(Q46116562)

19 December 2017

title

No association between general cognitive ability and rare copy number variation (English)

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19 December 2017

author

Allan F McRae

1

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19 December 2017

Margaret J. Wright

2

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19 December 2017

Narelle Hansell

3

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19 December 2017

Nick Martin

5

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19 December 2017

Grant W. Montgomery

object named as

Grant W Montgomery

4

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language of work or name

English

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publication date

17 February 2013

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19 December 2017

published in

Behavior Genetics

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19 December 2017

volume

43

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19 December 2017

issue

3

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19 December 2017

page(s)

202-207

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19 December 2017

https://scigraph.springernature.com/pub.10.1007/s10519-013-9587-9

exact match

0 references

cites work

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

1 reference

https://api.crossref.org/works/10.1007%2FS10519-013-9587-9

A copy number variation morbidity map of developmental delay

21 January 2018

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Genome-wide association studies establish that human intelligence is highly heritable and polygenic

21 January 2018

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21 January 2018

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Genetic foundations of human intelligence

21 January 2018

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

21 January 2018

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Rare structural variation of synapse and neurotransmission genes in autism

21 January 2018

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Intelligence in early adulthood and subsequent hospitalization for mental disorders.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10519-013-9587-9

Relative burden of large CNVs on a range of neurodevelopmental phenotypes

21 January 2018

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

21 January 2018

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

21 January 2018

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A genetic investigation of the covariation among inspection time, choice reaction time, and IQ subtest scores

21 January 2018

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X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.

21 January 2018

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Common variants in the trichohyalin gene are associated with straight hair in Europeans

21 January 2018

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Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

21 January 2018

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

21 January 2018

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X-linked mental retardation

21 January 2018

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Strong association of de novo copy number mutations with autism

21 January 2018

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Large recurrent microdeletions associated with schizophrenia

21 January 2018

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Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

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Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis

21 January 2018

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

21 January 2018

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Genetics of cognition: outline of a collaborative twin study

21 January 2018

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Rare copy number deletions predict individual variation in intelligence

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10519-013-9587-9

Singleton deletions throughout the genome increase risk of bipolar disorder

21 January 2018

1 reference

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10.1007/S10519-013-9587-9

21 January 2018

Identifiers

DOI

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19 December 2017

1 reference

19 December 2017