Evidence map›Paper›PMID 37072235›Full record

ArticleCMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne2023

Ensuring timely genetic diagnosis in adults.

Hanna Faghfoury, Andrea Guerin

Abstract read
In one paragraph

Article in CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2025
    Article
  3. Closing gaps in care and knowledge for adults with complex genetic conditions.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2024
    Article
  4. Review
  5. Autoinflammatory gene mutations associated with eosinophilia and asthma.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2023
    Article
  6. 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

2 authors.

Hanna FaghfouryDepartment of Medicine (Faghfoury), Mount Sinai Hospital and University Health Network, University of Toronto, Toronto, Ont.; Division of Medical Genetics (Guerin), Department of Pediatrics, Queen's University, Kingston, Ont.
Andrea GuerinDepartment of Medicine (Faghfoury), Mount Sinai Hospital and University Health Network, University of Toronto, Toronto, Ont.; Division of Medical Genetics (Guerin), Department of Pediatrics, Queen's University, Kingston, Ont. ag151@queensu.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Diseases, InbornAdultHumans

Identifiers

PMID37072235
PMCPMC10120577

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.