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Nature Medicine|July 27, 2026
Longitudinal plasma proteomics predict phenoconversion to clinically manifest ALSXiming Ran, Joanne Wuu, Zhaohui S Qin, et al.
BMC Medical Genomics|January 14, 2025
Evaluation of a biomarker for amyotrophic lateral sclerosis derived from a hypomethylated DNA signature of human motor neuronsCalum Harvey, Alicja Nowak, Sai Zhang, et al.
Research Square|December 9, 2024
Evaluation of a biomarker for amyotrophic lateral sclerosis derived from a hypomethylated DNA signature of human motor neuronsCalum Harvey, Alicja Nowak, Sai Zhang, et al.
Human Molecular Genetics|February 4, 2017
C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of PtenMatthew J Stopford, Adrian Higginbottom, Guillaume M Hautbergue, et al.
Biorxiv : the Preprint Server for Biology|July 14, 2025
TDP-43 toxic gain of function links ALS, FTD and Alzheimer's Disease through splicing dysregulationWelmoed Van Zuiden, Thea D Meimoun, Chen Bar, et al.
Acta Neuropathologica Communications|March 18, 2017
A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosisJohnathan Cooper-Knock, Claire Green, Gabriel Altschuler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2012
Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72Azza Ismail, Johnathan Cooper-Knock, J Robin Highley, et al.
Nature Biotechnology|July 27, 2025
Single-cell polygenic risk scores dissect cellular and molecular heterogeneity of complex human diseasesSai Zhang, Hantao Shu, Jingtian Zhou, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 21, 2024
Guidance for clinical management of pathogenic variant carriers at elevated genetic risk for ALS/FTDMichael Benatar, Terry D Heiman-Patterson, Johnathan Cooper-Knock, et al.
Biorxiv : the Preprint Server for Biology|May 27, 2024
Deconvolution of polygenic risk score in single cells unravels cellular and molecular heterogeneity of complex human diseasesSai Zhang, Hantao Shu, Jingtian Zhou, et al.
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