Temperament and brain networks of attention DOI Open Access
Michael I. Posner,

Mary K. Rothbart

Philosophical Transactions of the Royal Society B Biological Sciences, Journal Year: 2018, Volume and Issue: 373(1744), P. 20170254 - 20170254

Published: Feb. 26, 2018

The attention networks of the human brain are important control systems that develop from infancy into adulthood. While they common to everyone, differ in efficiency, forming basis individual differences attention. We have developed methods for measuring efficiency these older children and adults also examined their development infancy. During alerting orienting dominant infant's actions, but later an executive network dominates. Each has been associated with its main neuromodulator led associations genes related neuromodulator. links between parent reports child's effortful allow us associate molecular mechanisms fundamental behavioural outcomes. This article is part theme issue ‘Diverse perspectives on diversity: multi-disciplinary approaches taxonomies differences’.

Language: Английский

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences DOI
Richard Karlsson Linnér, Pietro Biroli, Edward Kong

et al.

Nature Genetics, Journal Year: 2019, Volume and Issue: 51(2), P. 245 - 257

Published: Jan. 9, 2019

Language: Английский

Citations

714

GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability DOI
Joëlle A. Pasman, Karin J. H. Verweij, Zachary F. Gerring

et al.

Nature Neuroscience, Journal Year: 2018, Volume and Issue: 21(9), P. 1161 - 1170

Published: Aug. 24, 2018

Language: Английский

Citations

499

Genetic architecture: the shape of the genetic contribution to human traits and disease DOI
Nicholas J. Timpson, Celia M.T. Greenwood, Nicole Soranzo

et al.

Nature Reviews Genetics, Journal Year: 2017, Volume and Issue: 19(2), P. 110 - 124

Published: Dec. 11, 2017

Language: Английский

Citations

416

Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117) DOI Creative Commons
Toni‐Kim Clarke, Mark J. Adams, Gail Davies

et al.

Molecular Psychiatry, Journal Year: 2017, Volume and Issue: 22(10), P. 1376 - 1384

Published: July 25, 2017

Alcohol consumption has been linked to over 200 diseases and is responsible for 5% of the global disease burden. Well-known genetic variants in alcohol metabolizing genes, example, ALDH2 ADH1B, are strongly associated with but have limited impact European populations where they found at low frequency. We performed a genome-wide association study (GWAS) self-reported 112 117 individuals UK Biobank (UKB) sample white British individuals. report significant associations 14 loci. These include single-nucleotide polymorphisms (SNPs) genes (ADH1B/ADH1C/ADH5) two loci KLB, gene recently consumption. also identify SNPs novel including GCKR, CADM2 FAM69C. Gene-based analyses implicated neurobiology substance use (DRD2, PDE4B). GCTA SNP-based heritability 13% (se=0.01). Sex-specific largely overlapping GWAS correlation (rG) between male female was 0.90 (s.e.=0.09, P-value=7.16 × 10-23). Using LD score regression, overlap years schooling (rG=0.18, s.e.=0.03), high-density lipoprotein cholesterol (rG=0.28, s.e.=0.05), smoking (rG=0.40, s.e.=0.06) various anthropometric traits (for overweight, rG=-0.19, s.e.=0.05). This replicates identifies that should be focus future studies investigating

Language: Английский

Citations

410

Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE DOI
Yann C. Klimentidis, David A. Raichlen, Jennifer W. Bea

et al.

International Journal of Obesity, Journal Year: 2018, Volume and Issue: 42(6), P. 1161 - 1176

Published: June 1, 2018

Language: Английский

Citations

336

Genome-wide analysis identifies 12 loci influencing human reproductive behavior DOI
Nicola Barban, Rick Jansen, Ronald de Vlaming

et al.

Nature Genetics, Journal Year: 2016, Volume and Issue: 48(12), P. 1462 - 1472

Published: Oct. 31, 2016

Language: Английский

Citations

324

BECon: a tool for interpreting DNA methylation findings from blood in the context of brain DOI Creative Commons
Rachel D. Edgar, Meaghan J. Jones, Michael J. Meaney

et al.

Translational Psychiatry, Journal Year: 2017, Volume and Issue: 7(8), P. e1187 - e1187

Published: Aug. 1, 2017

Tissue differences are one of the largest contributors to variability in human DNA methylome. Despite tissue-specific nature methylation, inaccessibility brain samples necessitates frequent use surrogate tissues such as blood, studies associations between methylation and function health. Results from humans difficult interpret this context, connection blood-brain is tenuous not well-documented. Here, we aimed provide a resource community aid interpretation blood-based results context tissue. We used paired 16 individuals three regions whole run on Illumina 450 K Human Methylation Array quantify concordance tissues. From these data, have made available metrics on: cytosine-phosphate-guanine dinucleotides (CpGs) our blood samples, CpGs brain, estimations how strongly CpG affected by cell composition both through web application BECon (Blood-Brain Epigenetic Concordance; https://redgar598.shinyapps.io/BECon/). anticipate that will enable biological results, brain.

Language: Английский

Citations

217

Elucidating the genetic basis of social interaction and isolation DOI Creative Commons
Felix R. Day, Ken K. Ong, John R. B. Perry

et al.

Nature Communications, Journal Year: 2018, Volume and Issue: 9(1)

Published: June 19, 2018

The negative impacts of social isolation and loneliness on health are well documented. However, little is known about their possible biological determinants. In up to 452,302 UK Biobank study participants, we perform genome-wide association analyses for regular participation in activities. We identify 15 genomic loci (P < 5 × 10-8) loneliness, demonstrate a likely causal between adiposity increased susceptibility depressive symptoms. Further were identified attendance at sports club or gym (N = 6 loci), pub 13) religious group 18). Across these traits there was strong enrichment genes expressed brain regions that control emotional expression behaviour. aetiological mechanisms specific each trait, addition identifying pleiotropic across multiple complex traits. may novel modifiable risk factors associated with withdrawal isolation.

Language: Английский

Citations

196

Selection against variants in the genome associated with educational attainment DOI Open Access
Augustine Kong, Michael L. Frigge, Guðmar Þorleifsson

et al.

Proceedings of the National Academy of Sciences, Journal Year: 2017, Volume and Issue: 114(5)

Published: Jan. 17, 2017

Epidemiological and genetic association studies show that genetics play an important role in the attainment of education. Here, we investigate effect this component on reproductive history 109,120 Icelanders consequent impact gene pool over time. We educational polygenic score, POLYEDU, constructed from results a recent study is associated with delayed reproduction (P < 10-100) fewer children overall. The stronger for women remains highly significant after adjusting attainment. Based 129,808 born between 1910 1990, find average POLYEDU has been declining at rate ∼0.010 standard units per decade, which substantial evolutionary timescale. Most importantly, because only captures fraction overall underlying latter could be two to three times faster.

Language: Английский

Citations

183

Using genetics for social science DOI
K. Paige Harden, Philipp Koellinger

Nature Human Behaviour, Journal Year: 2020, Volume and Issue: 4(6), P. 567 - 576

Published: May 11, 2020

Language: Английский

Citations

157