Predictive Cellular Signatures from Live Human Motor Neurons Distinguish TDP-43 ALS and Enable ALS Subtype Stratification

or derived from sALS revealed both overlapping and distinguishable signatures, suggesting shared yet distinct mechanistic pathways. Together, these findings establish ML-driven phenotypic profiling as a powerful approach to stratify people with ALS, help disentangle the molecular heterogeneity of ALS and produce a more holistic phenotypic definition in cell-based models, and ultimately find causes and treatments. This strategy offers a scalable and innovative paradigm for uncovering early disease mechanisms not only in ALS but potentially across a spectrum of neurodegenerative and sporadic disorders.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-04-24
DOI
https://doi.org/10.64898/2026.04.22.719920
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Predictive Cellular Signatures from Live Human Motor Neurons Distinguish TDP-43 ALS and Enable ALS Subtype Stratification

Noura Al Bistami, Reuben Thomas, Zohreh Faghihmonzavi, Edward Vertudes et al.
bioRxiv (Cold Spring Harbor Laboratory)
Amyotrophic Lateral Sclerosis Research
article

Predictive Cellular Signatures from Live Human Motor Neurons Distinguish TDP-43 ALS and Enable ALS Subtype Stratification

Noura Al Bistami, Reuben Thomas, Zohreh Faghihmonzavi, Edward Vertudes, Krishna Raja, Naufa Amirani, Julia Kaye, Úna Chan, Ana Jovičić, Mariya Barch, Wesley Robinson, Drew Linsley, Steve Finkbeiner
article en

Abstract

or derived from sALS revealed both overlapping and distinguishable signatures, suggesting shared yet distinct mechanistic pathways. Together, these findings establish ML-driven phenotypic profiling as a powerful approach to stratify people with ALS, help disentangle the molecular heterogeneity of ALS and produce a more holistic phenotypic definition in cell-based models, and ultimately find causes and treatments. This strategy offers a scalable and innovative paradigm for uncovering early disease mechanisms not only in ALS but potentially across a spectrum of neurodegenerative and sporadic disorders.

bioRxiv (Cold Spring Harbor Laboratory)
Gladstone Institutes (US), University of California, San Francisco (US), Brown University (US), Taube Koret Center (US), Sunesis (United States) (US)
California Institute for Regenerative Medicine
Reduced inequalities
Openalex Percentile: Top 10%
Amyotrophic Lateral Sclerosis Research
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