Evidence map›Paper›PMID 26955885›Full record

ArticleNature communications2016

Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank.

Jacqueline M Lane, Irma Vlasac, Simon G Anderson, Simon D Kyle, William G Dixon, David A Bechtold, Shubhroz Gill, Max A Little, Annemarie Luik, Andrew Loudon and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 165 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed, 6 pooled it
19.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

165 citing papers in PubMed, 6 syntheses or guidelines pooled it, 314 citations in OpenAlex.

  1. Pooled it
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  10. Chrononutrition-based dietary strategies for effective weight loss.European journal of clinical nutrition · 2026
    Article
  11. Circadian rhythms regulate refractive development across species.bioRxiv : the preprint server for biology · 2026
    Article
  12. Review
  13. Article
  14. Assessing the causal impact of leisure-time physical activity and screen time on lifespan: a Mendelian randomization study.European review of aging and physical activity : official journal of the European Group for Research into Elderly and Physical Activity · 2026
    Article
  15. CircadianiScience · 2026
    Article
  16. Article
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105 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 3 countries.

Jacqueline M LaneCenter for Human Genetic Research Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Irma VlasacCenter for Human Genetic Research Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Simon G AndersonCardiovascular Research Group, Institute of Cardiovascular Sciences, The University of Manchester, Manchester M139PL, UK.ORCID http://orcid.org/0000-0002-8896-073X
Simon D KyleSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX12JD, UK.
William G DixonCentre for Musculoskeletal Research Institute of Inflammation and Repair, The University of Manchester, Manchester M139PL, UK.ORCID http://orcid.org/0000-0001-5881-4857
David A BechtoldFaculty of Life Sciences, The University of Manchester, Manchester M139PL, UK.
Shubhroz GillChemical Biology Program, Broad Institute, Cambridge, Massachusetts 02142, USA.
Max A LittleDepartment of Mathematics, Engineering and Applied Science, Aston University, Birmingham B47ET, UK.
Annemarie LuikSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX12JD, UK.
Andrew LoudonFaculty of Life Sciences, The University of Manchester, Manchester M139PL, UK.
Richard EmsleyInstitute of Population Health, The University of Manchester, Manchester M139PL, UK.
Frank A J L ScheerDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
Deborah A LawlorMRC Integrative Epidemiology Unit at the University of Bristol, Bristol BS81TH, UK.
Susan RedlineDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
David W RayCentre for Endocrinology and Diabetes, Institute of Human Development, The University of Manchester, Manchester M139PL, UK.
Martin K RutterCentre for Endocrinology and Diabetes, Institute of Human Development, The University of Manchester, Manchester M139PL, UK.
Richa SaxenaCenter for Human Genetic Research Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
University of Manchester · GBBroad Institute · USBrigham and Women's Hospital · USUniversity of Oxford · GBAston University · GBManchester Academic Health Science Centre · GBUniversity of Bristol · GB

Funding

Leveraging Family Data to Identify Genetic Variants for Sleep ApneaR01HL113338 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LIN, XIHONG, REDLINE, SUSAN S. · 2012 to 2016
$4.4M
Melatonin and Receptor Gene Variant: Linking Circadian System and Type 2 DiabetesR01DK102696 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI SAXENA, RICHA, SCHEER, FRANK A · 2015 to 2019
$3.8M
Discovery of genes for sleep traitsR21HL121728 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SAXENA, RICHA · 2014 to 2015
$259k
Impact of genetic variants on sleep timing and type 2 diabetes riskF32DK102323 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI LANE, JACQUELINE MARIE · 2015 to 2016
$116k
Medical Research Council G0902272Medical Research Council MC_PC_13042Medical Research Council MC_PC_15018Medical Research Council MC_QA137853Medical Research Council MC_UU_12013/5Medical Research Council MR/K006665/1Medical Research Council MR/L010240/1Medical Research Council MR/M008908/1NHLBI NIH HHS R01 HL113338NHLBI NIH HHS R01HL113338-04NHLBI NIH HHS R21 HL121728NHLBI NIH HHS R21HL121728-02NIDDK NIH HHS F32 DK102323NIDDK NIH HHS F32DK102323-01A1NIDDK NIH HHS R01 DK102696Parkinson's UK J-0901Wellcome Trust 107851/Z/15/Z
6 · The paper itself

Abstract

Our sleep timing preference, or chronotype, is a manifestation of our internal biological clock. Variation in chronotype has been linked to sleep disorders, cognitive and physical performance, and chronic disease. Here we perform a genome-wide association study of self-reported chronotype within the UK Biobank cohort (n=100,420). We identify 12 new genetic loci that implicate known components of the circadian clock machinery and point to previously unstudied genetic variants and candidate genes that might modulate core circadian rhythms or light-sensing pathways. Pathway analyses highlight central nervous and ocular systems and fear-response-related processes. Genetic correlation analysis suggests chronotype shares underlying genetic pathways with schizophrenia, educational attainment and possibly BMI. Further, Mendelian randomization suggests that evening chronotype relates to higher educational attainment. These results not only expand our knowledge of the circadian system in humans but also expose the influence of circadian characteristics over human health and life-history variables such as educational attainment.

Indexed as

Circadian RhythmGenetic LociGenome, HumanAdultAgedCohort StudiesFemaleGenome-Wide Association StudyHumansMaleMiddle AgedUnited KingdomWhite People

Identifiers

PMID26955885
PMCPMC4786869
OpenAlexW2413730192

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.