Evidence map›Paper›PMID 38585669›Full record

ArticleBrain communications2024

Repeat expansions in

Camilla Novy, Øyvind L Busk, Ole-Bjørn Tysnes, Sigve S Landa, Tori N Aanjesen, Karl B Alstadhaug, Tale L Bjerknes, Ingrid K Bjørnå, Geir Bråthen, Elin Dahl and 19 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Brain communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. ALS and Huntington Disease: Unraveling the Connections between TDP-43 and Huntingtin.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Review
  3. Article
  4. Review
  5. 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

29 authors.

Camilla NovyDepartment of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway.ORCID https://orcid.org/0009-0008-0089-3669
Øyvind L BuskDepartment of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway.
Ole-Bjørn TysnesNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5009 Bergen, Norway.
Sigve S LandaDepartment of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway.
Tori N AanjesenDepartment of Neurology, Akershus University Hospital, 1478 Lørenskog, Norway.
Karl B AlstadhaugDepartment of Neurology, Nordland Hospital Trust, 8005 Bodø, Norway.
Tale L BjerknesNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5009 Bergen, Norway.
Ingrid K BjørnåDepartment of Neurology, Vestre Viken Hospital Trust, 3004 Drammen, Norway.
Geir BråthenDepartment of Neurology and Clinical Neurophysiology, St. Olavs Hospital, Trondheim University Hospital, 7030 Trondheim, Norway.
Elin DahlDepartment of Neurology, Telemark Hospital Trust, 3710 Skien, Norway.
Natasha DemicDepartment of Neurology, Vestfold Hospital Trust, 3103 Tønsberg, Norway.
Maria FahlströmDepartment of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway.
Heidi Ø FlemmenDepartment of Neurology, Telemark Hospital Trust, 3710 Skien, Norway.
Erika HallerstigDepartment of Neurology, Østfold Hospital Trust, 1714 Grålum, Norway.
Ineke HogenEschDepartment of Neurology, Fonna Hospital Trust, 5528 Haugesund, Norway.
Margitta T KampmanDepartment of Neurology, University Hospital of North Norway, 9019 Tromsø, Norway.
Grethe KlevelandDepartment of Neurology, Innlandet Hospital Trust, 2609 Lillehammer, Norway.
Helene B KvernmoDepartment of Neurology and Clinical Neurophysiology, St. Olavs Hospital, Trondheim University Hospital, 7030 Trondheim, Norway.
Unn LjøstadInstitute of Clinical Medicine, University of Bergen, 5007 Bergen, Norway.
Angelina ManiaolDepartment of Neurology, Oslo University Hospital, 0450 Oslo, Norway.
Aase Hagen MorsundDepartment of Neurology, Molde Hospital, 6412 Molde, Norway.
Ola NakkenDepartment of Neurology, Akershus University Hospital, 1478 Lørenskog, Norway.
Cathrine G OlsenDepartment of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway.
Katrin SchlüterDepartment of Neurology, Stavanger University Hospital, 4019 Stavanger, Norway.
May-Sissel UtvikDepartment of Neurology, Namsos Hospital Trust, 7803 Namsos, Norway.
Ryaz YaseenDepartment of Neurology, Oslo University Hospital, 0450 Oslo, Norway.
Øystein L HollaDepartment of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway.
Trygve HolmøyFaculty of Medicine, Institute of Clinical Medicine, University of Oslo, 0316 Oslo, Norway.
Helle HøyerDepartment of Medical Genetics, Telemark Hospital Trust, 3710 Skien, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic repeat expansions cause neuronal degeneration in amyotrophic lateral sclerosis as well as other neurodegenerative disorders such as spinocerebellar ataxia, Huntington's disease and Kennedy's disease. Repeat expansions in the same gene can cause multiple clinical phenotypes. We aimed to characterize repeat expansions in a Norwegian amyotrophic lateral sclerosis cohort. Norwegian amyotrophic lateral sclerosis patients (

Indexed as

amyotrophic lateral sclerosisgenetic risk factorNorwaypopulation-based study

Identifiers

PMID38585669
PMCPMC10998343

What OpenQuestion holds

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Registered trials

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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.