7 July 2018

1 reference

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Strong association of de novo copy number mutations with sporadic schizophrenia

7 July 2018

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Disruption of contactin 4 in three subjects with autism spectrum disorder

7 July 2018

1 reference

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Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen

7 July 2018

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Structural variation of chromosomes in autism spectrum disorder

7 July 2018

1 reference

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Association between microdeletion and microduplication at 16p11.2 and 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=3530597

Disruption of neurexin 1 associated with autism spectrum 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=3530597

Recurrent 16p11.2 microdeletions in 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=3530597

Psoriasis is associated with increased beta-defensin genomic copy number

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

The Lothian Birth Cohort 1936: a study to examine influences on cognitive ageing from age 11 to age 70 and beyond

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

Contribution of SHANK3 mutations to autism spectrum 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=3530597

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=3530597

Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

Methods and strategies for analyzing copy number variation using DNA microarrays

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

BRIP1 (BACH1) variants and familial breast cancer risk: a case-control 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=3530597

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using 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=3530597

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

Global variation in copy number in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

Structural variation in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

Detection of large-scale variation in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

The impact of childhood intelligence on later life: following up the Scottish mental surveys of 1932 and 1947.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

alpha-Synuclein locus triplication causes Parkinson's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530597

"General Intelligence," Objectively Determined and Measured

7 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Still just 1 g: Consistent results from five test batteries

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Sizing up human height variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Gene copy-number polymorphism in nature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Evidence for an influence of chemokine ligand 3-like 1 (CCL3L1) gene copy number on susceptibility to rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Neuropsychological dysfunction in antipsychotic-naive first-episode unipolar psychotic depression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Just one g: consistent results from three test batteries

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

The University of Manchester Longitudinal Study of Cognition in Normal Healthy Old Age, 1983 through 2003

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037385

Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23300510

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0037385

1 reference

2 August 2017

0 references

1 reference

2 August 2017

1 reference