Evidence map›Paper›PMID 39857601›Full record

ReviewBiomedicines2024

Exploring

Benjamin Y Q Tan, Charlene H P Kok, Megan B J Ng, Shaun Loong, Eric Jou, Leonard L L Yeo, Weiping Han, Christopher D Anderson, Chiea Chuen Khor, Poh San Lai

Abstract readReview
In one paragraph

Review in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. An Overview of Genetics of Moyamoya: BeyondInternational journal of molecular sciences · 2026
    Review
  4. Review
  5. A STOP-Gain RNF213 Variant Causes Chorea, Stroke-Like Episodes, and Leigh Syndrome-Like Encephalopathy.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. 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

10 authors.

Benjamin Y Q TanDivision of Neurology, Department of Medicine, National University Hospital, Singapore 119074, Singapore.ORCID 0000-0003-1824-9077
Charlene H P KokFaculty of Medicine, Imperial College London, London SW7 2AZ, UK.ORCID 0009-0001-1184-2065
Megan B J NgDivision of Neurology, Department of Medicine, National University Hospital, Singapore 119074, Singapore.ORCID 0000-0002-1196-6164
Shaun LoongDepartment of Medicine, Yong Loo Lin School of Medicine, Singapore 117597, Singapore.ORCID 0000-0002-2846-9092
Eric JouDepartment of Oncology, University of Oxford, Oxford OX3 7DQ, UK.
Leonard L L YeoDivision of Neurology, Department of Medicine, National University Hospital, Singapore 119074, Singapore.ORCID 0000-0002-4249-0402
Weiping HanInstitute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore 138632, Singapore.
Christopher D AndersonProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.ORCID 0000-0002-0053-2002
Chiea Chuen KhorGenome Institute of Singapore (GIS), Agency for Science, Technology and Research (A*STAR), Singapore 138632, Singapore.
Poh San LaiDepartment of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.ORCID 0000-0003-3352-2000

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in stroke genetics have highlighted the critical role of rare genetic variants in cerebrovascular diseases, with

Indexed as

geneticsintracranial atherosclerotic diseaseintracranial stenosismoyamoyaRNF213stroke

Identifiers

PMID39857601
PMCPMC11762504

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.