Evidence map›Paper›PMID 42642362›Full record

ArticleNature communications2026

Transcript-aware rare genetic variant association analyses of cardiopulmonary traits in participants from the All of Us Research Program.

Jingwen Zhang, So-Hyeon Hong, Xin Wang, Sean J Jurgens, Ching-Ti Liu, Josée Dupuis, Patrick T Ellinor, George T O'Connor, Quanshun Mei, Seung Hoan Choi

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jingwen ZhangDepartment of Biostatistics, Boston University School of Public Health, Boston, MA, USA.ORCID http://orcid.org/0009-0009-6062-1523
So-Hyeon HongDivision of Endocrinology and Metabolism, Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, South Korea.
Xin WangCardiovascular Disease Initiative, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Sean J JurgensCardiovascular Disease Initiative, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-1605-9782
Ching-Ti LiuDepartment of Biostatistics, Boston University School of Public Health, Boston, MA, USA.ORCID http://orcid.org/0000-0002-0703-0742
Josée DupuisDepartment of Biostatistics, Boston University School of Public Health, Boston, MA, USA.ORCID http://orcid.org/0000-0003-2871-3603
Patrick T EllinorCardiovascular Disease Initiative, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
George T O'ConnorPulmonary Center, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
Quanshun Mei *Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA. qsmei@bu.edu.ORCID http://orcid.org/0009-0006-7502-8819
Seung Hoan Choi *Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA. seuchoi@bu.edu.ORCID http://orcid.org/0000-0002-2797-3190

Funding

Understanding airway mucus dysfunction in population-based studiesR01HL164824 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI DIAZ, ALEJANDRO · 2022 to 2025
$2.7M
NHLBI NIH HHS R01 HL164824U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 5R01HL164824
6 · The paper itself

Abstract

Gene-based rare variant analyses often lack statistical power and may overlook transcript-specific effects. Here, we present a transcript-aware aggregation framework. In simulation studies, the framework maintains appropriate false-positive rates and shows competitive power relative to standard single-transcript analyses, approaching the performance of the ideal case of knowing the most informative transcript in advance. We then apply the approach to 129 cardiopulmonary traits in over 240,000 whole-genome-sequenced All of Us participants. By leveraging transcript-specific annotations, we identify 11 novel associations and recover 47 reported associations, including potentially pleiotropic genes linked to plasma lipid traits (PPARG) and body habitus (TCF12). Notably, for TTN, a gene known for its transcript-specific effects in cardiomyopathy, our framework strengthens the association signal and pinpoints the N2B isoform, which shows a stronger association with cardiomyopathy than other transcripts. These findings highlight the value of a transcript-aware framework for improving rare variant association studies.

Indexed as

CardiomyopathiesGenetic VariationConnectinGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPhenotypePolymorphism, Single NucleotideUnited StatesWhole Genome SequencingConnectin

Identifiers

PMID42642362
PMCPMC13507129

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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.