Resting state sensorimotor functional connectivity in multiple sclerosis inversely correlates with transcallosal motor pathway transverse diffusivity

The assessment and analysis of handedness: The Edinburgh inventory

Oldfield, R. C. (1971) · Neuropsychologia · doi:10.1016/0028-3932(71)90067-4 · Cited by 35,900 · 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

AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages

Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913 · see citing works

Numerical Recipes, The Art of Scientific Computing

Press, W. H., Flannery, B. P., Teukolsky, S. A., Vetterling, W. T., & Gould, H. (1987) · American Journal of Physics · doi:10.1119/1.14981 · Cited by 10,032 · see citing works

Functional connectivity in the motor cortex of resting human brain using echo‐planar mri

Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812 · see citing works

Numerical Recipes: The Art of Scientific Computing

Ziegel, E. R., Press, W. H., Flannery, B. P., Teukolsky, S. A., & Vetterling, W. T. (1987) · Technometrics · doi:10.2307/1269484 · Cited by 6,704 · see citing works

Axonal transection in the lesions of multiple sclerosis

Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029 · see citing works

Default-mode network activity distinguishes Alzheimer’s disease from healthy aging: evidence from functional MRI

Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684 · see citing works

Dysmyelination revealed through MRI as increased radial (but unchanged axial) diffusion of water

Song, S.-K., Sun, S.-W., Ramsbottom, M. J., Chang, C., Russell, J., & Cross, A. H. (2002) · NeuroImage · doi:10.1006/nimg.2002.1267 · Cited by 2,582 · see citing works

Diffusion tensor imaging detects and differentiates axon and myelin degeneration in mouse optic nerve after retinal ischemia

Song, S.-K., Sun, S.-W., Ju, W.-K., Lin, S.-J., Cross, A. H., & Neufeld, A. H. (2003) · NeuroImage · doi:10.1016/j.neuroimage.2003.07.005 · Cited by 1,738 · see citing works

Demyelination increases radial diffusivity in corpus callosum of mouse brain

Song, S.-K., Yoshino, J., Le, T. Q., Lin, S.-J., Sun, S.-W., Cross, A. H., & Armstrong, R. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.01.028 · Cited by 1,658 · see citing works

Axonal damage in acute multiple sclerosis lesions

Ferguson, B. (1997) · Brain · doi:10.1093/brain/120.3.393 · Cited by 1,532 · see citing works

Frequencies contributing to functional connectivity in the cerebral cortex in "resting-state" data.

Cordes, D., Haughton, V. M., Arfanakis, K., Carew, J. D., Turski, P. A., Moritz, C. H., Quigley, M., & Meyerand, M. E. (2001) · PubMed Central · Cited by 1,402 · see citing works

Functional connectivity in single and multislice echoplanar imaging using resting-state fluctuations

Lowe, M. J., Mock, B. J., & Sorenson, J. A. (1998) · NeuroImage · doi:10.1006/nimg.1997.0315 · Cited by 1,394 · see citing works

Electroencephalographic signatures of attentional and cognitive default modes in spontaneous brain activity fluctuations at rest

Laufs, H., Krakow, K., Sterzer, P., Eger, E., Beyerle, A., Salek-Haddadi, A., & Kleinschmidt, A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1831638100 · Cited by 1,028 · see citing works

Spontaneously emerging cortical representations of visual attributes

Kenet, T., Bibitchkov, D., Tsodyks, M., Grinvald, A., & Arieli, A. (2003) · Nature · doi:10.1038/nature02078 · Cited by 924 · see citing works

Multiple Sclerosis and Chronic Autoimmune Encephalomyelitis

Kornek, B., Storch, M. K., Weissert, R., Wallstroem, E., Stefferl, A., Olsson, T. P., Linington, C., Schmidbauer, M., & Lassmann, H. (2000) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64537-3 · Cited by 914 · see citing works

Brain connectivity related to working memory performance

Hampson, M., Driesen, N. R., Skudlarski, P., Gore, J. C., & Constable, R. T. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3408-06.2006 · Cited by 853 · see citing works

Activity and Connectivity of Brain Mood Regulating Circuit in Depression: A Functional Magnetic Resonance Study

Anand, A., Li, Y., Wang, Y., Wu, J., Gao, S., Bukhari, L., Mathews, V. P., Kalnin, A., & Lowe, M. J. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.02.021 · Cited by 787 · see citing works

Three-dimensional locations and boundaries of motor and premotor cortices as defined by functional brain imaging: A meta-analysis

Mayka, M. A., Corcos, D. M., Leurgans, S. E., & Vaillancourt, D. E. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.02.004 · Cited by 731 · see citing works

Very Slow Activity Fluctuations in Monkey Visual Cortex: Implications for Functional Brain Imaging

Leopold, D. A. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.4.422 · Cited by 675 · see citing works

Diffusion tensor imaging of lesions and normal-appearing white matter in multiple sclerosis

Werring, D. J., Clark, C. A., Barker, G. J., Thompson, A. J., & Miller, D. H. (1999) · Neurology · doi:10.1212/wnl.52.8.1626 · Cited by 621 · see citing works

Axonal loss in the pathology of MS: consequences for understanding the progressive phase of the disease

Bjartmar, C., Wujek, J. R., & Trapp, B. D. (2003) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(02)00069-2 · Cited by 573 · see citing works

Diffusion tensor magnetic resonance imaging in multiple sclerosis

Filippi, M., Cercignani, M., Inglese, M., Horsfield, M. A., & Comi, G. (2001) · Neurology · doi:10.1212/wnl.56.3.304 · Cited by 545 · see citing works

Regional coherence changes in the early stages of Alzheimer’s disease: A combined structural and resting-state functional MRI study

Yong He, A., Wang, L. Y., Zang, Y., Tian, L., Zhang, X., Li, K., & Jiang, T. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.11.042 · Cited by 542 · see citing works

Axonal and neuronal degeneration in multiple sclerosis: mechanisms and functional consequences

Bjartmar, C., & Trapp, B. D. (2001) · Current Opinion in Neurology · doi:10.1097/00019052-200106000-00003 · Cited by 479 · see citing works

Diffusion tensor imaging can detect and quantify corticospinal tract degeneration after stroke

Werring, D. J. (2000) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.69.2.269 · Cited by 396 · see citing works

A histological, histochemical and biochemical study of the macroscopically normal white matter in multiple sclerosis

Allen, I. V., & McKEOWN, S. R. (1979) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(79)90142-4 · Cited by 362 · see citing works

Axonal changes in chronic demyelinated cervical spinal cord plaques

Lovas, G., Szilágyi, N., Majtényi, K., Palkovits, M., & Komoly, S. (2000) · Brain · doi:10.1093/brain/123.2.308 · Cited by 356 · see citing works

Investigation of MS normal-appearing brain using diffusion tensor MRI with clinical correlations

Ciccarelli, O., Werring, D. J., Wheeler‐Kingshott, C. A. M. G., Barker, G. J., Parker, G. J. M., Thompson, A. J., & Miller, D. H. (2001) · Neurology · doi:10.1212/wnl.56.7.926 · Cited by 342 · see citing works

DTI mapping of human brain connectivity: Statistical fibre tracking and virtual dissection

Hagmann, P., Thiran, J.-P., Jonasson, L., Vandergheynst, P., Clarke, S., Maeder, P., & Meuli, R. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00142-3 · Cited by 326 · see citing works

The pathogenesis of lesions and normal-appearing white matter changes in multiple sclerosis: A serial diffusion MRI study

Werring, D. J. (2000) · Brain · doi:10.1093/brain/123.8.1667 · Cited by 323 · see citing works

Axonal loss in normal-appearing white matter in a patient with acute MS

Bjartmar, C., Kinkel, R. P., Kidd, G. J., Rudick, R. A., & Trapp, B. D. (2001) · Neurology · doi:10.1212/wnl.57.7.1248 · Cited by 281 · see citing works

Imaging brain connectivity in children with diverse reading ability

Beaulieu, C., Plewes, C., Paulson, L. A. D., Roy, D., Snook, L., Concha, L., & Phillips, L. M. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.053 · Cited by 279 · see citing works

Multiple Sclerosis: Low-Frequency Temporal Blood Oxygen Level–Dependent Fluctuations Indicate Reduced Functional Connectivity—Initial Results

Lowe, M. J., Phillips, M. D., Lurito, J. T., Mattson, D. H., Džemidžić, M., & Mathews, V. P. (2002) · Radiology · doi:10.1148/radiol.2241011005 · Cited by 256 · see citing works

Investigation of apparent diffusion coefficient and diffusion tensor anisotrophy in acute and chronic multiple sclerosis lesions.

Tievsky, A. L., Ptak, T., & Farkas, J. E. (1999) · PubMed · Cited by 251 · see citing works

Temporal-callosal pathway diffusivity predicts phonological skills in children

Dougherty, R. F., Ben-Shachar, M., Deutsch, G. K., Hernandez, A., Fox, G. R., & Wandell, B. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608961104 · Cited by 230 · see citing works

Cognitive dysfunction in patients with mildly disabling relapsing–remitting multiple sclerosis: an exploratory study with diffusion tensor MR imaging

Rovaris, M., Iannucci, G., Falautano, M., Possa, F., Martinelli, V., Comi, G., & Filippi, M. (2002) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(01)00690-6 · Cited by 216 · see citing works

Spinal cord axonal loss in multiple sclerosis: a post‐mortem study

Ganter, Prince, & Esiri (1999) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.1999.00205.x · Cited by 202 · see citing works

Axonal Pathology in Multiple Sclerosis. A Historical Note

Kornek, B., & Lassmann, H. (1999) · Brain Pathology · doi:10.1111/j.1750-3639.1999.tb00547.x · Cited by 197 · see citing works

In vivo evidence for axonal dysfunction remote from focal cerebral demyelination of the type seen in multiple sclerosis.

de Stefano, N., Narayanan, S., Matthews, P. M., Francis, G., Antel, J. P., & Arnold, D. (1999) · Brain : a journal of neurology · doi:10.1093/brain/122.10.1933 · Cited by 196 · see citing works

Multiple Sclerosis: Diffusion Tensor MR Imaging for Evaluation of Normal-appearing White Matter

Guo, A. C., MacFall, J. R., & Provenzale, J. M. (2002) · Radiology · doi:10.1148/radiol.2223010311 · Cited by 190 · see citing works

Connectivity-behavior analysis reveals that functional connectivity between left BA39 and Broca’s area varies with reading ability

Hampson, M., Tokoglu, F., Sun, Z., Schafer, R. J., Skudlarski, P., Gore, J. C., & Constable, R. T. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.040 · Cited by 181 · see citing works

Hypercapnia Reversibly Suppresses Low-Frequency Fluctuations in the Human Motor Cortex during Rest Using Echo–Planar MRI

Biswal, B. B., Hudetz, A. G., Yetkin, F. Z., Haughton, V. M., & Hyde, J. S. (1997) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-199703000-00007 · Cited by 171 · see citing works

Diffusion tensor imaging detects age-dependent white matter changes in a transgenic mouse model with amyloid deposition

Song, S.-K., Kim, J. H., Lin, S.-J., Brendza, R. P., & Holtzman, D. M. (2004) · Neurobiology of Disease · doi:10.1016/j.nbd.2003.12.003 · Cited by 170 · see citing works

Optic nerve diffusion tensor imaging in optic neuritis

Trip, S. A., Wheeler‐Kingshott, C. A. M. G., JONES, S. J., Yu, W., Barker, G. J., Thompson, A. J., Plant, G. T., & Miller, D. H. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.09.024 · Cited by 166 · see citing works

Isolating physiologic noise sources with independently determined spatial measures

Beall, E. B., & Lowe, M. J. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.004 · Cited by 157 · see citing works

BrainVISA: Software platform for visualization and analysis of multi-modality brain data

Cointepas, Y., Mangin, J., Garnero, L., Poline, J., & Benali, H. (2001) · NeuroImage · doi:10.1016/s1053-8119(01)91441-7 · Cited by 142 · see citing works

A Wallerian degeneration pattern in patients at risk for MS

Simon, J. H., Kinkel, R. P., Jacobs, L., Bub, L., & Simonian, N. A. (2000) · Neurology · doi:10.1212/wnl.54.5.1155 · Cited by 142 · see citing works

Spatially filtering functional magnetic resonance imaging data

Lowe, M. J., & Sorenson, J. A. (1997) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910370514 · Cited by 135 · see citing works

Demyelinating plaques in relapsing-remitting and secondary-progressive multiple sclerosis: assessment with diffusion MR imaging.

Scanderbeg, A. C., Tomaiuolo, F., Sabatini, U., Nocentini, U., Grasso, M. G., & Caltagirone, C. (2000) · PubMed Central · Cited by 105 · see citing works

Axonal degeneration and progressive neurologic disability in multiple sclerosis

Bjartmar, C., & Trapp, B. (2009) · Neurotoxicity research · doi:10.1007/bf03033380 · Cited by 104 · see citing works

T2* Dependence of Low Frequency Functional Connectivity

Peltier, S. J. (2002) · NeuroImage · doi:10.1006/nimg.2002.1141 · Cited by 102 · see citing works

Treatment of Baseline Drifts in fMRI Time Series Analysis

Lowe, M. J., & Russell, D. P. (1999) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199905000-00025 · Cited by 101 · see citing works

Preferential occult injury of corpus callosum in multiple sclerosis measured by diffusion tensor imaging

Ge, Y., Law, M., Johnson, G., Herbert, J., Babb, J. S., Mannon, L. J., & Grossman, R. I. (2004) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.20083 · Cited by 93 · see citing works

Analysis of normal-appearing white matter in multiple sclerosis: comparison of diffusion tensor MR imaging and magnetization transfer imaging.

Guo, A. C., Jewells, V. L., & Provenzale, J. M. (2001) · PubMed Central · Cited by 91 · see citing works

Directional diffusion in relapsing‐remitting multiple sclerosis: A possible in vivo signature of Wallerian degeneration

Henry, R. G., Oh, J., Nelson, S. J., & Pelletier, D. (2003) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.10379 · Cited by 77 · see citing works

Mechanisms of normal appearing corpus callosum injury related to pericallosal T1 lesions in multiple sclerosis using directional diffusion tensor and 1H MRS imaging

Oh, J. (2004) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2004.039032 · Cited by 68 · see citing works

Quantitative Diffusion Measurements in Focal Multiple Sclerosis Lesions

Nusbaum, A. O., Lu, D., Tang, C. Y., & Atlas, S. W. (2000) · American Journal of Roentgenology · doi:10.2214/ajr.175.3.1750821 · Cited by 63 · see citing works

Functional pathway-defined MRI diffusion measures reveal increased transverse diffusivity of water in multiple sclerosis

Lowe, M. J., Horenstein, C. I., Hirsch, J. G., Marrie, R. A., Stone, L. A., Bhattacharyya, P. K., Gass, A., & Phillips, M. D. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.04.208 · Cited by 60 · see citing works

Multiple sclerosis pathology in the normal and abnormal appearing white matter of the corpus callosum by diffusion tensor imaging

Coombs, B., Best, A. C., Brown, M. S., Miller, D. E., Corboy, J., Baier, M., & Simon, J. (2004) · Multiple Sclerosis · doi:10.1191/1352458504ms1053oa · Cited by 59 · see citing works

An objective method for regularization of fiber orientation distributions derived from diffusion-weighted MRI

Sakaie, K., & Lowe, M. J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.08.034 · Cited by 58 · see citing works

Occult tissue damage in patients with primary progressive multiple sclerosis is independent of T2-visible lesions

Rocca, M., Iannucci, G., Rovaris, M., Comi, G., & Filippi, M. (2003) · Journal of Neurology · doi:10.1007/s00415-003-1024-1 · Cited by 52 · see citing works

Untitled work

Cann, S. A. H., Netten, J. P. V., & Netten, C. V. (2000) · Pure Amsterdam UMC · doi:10.1002/1531-8249(200003)47:3

Untitled work

Basser (2000) · doi:10.1002/1522-2594(200010)44:4

Untitled work

Biswal (1997) · doi:10.1002/(sici)1099-1492(199706/08)10:4/5

Untitled work

Glover (2000) · doi:10.1002/1522-2594(200007)44:1

Auditory and visual word processing studied with fMRI

(1999) · doi:10.1002/(sici)1097-0193(1999)7:1

Exploring the brain network: A review on resting-state fMRI functional connectivity

van den Heuvel, M. P., & Hulshoff Pol, H. E. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2010.03.008 · Cited by 3,326 · see citing works

Functionally linked resting‐state networks reflect the underlying structural connectivity architecture of the human brain

van den Heuvel, M. P., Mandl, R. C. W., Kahn, R. S., & Hulshoff Pol, H. E. (2009) · Human Brain Mapping · doi:10.1002/hbm.20737 · Cited by 987 · see citing works

The Resting Brain: Unconstrained yet Reliable

Shehzad, Z. E., Kelly, C. A. M., Reiss, P. T., Gee, D. G., Gotimer, K., Uddin, L. Q., Lee, S. H., Margulies, D. S., Roy, A. K., Biswal, B. B., et al. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn256 · Cited by 913 · see citing works

Disease and the brain's dark energy

Zhang, D., & Raichle, M. E. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2009.198 · Cited by 903 · see citing works

Greater than the sum of its parts: a review of studies combining structural connectivity and resting-state functional connectivity

Damoiseaux, J. S., & Greicius, M. D. (2009) · Brain Structure and Function · doi:10.1007/s00429-009-0208-6 · Cited by 897 · see citing works

Correlations and anticorrelations in resting-state functional connectivity MRI: A quantitative comparison of preprocessing strategies

Weissenbacher, A., Kasess, C., Gerstl, F., Lanzenberger, R., Moser, E., & Windischberger, C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.005 · Cited by 776 · see citing works

Growing Together and Growing Apart: Regional and Sex Differences in the Lifespan Developmental Trajectories of Functional Homotopy

Zuo, X., Kelly, C. A. M., Martino, A. D., Mennes, M., Margulies, D. S., Bangaru, S. D., Grzadzinski, R., Evans, A. C., Zang, Y., Castellanos, F. X., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2612-10.2010 · Cited by 741 · see citing works

Small-world and scale-free organization of voxel-based resting-state functional connectivity in the human brain

van den Heuvel, M. P., Stam, C. J., Boersma, M., & Pol, H. E. H. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.08.010 · Cited by 720 · see citing works

Schizophrenia, neuroimaging and connectomics

Fornito, A., Zalesky, A., Pantelis, C., & Bullmore, E. T. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.090 · Cited by 716 · see citing works

Topological correlations of structural and functional networks in patients with traumatic brain injury

Caeyenberghs, K., Leemans, A., Leunissen, I., Michiels, K., & Swinnen, S. P. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00726 · Cited by 462 · see citing works

Impaired small-world efficiency in structural cortical networks in multiple sclerosis associated with white matter lesion load

Yong He, A., Dagher, A., Chen, Z., Charil, A., Zijdenbos, A. P., Worsley, K. J., & Evans, A. C. (2009) · Brain · doi:10.1093/brain/awp089 · Cited by 454 · see citing works

Measuring and manipulating brain connectivity with resting state functional connectivity magnetic resonance imaging (fcMRI) and transcranial magnetic stimulation (TMS)

Fox, M. D., Halko, M. A., Eldaief, M. C., & Pascual-Leone, A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.035 · Cited by 395 · see citing works

Unraveling the Miswired Connectome: A Developmental Perspective

Martino, A. D., Fair, D. A., Kelly, C. A. M., Satterthwaite, T. D., Castellanos, F. X., Thomason, M. E., Craddock, R. C., Luna, B., LEVENTHAL, B. L., Zuo, X., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.050 · Cited by 346 · see citing works

Regional Variation in Interhemispheric Coordination of Intrinsic Hemodynamic Fluctuations

Stark, D. E., Margulies, D. S., Shehzad, Z. E., Reiss, P. T., Kelly, C. A. M., Uddin, L. Q., Gee, D. G., Roy, A. K., Banich, M. T., Castellanos, F. X., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4544-08.2008 · Cited by 314 · see citing works

Diffusion Tensor Tractography Reveals Disrupted Topological Efficiency in White Matter Structural Networks in Multiple Sclerosis

Shu, N., Liu, Y., Li, K., Duan, Y., Wang, J., Yu, C., Dong, H., Ye, J., & Yong He, A. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr039 · Cited by 315 · see citing works

Graph theoretical analysis of structural and functional connectivity MRI in normal and pathological brain networks

Guye, M., Bettus, G., Bartoloméi, F., & Cozzone, P. J. (2010) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-010-0205-z · Cited by 298 · see citing works

Changes of Brain Structure and Function in ADHD Children

Qiu, M., Ye, Z., Li, Q., Liu, G., Xie, B., & Wang, J. (2010) · Brain Topography · doi:10.1007/s10548-010-0168-4 · Cited by 274 · see citing works

Hyperconnectivity is a fundamental response to neurological disruption.

Hillary, F. G., Román, C. A. F., Venkatesan, U. M., Rajtmajer, S. M., Bajo, R., & Castellanos, N. P. (2014) · Neuropsychology · doi:10.1037/neu0000110 · Cited by 248 · see citing works

Functional connectivity MRI in infants: Exploration of the functional organization of the developing brain

Smyser, C. D., Snyder, A. Z., & Neil, J. J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.073 · Cited by 241 · see citing works

What's New in Neuroimaging Methods?

Bandettini, P. A. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04420.x · Cited by 219 · see citing works

Reproducibility of Single-Subject Functional Connectivity Measurements

Anderson, J. S., Ferguson, M. A., Lopez-Larson, M. P., & Yurgelun-Todd, D. A. (2011) · American Journal of Neuroradiology · doi:10.3174/ajnr.a2330 · Cited by 195 · see citing works

Motor Network Degeneration in Amyotrophic Lateral Sclerosis: A Structural and Functional Connectivity Study

Verstraete, E., van den Heuvel, M. P., Veldink, J. H., Blanken, N., Mandl, R. C. W., Pol, H. E. H., & van den Berg, L. H. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013664 · Cited by 179 · see citing works

Neuroplasticity and functional recovery in multiple sclerosis

Tomassini, V., Matthews, P. M., Thompson, A. J., Fuglø, D., Geurts, J. J. G., Johansen‐Berg, H., Jones, D. K., Rocca, M. A., Wise, R. G., Barkhof, F., et al. (2012) · Nature Reviews Neurology · doi:10.1038/nrneurol.2012.179 · Cited by 166 · see citing works

Examination of the neural substrates activated in memories of experiences with resonant and dissonant leaders

Boyatzis, R. E., Passarelli, A. M., Koenig, K. A., Lowe, M. J., Mathew, B., Stoller, J. K., & Phillips, M. (2011) · The Leadership Quarterly · doi:10.1016/j.leaqua.2011.08.003 · Cited by 161 · see citing works

Functional implications of age differences in motor system connectivity

Langan, J. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00017 · Cited by 159 · see citing works

Structural substrates for resting network disruption in temporal lobe epilepsy

Voets, N., Beckmann, C. F., Cole, D. M., Hong, S., Bernasconi, A., & Bernasconi, N. (2012) · Brain · doi:10.1093/brain/aws137 · Cited by 150 · see citing works

Monkey in the middle: why non-human primates are needed to bridge the gap in resting-state investigations

Hutchison, R. M., & Everling, S. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00029 · Cited by 140 · see citing works

Imaging biomarkers in multiple sclerosis

Filippi, M., & Agosta, F. (2010) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.22102 · Cited by 141 · see citing works

Fusing DTI and fMRI data: A survey of methods and applications

Zhu, D., Zhang, T., Jiang, X., Hu, X., Chen, H., Yang, N., Lv, J., Han, J., Guo, L., & Liu, T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.071 · Cited by 133 · see citing works

Physical exercise keeps the brain connected: biking increases white matter integrity in patients with schizophrenia and healthy controls.

Svatkova, A., Mandl, R. C. W., Scheewe, T. W., Cahn, W., Kahn, R. S., & Hulshoff Pol, H. E. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv033 · Cited by 120 · see citing works

Cognitive state and connectivity effects of the genome-wide significant psychosis variant in ZNF804A

Esslinger, C., Kirsch, P., Haddad, L., Mier, D. U., Sauer, C., Erk, S., Schnell, K., Arnold, C., Witt, S. H., Rietschel, M., et al. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.10.012 · Cited by 120 · see citing works

Stable long-range interhemispheric coordination is supported by direct anatomical projections

Shen, K., Mišić, B., Cipollini, B., Bezgin, G., Buschkuehl, M., Hutchison, R. M., Jaeggi, S. M., Kross, E. F., Peltier, S., Everling, S., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503436112 · Cited by 119 · see citing works

Relationship between structural and functional connectivity change across the adult lifespan: A longitudinal investigation

Fjell, A. M., Sneve, M. H., Grydeland, H., Storsve, A. B., Amlien, I. K., Yendiki, A., & Walhovd, K. B. (2016) · Human Brain Mapping · doi:10.1002/hbm.23403 · Cited by 113 · see citing works

Basal functional connectivity within the anterior temporal network is associated with performance on declarative memory tasks

Gour, N., Ranjeva, J., Ceccaldi, M. P., Sylviane Confort-gouny, A., Barbeau, E. J., Soulier, E., Guye, M., Didic, M., & Félician, O. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.090 · Cited by 104 · see citing works

Classifying minimally disabled multiple sclerosis patients from resting state functional connectivity

Richiardi, J., Gschwind, M., Simioni, S., Annoni, J., Greco, B. M., Hagmann, P., Schluep, M., Vuilleumier, P. O., & Ville, D. V. D. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.05.078 · Cited by 97 · see citing works

The Explanatory Power of Network Models

Craver, C. F. (2016) · Philosophy of Science · doi:10.1086/687856 · Cited by 94 · see citing works

Functional Connectivity in Multiple Sclerosis: Recent Findings and Future Directions

Tahedl, M., Levine, S. M., Greenlee, M. W., Weissert, R., & Schwarzbach, J. V. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00828 · Cited by 95 · see citing works

Confirming white matter fMRI activation in the corpus callosum: Co-localization with DTI tractography

Mazerolle, E. L., Beyea, S., Gawryluk, J. R., Brewer, K., Bowen, C. V., & D’Arcy, R. C. N. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.102 · Cited by 91 · see citing works

Exploring brain functional connectivity in rest and sleep states: a fNIRS study

Nguyen, T. H., Babawale, O., Kim, T., Jo, H. J., Liu, H., & Kim, J. G. (2018) · Scientific Reports · doi:10.1038/s41598-018-33439-2 · Cited by 89 · see citing works

Evaluation of machine learning algorithms performance for the prediction of early multiple sclerosis from resting-state FMRI connectivity data

Saccà, V., Sarica, A., Novellino, F., Barone, S., Tallarico, T., Filippelli, E., Granata, A., Chiriaco, C., Bossio, R. B., Valentino, P., et al. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-018-9926-9 · Cited by 86 · see citing works

Direct Comparison of Spontaneous Functional Connectivity and Effective Connectivity Measured by Intracortical Microstimulation: An fMRI Study in Macaque Monkeys

Matsui, T., Tamura, K., Koyano, K. W., Takeuchi, D., Adachi, Y., Osada, T., & Miyashita, Y. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr019 · Cited by 82 · see citing works

Meta-Connectomic Analysis Reveals Commonly Disrupted Functional Architectures in Network Modules and Connectors across Brain Disorders

Sha, Z., Xia, M., Lin, Q., Cao, M., Tang, Y., Xu, K., Song, H., Wang, Z., Wang, F., Fox, P. T., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx273 · Cited by 81 · see citing works

Linking Functional Connectivity and Structural Connectivity Quantitatively: A Comparison of Methods

Huang, H., & Ding, M. (2015) · Brain Connectivity · doi:10.1089/brain.2015.0382 · Cited by 84 · see citing works

Specific somatotopic organization of functional connections of the primary motor network during resting state

van den Heuvel, M. P., & Pol, H. E. H. (2009) · Human Brain Mapping · doi:10.1002/hbm.20893 · Cited by 77 · see citing works

Corpus callosal diffusivity predicts motor impairment in relapsing–remitting multiple sclerosis: A TBSS and tractography study

Kern, K. C., Sarcona, J., Montag, M. J., Giesser, B. S., & Sicotte, N. L. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.10.077 · Cited by 78 · see citing works

Assessment of Inter-Hemispheric Imbalance Using Imaging and Noninvasive Brain Stimulation in Patients With Chronic Stroke

Cunningham, D. A., Machado, A. G., Janini, D., Varnerin, N. M., Bonnett, C. E., Yue, G. H., Jones, S., Lowe, M. J., Beall, E. B., Sakaie, K., et al. (2014) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2014.07.419 · Cited by 76 · see citing works

Functional and Structural Connectivity of the Motor Network in Pediatric and Adult-Onset Relapsing-Remitting Multiple Sclerosis

Rocca, M. A., Absinta, M., Moiola, L., Ghezzi, A., Colombo, B., Martinelli, V., Comı, G., & Filippi, M. (2010) · Radiology · doi:10.1148/radiol.09090463 · Cited by 76 · see citing works

Exercise Therapy for Parkinson's Disease: Pedaling Rate Is Related to Changes in Motor Connectivity

Shah, C., Beall, E. B., Frankemolle‐Gilbert, A. M., Penko, A. L., Phillips, M. D., Lowe, M. J., & Alberts, J. L. (2015) · Brain Connectivity · doi:10.1089/brain.2014.0328 · Cited by 76 · see citing works

The Effect of Forced-Exercise Therapy for Parkinson's Disease on Motor Cortex Functional Connectivity

Beall, E. B., Lowe, M. J., Alberts, J. L., Frankemolle‐Gilbert, A. M., Thota, A. K., Shah, C., & Phillips, M. D. (2013) · Brain Connectivity · doi:10.1089/brain.2012.0104 · Cited by 75 · see citing works

Relationships of brain white matter microstructure with clinical and MR measures in relapsing‐remitting multiple sclerosis

Giorgio, A., Palace, J. A., Johansen‐Berg, H., Smith, S. M., Ropele, S., Fuchs, S., Wallner-Blazek, M., Enzinger, C., & Fazekas, F. (2010) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.22062 · Cited by 71 · see citing works

A Tensor Decomposition-Based Approach for Detecting Dynamic Network States From EEG

Mahyari, A., Zoltowski, D. M., Bernat, E. M., & Aviyente, S. (2016) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2016.2553960 · Cited by 66 · see citing works

Abnormal connectivity of the sensorimotor network in patients with MS: A multicenter fMRI study

Rocca, M. A., Absinta, M., Valsasina, P., Ciccarelli, O., Marino, S., Rovira, À., Gass, A., Wegner, C., Enzinger, C., Korteweg, T., et al. (2008) · Human Brain Mapping · doi:10.1002/hbm.20679 · Cited by 67 · see citing works

Stratifying chronic stroke patients based on the influence of contralesional motor cortices: An inter-hemispheric inhibition study

Lin, Y., Potter–Baker, K. A., Cunningham, D. A., Li, M., Sankarasubramanian, V., Lee, J., Jones, S., Sakaie, K., Wang, X., Machado, A. G., et al. (2020) · Clinical Neurophysiology · doi:10.1016/j.clinph.2020.06.016 · Cited by 66 · see citing works

Abnormalities of Resting State Functional Connectivity Are Related to Sustained Attention Deficits in MS

Loitfelder, M., Filippi, M., Rocca, M. A., Valsasina, P., Ropele, S., Jehna, M., Fuchs, S., Schmidt, R., Neuper, C., Fazekas, F., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042862 · Cited by 65 · see citing works

Transcranial Direct Current Stimulation Targeting Primary Motor Versus Dorsolateral Prefrontal Cortices: Proof-of-Concept Study Investigating Functional Connectivity of Thalamocortical Networks Specific to Sensory-Affective Information Processing

Sankarasubramanian, V., Cunningham, D. A., Potter–Baker, K. A., Beall, E. B., Roelle, S. M., Varnerin, N. M., Machado, A. G., Jones, S. E., Lowe, M. J., & Plow, E. B. (2017) · Brain Connectivity · doi:10.1089/brain.2016.0440 · Cited by 65 · see citing works

Integrating Functional and Diffusion Magnetic Resonance Imaging for Analysis of Structure-Function Relationship in the Human Language Network

Morgan, V. L., Mishra, A., Newton, A. T., Gore, J. C., & Ding, Z. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006660 · Cited by 60 · see citing works

Low frequency fluctuations reveal integrated and segregated processing among the cerebral hemispheres

Gee, D. G., Biswal, B. B., Kelly, C. A. M., Stark, D. E., Margulies, D. S., Shehzad, Z. E., Uddin, L. Q., Klein, D. F., Banich, M. T., Castellanos, F. X., et al. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.073 · Cited by 60 · see citing works

Altered Inter-Subregion Connectivity of the Default Mode Network in Relapsing Remitting Multiple Sclerosis: A Functional and Structural Connectivity Study

Zhou, F., Zhuang, Y., Gong, H., Wang, B., Wang, X., Chen, Q., Wu, L., & Wan, H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101198 · Cited by 59 · see citing works

Adaptive cyclic physiologic noise modeling and correction in functional MRI

Beall, E. B. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.01.013 · Cited by 59 · see citing works

Topological organization of connectivity strength in the rat connectome

van den Heuvel, M. P., Scholtens, L. H., & de Reus, M. A. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-0999-6 · Cited by 56 · see citing works

Resting-State Networks and the Functional Connectome of the Human Brain in Agenesis of the Corpus Callosum

Owen, J. P., Li, Y., Yang, F., Shetty, C., Bukshpun, P., Vora, S., Wakahiro, M. L. J., Hinkley, L. B. N., Nagarajan, S. S., Sherr, E. H., et al. (2013) · Brain Connectivity · doi:10.1089/brain.2013.0175 · Cited by 56 · see citing works

Development of biomarkers for multiple sclerosis as a neurodegenerative disorder

Ziemann, U., Wahl, M., Hattingen, E., & Tumani, H. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.04.007 · Cited by 54 · see citing works

Functional connectivity changes and their relationship with clinical disability and white matter integrity in patients with relapsing–remitting multiple sclerosis

Sbardella, E., Tona, F., Petsas, N., Upadhyay, N., Piattella, M. C., Filippini, N., Prosperini, L., Pozzilli, C., & Pantano, P. (2015) · Multiple Sclerosis Journal · doi:10.1177/1352458514568826 · Cited by 51 · see citing works

Resting-state fMRI functional connectivity: a new perspective to evaluate pain modulation in migraine?

Colombo, B., Rocca, M. A., Messina, R., Guerrieri, S., & Filippi, M. (2015) · Neurological Sciences · doi:10.1007/s10072-015-2145-x · Cited by 50 · see citing works

Functional MR Imaging in Multiple Sclerosis

Filippi, M., & Rocca, M. A. (2008) · Neuroimaging Clinics of North America · doi:10.1016/j.nic.2008.08.004 · Cited by 49 · see citing works

Influence of Corticospinal Tracts from Higher Order Motor Cortices on Recruitment Curve Properties in Stroke

Potter–Baker, K. A., Varnerin, N. M., Cunningham, D. A., Roelle, S. M., Sankarasubramanian, V., Bonnett, C. E., Machado, A. G., Conforto, A. B., Sakaie, K., & Plow, E. B. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00079 · Cited by 46 · see citing works

Expanded functional coupling of subcortical nuclei with the motor resting-state network in multiple sclerosis

Dogonowski, A.-M., Siebner, H. R., Sørensen, P. S., Wu, X., Biswal, B. B., Paulson, O. B., Dyrby, T. B., Skimminge, A., Blinkenberg, M., & Madsen, K. H. (2012) · Multiple Sclerosis Journal · doi:10.1177/1352458512460416 · Cited by 45 · see citing works

Le réseau cérébral par défaut : rôle cognitif et perturbations dans la pathologie

Mevel, K., Grassiot, B., Chételat, G., Defer, G. L., Desgranges, B., & Eustache, F. (2010) · Revue Neurologique · doi:10.1016/j.neurol.2010.01.008 · Cited by 43 · see citing works

Comparison of Diffusion Tensor‐Based Tractography and Quantified Brain Atrophy for Analyzing Demyelination and Axonal Loss in MS

Fink, F., Klein, J., Lanz, M., Mitrovics, T., Lentschig, M. G., Hahn, H. K., & Hildebrandt, H. (2009) · Journal of Neuroimaging · doi:10.1111/j.1552-6569.2009.00377.x · Cited by 43 · see citing works

A Systematic Review of Resting-State Functional MRI Connectivity Changes and Cognitive Impairment in Multiple Sclerosis

Jandric, D., Doshi, A., Scott, R., Paling, D., Rog, D. J., Chataway, J., Schoonheim, M. M., Parker, G. J. M., & Muhlert, N. (2021) · Brain Connectivity · doi:10.1089/brain.2021.0104 · Cited by 42 · see citing works

Sensorimotor Cortex Gamma-Aminobutyric Acid Concentration Correlates with Impaired Performance in Patients with MS

Bhattacharyya, P. K., Phillips, M. D., Stone, L. A., Bermel, R. A., & Lowe, M. J. (2013) · American Journal of Neuroradiology · doi:10.3174/ajnr.a3483 · Cited by 42 · see citing works

Functional Homotopic Changes in Multiple Sclerosis with Resting-State Functional MR Imaging

Zhou, Y., Milham, M. P., Zuo, X., Kelly, C. A. M., Jaggi, H., Herbert, J., Grossman, R. I., & Ge, Y. (2013) · American Journal of Neuroradiology · doi:10.3174/ajnr.a3386 · Cited by 42 · see citing works

Characterizing Rapid Fluctuations of Resting State Functional Connectivity in Demyelinating, Neurodegenerative, and Psychiatric Conditions: From Static to Time-Varying Analysis

Valsasina, P., de la Cruz, M. H., Filippi, M., & Rocca, M. A. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00618 · Cited by 42 · see citing works

Cerebellar White Matter Damage Is Associated With Postural Sway Deficits in People With Multiple Sclerosis

Gera, G., Fling, B. W., & Horak, F. B. (2019) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2019.07.011 · Cited by 42 · see citing works

The diminished interhemispheric connectivity correlates with negative symptoms and cognitive impairment in first-episode schizophrenia

Mwansisya, T. E., Wang, Z., Tao, H., Zhang, H., Hu, A., Guo, S., & Liu, Z. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.07.018 · Cited by 41 · see citing works

Functional Brain Network Changes Associated with Maintenance of Cognitive Function in Multiple Sclerosis

Helekar, S. A., Shin, J. C., Mattson, B. J., Bartley, K. A., Stosic, M., Saldana-King, T., Montague, P. R., & Hutton, G. J. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00219 · Cited by 41 · see citing works

Electroencephalography-Derived Sensory and Motor Network Topology in Multiple Sclerosis Fatigue

Vecchio, F., Miraglia, F., Porcaro, C., Cottone, C., Cancelli, A., Rossini, P. M., & Tecchio, F. (2016) · Neurorehabilitation and neural repair · doi:10.1177/1545968316656055 · Cited by 41 · see citing works

How changes in brain activity and connectivity are associated with motor performance in people with MS

Peterson, D. S., & Fling, B. W. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.09.019 · Cited by 40 · see citing works

Altered likelihood of brain activation in attention and working memory networks in patients with multiple sclerosis: An ALE meta-analysis

Kollndorfer, K., Krajnik, J., Woitek, R., Freiherr, J., Prayer, D., & Schöpf, V. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.09.005 · Cited by 40 · see citing works

Structural and functional magnetic resonance imaging correlates of motor network dysfunction in primary progressive multiple sclerosis

Ceccarelli, A., Rocca, M. A., Valsasina, P., Rodegher, M., Falini, A., Comi, G., & Filippi, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07147.x · Cited by 40 · see citing works

Cross‐sectional and longitudinal multimodal structural imaging in prodromal Huntington's disease

Harrington, D. L., Long, J. D., Durgerian, S., Mourany, L., Koenig, K. A., Bonner‐Jackson, A., Paulsen, J. S., for the PREDICT‐HD Investigators of the Huntington Study Group, & Rao, S. M. (2016) · Movement Disorders · doi:10.1002/mds.26803 · Cited by 39 · see citing works

The relationship between BOLD fMRI response and the underlying white matter as measured by fractional anisotropy (FA): A systematic review

Warbrick, T., Rosenberg, J., & Shah, N. J. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.075 · Cited by 39 · see citing works

Advanced MRI in Multiple Sclerosis: Current Status and Future Challenges

Fox, R. J., Beall, E. B., Bhattacharyya, P. K., Chen, J. T., & Sakaie, K. (2011) · Neurologic Clinics · doi:10.1016/j.ncl.2010.12.011 · Cited by 38 · see citing works

Bayesian vector autoregressive model for multi‐subject effective connectivity inference using multi‐modal neuroimaging data

Chiang, S., Guindani, M., Yeh, H. J., Haneef, Z., Stern, J. M., & Vannucci, M. (2016) · Human Brain Mapping · doi:10.1002/hbm.23456 · Cited by 36 · see citing works

Scan-rescan repeatability and cross-scanner comparability of DTI metrics in healthy subjects in the SPRINT-MS multicenter trial

Zhou, X., Sakaie, K., Debbins, J. P., Narayanan, S., Fox, R. J., & Lowe, M. J. (2018) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2018.07.011 · Cited by 36 · see citing works

Resting-state connectivity of pre-motor cortex reflects disability in multiple sclerosis

Dogonowski, A.-M., Siebner, H. R., Sørensen, P. S., Paulson, O. B., Dyrby, T. B., Blinkenberg, M., & Madsen, K. H. (2013) · Acta Neurologica Scandinavica · doi:10.1111/ane.12121 · Cited by 36 · see citing works

The emergence of doing “nothing” as a viable paradigm design

Lowe, M. J. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.014 · Cited by 35 · see citing works

A historical perspective on the evolution of resting-state functional connectivity with MRI

Lowe, M. J. (2010) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-010-0230-y · Cited by 35 · see citing works

A multicentre study of motor functional connectivity changes in patients with multiple sclerosis

Valsasina, P., Rocca, M. A., Absinta, M., Sormani, M. P., Mancini, L., Stefano, N. D., Rovira, À., Gass, A., Enzinger, C., Barkhof, F., et al. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07623.x · Cited by 34 · see citing works

Abnormal functional connectivity during visuospatial processing is associated with disrupted organisation of white matter in autism

McGrath, J., Johnson, K. A., O’Hanlon, E., Garavan, H., Leemans, A., & Gallagher, L. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00434 · Cited by 33 · see citing works

Alterations in Functional and Structural Connectivity in Pediatric-Onset Multiple Sclerosis

Akbar, N., Giorgio, A., Till, C., Sled, J. G., Doesburg, S. M., Stefano, N. D., & Banwell, B. (2016) · PLoS ONE · doi:10.1371/journal.pone.0145906 · Cited by 34 · see citing works

Endogenous oscillations and networks in functional magnetic resonance imaging

Bandettini, P. A., & Bullmore, E. T. (2008) · Human Brain Mapping · doi:10.1002/hbm.20607 · Cited by 32 · see citing works

Stimulation of the Premotor Cortex Enhances Interhemispheric Functional Connectivity in Association with Upper Limb Motor Recovery in Moderate-to-Severe Chronic Stroke

Unger, R. H., Lowe, M. J., Beall, E. B., Béthoux, F., Jones, S. E., Machado, A. G., Plow, E. B., & Cunningham, D. A. (2023) · Brain Connectivity · doi:10.1089/brain.2022.0064 · Cited by 31 · see citing works

The resting‐state neurovascular coupling relationship: rapid changes in spontaneous neural activity in the somatosensory cortex are associated with haemodynamic fluctuations that resemble stimulus‐evoked haemodynamics

Bruyns‐Haylett, M., Harris, S., Boorman, L. W., Zheng, Y., Berwick, J., & Jones, M. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12295 · Cited by 30 · see citing works

Regions of interest for resting-state fMRI analysis determined by inter-voxel cross-correlation

Golestani, A., & Goodyear, B. G. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.038 · Cited by 29 · see citing works

Corpus Callosum Atrophy Correlates with Gray Matter Atrophy in Patients with Multiple Sclerosis

Klawiter, E. C., Ceccarelli, A., Arora, A., Jackson, J. S., Bakshi, S., Kim, G., Miller, J. R., Tauhid, S., von Gizycki, C., Bakshi, R., et al. (2014) · Journal of Neuroimaging · doi:10.1111/jon.12124 · Cited by 29 · see citing works

Effectiveness and neural mechanisms associated with tDCS delivered to premotor cortex in stroke rehabilitation: study protocol for a randomized controlled trial

Plow, E. B., Cunningham, D. A., Beall, E. B., Jones, S., Wyant, A., Bonnett, C. E., Yue, G. H., Lowe, M. J., Wang, X., Sakaie, K., et al. (2013) · Trials · doi:10.1186/1745-6215-14-331 · Cited by 30 · see citing works

Modern Methods for Interrogating the Human Connectome

Lowe, M. J., Sakaie, K., Beall, E. B., Calhoun, V. D., Bridwell, D. A., Rubinov, M., & Rao, S. M. (2016) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617716000060 · Cited by 28 · see citing works

Effect of MAOA Genotype on Resting-State Networks in Healthy Participants

Clemens, B., Voss, B., Pawliczek, C. M., Mingoia, G., Weyer, D., Repple, J., Eggermann, T., Zerres, K., Reetz, K., & Habel, U. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht366 · Cited by 27 · see citing works

SEVEN TOPICS IN FUNCTIONAL MAGNETIC RESONANCE IMAGING

Bandettini, P. A. (2009) · Journal of Integrative Neuroscience · doi:10.1142/s0219635209002186 · Cited by 28 · see citing works

Functional pathway-defined MRI diffusion measures reveal increased transverse diffusivity of water in multiple sclerosis

Lowe, M. J., Horenstein, C. I., Hirsch, J. G., Marrie, R. A., Stone, L. A., Bhattacharyya, P. K., Gass, A., & Phillips, M. D. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.04.208 · Cited by 60 · see citing works

Anatomic Connectivity Assessed Using Pathway Radial Diffusivity Is Related to Functional Connectivity in Monosynaptic Pathways

Lowe, M. J., Koenig, K. A., Beall, E. B., Sakaie, K., Stone, L. A., Bermel, R. A., & Phillips, M. D. (2014) · Brain Connectivity · doi:10.1089/brain.2014.0265 · Cited by 16 · see citing works

Functional connectivity in the dorsal network of the cervical spinal cord is correlated with diffusion tensor imaging indices in relapsing-remitting multiple sclerosis

Combes, A. J. E., O’Grady, K. P., Rogers, B. P., Schilling, K. G., Lawless, R. D., Visagie, M., Houston, D., Prock, L. E., Malone, S., Satish, S., et al. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.103127 · Cited by 18 · see citing works

Abnormal functional connectivity and cortical integrity influence dominant hand motor disability in multiple sclerosis: a multimodal analysis

zhong, J., Nantes, J. C., Holmes, S. A., Gallant, S., Narayanan, S., & Koski, L. M. (2016) · Human Brain Mapping · doi:10.1002/hbm.23307 · Cited by 27 · see citing works

Characterizing multiple sclerosis disease progression using a combined structural and functional connectivity metric

Bhattacharyya, P. K., Fox, R. J., Sakaie, K., Bena, J., Harvey, T., Raska, P., Lin, J. Y., & Lowe, M. J. (2023) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2023.07.016 · Cited by 4 · see citing works