An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets

Statistical parametric maps in functional imaging: A general linear approach

Friston, K. J., Holmes, A. P., Worsley, K. J., Poline, J. ‐., Frith, C. D., & Frackowiak, R. S. J. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020402 · Cited by 9,688

Conn : A Functional Connectivity Toolbox for Correlated and Anticorrelated Brain Networks

Whitfield-Gabrieli, S., & Nieto-Castanon, A. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0073 · Cited by 4,885

A new SPM toolbox for combining probabilistic cytoarchitectonic maps and functional imaging data

Eickhoff, S. B., Stephan, K. E., Mohlberg, H., Grefkes, C., Fink, G. R., Amunts, K., & Zilles, K. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.034 · Cited by 4,033

Functional Neuroimaging of Anxiety: A Meta-Analysis of Emotional Processing in PTSD, Social Anxiety Disorder, and Specific Phobia

Etkin, A., & Wager, T. D. (2007) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2007.07030504 · Cited by 3,391

Mindfulness practice leads to increases in regional brain gray matter density

Hölzel, B. K., Carmody, J., Vangel, M., Congleton, C., Yerramsetti, S. M., Gard, T., & Lazar, S. W. (2011) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2010.08.006 · Cited by 1,914

Hyperactivity and hyperconnectivity of the default network in schizophrenia and in first-degree relatives of persons with schizophrenia

Whitfield-Gabrieli, S., Thermenos, H. W., Milanovic, S., Tsuang, M. T., Faraone, S. V., McCarley, R. W., Shenton, M. E., Green, A. I., Nieto-Castanon, A., LaViolette, P., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809141106 · Cited by 1,435

Resolving emotional conflict: a role for the rostral anterior cingulate cortex in modulating activity in the amygdala

Etkin, A., Egner, T., Peraza, D. M., Kandel, E. R., & Hirsch, J. (2006) · Neuron · doi:10.1016/j.neuron.2006.07.029 · Cited by 1,360

The precuneus/posterior cingulate cortex plays a pivotal role in the default mode network: Evidence from a partial correlation network analysis

Fransson, P., & Marrelec, G. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.05.059 · Cited by 1,213

BOLD correlates of EEG topography reveal rapid resting-state network dynamics

Britz, J., Van De Ville, D., & Michel, C. M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.052 · Cited by 1,070

Aberrant “Default Mode” Functional Connectivity in Schizophrenia

Garrity, A. G., Pearlson, G. D., McKiernan, K., Lloyd, D., Kiehl, K. A., & Calhoun, V. D. (2007) · American Journal of Psychiatry · doi:10.1176/ajp.2007.164.3.450 · Cited by 1,114

Limbic scars: long-term consequences of childhood maltreatment revealed by functional and structural magnetic resonance imaging

Dannlowski, U., Stuhrmann, A., Beutelmann, V., Zwanzger, P., Lenzen, T., Grotegerd, D., Domschke, K., Hohoff, C., Ohrmann, P., Bauer, J., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.10.021 · Cited by 954

Episodic future thinking reduces reward delay discounting through an enhancement of prefrontal–mediotemporal interactions

Peters, J., & Büchel, C. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.026 · Cited by 871

The brain-derived neurotrophic factor Val66Met polymorphism and variation in human cortical morphology

Pezawas, L., Verchinski, B. A., Mattay, V. S., Callicott, J. H., Kolachana, B. S., Straub, R. E., Egan, M. F., Meyer-Lindenberg, A., & Weinberger, D. R. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.2680-04.2004 · Cited by 890

Is meditation associated with altered brain structure? A systematic review and meta-analysis of morphometric neuroimaging in meditation practitioners

Fox, K. C. R., Nijeboer, S., Dixon, M. L., Floman, J. L., Ellamil, M., Rumak, S. P., Sedlmeier, P., & Christoff, K. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.03.016 · Cited by 804

Probiotic Bifidobacterium longum NCC3001 reduces depression scores and alters brain activity: a pilot study in patients with irritable bowel syndrome

Pinto-Sanchez, M. I., Hall, G. B., Ghajar, K., Nardelli, A., Bolino, C., Lau, J. T., Martin, F.-P., Cominetti, O., Welsh, C., Rieder, A., et al. (2017) · Gastroenterology · doi:10.1053/j.gastro.2017.05.003 · Cited by 821

A specific role for posterior dorsolateral striatum in human habit learning

Tricomi, E., Balleine, B. W., & O’Doherty, J. P. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06796.x · Cited by 769

Temporal and spatial dynamics of brain structure changes during extensive learning

Draganski, B., Gaser, C., Kempermann, G., Kuhn, H. G., Winkler, J., Buchel, C., & May, A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4628-05.2006 · Cited by 765

Identifying major depression using whole-brain functional connectivity: a multivariate pattern analysis

Zeng, L.-L., Shen, H., Liu, L., Wang, L., Li, B., Fang, P., Zhou, Z., Li, Y., & Hu, D. (2012) · Brain · doi:10.1093/brain/aws059 · Cited by 748

Functional neuroimaging of autobiographical memory

Cabeza, R., & St Jacques, P. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.02.005 · Cited by 736

The wandering brain: meta-analysis of functional neuroimaging studies of mind-wandering and related spontaneous thought processes

Fox, K. C. R., Spreng, R. N., Ellamil, M., Andrews-Hanna, J. R., & Christoff, K. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.02.039 · Cited by 690

Differential activation of the dorsal striatum by high-calorie visual food stimuli in obese individuals

Rothemund, Y., Preuschhof, C., Bohner, G., Bauknecht, H.-C., Klingebiel, R., Flor, H., & Klapp, B. F. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.05.008 · Cited by 679

Functional neuroanatomy of meditation: a review and meta-analysis of 78 functional neuroimaging investigations.

Fox, K. C. R., Dixon, M. L., Nijeboer, S., Girn, M., Floman, J. L., Lifshitz, M., Ellamil, M., Sedlmeier, P., & Christoff, K. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.03.021 · Cited by 656

Abnormal functional connectivity of default mode sub-networks in autism spectrum disorder patients

Assaf, M., Jagannathan, K., Calhoun, V. D., Miller, L., Stevens, M. C., Sahl, R., O'Boyle, J. G., Schultz, R. T., & Pearlson, G. D. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.067 · Cited by 680

A direct brainstem–amygdala–cortical ‘alarm’system for subliminal signals of fear.

Liddell, B. J., Brown, K. J., Kemp, A. H., Barton, M. J., Das, P., Peduto, A., Gordon, E., & Williams, L. M. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.08.016 · Cited by 670

Applications of machine learning to diagnosis and treatment of neurodegenerative diseases

Myszczynska, M. A., Ojamies, P. N., Lacoste, A. M. B., Neil, D., Saffari, A., Mead, R., Hautbergue, G. M., Holbrook, J. D., & Ferraiuolo, L. (2020) · Nature Reviews Neurology · doi:10.1038/s41582-020-0377-8 · Cited by 595

Inflammation-Induced Anhedonia: Endotoxin Reduces Ventral Striatum Responses to Reward

Eisenberger, N. I., Berkman, E. T., Inagaki, T. K., Rameson, L. T., Mashal, N. M., & Irwin, M. R. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.06.010 · Cited by 596

Abnormalities of intrinsic functional connectivity in autism spectrum disorders

Monk, C. S., Peltier, S. J., Wiggins, J. L., Weng, S.-J., Carrasco, M., Risi, S., & Lord, C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.04.069 · Cited by 578

A Meta-analysis of Executive Components of Working Memory

Nee, D. E., Brown, J. W., Askren, M. K., Berman, M. G., Demiralp, E., Krawitz, A., & Jonides, J. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs007 · Cited by 544

Failure of anterior cingulate activation and connectivity with the amygdala during implicit regulation of emotional processing in generalized anxiety disorder

Etkin, A., Prater, K. E., Hoeft, F., Menon, V., & Schatzberg, A. F. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2009.09070931 · Cited by 550

Gender differences in brain networks supporting empathy

Schulte-Rüther, M., Markowitsch, H. J., Shah, N. J., Fink, G. R., & Piefke, M. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.04.180 · Cited by 536

Neuroanatomical correlates of behavioural disorders in dementia

Rosen, H. J., Allison, S. C., Schauer, G. F., Gorno-Tempini, M. L., Weiner, M. W., & Miller, B. L. (2005) · Brain · doi:10.1093/brain/awh628 · Cited by 497

Old brains come uncoupled in sleep: slow wave-spindle synchrony, brain atrophy, and forgetting

Helfrich, R. F., Mander, B. A., Jagust, W. J., Knight, R. T., & Walker, M. P. (2018) · Neuron · doi:10.1016/j.neuron.2017.11.020 · Cited by 497

Disrupted prediction-error signal in psychosis: Evidence for an associative account of delusions

Corlett, P. R., Murray, G. K., Honey, G. D., Aitken, M. R. F., Shanks, D. R., Robbins, T. W., Bullmore, E. T., Dickinson, A., & Fletcher, P. C. (2007) · Brain · doi:10.1093/brain/awm173 · Cited by 460

Neural correlates of sexual cue reactivity in individuals with and without compulsive sexual behaviours

Voon, V., Mole, T. B., Banca, P., Porter, L., Morris, L., Mitchell, S., Lapa, T. R., Karr, J., Harrison, N. A., Potenza, M. N., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102419 · Cited by 462

Decreased interhemispheric functional connectivity in autism

Anderson, J. S., Druzgal, T. J., Froehlich, A., DuBray, M. B., Lange, N., Alexander, A. L., Abildskov, T., Nielsen, J. A., Cariello, A. N., Cooperrider, J. R., et al. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq190 · Cited by 438

The structural integrity of an amygdala-prefrontal pathway predicts trait anxiety

Kim, M. J., & Whalen, P. J. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2335-09.2009 · Cited by 433

A neural mechanism mediating the impact of episodic prospection on farsighted decisions

Benoit, R. G., Gilbert, S. J., & Burgess, P. W. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6559-10.2011 · Cited by 422

Adolescent impulsivity phenotypes characterized by distinct brain networks

the IMAGEN Consortium, Whelan, R., Conrod, P. J., Poline, J.-B., Lourdusamy, A., Banaschewski, T., Barker, G. J., Bellgrove, M. A., Büchel, C., Byrne, M., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3092 · Cited by 420

Neural sensitivity to social rejection is associated with inflammatory responses to social stress

Slavich, G. M., Way, B. M., Eisenberger, N. I., & Taylor, S. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009164107 · Cited by 418

Gambling near-misses enhance motivation to gamble and recruit win-related brain circuitry

Clark, L., Lawrence, A. J., Astley-Jones, F., & Gray, N. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.031 · Cited by 410

Association of plasma clusterin concentration with severity, pathology, and progression in Alzheimer disease

Thambisetty, M., Simmons, A., Velayudhan, L., Hye, A., Campbell, J., Zhang, Y., Wahlund, L.-O., Westman, E., Kinsey, A., Güntert, A., et al. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.78 · Cited by 405

Both the Middle Temporal Gyrus and the Ventral Anterior Temporal Area Are Crucial for Multimodal Semantic Processing: Distortion-corrected fMRI Evidence for a Double Gradient of Information Convergence in the Temporal Lobes

Visser, M., Jefferies, E., Embleton, K. V., & Lambon Ralph, M. A. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00244 · Cited by 369

Amygdala response to preattentive masked fear in children with conduct problems: the role of callous–unemotional traits

Viding, E., Sebastian, C. L., Dadds, M. R., Lockwood, P. L., Cecil, C. A. M., De Brito, S. A., & McCrory, E. J. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.12020191 · Cited by 368

Diminished neural processing of aversive and rewarding stimuli during selective serotonin reuptake inhibitor treatment

McCabe, C., Mishor, Z., Cowen, P. J., & Harmer, C. J. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.11.001 · Cited by 365

Hippocampal hypometabolism predicts cognitive decline from normal aging

Mosconi, L., De Santi, S., Li, J., Tsui, W. H., Li, Y., Boppana, M., Laska, E., Rusinek, H., & de Leon, M. J. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.12.008 · Cited by 360

Amygdala Responses to Fearful and Happy Facial Expressions under Conditions of Binocular Suppression

Williams, M. A., Morris, A. P., McGlone, F., Abbott, D. F., & Mattingley, J. B. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.4977-03.2004 · Cited by 362

Neuroprotective Effects of Cognitive Enhancement Therapy Against Gray Matter Loss in Early Schizophrenia: Results From a 2-Year Randomized Controlled Trial

Eack, S. M., Hogarty, G. E., Cho, R. Y., Prasad, K. M. R., Greenwald, D. P., Hogarty, S. S., & Keshavan, M. S. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.63 · Cited by 360

Fasting biases brain reward systems towards high‐calorie foods

Goldstone, A. P., Prechtl de Hernandez, C. G., Beaver, J. D., Muhammed, K., Croese, C., Bell, G., Durighel, G., Hughes, E., Waldman, A. D., Frost, G., et al. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06949.x · Cited by 356

Cumulative adversity and smaller gray matter volume in medial prefrontal, anterior cingulate, and insula regions

Ansell, E. B., Rando, K., Tuit, K., Guarnaccia, J., & Sinha, R. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.11.022 · Cited by 354

Father’s brain is sensitive to childcare experiences

Abraham, E., Hendler, T., Shapira-Lichter, I., Kanat-Maymon, Y., Zagoory-Sharon, O., & Feldman, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402569111 · Cited by 343

Interleukin-6 Covaries Inversely with Hippocampal Grey Matter Volume in Middle-Aged Adults

Marsland, A. L., Gianaros, P. J., Abramowitch, S. M., Manuck, S. B., & Hariri, A. R. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.04.016 · Cited by 348

The Brain’s Response to Reward Anticipation and Depression in Adolescence: Dimensionality, Specificity, and Longitudinal Predictions in a Community-Based Sample

Stringaris, A., Vidal-Ribas Belil, P., Artiges, E., Lemaitre, H., Gollier-Briant, F., Wolke, S., Vulser, H., Miranda, R., Penttilä, J., Struve, M., et al. (2015) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2015.14101298 · Cited by 322

Resting-state functional connectivity in treatment-resistant depression

Lui, S., Wu, Q., Qiu, L., Yang, X., Kuang, W., Chan, R. C. K., Huang, X., Kemp, G. J., Mechelli, A., & Gong, Q. (2011) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.10101419 · Cited by 336

Automatic Mood-Congruent Amygdala Responses to Masked Facial Expressions in Major Depression

Suslow, T., Konrad, C., Kugel, H., Rumstadt, D., Zwitserlood, P., Schöning, S., Ohrmann, P., Bauer, J., Pyka, M., Kersting, A., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.07.023 · Cited by 328

Common and differential neural networks of emotion regulation by detachment, reinterpretation, distraction, and expressive suppression: a comparative fMRI investigation

Dörfel, D., Lamke, J.-P., Hummel, F., Wagner, U., Erk, S., & Walter, H. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.06.051 · Cited by 322

Prospective reports of chronic life stress predict decreased grey matter volume in the hippocampus

Gianaros, P. J., Jennings, J. R., Sheu, L. K., Greer, P. J., Kuller, L. H., & Matthews, K. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.10.045 · Cited by 324

Psilocybin-induced decrease in amygdala reactivity correlates with enhanced positive mood in healthy volunteers

Kraehenmann, R., Preller, K. H., Scheidegger, M., Pokorny, T., Bosch, O. G., Seifritz, E., & Vollenweider, F. X. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.04.010 · Cited by 323

Reduced spontaneous but relatively normal deliberate vicarious representations in psychopathy

Meffert, H., Gazzola, V., den Boer, J. A., Bartels, A. A. J., & Keysers, C. (2013) · Brain · doi:10.1093/brain/awt190 · Cited by 318

Using network science to evaluate exercise-associated brain changes in older adults.

Burdette (2010) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2010.00023 · Cited by 320

Fiber density asymmetry of the arcuate fasciculus in relation to functional hemispheric language lateralization in both right- and left-handed healthy subjects: a combined fMRI and DTI study

Vernooij, M. W., Smits, M., Wielopolski, P. A., Houston, G. C., Krestin, G. P., & van der Lugt, A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.12.041 · Cited by 316

Global fiber reconstruction becomes practical

Reisert, M., Mader, I., Anastasopoulos, C., Weigel, M., Schnell, S., & Kiselev, V. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.016 · Cited by 312

Alterations in resting-state functional connectivity link mindfulness meditation with reduced interleukin-6: a randomized controlled trial

Creswell, J. D., Taren, A. A., Lindsay, E. K., Greco, C. M., Gianaros, P. J., Fairgrieve, A., Marsland, A. L., Brown, K. W., Way, B. M., Rosen, R. K., et al. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.01.008 · Cited by 299

Behavioral and neuroimaging evidence for overreliance on habit learning in alcohol-dependent patients

Sjoerds, Z., de Wit, S., van den Brink, W., Robbins, T. W., Beekman, A. T. F., Penninx, B. W. J. H., & Veltman, D. J. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.107 · Cited by 312

Common abnormalities and disorder-specific compensation during implicit regulation of emotional processing in generalized anxiety and major depressive disorders

Etkin, A., & Schatzberg, A. F. (2011) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2011.10091290 · Cited by 311

Bridging language and attention: brain basis of the impact of bilingualism on cognitive control

Garbin, G., Sanjuan, A., Forn, C., Bustamante, J. C., Rodriguez-Pujadas, A., Belloch, V., Hernandez, M., Costa, A., & Ávila, C. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.078 · Cited by 309

Resting state default-mode network connectivity in early depression using a seed region-of-interest analysis: decreased connectivity with caudate nucleus

Bluhm, R., Williamson, P., Lanius, R., Théberge, J., Densmore, M., Bartha, R., Neufeld, R., & Osuch, E. (2009) · Psychiatry and Clinical Neurosciences · doi:10.1111/j.1440-1819.2009.02030.x · Cited by 294

A Dual Role for Prediction Error in Associative Learning

den Ouden, H. E. M., Friston, K. J., Daw, N. D., McIntosh, A. R., & Stephan, K. E. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn161 · Cited by 306

Highly religious participants recruit areas of social cognition in personal prayer

Schjoedt, U., Stødkilde-Jørgensen, H., Geertz, A. W., & Roepstorff, A. (2009) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsn050 · Cited by 305

Striatal Prediction Error Modulates Cortical Coupling

den Ouden, H. E. M., Daunizeau, J., Roiser, J., Friston, K. J., & Stephan, K. E. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4458-09.2010 · Cited by 304

Mapping neuroplastic potential in brain-damaged patients

Herbet, G., Maheu, M., Costi, E., Lafargue, G., & Duffau, H. (2016) · Brain · doi:10.1093/brain/awv394 · Cited by 289

Neuroticism modulates amygdala—prefrontal connectivity in response to negative emotional facial expressions

Cremers, H. R., Demenescu, L. R., Aleman, A., Renken, R., van Tol, M.-J., van der Wee, N. J. A., Veltman, D. J., & Roelofs, K. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.08.023 · Cited by 288

Widespread age-related differences in the human brain microstructure revealed by quantitative magnetic resonance imaging

Callaghan, M. F., Freund, P., Draganski, B., Anderson, E., Cappelletti, M., Chowdhury, R., Diedrichsen, J., FitzGerald, T. H. B., Smittenaar, P., Helms, G., et al. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.02.008 · Cited by 292

White matter damage in Alzheimer disease and its relationship to gray matter atrophy

Agosta, F., Pievani, M., Sala, S., Geroldi, C., Galluzzi, S., Frisoni, G. B., & Filippi, M. (2011) · Radiology · doi:10.1148/radiol.10101284 · Cited by 288

State-dependent changes in hippocampal grey matter in depression

Arnone, D., McKie, S., Elliott, R., Juhasz, G., Thomas, E. J., Downey, D., Williams, S., Deakin, J. F. W., & Anderson, I. M. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.150 · Cited by 287

Abnormally high degree connectivity of the orbitofrontal cortex in obsessive-compulsive disorder

Beucke, J. C., Sepulcre, J., Talukdar, T., Linnman, C., Zschenderlein, K., Endrass, T., Kaufmann, C., & Kathmann, N. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.173 · Cited by 280

A larynx area in the human motor cortex

Brown, S., Ngan, E., & Liotti, M. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm131 · Cited by 286

The neural correlates of empathy: experience, automaticity, and prosocial behavior

Rameson, L. T., Morelli, S. A., & Lieberman, M. D. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00130 · Cited by 279

Functional neuroimaging of avoidance habits in obsessive-compulsive disorder

Gillan, C. M., Apergis-Schoute, A. M., Morein-Zamir, S., Urcelay, G. P., Sule, A., Fineberg, N. A., Sahakian, B. J., & Robbins, T. W. (2015) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2014.14040525 · Cited by 265

Elevated striatal and decreased dorsolateral prefrontal cortical activity in response to emotional stimuli in euthymic bipolar disorder: no associations with psychotropic medication load

Hassel, S., Almeida, J. R., Kerr, N., Nau, S., Ladouceur, C. D., Fissell, K., Kupfer, D. J., & Phillips, M. L. (2008) · Bipolar Disorders · doi:10.1111/j.1399-5618.2008.00641.x · Cited by 277

Glucose metabolism, gray matter structure, and memory decline in subjective memory impairment

Scheef, L., Spottke, A., Daerr, M., Joe, A., Striepens, N., Kölsch, H., Popp, J., Daamen, M., Gorris, D., Heneka, M. T., et al. (2012) · Neurology · doi:10.1212/wnl.0b013e31826c1a8d · Cited by 277

Processing of the incentive for social approval in the ventral striatum during charitable donation

Izuma, K., Saito, D. N., & Sadato, N. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21228 · Cited by 276

Loss of imagery phenomenology with intact visuo-spatial task performance: a case of 'blind imagination'

Zeman, A. Z. J., Della Sala, S., Torrens, L. A., Gountouna, V.-E., McGonigle, D. J., & Logie, R. H. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.08.024 · Cited by 273

Progesterone selectively increases amygdala reactivity in women

van Wingen, G. A., van Broekhoven, F., Verkes, R. J., Petersson, K. M., Bäckström, T., Buitelaar, J. K., & Fernández, G. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002030 · Cited by 273

Default mode network connectivity as a predictor of post‐traumatic stress disorder symptom severity in acutely traumatized subjects

Lanius, R. A., Bluhm, R. L., Coupland, N. J., Hegadoren, K. M., Rowe, B., Théberge, J., Neufeld, R. W. J., Williamson, P. C., & Brimson, M. (2010) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.2009.01391.x · Cited by 273

The neurobiology of emotion regulation in posttraumatic stress disorder: amygdala downregulation via real‐time fMRI neurofeedback

Nicholson, A. A., Rabellino, D., Densmore, M., Frewen, P. A., Paret, C., Kluetsch, R., Schmahl, C., Théberge, J., Neufeld, R. W. J., McKinnon, M. C., et al. (2017) · Human Brain Mapping · doi:10.1002/hbm.23402 · Cited by 273

Individual differences in typical reappraisal use predict amygdala and prefrontal responses

Drabant, E. M., McRae, K., Manuck, S. B., Hariri, A. R., & Gross, J. J. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.09.007 · Cited by 270

Neural Hyporesponsiveness and Hyperresponsiveness During Immediate and Delayed Reward Processing in Adult Attention-Deficit/Hyperactivity Disorder

Plichta, M. M., Vasic, N., Wolf, R. C., Lesch, K.-P., Brummer, D., Jacob, C., Fallgatter, A. J., & Grön, G. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.07.008 · Cited by 272

The Link between Facial Feedback and Neural Activity within Central Circuitries of Emotion—New Insights from Botulinum Toxin–Induced Denervation of Frown Muscles

Hennenlotter, A., Dresel, C., Castrop, F., Ceballos-Baumann, A. O., Wohlschläger, A. M., & Haslinger, B. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn104 · Cited by 269

Variation in the μ-opioid receptor gene ( OPRM1 ) is associated with dispositional and neural sensitivity to social rejection

Way, B. M., Taylor, S. E., & Eisenberger, N. I. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812612106 · Cited by 264

Blunted response to feedback information in depressive illness

Steele, J. D., Kumar, P., & Ebmeier, K. P. (2007) · Brain · doi:10.1093/brain/awm150 · Cited by 261

Predicting treatment response in social anxiety disorder from functional magnetic resonance imaging.

Doehrmann, O., Ghosh, S. S., Polli, F. E., Reynolds, G. O., Horn, F., Keshavan, A., Triantafyllou, C., Saygin, Z. M., Whitfield-Gabrieli, S., Hofmann, S. G., et al. (2013) · JAMA Psychiatry · doi:10.1001/2013.jamapsychiatry.5 · Cited by 262

Resting-state functional and structural connectivity within an insula–amygdala route specifically index state and trait anxiety

Baur, V., Hänggi, J., Langer, N., & Jäncke, L. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.06.003 · Cited by 258

Converging evidence for the neuroanatomic basis of combinatorial semantics in the angular gyrus

Price, A. R., Bonner, M. F., Peelle, J. E., & Grossman, M. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3446-14.2015 · Cited by 262

Exenatide once weekly for alcohol use disorder investigated in a randomized, placebo-controlled clinical trial

Klausen, M. K., Jensen, M. E., Møller, M., Le Dous, N., Jensen, A.-M. Ø., Zeeman, V. A., Johannsen, C.-F., Lee, A., Thomsen, G. K., Macoveanu, J., et al. (2022) · JCI Insight · doi:10.1172/jci.insight.159863 · Cited by 262

The neural substrates of cognitive control deficits in autism spectrum disorders

Solomon, M., Ozonoff, S. J., Ursu, S., Ravizza, S., Cummings, N., Ly, S., & Carter, C. S. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.04.019 · Cited by 263

Structural MRI correlates for vulnerability and resilience to major depressive disorder

Amico, F. (2011) · Journal of Psychiatry & Neuroscience · doi:10.1503/jpn.090186 · Cited by 256

Oxytocin facilitates protective responses to aversive social stimuli in males

Striepens, N., Scheele, D., Kendrick, K. M., Becker, B., Schäfer, L., Schwalba, K., Reul, J., Maier, W., & Hurlemann, R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208852109 · Cited by 242

Neural substrates of abstinence-induced cigarette cravings in chronic smokers

Wang, Z., Faith, M., Patterson, F., Tang, K., Kerrin, K., Wileyto, E. P., Detre, J. A., & Lerman, C. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2966-07.2007 · Cited by 256

The Neural Basis of Human Social Values: Evidence from Functional MRI

Zahn, R., Moll, J., Paiva, M., Garrido, G., Krueger, F., Huey, E. D., & Grafman, J. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn080 · Cited by 328

Enhanced resting-state connectivity of amygdala in the immediate aftermath of acute psychological stress

van Marle, H. J. F., Hermans, E. J., Qin, S., & Fernández, G. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.070 · Cited by 251

Developmental influences on the neural bases of responses to social rejection: Implications of social neuroscience for education

Sebastian, C. L., Tan, G. C. Y., Roiser, J. P., Viding, E., Dumontheil, I., & Blakemore, S.-J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.063 · Cited by 250