Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
21826061
TITLE
Genome-wide association studies establish that human intelligence is highly heritable and polygenic.
ABSTRACT
General intelligence is an important human quantitative trait that accounts for much of the variation in diverse cognitive abilities. Individual differences in intelligence are strongly associated with many important life outcomes, including educational and occupational attainments, income, health and lifespan. Data from twin and family studies are consistent with a high heritability of intelligence, but this inference has been controversial. We conducted a genome-wide analysis of 3511 unrelated adults with data on 549,692 single nucleotide polymorphisms (SNPs) and detailed phenotypes on cognitive traits. We estimate that 40% of the variation in crystallized-type intelligence and 51% of the variation in fluid-type intelligence between individuals is accounted for by linkage disequilibrium between genotyped common SNP markers and unknown causal variants. These estimates provide lower bounds for the narrow-sense heritability of the traits. We partitioned genetic variation on individual chromosomes and found that, on average, longer chromosomes explain more variation. Finally, using just SNP data we predicted ∼1% of the variance of crystallized and fluid cognitive phenotypes in an independent sample (P=0.009 and 0.028, respectively). Our results unequivocally confirm that a substantial proportion of individual differences in human intelligence is due to genetic variation, and are consistent with many genes of small effects underlying the additive genetic influences on intelligence.
DATE PUBLISHED
2011 Oct
HISTORY
PUBSTATUS PUBSTATUSDATE
aheadofprint 2011/08/09
entrez 2011/08/10 06:00
pubmed 2011/08/10 06:00
medline 2012/02/04 06:00
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Davies G Davies G G Department of Psychology, University of Edinburgh, Edinburgh, Scotland, UK.
Tenesa A Tenesa A A
Payton A Payton A A
Yang J Yang J J
Harris SE Harris S E SE
Liewald D Liewald D D
Ke X Ke X X
Le Hellard S Le Hellard S S
Christoforou A Christoforou A A
Luciano M Luciano M M
McGhee K McGhee K K
Lopez L Lopez L L
Gow AJ Gow A J AJ
Corley J Corley J J
Redmond P Redmond P P
Fox HC Fox H C HC
Haggarty P Haggarty P P
Whalley LJ Whalley L J LJ
McNeill G McNeill G G
Goddard ME Goddard M E ME
Espeseth T Espeseth T T
Lundervold AJ Lundervold A J AJ
Reinvang I Reinvang I I
Pickles A Pickles A A
Steen VM Steen V M VM
Ollier W Ollier W W
Porteous DJ Porteous D J DJ
Horan M Horan M M
Starr JM Starr J M JM
Pendleton N Pendleton N N
Visscher PM Visscher P M PM
Deary IJ Deary I J IJ
INVESTIGATORS
JOURNAL
VOLUME: 16
ISSUE: 10
TITLE: Molecular psychiatry
ISOABBREVIATION: Mol. Psychiatry
YEAR: 2011
MONTH: Oct
DAY:
MEDLINEDATE:
SEASON:
CITEDMEDIUM: Internet
ISSN: 1476-5578
ISSNTYPE: Electronic
MEDLINE JOURNAL
MEDLINETA: Mol Psychiatry
COUNTRY: England
ISSNLINKING: 1359-4184
NLMUNIQUEID: 9607835
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
Meta-Analysis
Research Support, Non-U.S. Gov't
COMMENTS AND CORRECTIONS
REFTYPE REFSOURCE REFPMID NOTE
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GRANTS
GRANTID AGENCY COUNTRY
064359 Wellcome Trust United Kingdom
BB/F019394/1 Biotechnology and Biological Sciences Research Council United Kingdom
BB/F022441/1 Biotechnology and Biological Sciences Research Council United Kingdom
CZB/4/505 Chief Scientist Office United Kingdom
ETM/55 Chief Scientist Office United Kingdom
G0100594 Medical Research Council United Kingdom
G0400546 Medical Research Council United Kingdom
G0700704 Medical Research Council United Kingdom
G0700704(84698) Medical Research Council United Kingdom
G0901461 Medical Research Council United Kingdom
SAG09977 Biotechnology and Biological Sciences Research Council United Kingdom
Biotechnology and Biological Sciences Research Council United Kingdom
Chief Scientist Office United Kingdom
Medical Research Council United Kingdom
Wellcome Trust United Kingdom
GENERAL NOTE
KEYWORDS
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
Adolescent
Adult
Aged
Aged, 80 and over
Child
Cohort Studies
Female
Genome, Human
Genome-Wide Association Study
Humans
Intelligence genetics
Longitudinal Studies genetics
Male genetics
Middle Aged genetics
Multifactorial Inheritance genetics
Polymorphism, Single Nucleotide genetics
Quantitative Trait, Heritable genetics
Reference Values genetics
Young Adult genetics
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
OTHER ID's
OTHERID SOURCE
PMC3182557 NLM
UKMS35731 NLM