A transcriptome-guided framework for linking multicellular disease signatures to candidate therapeutic strategies in refractory epilepsy is established, and four compounds reduced seizure-like activity in vivo, as assessed by behavioral assays and local field potential recordings.
This dataset defines transcriptomic programs underlying key cellular alterations in TLE, enabling mechanistic dissection of epileptogenesis, and term this microglia population epilepsy-associated microglia (EAM).
Victoria Ho, Ruth Tjondropurnomo, Jennifer Nguyen et al.· iScience· 0 citations
Interindividual heterogeneity in Alzheimer’s disease (AD) remains poorly understood, as disparate single-cell studies leave it unclear whether findings reflect shared architecture or dataset-specific idiosyncrasies. Here, we present panAD, a transcriptomic atlas of >3 million nuclei from 791 individuals across 13 studi...
Negin Rahimzadeh, S. Morabito, S. Khullar et al.· bioRxiv· 0 citations
It is demonstrated that pathology-defined cell states provide a more reproducible framework for studying ALS transcriptomic alterations than conventional case-control comparisons and an interactive browser is provided to facilitate exploration and comparison of ALS snRNA-seq datasets.
C. V. van Dijk, Sam Bonsall, A. Giani et al.· bioRxiv· 0 citations
It is shown that depletion of these AD risk genes disrupts baseline morpho-transcriptomic coupling and fundamentally alters microglial phagocytic capacity, revealing how AD GWAS genes may drive microglia into dysfunctional states characterized by altered morphology, distinct multi-omic signatures, and impaired function...
Ying-Jie Zhang, Ai Zhang, Sang Seo et al.· bioRxiv· 0 citations
Findings reveal distinct, reproducible dysregulation of peripheral-central functional coupling in SCZ, offering a multi-scale framework for understanding its pathophysiology and highlighting the potential of trans-scale features as candidate biomarkers for diagnosis and mechanistic insight.
Yu-Sha Ji, Yi-Feng Liu, Zhi-Qiang Mu et al.· Molecular Psychiatry· 0 citations
A framework for understanding how early-established genomic backbones and regional transcriptional plasticity jointly drive phenotypic diversity is provided for understanding how genomic diversification intersects with transcriptional plasticity remains incompletely understood.
Serafiina Ohlsbom, S. Mäntylä, R. Nätkin et al.· bioRxiv· 0 citations
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