Temporal Autocorrelation in Univariate Linear Modeling of FMRI Data

SUSAN—a new approach to low level image processing

Smith, S. M., & Brady, J. M. (1997) · International Journal of Computer Vision · doi:10.1023/a:1007963824710 · Cited by 3,333

Distracted and down: neural mechanisms of affective interference in subclinical depression

Kaiser, R. H., Andrews-Hanna, J. R., Spielberg, J. M., Warren, S. L., Sutton, B. P., Miller, G. A., Heller, W., & Banich, M. T. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu100 · Cited by 147

Being right is its own reward: load and performance related ventral striatum activation to correct responses during a working memory task in youth

Satterthwaite, T. D., Ruparel, K., Loughead, J., Elliott, M. A., Gerraty, R. T., Calkins, M. E., Hakonarson, H., Gur, R. C., Gur, R. E., & Wolf, D. H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.060 · Cited by 148

A functional magnetic resonance imaging investigation of uncertainty in adolescents with anxiety disorders

Krain, A. L., Gotimer, K., Hefton, S., Ernst, M., Castellanos, F. X., Pine, D. S., & Milham, M. P. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.06.011 · Cited by 147

Glucocorticoids Decrease Hippocampal and Prefrontal Activation during Declarative Memory Retrieval in Young Men

Oei, N. Y. L., Elzinga, B. M., Wolf, O. T., de Ruiter, M. B., Damoiseaux, J. S., Kuijer, J. P. A., Veltman, D. J., Scheltens, P., & Rombouts, S. A. R. B. (2007) · Brain Imaging and Behavior · doi:10.1007/s11682-007-9003-2 · Cited by 146

Multiple Somatotopic Representations of Heat and Mechanical Pain in the Operculo-Insular Cortex: A High-Resolution fMRI Study

Baumgärtner, U., Iannetti, G. D., Zambreanu, L., Stoeter, P., Treede, R.-D., & Tracey, I. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00253.2010 · Cited by 145

Neurological correlates of reward responding in adolescents with and without externalizing behavior disorders

Gatzke-Kopp, L. M., Beauchaine, T. P., Shannon, K. E., Chipman, J., Fleming, A. P., Crowell, S. E., Liang, O., Johnson, L. C., & Aylward, E. (2009) · Journal of Abnormal Psychology · doi:10.1037/a0014378 · Cited by 137

Brain Mechanisms Supporting Discrimination of Sensory Features of Pain: A New Model

Oshiro, Y., Quevedo, A. S., McHaffie, J. G., Kraft, R. A., & Coghill, R. C. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5538-08.2009 · Cited by 133

Co-occurring anxiety influences patterns of brain activity in depression

Engels, A. S., Heller, W., Spielberg, J. M., Warren, S. L., Sutton, B. P., Banich, M. T., & Miller, G. A. (2010) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.10.1.141 · Cited by 133

Measuring neural representations with fMRI: practices and pitfalls

Davis, T., & Poldrack, R. A. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12156 · Cited by 132

Neural systems for executive and emotional processing are modulated by symptoms of posttraumatic stress disorder in Iraq War veterans

Morey, R. A., Petty, C. M., Cooper, D. A., LaBar, K. S., & McCarthy, G. (2008) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2007.07.007 · Cited by 131

Neural correlates of craving and resisting craving for tobacco in nicotine dependent smokers

Hartwell, K. J., Johnson, K. A., Li, X., Myrick, H., LeMatty, T., George, M. S., & Brady, K. T. (2011) · Addiction Biology · doi:10.1111/j.1369-1600.2011.00340.x · Cited by 129

Brain Mechanisms Supporting Spatial Discrimination of Pain

Oshiro, Y., Quevedo, A. S., McHaffie, J. G., Kraft, R. A., & Coghill, R. C. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5128-06.2007 · Cited by 128

Effect of baseline cannabis use and working‐memory network function on changes in cannabis use in heavy cannabis users: a prospective fMRI study

Cousijn, J., Wiers, R. W., Ridderinkhof, K. R., van den Brink, W., Veltman, D. J., & Goudriaan, A. E. (2014) · Human Brain Mapping · doi:10.1002/hbm.22342 · Cited by 125

Exciting fear in adolescence: does pubertal development alter threat processing?

Spielberg, J. M., Olino, T. M., Forbes, E. E., & Dahl, R. E. (2014) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2014.01.004 · Cited by 123

Practice effects in the brain: Changes in cerebral activation after working memory practice depend on task demands

Jolles, D. D., Grol, M. J., Van Buchem, M. A., Rombouts, S. A. R. B., & Crone, E. A. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.04.028 · Cited by 122

Risk for depression and neural responses to fearful facial expressions of emotion

Chan, S. W. Y., Norbury, R., Goodwin, G. M., & Harmer, C. J. (2009) · British Journal of Psychiatry · doi:10.1192/bjp.bp.107.047993 · Cited by 117

Down but not out in posterior cingulate cortex: Deactivation yet functional coupling with prefrontal cortex during demanding semantic cognition

Krieger-Redwood, K., Jefferies, E., Karapanagiotidis, T., Seymour, R., Nunes, A., Ang, J. W. A., Majernikova, V., Mollo, G., & Smallwood, J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.07.060 · Cited by 106

Neural pattern similarity predicts long-term fear memory

Visser, R. M., Scholte, H. S., Beemsterboer, T., & Kindt, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3345 · Cited by 118

Brain networks predicting placebo analgesia in a clinical trial for chronic back pain

Hashmi, J. A., Baria, A. T., Baliki, M. N., Huang, L., Schnitzer, T. J., & Apkarian, V. A. (2012) · Pain · doi:10.1016/j.pain.2012.08.008 · Cited by 115

Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism

Gordon, I., Jack, A., Pretzsch, C. M., Vander Wyk, B., Leckman, J. F., Feldman, R., & Pelphrey, K. A. (2016) · Scientific Reports · doi:10.1038/srep35054 · Cited by 114

The cortical connectivity of the periaqueductal gray and the conditioned response to the threat of breathlessness

Faull, O. K., & Pattinson, K. T. (2017) · eLife · doi:10.7554/elife.21749 · Cited by 110

Short-term antidepressant treatment modulates amygdala response to happy faces

Norbury, R., Taylor, M. J., Selvaraj, S., Murphy, S. E., Harmer, C. J., & Cowen, P. J. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1597-1 · Cited by 109

Adaptive coding of action values in the human rostral cingulate zone

Jocham, G., Neumann, J., Klein, T. A., Danielmeier, C., & Ullsperger, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0349-09.2009 · Cited by 106

fMRI activation in the amygdala and the orbitofrontal cortex in unmedicated subjects with major depressive disorder

Townsend, J. D., Eberhart, N. K., Bookheimer, S. Y., Eisenberger, N. I., Foland-Ross, L. C., Cook, I. A., Sugar, C. A., & Altshuler, L. L. (2010) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2010.06.001 · Cited by 105

A Basal Forebrain-Cingulate Circuit in Macaques Decides It Is Time to Act

Khalighinejad, N., Bongioanni, A., Verhagen, L., Folloni, D., Attali, D., Aubry, J.-F., Sallet, J., & Rushworth, M. F. S. (2020) · Neuron · doi:10.1016/j.neuron.2019.10.030 · Cited by 90

Extended self: medial prefrontal activity during transient association of self and objects

Kim, K., & Johnson, M. K. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq096 · Cited by 104

Influence of attentional demands on the processing of emotional facial expressions in the amygdala

Silvert, L., Lepsien, J., Fragopanagos, N., Goolsby, B., Kiss, M., Taylor, J. G., Raymond, J. E., Shapiro, K. L., Eimer, M., & Nobre, A. C. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.023 · Cited by 104

Low dose intranasal oxytocin delivered with Breath Powered device dampens amygdala response to emotional stimuli: A peripheral effect-controlled within-subjects randomized dose-response fMRI trial

Quintana, D. S., Westlye, L. T., Alnæs, D., Rustan, Ø. G., Kaufmann, T., Smerud, K. T., Mahmoud, R. A., Djupesland, P. G., & Andreassen, O. A. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.04.010 · Cited by 102

The Incentive Salience of Alcohol: Translating the Effects of Genetic Variant in CNR1

Hutchison, K. E., Haughey, H., Niculescu, M., Schacht, J., Kaiser, A., Stitzel, J., Horton, W. J., & Filbey, F. (2008) · Archives of General Psychiatry · doi:10.1001/archpsyc.65.7.841 · Cited by 102

Elevated response of human amygdala to neutral stimuli in mild post traumatic stress disorder: neural correlates of generalized emotional response

Brunetti, M., Sepede, G., Mingoia, G., Catani, C., Ferretti, A., Merla, A., Del Gratta, C., Romani, G. L., & Babiloni, C. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.024 · Cited by 101

Increased Amygdala Response to Positive Social Feedback in Young People with Major Depressive Disorder

Davey, C. G., Allen, N. B., Harrison, B. J., & Yücel, M. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.12.004 · Cited by 98

Affective context interferes with cognitive control in unipolar depression: an fMRI investigation

Dichter, G. S., Felder, J. N., & Smoski, M. J. (2009) · Journal of Affective Disorders · doi:10.1016/j.jad.2008.06.027 · Cited by 99

An fMRI examination of developmental differences in the neural correlates of uncertainty and decision‐making

Krain, A. L., Hefton, S., Pine, D. S., Ernst, M., Xavier Castellanos, F., Klein, R. G., & Milham, M. P. (2006) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2006.01677.x · Cited by 94

Reward-Guided Learning with and without Causal Attribution

Jocham, G., Brodersen, K. H., Constantinescu, A. O., Kahn, M. C., Ianni, A. M., Walton, M. E., Rushworth, M. F. S., & Behrens, T. E. J. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.018 · Cited by 92

Major depressive disorder is characterized by greater reward network activation to monetary than pleasant image rewards

Smoski, M. J., Rittenberg, A., & Dichter, G. S. (2011) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2011.06.012 · Cited by 91

The good, the bad, and the irrelevant: Neural mechanisms of learning real and hypothetical rewards and effort

Scholl, J., Kolling, N., Nelissen, N., Wittmann, M. K., Harmer, C. J., & Rushworth, M. F. S. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0396-15.2015 · Cited by 85

Smoking impacts on prefrontal attentional network function in young adult brains

Musso, F., Bettermann, F., Vucurevic, G., Stoeter, P., Konrad, A., & Winterer, G. (2007) · Psychopharmacology · doi:10.1007/s00213-006-0499-8 · Cited by 93

Inverse effects of oxytocin on attributing mental activity to others in depressed and healthy subjects: a double-blind placebo controlled FMRI study

Pincus, D. (2010) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2010.00134 · Cited by 91

Decoding developmental differences and individual variability in response inhibition through predictive analyses across individuals

Cohen, J. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00047 · Cited by 89

The neural architecture of executive functions is established by middle childhood

Engelhardt, L. E., Harden, K. P., Tucker-Drob, E. M., & Church, J. A. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.024 · Cited by 87

Approach-bias predicts development of cannabis problem severity in heavy cannabis users: results from a prospective FMRI study

Cousijn, J., Goudriaan, A. E., Ridderinkhof, K. R., van den Brink, W., Veltman, D. J., & Wiers, R. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042394 · Cited by 85

Mapping Human Laryngeal Motor Cortex during Vocalization

Eichert, N., Papp, D., Mars, R. B., & Watkins, K. E. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa182 · Cited by 89

Remitted major depression is characterized by reduced prefrontal cortex reactivity to reward loss

Schiller, C. E., Minkel, J., Smoski, M. J., & Dichter, G. S. (2013) · Journal of Affective Disorders · doi:10.1016/j.jad.2013.06.016 · Cited by 89

Expertise with artificial nonspeech sounds recruits speech-sensitive cortical regions

Leech, R., Holt, L. L., Devlin, J. T., & Dick, F. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5758-08.2009 · Cited by 83

A brain network instantiating approach and avoidance motivation

Spielberg, J. M., Miller, G. A., Warren, S. L., Engels, A. S., Crocker, L. D., Banich, M. T., Sutton, B. P., & Heller, W. (2012) · Psychophysiology · doi:10.1111/j.1469-8986.2012.01443.x · Cited by 84

Extended-release naltrexone (XR-NTX) attenuates brain responses to alcohol cues in alcohol-dependent volunteers: a bold FMRI study

Lukas, S. E., Lowen, S. B., Lindsey, K. P., Conn, N., Tartarini, W., Rodolico, J., Mallya, G., Palmer, C., & Penetar, D. M. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.055 · Cited by 83

Neural mechanisms supporting the relationship between dispositional mindfulness and pain

Zeidan, F., Salomons, T., Farris, S. R., Emerson, N. M., Adler-Neal, A., Jung, Y., & Coghill, R. C. (2018) · Pain · doi:10.1097/j.pain.0000000000001344 · Cited by 77

A developmental reduction of the excitation:inhibition ratio in association cortex during adolescence

Larsen, B., Cui, Z., Adebimpe, A., Pines, A., Alexander-Bloch, A., Bertolero, M., Calkins, M. E., Gur, R. E., Gur, R. C., Mahadevan, A. S., et al. (2022) · Science Advances · doi:10.1126/sciadv.abj8750 · Cited by 80

Conditioned respiratory threat in the subdivisions of the human periaqueductal gray

Faull, O. K., Jenkinson, M., Ezra, M., & Pattinson, K. T. (2016) · eLife · doi:10.7554/elife.12047 · Cited by 77

Predicting rapid response to cognitive-behavioural treatment for panic disorder: The role of hippocampus, insula, and dorsolateral prefrontal cortex

Reinecke, A., Thilo, K., Filippini, N., Croft, A., & Harmer, C. J. (2014) · Behaviour Research and Therapy · doi:10.1016/j.brat.2014.07.017 · Cited by 75

Frontoparietal mechanisms supporting attention to location and intensity of painful stimuli

Lobanov, O. V., Quevedo, A. S., Hadsel, M. S., Kraft, R. A., & Coghill, R. C. (2013) · Pain · doi:10.1016/j.pain.2013.05.030 · Cited by 65

Intermittent theta burst stimulation of cerebellar vermis enhances fronto-cerebellar resting state functional connectivity in schizophrenia with predominant negative symptoms: A randomized controlled trial

Basavaraju, R., Ithal, D., Thanki, M. V., Ramalingaiah, A. H., Thirthalli, J., Reddy, R. P., Brady, R. O., Halko, M. A., Bolo, N. R., Keshavan, M. S., et al. (2021) · Schizophrenia Research · doi:10.1016/j.schres.2021.10.005 · Cited by 70

Depression and anxious apprehension distinguish frontocingulate cortical activity during top-down attentional control.

Silton, R. L., Heller, W., Engels, A. S., Towers, D. N., Spielberg, J. M., Edgar, J. C., Sass, S. M., Stewart, J. L., Sutton, B. P., Banich, M. T., et al. (2011) · Journal of Abnormal Psychology · doi:10.1037/a0023204 · Cited by 70

Stress Impairs Episodic Retrieval by Disrupting Hippocampal and Cortical Mechanisms of Remembering

Gagnon, S. A., Waskom, M. L., Brown, T. I., & Wagner, A. D. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy162 · Cited by 69

A single dose of mirtazapine modulates neural responses to emotional faces in healthy people

Rawlings, N. B., Norbury, R., Cowen, P. J., & Harmer, C. J. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1983-8 · Cited by 65

Neural correlates of cognitive and affective processing in maltreated youth with posttraumatic stress symptoms: Does gender matter?

Crozier, J. C., Wang, L., Huettel, S. A., & De Bellis, M. D. (2014) · Development and Psychopathology · doi:10.1017/s095457941400008x · Cited by 64

Morphological and functional variability in central and subcentral motor cortex of the human brain

Eichert, N., Watkins, K. E., Mars, R. B., & Petrides, M. (2021) · Brain Structure and Function · doi:10.1007/s00429-020-02180-w · Cited by 58

Frontolimbic responses to emotional faces in young people at familial risk of depression

Mannie, Z. N., Taylor, M. J., Harmer, C. J., Cowen, P. J., & Norbury, R. (2011) · Journal of Affective Disorders · doi:10.1016/j.jad.2010.09.030 · Cited by 62

Increased neural response to fear in patients recovered from depression: a 3T functional magnetic resonance imaging study

Norbury, R., Selvaraj, S., Taylor, M. J., Harmer, C., & Cowen, P. J. (2010) · Psychological Medicine · doi:10.1017/s0033291709990596 · Cited by 62

A comparison of sensory-motor activity during speech in first and second languages

Simmonds, A. J., Wise, R. J. S., Dhanjal, N. S., & Leech, R. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00343.2011 · Cited by 56

Representational similarity analysis offers a preview of the noradrenergic modulation of long-term fear memory at the time of encoding

Visser, R. M., Kunze, A. E., Westhoff, B., Scholte, H. S., & Kindt, M. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.01.021 · Cited by 52

Effective emotion regulation strategies improve fMRI and ECG markers of psychopathology in panic disorder: Implications for psychological treatment action

Reinecke, A., Filippini, N., Berna, C., Western, D. G., Hanson, B., Cooper, M. J., Taggart, P., & Harmer, C. J. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.160 · Cited by 54

Striatal action-value neurons reconsidered

Elber-Dorozko, L., & Loewenstein, Y. (2018) · eLife · doi:10.7554/elife.34248 · Cited by 53

Dynamic functional reorganizations and relationship with working memory performance in healthy aging

Sala-Llonch, R., Arenaza-Urquijo, E. M., Valls-Pedret, C., Vidal-Piñeiro, D., Bargalló, N., Junqué, C., & Bartrés-Faz, D. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00152 · Cited by 54

Sound the Alarm: The Effect of Narcissism on Retaliatory Aggression Is Moderated by dACC Reactivity to Rejection

Chester, D. S., & DeWall, C. N. (2016) · Journal of Personality · doi:10.1111/jopy.12164 · Cited by 54

Deep brain stimulation of the nucleus accumbens in the treatment of severe alcohol use disorder: A phase I pilot trial

Davidson, B., Giacobbe, P., George, T. P., Nestor, S. M., Rabin, J. S., Goubran, M., Nyman, A. J., Baskaran, A., Meng, Y., Pople, C. B., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01677-6 · Cited by 52

A collaborative resource platform for non-human primate neuroimaging

Messinger, A., Sirmpilatze, N., Heuer, K., Loh, K. K., Mars, R. B., Sein, J., Xu, T., Glen, D., Jung, B., Seidlitz, J., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2020.117519 · Cited by 52

Relationships between Brain Activity, Tryptophan-Related Gut Metabolites, and Autism Symptomatology

Aziz-Zadeh, L., Ringold, S. M., Jayashankar, A., Kilroy, E., Butera, C., Jacobs, J. P., Tanartkit, S., Mahurkar-Joshi, S., Bhatt, R. R., Dapretto, M., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-58459-1 · Cited by 51

Amygdala reactivity in healthy adults is correlated with prefrontal cortical thickness

Foland-Ross, L. C., Altshuler, L. L., Bookheimer, S. Y., Lieberman, M. D., Townsend, J., Penfold, C., Moody, T., Ahlf, K., Shen, J. K., Madsen, S. K., et al. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4578-09.2010 · Cited by 49

The Left Intraparietal Sulcus Modulates the Selection of Low Salient Stimuli

Mevorach, C., Shalev, L., Allen, H. A., & Humphreys, G. W. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21044 · Cited by 51

Neural indicators of emotion regulation via acceptance vs reappraisal in remitted major depressive disorder

Smoski, M. J., Keng, S.-L., Ji, J. L., Moore, T., Minkel, J., & Dichter, G. S. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv003 · Cited by 51

Academic stress and personality interact to increase the neural response to high-calorie food cues

Neseliler, S., Tannenbaum, B., Zacchia, M., Larcher, K., Coulter, K., Lamarche, M., Marliss, E. B., Pruessner, J., & Dagher, A. (2017) · Appetite · doi:10.1016/j.appet.2017.05.016 · Cited by 49

Age‐related differences in working memory deficits during nicotine withdrawal

Falcone, M., Wileyto, E. P., Ruparel, K., Gerraty, R. T., LaPrate, L., Detre, J. A., Gur, R., Loughead, J., & Lerman, C. (2014) · Addiction Biology · doi:10.1111/adb.12051 · Cited by 48

Neural response to emotional stimuli associated with successful antidepressant treatment and behavioral activation

Rizvi, S. J., Salomons, T. V., Konarski, J. Z., Downar, J., Giacobbe, P., McIntyre, R. S., & Kennedy, S. H. (2013) · Journal of Affective Disorders · doi:10.1016/j.jad.2013.06.050 · Cited by 45

Brain activation patterns underlying fast habituation to painful laser stimuli

Mobascher, A., Brinkmeyer, J., Warbrick, T., Musso, F., Schlemper, V., Wittsack, H. J., Saleh, A., Schnitzler, A., & Winterer, G. (2010) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2009.10.008 · Cited by 48

Cortical organization of inhibition-related functions and modulation by psychopathology

Warren, S. L., Crocker, L. D., Spielberg, J. M., Engels, A. S., Banich, M. T., Sutton, B. P., Miller, G. A., & Heller, W. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00271 · Cited by 48

Development of the action observation network during early adolescence: a longitudinal study

Shaw, D. J., Grosbras, M.-H., Leonard, G., Pike, G. B., & Paus, T. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq105 · Cited by 47

Risk for depression is associated with neural biases in emotional categorisation

Chan, S. W. Y., Harmer, C. J., Goodwin, G. M., & Norbury, R. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.05.030 · Cited by 46

Brain mechanisms supporting violated expectations of pain

Zeidan, F., Lobanov, O. V., Kraft, R. A., & Coghill, R. C. (2015) · Pain · doi:10.1097/j.pain.0000000000000231 · Cited by 41

From cue to meaning: Brain mechanisms supporting the construction of expectations of pain

Lobanov, O. V., Zeidan, F., McHaffie, J. G., Kraft, R. A., & Coghill, R. C. (2014) · Pain · doi:10.1016/j.pain.2013.09.014 · Cited by 38

Erythropoietin modulates neural and cognitive processing of emotional information in biomarker models of antidepressant drug action in depressed patients

Miskowiak, K. W., Favaron, E., Hafizi, S., Inkster, B., Goodwin, G. M., Cowen, P. J., & Harmer, C. J. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1842-7 · Cited by 40

L-Theanine and Caffeine Improve Target-Specific Attention to Visual Stimuli by Decreasing Mind Wandering: A Human Functional Magnetic Resonance Imaging Study

Kahathuduwa, C. N., Dhanasekara, C. S., Chin, S.-H., Davis, T., Weerasinghe, V. S., Dassanayake, T. L., & Binks, M. (2018) · Nutrition Research · doi:10.1016/j.nutres.2017.11.002 · Cited by 46

Functional imaging changes in the medial prefrontal cortex in adult ADHD

Salavert, J., Ramos-Quiroga, J. A., Moreno-Alcázar, A., Caseras, X., Palomar, G., Radua, J., Bosch, R., Salvador, R., McKenna, P. J., Casas, M., et al. (2018) · Journal of Attention Disorders · doi:10.1177/1087054715611492 · Cited by 39

The single-epoch fMRI design: validation of a simplified paradigm for the collection of subjective ratings

Koyama, T., McHaffie, J. G., Laurienti, P. J., & Coghill, R. C. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00119-8 · Cited by 37

A habenula-insular circuit encodes the willingness to act

Khalighinejad, N., Garrett, N., Priestley, L., Lockwood, P., & Rushworth, M. F. S. (2021) · Nature Communications · doi:10.1038/s41467-021-26569-1 · Cited by 32

Changes in alcohol-related brain networks across the first year of college: a prospective pilot study using fMRI effective connectivity mapping

Beltz, A. M., Gates, K. M., Engels, A. S., Molenaar, P. C. M., Pulido, C., Turrisi, R., Berenbaum, S. A., Gilmore, R. O., & Wilson, S. J. (2013) · Addictive Behaviors · doi:10.1016/j.addbeh.2012.12.023 · Cited by 36

Neural correlates of psychotic-like experiences during spiritual-trance state

Mainieri, A. G., Peres, J. F. P., Moreira-Almeida, A., Mathiak, K., Habel, U., & Kohn, N. (2017) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2017.06.006 · Cited by 35

Connectomic consistency: a systematic stability analysis of structural and functional connectivity

Osmanlıoğlu, Y., Alappatt, J. A., Parker, D., & Verma, R. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/ab947b · Cited by 33

Effects of a 7-Day Meditation Retreat on the Brain Function of Meditators and Non-Meditators During an Attention Task

Kozasa, E. H., Balardin, J. B., Sato, J. R., Chaim, K. T., Lacerda, S. S., Radvany, J., Mello, L. E. A. M., & Amaro, E. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00222 · Cited by 32

The auditory dorsal stream plays a crucial role in projecting hallucinated voices into external space

Looijestijn, J., Diederen, K. M. J., Goekoop, R., Sommer, I. E. C., Daalman, K., Kahn, R. S., Hoek, H. W., & Blom, J. D. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.02.004 · Cited by 31

Frontolimbic responses to emotional face memory: The neural correlates of first impressions

Satterthwaite, T. D., Wolf, D. H., Gur, R. C., Ruparel, K., Valdez, J. N., Gur, R. E., & Loughead, J. (2009) · Human Brain Mapping · doi:10.1002/hbm.20803 · Cited by 29

Resting‐state connectivity within and across neural circuits in anorexia nervosa

Uniacke, B., Wang, Y., Biezonski, D., Sussman, T., Lee, S., Posner, J., & Steinglass, J. (2019) · Brain and Behavior · doi:10.1002/brb3.1205 · Cited by 31

DeepPrep: an accelerated, scalable and robust pipeline for neuroimaging preprocessing empowered by deep learning

Ren, J., An, N., Lin, C., Zhang, Y., Sun, Z., Zhang, W., Li, S., Guo, N., Cui, W., Hu, Q., et al. (2025) · Nature Methods · doi:10.1038/s41592-025-02599-1 · Cited by 29

NK1 receptor antagonism and the neural processing of emotional information in healthy volunteers

McCabe, C., Cowen, P. J., & Harmer, C. J. (2009) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145709990150 · Cited by 27

Neural responses to reward anticipation and feedback in adult and adolescent cannabis users and controls

Skumlien, M., Mokrysz, C., Freeman, T. P., Wall, M. B., Bloomfield, M., Lees, R., Borissova, A., Petrilli, K., Carson, J., Coughlan, T., et al. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01316-2 · Cited by 27

Imaging brain function with simultaneous BOLD and viscoelasticity contrast: fMRI/fMRE

Lan, P. S., Glaser, K. J., Ehman, R. L., & Glover, G. H. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116592 · Cited by 26

Exploring the neural basis for paternal protection: An investigation of the neural response to infants in danger

van ‘t Veer, A. E., Thijssen, S., Witteman, J., van IJzendoorn, M. H., & Bakermans-Kranenburg, M. J. (2019) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsz018 · Cited by 25

Increased anti-correlation between the left dorsolateral prefrontal cortex and the default mode network following Stanford Neuromodulation Therapy (SNT): analysis of a double-blinded, randomized, sham-controlled trial

Gajawelli, N., Geoly, A. D., Batail, J.-M., Xiao, X., Maron-Katz, A., Cole, E., Azeez, A., Kratter, I. H., Saggar, M., & Williams, N. R. (2024) · npj Mental Health Research · doi:10.1038/s44184-024-00073-y · Cited by 18

Human hippocampus and dorsomedial prefrontal cortex infer and update latent causes during social interaction

Mahmoodi, A., Luo, S., Harbison, C., Piray, P., & Rushworth, M. F. S. (2024) · Neuron · doi:10.1016/j.neuron.2024.09.001 · Cited by 17

Maternal psychological distress associates with alterations in resting‐state low‐frequency fluctuations and distal functional connectivity of the neonate medial prefrontal cortex

Rajasilta, O., Häkkinen, S., Björnsdotter, M., Scheinin, N. M., Lehtola, S. J., Saunavaara, J., Parkkola, R., Lähdesmäki, T., Karlsson, L., Karlsson, H., et al. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.15882 · Cited by 15