Evidence map›Paper›PMID 40865030›Full record

ArticleJCO precision oncology2025

Association of

Jennifer Herrera-Mullar, Cassidy Carraway, Ashley P L Marsh, Felicia Hernandez, Emily Kudalkar, Marcy E Richardson

Erratum issuedAbstract read
In one paragraph

Article in JCO precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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

5 · Who and what money

Authors and funding

6 authors.

Jennifer Herrera-MullarAmbry Genetics Corporation, Aliso Viejo, CA.ORCID 0009-0001-7861-178X
Cassidy CarrawayAmbry Genetics Corporation, Aliso Viejo, CA.
Ashley P L MarshAmbry Genetics Corporation, Aliso Viejo, CA.ORCID 0000-0001-6049-6931
Felicia HernandezAmbry Genetics Corporation, Aliso Viejo, CA.
Emily KudalkarAmbry Genetics Corporation, Aliso Viejo, CA.
Marcy E RichardsonAmbry Genetics Corporation, Aliso Viejo, CA.ORCID 0000-0002-4626-4920

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose

methodsRetrospective review of approximately 950,000 individuals undergoing multigene panel testing (MGPT) for cancer predisposition identified 36 individuals with pLoF variants in

resultsThirty-six individuals (0.004%) had 28 unique pLoF variants in

conclusion

Indexed as

Colorectal NeoplasmsLoss of Function MutationRibosomal ProteinsAdultAgedCohort StudiesColorectal Neoplasms, Hereditary NonpolyposisFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedRetrospective StudiesRibosomal Proteins

Identifiers

PMID40865030
PMCPMC12406993

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.