Evidence map›Paper›PMID 41184541›Full record

ArticleNature genetics2025

Liability threshold model-based disease risk prediction based on electronic health record phenotypes.

Cue Hyunkyu Lee, Atlas Khan, Chen Wang, Chunhua Weng, Joseph D Buxbaum, Krzysztof Kiryluk, Iuliana Ionita-Laza

Abstract read
In one paragraph

Article in Nature genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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.

Cue Hyunkyu LeeDepartment of Biostatistics, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-4482-5640
Atlas KhanDepartment of Medicine, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-6651-2725
Chen WangDepartment of Biostatistics, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0001-9127-0054
Chunhua WengDepartment of Biomedical Informatics, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-9624-0214
Joseph D BuxbaumDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0001-8898-8313
Krzysztof KirylukDepartment of Medicine, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0002-5047-6715
Iuliana Ionita-LazaDepartment of Biostatistics, Columbia University, New York, NY, USA. ii2135@cumc.columbia.edu.ORCID http://orcid.org/0000-0002-9001-2026

Funding

Novel Statistical methods for DNA Sequencing Data, and applications to Autism.R01MH095797 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IONITA, IULIANA · 2012 to 2022
$3.1M
Multi-omics approaches for gene discovery in Alzheimer's Disease.RF1AG072272 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IONITA, IULIANA, WEI, YING · 2021 to 2021
$1.6M
Multi-omics approaches for gene discovery in Alzheimer's Disease.R01AG072272 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IONITA, IULIANA, WEI, YING · 2024 to 2024
$552k
Quantitative disease risk scores for common diseases, with applications to eMERGER21HG012345 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IONITA, IULIANA · 2021 to 2021
$446k
Multi-Trait Analysis in Large-Scale Biobank Datasets Linked to Electronic Health Records.K99HG013546 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LEE, HYUNKYU · 2024 to 2025
$244k
NHGRI NIH HHS K99 HG013546NHGRI NIH HHS R21 HG012345NIA NIH HHS R01 AG072272NIA NIH HHS RF1 AG072272NIMH NIH HHS R01 MH095797U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) HG012345
6 · The paper itself

Abstract

Electronic health records have been increasingly adopted as useful resources for genomic research. However, case-control labeling of clinical data from electronic health records is challenging and most studies utilize phenotype codes to define case/control labels, resulting in suboptimal downstream analyses. Here we describe the liability threshold phenotypic integration, a method combining genetic relatedness with phenotypic data, including binary and continuous traits such as diagnosis codes, family disease history, laboratory measurements and biomarkers, to derive new continuous phenotypes for target diseases. The model utilizes an automatic trait selection algorithm that increases performance in disease risk prediction and provides insights into nontarget traits associated with the target disease. Our simulations and applications to the eMERGE network and the UK Biobank data demonstrate consistent performance gains in disease risk prediction and genome-wide association study power compared to conventional phenotype codes, models that solely incorporate family history and the phenotype imputation method SoftImpute, with similar false-positive rate control.

Indexed as

Electronic Health RecordsGenetic Predisposition to DiseaseAlgorithmsCase-Control StudiesGenome-Wide Association StudyHumansModels, GeneticPhenotypeRisk Factors

Identifiers

PMID41184541
PMCPMC12597826

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.