Evidence map›Paper›PMID 41445655›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Phenome-wide analysis of genetically imputed neuroimaging phenotypes reveals associations with psychiatric traits in a multi-ancestry cohort.

Lina Chihoub, Corinde E Wiers, Joel Gelernter, Bingxin Zhao, Christal N Davis, Henry R Kranzler

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Lina Chihoubepartment of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.
Corinde E Wiersepartment of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.ORCID 0000-0002-2934-8794
Joel GelernterDepartment of Psychiatry, Yale School of Medicine, New Haven, CT 06511 and VA Connecticut Healthcare Center, West Haven, CT 06516.ORCID 0000-0002-4067-1859
Bingxin ZhaoDepartment of Statistics and Data Science, University of Pennsylvania, Philadelphia, PA 19104.
Christal N Davisepartment of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.ORCID 0000-0003-3974-5598
Henry R Kranzlerepartment of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.ORCID 0000-0002-1018-0450

Funding

Leveraging GWAS Findings to Map Variants and Identify Novel Effector Genes for Alcohol-Related TraitsR01AA030056 · NIAAA · UNIVERSITY OF PENNSYLVANIA · PI Struan F A Grant, MATTHEW S KAYSER · 2023 to 2026
$2.5M
BLRD VA I01 BX004820NIAAA NIH HHS R01 AA030056
6 · The paper itself

Abstract

Background: Understanding how variation in brain structure and function contributes to psychiatric and behavioral phenotypes remains a key challenge. The absence of neuroimaging data in many study samples limits this effort. Methods: We used genome-wide association study (GWAS) summary statistics from the UK Biobank to impute 301 brain imaging-derived phenotype (IDP) genetic scores (IGS) in the Yale-Penn cohort, which is enriched for substance use disorders (n = 10,275; 52.8% European-like [EUR] and 47.2% African-like [AFR] genetic ancestry). The brain IDPs include white matter microstructure, regional volume, and resting-state functional connectivity measures, for which we generated IGS in the Yale-Penn participants. We then conducted a brain-wide phenome-wide association study (pheWAS) of the 301 IGS across 692 behavioral, psychiatric, and environmental traits. Results: Among EUR individuals, we identified 19 IGS with significant associations that survived within-trait corrections for multiple testing. These included links between genetically predicted white matter integrity and sedative abuse, tobacco withdrawal, attention deficit hyperactivity disorder (ADHD); structural brain volumes and cocaine dependence, ADHD, and conduct disorder; and functional connectivity with substance-related symptoms and social phobia. Among AFR individuals, we identified 15 IDPs with significant associations, including associations between genetically predicted white matter integrity and stimulant use disorder, regional brain volumes and opioid withdrawal/dependence, and functional connectivity and cocaine craving. Conclusions: Genetically imputed brain features capture biological variation associated with psychiatric traits. This work provides a framework for leveraging genetic data to link neuroimaging measures to substance use and mental health outcomes in samples that lack imaging data.

Indexed as

Imaging-derived PhenotypesImputed Brain FeaturesMulti-ancestry AnalysisPhenome-wide Association StudyYale-Penn Sample

Identifiers

PMID41445655
PMCPMC12723762

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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.