Evidence map›Paper›PMID 41411243›Full record

ArticlePLoS genetics2025

PERADIGM: Phenotype embedding similarity-based rare disease gene mapping.

Wangjie Zheng, Yuhan Xie, Jianlei Gu, Hongyu Li, Stefan Somlo, Whitney Besse, Hongyu Zhao

Abstract read
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Article in PLoS genetics, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Wangjie ZhengDepartment of Biostatistics, Yale University, New Haven, Connecticut, United States of America.
Yuhan XieDepartment of Biostatistics, Yale University, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0000-0002-1738-0885
Jianlei GuDepartment of Biostatistics, Yale University, New Haven, Connecticut, United States of America.
Hongyu LiDepartment of Biostatistics, Yale University, New Haven, Connecticut, United States of America.
Stefan SomloDepartment of Internal Medicine, Section of Nephrology, Yale School of Medicine, New Haven, Connecticut, United States of America.
Whitney BesseDepartment of Internal Medicine, Section of Nephrology, Yale School of Medicine, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0000-0002-8283-1507
Hongyu ZhaoDepartment of Biostatistics, Yale University, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0000-0003-1195-9607

Funding

Statistical Methods for Genetic Risk Predictions across Diverse PopulationsR01HG012735 · NHGRI · YALE UNIVERSITY · PI ZHAO, HONGYU · 2022 to 2025
$2.4M
NHGRI NIH HHS R01 HG012735
6 · The paper itself

Abstract

Identifying genes associated with rare diseases remains challenging due to the scarcity of patients and the limited statistical power of traditional association methods. Here, we introduce PERADIGM ( Phenotype Embedding similarity-based RAre DIsease Gene Mapping), a novel framework that leverages natural language processing techniques to integrate comprehensive phenotype information from electronic health records for rare disease gene discovery. PERADIGM employs an embedding model to capture relationships between ICD-10 codes, providing a nuanced representation of individual phenotypes. By utilizing patient similarity scores, it enhances the identification of candidate genes associated with disease-specific phenotypes, surpassing conventional methods that rely on binary disease status. We applied PERADIGM to the UK Biobank dataset for three rare diseases: autosomal dominant polycystic kidney disease (ADPKD), Marfan syndrome, and neurofibromatosis type 1 (NF1). PERADIGM identified additional candidate genes associated with ADPKD-related and Marfan syndrome-related phenotypes, some of which are supported by existing literature, and demonstrated enhanced signal detection for NF1-specific phenotypes beyond traditional methods. Our findings demonstrate the potential of PERADIGM to identify genes associated with rare diseases and related phenotypes by incorporating phenotype embeddings and patient similarity, providing a powerful tool for precision medicine and a deeper understanding of rare disease genetics and clinical manifestations.

Indexed as

Chromosome MappingMarfan SyndromeNeurofibromatosis 1Polycystic Kidney, Autosomal DominantRare DiseasesElectronic Health RecordsGenetic Association StudiesGenetic Predisposition to DiseaseHumansPhenotype

Identifiers

PMID41411243
PMCPMC12714201

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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.