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V. Drory

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Open access Sep 2026

Data-driven identification of repurposable drugs for ALS

Amyotrophic lateral sclerosis (ALS) is a severe disease that causes thousands of deaths annually. Current treatments are either limited in effectiveness or not broadly applicable. To discover new options, we conducted a genetics-based screen to identify drugs that could be repurposed for ALS. We analyzed genome-wid...

S. Saez-Atienzar, Luis A. Rojas-Colón, Ruth Chia et al. · 0 citations
Open access Sep 2026

Towards a deep-learning genomic tool for risk stratification and diagnostic support in sporadic ALS

A new model is developed that is validated across diverse ALS populations, can handle discrepancies between genotyping technologies, and is applicable to individual external samples, and has the potential to extend genetic risk assessment to all individuals, regardless of their family history or the presence of known A...

Jia-Jing Hu, Oliver Pain, A. Al Khleifat et al. · 0 citations
Open access Jul 2026

Circulating protein profiling identifies prognostic biomarkers in amyotrophic lateral Sclerosis

The utility of multiple proteins reflecting diverse biological pathways in refining survival stratification is indicates the utility of multiple proteins reflecting diverse biological pathways in refining survival stratification and highlights systemic factors in ALS progression.

H. Klimovski, M. Weinreich, A. Strange et al. · 0 citations
Open access Jul 2026

A proteomic signature for prognostic stratification in amyotrophic lateral sclerosis

This work indicates the utility of multiple proteins reflecting diverse biological pathways in refining survival stratification and highlights systemic factors in ALS progression, highlighting their potential role in measuring disease progression.

D. Lester, P. Piazza, E. Dellar et al. · 0 citations

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