Evidence map›Paper›PMID 42625059›Full record

ReviewNature genetics2026

Toward the clinical application of long-read sequencing in repeat-expansion disorders.

Louise Benarroch, Jovan Pešović, Marzia Rossato, Zhongbo Chen, Morghan C Lucas, Guillaume Cogan, Indhu-Shree Rajan-Babu, Vitus Prokosch, Christina Zarouchlioti, Marco Carlomagno and 27 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

37 authors.

Louise BenarrochSorbonne Université, Inserm, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.ORCID http://orcid.org/0000-0003-2805-9170
Jovan PešovićUniversity of Belgrade-Faculty of Biology, Center for Human Molecular Genetics, Belgrade, Serbia.ORCID http://orcid.org/0000-0002-8304-2067
Marzia RossatoDepartment of Biotechnology, University of Verona, Verona, Italy.ORCID http://orcid.org/0000-0002-6101-1550
Zhongbo ChenCentre for Preventive Neurology, Wolfson Institute of Population Health, Queen Mary University London, London, UK.ORCID http://orcid.org/0000-0001-6668-7202
Morghan C LucasMGZ-Medical Genetics Center, Munich, Germany.ORCID http://orcid.org/0000-0001-7654-9137
Guillaume CoganSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, INSERM U1127, CNRS UMR7225, APHP, Paris, France.
Indhu-Shree Rajan-BabuDepartment of Medical Genetics, University of British Columbia, BC Children's and Women's Hospital, Vancouver, British Columbia, Canada.
Vitus ProkoschMGZ-Medical Genetics Center, Munich, Germany.ORCID http://orcid.org/0009-0008-5791-3536
Christina ZarouchliotiUCL Institute of Ophthalmology, London, UK.ORCID http://orcid.org/0000-0002-5096-177X
Marco CarlomagnoDepartment of Biotechnology, University of Verona, Verona, Italy.ORCID http://orcid.org/0009-0009-7079-5797
Ida HöijerDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-3915-3384
Mayra SauerMGZ-Medical Genetics Center, Munich, Germany.
Ismail JamailInstitut Curie, PSL University, CurieCoreTech Next-Generation Sequencing (ICGex), Paris, France.
Shota ShibataCenter for Genomic Medicine, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-9131-5408
Glen Lester SequieraDepartment of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, The University of British Columbia, Vancouver, British Columbia, Canada.
Benjamin P KleinstiverCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-5469-0655
Sonia LameirasInstitut Curie, PSL University, CurieCoreTech Next-Generation Sequencing (ICGex), Paris, France.
Ricardo Mouro PintoCenter for Genomic Medicine, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0001-6744-2805
Giuseppe NovelliDepartment of Biomedicine and Prevention, University of Rome 'Tor Vergata', Rome, Italy.ORCID http://orcid.org/0000-0002-7781-602X
Davina Hensman MossSt George's, University of London, London, UK.ORCID http://orcid.org/0000-0003-2467-0917
Natalia DominikDepartment of Neuromuscular Diseases, Queen Square Institute of Neurology, UCL, London, UK.
Mathieu BarbierParis Brain Institute-Institut du Cerveau-ICM, Sorbonne Université, Inserm U1127, CNRS UMR 7225, AP-HP-Hôpital Pitié-Salpêtrière, Paris, France.ORCID http://orcid.org/0000-0002-5154-2163
Isabelle Le BerParis Brain Institute-Institut du Cerveau-ICM, Sorbonne Université, Inserm U1127, CNRS UMR 7225, AP-HP-Hôpital Pitié-Salpêtrière, Paris, France.
Guillaume BassezSorbonne Université, Inserm, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.
Denis FurlingSorbonne Université, Inserm, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.ORCID http://orcid.org/0000-0001-7912-4409
Massimo DelledonneDepartment of Biotechnology, University of Verona, Verona, Italy.ORCID http://orcid.org/0000-0002-7100-4581
Karen UsdinLaboratory of Cell and Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
Sylvain BaulandeInstitut Curie, PSL University, CurieCoreTech Next-Generation Sequencing (ICGex), Paris, France.ORCID http://orcid.org/0000-0003-3104-1684
Geneviève GourdonSorbonne Université, Inserm, Institut de Myologie, Centre de Recherche en Myologie, Paris, France.
Birgitt SchüleDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Dušanka Savić-PavićevićUniversity of Belgrade-Faculty of Biology, Center for Human Molecular Genetics, Belgrade, Serbia.ORCID http://orcid.org/0000-0002-2079-4077
Annalisa BottaDepartment of Biomedicine and Prevention, University of Rome 'Tor Vergata', Rome, Italy.ORCID http://orcid.org/0000-0003-4031-5624
Alice E DavidsonUCL Institute of Ophthalmology, London, UK.ORCID http://orcid.org/0000-0002-1816-6151
Adam AmeurDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-6085-6749
Vincent DionUK Dementia Research Institute at Cardiff University, Cardiff, UK.ORCID http://orcid.org/0000-0003-4953-7637
Stéphanie ToméSorbonne Université, Inserm, Institut de Myologie, Centre de Recherche en Myologie, Paris, France. stephanie.tome@inserm.fr.ORCID http://orcid.org/0000-0002-0135-9256
LRS-RED Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Repeat-expansion disorders (REDs) are a mechanistically and clinically well-defined subgroup of rare diseases caused by the expansion of short tandem repeats (STRs). These expansions can exceed several kilobases and show complex features, such as noncanonical secondary structures, somatic instability, repeat interruptions and allele-specific methylation. These characteristics are highly relevant for understanding disease mechanisms, clinical variability, prognosis and potentially therapeutic decision-making, but cannot be fully resolved using traditional diagnostic methods or short-read sequencing technologies. By contrast, long-read sequencing (LRS) enables accurate investigation of STR complexity in a single assay, facilitates the discovery of new pathogenic repeat expansions and drives advances in diagnostics, clinical and basic research, which may allow for better patient stratification in future clinical trials. This Perspective discusses recent LRS-driven discoveries, methodological and bioinformatic advances, and emerging diagnostic applications to illustrate the potential of LRS in reshaping both research and clinical practice.

Indexed as

DNA Repeat ExpansionHigh-Throughput Nucleotide SequencingMicrosatellite RepeatsSequence Analysis, DNAHumans

Identifiers

What OpenQuestion holds

Textmetadata
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.