Functional neuroanatomy of peripheral inflammatory physiology: A meta-analysis of human neuroimaging studies

Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482 · see citing works

The moderator–mediator variable distinction in social psychological research: Conceptual, strategic, and statistical considerations.

Baron, R. M., & Kenny, D. A. (1986) · Journal of Personality and Social Psychology · doi:10.1037//0022-3514.51.6.1173 · Cited by 91,542 · see citing works

The moderator-mediator variable distinction in social psychological research: Conceptual, strategic, and statistical considerations

Baron, R. M., & Kenny, D. A. (1986) · Journal of Personality and Social Psychology · doi:10.1037/0022-3514.51.6.1173 · Cited by 91,532 · see citing works

Preferred Reporting Items for Systematic Reviews and Meta-Analyses: the PRISMA statement

Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G., & for the PRISMA Group (2009) · BMJ · doi:10.1136/bmj.b2535 · Cited by 83,823 · see citing works

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement.

(2009) · PubMed Central · Cited by 44,859 · see citing works

Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement

Moher, D., Liberati, A., Tetzlaff, J., & Altman, D. G. (2009) · Journal of Clinical Epidemiology · doi:10.1016/j.jclinepi.2009.06.005 · Cited by 19,575 · see citing works

Inflammation and metabolic disorders

Hotamisligil, G. S. (2006) · Nature · doi:10.1038/nature05485 · Cited by 9,199 · see citing works

The organization of the human cerebral cortex estimated by intrinsic functional connectivity

Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182 · see citing works

Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity

Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023 · see citing works

Glutamate neurotoxicity and diseases of the nervous system

Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,152 · see citing works

Inflammation and Atherosclerosis

Libby, P., Ridker, P. M., & Maseri, A. (2002) · Circulation · doi:10.1161/hc0902.104353 · Cited by 7,724 · see citing works

Power failure: why small sample size undermines the reliability of neuroscience

Button, K. S., Ioannidis, J. P. A., Mokrysz, C., Nosek, B. A., Flint, J., Robinson, E. S. J., & Munafò, M. R. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3475 · Cited by 7,641 · cited 1× · see citing works

Dissociable intrinsic connectivity networks for salience processing and executive control

Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426 · see citing works

From inflammation to sickness and depression: when the immune system subjugates the brain

Dantzer, R., O'Connor, J. C., Freund, G. G., Johnson, R. W., & Kelley, K. W. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2297 · Cited by 7,395 · see citing works

The organization of the human cerebellum estimated by intrinsic functional connectivity

Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304 · see citing works

How do you feel — now? The anterior insula and human awareness

(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657 · see citing works

How do you feel? Interoception: The sense of the physiological condition of the body

Craig, A. D. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn894 · Cited by 6,006 · see citing works

Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin

Borovikova, L. V., Ivanova, S., Zhang, M., Yang, H., Botchkina, G. I., Watkins, L. R., Wang, H., Abumrad, N., Eaton, J. W., & Tracey, K. J. (2000) · Nature · doi:10.1038/35013070 · Cited by 4,211 · 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

Mechanisms underlying inflammation in neurodegeneration

Glass, C. K., Saijo, K., Winner, B., Marchetto, M. C., & Gage, F. H. (2010) · Cell · doi:10.1016/j.cell.2010.02.016 · Cited by 3,580 · see citing works

Cluster failure: why fMRI inferences for spatial extent have inflated false-positive rates

Eklund, A., Nichols, T. E., & Knutsson, H. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1602413113 · Cited by 3,487 · see citing works

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 · see citing works

A meta-analysis of heart rate variability and neuroimaging studies: implications for heart rate variability as a marker of stress and health

Thayer, J. F., Åhs, F., Fredrikson, M., Sollers, J. J., & Wager, T. D. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.11.009 · Cited by 3,224 · see citing works

Distinct brain networks for adaptive and stable task control in humans

Dosenbach, N. U. F., Fair, D. A., Miezin, F. M., Cohen, A. L., Wenger, K. K., Dosenbach, R. A. T., Fox, M. D., Snyder, A. Z., Vincent, J. L., Raichle, M. E., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704320104 · Cited by 2,632 · see citing works

The Organization of Networks within the Orbital and Medial Prefrontal Cortex of Rats, Monkeys and Humans

Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627 · see citing works

Interoception: the sense of the physiological condition of the body

(Bud) Craig, A. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00090-4 · Cited by 2,556 · see citing works

The brain basis of emotion: a meta-analytic review

Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320 · see citing works

Large-Scale Network Dysfunction in Major Depressive Disorder: A Meta-analysis of Resting-State Functional Connectivity

Kaiser, R. H., Andrews-Hanna, J. R., Wager, T. D., & Pizzagalli, D. A. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.0071 · Cited by 2,281 · see citing works

Biological basis of the behavior of sick animals

Hart, B. L. (1988) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(88)80004-6 · Cited by 2,223 · see citing works

Nonresolving Inflammation

Nathan, C., & Ding, A. (2010) · Cell · doi:10.1016/j.cell.2010.02.029 · Cited by 2,183 · see citing works

Immune attack: the role of inflammation in Alzheimer disease

Heppner, F. L., Ransohoff, R. M., & Becher, B. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3880 · Cited by 2,134 · see citing works

Valid conjunction inference with the minimum statistic

Nichols, T. E., Brett, M., Andersson, J., Wager, T. D., & Poline, J. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.005 · Cited by 1,885 · see citing works

Interoceptive predictions in the brain

Barrett, L. F., & Simmons, W. K. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3950 · Cited by 1,766 · see citing works

An fMRI-Based Neurologic Signature of Physical Pain

Wager, T. D., Atlas, L. Y., Lindquist, M. A., Roy, M., Woo, C.-W., & Kross, E. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1204471 · Cited by 1,597 · see citing works

Differential projections of the infralimbic and prelimbic cortex in the rat

Vertes, R. P. (2004) · Synapse · doi:10.1002/syn.10279 · Cited by 1,550 · see citing works

Immune modulation of learning, memory, neural plasticity and neurogenesis

Yirmiya, R., & Goshen, I. (2011) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2010.10.015 · Cited by 1,483 · see citing works

A probabilistic MR atlas of the human cerebellum

Diedrichsen, J., Balsters, J. H., Flavell, J. C., Cussans, E., & Ramnani, N. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.01.045 · Cited by 1,370 · see citing works

Cytokine-Associated Emotional and Cognitive Disturbances in Humans

Reichenberg, A., Yirmiya, R., Schuld, A., Kraus, T., Haack, M., Morag, A., & Pollmächer, T. (2001) · Archives of General Psychiatry · doi:10.1001/archpsyc.58.5.445 · Cited by 1,365 · see citing works

Prefrontal cortex in the rat: Projections to subcortical autonomic, motor, and limbic centers

Gabbott, P. L. A., Warner, T. A., Jays, P. R. L., Salway, P., & Busby, S. J. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20738 · Cited by 1,227 · see citing works

Chronic stress and age-related increases in the proinflammatory cytokine IL-6.

Kiecolt-Glaser, J. K., Preacher, K. J., MacCallum, R. C., Atkinson, C., Malarkey, W. B., & Glaser, R. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1531903100 · Cited by 1,220 · see citing works

Construction of a 3D probabilistic atlas of human cortical structures

Shattuck, D. W., Mirza, M., Adisetiyo, V., Hojatkashani, C., Salamon, G., Narr, K. L., Poldrack, R. A., Bilder, R. M., & Toga, A. W. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.031 · Cited by 1,208 · see citing works

Immune system to brain signaling: Neuropsychopharmacological implications

Capuron, L., & Miller, A. H. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.01.014 · Cited by 1,195 · see citing works

Visceral influences on brain and behavior

Critchley, H. D., & Harrison, N. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.02.008 · Cited by 1,177 · see citing works

Reflex control of immunity

Tracey, K. J. (2009) · Nature Reviews Immunology · doi:10.1038/nri2566 · Cited by 1,154 · cited 2× · see citing works

Functional grouping and cortical–subcortical interactions in emotion: a meta-analysis of neuroimaging studies

Kober, H., Barrett, L. F., Joseph, J., Bliss-Moreau, E., Lindquist, K., & Wager, T. D. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.03.059 · Cited by 1,144 · see citing works

Neural regulation of innate immunity: a coordinated nonspecific host response to pathogens

Sternberg, E. M. (2006) · Nature Reviews Immunology · doi:10.1038/nri1810 · Cited by 1,064 · see citing works

Social stress induces neurovascular pathology promoting depression

Menard, C., Pfau, M. L., Hodes, G. E., Kana, V., Wang, V. X., Bouchard, S., Takahashi, A., Flanigan, M. E., Aleyasin, H., LeClair, K. B., et al. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0010-3 · Cited by 1,028 · see citing works

Psychoneuroimmunology Meets Neuropsychopharmacology: Translational Implications of the Impact of Inflammation on Behavior

Haroon, E., Raison, C. L., & Miller, A. H. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2011.205 · Cited by 1,000 · see citing works

The habenula: from stress evasion to value-based decision-making

Hikosaka, O. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2866 · Cited by 955 · see citing works

Depressive rumination, the default-mode network, and the dark matter of clinical neuroscience

Hamilton, J. P., Farmer, M., Fogelman, P., & Gotlib, I. H. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.02.020 · Cited by 952 · see citing works

The Autonomic Brain: An Activation Likelihood Estimation Meta-Analysis for Central Processing of Autonomic Function

Beissner, F., Meissner, K., Bar, K.-J., & Napadow, V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1103-13.2013 · Cited by 920 · see citing works

CYTOKINE TARGETS IN THE BRAIN: IMPACT ON NEUROTRANSMITTERS AND NEUROCIRCUITS: Review: Cytokine Targets in the Brain

Miller, A. H., Haroon, E., Raison, C. L., & Felger, J. C. (2013) · Depression and Anxiety · doi:10.1002/da.22084 · Cited by 892 · see citing works

The central autonomic nervous system: conscious visceral perception and autonomic pattern generation

Saper, C. B. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.032502.111311 · Cited by 837 · see citing works

Multidimensional Scaling, Tree-Fitting, and Clustering

Shepard, R. (1980) · Science · doi:10.1126/science.210.4468.390 · Cited by 826 · see citing works

Ten simple rules for neuroimaging meta-analysis

Müller, V. I., Cieslik, E. C., Laird, A. R., Fox, P. T., Radua, J., Mataix-Cols, D., Tench, C. R., Yarkoni, T., Nichols, T. E., Turkeltaub, P. E., et al. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.11.012 · Cited by 805 · see citing works

Inflammation Causes Mood Changes Through Alterations in Subgenual Cingulate Activity and Mesolimbic Connectivity

Harrison, N. A., Brydon, L., Walker, C., Gray, M. A., Steptoe, A., & Critchley, H. D. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.03.015 · Cited by 756 · see citing works

Evidence for a viscerotopic sensory representation in the cortex and thalamus in the rat

Cechetto, D. F., & Saper, C. B. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902620104 · Cited by 703 · see citing works

Unexpected role of interferon-γ in regulating neuronal connectivity and social behaviour

Filiano, A. J., Xu, Y., Tustison, N. J., Marsh, R. L., Baker, W., Smirnov, I., Overall, C. C., Gadani, S. P., Turner, S. D., Weng, Z., et al. (2016) · Nature · doi:10.1038/nature18626 · Cited by 697 · see citing works

The effects of acute psychological stress on circulating and stimulated inflammatory markers: a systematic review and meta-analysis

Marsland, A. L., Walsh, C., Lockwood, K., & John-Henderson, N. A. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2017.01.011 · Cited by 691 · see citing works

Early-Life Adversity and Physical and Emotional Health Across the Lifespan: A Neuroimmune Network Hypothesis

Nusslock, R., & Miller, G. E. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.05.017 · Cited by 672 · see citing works

Integrating neuroimmune systems in the neurobiology of depression

Wohleb, E. S., Franklin, T., Iwata, M., & Duman, R. S. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.69 · Cited by 668 · see citing works

Dynamic microglial alterations underlie stress-induced depressive-like behavior and suppressed neurogenesis

Kreisel, T., Frank, M. G., Licht, T., Reshef, R., Ben-Menachem-Zidon, O., Baratta, M. V., Maier, S. F., & Yirmiya, R. (2014) · Molecular Psychiatry · doi:10.1038/mp.2013.155 · Cited by 663 · see citing works

The role of peripheral immune cells in the CNS in steady state and disease

Prinz, M., & Priller, J. (2017) · Nature Neuroscience · doi:10.1038/nn.4475 · Cited by 657 · see citing works

Evidence for a large-scale brain system supporting allostasis and interoception in humans

Kleckner, I. R., Zhang, J., Touroutoglou, A., Chanes, L., Xia, C., Simmons, W. K., Quigley, K. S., Dickerson, B. C., & Feldman Barrett, L. (2017) · Nature Human Behaviour · doi:10.1038/s41562-017-0069 · Cited by 641 · see citing works

Stress-related noradrenergic activity prompts large-scale neural network reconfiguration

Hermans, E. J., van Marle, H. J. F., Ossewaarde, L., Henckens, M. J. A. G., Qin, S., van Kesteren, M. T. R., Schoots, V. C., Cousijn, H., Rijpkema, M., Oostenveld, R., et al. (2011) · Science · doi:10.1126/science.1209603 · Cited by 627 · see citing works

Brain-immune communication pathways

Quan, N., & Banks, W. A. (2007) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2007.05.005 · Cited by 626 · see citing works

Inflammation is associated with decreased functional connectivity within corticostriatal reward circuitry in depression

Felger, J. C., Li, Z., Haroon, E., Woolwine, B. J., Jung, M. Y., Hu, X., & Miller, A. H. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.168 · Cited by 620 · see citing works

Acute Systemic Inflammation Impairs Endothelium-Dependent Dilatation in Humans

Hingorani, A. D., Cross, J. M., Kharbanda, R. K., Mullen, M. J., Bhagat, K., Taylor, M., Donald, A. E., Palacios‐Callender, M., Griffin, G. E., Deanfield, J. E., et al. (2000) · Circulation · doi:10.1161/01.cir.102.9.994 · Cited by 605 · see citing works

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 · see citing works

Social neuroscience and health: neurophysiological mechanisms linking social ties with physical health

Eisenberger, N. I., & Cole, S. W. (2012) · Nature Neuroscience · doi:10.1038/nn.3086 · Cited by 590 · see citing works

Functional–Anatomical Validation and Individual Variation of Diffusion Tractography-based Segmentation of the Human Thalamus

Johansen‐Berg, H., Behrens, T. E. J., Sillery, E., Ciccarelli, O., Thompson, A. J., Smith, S. M., & Matthews, P. M. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh105 · Cited by 563 · see citing works

NeuroVault.org: a web-based repository for collecting and sharing unthresholded statistical maps of the human brain

Gorgolewski, K. J., Varoquaux, G. P., Rivera, G., Schwarz, Y., Ghosh, S., Maumet, C., Sochat, V., Nichols, T. E., Poldrack, R. A., Poline, J., et al. (2015) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2015.00008 · Cited by 554 · see citing works

Interleukin-6 and risk of cognitive decline: MacArthur Studies of Successful Aging

Weaver, J. D., Huang, M.-H., Albert, M., Harris, T., Rowe, J. W., & Seeman, T. E. (2002) · Neurology · doi:10.1212/wnl.59.3.371 · Cited by 536 · see citing works

Neural regulation of immunity: molecular mechanisms and clinical translation

Pavlov, V. A., & Tracey, K. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4477 · Cited by 534 · see citing works

Vagal immune-to-brain communication: a visceral chemosensory pathway

Goehler, L. E., Gaykema, R. P. A., Hansen, M. K., Anderson, K., Maier, S. F., & Watkins, L. R. (2000) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00219-8 · Cited by 525 · see citing works

Is depression an inflammatory disorder?

Raison, C. L., & Miller, A. H. (2011) · Current Psychiatry Reports · doi:10.1007/s11920-011-0232-0 · Cited by 524 · see citing works

Inflammation Effects on Motivation and Motor Activity: Role of Dopamine

Felger, J. C., & Treadway, M. T. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.143 · Cited by 453 · see citing works

Mechanisms of Disease: oxidative stress and inflammation in the pathogenesis of hypertension

Vaziri, N. D., & Rodríguez-Iturbe, B. (2006) · Nature Clinical Practice Nephrology · doi:10.1038/ncpneph0283 · Cited by 442 · see citing works

Lipopolysaccharide induces delayed FosB/DeltaFosB immunostaining within the mouse extended amygdala, hippocampus and hypothalamus, that parallel the expression of depressive-like behavior

Frenois, F., Moreau, M., O’Connor, J., Lawson, M., Micon, C., Lestage, J., Kelley, K. W., Dantzer, R., & Castanon, N. (2007) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2007.03.005 · Cited by 438 · see citing works

Meta-analysis of functional neuroimaging data: current and future directions

Wager, T. D., Lindquist, M., & Kaplan, L. (2007) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsm015 · Cited by 434 · see citing works

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 · see citing works

Emotional valence modulates brain functional abnormalities in depression: Evidence from a meta-analysis of fMRI studies

Groenewold, N. A., Opmeer, E. M., de Jonge, P., Aleman, A., & Costafreda, S. G. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.11.015 · Cited by 417 · see citing works

Brain mediators of cardiovascular responses to social threat

Wager, T. D., Waugh, C. E., Lindquist, M., Noll, D. C., Fredrickson, B. L., & Taylor, S. F. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.043 · Cited by 402 · see citing works

Neuroimaging of the periaqueductal gray: State of the field

Linnman, C., Moulton, E. A., Barmettler, G., Becerra, L. R., & Borsook, D. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.095 · Cited by 402 · see citing works

Neural and humoral pathways of communication from the immune system to the brain: parallel or convergent?

Dantzer, R., Konsman, J.-P., Bluthé, R.-M., & Kelley, K. W. (2000) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00220-4 · Cited by 400 · see citing works

The dorsal posterior insula subserves a fundamental role in human pain

Segerdahl, A. R., Mezue, M., Okell, T. W., Farrar, J. T., & Tracey, I. (2015) · Nature Neuroscience · doi:10.1038/nn.3969 · Cited by 393 · see citing works

Meta-analysis of neuroimaging data: a comparison of image-based and coordinate-based pooling of studies

Salimi-Khorshidi, G., Smith, S. M., Keltner, J. R., Wager, T. D., & Nichols, T. E. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.12.039 · Cited by 388 · see citing works

The Pain of Being Sick: Implications of Immune-to-Brain Communication for Understanding Pain

Watkins, L. R., & Maier, S. F. (2000) · Annual Review of Psychology · doi:10.1146/annurev.psych.51.1.29 · Cited by 388 · see citing works

Dopaminergic Mechanisms of Reduced Basal Ganglia Responses to Hedonic Reward During Interferon Alfa Administration

Capuron, L., Pagnoni, G., Drake, D. F., Woolwine, B. J., Spivey, J. R., Crowe, R. J., Votaw, J. R., Goodman, M. M., & Miller, A. H. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.2094 · Cited by 382 · see citing works

Peripheral inflammation is associated with altered substantia nigra activity and psychomotor slowing in humans

Brydon, L., Harrison, N. A., Walker, C., Steptoe, A., & Critchley, H. D. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.12.007 · Cited by 381 · see citing works

Immune and neuroendocrine mechanisms of stress vulnerability and resilience

Ménard, C., Pfau, M. L., Hodes, G. E., & Russo, S. J. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.90 · Cited by 374 · see citing works

Activation of Vagal Afferents after Intravenous Injection of Interleukin-1β: Role of Endogenous Prostaglandins

Ek, M., Kurosawa, M., Lundeberg, T., & Ericsson, A. B. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-22-09471.1998 · Cited by 370 · see citing works

The limbic lobe and its output channels: implications for emotional functions and adaptive behavior

Heimer, L., & Van Hoesen, G. W. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.06.006 · Cited by 366 · see citing works

Mixed-Affinity Binding in Humans with 18-kDa Translocator Protein Ligands

Owen, D. R., Gunn, R. N., Rabiner, E. A., Bennacef, I., Fujita, M., Kreisl, W. C., Innis, R. B., Pike, V. W., Reynolds, R., Matthews, P. M., et al. (2010) · Journal of Nuclear Medicine · doi:10.2967/jnumed.110.079459 · Cited by 361 · see citing works

Imaging robust microglial activation after lipopolysaccharide administration in humans with PET

Sandiego, C. M., Gallezot, J.-D., Pittman, B., Nabulsi, N., Lim, K., Lin, S.-F., Matuskey, D., Lee, J.-Y., O’Connor, K. C., Huang, Y., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1511003112 · Cited by 356 · see citing works

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 · see citing works

Brain correlates of autonomic modulation: Combining heart rate variability with fMRI

Napadow, V., Dhond, R. P., Conti, G., Makris, N., Brown, E. N., & Barbieri, R. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.04.238 · Cited by 347 · see citing works

Neural Origins of Human Sickness in Interoceptive Responses to Inflammation

Harrison, N. A., Brydon, L., Walker, C., Gray, M. A., Steptoe, A., Dolan, R. J., & Critchley, H. D. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.03.007 · Cited by 345 · see citing works

The relation between statistical power and inference in fMRI

Cremers, H. R., Wager, T. D., & Yarkoni, T. (2017) · PLoS ONE · doi:10.1371/journal.pone.0184923 · Cited by 336 · see citing works

Psychosocial and Behavioral Predictors of Inflammation in Middle-Aged and Older Adults: The Chicago Health, Aging, and Social Relations Study

McDade, T. W., Hawkley, L. C., & Cacioppo, J. T. (2006) · Psychosomatic Medicine · doi:10.1097/01.psy.0000221371.43607.64 · Cited by 326 · see citing works

Neural–immune interactions: An integrative view of the bidirectional relationship between the brain and immune systems

Wrona, D. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2005.10.017 · Cited by 322 · see citing works

Brain morphology links systemic inflammation to cognitive function in midlife adults

Marsland, A. L., Gianaros, P. J., Kuan, D. C.-H., Sheu, L. K., Krajina, K., & Manuck, S. B. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2015.03.015 · Cited by 321 · see citing works

An fMRI study of cytokine-induced depressed mood and social pain: The role of sex differences

Eisenberger, N. I., Inagaki, T. K., Rameson, L. T., Mashal, N. M., & Irwin, M. R. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.04.040 · Cited by 313 · see citing works

Untitled work

(1994) · PubMed · Cited by 294 · see citing works

Brain-Body Pathways Linking Psychological Stress and Physical Health

Gianaros, P. J., & Wager, T. D. (2015) · Current Directions in Psychological Science · doi:10.1177/0963721415581476 · Cited by 290 · see citing works

Activation of the reward system boosts innate and adaptive immunity

Ben-Shaanan, T. L., Azulay-Debby, H., Dubovik, T., Starosvetsky, E., Korin, B., Schiller, M., Green, N. L., Admon, Y., Hakim, F., Shen-Orr, S. S., et al. (2016) · Nature Medicine · doi:10.1038/nm.4133 · Cited by 272 · see citing works

Using the talairach atlas with the MNI template

Brett, M., Kalina Christoff, A., Cusack, R., & Lancaster, J. L. (2001) · NeuroImage · doi:10.1016/s1053-8119(01)91428-4 · Cited by 271 · see citing works

Inflammation selectively enhances amygdala activity to socially threatening images

Inagaki, T. K., Muscatell, K. A., Irwin, M. R., Cole, S. W., & Eisenberger, N. I. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.090 · Cited by 264 · see citing works

Brain mediators of cardiovascular responses to social threat, part II: prefrontal–subcortical pathways and relationship with anxiety

Wager, T. D., van Ast, V. A., Hughes, B. L., Davidson, M. L., Lindquist, M. A., & Ochsner, K. N. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.044 · Cited by 264 · see citing works

Evaluating the consistency and specificity of neuroimaging data using meta-analysis

Wager, T. D., Lindquist, M. A., Nichols, T. E., Kober, H., & Van Snellenberg, J. X. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.10.061 · Cited by 242 · see citing works

Greater amygdala activity and dorsomedial prefrontal–amygdala coupling are associated with enhanced inflammatory responses to stress

Muscatell, K. A., Dedovic, K., Slavich, G. M., Jarcho, M. R., Breen, E. C., Bower, J. E., Irwin, M. R., & Eisenberger, N. I. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.06.201 · Cited by 240 · see citing works

Basal Ganglia Hypermetabolism and Symptoms of Fatigue during Interferon-α Therapy

Capuron, L., Pagnoni, G., Demetrashvili, M. F., Lawson, D. H., Fornwalt, F. B., Woolwine, B., Berns, G. S., Nemeroff, C. B., & Miller, A. H. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301362 · Cited by 229 · see citing works

Anterior Cingulate Activation and Error Processing During Interferon-Alpha Treatment

Capuron, L., Pagnoni, G., Demetrashvili, M., Woolwine, B. J., Nemeroff, C. B., Berns, G. S., & Miller, A. H. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.03.033 · Cited by 222 · see citing works

Endotoxin-induced systemic inflammation activates microglia: [11C]PBR28 positron emission tomography in nonhuman primates

Hannestad, J. O., Gallezot, J., Schafbauer, T., Lim, K., Kloczynski, T., Morris, E. D., Carson, R. E., Ding, Y., & Cosgrove, K. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.055 · Cited by 213 · see citing works

Suppression of fever after lesions of the anteroventral third ventricle in guinea pigs

Blatteis, C. M., Bealer, S. L., Hunter, W. S., Llanos, J.-Q., Ahokas, R. A., & Mashburn, T. A. (1983) · Brain Research Bulletin · doi:10.1016/0361-9230(83)90124-7 · Cited by 213 · see citing works

Kinetic analysis in healthy humans of a novel positron emission tomography radioligand to image the peripheral benzodiazepine receptor, a potential biomarker for inflammation

Fujita, M., Imaizumi, M., Zoghbi, S. S., Fujimura, Y., Farris, A. G., Suhara, T., Hong, J. S., Pike, V. W., & Innis, R. B. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.11.011 · Cited by 213 · see citing works

Proinflammatory milieu in combat-related PTSD is independent of depression and early life stress

Lindqvist, D., Wolkowitz, O. M., Mellon, S., Yehuda, R., Flory, J. D., Henn-Haase, C., Bierer, L. M., Abu-Amara, D., Coy, M., Neylan, T. C., et al. (2014) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.06.003 · Cited by 213 · see citing works

Neural aspects of immunomodulation: Focus on the vagus nerve

Thayer, J. F., & Sternberg, E. M. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.07.247 · Cited by 200 · see citing works

Regional specialization within the human striatum for diverse psychological functions

Pauli, W. M., O’Reilly, R. C., Yarkoni, T., & Wager, T. D. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1507610113 · Cited by 198 · see citing works

Endotoxin-induced experimental systemic inflammation in humans: A model to disentangle immune-to-brain communication

Schedlowski, M., Engler, H., & Grigoleit, J.-S. (2014) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2013.09.015 · Cited by 195 · see citing works

The insular cortex and the regulation of cardiac function

Oppenheimer, S., & Cechetto, D. (2016) · Comprehensive Physiology · doi:10.1002/cphy.c140076 · Cited by 191 · see citing works

Motor, cognitive, and affective areas of the cerebral cortex influence the adrenal medulla

Dum, R. P., Levinthal, D. J., & Strick, P. L. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1605044113 · Cited by 188 · see citing works

Ascending visceral regulation of cortical affective information processing

Berntson, G. G., Sarter, M. F., & Cacioppo, J. T. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02967.x · Cited by 185 · see citing works

A review of neuroimaging studies of stressor-evoked blood pressure reactivity: Emerging evidence for a brain-body pathway to coronary heart disease risk

Gianaros, P. J., & Sheu, L. K. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.04.073 · Cited by 180 · see citing works

Blood to brain transport of interleukin links the immune and central nervous systems

Banks, W. A., & Kastin, A. J. (1991) · Life Sciences · doi:10.1016/0024-3205(91)90385-o · Cited by 177 · see citing works

Nonparametric Measures of Association

Gibbons, J. D. (1993) · Sage eBooks · doi:10.4135/9781412985291 · Cited by 170 · see citing works

Peripheral and central mechanisms of stress resilience

Pfau, M. L., & Russo, S. J. (2015) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.09.004 · Cited by 170 · see citing works

Cardiovascular and autonomic reactivity to psychological stress: Neurophysiological substrates and links to cardiovascular disease

Ginty, A. T., Kraynak, T. E., Fisher, J. P., & Gianaros, P. J. (2017) · Autonomic Neuroscience · doi:10.1016/j.autneu.2017.03.003 · Cited by 168 · see citing works

Brain systems for baroreflex suppression during stress in humans

Gianaros, P. J., Onyewuenyi, I. C., Sheu, L. K., Christie, I. C., & Critchley, H. D. (2012) · Human Brain Mapping · doi:10.1002/hbm.21315 · Cited by 166 · see citing works

Pooling fMRI data: meta-analysis, mega-analysis and multi-center studies

Costafreda, S. G. (2009) · Frontiers in Neuroinformatics · doi:10.3389/neuro.11.033.2009 · Cited by 156 · see citing works

IFN-Alpha-Induced Cortical and Subcortical Glutamate Changes Assessed by Magnetic Resonance Spectroscopy

Haroon, E., Woolwine, B. J., Chen, X., Pace, T. W., Parekh, S., Spivey, J. R., Hu, X. P., & Miller, A. H. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.25 · Cited by 154 · see citing works

Therapeutic Implications of Brain–Immune Interactions: Treatment in Translation

Miller, A. H., Haroon, E., & Felger, J. C. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.167 · Cited by 152 · see citing works

Prefrontal cortical hypometabolism during low-dose interferon alpha treatment

Juengling, F. D., Ebert, D., Gut, O., Engelbrecht, M. A., Rasenack, J., Nitzsche, E. U., Bauer, J., & Lieb, K. (2000) · Psychopharmacology · doi:10.1007/s002130000549 · Cited by 149 · see citing works

Exposure to an inflammatory challenge enhances neural sensitivity to negative and positive social feedback.

Muscatell, K. A., Moieni, M., Inagaki, T. K., Dutcher, J. M., Jevtic, I., Breen, E. C., Irwin, M. R., & Eisenberger, N. I. (2016) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.03.022 · Cited by 146 · see citing works

Functional connectivity and network analysis of midbrain and brainstem nuclei

Bär, K.-J., de la Cruz, F., Schumann, A., Koehler, S., Sauer, H., Critchley, H., & Wagner, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.071 · Cited by 134 · see citing works

Systemic inflammation and resting state connectivity of the default mode network

Marsland, A. L., Kuan, D. C.-H., Sheu, L. K., Krajina, K., Kraynak, T. E., Manuck, S. B., & Gianaros, P. J. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.01.013 · Cited by 134 · see citing works

NEUROIMMUNOMODULATION VIA LIMBIC STRUCTURES — THE NEUROANATOMY OF PSYCHOIMMUNOLOGY

Haas, H. S., & Schauenstein, K. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(96)00055-x · Cited by 133 · see citing works

Visceral cortex: Integration of the mucosal senses with limbic information in the rat agranular insular cortex

Krushel, L. A., & van der Kooy, D. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902700105 · Cited by 132 · see citing works

The role of the ventral striatum in inflammatory-induced approach toward support figures

Inagaki, T. K., Muscatell, K. A., Irwin, M. R., Moieni, M., Dutcher, J. M., Jevtic, I., Breen, E. C., & Eisenberger, N. I. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.10.006 · Cited by 132 · see citing works

Identification of discrete functional subregions of the human periaqueductal gray

Satpute, A. B., Wager, T. D., Cohen-Adad, J., Bianciardi, M., Choi, J.-K., Buhle, J. T., Wald, L. L., & Barrett, L. F. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1306095110 · Cited by 131 · see citing works

Quantitative magnetization transfer imaging as a biomarker for effects of systemic inflammation on the brain

Harrison, N. A., Cooper, E., Dowell, N. G., Keramida, G., Voon, V., Critchley, H. D., & Cercignani, M. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.09.023 · Cited by 129 · see citing works

Inflammatory Pathways Link Socioeconomic Inequalities to White Matter Architecture

Gianaros, P. J., Marsland, A. L., Sheu, L. K., Erickson, K. I., & Verstynen, T. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs191 · Cited by 125 · see citing works

Ascending mechanisms of stress integration: Implications for brainstem regulation of neuroendocrine and behavioral stress responses

Myers, B., Scheimann, J. R., Franco, A. C. G., & Herman, J. P. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.011 · Cited by 125 · see citing works

When grief heats up: Pro-inflammatory cytokines predict regional brain activation

O'Connor, M.-F., Irwin, M. R., & Wellisch, D. K. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.049 · Cited by 123 · see citing works

The association between pro-inflammatory cytokines, regional cerebral metabolism, and cognitive complaints following adjuvant chemotherapy for breast cancer

Pomykala, K. L., Ganz, P. A., Bower, J. E., Kwan, L. C., Castellon, S. A., Mallam, S., Cheng, I., Ahn, R., Breen, E. C., Irwin, M. R., et al. (2013) · Brain Imaging and Behavior · doi:10.1007/s11682-013-9243-2 · Cited by 122 · see citing works

An Inflammatory Pathway Links Atherosclerotic Cardiovascular Disease Risk to Neural Activity Evoked by the Cognitive Regulation of Emotion

Gianaros, P. J., Marsland, A. L., Kuan, D. C.-H., Schirda, B. L., Jennings, J. R., Sheu, L. K., Hariri, A. R., Gross, J. J., & Manuck, S. B. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.10.012 · Cited by 119 · see citing works

Peripheral Inflammation Acutely Impairs Human Spatial Memory via Actions on Medial Temporal Lobe Glucose Metabolism

Harrison, N. A., Doeller, C. F., Voon, V., Burgess, N., & Critchley, H. D. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.01.005 · Cited by 118 · see citing works

Inflammatory Factors Contribute to Depression and Its Comorbid Conditions

Anisman, H., & Hayley, S. P. (2012) · Science Signaling · doi:10.1126/scisignal.2003579 · Cited by 117 · see citing works

Glucose Metabolism in the Insula and Cingulate Is Affected by Systemic Inflammation in Humans

Hannestad, J., Subramanyam, K., DellaGioia, N., Planeta-Wilson, B., Weinzimmer, D., Pittman, B., & Carson, R. E. (2012) · Journal of Nuclear Medicine · doi:10.2967/jnumed.111.097014 · Cited by 113 · see citing works

Langerhans cells β2-adrenoceptors: role in migration, cytokine production, Th priming and contact hypersensitivity

Maestroni, G. J. M., & Mazzola, P. (2003) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2003.08.039 · Cited by 112 · see citing works

Multivariate Brain Prediction of Heart Rate and Skin Conductance Responses to Social Threat

Eisenbarth, H., Chang, L. J., & Wager, T. D. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3672-15.2016 · Cited by 111 · see citing works

Are There Neurophenotypes for Asthma? Functional Brain Imaging of the Interaction between Emotion and Inflammation in Asthma

Rosenkranz, M. A., Busse, W. W., Sheridan, J. F., Crisafi, G. M., & Davidson, R. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040921 · Cited by 109 · see citing works

Adrenergic receptors mediate stress-induced elevations in extracellular Hsp72

Johnson, J. D., Campisi, J., Sharkey, C. M., Kennedy, S. L., Nickerson, M., & Fleshner, M. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00390.2005 · Cited by 108 · see citing works

Common representation of pain and negative emotion in the midbrain periaqueductal gray

Buhle, J. T., Kober, H., Ochsner, K. N., Mende-Siedlecki, P., Weber, J., Hughes, B. L., Kross, E., Atlas, L. Y., McRae, K., & Wager, T. D. (2013) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nss038 · Cited by 100 · see citing works

Visceral sensory inputs to the endocrine hypothalamus

Rinaman, L. (2007) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2007.02.002 · Cited by 97 · see citing works

Human cerebral circuitry related to cardiac control: a neuroimaging meta-analysis

Ruiz Vargas, E., Sörös, P., Shoemaker, J. K., & Hachinski, V. (2016) · Annals of Neurology · doi:10.1002/ana.24642 · Cited by 94 · see citing works

Neural response to emotional stimuli during experimental human endotoxemia: Neural Response During Acute Inflammation

Kullmann, J. S., Grigoleit, J.-S., Lichte, P., Kobbe, P., Rosenberger, C., Banner, C., Wolf, O. T., Engler, H., Oberbeck, R., Elsenbruch, S., et al. (2013) · Human Brain Mapping · doi:10.1002/hbm.22063 · Cited by 93 · cited 1× · see citing works

Future directions in the study of early-life stress and physical and emotional health: implications of the neuroimmune network hypothesis.

Hostinar, C. E., Nusslock, R., & Miller, G. E. (2018) · Journal of Clinical Child & Adolescent Psychology · doi:10.1080/15374416.2016.1266647 · Cited by 90 · see citing works

Effects of Inflammation on Hippocampus and Substantia Nigra Responses to Novelty in Healthy Human Participants

Harrison, N. A., Cercignani, M., Voon, V., & Critchley, H. D. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.222 · Cited by 89 · see citing works

Gender differences in stimulated cytokine production following acute psychological stress

Prather, A. A., Carroll, J., Fury, J. M., McDade, K. K., Ross, D. C., & Marsland, A. L. (2008) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2008.11.004 · Cited by 80 · see citing works

Competing physiological pathways link individual differences in weight and abdominal adiposity to white matter microstructure

Verstynen, T., Weinstein, A. M., Erickson, K. I., Sheu, L. K., Marsland, A. L., & Gianaros, P. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.075 · Cited by 77 · see citing works

Central autonomic network mediates cardiovascular responses to acute inflammation: relevance to increased cardiovascular risk in depression?

Harrison, N. A., Cooper, E., Voon, V., Miles, K., & Critchley, H. D. (2013) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2013.02.001 · Cited by 76 · see citing works

Mind-body interactions in the regulation of airway inflammation in asthma: A PET study of acute and chronic stress

Rosenkranz, M. A., Esnault, S. J., Christian, B. T., Crisafi, G. M., Gresham, L. K., Higgins, A. T., Moore, M. N., Moore, S. M., Weng, H. Y., Salk, R. H., et al. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.03.024 · Cited by 76 · see citing works

Acute Changes in Striatal Microstructure Predict the Development of Interferon-Alpha Induced Fatigue

Dowell, N. G., Cooper, E. A., Tibble, J., Voon, V., Critchley, H. D., Cercignani, M., & Harrison, N. A. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.05.015 · Cited by 74 · see citing works

Meta-analysis of neuroimaging data

Kober, H., & Wager, T. D. (2010) · WIREs Cognitive Science · doi:10.1002/wcs.41 · Cited by 74 · see citing works

Brain structures implicated in inflammation-associated depression

Harrison, N. A. (2016) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2016_30 · Cited by 74 · see citing works

Intrinsic functional connectivity of insular cortex and symptoms of sickness during acute experimental inflammation

Lekander, M., Karshikoff, B., Johansson, E., Soop, A., Fransson, P., Lundström, J. N., Andréasson, A., Ingvar, M., Petrović, P., Axelsson, J., et al. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.12.018 · Cited by 73 · see citing works

Interferon-α acutely impairs whole-brain functional connectivity network architecture – A preliminary study

Dipasquale, O., Cooper, E. A., Tibble, J. A., Voon, V., Baglio, F., Baselli, G., Cercignani, M., & Harrison, N. A. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.12.011 · Cited by 71 · see citing works

A Brain Phenotype for Stressor‐Evoked Blood Pressure Reactivity

Gianaros, P., Lei, S. K., Uyar, F., Koushik, J., Jennings, J., Wager, T., Singh, A., & Verstynen, T. (2017) · Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease · doi:10.1161/jaha.117.006053 · Cited by 67 · see citing works

Links between inflammation, amygdala reactivity, and social support in breast cancer survivors

Muscatell, K. A., Eisenberger, N. I., Dutcher, J. M., Cole, S. W., & Bower, J. E. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.09.008 · Cited by 60 · see citing works

In vivo evidence of a functional association between immune cells in blood and brain in healthy human subjects

Kanegawa, N., Collste, K., Forsberg, A., Schain, M., Arakawa, R., Jučaitė, A., Lekander, M., Höglund, C. O., Kosek, E., Lampa, J., et al. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.01.019 · Cited by 60 · see citing works

Visceral brain–body information transfer

Cameron, O. G. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.010 · Cited by 58 · see citing works

Large-scale brain networks in affective and social neuroscience: Towards an integrative functional architecture of the brain

Barrett, L. F., & Satpute, A. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.12.012 · Cited by 58 · see citing works

Experimental human endotoxemia enhances brain activity during social cognition

Kullmann, J. S., Grigoleit, J., Wolf, O. T., Engler, H., Oberbeck, R., Elsenbruch, S., Forsting, M., Schedlowski, M., & Gizewski, E. R. (2013) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst049 · Cited by 53 · see citing works

Depressive Behavior in Mice Due to Immune Stimulation is Accompanied by Reduced Neural Activity in Brain Regions Involved in Positively Motivated Behavior

Stone, E. A., Lehmann, M. L., Lin, Y., & Quartermain, D. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.04.020 · Cited by 52 · see citing works

Associations among central nervous, endocrine, and immune activities when positive emotions are elicited by looking at a favorite person

Matsunaga, M., Isowa, T., Kimura, K., Miyakoshi, M., Kanayama, N., Murakami, H., Sato, S., Konagaya, T., NOGIMORI, T., Fukuyama, S., et al. (2007) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2007.09.008 · Cited by 49 · see citing works

Ascending caudal medullary catecholamine pathways drive sickness-induced deficits in exploratory behavior: Brain substrates for fatigue?

Gaykema, R. P. A., & Goehler, L. E. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.11.005 · Cited by 49 · see citing works

Vagal nerve activity as a moderator of brain-immune relationships

Ohira, H., Matsunaga, M., Osumi, T., Fukuyama, S., Shinoda, J., Yamada, J., & Gidron, Y. (2013) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2013.04.011 · Cited by 47 · see citing works

Imaging brain and immune association accompanying cognitive appraisal of an acute stressor

Ohira, H., Isowa, T., Nomura, M., Ichikawa, N., Kimura, K., Miyakoshi, M., Iidaka, T., Fukuyama, S., Nakajima, T., & Yamada, J. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.017 · Cited by 45 · see citing works

Threat-related amygdala activity is associated with peripheral CRP concentrations in men but not women

Swartz, J. R., Prather, A. A., & Hariri, A. R. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.01.024 · Cited by 42 · see citing works

Inference for Contingency Tables

Agresti, A. (2002) · Wiley series in probability and statistics · doi:10.1002/0471249688.ch3 · Cited by 40 · see citing works

Regulation of natural killer cell redistribution by prefrontal cortex during stochastic learning

Ohira, H., Fukuyama, S., Kimura, K., Nomura, M., Isowa, T., Ichikawa, N., Matsunaga, M., Shinoda, J., & Yamada, J. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.04.088 · Cited by 37 · see citing works

Peripheral inflammation related to lower fMRI activation during a working memory task and resting functional connectivity among older adults: a preliminary study

Dev, S. I., Moore, R. C., Soontornniyomkij, B., Achim, C. L., Jeste, D. V., & Eyler, L. T. (2016) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.4482 · Cited by 36 · see citing works

Neural-Immune Interactions in Brain Function and Alcohol Related Disorders

Cui, C.-H., Grandison, L., & Noronha, A. (2013) · Springer US · doi:10.1007/978-1-4614-4729-0 · Cited by 35 · see citing works

Relationship between trait anxiety, brain activity and natural killer cell activity in cancer patients: a preliminary PET study

Tashiro, M., Itoh, M., Kubota, K., Kumano, H., Masud, M., Moser, E. A., Arai, H., & Sasaki, H. (2001) · Psycho-Oncology · doi:10.1002/pon.548 · Cited by 34 · see citing works

Nonparametric Measures of Association.

Podgor, M. J., & Gibbons, J. D. (1994) · Journal of the American Statistical Association · doi:10.2307/2290888 · Cited by 14 · see citing works

Human Brain–Immune Relationships: A PET Study

Wik, G., Lekander, M., & Fredrikson, M. (1998) · Brain Behavior and Immunity · doi:10.1006/brbi.1998.0529 · Cited by 12 · see citing works

Neuroimaging and Clinical Studies on Brain–Immune Interactions

Hannestad, J. O. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4729-0_4 · Cited by 1 · see citing works

Comparison of bacterial lipopolysaccharide-induced sickness behavior in rodents and humans: Relevance for symptoms of anxiety and depression

Lasselin, J., Schedlowski, M., Karshikoff, B., Engler, H., Lekander, M., & Konsman, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.05.001 · Cited by 165 · see citing works

Linking atypical depression and insulin resistance-related disorders via low-grade chronic inflammation: Integrating the phenotypic, molecular and neuroanatomical dimensions

Sen, Z. D., Danyeli, L. V., Woelfer, M., Lamers, F., Wagner, G., Sobanski, T., & Walter, M. (2021) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2020.12.020 · Cited by 65 · see citing works

Neuroimmune modulation of pain across the developmental spectrum

Karshikoff, B., Tadros, M. A., Mackey, S., & Zouikr, I. (2019) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2019.01.010 · Cited by 21 · see citing works

Towards an Integrative Account of Potential Mechanisms Mediating the Path From Sleep Dysfunction to Hallucinations

Sheaves, B., Cropley, V. L., Moseley, P., Woodruff, P. W. R., Punton, G., Speth, C., Speth, J., Meerlo, P., & Brederoo, S. G. (2025) · Schizophrenia Bulletin · doi:10.1093/schbul/sbaf107 · Cited by 6 · see citing works

Baseline Pro-Inflammatory Cytokine Levels Moderate Psychological Inflexibility in Behavioral Treatment for Chronic Pain

Karshikoff, B., Åström, J., Holmström, L., Lekander, M., Kemani, M. K., & Wicksell, R. K. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11092285 · Cited by 6 · see citing works

Review for "Posterior cingulate cortex targeted real‐time fMRI neurofeedback recalibrates functional connectivity with the amygdala, posterior insula, and default‐mode network in PTSD"

(2022) · doi:10.1002/brb3.2883/v2/review1

Decision letter for "Posterior cingulate cortex targeted real‐time fMRI neurofeedback recalibrates functional connectivity with the amygdala, posterior insula, and default‐mode network in PTSD"

(2022) · doi:10.1002/brb3.2883/v2/decision1

Review for "Posterior cingulate cortex targeted real‐time fMRI neurofeedback recalibrates functional connectivity with the amygdala, posterior insula, and default‐mode network in PTSD"

(2022) · doi:10.1002/brb3.2883/v1/review2

The role of default network deactivation in cognition and disease

Anticevic, A., Cole, M. W., Murray, J. D., Corlett, P. R., Wang, X.-J., & Krystal, J. H. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.10.008 · Cited by 978 · see citing works

In praise of tedious anatomy

Devlin, J. T., & Poldrack, R. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.09.055 · Cited by 195 · see citing works