What affects detectability of lesion-deficit relationships in lesion studies?
Open accessAbstract
Elucidating the brain basis for psychological processes and behavior is a fundamental aim of cognitive neuroscience. The lesion method, using voxel-based statistical analysis, is an important approach to this goal, identifying neural structures that are necessary for the support of specific mental operations, and complementing the strengths of functional imaging techniques. Lesion coverage in a population is by nature spatially heterogeneous and biased, systematically affecting the ability of lesion-deficit correlation methods to detect and localize functional associations. We have developed a simulator that allows investigators to model parameters in a lesion-deficit study and characterize the statistical bias in lesion deficit detection coverage that will result from specific assumptions. We used the simulator to assess the signal detection properties and localization accuracy of standard lesion-deficit correlation methods, under a simple truth model - that a critical region of interest (CR), when damaged, gives rise to a deficit. We considered voxel-based lesion-symptom mapping (VLSM) and proportional MAP-3 (PM3). Using regression analysis, we examined if the pattern of outcome statistics can be explained by simulation parameters, factors that are inherent to anatomic parcels, and lesion coverage of the population, which consisted of a representative sample of 351 subjects drawn from the Iowa Patient Registry. We examined the effect of using nonparametric versus parametric statistics to obtain thresholded maps and the effect of correcting for multiple comparisons using false discovery rate or cluster-based correction. Our results, which are derived from samples of realistic lesions, indicate that even a simple truth model yields localization errors that are systematic and pervasive, averaging 2 cm in the standard anatomic space, and tending to be directed towards areas of greater anatomic coverage. This displacement positions the center of mass of the detected region in a different anatomical region 87% of the time. This basic result is not affected by the choice of PM3 vs VLSM as the fundamental approach, nor is localization error ameliorated by incorporation of lesion size as a covariate in the VLSM approach, or by data distribution-driven approaches to controlling multiple spatial comparisons (false discovery rate or cluster-based correction approaches). Our simulations offer a quantitative basis for interpreting lesion studies in cognitive neuroscience. We suggest ways in which lesion simulation and analysis frameworks could be productively extended.
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?
It is difficult to determine which part of the lesion site is driving observed behavioural effects.
“In all cases, it is therefore difficult to determine which part of the lesion site is driving the observed behavioural effects”
From Damage to Broca’s area does not contribute to long-term speech production outcome after stroke (2021) · cites this paper as Inoue et al., 2014
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
Desikan, R. S., Ségonne, F., Fischl, B., Quinn, B. T., Dickerson, B. C., Blacker, D., Buckner, R. L., Dale, A. M., Maguire, R. P., Hyman, B. T., et al. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.021 · Cited by 13,324 · see citing works
Voxel-based lesion-symptom mapping
Bates, E., Wilson, S. M., Saygin, A. P., Dick, F., Sereno, M. I., Knight, R. T., & Dronkers, N. F. (2003) · Nature Neuroscience · doi:10.1038/nn1050 · Cited by 1,457 · see citing works
Improving Lesion-Symptom Mapping
Rorden, C., Karnath, H., & Bonilha, L. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.7.1081 · Cited by 1,347 · see citing works
Adolphs, R., Damasio, H., Tranel, D., Cooper, G., & Damasio, A. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02683.2000 · Cited by 1,095 · see citing works
Lesion analysis in neuropsychology
Damásio, H., & Damásio, A. R. (1989) · Oxford University Press eBooks · Cited by 881 · see citing works
Neural systems behind word and concept retrieval
Damasio, H., Tranel, D., Grabowski, T. J., Adolphs, R., & Damásio, A. R. (2004) · Cognition · doi:10.1016/j.cognition.2002.07.001 · Cited by 762 · see citing works
A neural basis for the retrieval of conceptual knowledge
Tranel, D., Damásio, H., & Damásio, A. R. (1997) · Neuropsychologia · doi:10.1016/s0028-3932(97)00085-7 · Cited by 633 · see citing works
The Anatomy of Spatial Neglect based on Voxelwise Statistical Analysis: A Study of 140 Patients
Karnath, H. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh076 · Cited by 573 · see citing works
Lesion Analysis in Neuropsychology
Poeck, K. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90028-9 · Cited by 528 · see citing works
NEURAL CORRELATES OF CONCEPTUAL KNOWLEDGE FOR ACTIONS
Tranel, D., Kemmerer, D. L., Adolphs, R., Damásio, H., & Damásio, A. R. (2003) · Cognitive Neuropsychology · doi:10.1080/02643290244000248 · Cited by 340 · see citing works
Human brain lesion-deficit inference remapped
Mah, Y.-H., Husain, M., Rees, G., & Nachev, P. (2014) · Brain · doi:10.1093/brain/awu164 · Cited by 336 · see citing works
Brainvox: An Interactive, Multimodal Visualization and Analysis System for Neuroanatomical Imaging
Frank, R. J., Damasio, H., & Grabowski, T. J. (1997) · NeuroImage · doi:10.1006/nimg.1996.0250 · Cited by 273 · see citing works
A Neural Basis for the Retrieval of Words for Actions
Tranel, D., Adolphs, R., Damásio, H., & Damásio, A. R. (2001) · Cognitive Neuropsychology · doi:10.1080/02643290126377 · Cited by 269 · see citing works
Kemmerer, D. L., Rudrauf, D., Manzel, K., & Tranel, D. (2010) · Cortex · doi:10.1016/j.cortex.2010.11.001 · Cited by 268 · see citing works
Three-dimensional In Vivo Mapping of Brain Lesions in Humans
Damasio, H., & Frank, R. (1992) · Archives of Neurology · doi:10.1001/archneur.1992.00530260037016 · Cited by 240 · see citing works
Neural systems for recognition of emotional prosody: A 3-D lesion study.
Adolphs, R., Damásio, H., & Tranel, D. (2002) · Emotion · doi:10.1037/1528-3542.2.1.23 · Cited by 237 · see citing works
Damage to Ventromedial Prefrontal Cortex Impairs Judgment of Harmful Intent
Young, L., Bechara, A., Tranel, D., Damásio, H., HAUSER, M. D., & Damásio, A. R. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.003 · Cited by 224 · see citing works
An evaluation of traditional and novel tools for lesion behavior mapping
Rorden, C., Fridriksson, J., & Karnath, H. ‐. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.031 · Cited by 161 · see citing works
Degenerate neuronal systems sustaining cognitive functions
Noppeney, U., Friston, K. J., & Price, C. J. (2004) · Journal of Anatomy · doi:10.1111/j.0021-8782.2004.00343.x · Cited by 153 · see citing works
Damage to the default mode network disrupts autobiographical memory retrieval
Philippi, C. L., Tranel, D., Duff, M. C., & Rudrauf, D. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu070 · Cited by 146 · see citing works
Tranel, D., Vianna, E., Manzel, K. W., Damásio, H., & Grabowski, T. J. (2008) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803390802317542 · Cited by 125 · see citing works
Inappropriate usage of the Brunner–Munzel test in recent voxel-based lesion-symptom mapping studies
Medina, J., Kimberg, D. Y., Chatterjee, A. K., & Coslett, H. B. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.09.016 · Cited by 109 · see citing works
Disconnection's renaissance takes shape: Formal incorporation in group-level lesion studies
Rudrauf, D., MEHTA, S., & Grabowski, T. J. (2008) · Cortex · doi:10.1016/j.cortex.2008.05.005 · Cited by 92 · see citing works
Does the Clock Drawing Test have focal neuroanatomical correlates?
Tranel, D., Rudrauf, D., Vianna, E., & Damásio, H. (2008) · Neuropsychology · doi:10.1037/0894-4105.22.5.553 · Cited by 78 · see citing works
Friston, K. J., & Price, C. J. (2011) · Cognitive Neuropsychology · doi:10.1080/02643294.2011.558835 · Cited by 61 · see citing works
Kinkingnéhun, S., Emmanuelle Volle, C., Pélégrini‐Issac, M., Golmard, J., Lehéricy, S., Boisguéheneuc, F. D., Zhang-Nunes, S., Sosson, D., Duffau, H., Samson, Y., et al. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.06.027 · Cited by 48 · see citing works
Caviness, V. S., Makris, N., Montinaro, E., Sahin, N. T., Bates, J. F., Schwamm, L. H., Caplan, D. N., & Kennedy, D. N. (2002) · Stroke · doi:10.1161/01.str.0000036084.82955.c7 · Cited by 11 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Improved accuracy of lesion to symptom mapping with multivariate sparse canonical correlations
Pustina, D., Avants, B., Faseyitan, O. K., Medaglia, J. D., & Coslett, H. B. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.08.027 · Cited by 183 · see citing works
Mapping human brain lesions and their functional consequences
Karnath, H., Sperber, C., & Rorden, C. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.10.028 · Cited by 176 · see citing works
Damage to Broca’s area does not contribute to long-term speech production outcome after stroke
Gajardo-Vidal, A., Lorca-Puls, D. L., team, P., Warner, H., Pshdary, B., Crinion, J. T., Leff, A. P., Hope, T. M. H., Geva, S., Seghier, M. L., et al. (2021) · Brain · doi:10.1093/brain/awaa460 · Cited by 150 · see citing works
The neuroanatomical–functional paradox in spinal cord injury
Fouad, K., Popovich, P. G., Kopp, M. A., & Schwab, J. M. (2020) · Nature Reviews Neurology · doi:10.1038/s41582-020-00436-x · Cited by 160 · see citing works
Impact of correction factors in human brain lesion‐behavior inference
Sperber, C., & Karnath, H. (2017) · Human Brain Mapping · doi:10.1002/hbm.23490 · Cited by 136 · see citing works
A hitchhiker's guide to lesion‐behaviour mapping
de Haan, B., & Karnath, H. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.10.021 · Cited by 109 · see citing works
Connectome-based lesion-symptom mapping (CLSM): A novel approach to map neurological function
Gleichgerrcht, E. L., Fridriksson, J., Rorden, C., & Bonilha, L. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.08.018 · Cited by 105 · see citing works
Post-stroke outcomes predicted from multivariate lesion-behaviour and lesion network mapping
Bowren, M. D., Bruss, J., Manzel, K. W., Edwards, D. J., Liu, C. Y., Corbetta, M., Tranel, D., & Boes, A. D. (2022) · Brain · doi:10.1093/brain/awac010 · Cited by 110 · see citing works
Thye, M. D., & Mirman, D. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.10.017 · Cited by 99 · see citing works
Ten problems and solutions when predicting individual outcome from lesion site after stroke
Price, C. J., Hope, T. M. H., & Seghier, M. L. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.08.006 · Cited by 97 · see citing works
Predicting language outcomes after stroke: Is structural disconnection a useful predictor?
Hope, T. M. H., Leff, A. P., & Price, C. J. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.03.037 · Cited by 85 · see citing works
The impact of sample size on the reproducibility of voxel-based lesion-deficit mappings
Lorca‐Puls, D. L., Gajardo‐Vidal, A., White, J., Seghier, M. L., Leff, A. P., Green, D. W., Crinion, J., Ludersdorfer, P., Hope, T. M. H., Bowman, H., et al. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.03.014 · Cited by 82 · see citing works
Ivanova, M. V., Herron, T. J., Dronkers, N. F., & Baldo, J. V. (2020) · Human Brain Mapping · doi:10.1002/hbm.25278 · Cited by 79 · see citing works
An empirical evaluation of multivariate lesion behaviour mapping using support vector regression
Sperber, C., Wiesen, D., & Karnath, H. (2018) · Human Brain Mapping · doi:10.1002/hbm.24476 · Cited by 74 · see citing works
On the validity of lesion-behaviour mapping methods
Sperber, C., & Karnath, H. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.07.035 · Cited by 73 · see citing works
The dimensionalities of lesion-deficit mapping
Xu, T., Jha, A., & Nachev, P. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.09.007 · Cited by 55 · see citing works
Dronkers, N. F., Ivanova, M. V., & Baldo, J. V. (2017) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617717001126 · Cited by 55 · see citing works
Sperber, C. (2020) · Cortex · doi:10.1016/j.cortex.2020.01.004 · Cited by 47 · see citing works
Mapping correlated neurological deficits after stroke to distributed brain networks
Siegel, J. S., Shulman, G. L., & Corbetta, M. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02525-7 · Cited by 44 · see citing works
Lesion-symptom mapping in the study of spoken language understanding
Wilson, S. M. (2016) · Language Cognition and Neuroscience · doi:10.1080/23273798.2016.1248984 · Cited by 44 · see citing works
Mapping psycholinguistic features to the neuropsychological and lesion profiles in aphasia
Alyahya, R. S. W., Halai, A. D., Conroy, P., & Ralph, M. A. L. (2019) · Cortex · doi:10.1016/j.cortex.2019.12.002 · Cited by 40 · see citing works
Toba, M. N., Godefroy, O., Rushmore, J., Zavaglia, M., Maatoug, R., Hilgetag, C. C., & Valero‐Cabré, A. (2019) · Brain · doi:10.1093/brain/awz343 · Cited by 39 · see citing works
Evaluating the granularity and statistical structure of lesions and behaviour in post-stroke aphasia
Zhao, Y., Halai, A. D., & Ralph, M. A. L. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa062 · Cited by 39 · see citing works
Graph lesion-deficit mapping of fluid intelligence
Cipolotti, L., Ruffle, J. K., Mole, J. A., Xu, T., Hyare, H., Shallice, T., Chan, E., & Nachev, P. (2022) · Brain · doi:10.1093/brain/awac304 · Cited by 51 · see citing works
The cognitive and neural underpinnings of discourse coherence in post-stroke aphasia
Alyahya, R. S. W., Ralph, M. A. L., Halai, A. D., & Hoffman, P. (2022) · Brain Communications · doi:10.1093/braincomms/fcac147 · Cited by 32 · see citing works
How distributed processing produces false negatives in voxel-based lesion-deficit analyses
Gajardo‐Vidal, A., Lorca‐Puls, D. L., Crinion, J., White, J., Seghier, M. L., Leff, A. P., Hope, T. M. H., Ludersdorfer, P., Green, D. W., Bowman, H., et al. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.02.025 · Cited by 32 · see citing works
Maffei, V., Mazzarella, E., Piras, F., Spalletta, G., Caltagirone, C., Lacquaniti, F., & Daprati, E. (2016) · Cortex · doi:10.1016/j.cortex.2016.02.004 · Cited by 29 · see citing works
Exoskeleton-Robot Assisted Therapy in Stroke Patients: A Lesion Mapping Study
Cerasa, A., Pignolo, L., Gramigna, V., Serra, S., Olivadese, G., Rocca, F., Perrotta, P., Dolce, G., Quattrone, A., & Tonin, P. (2018) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2018.00044 · Cited by 29 · see citing works
Lesion mapping in neuropsychological research: A practical and conceptual guide
Moore, M. J., Demeyere, N., Rorden, C., & Mattingley, J. B. (2023) · Cortex · doi:10.1016/j.cortex.2023.10.001 · Cited by 28 · see citing works
Arnoux, A., Toba, M. N., Duering, M., Diouf, M., Daouk, J., Constans, J., Puy, L., Barbay, M., & Godefroy, O. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.10.003 · Cited by 26 · see citing works
The strange role of brain lesion size in cognitive neuropsychology
Sperber, C. (2021) · Cortex · doi:10.1016/j.cortex.2021.11.005 · Cited by 26 · see citing works
Mapping spoken language and cognitive deficits in post-stroke aphasia
Akkad, H., Hope, T. M. H., Howland, C., Ondobaka, S., Pappa, K., Nardo, D., Duncan, J., Leff, A. P., & Crinion, J. (2023) · NeuroImage Clinical · doi:10.1016/j.nicl.2023.103452 · Cited by 25 · see citing works
Achilles, E. I. S., Weiss, P. H., Fink, G. R., Binder, E., Price, C. J., & Hope, T. M. H. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.08.036 · Cited by 24 · see citing works
Multivariate Approaches to Understanding Aphasia and its Neural Substrates
Wilson, S. M., & Hula, W. D. (2019) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-019-0971-6 · Cited by 23 · see citing works
Multi-model mapping of phonemic fluency
Lisa Cipolotti, A., Xu, T., Harry, B. B., Mole, J. A., Lakey, G., Shallice, T., Chan, E., & Nachev, P. (2021) · Brain Communications · doi:10.1093/braincomms/fcab232 · Cited by 22 · see citing works
Lesion symptom mapping at the regional level in patients with a meningioma.
Baene, W. D., Rijnen, S. J. M., Gehring, K., Meskal, I., Rutten, G.-J. M., & Sitskoorn, M. M. (2018) · Neuropsychology · doi:10.1037/neu0000490 · Cited by 22 · see citing works
Lorca‐Puls, D. L., Gajardo‐Vidal, A., Seghier, M. L., Leff, A. P., Sethi, V., Prejawa, S., Hope, T. M. H., Devlin, J. T., & Price, C. J. (2017) · Brain · doi:10.1093/brain/awx087 · Cited by 19 · see citing works
Post‐stroke cognitive deficits rarely come alone: Handling co‐morbidity in lesion‐behaviour mapping
Sperber, C., Nolingberg, C., & Karnath, H. (2019) · Human Brain Mapping · doi:10.1002/hbm.24885 · Cited by 19 · see citing works
Wilmskoetter, J., Fridriksson, J., Gleichgerrcht, E. L., Stark, B. C., Gaizo, J. D., Hickok, G. S., Vaden, K. I., Hillis, A. E., Rorden, C., & Bonilha, L. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101961 · Cited by 19 · see citing works
Voxel-Based Lesion Symptom Mapping
Baldo, J. V., Ivanova, M. V., Herron, T. J., Wilson, S. M., & Dronkers, N. F. (2022) · Neuromethods · doi:10.1007/978-1-0716-2225-4_5 · Cited by 19 · see citing works
Metabolic lesion-deficit mapping of human cognition
Jha, A., Teotónio, R., Smith, A.-L., Bomanji, J. B., Dickson, J. C., Diehl, B., Duncan, J. S., & Nachev, P. (2020) · Brain · doi:10.1093/brain/awaa032 · Cited by 17 · see citing works
Functional anomaly mapping reveals local and distant dysfunction caused by brain lesions
DeMarco, A. T., & Turkeltaub, P. E. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116806 · Cited by 16 · see citing works
Reprint of: Mapping human brain lesions and their functional consequences
Karnath, H., Sperber, C., & Rorden, C. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.01.044 · Cited by 14 · see citing works
Ground-truth validation of uni- and multivariate lesion inference approaches
Zavaglia, M., Malherbe, C., Schlaadt, S., Nachev, P., & Hilgetag, C. C. (2024) · Brain Communications · doi:10.1093/braincomms/fcae251 · Cited by 12 · see citing works
Interpreting and validating complexity and causality in lesion-symptom prognoses
Seghier, M. L., & Price, C. J. (2023) · Brain Communications · doi:10.1093/braincomms/fcad178 · Cited by 9 · see citing works
Ofir, S., Meilijson, I., Frenkel‐Toledo, S., & Soroker, N. (2022) · Human Brain Mapping · doi:10.1002/hbm.26105 · Cited by 7 · see citing works
Stable multivariate lesion symptom mapping
Teghipco, A., Newman‐Norlund, R., Gibson, M., Bonilha, L., Absher, J. R., Fridriksson, J., & Rorden, C. (2024) · Aperture Neuro · doi:10.52294/001c.117311 · Cited by 4 · see citing works
Academic skills after brain injury: A lifespan perspective.
Sullivan, A. W., Bowren, M. D., Bruss, J., Tranel, D., & Demir‐Lira, Ö. E. (2022) · Neuropsychology · doi:10.1037/neu0000806 · Cited by 4 · see citing works
Extension of voxel-based lesion mapping to multidimensional neurophysiological data
Hardstone, R., Ostrowski, L. M., Dusang, A. N., López‐Larraz, E., Jesser, J., Cash, S. S., Cramer, S. C., Hochberg, L. R., Ramos‐Murguialday, A., & Lin, D. J. (2025) · Scientific Reports · doi:10.1038/s41598-025-17247-z · Cited by 2 · see citing works
Kropp, E., Varkanitsa, M., Carvalho, N., Falconer, I., Billot, A., Al-Dabbagh, M., & Kiran, S. (2025) · Cortex · doi:10.1016/j.cortex.2025.04.015 · Cited by 3 · see citing works
Moore, M. J., Rorden, C., Robinson, G. A., Mattingley, J. B., & Demeyere, N. (2026) · Human Brain Mapping · doi:10.1002/hbm.70619 · Cited by 1 · see citing works
Spatial Correlates of Dementia and Disability After Intracerebral Hemorrhage
Chen, Y., Rivier, C. A., Mora, S. A., Lopez, V. M. T., Payabvash, S., Sheth, K. N., Harloff, A., Falcone, G. J., Rosand, J. M., Mayerhofer, E., et al. (2025) · Journal of the American Heart Association · doi:10.1161/jaha.124.037930 · Cited by 1 · see citing works
Mapping language and non-language cognitive deficits in post-stroke anomic aphasiaPreprint
Akkad, H., Hope, T. M. H., Howland, C., Ondobaka, S., Pappa, K., Nardo, D., Duncan, J., Leff, A. P., & Crinion, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.15.431293 · Cited by 1 · see citing works
Lack of statistical significance is not evidence against modularity in visual feature processing
Griffis, J. C., & Boes, A. D. (2025) · Brain · doi:10.1093/brain/awaf352 · Cited by 1 · see citing works
3D generalization of brain model to visualize and analyze neuroanatomical data
Abedin, S. (2016) · D-Scholarship@Pitt (University of Pittsburgh)
Puls, L., & Diego, L. (2019) · UCL Discovery (University College London)
Lesion-Symptom Mapping in Speech and Language Disorders: A Translational Perspective
Argyropoulos, G. P. D. (2020) · Contemporary clinical neuroscience · doi:10.1007/978-3-030-35687-3_11
Critical‐Network Lesion‐Symptom Mapping
Walker, G. M., Kurteff, G., Hussain, A., Rorden, C., Bonilha, L., Fridriksson, J., & Hickok, G. S. (2026) · Human Brain Mapping · doi:10.1002/hbm.70644
- Authors
- Inoue, K., Madhyastha, T., Rudrauf, D., Mehta, S., & Grabowski, T.
- Affiliations
- University of Washington (US)
- Inserm (FR)
- Corresponding author
- Madhyastha, Tara
- Venue
- NeuroImage Clinical
- Publisher
- Elsevier BV
- Published
- 2014
- Volume
- 6
- Pages
- 388-397
- ISSN
- 2213-1582 (ISSN-L)
- PMC
- PMC4218935
- OpenAlex
- W2060198695
- Cited by
- 59
- References
- 27
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 2 · 2023: 3 · 2022: 7 · 2021: 3 · 2020: 8 · 2019: 8 · 2018: 8 · 2017: 10 · 2016: 4
- FWCI
- 2.60
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- NeuroImage Clinical (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- NINDS (R01 NS058658, P50 NS019632)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- voxel-based lesion-symptom mapping, lesion simulation, positioning accuracy, signal detection, multiple testing correction, false discovery rate
- MeSH terms
- Brain, Brain Injuries, Computer Simulation, Data Interpretation, Statistical, Diagnosis, Computer-Assisted, Humans
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