Evidence map›Paper›PMID 40265723›Full record

ReviewMovement disorders : official journal of the Movement Disorder Society2025

Long-Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia.

Thomas Wirth, Kishore R Kumar, Michael Zech

Abstract readReview
In one paragraph

Review in Movement disorders : official journal of the Movement Disorder Society, 2025. 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. Genetic Etiologies of Dystonia with Anarthria/Aphonia.Movement disorders clinical practice · 2026
    Article
  2. Article
  3. Article
  4. Integrating Long-Read Nanopore Sequencing for Precision Resolution of Genomic Variants in Dystonia.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  5. 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

3 authors.

Thomas WirthNeurology Department, Strasbourg University Hospital, Strasbourg, France.ORCID 0000-0002-4427-5765
Kishore R KumarTranslational Neurogenomics Group, Genomics and Inherited Disease Program, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.ORCID 0000-0003-3482-6962
Michael ZechInstitute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.ORCID 0000-0001-8112-9153

Funding

APTESDFG 458949627DFG ZE 1213/2-1Dystonia Genetic Research MissionDystonia Medical Research FoundationFederal Ministry of Education and ResearchFondation PlaniolFrench Ministry of HealthGerman Federal Ministry of Education and ResearchInternational Cerebral Palsy Genomics ConsortiumKröner-Fresenius-Stiftung 2022_EKSE.185Medical Research Future FundPreDYTTechnical University of Munich
6 · The paper itself

Abstract

Long-read sequencing methodologies provide powerful capacity to identify all types of genomic variations in a single test. Long-read platforms such as Oxford Nanopore and PacBio have the potential to revolutionize molecular diagnostics by reaching unparalleled accuracies in genetic discovery and long-range phasing. In the field of dystonia, promising results have come from recent pilot studies showing improved detection of disease-causing structural variants and repeat expansions. Increases in throughput and ongoing reductions in cost will facilitate the incorporation of long-read approaches into mainstream diagnostic practice. Although these developments are likely to transform clinical care, there is currently a discrepancy between the potential benefits of long-read sequencing and the application of this technique to dystonia. In this review we highlight current opportunities and limitations of adopting long-read sequencing methods for the investigation of patients with dystonia. We provide examples of long-read sequencing integration into diagnostic evaluation and the study of pathomechanisms in individuals with dystonic disorders. The goal of this article is to stimulate research into the application and optimization of long-read analysis strategies in dystonia, thus enabling more precise understanding of the underlying etiology in the future. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

DystoniaDystonic DisordersGenetic TestingHigh-Throughput Nucleotide SequencingHumansdystonialong‐range haplotype phasinglong‐read sequencingOxford NanoporePacBiorepeat expansionsstructural variants

Identifiers

PMID40265723
PMCPMC12160967

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.