Lattice physics approaches for neural networks
Open accessAbstract
Modern neuroscience has evolved into a frontier field that draws on numerous disciplines, resulting in the flourishing of novel conceptual frames primarily inspired by physics and complex systems science. Contributing in this direction, we recently introduced a mathematical framework to describe the spatiotemporal interactions of systems of neurons using lattice field theory, the reference paradigm for theoretical particle physics. In this note, we provide a concise summary of the basics of the theory, aiming to be intuitive to the interdisciplinary neuroscience community. We contextualize our methods, illustrating how to readily connect the parameters of our formulation to experimental variables using well-known renormalization procedures. This synopsis yields the key concepts needed to describe neural networks using lattice physics. Such classes of methods are attention-worthy in an era of blistering improvements in numerical computations, as they can facilitate relating the observation of neural activity to generative models underpinned by physical principles.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Lattice field theory has been adapted to model spatiotemporal neural dynamics by discretizing neural activity on a spacetime lattice.
“In particular, lattice field theory, originally developed in quantum field theory and particle physics, has been adapted to model spatiotemporal neural dynamics by discretizing neural activity on a spacetime lattice [44].”
From Quantum-Inspired and Non-Classical Approaches to Consciousness: Models, Evidence and Constraints (2026) · cites this paper as [44]
Lattice field theory-based approaches remain primarily theoretical and computational, providing a principled formalism rather than demonstrating biologically instantiated quantum processes.
“Despite these promising features, it is important to emphasize that lattice field theory-based approaches remain primarily theoretical and computational. Their current contribution lies in providing a principled formalism for describing emergent spatiotemporal structure in neural activity, rather than in demonstrating biologically instantiated quantum processes.”
From Quantum-Inspired and Non-Classical Approaches to Consciousness: Models, Evidence and Constraints (2026) · cites this paper as [44]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Zadeh, L. A. (1965) · Information and Control · doi:10.1016/s0019-9958(65)90241-x · Cited by 67,855 · see citing works
Neural networks and physical systems with emergent collective computational abilities.
Hopfield, J. J. (1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.8.2554 · Cited by 19,270 · see citing works
The free-energy principle: a unified brain theory?
Friston, K. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2787 · Cited by 8,120 · cited 2× · see citing works
“Although these two strategies are the most popular, their fragmented view falls short of formally reconciling with general physical principles 36 .”
BackgroundMethodFriston, K. J., Harrison, L., & Penny, W. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00202-7 · Cited by 4,583 · see citing works
Wilson, K. G. (1974) · Physical review. D. Particles, fields, gravitation, and cosmology/Physical review. D. Particles and fields · doi:10.1103/physrevd.10.2445 · Cited by 4,580 · see citing works
The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes
Buzsáki, G., Anastassiou, C. A., & Koch, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3241 · Cited by 4,225 · see citing works
Excitatory and Inhibitory Interactions in Localized Populations of Model Neurons
Wilson, H. R., & Cowan, J. D. (1972) · Biophysical Journal · doi:10.1016/s0006-3495(72)86068-5 · Cited by 3,579 · see citing works
Functional and Effective Connectivity: A Review
Friston, K. J. (2011) · Brain Connectivity · doi:10.1089/brain.2011.0008 · Cited by 3,415 · see citing works
A maximum entropy approach to natural language processing
Berger, A. L., Pietra, V. J. D., & Pietra, S. A. D. (1996) · doi:10.5555/234285.234289 · Cited by 3,083 · see citing works
Internal models for motor control and trajectory planning.
Kawato, M. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)00028-8 · Cited by 2,685 · see citing works
Canonical Microcircuits for Predictive Coding
Bastos, A. M., Usrey, W. M., Adams, R. A., Mangun, G. R., Fries, P., & Friston, K. J. (2012) · Neuron · doi:10.1016/j.neuron.2012.10.038 · Cited by 2,421 · cited 2× · see citing works
“Nonetheless, the columnar organization is the most accepted view for the structural and operational components of neural circuitry 114 .”
BackgroundMethodShadlen, M. N., & Newsome, W. T. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03870.1998 · Cited by 2,178 · see citing works
Dynamics of pattern formation in lateral-inhibition type neural fields
Амари, Ш.-И. (1977) · Biological Cybernetics · doi:10.1007/bf00337259 · Cited by 2,086 · see citing works
Fredkin, E., & Toffoli, T. (1982) · International Journal of Theoretical Physics · doi:10.1007/bf01857727 · Cited by 1,896 · see citing works
A mathematical theory of the functional dynamics of cortical and thalamic nervous tissue
Wilson, H. R., & Cowan, J. D. (1973) · Kybernetik · doi:10.1007/bf00288786 · Cited by 1,823 · see citing works
Context-dependent computation by recurrent dynamics in prefrontal cortex
Mante, V., Sussillo, D., Shenoy, K. V., & Newsome, W. T. (2013) · Nature · doi:10.1038/nature12742 · Cited by 1,807 · see citing works
Neural correlations, population coding and computation
Averbeck, B. B., Latham, P. E., & Pouget, A. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1888 · Cited by 1,743 · see citing works
Weak pairwise correlations imply strongly correlated network states in a neural population
Schneidman, E., Berry, M. J., Segev, R., & Bialek, W. (2006) · Nature · doi:10.1038/nature04701 · Cited by 1,701 · see citing works
The renormalization group and critical phenomena
Wilson, K. G. (1983) · Reviews of Modern Physics · doi:10.1103/revmodphys.55.583 · Cited by 1,685 · see citing works
A free energy principle for the brain
Friston, K., Kilner, J., & Harrison, L. (2006) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2006.10.001 · Cited by 1,369 · see citing works
Discreteness of area and volume in quantum gravity
Rovelli, C., & Smolin, L. (1995) · Nuclear Physics B · doi:10.1016/0550-3213(95)00150-q · Cited by 1,365 · cited 1× · see citing works
“Many authors 23,24,84,85 have agreed that expressing physical theories in these terms still guarantees the symmetries and conservation laws of continuous formulations.”
BackgroundProbabilistic decision making by slow reverberation in cortical circuits
Wang, X.-J. (2002) · Neuron · doi:10.1016/s0896-6273(02)01092-9 · Cited by 1,242 · see citing works
An Integrated Brain-Machine Interface Platform With Thousands of Channels
Musk, E., & Neuralink (2019) · Journal of Medical Internet Research · doi:10.2196/16194 · Cited by 1,206 · see citing works
Neuropixels 2.0: A miniaturized high-density probe for stable, long-term brain recordings.
Steinmetz, N. A., Aydin, C., Lebedeva, A., Okun, M., Pachitariu, M., Bauza, M., Beau, M., Bhagat, J., Böhm, C., Broux, M., et al. (2021) · Science · doi:10.1126/science.abf4588 · Cited by 1,173 · see citing works
The dynamic brain: from spiking neurons to neural masses and cortical fields
Deco, G., Jirsa, V. K., Robinson, P. A., Breakspear, M., & Friston, K. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000092 · Cited by 1,084 · see citing works
Dynamics of neuronal firing correlation: modulation of "effective connectivity"
Aertsen, A. M. H. J., Gerstein, G. L., Habib, M., & Palm, G. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.5.900 · Cited by 1,073 · see citing works
Storing Infinite Numbers of Patterns in a Spin-Glass Model of Neural Networks
Amit, D. J., Gutfreund, H., & Sompolinsky, H. (1985) · Physical Review Letters · doi:10.1103/physrevlett.55.1530 · Cited by 1,063 · see citing works
Amit, D. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.3.237 · Cited by 1,061 · see citing works
The columnar organization of the neocortex.
Mountcastle, V. B. (1997) · Brain : a journal of neurology · doi:10.1093/brain/120.4.701 · Cited by 941 · see citing works
Itzykson, C., & Drouffe, J.-M. (1989) · doi:10.1017/cbo9780511622779 · Cited by 885 · see citing works
Fast Global Oscillations in Networks of Integrate-and-Fire Neurons with Low Firing Rates
Brunel, N., & Hakim, V. (1999) · Neural Computation · doi:10.1162/089976699300016179 · Cited by 881 · see citing works
Zur Formulierung quantisierter Feldtheorien
Lehmann, H., Symanzik, K., & Zimmermann, W. (1955) · Il Nuovo Cimento · doi:10.1007/bf02731765 · Cited by 868 · see citing works
Comparing dynamic causal models.
Penny, W. D., Stephan, K. E., Mechelli, A., & Friston, K. J. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.03.026 · Cited by 848 · see citing works
Dynamics of neuronal interactions in monkey cortex in relation to behavioural events
Vaadia, E., Haalman, I., Abeles, M., Bergman, H., Prut, Y., Slovin, H., & Aertsen, A. (1995) · Nature · doi:10.1038/373515a0 · Cited by 802 · see citing works
Linking Structure and Function in Macroscale Brain Networks
Suárez, L. E., Markello, R. D., Betzel, R. F., & Mišić, B. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.01.008 · Cited by 745 · see citing works
Abeles, M. (1982) · Studies of brain function · doi:10.1007/978-3-642-81708-3 · Cited by 686 · see citing works
Neural Manifolds for the Control of Movement
Gallego, J. Á., Perich, M. G., Miller, L. E., & Solla, S. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.025 · Cited by 676 · see citing works
Computation Through Neural Population Dynamics
Vyas, S., Golub, M. D., Sussillo, D., & Shenoy, K. V. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-092619-094115 · Cited by 671 · see citing works
Probabilistic brains: knowns and unknowns
Pouget, A., Beck, J. M., Ma, W. J., & Latham, P. E. (2013) · Nature Neuroscience · doi:10.1038/nn.3495 · Cited by 615 · see citing works
Demixed principal component analysis of neural population data
Kobak, D., Brendel, W., Constantinidis, C., Feierstein, C. E., Kepecs, Á., Mainen, Z. F., Qi, X.-L., Romo, R., Uchida, N., & Machens, C. K. (2016) · eLife · doi:10.7554/elife.10989 · Cited by 602 · see citing works
A neural network that finds a naturalistic solution for the production of muscle activity
Sussillo, D., Churchland, M. M., Kaufman, M. T., & Shenoy, K. V. (2015) · Nature Neuroscience · doi:10.1038/nn.4042 · Cited by 598 · see citing works
The cortical column: a structure without a function
Horton, J. C., & Adams, D. L. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1623 · Cited by 597 · see citing works
The minicolumn hypothesis in neuroscience
Buxhoeveden, D. P., & Casanova, M. F. (2002) · Brain · doi:10.1093/brain/awf110 · Cited by 496 · see citing works
Explainable Deep Learning: A Field Guide for the Uninitiated
Ras, G., Xie, N., van Gerven, M. A. J., & Doran, D. (2022) · Journal of Artificial Intelligence Research · doi:10.1613/jair.1.13200 · Cited by 486 · see citing works
Bump attractor dynamics in prefrontal cortex explains behavioral precision in spatial working memory
Wimmer, K., Nykamp, D. Q., Constantinidis, C., & Compte, A. (2014) · Nature Neuroscience · doi:10.1038/nn.3645 · Cited by 453 · see citing works
Diverse coupling of neurons to populations in sensory cortex
Okun, M., Steinmetz, N. A., Cossell, L., Iacaruso, M. F., Ko, H., Barthó, P., Moore, T., Hofer, S. B., Mrsic‐Flogel, T. D., Carandini, M., et al. (2015) · Nature · doi:10.1038/nature14273 · Cited by 428 · see citing works
Simultaneously Recorded Trains of Action Potentials: Analysis and Functional Interpretation
Gerstein, G. L., & Perkel, D. H. (1969) · Science · doi:10.1126/science.164.3881.828 · Cited by 417 · see citing works
A neural interface for a cortical vision prosthesis
Normann, R. A., Maynard, E. M., Rousche, P. J., & Warren, D. J. (1999) · Vision Research · doi:10.1016/s0042-6989(99)00040-1 · Cited by 411 · see citing works
Linking Connectivity, Dynamics, and Computations in Low-Rank Recurrent Neural Networks
Mastrogiuseppe, F., & Ostojic, S. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.003 · Cited by 394 · see citing works
The Cellular Automaton Interpretation of Quantum Mechanics
Hooft, G. ’. (2016) · Fundamental theories of physics · doi:10.1007/978-3-319-41285-6 · Cited by 391 · see citing works
Properties of a mass of cells capable of regenerating pulses
Beurle, R. L. (1956) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1956.0012 · Cited by 386 · see citing works
Murray, J. D., Bernacchia, A., Roy, N. A., Constantinidis, C., Romo, R., & Wang, X. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619449114 · Cited by 381 · see citing works
A guide to group effective connectivity analysis, part 1: First level analysis with DCM for fMRI
Zeidman, P., Jafarian, A., Corbin, N., Seghier, M. L., Razi, A., Price, C. J., & Friston, K. J. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.06.031 · Cited by 369 · see citing works
A biohybrid synapse with neurotransmitter-mediated plasticity
Keene, S. T., Lubrano, C., Kazemzadeh, S., Melianas, A., Tuchman, Y., Polino, G., Scognamiglio, P., Cinà, L., Salleo, A., van de Burgt, Y., et al. (2020) · Nature Materials · doi:10.1038/s41563-020-0703-y · Cited by 369 · see citing works
Chaudhuri, R., Gerçek, B., Pandey, B., Peyrache, A., & Fiete, I. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0460-x · Cited by 367 · see citing works
Recurrent network models of sequence generation and memory
Rajan, K., Harvey, C. D., & Tank, D. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.009 · Cited by 351 · see citing works
Brain organoids for the study of human neurobiology at the interface of in vitro and in vivo
Chiaradia, I., & Lancaster, M. A. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-00730-3 · Cited by 343 · see citing works
Correlations and the encoding of information in the nervous system
Panzeri, S., Schultz, S. R., Treves, A., & Rolls, E. T. (1999) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1999.0736 · Cited by 341 · see citing works
Damgaard, P. H., & Hüffel, H. (1987) · Physics Reports · doi:10.1016/0370-1573(87)90144-x · Cited by 341 · see citing works
The P(φ) 2 Euclidean Quantum Field Theory as Classical Statistical Mechanics
Guerra, F., Rosen, L., & Simon, B. (1975) · Annals of Mathematics · doi:10.2307/1970988 · Cited by 327 · see citing works
Characteristics of Random Nets of Analog Neuron-Like Elements
Amarimber, S.-I. (1972) · IEEE Transactions on Systems Man and Cybernetics · doi:10.1109/tsmc.1972.4309193 · Cited by 304 · see citing works
Cortical activity flips among quasi-stationary states.
Abeles, M., Bergman, H., Gat, I., Meilijson, I., Seidemann, E., Tishby, N., & Vaadia, E. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.19.8616 · Cited by 295 · see citing works
Inverse statistical problems: from the inverse Ising problem to data science
Nguyen, H. C., Zecchina, R., & Berg, J. (2017) · Advances In Physics · doi:10.1080/00018732.2017.1341604 · Cited by 284 · see citing works
Collective properties of neural networks: A statistical physics approach
Peretto, P. (1984) · Biological Cybernetics · doi:10.1007/bf00317939 · Cited by 266 · see citing works
Training deep neural density estimators to identify mechanistic models of neural dynamics
Gonçalves, P. J., Lueckmann, J.-M., Deistler, M., Nonnenmacher, M., Öcal, K., Bassetto, G., Chintaluri, C., Podlaski, W. F., Haddad, S. A., Vogels, T. P., et al. (2020) · eLife · doi:10.7554/elife.56261 · Cited by 252 · see citing works
Searching for Collective Behavior in a Large Network of Sensory Neurons
Tkačik, G., Marre, O., Amodei, D., Schneidman, E., Bialek, W., & Berry, M. J. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003408 · Cited by 248 · see citing works
Excitatory signal flow and connectivity in a cortical column: focus on barrel cortex.
Lübke, J., & Feldmeyer, D. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0144-2 · Cited by 233 · see citing works
Microcolumns in the cerebral cortex
Jones, E. G. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.10.5019 · Cited by 233 · see citing works
Landscape and flux theory of non-equilibrium dynamical systems with application to biology
Wang, J. (2015) · Advances In Physics · doi:10.1080/00018732.2015.1037068 · Cited by 229 · see citing works
Working memory, attention, and salience in active inference
Parr, T., & Friston, K. J. (2017) · Scientific Reports · doi:10.1038/s41598-017-15249-0 · Cited by 226 · see citing works
Functional neuronal circuitry and oscillatory dynamics in human brain organoids
Sharf, T., van der Molen, T., Glasauer, S. M. K., Guzman, E., Buccino, A., Luna, G., Cheng, Z., Audouard, M., Ranasinghe, K., Kudo, K., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32115-4 · Cited by 218 · see citing works
Two views on the cognitive brain
Barack, D. L., & Krakauer, J. W. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00448-6 · Cited by 214 · see citing works
A unifying perspective on neural manifolds and circuits for cognition
Langdon, C., Genkin, M., & Engel, T. A. (2023) · Nature reviews. Neuroscience · doi:10.1038/s41583-023-00693-x · Cited by 210 · see citing works
Field-theoretic approach to fluctuation effects in neural networks
Buice, M. A., & Cowan, J. D. (2007) · Physical Review E · doi:10.1103/physreve.75.051919 · Cited by 199 · see citing works
Massively parallel microwire arrays integrated with CMOS chips for neural recording
Obaid, A., Hanna, M.-E., Wu, Y., Köllő, M., Rácz, R., Angle, M. R., Müller, J., Brackbill, N., Wray, W., Franke, F., et al. (2020) · Science Advances · doi:10.1126/sciadv.aay2789 · Cited by 195 · see citing works
Jazayeri, M., & Ostojic, S. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.08.002 · Cited by 193 · see citing works
Formulation of lattice gauge theories for quantum simulations
Zohar, E., & Burrello, M. (2015) · Physical review. D. Particles, fields, gravitation, and cosmology/Physical review. D. Particles and fields · doi:10.1103/physrevd.91.054506 · Cited by 192 · see citing works
Gauge fields on a lattice. I. General outlook
Balian, R., Drouffe, J.-M., & Itzykson, C. (1974) · Physical review. D. Particles, fields, gravitation, and cosmology/Physical review. D. Particles and fields · doi:10.1103/physrevd.10.3376 · Cited by 192 · see citing works
Can time be a discrete dynamical variable?
Lee, T. D. (1983) · Physics Letters B · doi:10.1016/0370-2693(83)90687-1 · Cited by 191 · see citing works
Fuzzy Logic = Computing with Words
Zadeh, L. A. (1999) · Studies in fuzziness and soft computing · doi:10.1007/978-3-7908-1873-4_1 · Cited by 189 · see citing works
SiNAPS: An implantable active pixel sensor CMOS-probe for simultaneous large-scale neural recordings
Angotzi, G. N., Boi, F., Lecomte, A., Miele, E., Malerba, M., Zucca, S., Casile, A., & Berdondini, L. (2018) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2018.10.032 · Cited by 177 · see citing works
Collective Behavior of Networks with Linear (VLSI) Integrate-and-Fire Neurons
Fusi, S., & Mattia, M. (1999) · Neural Computation · doi:10.1162/089976699300016601 · Cited by 163 · see citing works
Spin glass model of learning by selection.
Toulouse, G., Dehaene, S., & Changeux, J. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.6.1695 · Cited by 157 · see citing works
Spike-based dynamic computing with asynchronous sensing-computing neuromorphic chip
Yao, M., Richter, O., Zhao, G., Qiao, N., Xing, Y., Wang, D., Hu, T., Fang, W., Demirci, T., Marchi, M. D., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-47811-6 · Cited by 152 · see citing works
Adaptive Cluster Expansion for Inferring Boltzmann Machines with Noisy Data
Cocco, S., & Monasson, R. (2011) · Physical Review Letters · doi:10.1103/physrevlett.106.090601 · Cited by 142 · see citing works
Attractor dynamics gate cortical information flow during decision-making
Finkelstein, A., Fontolan, L., Economo, M. N., Li, N., Romani, S., & Svoboda, K. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00840-6 · Cited by 130 · see citing works
Modeling Compositionality by Dynamic Binding of Synfire Chains
Abeles, M., Hayon, G., & Lehmann, D. J. (2004) · Journal of Computational Neuroscience · doi:10.1023/b:jcns.0000037682.18051.5f · Cited by 122 · see citing works
Monte Carlo Calculation of Renormalized Coupling Parameters
Swendsen, R. H. (1984) · Physical Review Letters · doi:10.1103/physrevlett.52.1165 · Cited by 115 · see citing works
High-resolution data-driven model of the mouse connectome
Knox, J. E., Harris, K. D., Graddis, N., Whitesell, J. D., Zeng, H., Harris, J. A., Shea‐Brown, E., & Mihalaş, Ş. (2018) · Network Neuroscience · doi:10.1162/netn_a_00066 · Cited by 113 · see citing works
Feynman's Thesis — A New Approach to Quantum Theory
Brown, L. M. (2005) · WORLD SCIENTIFIC eBooks · doi:10.1142/5852 · Cited by 110 · see citing works
Real-space renormalization in statistical mechanics
Efrati, E., Wang, Z., Kolan, A. J., et al. (2014) · Reviews of Modern Physics · doi:10.1103/revmodphys.86.647 · Cited by 108 · see citing works
Memristive synapses connect brain and silicon spiking neurons
Serb, A., Corna, A., George, R., Khiat, A., Rocchi, F., Reato, M., Maschietto, M., Mayr, C., Indiveri, G., Vassanelli, S., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-58831-9 · Cited by 102 · see citing works
Nonequilibrium landscape theory of neural networks
Yan, H., Zhao, L., Hu, L. Q., Wang, X., Wang, E., & Wang, J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310692110 · Cited by 100 · see citing works
Lattice quantum electrodynamics in (3+1)-dimensions at finite density with tensor networks
Magnifico, G., Felser, T., Silvi, P., & Montangero, S. (2021) · Nature Communications · doi:10.1038/s41467-021-23646-3 · Cited by 91 · see citing works
Parcels and particles: Markov blankets in the brain
Friston, K. J., Fagerholm, E. D., Zarghami, T. S., Parr, T., Hipólito, I., Magrou, L., & Razi, A. (2020) · Network Neuroscience · doi:10.1162/netn_a_00175 · Cited by 90 · see citing works
How particular is the physics of the free energy principle?
Aguilera, M., Millidge, B., Tschantz, A., & Buckley, C. L. (2021) · Physics of Life Reviews · doi:10.1016/j.plrev.2021.11.001 · Cited by 88 · see citing works
Statistical Field Theory for Neural Networks
Helias, M., & Dahmen, D. (2020) · Lecture notes in physics · doi:10.1007/978-3-030-46444-8 · Cited by 86 · see citing works
Path integral approach to random neural networks
Crisanti, A., & Sompolinsky, H. (2018) · Physical review. E · doi:10.1103/physreve.98.062120 · Cited by 84 · see citing works
How particular is the physics of the free energy principle?
Millidge, B. (2022) · Sussex Research Online (University of Sussex) · Cited by 83 · see citing works
Feynman's Thesis - A New Approach to Quantum Theory
(2005) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789812567635 · Cited by 81 · see citing works
Difference equations and conservation laws
Lee, T. D. (1987) · Journal of Statistical Physics · doi:10.1007/bf01011145 · Cited by 78 · see citing works
Vassanelli, S., & Mahmud, M. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00438 · Cited by 78 · see citing works
A Neuromorphic Prosthesis to Restore Communication in Neuronal Networks
Buccelli, S., Bornat, Y., Colombi, I., Ambroise, M., Martines, L., Pasquale, V., Bisio, M., Tessadori, J., Nowak, P., Grassia, F., et al. (2019) · iScience · doi:10.1016/j.isci.2019.07.046 · Cited by 77 · see citing works
Laplacian renormalization group for heterogeneous networks
Villegas, P., Gili, T., Caldarelli, G., et al. (2023) · Nature Physics · doi:10.1038/s41567-022-01866-8 · Cited by 76 · see citing works
Detecting Synfire Chain Activity Using Massively Parallel Spike Train Recording
Schrader, S., Grün, S., Diesmann, M., & Gerstein, G. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01245.2007 · Cited by 69 · see citing works
Lattice quantum electrodynamics in (3+1)-dimensions at finite density with tensor networks
Magnifico, G., Felser, T., Silvi, P., & Montangero, S. (2021) · RePEc: Research Papers in Economics · Cited by 67 · see citing works
Metastable states in asymmetrically diluted Hopfield networks
Treves, A., & Amit, D. J. (1988) · Journal of Physics A Mathematical and General · doi:10.1088/0305-4470/21/14/016 · Cited by 65 · see citing works
Cell assemblies at multiple time scales with arbitrary lag constellations
Russo, E., & Durstewitz, D. (2017) · eLife · doi:10.7554/elife.19428 · Cited by 65 · see citing works
Metastable dynamics of neural circuits and networks
Brinkman, B. A. W., Yan, H., Maffei, A., Park, I. M., Fontanini, A., Wang, J., & La Camera, G. (2022) · Applied Physics Reviews · doi:10.1063/5.0062603 · Cited by 64 · see citing works
Morphological differences between minicolumns in human and nonhuman primate cortex
Buxhoeveden, D. P., Switala, A. E., Roy, E., Litaker, M. S., & Casanova, M. F. (2001) · American Journal of Physical Anthropology · doi:10.1002/ajpa.1092 · Cited by 62 · see citing works
Neural Activity in Frontal Cortical Cell Layers: Evidence for Columnar Sensorimotor Processing
Opriș, I. C., Hampson, R. E., Stanford, T. R., Gerhardt, G. A., & Deadwyler, S. A. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21534 · Cited by 62 · see citing works
Phantom oscillations in principal component analysis
Shinn, M. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2311420120 · Cited by 61 · see citing works
Weizcsäcker, C. F. V. (1984) · Boston studies in the philosophy of science · doi:10.1007/978-94-009-7178-3_13 · Cited by 58 · see citing works
Beyond mean field theory: statistical field theory for neural networks
Buice, M. A., & Chow, C. C. (2013) · Journal of Statistical Mechanics Theory and Experiment · doi:10.1088/1742-5468/2013/03/p03003 · Cited by 56 · see citing works
On the microscopic foundation of scaling laws
Castro, C. D., & Jona-Lasinio, G. (1969) · Physics Letters A · doi:10.1016/0375-9601(69)90148-0 · Cited by 54 · see citing works
The emergence of synchrony in networks of mutually inferring neurons
Palacios, E. R., Isomura, T., Parr, T., & Friston, K. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-42821-7 · Cited by 54 · see citing works
The effect of nonstationarity on models inferred from neural data
Tyrcha, J., Roudi, Y., Marsili, M., et al. (2013) · Journal of Statistical Mechanics Theory and Experiment · doi:10.1088/1742-5468/2013/03/p03005 · Cited by 53 · see citing works
A primer on Variational Laplace (VL)
Zeidman, P., Friston, K. J., & Parr, T. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120310 · Cited by 52 · see citing works
Sparse DCM for whole-brain effective connectivity from resting-state fMRI data
Prando, G., Zorzi, M., Bertoldo, A., Corbetta, M., Zorzi, M., & Chiuso, A. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116367 · Cited by 50 · see citing works
Plasticity and Adaptation in Neuromorphic Biohybrid Systems
George, R., Chiappalone, M., Giugliano, M., Levi, T., Vassanelli, S., Partzsch, J., & Mayr, C. (2020) · iScience · doi:10.1016/j.isci.2020.101589 · Cited by 50 · see citing works
Neural Field Models: A mathematical overview and unifying framework
Cook, B. J., Peterson, A. D. H., Woldman, W., & Terry, J. R. (2022) · Mathematical Neuroscience and Applications · doi:10.46298/mna.7284 · Cited by 48 · see citing works
Relating theories via renormalization
Kadanoff, L. P. (2012) · Studies in History and Philosophy of Science Part B Studies in History and Philosophy of Modern Physics · doi:10.1016/j.shpsb.2012.05.002 · Cited by 44 · see citing works
A unifying framework for mean-field theories of asymmetric kinetic Ising systems
Aguilera, M., Moosavi, S. A., & Shimazaki, H. (2021) · Nature Communications · doi:10.1038/s41467-021-20890-5 · Cited by 44 · see citing works
Analysis of neuronal ensemble activity reveals the pitfalls and shortcomings of rotation dynamics
Lebedev, M., Ossadtchi, A. E., Mill, N. A., Urpí, N. A., Cervera, M. R., & Nicolelis, M. A. L. (2019) · Scientific Reports · doi:10.1038/s41598-019-54760-4 · Cited by 43 · see citing works
Engineering recurrent neural networks from task-relevant manifolds and dynamics
Pollock, E., & Jazayeri, M. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008128 · Cited by 43 · see citing works
Multimodal 3D atlas of the macaque monkey motor and premotor cortex
Rapan, L., Froudist‐Walsh, S., Niu, M., Xu, T., Funck, T., Zilles, K., & Palomero‐Gallagher, N. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117574 · Cited by 42 · see citing works
Input space bifurcation manifolds of recurrent neural networks
Haschke, R., & Steil, J. J. (2005) · Neurocomputing · doi:10.1016/j.neucom.2004.11.030 · Cited by 40 · see citing works
Long term performance of porous platinum coated neural electrodes
Leber, M., Bhandari, R., Mize, J. T., Warren, D. J., Shandhi, M. M. H., Solzbacher, F., & Negi, S. (2017) · Biomedical Microdevices · doi:10.1007/s10544-017-0201-4 · Cited by 40 · see citing works
Attractor dynamics reflect decision confidence in macaque prefrontal cortex
Wang, S., Falcone, R., Richmond, B. J., & Averbeck, B. B. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01445-x · Cited by 40 · see citing works
Tavoni, G., Ferrari, U., Battaglia, F. P., Cocco, S., & Monasson, R. (2017) · Network Neuroscience · doi:10.1162/netn_a_00014 · Cited by 38 · see citing works
A unifying framework for mean-field theories of asymmetric kinetic Ising systems
Aguilera, M., Moosavi, S. A., & Shimazaki, H. (2021) · Sussex Research Online (University of Sussex) · Cited by 35 · see citing works
Quantum field theory of binary alternatives
G�rnitz, T., Graudenz, D., & Weizs�cker, C. F. V. (1992) · International Journal of Theoretical Physics · doi:10.1007/bf00671965 · Cited by 33 · see citing works
ASSET: Analysis of Sequences of Synchronous Events in Massively Parallel Spike Trains
Torre, E., Canova, C., Denker, M., Gerstein, G. L., Helias, M., & Grün, S. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004939 · Cited by 33 · see citing works
Shi, Y.-L., Steinmetz, N. A., Moore, T., Boahen, K. A., & Engel, T. A. (2022) · Nature Communications · doi:10.1038/s41467-021-27724-4 · Cited by 31 · see citing works
Cruz, L., Buldyrev, S. V., Peng, S., Roe, D. L., Urbanc, B., Stanley, E., & Rosene, D. L. (2004) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2004.09.005 · Cited by 28 · see citing works
Ye, Z., Shelton, A. M., Shaker, J. R., Boussard, J., Colonell, J. I., Birman, D., Manavi, S., Chen, S., Windolf, C., Hurwitz, C., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.23.554527 · Cited by 28 · see citing works
Are spin-glass effects relevant to understanding realistic auto-associative networks?
Treves, A. (1991) · Journal of Physics A Mathematical and General · doi:10.1088/0305-4470/24/11/029 · Cited by 27 · see citing works
Neuronal population dynamics during motor plan cancellation in nonhuman primates
Pani, P., Giamundo, M., Giarrocco, F., Mione, V., Fontana, R., Brunamonti, E., Mattia, M., & Ferraina, S. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2122395119 · Cited by 26 · see citing works
Self-citationStochastic quantisation of Yang–Mills–Higgs in 3D
Chandra, A., Chevyrev, I., Hairer, M., & Shen, H. (2024) · Inventiones mathematicae · doi:10.1007/s00222-024-01264-2 · Cited by 26 · see citing works
The Complexity of Dynamics in Small Neural Circuits
Fasoli, D., Cattani, A., & Panzeri, S. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004992 · Cited by 25 · see citing works
Methods for identification of spike patterns in massively parallel spike trains
Quaglio, P., Rostami, V., Torre, E., & Grün, S. (2018) · Biological Cybernetics · doi:10.1007/s00422-018-0755-0 · Cited by 25 · see citing works
Learning non-stationary Langevin dynamics from stochastic observations of latent trajectories
Genkin, M., Hughes, O., & Engel, T. A. (2021) · Nature Communications · doi:10.1038/s41467-021-26202-1 · Cited by 25 · see citing works
Interfacing brain organoids with precision medicine and machine learning
Zheng, H., Feng, Y., Tang, J., & Ma, S. (2022) · Cell Reports Physical Science · doi:10.1016/j.xcrp.2022.100974 · Cited by 25 · see citing works
Functional networks from inverse modeling of neural population activity
Cocco, S., Monasson, R., Posani, L., & Tavoni, G. (2017) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2017.04.017 · Cited by 23 · see citing works
Gell-Mann–Low Criticality in Neural Networks
Tiberi, L., Stapmanns, J., Kühn, T., Luu, T., Dahmen, D., & Helias, M. (2022) · Physical Review Letters · doi:10.1103/physrevlett.128.168301 · Cited by 22 · see citing works
Statistical Physics through the Lens of Real-Space Mutual Information
Gökmen, D. E., Ringel, Z., Huber, S. D., et al. (2021) · Physical Review Letters · doi:10.1103/physrevlett.127.240603 · Cited by 21 · see citing works
Theory of Brain Function, Quantum Mechanics and SuperstringsPreprint
Nanopoulos, D. V. (1995) · arXiv (Cornell University) · doi:10.48550/arxiv.hep-ph/9505374 · Cited by 20 · see citing works
Yan, H., & Wang, J. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008209 · Cited by 20 · see citing works
Emergence of associative learning in a neuromorphic inference network
Gandolfi, D., Puglisi, F. M., Boiani, G. M., Pagnoni, G., Friston, K. J., D'Angelo, E. U., & Mapelli, J. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac6ca7 · Cited by 18 · see citing works
Self-Consistent Stochastic Dynamics for Finite-Size Networks of Spiking Neurons
Vinci, G. V., Benzi, R., & Mattia, M. (2023) · Physical Review Letters · doi:10.1103/physrevlett.130.097402 · Cited by 18 · see citing works
Renormalization group approach to spin glass systems
Parisi, G., Petronzio, R., & Rosati, F. (2001) · The European Physical Journal B · doi:10.1007/s100510170171 · Cited by 17 · see citing works
Neural assemblies revealed by inferred connectivity-based models of prefrontal cortex recordings
Tavoni, G., Cocco, S., & Monasson, R. (2016) · Journal of Computational Neuroscience · doi:10.1007/s10827-016-0617-5 · Cited by 17 · see citing works
Swan, M., dos Santos, R. P., & Witte, F. (2022) · Quantum Reports · doi:10.3390/quantum4010008 · Cited by 16 · see citing works
Predictive Coding, Cortical Feedback, and Spike-Timing Dependent Plasticity
Rao, R. P. N., & Sejnowski, T. J. (2002) · The MIT Press eBooks · doi:10.7551/mitpress/5583.003.0021 · Cited by 16 · see citing works
Spatial and temporal correlations in neural networks with structured connectivity
Shi, Y.-L., Zeraati, R., Levina, A., & Engel, T. A. (2023) · Physical Review Research · doi:10.1103/physrevresearch.5.013005 · Cited by 16 · see citing works
Friston, K. J. (2023) · Frontiers in Science · doi:10.3389/fsci.2023.1147911 · Cited by 16 · see citing works
Helmholtz's inverse problem of the discrete calculus of variations
Bourdin, L., & Cresson, J. (2013) · The Journal of Difference Equations and Applications · doi:10.1080/10236198.2012.754435 · Cited by 15 · see citing works
Neural Activity in Quarks Language: Lattice Field Theory for a Network of Real Neurons
Bardella, G., Franchini, S., Pan, L., Balzan, R., Ramawat, S., Brunamonti, E., Pani, P., & Ferraina, S. (2024) · Entropy · doi:10.3390/e26060495 · Cited by 15 · see citing works
Self-citationFischer, B. (1973) · Bulletin of Mathematical Biology · doi:10.1016/s0092-8240(73)80034-5 · Cited by 13 · see citing works
Solving Inverse Problems with Latent Diffusion Models via Hard Data ConsistencyPreprint
Song, B., Kwon, S. M., Zhang, Z., et al. (2023) · arXiv (Cornell University) · doi:10.48550/arxiv.2307.08123 · Cited by 13 · see citing works
Neuronal travelling waves explain rotational dynamics in experimental datasets and modelling
Kuzmina, E., Kriukov, D. V., & Lebedev, M. (2024) · Scientific Reports · doi:10.1038/s41598-024-53907-2 · Cited by 13 · see citing works
Decomposing neural networks as mappings of correlation functions
Fischer, K., René, A., Keup, C., et al. (2022) · Physical Review Research · doi:10.1103/physrevresearch.4.043143 · Cited by 12 · see citing works
Neuronal tuning and population representations of shape and category in human visual cortex
Bougou, V., Vanhoyland, M., Bertrand, A., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-49078-3 · Cited by 11 · see citing works
Parameter Estimation in the Age of Degeneracy and Unidentifiability
Lederman, D., Patel, R., Itani, O., & Rotstein, H. G. (2022) · Mathematics · doi:10.3390/math10020170 · Cited by 10 · see citing works
An Action Principle for Biological Systems
Summers, R. L. (2021) · Journal of Physics Conference Series · doi:10.1088/1742-6596/2090/1/012109 · Cited by 9 · see citing works
Lagrangians and integrability for additive fourth-order difference equations
Gubbiotti, G. (2020) · Iris (Roma Tre University) · doi:10.1140/epjp/s13360-020-00858-y · Cited by 8 · see citing works
Linking network- and neuron-level correlations by renormalized field theory
Dick, M. I., van Meegen, A., & Helias, M. (2024) · Physical Review Research · doi:10.1103/physrevresearch.6.033264 · Cited by 8 · see citing works
Replica Symmetry Breaking without replicas
Franchini, S. (2023) · Annals of Physics · doi:10.1016/j.aop.2023.169220 · Cited by 7 · see citing works
Self-citationOptimized brute-force algorithms for the bifurcation analysis of a binary neural network model
Fasoli, D., & Panzeri, S. (2019) · Physical review. E · doi:10.1103/physreve.99.012316 · Cited by 6 · see citing works
Parametrized Equation of State for QCD from 3D Ising Model
Parotto, P. (2018) · doi:10.22323/1.311.0036 · Cited by 6 · see citing works
Rendering neuronal state equations compatible with the principle of stationary action
Fagerholm, E. D., Foulkes, W. M. C., Friston, K. J., et al. (2021) · The Journal of Mathematical Neuroscience · doi:10.1186/s13408-021-00108-0 · Cited by 6 · see citing works
Learning Interacting Theories from Data
Merger, C., René, A., Fischer, K., et al. (2023) · Physical Review X · doi:10.1103/physrevx.13.041033 · Cited by 6 · see citing works
On the inverse problem of the discrete calculus of variations
Gubbiotti, G. (2019) · Journal of Physics A Mathematical and Theoretical · doi:10.1088/1751-8121/ab2919 · Cited by 6 · see citing works
Space-time generated from a set of binary units
Peretto, P. (2004) · The European Physical Journal C · doi:10.1140/epjc/s2004-01826-1 · Cited by 4 · see citing works
van Hemmen, J. L., Schüz, A., & Aertsen, A. (2014) · Biological Cybernetics · doi:10.1007/s00422-014-0630-6 · Cited by 4 · see citing works
Franchini, S. (2021) · Communications in Theoretical Physics · doi:10.1088/1572-9494/abde32 · Cited by 4 · see citing works
Self-citationIntroduction to lattice field theory
Ydri, B. (2019) · Institute of Physics eBooks · doi:10.1088/2053-2563/ab0548ch2 · Cited by 4 · see citing works
Field theory for biophysical neural networksPreprint
Qiu, S.-W., & Chow, C. C. (2014) · arXiv (Cornell University) · doi:10.48550/arxiv.1411.1400 · Cited by 3 · see citing works
A Noether Theorem for discrete Covariant MechanicsPreprint
D’Ambrosio, F. (2019) · arXiv (Cornell University) · doi:10.48550/arxiv.1902.08997 · Cited by 2 · see citing works
Exploring Quantum Field Theories with Qubit Lattice Models
Singh, H. (2020) · Cited by 2 · see citing works
Rosetta stone for the population dynamics of spiking neuron networks
Vinci, G. V., & Mattia, M. (2024) · Physical review. E · doi:10.1103/physreve.110.034303 · Cited by 2 · see citing works
Grimmer, D. (2022) · PhilSci-Archive (University of Pittsburgh) · doi:10.48550/arxiv.2205.07701 · Cited by 2 · see citing works
Hill, S. (2015) · Encyclopedia of Computational Neuroscience · doi:10.1007/978-1-4614-6675-8_571 · Cited by 1 · see citing works
Statistical Field Theory and Networks of Spiking NeuronsPreprint
Gosselin, P., Lotz, A., & Wambst, M. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2009.14744 · Cited by 1 · see citing works
Effective Theories and Elementary Particle Masses
Wells, J. D. (2012) · SpringerBriefs in physics · doi:10.1007/978-3-642-34892-1_4 · Cited by 1 · see citing works
Statistical mechanics for networks of real neuronsPreprint
Meshulam, L., & Bialek, W. (2024) · arXiv (Cornell University) · doi:10.48550/arxiv.2409.00412 · Cited by 1 · see citing works
Hill, S. (2014) · Encyclopedia of Computational Neuroscience · doi:10.1007/978-1-4614-7320-6_571-1 · Cited by 1 · see citing works
Building Quantum Field Theories Out of NeuronsPreprint
Halverson, J. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2112.04527
Qubit Field TheoryPreprint
Deutsch, D. (2004) · arXiv (Cornell University) · doi:10.48550/arxiv.quant-ph/0401024
Flagged first, then by citations
Research works printed but not linked: 2
- [24]Penrose R. Emperor’s New Mind 1999 Oxford University Press UK
- [163]Hoover B. Liang Y. Pham B. Panda R. Strobelt H. Chau D.H. Zaki M.J. Krotov D. Energy transformer arXiv 2023 2302.07253
Cited by
Sorted by citations
Quantum-Inspired and Non-Classical Approaches to Consciousness: Models, Evidence and Constraints
Arias-Carrión, O., Ortega-Robles, E., & Manjarrez, E. (2026) · Brain Sciences · doi:10.3390/brainsci16040386 · Cited by 1 · see citing works
“This representation allows the construction of effective theories through coarse-graining procedures, in which macroscopic neural dynamics emerge from underlying discrete interactions, conceptually paralleling renormalisation approaches in statistical and quantum field theory [44].”
Influential
- Authors
- Bardella, G., Franchini, S., Pani, P., & Ferraina, S.
- Affiliations
- Sapienza University of Rome (IT)
- Corresponding author
- Bardella, Giampiero
- Franchini, Simone
- Venue
- iScience
- Publisher
- Elsevier BV
- Published
- 2024-12
- Volume
- 27
- Issue
- 12
- Pages
- 111390
- ISSN
- 2589-0042 (ISSN-L)
- PMC
- PMC11638618
- OpenAlex
- W4404397493
- Cited by
- 17
- References
- 190
- Citations by year
- 2026: 2 · 2025: 14 · 2024: 1
- FWCI
- 1.10
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- iScience (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- arXiv (Cornell University) (submittedVersion, cc-by-nc-nd)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion, cc-by-nc-nd)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
- arXiv (Cornell University)
- Funders
- University of Rome La Sapienza (PH11715C823A9528, RM12117A8AD27DB1)
- Università degli Studi di Pavia
- European Commission (CUP B51E22000150006, IR0000011)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Physical Sciences › Physics and Astronomy › Condensed Matter Physics › Theoretical and Computational Physics
- Physical Sciences › Computer Science › Artificial Intelligence › Neural Networks and Applications
- Keywords
- lattice field theory, artificial neural networks, renormalization, complex systems
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review