Evidence map›Paper›PMID 31421235›Full record

ArticleJournal of the American Academy of Child and Adolescent Psychiatry2020

Translating Discoveries in Attention-Deficit/Hyperactivity Disorder Genomics to an Outpatient Child and Adolescent Psychiatric Cohort.

Pieter J Vuijk, Joanna Martin, Ellen B Braaten, Giulio Genovese, Michael R Capawana, Sheila M O'Keefe, B Andi Lee, Hannah S Lind, Jordan W Smoller, Stephen V Faraone and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of the American Academy of Child and Adolescent Psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 3 pooled it
3.0field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 3 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Pooled it
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  3. Polygenic Scores for ADHD: A Meta-Analysis.Research on child and adolescent psychopathology · 2021
    Pooled it
  4. Article
  5. Association Between the Genetic Risk for Attention-Deficit/Hyperactivity Disorder and Cognitive Function in Older Age: The MYHAT Population-Based Study.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Pieter J VuijkCenter for Genomic Medicine, Massachusetts General Hospital, Boston.
Joanna MartinMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, UK; Stanley Center for Psychiatric Research, Broad Institute, Cambridge, MA.
Ellen B BraatenMassachusetts General Hospital and Harvard Medical School, Massachusetts General Hospital, Boston.
Giulio GenoveseStanley Center for Psychiatric Research, Broad Institute, Cambridge, MA.
Michael R CapawanaMassachusetts General Hospital and Harvard Medical School, Massachusetts General Hospital, Boston.
Sheila M O'KeefeMassachusetts General Hospital and Harvard Medical School, Massachusetts General Hospital, Boston.
B Andi LeeCenter for Genomic Medicine, Massachusetts General Hospital, Boston.
Hannah S LindCenter for Genomic Medicine, Massachusetts General Hospital, Boston.
Jordan W SmollerCenter for Genomic Medicine, Massachusetts General Hospital, Boston; Stanley Center for Psychiatric Research, Broad Institute, Cambridge, MA; Massachusetts General Hospital and Harvard Medical School, Massachusetts General Hospital, Boston.
Stephen V FaraoneSUNY Upstate Medical University, Syracuse, NY.
Roy H PerlisCenter for Genomic Medicine, Massachusetts General Hospital, Boston; Stanley Center for Psychiatric Research, Broad Institute, Cambridge, MA; Massachusetts General Hospital and Harvard Medical School, Massachusetts General Hospital, Boston; Center for Experimental Drugs and Diagnostics, Massachusetts General Hospital, Boston.
Alysa E DoyleCenter for Genomic Medicine, Massachusetts General Hospital, Boston; Stanley Center for Psychiatric Research, Broad Institute, Cambridge, MA; Massachusetts General Hospital and Harvard Medical School, Massachusetts General Hospital, Boston. Electronic address: doylea@helix.mgh.harvard.edu.
Broad Institute · USHarvard University · USMassachusetts General Hospital · USSUNY Upstate Medical University · US

Funding

Longitudinal Family/Molecular Genetic Study to Validate Research Domain CriteriaR01MH101519 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI FARAONE, STEPHEN V, GLATT, STEPHEN J · 2014 to 2018
$3.5M
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
Psychosis risk variants and cognitive control in clinically-referred youthR03MH106862 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI DOYLE, ALYSA E · 2015 to 2016
$249k
NIMH NIH HHS R01 MH101519NIMH NIH HHS R03 MH106862NIMH NIH HHS U01 MH109536Wellcome TrustWellcome Trust 106047
6 · The paper itself

Abstract

objectiveGenomic discoveries should be investigated in generalizable child psychiatric samples in order to justify and inform studies that will evaluate their use for specific clinical purposes. In youth consecutively referred for neuropsychiatric evaluation, we examined 1) the convergent and discriminant validity of attention-deficit/hyperactivity disorder (ADHD) polygenic risk scores (PRSs) in relation to DSM-based ADHD phenotypes; 2) the association of ADHD PRSs with phenotypes beyond ADHD that share its liability and have implications for outcome; and 3) the extent to which youth with high ADHD PRSs manifest a distinctive clinical profile.

methodParticipants were 433 youth, ages 7-18 years, from the Longitudinal Study of Genetic Influences on Cognition. We used logistic/linear regression and mixed effects models to examine associations with ADHD-related polygenic variation from the largest ADHD genome-wide association study to date. We replicated key findings in 5,140 adult patients from a local health system biobank.

resultsAmong referred youth, ADHD PRSs were associated with ADHD diagnoses, cross-diagnostic ADHD symptoms and academic impairment (odds ratios ∼1.4; R

conclusionAmong child and adolescent outpatients, ADHD polygenic risk was associated with ADHD and related phenotypes as well as clinical severity. These results extend the scientific foundation for studies of ADHD polygenic risk in the clinical setting and highlight directions for further research.

Indexed as

Attention Deficit Disorder with HyperactivityAdolescentAdultChildGenome-Wide Association StudyGenomicsHumansLongitudinal StudiesOutpatientsADHDclinical translationgenomic medicinepolygenic risk

Identifiers

PMID31421235
PMCPMC7408479
OpenAlexW2966964292

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.