Evidence map›Paper›PMID 37621409›Full record

ArticleBrain communications2023

Carolin K Scriba, Igor Stevanovski, Sanjog R Chintalaphani, Hasindu Gamaarachchi, Roula Ghaoui, Darshan Ghia, Robert D Henderson, Nerissa Jordan, Antony Winkel, Phillipa J Lamont and 7 more

Open access · goldAbstract read
In one paragraph

Article in Brain communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Novel, complex configurations of theBrain communications · 2025
    Article
  9. Article
  10. Pseudodominance in RFC1-Spectrum Disorder.Cerebellum (London, England) · 2024
    Article
  11. Review
  12. Neurology. Genetics · 2024
    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

17 authors at 11 institutions in 3 countries.

Carolin K ScribaRare Genetic Diseases and Functional Genomics Group, Centre for Medical Research, University of Western Australia, Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands, WA 6009, Australia.ORCID https://orcid.org/0000-0001-9874-3846
Igor StevanovskiGenomics Pillar, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia.
Sanjog R ChintalaphaniGenomics Pillar, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia.
Hasindu GamaarachchiGenomics Pillar, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia.
Roula GhaouiDepartment of Neurology, Royal Adelaide Hospital, Adelaide, SA 5000, Australia.
Darshan GhiaUWA Medical School, University of Western Australia, Perth, WA 6009, Australia.
Robert D HendersonCentre for Clinical Research, University of Queensland, Herston, QLD 4006, Australia.
Nerissa JordanDepartment of Neurology, Fiona Stanley Hospital, Perth, WA 6150, Australia.
Antony WinkelDepartment of Neurosciences, Griffith University, Sunshine Coast University Hospital, Mount Gravatt, QLD 4111, Australia.
Phillipa J LamontNeurogenetic Unit, Royal Perth Hospital, Perth, WA 6000, Australia.
Miriam J RodriguesNeurology Department, Auckland City Hospital, Auckland, New Zealand.
Richard H RoxburghCentre for Brain Research Neurogenetics Research Clinic, University of Auckland, Auckland, New Zealand.
Ben WeisburdProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Nigel G LaingPreventive Genetics Group, Centre for Medical Research, University of Western Australia, Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands, WA 6009, Australia.
Ira W DevesonGenomics Pillar, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia.ORCID https://orcid.org/0000-0003-3861-0472
Mark R DavisNeurogenetics Laboratory, Department of Diagnostic Genomics, PP Block, QEII Medical Centre, Nedlands, WA 6009, Australia.
Gianina RavenscroftRare Genetic Diseases and Functional Genomics Group, Centre for Medical Research, University of Western Australia, Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands, WA 6009, Australia.
Garvan Institute of Medical Research · AUThe University of Western Australia · AUAuckland City Hospital · NZBroad Institute · USFiona Stanley Hospital · AUGriffith University · AUQueen Elizabeth II Medical Centre · AURoyal Adelaide Hospital · AURoyal Perth Hospital · AUThe University of Queensland · AUUniversity of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebellar ataxia, neuropathy and vestibular areflexia syndrome is a progressive, generally late-onset, neurological disorder associated with biallelic pentanucleotide expansions in Intron 2 of the

Indexed as

ataxiaCANVASRFC1sensory neuropathySTR

Identifiers

PMID37621409
PMCPMC10445415
OpenAlexW4385253161

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.