Evidence map›Paper›PMID 40026258›Full record

ReviewMovement disorders : official journal of the Movement Disorder Society2025

Exploration of Neurodegenerative Diseases Using Long-Read Sequencing and Optical Genome Mapping Technologies.

Guillaume Cogan, Kensuke Daida, Cornelis Blauwendraat, Kimberley Billingsley, Alexis Brice

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. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Screening of Hidden Pathogenic Structural Variants in PRKN.Movement disorders : official journal of the Movement Disorder Society · 2025
    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

5 authors.

Guillaume CoganLaboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-3505-7114
Kensuke DaidaLaboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.
Cornelis BlauwendraatLaboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-9358-8111
Kimberley BillingsleyLaboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-8003-4029
Alexis BriceInstitut National de la Recherche Médicale-U1127, Centre National de la Recherche Scientifique-UMR7225, APHP, Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Paris, France.

Funding

Long-read DNA sequencing of Alzheimers Disease and Related Dementias casesZIAAG000538 · NIA · NATIONAL INSTITUTE ON AGING · PI COOKSON, MARK · 2020 to 2025
$39.6M
Long-read DNA sequencing of Parkinson's disease and related disordersZIAAG000542 · NIA · NATIONAL INSTITUTE ON AGING · PI BLAUWENDRAAT, CORNELIS · 2023 to 2023
$270k
Intramural NIH HHS ZIA AG000538Intramural NIH HHS ZIA AG000542
6 · The paper itself

Abstract

Genetic factors play a central role in neurodegenerative disorders. Over the past few decades, significant progress has been made in identifying the causative genes of numerous monogenic disorders, largely due to the widespread adoption of next-generation sequencing (NGS) technologies in both research and clinical settings. However, many likely monogenic disorders still lack an accurate molecular diagnosis, primarily because conventional NGS methods are not effective at detecting structural variants and repeat expansions, both of which are crucial in many neurogenetic diseases. Recently, long-read sequencing (LRS) and optical genome mapping technologies have emerged as powerful tools, offering the ability to capture more complex genetic variations. These technologies have already led to the discovery of novel genes responsible for well-characterized neurodegenerative diseases (ND), enhancing the understanding of the biological underpinning of these conditions. Although currently LRS is mostly used in a research setting, we anticipate broader implementation of these methods in clinical laboratories in the near future. In this review, we explore the contributions of these technologies to ND research and highlight the remaining challenges for future advancements. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

Indexed as

Chromosome MappingHigh-Throughput Nucleotide SequencingNeurodegenerative DiseasesHumanslong‐read sequencingneurodegenerative diseasesoptical genome mapping

Identifiers

PMID40026258
PMCPMC12160994

What OpenQuestion holds

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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.