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Consistency-based thresholding of the human connectome
Abstract
Densely seeded probabilistic tractography yields weighted networks that are nearly fully connected, hence containing many spurious fibers. It is thus necessary to prune spurious connections from probabilistically-derived networks to obtain a more reliable overall estimate of the connectivity. A standard method is to threshold by weight, keeping only the strongest edges. Here, by measuring the consistency of edge weights across subjects, we propose a new thresholding method that aims to reduce the rate of false-positives in group-averaged connectivity matrices. Close inspection of the relationship between consistency, weight, and distance suggests that the most consistent edges are in fact those that are strong for their length, rather than simply strong overall. Hence retaining the most consistent edges preserves more long-distance connections than traditional weight-based thresholding, which penalizes long connections for being weak regardless of anatomy. By comparing our thresholded networks to mouse and macaque tracer data, we also show that consistency-based thresholding exhibits the species-invariant exponential decay of connection weights with distance, while weight-based thresholding does not. We also show that consistency-based thresholding can be used to identify highly consistent and highly inconsistent subnetworks across subjects, enabling more nuanced analyses of group-level connectivity than just the mean connectivity.
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“We note that inter-subject connectome consistency may also be improved using other approaches, e.g., consistency-based thresholding (Baum et al., 2018; Roberts et al., 2017).”
From Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review (2022) · cites this paper as Roberts et al., 2017
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Yang, H., Wu, G.-W., Li, Y.-X., Xu, X.-Y., Cong, J., Xu, H.-S., Ma, Y., Li, Y., Chen, R.-S., Pines, A., et al. (2023) · bioRxiv · doi:10.1101/2023.03.08.531800 · Cited by 11
“A consistency-based thresholding method was applied to reduce spurious connections (73), using the 75th percentile for edge weight coefficient of variation (52).”
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Similarity-guided multi-view functional brain network fusion
Li, Z., Liu, J., Sun, M., Zhang, F., Hu, B., & Dong, Q. (2025) · Medical Image Analysis · doi:10.1016/j.media.2025.103632 · Cited by 10
Interpretable AI for relating brain structural and functional connectomesPreprint
Yang, H., Winter, S., Zhang, Z., & Dunson, D. (2022) · arXiv (Cornell University) · doi:10.48550/arxiv.2210.05672 · Cited by 7
“Roberts et al. (2017) propose to use the masking-induced difference in predicted FC.”
BackgroundWhite matter, cognition and psychotic-like experiences in UK Biobank
Bosma, M. J., Cox, S. R., Ziermans, T. B., Buchanan, C. R., Shen, X., Tucker–Drob, E. M., Adams, M. J., Whalley, H. C., & Lawrie, S. M. (2021) · Psychological Medicine · doi:10.1017/s0033291721004244 · Cited by 10
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MethodCan hubs of the human connectome be identified consistently with diffusion MRI?
Gajwani, M., Oldham, S., Pang, J. C. S., Arnatkevičiūtė, A., Tiego, J., Bellgrove, M. A., & Fornito, A. (2023) · Network Neuroscience · doi:10.1162/netn_a_00324 · Cited by 20
“…the strongest or most frequently occurring across individuals (de Reus & van den Heuvel, 2013a), retaining edges that are the least variable across people (Roberts et al., 2017), or retaining edges that preserve a specific proportion of connections in different distance bins (Betzel et al., 2019).”
BackgroundGast, H., & Assaf, Y. (2023) · Network Neuroscience · doi:10.1162/netn_a_00342 · Cited by 10
“In brain networks, connection strength often decays with distance (Ercsey-Ravasz et al., 2013; Roberts et al., 2016; Rosen & Halgren, 2021), while FA shown to be positively correlate with edge length (Roberts et al., 2017).”
BackgroundStructural and functional connectivity of the inferior temporal numeral area
Conrad, B. N., Pollack, C., Yeo, D. J. S., & Price, G. R. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac492 · Cited by 9
“We chose a cutoff of the top 30% of connections in accordance with prior applications of this approach (Roberts et al. 2017; Buchanan et al. 2020).”
MethodA Robust Modular Automated Neuroimaging Pipeline for Model Inputs to TheVirtualBrain
Frazier-Logue, N., Wang, J. L., Wang, Z., Sodums, D. J., Khosla, A., Samson, A. D., McIntosh, A. R., & Shen, K. (2022) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2022.883223 · Cited by 11
“There are several thresholding methods to mitigate the effects of spurious connections (e.g., de Reus and van den Heuvel, 2013; Roberts et al., 2017; Shen et al., 2019b) and we leave it to users to decide the method that best suits their needs.”
Portoles, O., Blesa, M., van Vugt, M. V., Cao, M., & Borst, J. (2021) · bioRxiv · doi:10.1371/journal.pcbi.1009407 · Cited by 9
“Connectivity matrices were averaged across subjects, and the 10% of links with the highest coefficient of variation across subjects were set to zero[76].”
Robalo, B. M. D. B., Vlegels, N., Meier, J. M., Leemans, A., Biessels, G. J., Reijmer, Y. D., on Behalf of the Utrecht VCI Study Group, van den Berg, E., Biesbroek, J. M., Brundel, M., et al. (2020) · Brain Connectivity · doi:10.1089/brain.2019.0686 · Cited by 10
“We also found that a larger proportion of long-range connections was removed during thresholding, indicating that longer connections are often composed of low NOS (Roberts et al., 2017).”
Effects of parcellation and threshold on brainconnectivity measures
Lacy, T. C., & Robinson, P. A. (2020) · PLoS ONE · doi:10.1371/journal.pone.0239717 · Cited by 6
“To a first approximation, if R is large and θ is small, each region will be connected to all regions within a small sphere around it, with a volume approximately equal to θ times the volume of the brain, because θ is the proportion of connections present; again, to a first approximation, connections beyond this distan…”
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Zhang, Q.-Y., Su, C.-W., Luo, Q., Grebogi, C., Huang, Z., & Jiang, J. (2025) · Research · doi:10.34133/research.0648 · Cited by 6
“To enhance the reliability of connection fitting, it becomes imperative to trim these erroneous connections stemming from the probabilistically generated network [ 95 ].”
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Longitudinal alterations of cortical structural‐functional coupling in temporal lobe epilepsy
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“Complementarily, we propose a completely data-driven topological filtering scheme for extracting the backbone of a SBN on an individual level (scan-based) without attempting to find any consistency among control subjects of a specific age (Roberts et al., 2016).”
BackgroundComing up short: Generative network models fail to accurately capture long-range connectivity
Oldham, S., Fornito, A., & Ball, G. (2025) · Network Neuroscience · doi:10.1162/netn.a.35 · Cited by 5
“…involve the creation of a consensus matrix, which is then used as a mask for individuals (Betzel et al., 2019; de Reus & van den Heuvel, 2013; Roberts et al., 2017), but such approaches would minimize interindividual variability in network binary network topology and thus meaning there would…”
Abnormal wiring of the structural connectome in adults with ADHD
Tolonen, T., Roine, T., Alho, K., Leppämäki, S., Tani, P., Koski, A., Laine, M., & Salmi, J. (2023) · Network Neuroscience · doi:10.1162/netn_a_00326 · Cited by 10
McPherson, B., & Pestilli, F. (2021) · Communications Biology · doi:10.1038/s42003-021-02451-0 · Cited by 7
Predicted disconnectome associated with progressive periventricular white matter ischemia
Li, Z., Dolui, S., Habes, M., Bassett, D. S., Wolk, D. A., & Detre, J. A. (2021) · Cerebral Circulation - Cognition and Behavior · doi:10.1016/j.cccb.2021.100022 · Cited by 6
“For the network analysis, a group representative structural connectivity matrix mask was created by retaining edges with the 10% strongest consistency estimates [44], excluding edges between physically nearby ROIs (<20 mm) [45].”
MethodGenetic and neuroanatomical support for functional brain network dynamics in epilepsyPreprint
Reddy, P. G., Betzel, R. F., Khambhati, A. N., Shah, P., Kini, L. G., Litt, B., Lucas, T. H., Davis, K. A., & Bassett, D. S. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/412395 · Cited by 5
“This type of non-uniform consistency thresholding has been shown to be superior to other, more commonly used forms of thresholding [66].”
MethodA Symmetry-Based Method to Infer Structural Brain Networks from Probabilistic Tractography Data
Shadi, K., Bakhshi, S., Gutman, D. A., Mayberg, H. S., & Dovrolis, C. (2016) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2016.00046 · Cited by 9
Robinson, P. A. (2025) · Physical review. E · doi:10.1103/physreve.111.014404 · Cited by 4
Xu, X., Yang, H., Cong, J., Xu, H., Kai, J., Zhao, S., Li, Y., Shou, H., Wang, K., Sydnor, V. J., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-73072-6 · Cited by 12
Topological cluster statistic (TCS): Toward structural connectivity–guided fMRI cluster enhancement
Sina Mansour, L., Seguin, C., Winkler, A. M., Noble, S., & Zalesky, A. (2024) · Network Neuroscience · doi:10.1162/netn_a_00375 · Cited by 3
“While we maintain connectome density by averaging individual network densities, as recommended previously (Betzel et al., 2019; Roberts et al., 2017), the density threshold serves as a tunable parameter influencing TCS performance.”
BackgroundMethodChai, Y., Park, H. R., Jo, H., Seo, M. Y., Kim, H. Y., Joo, E. Y., & Kim, H. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1221290 · Cited by 7
“While the application of thresholds to connectivity matrices has been a common practice in network studies to reduce false positive connections (de Reus and van den Heuvel, 2013; Roberts et al., 2017; Buchanan et al., 2020), note that we employed a deterministic tensor-based tracking approach.”
BackgroundRobalo, B. M. D. B., Luca, A. D., Chen, C., Dewenter, A., Duering, M., Hilal, S., Koek, H. L., Kopczak, A., Lam, B. Y. K., Leemans, A., et al. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.103217 · Cited by 6
“Thresholding was performed on the group-level probability matrix by removing connections with low probability until a fixed network density of 15 % was achieved (de Reus & van den Heuvel, 2013; Roberts et al., 2017).”
InfluentialBetzel, R. F., Griffa, A., Hagmann, P., & Mišić, B. (2018) · bioRxiv · doi:10.1101/412346 · Cited by 6
Baum, G. L., Roalf, D., Cook, P. A., Ciric, R., Rosen, A. F. G., Xia, C., Elliot, M., Ruparel, K., Verma, R., Tunç, B., et al. (2017) · bioRxiv · doi:10.1101/185397 · Cited by 6
“36%), edge consistency was defined by the coefficient of variation for each edge weight across subjects (Roberts et al., 2017).”
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Seguin, C., L., S. M., Betzel, R., Chumin, E., Puxeddu, M. G., Lv, J.-L., Parkes, L., Fitzgerald, P. B., Cash, R. F. H., & Zalesky, A. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02248-6 · Cited by 5
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Yang, H., Wu, G., Li, Y., Xu, X., Cong, J., Xu, H., Ma, Y., Yang, L., Chen, R., Pines, A. R., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2420228122 · Cited by 22
“A consistency - based thresholding method was applied to reduce spurious connections (73), using the 75th percentile for edge weight coefficient of variation (52).”
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Bobyleva, A., Gorsky, A., Nechaev, S., Valba, O. V., & Pospelov, N. (2025) · Network Neuroscience · doi:10.1162/netn_a_00439 · Cited by 3
“When analyzing structural connectomes, it is unlikely that all eigenmodes are completely delocalized, as this would imply that the system is ergodic, making it difficult to observe persistent activity.”
The role of epidemic spreading in seizure dynamics and epilepsy surgery
Millán, A. P., van Straaten, E. V., Stam, C., Nissen, I. A., Idema, S., Baayen, J. C., van Mieghem, P., & Hillebrand, A. (2022) · Network Neuroscience · doi:10.1101/2022.08.22.22279085 · Cited by 5
Distance‐dependent distribution thresholding in probabilistic tractography
Chang, Y., Halai, A. D., & Ralph, M. A. L. (2023) · Human Brain Mapping · doi:10.1002/hbm.26330 · Cited by 10
“…al., 2003, 2007; Parker et al., 2003; Smith et al., 2013), only a handful of studies have developed thresholding approaches that make the resulting connectivity close to the ‘ ground true ’ or comparable across the species (Betzel et al., 2019; de Reus & van den Heuvel, 2013; Roberts et al., 2017).”
BackgroundInfluentialDiscrete spectral eigenmode-resonance network of brain dynamics and connectivity
Robinson, P. A. (2021) · Physical review. E · doi:10.1103/physreve.104.034411 · Cited by 6
Robinson, P. A., Gao, X., & Han, Y. (2021) · Biological Cybernetics · doi:10.1007/s00422-021-00871-z · Cited by 5
“A final observation is that the corticocortical interareal axonal length distribution has an approximately exponential fall-off, with a characteristic range re (Braitenberg and Schüz 1998; Roberts et al. 2016; Deco et al. 2008; Roberts et al. 2017; Henderson and Robinson 2013, 2014; Ercsey-Ravasz et al. 2013); often s…”
BackgroundInfluentialBenchmarking overlapping community detection methods for applications in human connectomicsPreprint
Bryant, A. G., Jha, A., Agarwal, S., Cahill, P., Lam, B., Oldham, S., Arnatkevic̆iūtė, A., Fornito, A., & Fulcher, B. D. (2025) · bioRxiv · doi:10.1101/2025.03.19.643839 · Cited by 4
“A representative group-level connectome was calculated from the individual-level data using consistency-based thresholding [69], retaining only the weights from edges that ranked in the lowest 15% for weight coefficient of variation (CV) across the entire cohort.”
Localization of epileptogenic zone based on time-varying effective networks
Yin, N., Han, Y., Wang, L., Yang, F., Li, J., & Xu, G. (2024) · Epilepsy Research · doi:10.1016/j.eplepsyres.2024.107409 · Cited by 3
Cocaine Use Prediction With Tensor-Based Machine Learning on Multimodal MRI Connectome Data
Zhang, A. R., Bell, R. P., Chen, A., Tang, R., Hall, S. A., Chan, C. C. W., Al‐Khalil, K., & Meade, C. S. (2023) · Neural Computation · doi:10.1162/neco_a_01623 · Cited by 3
“The matrix itself is sparse, as is expected in the human brain with estimates of 30% connection density for white matter [40, 41].”
BackgroundLi, M., Habes, M., Grabe, H. J., Kang, Y., Qi, S., & Detre, J. A. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1237198 · Cited by 5
Millán, A. P., van Straaten, E. V., Stam, C., Nissen, I. A., Idema, S., van Mieghem, P., & Hillebrand, A. (2023) · Network Neuroscience · doi:10.1101/2023.03.16.23287370 · Cited by 4
“Recent studies have corroborated this behavior also in human structural connectivity (Deco & Kringelbach, 2020; Deco et al., 2021; Roberts, Perry, Roberts, Mitchell, & Breakspear, 2017), although the EDR cannot capture all details of white matter connectivity, as this is not isotropic (Betzel &…”
Deep learning-based Desikan-Killiany parcellation of the brain using diffusion MRI
Sadegheih, Y., & Merhof, D. (2025) · Scientific Reports · doi:10.1038/s41598-026-54446-8 · Cited by 3
Neuroanatomical pathways of TMS therapy for depression
Seguin, C., Mansour, S., Betzel, R., Chumin, E., Puxeddu, M. G., Lv, J.-L., Parkes, L., Cocchi, L., Fitzgerald, P. B., Cash, R. F. H., et al. (2025) · medRxiv · doi:10.1101/2025.02.10.25322034 · Cited by 3
“As detailed below, we used an established method to generate normative connectomes that mitigates tractography biases and filters out individual-level artefacts [24,25].”
Robalo, B. M. D. B., Vlegels, N., Leemans, A., Reijmer, Y. D., & Biessels, G. J. (2022) · Brain and Behavior · doi:10.1002/brb3.2523 · Cited by 3
“Other scan–rescan studies have examined thresholding approaches that are not based on edge-weights but rather on grouplevel consistency and is less biased towards the length of streamlines (Buchanan et al., 2020; Roberts et al., 2017).”
BackgroundResultMcPherson, B., & Pestilli, F. (2020) · doi:10.1101/2020.09.24.312090 · Cited by 3
“Connections present in less than half of the subjects were eliminated (see also Supplemental Figure 2a; [99]).”
BackgroundAutomatic discovery of disease subgroups by contrasting with healthy controls
Louiset, R., Duchesnay, É., Dufumier, B., Grigis, A., & Gori, P. (2026) · Data Mining and Knowledge Discovery · doi:10.1007/s10618-026-01233-8
Baird, M. E., Yang, J. Y., Seal, M. L., Beare, R. A., & Anderson, J. F. I. (2026) · Journal of Neurotrauma · doi:10.1177/08977151251407626 · Cited by 2
Yu, F., Wu, G., Li, W., Wang, Y., Wang, J., Wang, M., Kong, D., Yang, J. G., Ren, X., Yang, Z., et al. (2025) · BMC Medicine · doi:10.1186/s12916-025-04556-3 · Cited by 2
“To reduce false-positive connections that can arise from densely-seeded probabilistic tractography, we applied a consistency-based thresholding procedure [73, 74].”
Quinones, J. F., Gießing, C., Heep, A., & Hildebrandt, A. (2025) · Imaging Neuroscience · doi:10.1162/imag.a.928
“It requires the computation of a coefficient of variation across participants ( Roberts et al., 2017).”
InfluentialShen, R. S., Parker, D., Chen, A. A., Yerys, B. E., Tunç, B., Roberts, T. P. L., Shinohara, R. T., & Verma, R. (2025) · Human Brain Mapping · doi:10.1002/hbm.70256 · Cited by 2
“…connectomes derived from probabilistic tractography may include numerous spurious connections that could affect downstream analysis, we applied consistency-based thresholding (Roberts et al. 2017) to filter out spurious connections and retained only the most consistent ones across the population.”
Delayed threshold and spatial diffusion in k-core percolation induced by long-range connectivity
Zhang, X.-Y., Yao, Y. Y., Han, Z., & Yan, G. F. (2025) · Communications Physics · doi:10.1038/s42005-025-02171-5 · Cited by 2
“This trade-off between wiring cost and functional bene fi thasinspiredavarietyofspatiallyembeddednetworkmodelsthataim to capture the geometric constraints and connectivity patterns observed in empirical connectomes 14 – 17 .”
Song, L., Wang, P., Li, H., Weiss, P. H., Fink, G. R., Zhou, X., & Chen, Q. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad351 · Cited by 3
“In contrast, the average correlation matrix obtained from a larger number of participants can mitigate the potentially noisy connections (Roberts et al. 2017; Betzel et al. 2019).”
BackgroundStructural connectome of the human vestibular, pre-motor, and navigation network
Indovina, I., Riccelli, R., Passamonti, L., Maffei, V., Bosco, G., Lacquaniti, F., & Toschi, N. (2018) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2018.8512399 · Cited by 2
“Another approach, based on consinstency across subjects has been proposed [17].”
BackgroundGradients in excitability generate hippocampal waves and shape their interactions with cortex
Behler, A., Phogat, R., Jones, D. T., Shine, J. M., & Breakspear, M. (2026) · bioRxiv · doi:10.64898/2026.05.27.728116 · Cited by 1
“Connection strengths within each surface decrease according to an exponential-distance rule (EDR), as widely observed in tracer (Horv´at et al., 2016) and Magnetic Resonance Imaging (MRI)-based (Roberts et al., 2017) studies (Fig.”
Self-citationStructural connectome dimension shapes brain dynamics in health and disease
Barzon, G., Allegra, M., Aarabi, M., Pini, L., Domenico, M. D., Corbetta, M., & Suweis, S. (2026) · bioRxiv · doi:10.1101/2025.06.30.662336 · Cited by 1
“The dense connectomes were then thresholded to retain the top 20% of connections, to improve the signal-to-noise ratio [99] and to ensure that the two groups had the same network density.”
Structural network topology and cognitive control in very preterm born young adults
Marek, M. J., Dieter Wolke, C., Sorg, C., Wendt, J., Menegaux, A., Hedderich, D. M., Bartmann, P., Burkhardt, M., Hildebrandt, A., & Heep, A. (2026) · NeuroImage Clinical · doi:10.1016/j.nicl.2026.103952 · Cited by 1
“We normalised edge weights by dividing the raw streamline count by tract length (Roberts et al., 2017).”
Xu, X.-Y., Fu, Z., Xu, H.-S., Zhang, K., Yang, H., Li, Y., Zhao, Y.-L., Zheng, X., Keller, A. S., Xu, T., et al. (2025) · bioRxiv · doi:10.1101/2025.11.20.689391 · Cited by 1
“To reduce false-positive streamlines in global tractography 65 , we applied a consistency-based thresholding method 66 on the region-level connectome.”
Wu, F., Wu, G., Dong, P., Deng, J., Gao, X., Li, P., Yuan, J., & Sun, H. (2025) · Scientific Reports · doi:10.1038/s41598-025-18003-z · Cited by 1
“To equalise graph density across participants, we applied proportional thresholds from 0.05 to 0.15 in 0.025 increments, retaining the strongest 5–15% of edges 46 .”
InfluentialOverlooked weak structural connections support human cognition under nonlinear connectome scaling
Wang, R., Chang, Z., Liu, X.-C., Kristanto, D., Gärtner, E., Liu, X.-Y., Liu, M.-X., Wu, Y., Lui, M., & Zhou, C. (2025) · doi:10.48550/arxiv.2505.24125 · Cited by 1
Ekenze, O. S., Seiler, S., Pinheiro, A., DeCarli, C. S., Parva, P., Habes, M., Charidimou, A., Maillard, P., Beiser, A., Seshadri, S. S., et al. (2024) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2025.02.007 · Cited by 2
Wang, Y., Jin, Z.-S., Huyang, S., Lian, Q., & Wu, D.-X. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70174 · Cited by 1
Alshehri, A., Koussis, N. C., Al‐iedani, O., Khormi, I. M., Lea, R. A., Ramadan, S. A., & Lechner‐Scott, J. (2024) · NMR in Biomedicine · doi:10.1002/nbm.5119 · Cited by 1
“37 Our results were also robust across different thresholds (see Figure S1 ).”
BackgroundResultSchulte, J., Senden, M., Deco, G., Kobeleva, X., & Zamora‐López, G. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.07.548139 · Cited by 1
“Since one of the limitations of tractography is that it overestimates shorter connections, the hard thresholding favours short-range links in detriment of long-range ones (Betzel et al., 2019; Roberts et al., 2017).”
BackgroundCoelho, A., Magalhães, R. J. D. S., Moreira, P. S., Amorim, L., Portugal‐Nunes, C., Castanho, T. C., Santos, N. C., Sousa, N., & Fernandes, H. M. (2022) · Human Brain Mapping · doi:10.1002/hbm.25773 · Cited by 3
Deterministic Tractography Analysis of Rat Brain Using SIGMA Atlas in 9.4T MRI
Im, S.-J., Suh, J., Shim, J., & Baek, H. (2021) · Brain Sciences · doi:10.3390/brainsci11121656 · Cited by 2
Small-World Propensity Reveals the Frequency Specificity of Resting State Networks
Iandolo, R., Semprini, M., Buccelli, S., Barban, F., Zhao, M., Samogin, J., Bonassi, G., Avanzino, L., Mantini, D., & Chiappalone, M. (2020) · IEEE Open Journal of Engineering in Medicine and Biology · doi:10.1109/ojemb.2020.2965323 · Cited by 6
Mangalam, M., Schlattmann, B., Deans, C. F., & Wellsandt, E. (2026) · Frontiers in Network Physiology · doi:10.3389/fnetp.2026.1916345
Ng, J., Feusner, J. D., & Hawco, C. S. (2026) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2026.1920417
“In the main analysis, we retained 50% of connection weights with the lowest variability across participants (Roberts et al., 2017).”
Debona, R., & Walz, R. (2026) · bioRxiv · doi:10.64898/2026.08.08.743682
“Consistency-based thresholding avoids the problem by a different route (Roberts et al. 2017); supply matching offers a check applicable to existing pipelines unchanged.”
Griffiths phase in clique percolation in random geometric graphs
Tiselko, V., Valba, O. V., & Gorsky, A. (2026) · doi:10.48550/arxiv.2608.01487
Ou, L., Yang, J., Shi, L.-F., Wang, X.-G., Ou, P.-L., Huang, Y.-H., Chen, H., Li, C., Fan, R., Wang, B.-J., et al. (2026) · Movement Disorders · doi:10.1002/mds.70402
“To exclude false-positive structural connections, consistency-based thresholding 31 was applied using a 20th percentile coef fi cient of variation threshold.”
Song, Y., Huang, B., Wu, J., Lin, J., Xin, K., Gao, B., Kemp, G. J., Guo, B., & Gong, Q. (2026) · Psychological Medicine · doi:10.1017/s0033291726104838
“We used a consistency-based threshold to reduce the effect of spurious connectivities by measuring the coefficient of variation (CV) across subjects (Roberts et al., 2017), removing the top 25% of SC with the largest CV (Baum et al., 2020).”
Yan, T., Wang, K., Han, Z., Ma, Y., Wang, X. G., Zhang, K., Yang, G., & Liu, T. (2026) · BMC Medicine · doi:10.1186/s12916-026-04919-4
“Second, a group-representative connec-tome was derived by selecting the top 30% of edges with the lowest coefficients of variation across participants [54, 55].”
Structure-function coupling in the human brainstem
Farahani, A., Koley, S., Hansen, J. Y., Hannanu, F. F., García-Gomar, M., Singh, K., Cauzzo, S., Milisav, F., Liu, Z.-Q., Bazinet, V., et al. (2026) · bioRxiv · doi:10.64898/2026.04.05.716603
“1a) was constructed using a distance-dependent consensus thresholding approach 58,176,177 .”
General cognitive function and the brain’s structural connectome
Buchanan, C. R., Moodie, J., Batziou, V., Conole, E., Maniega, S. M., Harris, M., Yeung, H.-W., Corley, J., Liewald, D., Redmond, P., et al. (2026) · bioRxiv · doi:10.64898/2026.03.30.715223
“First, consistency-thresholding 63 was independently performed for each cohort, retaining the top 30% most consistent connections based on findings from a large single-scanner study 50 .”
InfluentialShao, Z., Du, Z., Song, Q., Liu, S., Cai, S., Liu, D., & Yuan, K. (2026) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2026.03.025
Alterations of white matter connectivity in alopecia areata patients
Yang, F., Liao, W., & Duan, Y. (2026) · Brain Imaging and Behavior · doi:10.1007/s11682-026-01123-z
“The selection of FN > 3 as the effective connection cri - terion was based on methodological rigor: it aims to filter noise, reduce false positives, and enhance network reliability (Bauer et al., 2017; Buchanan et al., 2020; Roberts et al., 2017; Yeh et al., 2021).”
Pandian, S., & Mohana, N. (2026) · Results in Engineering · doi:10.1016/j.rineng.2026.109609
Keyvanfard, F. (2026) · Basic and Clinical Neuroscience Journal · doi:10.32598/bcn.2026.3928.3
“Furthermore, the effect of other thresholding approaches, such as consistency-thresholding (Roberts et al., 2017), can also be investigated.”
Hub nodes integrate memory and prediction in reservoir computing: insights from graphs to brains
He, M., Li, Q., Yan, Z., Gao, J., & Xiao, J. (2026) · Nonlinear dynamics · doi:10.1007/s11071-025-12162-4
Quantifying biases in reconstructed brain networks
Corso, A., d’Andrea, V., & Domenico, M. D. (2026) · Communications Physics · doi:10.1038/s42005-025-02460-z · Cited by 1
“…(see Supplementary Algorithm S-1), we reconstruct binary adjacency matrices of structural networks using a consistency-based thresholding approach 33 (see Supplementary Algorithm S-2), while for functional networks we use the percolation threshold approach 34 (see Supplementary Algorithm S-3).”
LearnAD: Learning Interpretable Rules for Brain Networks in Alzheimer's Disease Classification
Andrews, T., Law, M., Ahmadi-Abhari, S., & Russo, A. (2025) · arXiv.org · doi:10.48550/arxiv.2601.00877
“Modern neuroimaging techniques are unable to completely remove spurious brain connections, resulting in noisy connectomes [32].”
The role of white matter myelin in structural-functional network coupling
Nelson, M. C., Lu, W. D., Leppert, I. R., Shafiei, G., Hansen, H. A., Rowley, C. D., Mišić, B., & Tardif, C. L. (2026) · Communications Biology · doi:10.1038/s42003-026-09813-6 · Cited by 5
Ferritto, C., Lioi, G., Jonin, P., & Coloigner, J. (2025) · European Signal Processing Conference (EUSIPCO) · doi:10.23919/eusipco63237.2025.11226187
“Both connectivity matrices were then thresholded using a consistency-based method to retain only the top 25% most consistent edges [29].”
Ma, M. K.-H., Fong, M. C., & Wang, W. Y. (2025) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc58623.2025.11251614
“While thresholding was initially believed to be essential for revealing clear small-world topologies, the utility of weak connections has been increasingly recognized as they reflect unique individual differences [15], [18].”
Schulte, J., Senden, M., Deco, G., Kobeleva, X., & Zamora‐López, G. (2025) · arXiv (Cornell University) · doi:10.48550/arxiv.2505.22893
“Since one of the limitations of tractography is that it overestimates shorter connections, the hard thresholding favours short-range links in detriment of long-range ones 80,81 .”
Constructing representative group networks from tractography: lessons from a dynamical approach
Kritikaki, E., Mancini, M., Kyriazis, D. A., Sigala, N., Farmer, S. F., & Luc Berthouze, A. (2024) · Frontiers in Network Physiology · doi:10.3389/fnetp.2024.1457486
Structure-Function Coupling in the Human Connectome with Hypergraph Neural Networks
Yuan, Y., & Wang, Y. (2024) · International Conference on Signal Processing · doi:10.1109/icsp62129.2024.10846404
“To obtain reliable connectivity between brain regions, we adopted a group-consistency thresh-olding method [25] to remove spurious connections in the probabilistic tracking network.”
Quantifying sex differences in brain network topology by aggregating nodal centrality rankings
Chen, W., Zhan, L., Luo, Y., Qiu, J., & Jia, T. (2024) · doi:10.48550/arxiv.2410.05923
“First, we use the Power Atlas and Pearson correlation to construct brain networks, but recent research show that thresholding and weighting schemes [7, 46, 48] and the number of nodes and edges [40] significantly impact network topology.”
MethodWang, Y., Jin, Z.-S., Huyang, S., Lian, Q., & Wu, D.-X. (2024) · bioRxiv · doi:10.1101/2024.02.04.578219
“Further, a consistency-based method (coefficient of variation of each edge) was applied (Roberts et al., 2017) to reduce spurious connections induced by probabilistic tractography because the criteria contribute to retain consistent both short-and long-range connections across subject.”
MethodChen, P., Yang, H., Zheng, X., Jia, H., Hao, J., Xu, X.-Y., Li, C., He, X.-S., Chen, R., Okubo, T. S., et al. (2023) · bioRxiv · doi:10.1101/2023.11.22.568257
“To address potential issues with spurious SC edges arising from probabilistic tractography 82 , we adopted a group-consistency approach as in previous studies 10,83 .”
The specificity of different-distance connections in human structural connectomesPreprint
Yang, Y., Zheng, Y., Zhen, Y., Tang, S., Zheng, H., & Zheng, Z. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.09.499310
“A consensus adjacency matrix that preserved the density and the edge-length distribution of the individual participant matrices [35, 49, 25] was then estimated using a group-consensus approach [49, 50, 51].”
MethodDisconnectome Associated with Progressive Ischemic Periventricular White Matter LesionsPreprint
Li, Z., Dolui, S., Habes, M., Bassett, D. S., Wolk, D. A., & Detre, J. A. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2019.12.24.888081
Madole, J. W., Ritchie, S. J., Cox, S. R., Buchanan, C. R., Hernández, M. V., Maniega, S. M., Wardlaw, J. M., Harris, M. A., Bastin, M. E., Deary, I. J., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2019.12.13.875559
Váša, F. (2018) · doi:10.17863/cam.25157
“These approaches, initially developed in the context of sparse connectomes obtained from deterministic tractography, have been generalised to dense connectomes from probabilistic tractography by retaining consistently strong (rather than consistently present) edges (Roberts et al., 2017).”
BackgroundMultifactorial Dynamics of White Matter Connectivity During AdolescencePreprint
Tunç, B., Parker, D., Shinohara, R. T., Elliott, M. A., Ruparel, K., Gur, R. E., Gur, R. C., & Verma, R. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/215152
“In order to demonstrate the robustness of the reported results to such confounding factors, we used consistency based thresholding [27] to prune possibly spurious connections and repeated our experiments with different network density (threshold) levels.”
MethodStructural connectomics: Where we are and where we should be?
Verma, R., & Osmanlıoğlu, Y. (2021) · Advances in magnetic resonance technology and applications · doi:10.1016/b978-0-12-816633-8.00011-9
Metadata
- Authors
- Roberts, J. A., Perry, A., Roberts, G., Mitchell, P. B., & Breakspear, M.
- Affiliations
- QIMR Berghofer Medical Research Institute (AU)
- Black Dog Institute (AU)
- Corresponding author
- Roberts, James A.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2017-01
- Volume
- 145
- Issue
- Pt A
- Pages
- 118-129
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2523692751
- Cited by
- 189
- References
- 50
- Citations by year
- 2026: 18 · 2025: 19 · 2024: 19 · 2023: 23 · 2022: 25 · 2021: 20 · 2020: 19 · 2019: 17 · 2018: 20 · 2017: 8
- FWCI
- 13.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Health and Medical Research Council (1037196)
- Australian Research Council (CE140100007)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Physical Sciences › Physics and Astronomy › Statistical and Nonlinear Physics › Complex Network Analysis Techniques
- Keywords
- human connectome, probabilistic tractography, long-distance connections, false positives, white matter connectivity
- MeSH terms
- Adolescent, Adult, Animals, Female, Humans, Image Processing, Computer-Assisted, Male, Nerve Net, Neural Pathways, Young Adult, Diffusion Tensor Imaging, Connectome, White Matter
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