Evidence map›Paper›PMID 32585810›Full record

ReviewJournal of clinical medicine2020

Dominantly Inherited Hereditary Nonpolyposis Colorectal Cancer Not Caused by MMR Genes.

Mariona Terradas, Gabriel Capellá, Laura Valle

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Hereditary cancer syndromes.World journal of clinical oncology · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Molecular testing for colorectal cancer: Clinical applications.World journal of gastrointestinal oncology · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Article
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

3 authors at 1 institution in 1 country.

Mariona TerradasHereditary Cancer Program, Catalan Institute of Oncology, IDIBELL, Hospitalet de Llobregat, 08908 Barcelona, Spain.
Gabriel CapelláHereditary Cancer Program, Catalan Institute of Oncology, IDIBELL, Hospitalet de Llobregat, 08908 Barcelona, Spain.
Laura ValleHereditary Cancer Program, Catalan Institute of Oncology, IDIBELL, Hospitalet de Llobregat, 08908 Barcelona, Spain.ORCID 0000-0003-0371-0844
Institut d'Investigació Biomédica de Bellvitge · ES

Funding

Fundación Científica Asociación Española Contra el Cáncer AECC-INVES19022TERRFundación Olga Torres FOT Investigadors ConsolidatsGeneralitat de Catalunya AGAUR_2017SGR1282Generalitat de Catalunya CERCA ProgramInstituto de Salud Carlos III CIBERONC CB16/12/00234Ministerio de Ciencia e Innovación SAF2015-68016-RMinisterio de Ciencia e Innovación SAF2016-80888-R
6 · The paper itself

Abstract

In the past two decades, multiple studies have been undertaken to elucidate the genetic cause of the predisposition to mismatch repair (MMR)-proficient nonpolyposis colorectal cancer (CRC). Here, we present the proposed candidate genes according to their involvement in specific pathways considered relevant in hereditary CRC and/or colorectal carcinogenesis. To date, only pathogenic variants in

Indexed as

cancer geneticscancer predispositioncancer susceptibilitycolorectal cancerfamilial colorectal cancer type Xgene identificationhereditary cancermismatch repair proficiencymolecular pathways

Identifiers

PMID32585810
PMCPMC7355797
OpenAlexW3036289221

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.