Evidence map›Paper›PMID 40593511›Full record

ArticleNature communications2025

DrFARM: identification of pleiotropic genetic variants in genome-wide association studies.

Lap Sum Chan, Gen Li, Eric B Fauman, Xianyong Yin, Markku Laakso, Michael Boehnke, Peter X K Song

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

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

1 citing paper in PubMed.

  1. 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

7 authors.

Lap Sum ChanDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-3206-9064
Gen LiDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
Eric B FaumanInternal Medicine Research Unit, Pfizer Worldwide Research, Development and Medical, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-9739-0249
Xianyong YinDepartment of Epidemiology, Nanjing Medical University, Nanjing, Jiangsu, China.ORCID http://orcid.org/0000-0001-6454-2384
Markku LaaksoInstitute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Kuopio, Finland.ORCID http://orcid.org/0000-0002-3394-7749
Michael BoehnkeDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-6442-7754
Peter X K SongDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA. pxsong@umich.edu.ORCID http://orcid.org/0000-0001-7881-7182

Funding

Tensor Array Methods for RNA-Seq AnalysisR01HG010731 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, GEN · 2020 to 2024
$1.4M
Statistical methods for analysis of high-dimensional mediation pathwaysR01ES033656 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Karen Eileen Peterson, Peter Xuekun Song · 2023 to 2026
$1.4M
E3Gen: Multigenerational Influences of Social Structure on Toxicant Exposures and Life Course Health in the ELEMENT CohortU24ES028502 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PETERSON, KAREN EILEEN, SONG, PETER XUEKUN · 2023 to 2025
$1.0M
Academy of Finland (Suomen Akatemia) 321428NHGRI NIH HHS R01 HG010731NIEHS NIH HHS R01 ES033656NIEHS NIH HHS U24 ES028502U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R01HG010731U.S. Department of Health & Human Services | NIH | National Institute of Environmental Health Sciences (NIEHS) R01ES033656
6 · The paper itself

Abstract

In a standard analysis, pleiotropic variants are identified by running separate genome-wide association studies (GWAS) and combining results across traits. But such statistical approach based on marginal summary statistics may lead to spurious results. We propose a new statistical approach, Debiased-regularized Factor Analysis Regression Model (DrFARM), through a joint regression model for simultaneous analysis of high-dimensional genetic variants and multilevel dependencies. This joint modeling strategy controls overall error to permit universal false discovery rate (FDR) control. DrFARM uses the strengths of the debiasing technique and the Cauchy combination test, both being theoretically justified, to establish a valid post selection inference on pleiotropic variants. Through extensive simulations, we show that DrFARM appropriately controls overall FDR. Applying DrFARM to data on 1031 metabolites measured on 6135 men from the Metabolic Syndrome in Men (METSIM) study, we identify five first-time reported putative causal genes, none of which had been implicated in any prior metabolite GWAS (including the prior METSIM analysis).

Indexed as

Genetic PleiotropyGenetic VariationGenome-Wide Association StudyComputer SimulationHumansMaleMetabolic SyndromeModels, GeneticPolymorphism, Single NucleotideRegression Analysis

Identifiers

PMID40593511
PMCPMC12216935

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.