Evidence map›Paper›PMID 33327514›Full record

ReviewCancers2020

Germline

D Gareth Evans, Emma R Woodward, Svetlana Bajalica-Lagercrantz, Carla Oliveira, Thierry Frebourg

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 17% 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, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Somatic and germline mutations in endometrial cancer.Journal of medicine and life · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. Hereditary cancer syndromes.World journal of clinical oncology · 2023
    Review
  13. Review
  14. Article
  15. Melanoma in patients with Li-Fraumeni syndrome (Review).Experimental and therapeutic medicine · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Male Breast Cancer: Current Scenario and Future Perspectives.Technology in cancer research & treatment
    Review
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

5 authors at 4 institutions in 4 countries.

D Gareth EvansManchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, University of Manchester, Manchester M13 9WL, UK.ORCID 0000-0002-8482-5784
Emma R WoodwardManchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, University of Manchester, Manchester M13 9WL, UK.ORCID 0000-0002-6297-2855
Svetlana Bajalica-LagercrantzHereditary Cancer Unit, Department of Clinical Genetics, Karolinska University Hospital, SE-17176 Stockholm, Sweden.
Carla Oliveirai3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0001-8340-2264
Thierry FrebourgDepartment of Genetics, Rouen University Hospital, Normandy Centre for Genomic and Personalized Medicine, 76000 Rouen, France.
University of Manchester · GBInserm · FRKarolinska University Hospital · SEUniversidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germline

Indexed as

breast cancergene panelsheritable TP53-related cancer syndromeinterpretationLi-Fraumeni syndromeTP53variant

Identifiers

PMID33327514
PMCPMC7764913
OpenAlexW3112744503

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.