Evidence map›Paper›PMID 41981312›Full record

ArticleNature biomedical engineering2026

Phenotypic prediction of missense variants via deep contrastive learning.

Jun Wen, Sihang Zeng, Clara-Lea Bonzel, Shilpa Nadimpalli Kobren, Jiangchuan Du, Yi Chai, Hao Wang, Meng Zhu, Siwei Chen, Fangwei Leng and 8 more

Abstract read
In one paragraph

Article in Nature biomedical engineering, 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

18 authors.

Jun WenDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-5067-2647
Sihang ZengDepartment of Biomedical Informatics and Medical Education, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0009-0003-2921-829X
Clara-Lea BonzelDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Shilpa Nadimpalli KobrenDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Jiangchuan DuDepartment of Statistics, University of Chicago, Chicago, IL, USA.
Yi ChaiYong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Hao WangDepartment of Computer Science, Rutgers University, Piscataway, NJ, USA.
Meng ZhuDepartment of Genetics, Harvard Medical School, Boston, MA, USA.
Siwei ChenBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Fangwei LengHoward Hughes Medical Institute and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, USA.
Harrison G ZhangDepartment of Biomedical Data Science, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-6679-1464
Katherine P LiaoDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Kelly ChoVA Boston Healthcare System, Boston, MA, USA.
Isaac S KohaneDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Marinka ZitnikDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-8530-7228
Alexandre C PereiraBrigham and Women's Hospital, Boston, MA, USA.
Jun S LiuDepartment of Statistics and Data Science, Tsinghua University, Beijing, China.ORCID http://orcid.org/0000-0002-4450-7239
Tianxi CaiDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. tcai@hsph.harvard.edu.ORCID http://orcid.org/0000-0002-5379-2502

Funding

SCH: Counterfactual Explanations for AI-Assisted Cancer Diagnosis and SubtypingR01CA297832 · NCI · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI Hao Wang · 2024 to 2026
$849k
NCI NIH HHS R01 CA297832
6 · The paper itself

Abstract

Missense variants (MVs) influence clinical phenotypes, but our understanding of their phenotypic consequences remains constrained. Existing computational approaches to interpret MVs predominantly assess their pathogenicity, without considering phenotypic heterogeneity. We present a machine-learning-based method, PheMART, to predict the clinical phenotypic consequences of MVs. PheMART integrates comprehensive variant and phenotype characterizations by leveraging a robust combination of multiple resources involving protein language models, protein-protein interactions, protein domains, medical knowledge graphs and electronic health records. Exploiting contrastive learning, PheMART establishes connections between MVs and 4,179 phenotypes by jointly projecting them into a cohesive low-dimensional metric space where proximity signifies relevance. Besides substantially outperforming existing models, PheMART aids in diagnosing individuals with rare diseases by effectively pinpointing clinical diagnoses and causative MVs. As a resource to the community, we provide a database of phenotypic predictions for 5.1 million putative pathogenic amino acid alterations.

Identifiers

PMID41981312
PMCPMC13229611

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.