Authors
van den Heuvel, M., Libedinsky, I., Quiroz Monnens, S., Repple, J., Cocchi, L.
Abstract
Lesion Network Mapping (LNM) is a method used to map symptom-related circuits in the human brain. Recent work has raised concerns about the method and the specificity of LNM-derived networks, which often show high spatial overlap across unrelated conditions. Null models have been proposed to address the raised limitations1. Useful statistical tools in network neuroscience, they are reference procedures; in LNM, the normative connectome matrix C remains the source of the derived networks also under null modelling. Their broader role as a general solution for LNM therefore warrants careful evaluation. Here, we examine the proposed null models step-by-step and test them empirically across multiple datasets. We show that the proposed null-model correction effectively only replaces C with a transformed matrix C' (e.g., C' ~ C - mean(C)), one that is directly derived from C and retains much of its low-dimensional structure. Consequently, null-model-corrected LNM maps remain shaped by the same standard set of connectome-derived patterns and continue to show repetition and non-specificity across unrelated conditions. We discuss the scope and limitations of null models for LNM, showing that they can statistically benchmark LNMs, but that their application does not resolve the core limitation of non-specificity of LNM networks.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 30 Sep 2026.
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