Mapping Activity and Functional Organisation of the Motor and Visual Pathways Using ADC ‐ fMRI in the Human Brain
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Abstract
In contrast to blood‐oxygenation level‐dependent (BOLD) functional MRI (fMRI), which relies on changes in blood flow and oxygenation levels to infer brain activity, diffusion fMRI (DfMRI) investigates brain dynamics by monitoring alterations in the apparent diffusion coefficient (ADC) of water. These ADC changes may arise from fluctuations in neuronal morphology, providing a distinctive perspective on neural activity. The potential of ADC as an fMRI contrast (ADC‐fMRI) lies in its capacity to reveal neural activity independently of neurovascular coupling, thus yielding complementary insights into brain function. To demonstrate the specificity and value of ADC‐fMRI, both ADC‐ and BOLD‐fMRI data were collected at 3 T in human subjects during visual stimulation and motor tasks. The first aim of this study was to identify an acquisition design for ADC that minimises BOLD contributions. By examining the timings in responses, we report that ADC 0/1 timeseries (acquired with b values of 0 and 1 ms/) exhibit residual vascular contamination, while ADC 0.2/1 timeseries (with b values of 0.2 and 1 ms/) show minimal BOLD influence and higher sensitivity to neuromorphological coupling. Second, a general linear model was employed to identify activation clusters for ADC 0.2/1 and BOLD, from which the average ADC and BOLD responses were calculated. The negative ADC response exhibited a significantly reduced delay relative to the task onset and offset as compared to BOLD. This early onset further supports the notion that ADC is sensitive to neuromorphological rather than neurovascular coupling. Remarkably, in the group‐level analysis, positive BOLD activation clusters were detected in the visual and motor cortices, while the negative ADC clusters mainly highlighted pathways in white matter connected to the motor cortex. In the averaged individual level analysis, negative ADC activation clusters were also present in the visual cortex. This finding confirmed the reliability of negative ADC as an indicator of brain function, even in regions with lower vascularisation such as white matter. Finally, we established that ADC‐fMRI time courses yield the expected functional organisation of the visual system, including both grey and white matter regions of interest. Functional connectivity matrices were used to perform hierarchical clustering of brain regions, where ADC‐fMRI successfully reproduced the expected structure of the dorsal and ventral visual pathways. This organisation was not replicated with the b = 0.2 ms/ diffusion‐weighted time courses, which can be seen as a proxy for BOLD (via T 2 ‐weighting). These findings underscore the robustness of ADC time courses in functional MRI studies, offering complementary insights into BOLD‐fMRI regarding brain function and connectivity patterns.
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DfMRI may offer greater spatial and temporal precision than BOLD, including potential sensitivity in white matter, where BOLD fMRI is challenging.
“DfMRI may, therefore, offer greater spatial and temporal precision than BOLD, including potential sensitivity in white matter, where BOLD fMRI is challenging (de Riedmatten, Spencer, Nguyen-Duc, et al., 2025; Nguyen-Duc et al., 2025; Spencer et al., 2025).”
From 40 Years of diffusion MRI in the brain: From history to emerging frontiers (2026) · cites this paper as Nguyen-Duc et al., 2025
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On a Test of Whether one of Two Random Variables is Stochastically Larger than the Other
Mann, H. B., & Whitney, D. R. (1947) · The Annals of Mathematical Statistics · doi:10.1214/aoms/1177730491 · Cited by 14,320 · see citing works
Advances in functional and structural MR image analysis and implementation as FSL
Smith, S. M., Jenkinson, M., Woolrich, M. W., Beckmann, C. F., Behrens, T. E. J., Johansen-Berg, H., Bannister, P. R., De Luca, M., Drobnjak, I., Flitney, D. E., et al. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.07.051 · Cited by 13,630 · see citing works
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190 · see citing works
Jenkinson, M., Beckmann, C. F., Behrens, T. E. J., Woolrich, M. W., & Smith, S. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.015 · Cited by 11,314 · see citing works
Fischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.021 · Cited by 9,526 · see citing works
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783 · see citing works
Brain magnetic resonance imaging with contrast dependent on blood oxygenation.
Ogawa, S., Lee, T. M., Kay, A. R., & Tank, D. W. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.24.9868 · Cited by 6,483 · see citing works
A reproducible evaluation of ANTs similarity metric performance in brain image registration
Avants, B. B., Tustison, N. J., Song, G., Cook, P. A., Klein, A., & Gee, J. C. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.025 · Cited by 4,796 · see citing works
PsychoPy—Psychophysics software in Python
Peirce, J. W. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2006.11.017 · Cited by 4,728 · see citing works
Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.
Kwong, K. K., Belliveau, J. W., Chesler, D. A., Goldberg, I. E., Weisskoff, R. M., Poncelet, B. P., Kennedy, D. N., Hoppel, B. E., Cohen, M. S., & Turner, R. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5675 · Cited by 4,212 · see citing works
Andersson, J. L. R., Skare, S., & Ashburner, J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00336-7 · Cited by 3,469 · see citing works
Preface: Cerebral Cortex Has Come of Age
Goldman, P. S., & RAKIC, P. T. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1-a · Cited by 3,412 · see citing works
MRtrix3: A fast, flexible and open software framework for medical image processing and visualisation
Tournier, J.-D., Smith, R., Raffelt, D., Tabbara, R., Dhollander, T., Pietsch, M., Christiaens, D., Jeurissen, B., Yeh, C.-H., & Connelly, A. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116137 · Cited by 2,974 · see citing works
Object vision and spatial vision: Two cortical pathways
Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947 · see citing works
Temporal Autocorrelation in Univariate Linear Modeling of FMRI Data
Woolrich, M. W., Ripley, B. D., Brady, M., & Smith, S. M. (2001) · NeuroImage · doi:10.1006/nimg.2001.0931 · Cited by 2,859 · see citing works
Denoising of diffusion MRI using random matrix theory
Veraart, J., Novikov, D. S., Christiaens, D., Ades-aron, B., Sijbers, J., & Fieremans, E. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.08.016 · Cited by 1,905 · see citing works
Stereotaxic white matter atlas based on diffusion tensor imaging in an ICBM template
Mori, S., Oishi, K., Jiang, H., Jiang, L., Li, X., Akhter, K., Hua, K., Faria, A. V., Mahmood, A., Woods, R. P., et al. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.12.035 · Cited by 1,832 · see citing works
Salimi-Khorshidi, G., Douaud, G., Beckmann, C. F., Glasser, M. F., Griffanti, L., & Smith, S. M. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.046 · Cited by 1,770 · see citing works
Multilevel linear modelling for FMRI group analysis using Bayesian inference
Woolrich, M. W., Behrens, T. E. J., Beckmann, C. F., Jenkinson, M., & Smith, S. M. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.12.023 · Cited by 1,719 · see citing works
Gibbs-ringing artifact removal based on local subvoxel-shifts
Kellner, E., Dhital, B., Kiselev, V. G., & Reisert, M. (2016) · Magnetic Resonance in Medicine · doi:10.1002/mrm.26054 · Cited by 1,478 · see citing works
The Underpinnings of the BOLD Functional Magnetic Resonance Imaging Signal
Logothetis, N. K. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-03963.2003 · Cited by 1,024 · see citing works
Shmuel, A., Augath, M., Oeltermann, A., & Logothetis, N. K. (2006) · Nature Neuroscience · doi:10.1038/nn1675 · Cited by 898 · see citing works
BigBrain: An Ultrahigh-Resolution 3D Human Brain Model
Amunts, K., Lepage, C., Borgeat, L., Mohlberg, H., Dickscheid, T., Rousseau, M.-É., Bludau, S., Bazin, P., Lewis, L. B., Oros‐Peusquens, A., et al. (2013) · Science · doi:10.1126/science.1235381 · Cited by 879 · see citing works
Coupling Mechanism and Significance of the BOLD Signal: A Status Report
Hillman, E. M. C. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014111 · Cited by 615 · see citing works
Contour, color and shape analysis beyond the striate cortex
Desimone, R., Schein, S. J., Moran, J., & Ungerleider, L. G. (1985) · Vision Research · doi:10.1016/0042-6989(85)90069-0 · Cited by 535 · see citing works
Modern hierarchical, agglomerative clustering algorithms
Müllner, D. (2011) · arXiv · doi:10.48550/arxiv.1109.2378 · Cited by 529 · see citing works
Krucker, T., Siggins, G. R., & Halpain, S. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.100139797 · Cited by 374 · see citing works
Revealing mesoscopic structural universality with diffusion
Novikov, D. S., Jensen, J. H., Helpern, J. A., & Fieremans, E. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1316944111 · Cited by 348 · see citing works
Direct and fast detection of neuronal activation in the human brain with diffusion MRI
Le Bihan, D., Urayama, S.-I., Aso, T., Hanakawa, T., & Fukuyama, H. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600644103 · Cited by 272 · see citing works
Detection of synchronous brain activity in white matter tracts at rest and under functional loading
Ding, Z., Huang, Y., Bailey, S., Gao, Y., Cutting, L. E., Rogers, B. P., Newton, A. T., & Gore, J. C. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1711567115 · Cited by 255 · see citing works
Cell type specificity of neurovascular coupling in cerebral cortex
Uhlířová, H., Kılıç, K., Tian, P., Thunemann, M., Desjardins, M., Saisan, P. A., Sakadžić, S., Ness, T. V., Matéo, C., Cheng, Q., et al. (2016) · eLife · doi:10.7554/elife.14315 · Cited by 237 · see citing works
Swelling of Nerve Fibers Associated with Action Potentials
Iwasa, K., Tasaki, I., & Gibbons, R. C. (1980) · Science · doi:10.1126/science.7423196 · Cited by 225 · see citing works
Coupling of the cortical hemodynamic response to cortical and thalamic neuronal activity
Devor, A., Ulbert, I., Dunn, A. K., Narayanan, S. N., Jones, S. R., Andermann, M. L., Boas, D. A., & Dale, A. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407789102 · Cited by 222 · see citing works
Kawashima, R., O’Sullivan, B., & Roland, P. E. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.13.5969 · Cited by 214 · see citing works
How accurate is magnetic resonance imaging of brain function?
Uǧurbil, K., Toth, L. J., & Kim, D. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)00039-5 · Cited by 198 · see citing works
Transient decrease in water diffusion observed in human occipital cortex during visual stimulation
Darquié, A., Poline, J.-B., Poupon, C., Saint-Jalmes, H., & Le Bihan, D. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.151125698 · Cited by 194 · see citing works
Setsompop, K., Fan, Q., Stockmann, J., Bilgiç, B., Huang, S. Y., Cauley, S., Nummenmaa, A. R., Wang, F., Yogesh Rathi, A., Witzel, T., et al. (2017) · Magnetic Resonance in Medicine · doi:10.1002/mrm.26653 · Cited by 178 · see citing works
Microvasculature of the human cerebral white matter: Arteries of the deep white matter
Nonaka, H., Akima, M., Hatori, T., Nagayama, T., Zhang, Z., & Ihara, F. (2003) · Neuropathology · doi:10.1046/j.1440-1789.2003.00486.x · Cited by 137 · see citing works
Ling, T., Boyle, K. C., Zuckerman, V., Flores, T. A., Ramakrishnan, C., Deisseroth, K. A., & Palanker, D. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1920039117 · Cited by 110 · see citing works
Sheth, B. R., & Young, R. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2016.00037 · Cited by 108 · see citing works
Rapid Structural Changes in Nerve Fibers and Cells Associated with Their Excitation Processes.
Tasaki, I. (1999) · The Japanese Journal of Physiology · doi:10.2170/jjphysiol.49.125 · Cited by 100 · see citing works
Evidence for a vascular contribution to diffusion FMRI at high <i>b</i> value
Miller, K. L., Bulte, D. P., Devlin, H., Robson, M. D., Wise, R. G., Woolrich, M. W., Jezzard, P., & Behrens, T. E. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707257105 · Cited by 98 · see citing works
Water diffusion in brain cortex closely tracks underlying neuronal activity
Tsurugizawa, T., Ciobanu, L., & Le Bihan, D. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303178110 · Cited by 93 · see citing works
Negative BOLD fMRI Response in the Visual Cortex Carries Precise Stimulus-Specific Information
Bressler, D. W., Spotswood, N., & Whitney, D. C. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000410 · Cited by 78 · see citing works
Suppression of background gradients in (B0 gradient‐based) NMR diffusion experiments
Zheng, G. F., & Price, W. S. (2007) · Concepts in Magnetic Resonance Part A · doi:10.1002/cmr.a.20092 · Cited by 62 · see citing works
Cohen, L. B., Hille, B., & Keynes, R. D. (1969) · The Journal of Physiology · doi:10.1113/jphysiol.1969.sp008876 · Cited by 60 · see citing works
Schilling, K. G., Li, M., Rheault, F., Gao, Y., Cai, L. Y., Zhao, Y., Xu, L., Ding, Z., Anderson, A. W., Landman, B. A., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2219666120 · Cited by 50 · see citing works
Jin, T., Zhao, F., & Kim, S. (2006) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21074 · Cited by 44 · see citing works
Diffusion-weighted magnetic resonance imaging of neuronal activity in the hippocampal slice model
Flint, J., Hansen, B., Vestergaard-Poulsen, P., & Blackband, S. J. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.02.003 · Cited by 44 · see citing works
A rapid-onset diffusion functional MRI signal reflects neuromorphological coupling dynamics
Nunes, D., Gil, R., & Shemesh, N. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117862 · Cited by 43 · see citing works
Choi, S., Jeong, G., Kim, Y.-B., & Cho, Z. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117145 · Cited by 42 · see citing works
Yacoub, E. S., Uludaǧ, K., Uǧurbil, K., & Harel, N. (2008) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2008.01.046 · Cited by 38 · see citing works
Nunes, D., Ianuș, A., & Shemesh, N. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.09.050 · Cited by 37 · see citing works
Distinct neurochemical influences on fMRI response polarity in the striatum
Cerri, D. H., Albaugh, D. L., Walton, L. R., Katz, B. M., Wang, T.-W. W., Chao, T.-H. H., Zhang, W., Nonneman, R. J., Jiang, J., Lee, S., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46088-z · Cited by 37 · see citing works
Honey, I shrunk the extracellular space: Measurements and mechanisms of astrocyte swelling
Walch, E., & Fiacco, T. A. (2022) · Glia · doi:10.1002/glia.24224 · Cited by 36 · see citing works
Ades‐Aron, B., Lemberskiy, G., Veraart, J., Golfinos, J. G., Fieremans, E., Novikov, D. S., & Shepherd, T. M. (2020) · Radiology · doi:10.1148/radiol.2020200822 · Cited by 35 · see citing works
MP-PCA denoising for diffusion MRS data: promises and pitfalls
Mosso, J., Simičić, D., Şimşek, K., Kreis, R., Cudalbu, C., & Jelescu, I. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119634 · Cited by 35 · see citing works
Self-citationOrientation dependence of microcirculation‐induced diffusion signal in anisotropic tissues
Abdullah, O., Gomez, A. D., Merchant, S. S., Heidinger, M., Poelzing, S., & Hsu, E. W. (2015) · Magnetic Resonance in Medicine · doi:10.1002/mrm.25980 · Cited by 33 · see citing works
Pampel, A., Jochimsen, T. H., & Möller, H. E. (2010) · NMR in Biomedicine · doi:10.1002/nbm.1502 · Cited by 30 · see citing works
Martínez-Maestro, M., Labadie, C., & Möller, H. E. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18795426 · Cited by 30 · see citing works
White-matter diffusion fMRI of mouse optic nerve
Spees, W. M., Lin, T., & Song, S. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.021 · Cited by 28 · see citing works
Diffusion fMRI detects white-matter dysfunction in mice with acute optic neuritis
Lin, T., Spees, W. M., Chiang, C., Trinkaus, K. M., Cross, A. H., & Song, S. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.02.007 · Cited by 25 · see citing works
Ferreira, C. T., Ceccaldi, M. P., Giusiano, B., & Poncet, M. (1998) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.65.3.382 · Cited by 23 · see citing works
Physiological modeling of the BOLD signal and implications for effective connectivity: A primer
Uludaǧ, K. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120249 · Cited by 21 · see citing works
Computational neuroanatomy of human stratum proprium of interparietal sulcus
Uesaki, M., Takemura, H., & Ashida, H. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1492-1 · Cited by 20 · see citing works
High b -value diffusion-weighted fMRI in a rat forepaw electrostimulation model at 7 T
Autio, J. A., Kershaw, J., Shibata, S., Obata, T., Kanno, I., & Aoki, I. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.04.006 · Cited by 19 · see citing works
Rat superior colliculus encodes the transition between static and dynamic vision modes
Gil, R., Valente, M., & Shemesh, N. (2024) · Nature Communications · doi:10.1038/s41467-024-44934-8 · Cited by 19 · see citing works
Luca, A. D., Schlaffke, L., Siero, J. C. W., Froeling, M., & Leemans, A. (2019) · Human Brain Mapping · doi:10.1002/hbm.24758 · Cited by 18 · see citing works
Kuroiwa, D., Obata, T., Kawaguchi, H., Autio, J. A., Hirano, M., Aoki, I., Kanno, I., & Kershaw, J. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.04.050 · Cited by 15 · see citing works
Nicolas, R., Gros-Dagnac, H., Aubry, F., & Celsis, P. (2017) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2017.01.022 · Cited by 14 · see citing works
Yamasaki, T., & Tobimatsu, S. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00750 · Cited by 14 · see citing works
Possible links between the lag structure in visual cortex and visual streams using fMRI
Park, B., Shim, W. M., James, O., & Park, H. (2019) · Scientific Reports · doi:10.1038/s41598-019-40728-x · Cited by 13 · see citing works
Multi-echo investigations of positive and negative CBF and concomitant BOLD changes
Devi, R., Lepsien, J., Lorenz, K., Schlumm, T., Mildner, T., & Möller, H. E. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119661 · Cited by 11 · see citing works
Koike‐Tani, M., Tominaga, T., Oldenbourg, R., & Tani, T. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/523571 · Cited by 10 · see citing works
Razlighi, Q. R. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00067 · Cited by 9 · see citing works
Spatially congruent negative BOLD responses to different stimuli do not summate in visual cortex
Wilson, R., Thomas, A. T., & Mayhew, S. D. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116891 · Cited by 9 · see citing works
All-optical observation on activity-dependent nanoscale dynamics of myelinated axons
Kwon, J., Lee, S., Jo, Y., & Choi, M. (2023) · Neurophotonics · doi:10.1117/1.nph.10.1.015003 · Cited by 9 · see citing works
Olszowy, W., Diao, Y., & Jelescu, I. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.16.444253 · Cited by 8 · see citing works
Self-citationHertanu, A., Pavan, T., & Jelescu, I. (2025) · Imaging Neuroscience · doi:10.1162/imag_a_00445 · Cited by 8 · see citing works
Self-citationDiffusion functional MRI with isotropic b-tensor encoding
Spencer, A. P. C., de Riedmatten, I., Nguyen‐Duc, J., Szczepankiewicz, F., & Jelescu, I. (2024) · Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition · doi:10.58530/2024/3313 · Cited by 1 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 3
- Fischl, B. 2012. “ Freesurfer.” NeuroImage 62, no. 2: 774– 781. Epub 2012 Jan 10. 22248573 PMC3685476
- Jenkinson, M., C. F. Beckmann, T. E. J. Behrens, M. W. Woolrich, and S. M. Smith. 2012. “ Fsl.” NeuroImage 62, no. 2: 782– 790. 21979382
- Le Bihan, D. 2019. “ What Can We See With IVIM MRI?” Physiological and Quantitative MRI 187: 56– 67. 29277647
Cited by
Sorted by citations
de Riedmatten, I., Spencer, A. P. C., Olszowy, W., & Jelescu, I. O. (2025) · Communications Biology · doi:10.1038/s42003-025-07889-0 · Cited by 12 · see citing works
Self-citationMapping grey and white matter activity in the human brain with isotropic ADC-fMRI
Spencer, A. P. C., Nguyen-Duc, J., de Riedmatten, I., Szczepankiewicz, F., & Jelescu, I. O. (2025) · Nature Communications · doi:10.1038/s41467-025-60357-5 · Cited by 12 · see citing works
Self-citationHertanu, A., Pavan, T., & Jelescu, I. (2025) · Imaging Neuroscience · doi:10.1162/imag_a_00445 · Cited by 8 · see citing works
Self-citationThe nature and interpretation of BOLD signals in white matter - A review
Gore, J. C., Li, M., Schilling, K. G., Xu, L., Li, Y., Zu, Z., Anderson, A. W., Ding, Z., & Gao, Y. (2025) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2025.110596 · Cited by 8 · see citing works
Evaluating the dependence of ADC-fMRI on haemodynamics in breath-hold and resting-state conditions
de Riedmatten, I., Spencer, A. P. C., Nguyen-Duc, J., Pérot, J.-B., Szczepankiewicz, F., Esteban, O., & Jelescu, I. O. (2025) · Imaging Neuroscience · doi:10.1162/imag.a.1020 · Cited by 4 · see citing works
Self-citationMaiuro, A., Palombo, M., Macaluso, E., Genovese, G., Bozzali, M., Giove, F., & Capuani, S. (2025) · Applied Sciences · doi:10.3390/app15094930 · Cited by 3 · see citing works
Complementarity of BOLD and ADC‐fMRI in Mapping Brain Visual Processing in the Rat
Pérot, J., Hertanu, A., Spencer, A. P. C., Nguyen‐Duc, J., Molochidis, N., Zerbi, V., Yon, M., & Jelescu, I. (2026) · NMR in Biomedicine · doi:10.1002/nbm.70231 · Cited by 1 · see citing works
Self-citation40 Years of diffusion MRI in the brain: From history to emerging frontiers
Le Bihan, D. (2026) · Imaging Neuroscience · doi:10.1162/imag.a.1365
Pérot, J., Hertanu, A., Spencer, A. P. C., Nguyen‐Duc, J., Molochidis, N., Zerbi, V., Yon, M., & Jelescu, I. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.24.666486
Self-citationAmetepe, J. M., Gholam, J., Beltrachini, L., Cercignani, M., & Jones, D. K. (2026) · Magnetic Resonance in Medicine · doi:10.1002/mrm.70417
de Riedmatten, I., Spencer, A. P. C., Martuzzi, R., Rochas, V., Pérot, J., Szczepankiewicz, F., & Jelescu, I. (2026) · Human Brain Mapping · doi:10.1002/hbm.70629
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- Authors
- Nguyen‐Duc, J., de Riedmatten, I., Spencer, A. P. C., Perot, J., Olszowy, W., & Jelescu, I.
- Affiliations
- Centre Hospitalier Universitaire Vaudois (CH)
- Department of Radiology Lausanne University Hospital (CHUV) and University of Lausanne (UNIL) Lausanne Switzerland
- DSM (Switzerland) (CH)
- Corresponding author
- Nguyen‐Duc, Jasmine
- Venue
- Human Brain Mapping
- Publisher
- Wiley
- Published
- 2025-01-21
- Volume
- 46
- Issue
- 2
- Pages
- e70110-e70110
- ISSN
- 1065-9471 (ISSN-L)
- 1097-0193
- PMC
- PMC11747996
- OpenAlex
- W4406676801
- Cited by
- 11
- References
- 80
- Citations by year
- 2026: 4 · 2025: 7
- FWCI
- 6.34
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Human Brain Mapping (publishedVersion, cc-by-nc)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- SERVAL (Université de Lausanne) (acceptedVersion, cc-by-nc)
- IRIS (submittedVersion, cc-by-nc)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (190882)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Keywords
- apparent diffusion coefficient, diffusion MRI, BOLD fMRI, neurovascular coupling, motor cortex, visual cortex, dorsal visual pathway, ventral stream, white matter, functional connectivity, brain activation mapping, visual stimulation, motor tasks
- MeSH terms
- Adult, Brain, Brain Mapping, Efferent Pathways, Female, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Motor Cortex, Oxygen, Photic Stimulation, Visual Pathways, Diffusion Magnetic Resonance Imaging, Young Adult
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 ›
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