ArticleCommunications biology2023
Uncovering hidden network architecture from spiking activities using an exact statistical input-output relation of neurons.
Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 8 citations in OpenAlex.
- Charting higher-order models of brain function beyond pairwise interactions.Nature communications · 2026Article
- Comparing effective and functional connectivity.Scientific reports · 2026Article
- Spiking dynamics of individual neurons reflect changes in the structure and function of neuronal networks.Nature communications · 2025Article
- Explosive neural networks via higher-order interactions in curved statistical manifolds.Nature communications · 2025Article
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Authors and funding
4 authors at 3 institutions in 2 countries.
Funding
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Abstract
Identifying network architecture from observed neural activities is crucial in neuroscience studies. A key requirement is knowledge of the statistical input-output relation of single neurons in vivo. By utilizing an exact analytical solution of the spike-timing for leaky integrate-and-fire neurons under noisy inputs balanced near the threshold, we construct a framework that links synaptic type, strength, and spiking nonlinearity with the statistics of neuronal population activity. The framework explains structured pairwise and higher-order interactions of neurons receiving common inputs under different architectures. We compared the theoretical predictions with the activity of monkey and mouse V1 neurons and found that excitatory inputs given to pairs explained the observed sparse activity characterized by strong negative triple-wise interactions, thereby ruling out the alternative explanation by shared inhibition. Moreover, we showed that the strong interactions are a signature of excitatory rather than inhibitory inputs whenever the spontaneous rate is low. We present a guide map of neural interactions that help researchers to specify the hidden neuronal motifs underlying observed interactions found in empirical data.
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