Evidence map›Paper›PMID 35267422›Full record

ReviewCancers2022

Lynch-like Syndrome: Potential Mechanisms and Management.

Alejandro Martínez-Roca, Mar Giner-Calabuig, Oscar Murcia, Adela Castillejo, José Luis Soto, Anabel García-Heredia, Rodrigo Jover

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Alejandro Martínez-RocaServicio de Medicina Digestiva, Hospital General Universitario de Alicante, Instituto de Investigación Sanitaria, ISABIAL, Universidad Miguel Hernández, 03010 Alicante, Spain.ORCID 0000-0002-8337-4133
Mar Giner-CalabuigServicio de Medicina Digestiva, Hospital General Universitario de Alicante, Instituto de Investigación Sanitaria, ISABIAL, Universidad Miguel Hernández, 03010 Alicante, Spain.ORCID 0000-0002-6267-3708
Oscar MurciaServicio de Medicina Digestiva, Hospital General Universitario de Alicante, Instituto de Investigación Sanitaria, ISABIAL, Universidad Miguel Hernández, 03010 Alicante, Spain.
Adela CastillejoLaboratorio de Genética Molecular, Hospital General Universitario de Elche, FISABIO, 03203 Elche, Spain.
José Luis SotoLaboratorio de Genética Molecular, Hospital General Universitario de Elche, FISABIO, 03203 Elche, Spain.ORCID 0000-0003-0234-9188
Anabel García-HerediaServicio de Medicina Digestiva, Hospital General Universitario de Alicante, Instituto de Investigación Sanitaria, ISABIAL, Universidad Miguel Hernández, 03010 Alicante, Spain.ORCID 0000-0003-2876-1779
Rodrigo JoverServicio de Medicina Digestiva, Hospital General Universitario de Alicante, Instituto de Investigación Sanitaria, ISABIAL, Universidad Miguel Hernández, 03010 Alicante, Spain.
Hospital General Universitario de Alicante Doctor Balmis · ESFundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana · ESYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lynch syndrome is an autosomal dominant disorder caused by germline mutations in DNA mismatch repair (MMR) system genes, such as

Indexed as

colorectal cancerDNA mismatch repair geneshereditary cancerlynch-like syndromelynch syndrome

Identifiers

PMID35267422
PMCPMC8909420
OpenAlexW4213413884

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.