Cited by 1,080Functional Brain Connectivity StudiesMind wandering and attentionNeural and Behavioral Psychology Studies

The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.

A Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging

McKiernan, Kristen A., Kaufman, Jacqueline N., Kucera-Thompson, Jane, Binder, Jeffrey R.·2003·Journal of Cognitive Neuroscience

DOI 10.1162/089892903321593117

Open this paper in CoChat — free account

Abstract

Task-induced deactivation (TID) refers to a regional decrease in blood flow during an active task relative to a “resting” or “passive” baseline. We tested the hypothesis that TID results from a reallocation of processing resources by parametrically manipulating task difficulty within three factors: target discriminability, stimulus presentation rate, and short-term memory load. Subjects performed an auditory target detection task during functional magnetic resonance imaging (fMRI), responding to a single target tone or, in the short-term memory load conditions, to target sequences. Seven task conditions (a common version and two additional levels for each of the three factors) were each alternated with “rest” in a block design. Analysis of covariance identified brain regions in which TID occurred. Analyses of variance identified seven regions (left anterior cingulate/superior frontal gyrus, left middle frontal gyrus, right anterior cingulate gyrus, left and right posterior cingulate gyrus, left posterior parieto-occipital cortex, and right precuneus) in which TID magnitude varied across task levels within a factor. Follow-up tests indicated that for each of the three factors, TID magnitude increased with task difficulty. These results suggest that TID represents reallocation of processing resources from areas in which TID occurs to areas involved in task performance. Short-term memory load and stimulus rate also predict suppression of spontaneous thought, and many of the brain areas showing TID have been linked with semantic processing, supporting claims that TID may be due in part to suspension of spontaneous semantic processes that occur during “rest” (Binder et al., 1999). The concept that the typical “resting state” is actually a condition characterized by rich cognitive activity has important implications for the design and analysis of neuroimaging studies.

Integrity signals

Registry

Crossref · 10.1162/089892903321593117

Cites

56 of 56 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

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
The Principles of Psychology
James, W. (1891) · Personality Culture Society · doi:10.1037/11059-000 · Cited by 25,876
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
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
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
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
Book Reviews: Keppel, Geoffrey. Design and Analysis: A Researcher’s Handbook . Englewood Cliffs, N. J.: Prentice Hall, 1973. 658 + xiii pp. $13.95
Beaton, A. E., & Keppel, G. (1975) · American Educational Research Journal · doi:10.2307/1162588 · Cited by 5,857
Imaging Cognition II: An Empirical Review of 275 PET and fMRI Studies
Cabeza, R., & Nyberg, L. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/08989290051137585 · Cited by 3,598
Emotion, Decision Making and the Orbitofrontal Cortex
Bechara, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.295 · Cited by 3,589
Searching for a baseline: Functional imaging and the resting human brain
Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371

Show all 56 references

Research works printed but not linked: 3

10.2466/pms.1966.23.2.399 · DOI · Paper page
Ingvar D. H., 1985, Human Neurobiology, 4, 127
McGuire P. K., 1996, NeuroReport, 7, 2095

Sorted by citations

Items 601–700 of 999

Noradrenaline transporter blockade increases fronto-parietal functional connectivity relevant for working memory
Hernaus, D., Santa, M. M. C., Offermann, J. S., & van Amelsvoort, T. (2017) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2017.02.004 · Cited by 33
Precision functional mapping of human memory systems
Gilmore, A. W., Nelson, S. M., & McDermott, K. B. (2021) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2020.12.013 · Cited by 27
Neural correlates of temporal-order judgments versus those of spatial-location: Deactivation of hippocampus may facilitate spatial performance
Rekkas, P. V., Westerveld, M., Skudlarski, P., Zumer, J. M., Pugh, K. R., Spencer, D. D., & Constable, R. T. (2005) · Brain and Cognition · doi:10.1016/j.bandc.2005.05.013 · Cited by 32
Merging Clinical Neuropsychology and Functional Neuroimaging to Evaluate the Construct Validity and Neural Network Engagement of then-Back Task
Kearney-Ramos, T. E., Fausett, J. S., Gess, J. L., Reno, A. J., Peraza, J., Kilts, C., & James, G. A. (2014) · Journal of the International Neuropsychological Society · doi:10.1017/s135561771400054x · Cited by 33
Controlling for individual differences in fMRI brain activation to tones, syllables, and words
Rimol, L. M., Specht, K., & Hugdahl, K. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.10.021 · Cited by 29
Impaired temporoparietal deactivation with working memory load in antipsychotic-naïve patients with first-episode schizophrenia
Nejad, A. B., Ebdrup, B. H., Siebner, H. R., Rasmussen, H., Aggernæs, B., Glenthoj, B. Y., & Baaré, W. F. C. (2011) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2010.556199 · Cited by 31
Brain metabolism in patients with hepatic encephalopathy studied by PET and MR
Keiding, S., & Pavese, N. (2013) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2013.05.006 · Cited by 29
Menstrual cycle variations in the BOLD-response to a number bisection task: Implications for research on sex differences
Pletzer, B. A., Kronbichler, M., Ladurner, G., Nuerk, H., & Kerschbaum, H. (2011) · Brain Research · doi:10.1016/j.brainres.2011.08.058 · Cited by 29
Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia
Mothersill, O., Tangney, N., Morris, D. W., McCarthy, H., Frodl, T., Gill, M., Corvin, A. P., & Donohoe, G. J. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2016.11.043 · Cited by 31
Challenge to Promote Change: The Neural Basis of the Contextual Interference Effect in Young and Older Adults
Pauwels, L., Chalavi, S., Gooijers, J., Maes, C., Albouy, G., Sunaert, S. G., & Swinnen, S. P. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2640-17.2018 · Cited by 29
Response time as a proxy of ongoing mental state: A combined fMRI and pupillometry study in Generalized Anxiety Disorder
Makovac, E., Fagioli, S., Watson, D. R., Meeten, F., Smallwood, J., Critchley, H., & Ottaviani, C. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.02.038 · Cited by 29
Altered brain response without behavioral attention deficits in healthy siblings of schizophrenic patients
Sepede, G., Ferretti, A., Perrucci, M. G., Gambi, F., Donato, F. D., Nuccetelli, F., Gratta, C. D., Tartaro, A., Salerno, R. M., Ferro, F. M., et al. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.07.053 · Cited by 29
Default brain functionality in blind people
Burton, H., Snyder, A. Z., & Raichle, M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406676101 · Cited by 29
Event-related functional MRI investigation of vocal pitch variation☆
Peck, K. K., Galgano, J., Branski, R. C., Bogomolny, D., Ho, M., Holodny, A. I., & Kraus, D. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.08.034 · Cited by 30
‘Do I like this person?’ A network analysis of midline cortex during a social preference task
Chen, A. C., Welsh, R. C., Liberzon, I., & Taylor, S. F. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.044 · Cited by 30
An fMRI study of multimodal selective attention in schizophrenia
Mayer, A. R., Hanlon, F. M., Teshiba, T. M., Klimaj, S. D., Ling, J. M., Dodd, A. B., Calhoun, V. D., Bustillo, J., & Toulouse, T. (2015) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.114.155499 · Cited by 28
Stimulus pacing affects the activation of the medial temporal lobe during a semantic classification task: An fMRI study
Tieleman, A., Seurinck, R., Deblaere, K., Vandemaele, P., Vingerhoets, G., & Achten, E. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.02.017 · Cited by 28
Precuneus degeneration in nondemented elderly individuals with APOE ɛ4: Evidence from structural and functional MRI analyses
Chen, Y., Liu, Z., Zhang, J., Chen, K., Li, Y., Li, X., Gong, G., Wang, J., & Zhang, Z. (2016) · Human Brain Mapping · doi:10.1002/hbm.23359 · Cited by 29
Brain activity in struggling readers before intervention relates to future reading gains
Nugiel, T., Roe, M. A., Taylor, W. P., Cirino, P. T., Vaughn, S. R., Fletcher, J. M., Juranek, J. J., & Church, J. A. (2018) · Cortex · doi:10.1016/j.cortex.2018.11.009 · Cited by 27
Sex Differences in the Processing of Global vs. Local Stimulus Aspects in a Two-Digit Number Comparison Task – An fMRI Study
Pletzer, B. A., Kronbichler, M., Nuerk, H., & Kerschbaum, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053824 · Cited by 28
Activation of the Occipital Cortex and Deactivation of the Default Mode Network During Working Memory in the Early Blind
Park, H., Chun, J., Park, B., Park, H., Kim, J. I., Lee, J. D., & Kim, J. (2011) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617711000051 · Cited by 32
Brain Correlates of Mathematical Competence in Processing Mathematical Representations
Grabner, R. H., Reishofer, G., Koschutnig, K., & Ebner, F. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00130 · Cited by 29
Resting state default mode network connectivity in children and adolescents with ADHD after acute tryptophan depletion
Biskup, C. S., Helmbold, K., Baurmann, D., Klasen, M., Gaber, T. J., Bubenzer‐Busch, S., Königschulte, W., Fink, G. R., & Zepf, F. D. (2016) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12573 · Cited by 30
Effects of low- and high-intensity exercise on emotional face processing: an fMRI face-matching study
Schmitt, A., Martin, J. A., Rojas, S., Vafa, R., Scheef, L., Strüder, H. K., & Boecker, H. (2019) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsz042 · Cited by 28
Spontaneous fMRI activity during resting wakefulness and sleep
Duyn, J. H. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53839-0.00019-3 · Cited by 29
Brain activation and deactivation during location and color working memory tasks in 11-13-year-old children.
Vuontela, V., Steenari, M., Aronen, E., Korvenoja, A., Aronen, H., & Carlson, S. (2009) · Brain and Cognition · doi:10.1016/j.bandc.2008.05.010 · Cited by 30
Neural Correlates of Enhanced Memory for Meaningful Associations with Age
Amer, T., Giovanello, K. S., Nichol, D. R., Hasher, L., & Grady, C. L. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy334 · Cited by 28
Skill dependent audiovisual integration in the fusiform induces repetition suppression
McNorgan, C., & Booth, J. R. (2015) · Brain and Language · doi:10.1016/j.bandl.2014.12.002 · Cited by 26
Sleep deprivation reduces the rate of rapid picture processing
Kong, D., Asplund, C. L., & Chee, M. W. L. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.01.037 · Cited by 25
Brain network changes and memory decline in aging
Beason‐Held, L. L., Hohman, T. J., Venkatraman, V. K., An, Y., & Resnick, S. M. (2016) · Brain Imaging and Behavior · doi:10.1007/s11682-016-9560-3 · Cited by 26
Deep learning for sex classification in resting-state and task functional brain networks from the UK Biobank
Leming, M., & Suckling, J. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118409 · Cited by 20
Neural Correlates of Variation in Personal Space and Social Functioning in Schizophrenia and Healthy Individuals
Zapetis, S. L., Nasiriavanaki, Z., Luther, L., & Holt, D. J. (2022) · Schizophrenia Bulletin · doi:10.1093/schbul/sbac052 · Cited by 27
White matter microstructure contributes to age-related declines in task-induced deactivation of the default mode network
Brown, C. A., Hakun, J. G., Zhu, Z., Johnson, N. F., & Gold, B. T. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00194 · Cited by 26
Transverse patterning dissociates human EEG theta power and hippocampal BOLD activation
Meltzer, J. A., Fonzo, G. A., & Constable, R. T. (2008) · Psychophysiology · doi:10.1111/j.1469-8986.2008.00719.x · Cited by 26
Abnormal synchrony and effective connectivity in patients with schizophrenia and auditory hallucinations
de la Iglesia-Vayá, M., Escartí, M. J., Molina‐Mateo, J., Martí‐Bonmatí, L., Gadea, M., Castellanos, F. X., Aguilar, E. J., Robles, M., Biswal, B. B., & Sanjuán, J. (2014) · NeuroImage Clinical · doi:10.1016/j.nicl.2014.08.027 · Cited by 26
The Effect of Long-Acting Risperidone on Working Memory in Schizophrenia
Surguladze, S. A., Chu, E. M.-Y., Evans, A., Anilkumar, A. P., Patel, M. X., Timehin, C., & David, A. S. (2007) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0b013e31815a256c · Cited by 25
Beyond dopamine: functional MRI predictors of responsiveness to cognitive behaviour therapy for psychosis
Kumari, V. (2010) · Frontiers in Behavioral Neuroscience · doi:10.3389/neuro.08.004.2010 · Cited by 25
SEVEN TOPICS IN FUNCTIONAL MAGNETIC RESONANCE IMAGING
Bandettini, P. A. (2009) · Journal of Integrative Neuroscience · doi:10.1142/s0219635209002186 · Cited by 28
Are you listening? Brain activation associated with sustained nonspatial auditory attention in the presence and absence of stimulation
Seydell‐Greenwald, A., Greenberg, A. S., & Rauschecker, J. P. (2013) · Human Brain Mapping · doi:10.1002/hbm.22323 · Cited by 27
Default mode network deactivation during odor–visual association
Karunanayaka, P., Wilson, D. A., Tobia, M. J., Martinez, B., Meadowcroft, M. D., Eslinger, P. J., & Yang, Q. X. (2016) · Human Brain Mapping · doi:10.1002/hbm.23440 · Cited by 27
Brain processing of rectal sensation in adolescents with functional defecation disorders and healthy controls
Mugie, S., Koppen, I., van den Berg, M. M., Groot, P., Reneman, L., de Ruiter, M. D., & Benninga, M. A. (2018) · Neurogastroenterology and Motility · doi:10.1111/nmo.13228 · Cited by 23
Long reaction times are associated with delayed brain activity in lewy body dementia
Firbank, M., O'Brien, J. T., & Taylor, J. (2017) · Human Brain Mapping · doi:10.1002/hbm.23866 · Cited by 26
Done That: Short-term Repetition Related Modulations of Motor Cortex Activity as a Stable Signature for Overnight Motor Memory Consolidation
Gabitov, E., Manor, D., & Karni, A. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00675 · Cited by 26
fMRI investigation of working memory in adolescents with surgically treated congenital heart disease
King, T. Z., Smith, K. M., Burns, T. G., Sun, B., Shin, J., Jones, R. A., Drossner, D., & Mahle, W. T. (2017) · Applied Neuropsychology: Child · doi:10.1080/21622965.2015.1065185 · Cited by 25
The neural correlates of sex differences in left–right confusion
Hjelmervik, H., Westerhausen, R., Hirnstein, M., Specht, K., & Hausmann, M. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.02.066 · Cited by 25
Brain Metabolism in Substance-Induced Psychosis and Schizophrenia: A Preliminary PET Study
Dragogna, F., Mauri, M. C., Marotta, G., Armao, F. T., Brambilla, P., & Altamura, A. C. (2014) · Neuropsychobiology · doi:10.1159/000366485 · Cited by 27
Contributive sources analysis: A measure of neural networks' contribution to brain activations
Beldzik, E., Domagalik, A., Daselaar, S. M., Fąfrowicz, M., Froncisz, W., Ogińska, H., & Marek, T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.014 · Cited by 24
Reduced load-dependent default mode network deactivation across executive tasks in schizophrenia spectrum disorders
Haatveit, B. C., Jensen, J., Alnæs, D., Kaufmann, T., Brandt, C. L., Thoresen, C., Andreassen, O. A., Melle, I. S., Ueland, T., & Westlye, L. T. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.08.012 · Cited by 26
Functional Magnetic Resonance Imaging
Sweet, L. H. (2010) · Springer eBooks · doi:10.1007/978-1-4419-6373-4_3 · Cited by 26
Recency Effects in the Inferior Parietal Lobe during Verbal Recognition Memory
Buchsbaum, B. R., Ye, D., & D’Esposito, M. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00059 · Cited by 23
Effective connectivity among the working memory regions during preparation for and during performance of the n-back task
Manelis, A., & Reder, L. M. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00593 · Cited by 28
Regional cerebral blood flow increases during wakeful rest following cognitive training
Mazoyer, B. M., Houdé, O., Joliot, M., Mellet, E., & Tzourio‐Mazoyer, N. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.06.021 · Cited by 25
The Functional Topography and Temporal Dynamics of Overlapping and Distinct Brain Activations for Adaptive Task Control and Stable Task-set Maintenance during Performance of an fMRI-adapted Clinical Continuous Performance Test
Olsen, A., Brunner, J. F., Evensen, K. A. I., Garzón, B., Landrø, N. I., & Haberg, A. K. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00358 · Cited by 25
Overlapping but Divergent Neural Correlates Underpinning Audiovisual Synchrony and Temporal Order Judgments
Love, S., Petrini, K., Pernet, C. R., Latinus, M., & Pollick, F. E. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00274 · Cited by 25
Hello, is that me you are looking for? A re-examination of the role of the DMN in social and self relevant aspects of off-task thought
Murphy, C., Poerio, G. L., Sormaz, M., Wang, H.-T., Vatansever, D., Allen, M., Margulies, D. S., Jefferies, E., & Smallwood, J. (2019) · PLoS ONE · doi:10.1371/journal.pone.0216182 · Cited by 26
Resting-state brain network connectivity is an independent predictor of responsiveness to language therapy in chronic post-stroke aphasia
Falconer, I., Varkanitsa, M., & Kiran, S. (2024) · Cortex · doi:10.1016/j.cortex.2023.11.022 · Cited by 24
Characterizing nonlinear relationships in functional imaging data using eigenspace maximal information canonical correlation analysis (emiCCA)
Dong, L., Zhang, Y., Zhang, R., Zhang, X., Gong, D., Valdes-Sosa, P. A., Xu, P., Luo, C., & Yao, D. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.006 · Cited by 24
Emotion-related cerebral blood flow changes in the ventral medial prefrontal cortex: An NIRS study
Ozawa, S., Kanayama, N., & Hiraki, K. (2019) · Brain and Cognition · doi:10.1016/j.bandc.2019.05.001 · Cited by 26
Structural disconnectome mapping of cognitive function in poststroke patients
Kolskår, K. K., Ulrichsen, K. M., Richard, G., Dørum, E. S., de Schotten, M. T., Rokicki, J., Sánchez, J. M., Engvig, A., Hansen, H. I., Nordvik, J. E., et al. (2022) · Brain and Behavior · doi:10.1002/brb3.2707 · Cited by 24
The relationship between task‐related and subsequent memory effects
de Chastelaine, M., & Rugg, M. D. (2014) · Human Brain Mapping · doi:10.1002/hbm.22430 · Cited by 24
Functional neuroimaging study of performances on a Go/No-go task in 6- to 7-year-old preterm children: Impact of intrauterine growth restriction
Réveillon, M., Urben, S., Barisnikov, K., Tolsa, C. B., Hüppi, P. S., & Lazeyras, F. (2013) · NeuroImage Clinical · doi:10.1016/j.nicl.2013.10.007 · Cited by 25
The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals
Rose, E. J., Greene, C. M., Kelly, S., Morris, D. W., Robertson, I. H., Fahey, C., Jacobson, S. C., O’Doherty, J. P., Newell, F. N., McGrath, J., et al. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.054 · Cited by 24
Response to Comment on "Wandering Minds: The Default Network and Stimulus-Independent Thought"
Mason, M. F., Norton, M. I., Horn, J. D. V., Wegner, D. M., Grafton, S. T., & Macrae, C. N. (2007) · Science · doi:10.1126/science.1141078 · Cited by 24
Evidence for Corticostriatal Dysfunction During Cognitive Skill Learning in Adolescent Siblings of Patients With Childhood-Onset Schizophrenia
Wagshal, D., Knowlton, B. J., Suthana, N., Cohen, J. R., Poldrack, R. A., Bookheimer, S. Y., Bilder, R. M., & Asarnow, R. F. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt147 · Cited by 24
Increase of posterior connectivity in aging within the Ventral Attention Network: A functional connectivity analysis using independent component analysis
Deslauriers, J., Ansado, J., Marrelec, G., Provost, J.-S., & Joanette, Y. (2016) · Brain Research · doi:10.1016/j.brainres.2016.12.017 · Cited by 24
The Effects of Age, from Young to Middle Adulthood, and Gender on Resting State Functional Connectivity of the Dopaminergic Midbrain
Peterson, A. C., Zhang, S., Hu, S., Chao, H. H., & Li, C. R. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00052 · Cited by 25
Attention-Related Brain Activation Is Altered in Older Adults With White Matter Hyperintensities Using Multi-Echo fMRI
Atwi, S., Metcalfe, A. W. S., Robertson, A. D., Rezmovitz, J., Anderson, N. D., & MacIntosh, B. J. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00748 · Cited by 26
Prism adaptation enhances decoupling between the default mode network and the attentional networks
Wilf, M., Serino, A., Clarke, S., & Crottaz‐Herbette, S. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.06.050 · Cited by 24
Childhood urbanicity interacts with polygenic risk for depression to affect stress-related medial prefrontal function
Zhang, X., Yan, H., Yu, H., Zhao, X., Shah, S., Dong, Z., Yang, G., Zhang, X., Muse, T., Li, J., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01650-x · Cited by 25
Neural circuitry associated with two different approaches to novel word learning
Clements-Stephens, A. M., Materek, A., Eason, S. H., Scarborough, H. S., Pugh, K. R., Rimrodt, S. L., Pekar, J. J., & Cutting, L. E. (2011) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2011.06.001 · Cited by 23
All that glitters is not BOLD: inconsistencies in functional MRI
Renvall, V., Nangini, C., & Hari, R. (2014) · Scientific Reports · doi:10.1038/srep03920 · Cited by 23
The Default Mode Network Differentiates Biological From Non-Biological Motion
Dayan, E., Sella, I., Mukovskiy, A., Douek, Y., Giese, M. A., Malach, R., & Flash, T. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu199 · Cited by 27
Time-Perception Network and Default Mode Network Are Associated with Temporal Prediction in a Periodic Motion Task
Carvalho, F. M., Chaim, K. T., Sanchez, T. A., & de Araújo, D. B. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00268 · Cited by 23
Load-dependent hyperdeactivation of the default mode network in people with schizophrenia
Hahn, B., Harvey, A. N., Gold, J. M., Ross, T. J., & Stein, E. A. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.01.001 · Cited by 22
Default Network Activity Is Associated with Better Performance in a Vigilance Task
Bogler, C., Vowinkel, A., Zhutovsky, P., & Haynes, J. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00623 · Cited by 22
Functional MRI of Letter Cancellation Task Performance in Older Adults
Deng, I. D., Chung, L., Talwar, N. A., Tam, F., Churchill, N. W., Schweizer, T. A., & Graham, S. J. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00097 · Cited by 24
Differential effects of DAAO on regional activation and functional connectivity in schizophrenia, bipolar disorder and controls
Papagni, S. A., Mechelli, A., Prata, D. P., Kambeitz, J. P., Fu, C. H. Y., Picchioni, M., Walshe, M., Toulopoulou, T., Bramon, E., Murray, R. M., et al. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.037 · Cited by 22
Cognitive, Intervention, and Neuroimaging Perspectives on Executive Function in Children With Reading Disabilities
Church, J. A., Cirino, P. T., Miciak, J., Juranek, J. J., Vaughn, S. R., & Fletcher, J. M. (2019) · New Directions for Child and Adolescent Development · doi:10.1002/cad.20292 · Cited by 24
Scale Invariance in fNIRS as a Measurement of Cognitive Load
Zhuang, C., Meidenbauer, K. L., Kardan, O., Stier, A. J., Choe, K. W., Cardenas‐Iniguez, C., Huppert, T. J., & Berman, M. G. (2021) · Cortex · doi:10.1016/j.cortex.2022.05.009 · Cited by 23
Neural effects of cognitive control load on auditory selective attention
Sabri, M., Humphries, C., Verber, M., Liebenthal, E., Binder, J. R., Mangalathu-Arumana, J., & Desai, A. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.06.009 · Cited by 25
Self-citation
Dysfunctional neural networks associated with impaired social interactions in early psychosis: an ICA analysis
Mazza, M., Catalucci, A., Pino, M. C., Giusti, L., Nigri, A., Pollice, R., Roncone, R., CASACCHIA, M., & Gallucci, M. (2013) · Brain Imaging and Behavior · doi:10.1007/s11682-013-9223-6 · Cited by 22
Going Their Separate Ways: Dissociation of Hippocampal and Dorsolateral Prefrontal Activation during Episodic Retrieval and Post-retrieval Processing
Israel, S. L., Seibert, T. M., Black, M. L., & Brewer, J. B. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21198 · Cited by 22
Hyperdeactivation of the Default Mode Network in People With Schizophrenia When Focusing Attention in Space
Hahn, B., Harvey, A. N., Gold, J. M., Fischer, B. A., Keller, W. R., Ross, T. J., & Stein, E. A. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbw019 · Cited by 21
Gene Expression Correlates of the Cortical Network Underlying Sentence Processing
Kong, X., Tzourio‐Mazoyer, N., Joliot, M., Fedorenko, E. G., Liu, J., Fisher, S. E., & Francks, C. (2020) · Neurobiology of Language · doi:10.1162/nol_a_00004 · Cited by 24
Working memory in schizotypal personality disorder: fMRI activation and deactivation differences
Vu, M.-A. T., Thermenos, H. W., Terry, D. P., Wolfe, D. J., Voglmaier, M. M., Niznikiewicz, M. A., McCarley, R. W., Seidman, L. J., & Dickey, C. C. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.09.013 · Cited by 23
Brain processes in women and men in response to emotive sounds
Rigo, P., Pisapia, N. D., Bornstein, M. H., Putnick, D. L., Serra, M., Esposito, G., & Venuti, P. (2016) · Social Neuroscience · doi:10.1080/17470919.2016.1150341 · Cited by 22
Association of functional connectivity of the executive control network or default mode network with cognitive impairment in older adults with remitted major depressive disorder or mild cognitive impairment
Rashidi‐Ranjbar, N., Rajji, T. K., Hawco, C. S., Kumar, S., Herrmann, N., Mah, L., Flint, A. J., Fischer, C. E., Butters, M. A., Pollock, B. G., et al. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01308-2 · Cited by 23
Spatiotemporal consistency of local neural activities: A new imaging measure for functional MRI data
Dong, L., Luo, C., Cao, W., Zhang, R., Gong, J., Gong, D., & Yao, D. (2014) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.24831 · Cited by 23
An Event-Related fMRI Study of Phonological Verbal Working Memory in Schizophrenia
Kim, J., Matthews, N. L., & Park, S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012068 · Cited by 25
An external focus of attention is aconditio sine qua nonfor athletes: a response to Carson, Collins, and Toner (2015)
Wulf, G. (2016) · Journal of Sports Sciences · doi:10.1080/02640414.2015.1136746 · Cited by 21
Brain Activation and Psychomotor Speed in Middle-Aged Patients with Type 1 Diabetes: Relationships with Hyperglycemia and Brain Small Vessel Disease
Hwang, M., Tudorascu, D., Nunley, K. A., Karim, H. T., Aizenstein, H. J., Orchard, T. J., & Rosano, C. (2016) · Journal of Diabetes Research · doi:10.1155/2016/9571464 · Cited by 21
Functional brain networks involved in gaze and emotional processing
Ziaei, M., Ebner, N. C., & Burianová, H. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13464 · Cited by 21
Hypothalamic tumors impact gray and white matter volumes in fronto-limbic brain areas
Özyurt, J., Muller, H. L., Warmuth‐Metz, M., & Thiel, C. M. (2017) · Cortex · doi:10.1016/j.cortex.2017.01.017 · Cited by 21
General intelligence is associated with working memory-related brain activity: new evidence from a large sample study
Takeuchi, H., Taki, Y., Nouchi, R., Yokoyama, R., Kotozaki, Y., Nakagawa, S., Sekiguchi, A., Iizuka, K., Hanawa, S., Araki, T., et al. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1747-5 · Cited by 23
The left dorsal striatum is involved in the processing of neutral feedback
Behne, N., Scheich, H., & Brechmann, A. (2008) · Neuroreport · doi:10.1097/wnr.0b013e32830fe98c · Cited by 17
Disrupted functional connectivity of the default mode network due to acute vestibular deficit
Klingner, C. M., Volk, G. F., Brodoehl, S., Witte, O. W., & Guntinas‐Lichius, O. (2014) · NeuroImage Clinical · doi:10.1016/j.nicl.2014.08.022 · Cited by 22
Erratum: search-related suppression of hippocampus and default network activity during associative memory retrieval
Reas, E. T., Gimbel, S. I., Hales, J. B., & Brewer, J. B. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00002 · Cited by 22
The relationship between negative BOLD responses and ERS and ERD of alpha/beta oscillations in visual and motor cortex
Wilson, R., Mullinger, K. J., Francis, S., & Mayhew, S. D. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.06.009 · Cited by 19
The “two-brain” approach reveals the active role of task-deactivated default mode network in speech comprehension
Liu, L., Li, H., Ren, Z., Zhou, Q., Zhang, Y.-X., Lu, C., Qiu, J., Chen, H., & Ding, G. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab521 · Cited by 21
The effect of acute tryptophan depletion on emotional distraction and subsequent memory
Wang, L., Mullette-Gillman, O. A., Gadde, K. M., Kuhn, C. M., McCarthy, G., & Huettel, S. A. (2009) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsp025 · Cited by 21

Authors: McKiernan, K. A., Kaufman, J. N., Kucera-Thompson, J., & Binder, J. R.
Affiliations: Medical College of Wisconsin (US)
ORCID: Kaufman, Jacqueline N.
Binder, Jeffrey R.
Venue: Journal of Cognitive Neuroscience
Publisher: MIT Press
Published: 2003-04-01
Volume: 15
Issue: 3
Pages: 394-408
ISSN: 0898-929X (ISSN-L)
1530-8898
DOI: 10.1162/089892903321593117
OpenAlex: W2169605136
Cited by: 1,080
References: 56
Citations by year: 2026: 12 · 2025: 15 · 2024: 19 · 2023: 20 · 2022: 29 · 2021: 41 · 2020: 42 · 2019: 47 · 2018: 33 · 2017: 39 · 2016: 62 · 2015: 44 · 2014: 77 · 2013: 82 · 2012: 76
FWCI: 14.96
Type: journal article
Language: en
Open access: closed
Locations: Journal of Cognitive Neuroscience (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of Mental Health (P01MH051358, P0 MH51358)
National Institute of Neurological Disorders and Stroke (R01NS033576)
National Center for Research Resources (M01RR000058)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
Life Sciences › Neuroscience › Cognitive Neuroscience › Mind wandering and attention
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords: task-induced deactivation, resting state, task difficulty, stimulus presentation rate, auditory target detection, posterior cingulate cortex, precuneus, anterior cingulate cortex, semantic processing
MeSH terms: Acoustic Stimulation, Adult, Auditory Perception, Brain, Brain Mapping, Cerebrovascular Circulation, Female, Humans, Magnetic Resonance Imaging, Male, Memory, Short-Term, Mental Processes, Middle Aged

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

A Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks