Evidence map›Paper›PMID 28512748›Full record

ArticleAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2017

Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene-based tests, genome-wide variation, and SNP heritability.

L Cinnamon Bidwell, Joshua C Gray, Jessica Weafer, Abraham A Palmer, Harriet de Wit, James MacKillop

Registry-linked trialAbstract read
In one paragraph

Article in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07182344 (Effects of iTBS on Cognitive Control in Children With ADHD), which is not on this map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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.

NCT07182344 naenrolling by invitationnot on this mapstarted 2025, after this paper: background citation

Effects of iTBS on Cognitive Control in Children With ADHD: A Randomized, Sham-Controlled Study Integrating EEG During ANT, fNIRS, MRI, and Genetic Markers

TypeinterventionalSponsorNeurolab PlusRan2025 to 2026Enrolled40ConditionsADHD - Attention Deficit Disorder With HyperactivityArmsIntermittent Theta Burst Stimulation to Right DLPFC, Sham Intermittent Theta Burst Stimulation
3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. The Role of GCH1 Deficiency and Tetrahydrobiopterin in Mental Health.International journal of molecular sciences · 2025
    Article
  2. Editor's view: What makes science successful?Journal of global health · 2025
    Article
  3. Serotonin dysfunction in ADHD.Journal of neurodevelopmental disorders · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Mapping relationships between ADHD genetic liability, stressful life events, and ADHD symptoms in healthy adults.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Genomic evidence for MHC disassortative mating in humans.Proceedings. Biological sciences · 2019
    Article
  15. Review
  16. Article
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

6 authors.

L Cinnamon BidwellInstitute of Cognitive Science, University of Colorado at Boulder, Boulder, Colorado.
Joshua C GrayDepartment of Psychology, University of Georgia, Athens, Georgia.
Jessica WeaferDepartment of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, Illinois.
Abraham A PalmerDepartment of Psychiatry, University of California San Diego, San Diego, California.
Harriet de WitDepartment of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, Illinois.
James MacKillopPeter Boris Centre for Addictions Research, McMaster University/St. Joseph's Healthcare Hamilton, Hamilton, Canada.

Funding

The genetic basis of impulsive behavior in humansR01DA032015 · NIDA · UNIVERSITY OF CHICAGO · PI DE WIT, HARRIET · 2011 to 2015
$2.4M
Deconstructing the Smoking and ADHD Comorbidity: A Multilevel Genetic ApproachK23DA033302 · NIDA · UNIVERSITY OF COLORADO · PI BIDWELL, L. CINNAMON · 2012 to 2016
$871k
Neurobiological factors underlying sex differences in risk for alcohol abuseK01AA024519 · NIAAA · UNIVERSITY OF KENTUCKY · PI WEAFER, JESSICA J · 2016 to 2020
$598k
NIAAA NIH HHS K01 AA024519NIDA NIH HHS K23 DA033302NIDA NIH HHS R01 DA032015
6 · The paper itself

Abstract

Although the heritability of ADHD is estimated to be high, identifying specific genetic markers remains challenging. Most studies to date have examined the genetic basis of ADHD by employing dichotomous diagnostic phenotypes, but, as ADHD symptoms tend to be phenotypically dimensional, an alternative and potentially informative approach is to examine continuous indices of inattention and hyperactivity-impulsivity symptoms. The current study aimed to identify genetic effects on dimensionally-focused adult ADHD-related phenotypes in 990 individuals of European ancestry with intentionally low levels of substance misuse to avoid confounding. The study used four complementary approaches: (1) analysis of a priori candidate loci identified in prior meta-analytic work; (2) gene-based analysis; (3) hypothesis-free genome-wide association testing; and (4) single nucleotide polymorphism (SNP) heritability via genomic-relatedness-matrix restricted maximum likelihood analysis (GREML). The GREML analysis included a bivariate model to test whether the ADHD symptom dimensions index the same genetic liability. The results revealed significant differential associations between two a priori loci and ADHD phenotypes, rs6296 in HTR1B with inattention and rs3746544 in SNAP-25 with hyperactivity-impulsivity. No significant gene-based or genome-wide associations were detected, but SNP heritability revealed that a large portion of genetic variance was accounted for by common SNPs (44%, 55%, and 59% for inattention, hyperactivity-impulsivity, and total ADHD, respectively) and substantial shared genetic variance across inattention and hyperactivity-impulsivity (86%). These findings reveal both unique and common patterns of genetic influences across dimensional ADHD-related phenotypes. More broadly, these findings reveal the value in using multiple methods to understand the genetic etiology of ADHD.

Indexed as

Genetic MarkersGenetic Predisposition to DiseaseGenome-Wide Association StudyPolymorphism, Single NucleotideAdultAttention Deficit Disorder with HyperactivityFemaleGenetic TestingHumansMalePhenotypePrognosisReceptor, Serotonin, 5-HT1BSynaptosomal-Associated Protein 25Young AdultGenetic MarkersHTR1B protein, humanReceptor, Serotonin, 5-HT1BSNAP25 protein, humanSynaptosomal-Associated Protein 25ADHDgeneticsheritabilityhyperactivityimpulsivityinattention

Identifiers

PMID28512748
PMCPMC5690554

What OpenQuestion holds

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Registered trials

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.