Evidence map›Paper›PMID 39779847›Full record

ArticleNature2025

Site-saturation mutagenesis of 500 human protein domains.

Antoni Beltran, Xiang'er Jiang, Yue Shen, Ben Lehner

Abstract read
In one paragraph

Article in Nature, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing 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

70 citing papers in PubMed.

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  17. bioRxiv : the preprint server for biology · 2026
    Article
  18. Article
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  20. Functional dissection ofProceedings of the National Academy of Sciences of the United States of America · 2026
    Article

10 more citing papers are in PubMed but not listed here.

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

4 authors.

Antoni BeltranCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Xiang'er JiangBGI Research, Changzhou, China.
Yue ShenBGI Research, Changzhou, China.ORCID 0000-0002-3276-7295
Ben LehnerCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain. bl11@sanger.ac.uk.ORCID 0000-0002-8817-1124

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Missense variants that change the amino acid sequences of proteins cause one-third of human genetic diseases

Indexed as

MutagenesisMutation, MissenseProtein DomainsProteinsHumansModels, MolecularProtein StabilityProteins

Identifiers

PMID39779847
PMCPMC11754108

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.