Peter T. Nelson

Xinxing Wu, Chong Peng, Peter T. Nelson et al.

Alzheimer's disease (AD), as a progressive brain disease, affects cognition, memory, and behavior. Similarly, limbic-predominant age-related TDP-43 encephalopathy (LATE) is a recently defined common neurodegenerative disease that mimics the clinical symptoms of AD. At present, the risk factors implicated in LATE and those distinguishing LATE from AD are largely unknown. We leveraged an integrated feature selection-based algorithmic approach, to identify important factors differentiating subjects with LATE and/or AD from Control on significantly imbalanced data. We analyzed two datasets ROSMAP and NACC and discovered that alcohol consumption was a top lifestyle and environmental factor linked with LATE and AD and their associations were differential. In particular, we identified a specific subpopulation consisting of APOE e4 carriers. We found that, for this subpopulation, light-to-moderate alcohol intake was a protective factor against both AD and LATE, but its protective role against AD appeared stronger than LATE. The codes for our algorithms are available at https://github.com/xinxingwu-uk/PFV.

Mahmut S. Gokmen, Mitchell A. Klusty, Peter T. Nelson et al.

Whole-slide images (WSIs) contain tissue information distributed across multiple magnification levels, yet most self-supervised methods treat these scales as independent views. This separation prevents models from learning representations that remain stable when resolution changes, a key requirement for practical neuropathology workflows. This study introduces Magnification-Aware Distillation (MAD), a self-supervised strategy that links low-magnification context with spatially aligned high-magnification detail, enabling the model to learn how coarse tissue structure relates to fine cellular patterns. The resulting foundation model, MAD-NP, is trained entirely through this cross-scale correspondence without annotations. A linear classifier trained only on 10x embeddings maintains 96.7% of its performance when applied to unseen 40x tiles, demonstrating strong resolution-invariant representation learning. Segmentation outputs remain consistent across magnifications, preserving anatomical boundaries and minimizing noise. These results highlight the feasibility of scalable, magnification-robust WSI analysis using a unified embedding space