Evidence map›Paper›PMID 41803120›Full record

ArticleNature communications2026

Multi-modal dissection of cell-type specific TDP-43 pathology in the motor cortex.

Wolfgang P Ruf, Julia K Kühlwein, Laura Meier, Sarah J Brockmann, Jaehyun LeeBae, Ghazaleh Sadri-Vakili, Deniz Yilmazer-Hanke, Susanne Petri, Dietmar R Thal, Veselin Grozdanov and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Wolfgang P Ruf *Department of Neurology, University Clinic, University of Ulm, Ulm, Germany.
Julia K Kühlwein *Department of Neurology, University Clinic, University of Ulm, Ulm, Germany.
Laura MeierDepartment of Neurology, University Clinic, University of Ulm, Ulm, Germany.
Sarah J BrockmannDepartment of Neurology, University Clinic, University of Ulm, Ulm, Germany.
Jaehyun LeeBaeGerman Center for Neurodegenerative Diseases (DZNE), Ulm, Germany.ORCID 0009-0002-1983-0074
Ghazaleh Sadri-VakiliSean M. Healey & AMG Center for ALS at Mass General, Massachusetts General Hospital, Boston, MA, USA.
Deniz Yilmazer-HankeClinical Neuroanatomy, Department of Neurology, University Clinic, University of Ulm, Ulm, Germany.ORCID 0000-0003-1483-0286
Susanne PetriDepartment of Neurology, Hannover Medical School, 1, Carl-Neuberg-Strasse, Hannover, Germany.
Dietmar R ThalLaboratory for Neuropathology, Department of Imaging and Pathology and Leuven Brain Institute (LBI), KU-Leuven, Herestraat 49, Leuven, Belgium.ORCID 0000-0002-1036-1075
Veselin Grozdanov *Department of Neurology, University Clinic, University of Ulm, Ulm, Germany. veselin.grozdanov@uni-ulm.de.ORCID 0000-0002-0825-7383
Karin M Danzer *Department of Neurology, University Clinic, University of Ulm, Ulm, Germany. karin.danzer@dzne.de.ORCID 0000-0003-0133-7046

Funding

KU-Leuven internal fundingTarget ALS Grant
6 · The paper itself

Abstract

Cytoplasmic TDP-43 pathology is a pathological sign of ALS/ALS-FTD and a converging disease event across different genotypes, phenotypes and CNS areas. To understand this process and target it therapeutically, we need to define which cell types are affected and which cell-type specific effects make them particularly vulnerable. We coupled flow-cytometry nuclear sorting and sequencing with single-nucleus multi-omic ATAC-seq and RNA-seq and spatial transcriptomics to define the transcriptional cell type of affected neurons in the post-mortem ALS/ALS-FTD motor cortex (30 ALS, 20 ALS-FTD & 32 control samples). Here, we show that mainly excitatory cortical neurons are affected by TDP-43 pathology and define the cell types that are affected the most: intratelencephalic L2-L3-LINC00507-FREM3, L3-L5-RORB-LNX2, L3-L5-RORB-ADGRL4 & L6-THEMIS-LINC00343 neurons and extratelencephalic L5-FEZF2-NTNG1 neurons. Transcriptional aberrations by TDP-43 pathology, like cryptic exon inclusion, are cell-type specific and affect distinct gene sets in each cell type, highlighting the need to address TDP-43 pathology in a cell-type specific manner.

Indexed as

Amyotrophic Lateral SclerosisDNA-Binding ProteinsMotor CortexNeuronsFlow CytometryHumansSpatial TranscriptomicsDNA-Binding ProteinsTARDBP protein, human

Identifiers

PMID41803120
PMCPMC12982666

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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.