Evidence map›Paper›PMID 37748513›Full record

ArticleNature2023

A molnupiravir-associated mutational signature in global SARS-CoV-2 genomes.

Theo Sanderson, Ryan Hisner, I'ah Donovan-Banfield, Hassan Hartman, Alessandra Løchen, Thomas P Peacock, Christopher Ruis

Open access · hybridAbstract read
In one paragraph

Article in Nature, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 1 pooled it
37.9field-weighted citation impact, top 1% of its field
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

118 citing papers in PubMed, 1 synthesis or guideline pooled it, 193 citations in OpenAlex.

  1. Pooled it
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  15. CROI 2026: Acute and Postacute COVID-19.Topics in antiviral medicine · 2026
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58 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 3 countries.

Theo SandersonFrancis Crick Institute, London, UK. theo.sanderson@crick.ac.uk.ORCID 0000-0003-4177-2851
Ryan HisnerDepartment of Bioinformatics, University of Cape Town, Cape Town, South Africa.
I'ah Donovan-BanfieldDepartment of Infection Biology and Microbiomes, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.ORCID 0000-0002-5124-2427
Hassan HartmanUK Health Security Agency, London, UK.
Alessandra LøchenUK Health Security Agency, London, UK.
Thomas P PeacockDepartment of Infectious Disease, Imperial College London, London, UK.ORCID 0000-0001-7077-2928
Christopher RuisMolecular Immunity Unit, University of Cambridge Department of Medicine, Medical Research Council-Laboratory of Molecular Biology, Cambridge, UK. cr628@cam.ac.uk.ORCID 0000-0003-0977-5534
UK Health Security Agency · GBMRC Laboratory of Molecular Biology · GBThe Francis Crick Institute · GBThe Pirbright Institute · GBUniversity of Cape Town · ZAUniversity of Liverpool · GB

Funding

Medical Research Council MR/W005611/1Wellcome Trust FC001043
6 · The paper itself

Abstract

Molnupiravir, an antiviral medication widely used against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), acts by inducing mutations in the virus genome during replication. Most random mutations are likely to be deleterious to the virus and many will be lethal; thus, molnupiravir-induced elevated mutation rates reduce viral load

Indexed as

Antiviral AgentsCOVID-19CytidineHydroxylaminesMutagenesisMutationSARS-CoV-2COVID-19 Drug TreatmentEvolution, MolecularGenome, ViralHumansPhylogenyViral LoadVirus ReplicationAntiviral AgentsCytidineHydroxylaminesmolnupiravir

Identifiers

PMID37748513
PMCPMC10651478
OpenAlexW4387012671

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.