Evidence map›Paper›PMID 30940813›Full record

ArticleNature communications2019

Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations.

Henry R Kranzler, Hang Zhou, Rachel L Kember, Rachel Vickers Smith, Amy C Justice, Scott Damrauer, Philip S Tsao, Derek Klarin, Aris Baras, Jeffrey Reid and 10 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 343 papers, 17 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
343citing papers in PubMed, 17 pooled it
44.8field-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

343 citing papers in PubMed, 17 syntheses or guidelines pooled it, 524 citations in OpenAlex.

  1. Pooled it
  2. CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2026
    Guideline
  3. Screening for high-risk drinking and alcohol use disorder: update of the 2023 national clinical practice guideline.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2026
    Guideline
  4. Pooled it
  5. The genetics of cannabis lifetime use.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Pooled it
  6. Pooled it
  7. Pooled it
  8. Pooled it
  9. Pooled it
  10. Pooled it
  11. Pooled it
  12. Pooled it
  13. Pooled it
  14. Pooled it
  15. Pooled it
  16. Genome-wide meta-analysis of alcohol use disorder in East Asians.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Pooled it
  17. Pooled it
  18. Article
  19. Neuropsychiatry genetics in Africa.Nature communications · 2026
    Review
  20. Article

283 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 8 institutions in 1 country.

Henry R KranzlerUniversity of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA. kranzler@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0002-1018-0450
Hang ZhouYale School of Medicine, New Haven, CT, 06511, USA.ORCID http://orcid.org/0000-0002-7694-6391
Rachel L KemberUniversity of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
Rachel Vickers SmithCrescenz Veterans Affairs Medical Center, Philadelphia, PA, 19104, USA.ORCID http://orcid.org/0000-0002-7224-8916
Amy C JusticeYale School of Medicine, New Haven, CT, 06511, USA.ORCID http://orcid.org/0000-0003-0139-5502
Scott DamrauerUniversity of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
Philip S TsaoVA Palo Alto Health Care System, Palo Alto, CA, 94304, USA.
Derek KlarinMassachusetts General Hospital, Harvard Medical School, Boston, MA, 02114, USA.ORCID http://orcid.org/0000-0002-4636-5780
Aris BarasRegeneron Genetics Center, Tarrytown, NY, 10591, USA.
Jeffrey ReidRegeneron Genetics Center, Tarrytown, NY, 10591, USA.ORCID http://orcid.org/0000-0001-8645-4713
John OvertonRegeneron Genetics Center, Tarrytown, NY, 10591, USA.
Daniel J RaderUniversity of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
Zhongshan ChengYale School of Medicine, New Haven, CT, 06511, USA.
Janet P TateYale School of Medicine, New Haven, CT, 06511, USA.
William C BeckerYale School of Medicine, New Haven, CT, 06511, USA.
John ConcatoYale School of Medicine, New Haven, CT, 06511, USA.
Ke XuYale School of Medicine, New Haven, CT, 06511, USA.
Renato PolimantiYale School of Medicine, New Haven, CT, 06511, USA.
Hongyu ZhaoYale School of Medicine, New Haven, CT, 06511, USA.ORCID http://orcid.org/0000-0003-1195-9607
Joel GelernterYale School of Medicine, New Haven, CT, 06511, USA.ORCID http://orcid.org/0000-0002-4067-1859
Yale University · USRegeneron (United States) · USVeterans Health Administration · USHarvard University · USPhiladelphia VA Medical Center · USUniversity of Louisville · USUniversity of Pennsylvania · USVA Palo Alto Health Care System · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI JESSICA E SALVATORE · 1989 to 2026
$162.7M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
7/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109532 · NIMH · WASHINGTON UNIVERSITY · PI AGRAWAL, ARPANA, EDENBERG, HOWARD J · 2016 to 2020
$3.1M
3/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109536 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHARNEY, ALEXANDER W, HUCKINS, LAURA MARIANNE · 2016 to 2020
$2.7M
BLRD VA I01 BX003341NCATS NIH HHS UL1 TR001863NIAAA NIH HHS U10 AA008401NIMH NIH HHS U01 MH109532NIMH NIH HHS U01 MH109536
6 · The paper itself

Abstract

Alcohol consumption level and alcohol use disorder (AUD) diagnosis are moderately heritable traits. We conduct genome-wide association studies of these traits using longitudinal Alcohol Use Disorder Identification Test-Consumption (AUDIT-C) scores and AUD diagnoses in a multi-ancestry Million Veteran Program sample (N = 274,424). We identify 18 genome-wide significant loci: 5 associated with both traits, 8 associated with AUDIT-C only, and 5 associated with AUD diagnosis only. Polygenic Risk Scores (PRS) for both traits are associated with alcohol-related disorders in two independent samples. Although a significant genetic correlation reflects the overlap between the traits, genetic correlations for 188 non-alcohol-related traits differ significantly for the two traits, as do the phenotypes associated with the traits' PRS. Cell type group partitioning heritability enrichment analyses also differentiate the two traits. We conclude that, although heavy drinking is a key risk factor for AUD, it is not a sufficient cause of the disorder.

Indexed as

Genome-Wide Association StudyAdultAgedAged, 80 and overAlcohol DrinkingAlcoholismFemaleHumansLongitudinal StudiesMaleMiddle AgedMultifactorial InheritancePhenotypePolymorphism, Single NucleotideYoung Adult

Identifiers

PMID30940813
PMCPMC6445072
OpenAlexW2928966425

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.