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Neural correlates of interindividual differences in the subjective experience of pain

https://doi.org/10.1073/pnas.1430684100
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hbm.460010306openalex-snapshot
Assessing the significance of focal activations using their spatial extent
inferredcites →https://doi.org/10.1006/nimg.1999.0440openalex-snapshot
Areas 3a, 3b, and 1 of Human Primary Somatosensory Cortex
inferredcites →https://doi.org/10.1006/nimg.2001.0931openalex-snapshot
Temporal Autocorrelation in Univariate Linear Modeling of FMRI Data
inferredcites →https://doi.org/10.1016/0304-3959(94)00108-qopenalex-snapshot
The effect of past-injury on pain threshold and tolerance
inferredcites →https://doi.org/10.1016/0304-3959(94)90097-3openalex-snapshot
A comparison of pain measurement characteristics of mechanical visual analogue and simple numerical rating scales
inferredcites →https://doi.org/10.1016/0304-3959(95)00015-kopenalex-snapshot
Unilateral decrease in thalamic activity observed with positron emission tomography in patients with chronic neuropathic pain
inferredcites →https://doi.org/10.1016/0304-3959(95)00048-wopenalex-snapshot
Central representation of chronic ongoing neuropathic pain studied by positron emission tomography
inferredcites →https://doi.org/10.1016/s0079-6123(08)62141-xopenalex-snapshot
The medial pain system, cingulate cortex, and parallel processing of nociceptive information
inferredcites →https://doi.org/10.1016/s0304-3959(02)00048-9openalex-snapshot
Reproducibility of pain measurement and pain perception
inferredcites →https://doi.org/10.1016/s0304-3959(97)00138-3openalex-snapshot
Pain processing during three levels of noxious stimulation produces differential patterns of central activity
inferredcites →https://doi.org/10.1016/s0304-3959(99)00081-0openalex-snapshot
An analysis of factors that contribute to the magnitude of placebo analgesia in an experimental paradigm
inferredcites →https://doi.org/10.1016/s1361-8415(01)00036-6openalex-snapshot
A global optimisation method for robust affine registration of brain images
inferredcites →https://doi.org/10.1037//0096-3445.113.4.571openalex-snapshot
Individual differences in loudness processing and loudness scales.
inferredcites →https://doi.org/10.1038/jcbfm.1992.127openalex-snapshot
A Three-Dimensional Statistical Analysis for CBF Activation Studies in Human Brain
inferredcites →https://doi.org/10.1055/b-002-44939openalex-snapshot
Surgical Management of Pain
inferredcites →https://doi.org/10.1093/brain/60.4.389openalex-snapshot
SOMATIC MOTOR AND SENSORY REPRESENTATION IN THE CEREBRAL CORTEX OF MAN AS STUDIED BY ELECTRICAL STIMULATION
inferredcites →https://doi.org/10.1126/science.277.5328.968openalex-snapshot
Pain Affect Encoded in Human Anterior Cingulate But Not Somatosensory Cortex
inferredcites →https://doi.org/10.1152/jn.1993.69.3.703openalex-snapshot
Wide dynamic range but not nociceptive-specific neurons encode multidimensional features of prolonged repetitive heat pain
inferredcites →https://doi.org/10.1152/jn.1998.80.6.3312openalex-snapshot
Temporal and Intensity Coding of Pain in Human Cortex
inferredcites →https://doi.org/10.1152/jn.1999.82.4.1934openalex-snapshot
Pain Intensity Processing Within the Human Brain: A Bilateral, Distributed Mechanism
inferredcites →https://doi.org/10.1152/jn.2001.85.6.2602openalex-snapshot
Hemispheric Lateralization of Somatosensory Processing
inferredcites →https://doi.org/10.1152/jn.2001.86.1.402openalex-snapshot
Cortical Representation of the Sensory Dimension of Pain

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.2458528openalex-extracted
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inferred← citeshttps://doi.org/10.1002/14651858.cd008921openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/14651858.cd008921.pub2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470749357.refsopenalex-snapshot
References
inferred← citeshttps://doi.org/10.1002/9781118398890.ch3openalex-snapshot
Defining Human Pain Phenotypes for Genetic Association Studies
inferred← citeshttps://doi.org/10.1002/9781394259847.ch22openalex-snapshot
Naïve Realism v. Representationalism
inferred← citeshttps://doi.org/10.1002/acr.20005openalex-snapshot
Report of the American College of Rheumatology Pain Management Task Force
inferred← citeshttps://doi.org/10.1002/advs.202503373openalex-snapshot
A Replicable and Generalizable Neuroimaging‐Based Indicator of Pain Sensitivity Across Individuals
inferred← citeshttps://doi.org/10.1002/ana.21301openalex-snapshot
Functional neuroimaging of belief, disbelief, and uncertainty
inferred← citeshttps://doi.org/10.1002/art.37685openalex-snapshot
Alterations in resting‐state regional cerebral blood flow demonstrate ongoing pain in osteoarthritis: An arterial spin‐labeled magnetic resonance imaging study
inferred← citeshttps://doi.org/10.1002/art.37739openalex-snapshot
Review: Central pain mechanisms in the rheumatic diseases: Future directions
inferred← citeshttps://doi.org/10.1002/brb3.521openalex-snapshot
Altered regional brain function in the treatment‐naive patients with somatic symptom disorder: a resting‐state fMRI study
inferred← citeshttps://doi.org/10.1002/gps.5812openalex-snapshot
The pain and depressive symptoms cascade: A bidirectional analysis of the Mexican Health and Aging Study 2012–2015
inferred← citeshttps://doi.org/10.1002/hbm.20867openalex-snapshot
Individual sensitivity to pain expectancy is related to differential activation of the hippocampus and amygdala
inferred← citeshttps://doi.org/10.1002/hbm.21416openalex-snapshot
Localization of pain‐related brain activation: A meta‐analysis of neuroimaging data
inferred← citeshttps://doi.org/10.1002/hbm.22260openalex-snapshot
Differences in cortical coding of heat evoked pain beyond the perceived intensity: An fMRI and EEG study
inferred← citeshttps://doi.org/10.1002/hbm.22496openalex-snapshot
Placebo analgesia and reward processing: Integrating genetics, personality, and intrinsic brain activity
inferred← citeshttps://doi.org/10.1002/hbm.23220openalex-snapshot
Spectral and spatial changes of brain rhythmic activity in response to the sustained thermal pain stimulation
inferred← citeshttps://doi.org/10.1002/hbm.25659openalex-snapshot
Neural mechanisms of pain processing differ between endurance athletes and nonathletes: A functional connectivity magnetic resonance imaging study
inferred← citeshttps://doi.org/10.1002/hbm.25999openalex-snapshot
Neurotransmitter receptor densities are associated with changes in regional Cerebral blood flow during clinical ongoing pain
inferred← citeshttps://doi.org/10.1002/j.1532-2149.2012.00235.xopenalex-snapshot
On the moderating role of age in the relationship between pain and cognition
inferred← citeshttps://doi.org/10.1002/jmri.22814openalex-snapshot
Measuring the neural response to continuous intramuscular infusion of hypertonic saline by perfusion MRI
inferred← citeshttps://doi.org/10.1002/mrm.26455openalex-snapshot
Optimal echo time for functional MRI of the infant brain identified in response to noxious stimulation
inferred← citeshttps://doi.org/10.1002/neu.20085openalex-snapshot
Functional imaging of the human trigeminal system: Opportunities for new insights into pain processing in health and disease
inferred← citeshttps://doi.org/10.1007/0-387-25610-5_18openalex-snapshot
Confounding Effects of Pain, Psychoemotional Problems or Psychiatric Disorder, Premorbid Ability Structure, and Motivational or Other Factors on Neuropsychological Test Performance
inferred← citeshttps://doi.org/10.1007/3-540-26841-3_5openalex-snapshot
Psychosomatische Aspekte am Beispiel der Alexithymie und chronischer Schmerzen
inferred← citeshttps://doi.org/10.1007/88-470-0550-7_10openalex-snapshot
The Sensorimotor Side of Empathy for Pain
inferred← citeshttps://doi.org/10.1007/978-1-0716-3068-6_7openalex-snapshot
Qualia, Brain Waves, and Spinal Reflexes: The Study of Pain Perception by Means of Subjective Reports, Electroencephalography, and Electromyography
inferred← citeshttps://doi.org/10.1007/978-1-4419-0134-7_16openalex-snapshot
Neuroimaging in Understanding Chronic Pain Mechanisms and the Development of New Therapies
inferred← citeshttps://doi.org/10.1007/978-1-4419-1651-8_27openalex-snapshot
Pain Imaging
inferred← citeshttps://doi.org/10.1007/978-1-60327-323-7_21openalex-snapshot
RT-PCR Analysis of Pain Genes: Use of Gel-Based RT-PCR for Studying Induced and Tissue-Enriched Gene Expression
inferred← citeshttps://doi.org/10.1007/978-1-60327-919-2_25openalex-snapshot
Pharmacological Applications of fMRI
inferred← citeshttps://doi.org/10.1007/978-2-8178-0414-9_10openalex-snapshot
Why Does My Body Hurt? Somatoform Disorders and Pain
inferred← citeshttps://doi.org/10.1007/978-3-030-19201-3_2openalex-snapshot
Pain Disorder: A Biopsychosocial Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-04248-5_3openalex-snapshot
Pain
inferred← citeshttps://doi.org/10.1007/978-3-031-56541-0_5openalex-snapshot
Measuring Pain
inferred← citeshttps://doi.org/10.1007/978-3-211-99741-3_8openalex-snapshot
2.7 Neurobiological correlates of social exclusion and social pain
inferred← citeshttps://doi.org/10.1007/978-3-319-20322-5_3openalex-snapshot
Major Pain Theories and Factors Behind Chronic Pain
inferred← citeshttps://doi.org/10.1007/978-3-319-22858-7_2openalex-snapshot
Mechanisms of Arthritis Pain
inferred← citeshttps://doi.org/10.1007/978-3-319-44103-0_6openalex-snapshot
The Challenge of Measuring Pain in Humans
inferred← citeshttps://doi.org/10.1007/978-3-319-48046-6_11openalex-snapshot
Rheumatic Pain
inferred← citeshttps://doi.org/10.1007/978-3-319-48046-6_16openalex-snapshot
The Neuroimaging of Vicarious Pain
inferred← citeshttps://doi.org/10.1007/978-3-319-48046-6_4openalex-snapshot
Physiopathology of Pain
inferred← citeshttps://doi.org/10.1007/978-3-319-49022-9_11openalex-snapshot
Should Investigators Introspect on Their Own Pain Experiences as Study Co-Participants?
inferred← citeshttps://doi.org/10.1007/978-3-319-49022-9_7openalex-snapshot
A Scientific and Philosophical Analysis of Meanings of Pain in Studies of Pain and Suffering
inferred← citeshttps://doi.org/10.1007/978-3-319-74391-2_7openalex-snapshot
Suicide in Chronic Pain Patients: Risk Factors and Clinical Considerations
inferred← citeshttps://doi.org/10.1007/978-3-319-75112-2_15openalex-snapshot
Somatization and Bodily Distress Disorder
inferred← citeshttps://doi.org/10.1007/978-3-319-99124-5_36openalex-snapshot
Introspection and Measurement of Subjective Pain Experience
inferred← citeshttps://doi.org/10.1007/978-3-540-29805-2_3308openalex-snapshot
PET and fMRI Imaging in Parietal Cortex (SI, SII, Inferior Parietal Cortex BA40)
inferred← citeshttps://doi.org/10.1007/978-3-540-29805-2_729openalex-snapshot
Cingulate Cortex, Functional Imaging
inferred← citeshttps://doi.org/10.1007/978-3-642-19844-1_37openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-28753-4_729openalex-snapshot
Cingulate Cortex, Functional Imaging
inferred← citeshttps://doi.org/10.1007/978-3-642-32671-4_2openalex-snapshot
Schmerzstörung – Eine biopsychosoziale Erkrankung
inferred← citeshttps://doi.org/10.1007/978-3-642-37816-4_2openalex-snapshot
Pain Disorder: A Biopsychosocial Disease
inferred← citeshttps://doi.org/10.1007/978-3-662-45057-4_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-662-47765-6_19openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-662-58248-0_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-662-68956-1_22openalex-snapshot
Komplementäre Maßnahmen, nicht-medikamentöse Schmerztherapie mit Wickel und Kompressen, ätherischen Ölen, fetten Pflanzenölen und Heilpflanzen
inferred← citeshttps://doi.org/10.1007/978-3-7091-1841-2_20openalex-snapshot
Somatic Symptom and Related Disorders
inferred← citeshttps://doi.org/10.1007/978-88-470-0659-1_10openalex-snapshot
Il versante sensorimotorio dell’empatia per il dolore
inferred← citeshttps://doi.org/10.1007/978-90-481-9310-3_6openalex-snapshot
Do Our Economic Choices Make Us Happy?
inferred← citeshttps://doi.org/10.1007/978-94-007-6001-1_18openalex-snapshot
The Real Trouble with Phenomenal Externalism: New Empirical Evidence for a Brain-Based Theory of Consciousness
inferred← citeshttps://doi.org/10.1007/978-94-024-0965-9_1openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1007/978-94-024-0965-9_6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-024-0965-9_7openalex-snapshot
Objectifying Pain
inferred← citeshttps://doi.org/10.1007/s00112-013-2958-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00221-025-07176-8openalex-snapshot
Perception of first and second pain during offset analgesia
inferred← citeshttps://doi.org/10.1007/s00406-010-0113-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00429-016-1290-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00482-005-0405-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00482-010-0920-4openalex-snapshot
Schmerzempfindung bei Jugendlichen mit chronischen funktionellen Schmerzen
inferred← citeshttps://doi.org/10.1007/s00702-009-0348-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00729-008-0222-9openalex-snapshot
Somatoforme Schmerzen: hirnphysiologische Aspekte
inferred← citeshttps://doi.org/10.1007/s00737-018-0838-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10194-006-0309-zopenalex-snapshot
Outcome of transcutaneous electrical nerve stimulation in chronic pain: short-term results of a double-blind, randomised, placebo-controlled trial
inferred← citeshttps://doi.org/10.1007/s10548-013-0291-0openalex-snapshot
Individual Differences in Pain Sensitivity Vary as a Function of Precuneus Reactivity
inferred← citeshttps://doi.org/10.1007/s10549-008-0240-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10571-011-9737-7openalex-snapshot
The Striatum and Pain Modulation
inferred← citeshttps://doi.org/10.1007/s10877-018-0174-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10880-017-9515-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11064-008-9818-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11098-022-01907-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11229-017-1425-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11604-006-0035-0openalex-snapshot
Cerebral glucose metabolism change in patients with complex regional pain syndrome: a PET study
inferred← citeshttps://doi.org/10.1007/s11724-012-0319-3openalex-snapshot
Comment l’expérience de douleur est-elle « construite » par le cerveau ? Effets du contexte émotionnel sur la perception de douleur
inferred← citeshttps://doi.org/10.1007/s11916-020-00890-8openalex-snapshot
Neurophysiological Mechanisms Supporting Mindfulness Meditation–Based Pain Relief: an Updated Review
inferred← citeshttps://doi.org/10.1007/s11916-020-0844-3openalex-snapshot
Patient and Surgery-Related Predictors of Acute Postoperative Pain
inferred← citeshttps://doi.org/10.1007/s11920-008-0050-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11926-005-0018-7openalex-snapshot
Individual differences in pain responses
inferred← citeshttps://doi.org/10.1007/s12671-020-01323-8openalex-snapshot
Efficacy of Transcranial Direct Current Stimulation-Enhanced Mindfulness-Based Program for Chronic Pain: a Single-Blind Randomized Sham Controlled Pilot Study
inferred← citeshttps://doi.org/10.1007/s13164-013-0171-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b0-443-07287-6/50080-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-801851-4.00002-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-812202-0.00012-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-04743-2.50080-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-05541-3.00020-xopenalex-snapshot
The Pain of Childbirth and Its Effect on the Mother and the Fetus
inferred← citeshttps://doi.org/10.1016/b978-0-323-06489-7.00026-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-7020-3005-5.00012-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-7020-7489-9.00009-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-7216-0334-6.50022-4openalex-snapshot
The Measurement of Pain: Objectifying the Subjective
inferred← citeshttps://doi.org/10.1016/b978-008045046-9.01932-xopenalex-snapshot
Pain: Neuroimaging
inferred← citeshttps://doi.org/10.1016/b978-012370880-9.00209-7openalex-snapshot
Assessing Pain in Animals
inferred← citeshttps://doi.org/10.1016/b978-012419239-3/50045-xopenalex-snapshot
Imaging
inferred← citeshttps://doi.org/10.1016/b978-032304184-3.50046-7openalex-snapshot
Pain and Addictive Disorders: Challenge and Opportunity
inferred← citeshttps://doi.org/10.1016/b978-1-4160-6726-9.00104-8openalex-snapshot
Psychologic Strategies for Chronic Pain
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0721-2.00022-2openalex-snapshot
The Measurement of Pain
inferred← citeshttps://doi.org/10.1016/b978-3-437-21833-0.16001-2openalex-snapshot
Gesamtliteraturverzeichnis
inferred← citeshttps://doi.org/10.1016/b978-84-458-2037-7.00006-3openalex-snapshot
Un sustrato biológico para los trastornos somatomorfos
inferred← citeshttps://doi.org/10.1016/b978-84-8174-949-6.50075-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.irn.2020.09.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.irn.2024.10.008openalex-snapshot
Neuroanatomy of the nociceptive system: From nociceptors to brain networks
inferred← citeshttps://doi.org/10.1016/j.ajo.2023.12.004openalex-snapshot
FL-41 Tint Reduces Activation of Neural Pathways of Photophobia in Patients with Chronic Ocular Pain
inferred← citeshttps://doi.org/10.1016/j.bbr.2023.114552openalex-snapshot
The role of the male rat infralimbic cortex in distraction analgesia
inferred← citeshttps://doi.org/10.1016/j.biopsycho.2021.108192openalex-snapshot
Dysfunction of the anterior and intermediate hippocampal functional network in major depressive disorders across the adult lifespan
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2008.12.014openalex-snapshot
Forebrain pain mechanisms
inferred← citeshttps://doi.org/10.1016/j.cacc.2006.03.004openalex-snapshot
British Neuroscience Association (BNA) and British Pain Society joint 1-day symposium
inferred← citeshttps://doi.org/10.1016/j.clinph.2016.01.008openalex-snapshot
Higher pain rating results in lower variability of somatosensory cortex activation by painful mechanical stimuli: An fMRI study
inferred← citeshttps://doi.org/10.1016/j.cognition.2019.01.018openalex-snapshot
Metacognition across sensory modalities: Vision, warmth, and nociceptive pain
inferred← citeshttps://doi.org/10.1016/j.conb.2005.06.010openalex-snapshot
Nociceptive processing in the human brain
inferred← citeshttps://doi.org/10.1016/j.concog.2007.12.001openalex-snapshot
Pain, dissociation and subliminal self-representations
inferred← citeshttps://doi.org/10.1016/j.cophys.2020.12.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.copsyc.2018.12.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cortex.2025.03.009openalex-snapshot
Exploring insight into unfamiliar face recognition ability: The case from developmental prosopagnosia
inferred← citeshttps://doi.org/10.1016/j.douler.2011.01.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.drugalcdep.2008.01.012openalex-snapshot
Abnormal heat and pain perception in remitted heroin dependence months after detoxification from methadone-maintenance
inferred← citeshttps://doi.org/10.1016/j.ejpain.2004.12.006openalex-snapshot
Intracerebral pain processing in a Yoga Master who claims not to feel pain during meditation
inferred← citeshttps://doi.org/10.1016/j.ejpain.2006.09.008openalex-snapshot
Self‐reported pain sensitivity: Lack of correlation with pain threshold and tolerance
inferred← citeshttps://doi.org/10.1016/j.ejpain.2007.03.386openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejpain.2008.01.009openalex-snapshot
Is the interleukin‐6 haplotype a prognostic factor for sciatica?
inferred← citeshttps://doi.org/10.1016/j.ejpain.2008.06.010openalex-snapshot
Fibromyalgia pain and its modulation by hypnotic and non‐hypnotic suggestion: An fMRI analysis
inferred← citeshttps://doi.org/10.1016/j.ejphar.2004.03.041openalex-snapshot
Comparison of the antinociceptive effect of morphine, methadone, buprenorphine and codeine in two substrains of Sprague–Dawley rats
inferred← citeshttps://doi.org/10.1016/j.ejphar.2004.07.024openalex-snapshot
Striatal dopamine D2 receptors in modulation of pain in humans: a review
inferred← citeshttps://doi.org/10.1016/j.expneurol.2007.03.010openalex-snapshot
Striatal dopamine D2 receptors attenuate neuropathic hypersensitivity in the rat
inferred← citeshttps://doi.org/10.1016/j.ijotn.2017.10.003openalex-snapshot
The efficacy of high volume of local infiltration analgesia for postoperative pain relief after total hip arthroplasty under general anaesthesia - A randomised controlled trial
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2005.01.003openalex-snapshot
Sex differentiated responses to intranasal trigeminal stimuli
inferred← citeshttps://doi.org/10.1016/j.injury.2010.07.245openalex-snapshot
Psychological factors contributing to perceptions pain intensity after acute orthopaedic injury
inferred← citeshttps://doi.org/10.1016/j.janxdis.2010.09.015openalex-snapshot
Dental anxiety in relation to neuroticism and pain sensitivity. A twin study
inferred← citeshttps://doi.org/10.1016/j.jmpt.2005.04.001openalex-snapshot
The Use of Survival Analysis for the Evaluation of Musculoskeletal Therapy
inferred← citeshttps://doi.org/10.1016/j.jmpt.2005.12.010openalex-snapshot
The Efficiency of Multiple Impulse Therapy for Musculoskeletal Complaints
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2017.11.020openalex-snapshot
Prospective evaluation of chronic pain disorders and treatments
inferred← citeshttps://doi.org/10.1016/j.joca.2010.03.002openalex-snapshot
Psychological management of osteoarthritic pain
inferred← citeshttps://doi.org/10.1016/j.jpain.2004.02.226openalex-snapshot
Catastrophizing predicts changes in thermal pain responses after resolution of acute dental pain
inferred← citeshttps://doi.org/10.1016/j.jpain.2004.11.008openalex-snapshot
The A118G single nucleotide polymorphism of the μ-opioid receptor gene (OPRM1) is associated with pressure pain sensitivity in humans
inferred← citeshttps://doi.org/10.1016/j.jpain.2006.05.009openalex-snapshot
Sex and Pain-Related Psychological Variables Are Associated With Thermal Pain Sensitivity for Patients With Chronic Low Back Pain
inferred← citeshttps://doi.org/10.1016/j.jpain.2007.07.001openalex-snapshot
Maternal Separation Leads to Persistent Reductions in Pain Sensitivity in Female Rats
inferred← citeshttps://doi.org/10.1016/j.jpain.2007.08.008openalex-snapshot
The Effect of Subcutaneous Naloxone on Experimentally Induced Pain
inferred← citeshttps://doi.org/10.1016/j.jpain.2008.02.008openalex-snapshot
Neuroimaging of Pain: Advances and Future Prospects
inferred← citeshttps://doi.org/10.1016/j.jpain.2008.09.010openalex-snapshot
Individual Differences in Pain Sensitivity: Measurement, Causation, and Consequences
inferred← citeshttps://doi.org/10.1016/j.jpain.2009.04.001openalex-snapshot
Genetic Contributions to Clinical Pain and Analgesia: Avoiding Pitfalls in Genetic Research
inferred← citeshttps://doi.org/10.1016/j.jpain.2009.06.002openalex-snapshot
Translational Pain Research: Achievements and Challenges
inferred← citeshttps://doi.org/10.1016/j.jpain.2009.07.015openalex-snapshot
The Effects of Brief Mindfulness Meditation Training on Experimentally Induced Pain
inferred← citeshttps://doi.org/10.1016/j.jpain.2009.10.016openalex-snapshot
Comparison of the Cold Pressor Test and Contact Thermode-Delivered Cold Stimuli for the Assessment of Cold Pain Sensitivity
inferred← citeshttps://doi.org/10.1016/j.jpain.2010.03.014openalex-snapshot
Psychological and Sensory Predictors of Experimental Thermal Pain: A Multifactorial Model
inferred← citeshttps://doi.org/10.1016/j.jpain.2010.07.006openalex-snapshot
Combination Drug Therapy for Chronic Pain: A Call for More Clinical Studies
inferred← citeshttps://doi.org/10.1016/j.jpain.2012.05.007openalex-snapshot
Pain Measurement and Brain Activity: Will Neuroimages Replace Pain Ratings?
inferred← citeshttps://doi.org/10.1016/j.jpain.2014.06.011openalex-snapshot
Test-Retest Reliability of Pain-Related Brain Activity in Healthy Controls Undergoing Experimental Thermal Pain
inferred← citeshttps://doi.org/10.1016/j.jpain.2014.10.001openalex-snapshot
Spatial Summation of Pain in Humans Investigated Using Transcutaneous Electrical Stimulation
inferred← citeshttps://doi.org/10.1016/j.jpain.2018.03.002openalex-snapshot
Pain Adaptability in Individuals With Chronic Musculoskeletal Pain Is Not Associated With Conditioned Pain Modulation
inferred← citeshttps://doi.org/10.1016/j.jpain.2021.06.004openalex-snapshot
Slowing in Peak-Alpha Frequency Recorded After Experimentally-Induced Muscle Pain is not Significantly Different Between High and Low Pain-Sensitive Subjects
inferred← citeshttps://doi.org/10.1016/j.jpain.2022.07.007openalex-snapshot
To Calibrate or not to Calibrate? A Methodological Dilemma in Experimental Pain Research
inferred← citeshttps://doi.org/10.1016/j.jpain.2026.106231openalex-snapshot
Association of pain sensitization with prefrontal cortex activation and movement patterns during single- and dual-task walking in people with knee osteoarthritis
inferred← citeshttps://doi.org/10.1016/j.jpsychores.2010.02.001openalex-snapshot
Psychobiological differences between depression and somatization
inferred← citeshttps://doi.org/10.1016/j.jsams.2021.08.012openalex-snapshot
How sleep can help maximize human potential: The role of leaders
inferred← citeshttps://doi.org/10.1016/j.medcle.2014.08.002openalex-snapshot
Pain assessment using the Facial Action Coding System. A systematic review
inferred← citeshttps://doi.org/10.1016/j.medcli.2014.08.010openalex-snapshot
Evaluación del dolor mediante el Sistema de Codificación de la Acción Facial. Revisión sistemática
inferred← citeshttps://doi.org/10.1016/j.ncl.2007.01.009openalex-snapshot
Chronic Pain Management in Spine Disorders
inferred← citeshttps://doi.org/10.1016/j.nec.2004.03.001openalex-snapshot
Functional imaging and the neural systems of chronic pain
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2010.05.002openalex-snapshot
Individual differences in prefrontal cortex function and the transition from drug use to drug dependence
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2013.01.002openalex-snapshot
Localization of function in anterior cingulate cortex: From psychosurgery to functional neuroimaging
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2013.08.006openalex-snapshot
The downward spiral of chronic pain, prescription opioid misuse, and addiction: Cognitive, affective, and neuropsychopharmacologic pathways
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2018.11.006openalex-snapshot
Neurobiological mechanisms underlying the sleep-pain relationship in adolescence: A review
inferred← citeshttps://doi.org/10.1016/j.neucom.2017.07.045openalex-snapshot
A novel and effective fMRI decoding approach based on sliced inverse regression and its application to pain prediction
inferred← citeshttps://doi.org/10.1016/j.neulet.2012.02.076openalex-snapshot
Real-time fMRI applied to pain management
inferred← citeshttps://doi.org/10.1016/j.neulet.2012.03.082openalex-snapshot
Mindfulness meditation-related pain relief: Evidence for unique brain mechanisms in the regulation of pain
inferred← citeshttps://doi.org/10.1016/j.neulet.2012.04.043openalex-snapshot
Neuroimaging as a tool to investigate how cognitive factors influence analgesic drug outcomes
inferred← citeshttps://doi.org/10.1016/j.neulet.2014.11.032openalex-snapshot
Regional differences of repeatability on visual analogue scale with experimental mechanical pain stimuli
inferred← citeshttps://doi.org/10.1016/j.neuro.2021.02.004openalex-snapshot
Neurobehavioral and neurochemical effects in rats offspring co-exposed to arsenic and fluoride during development
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2004.01.021openalex-snapshot
Improvement of fMRI data processing of olfactory responses with a perception-based template
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2004.04.033openalex-snapshot
Cerebral activation during hypnotically induced and imagined pain
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2005.03.041openalex-snapshot
Somatotopic organisation of the human insula to painful heat studied with high resolution functional imaging
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2007.02.001openalex-snapshot
Capsaicin-induced thermal hyperalgesia and sensitization in the human trigeminal nociceptive pathway: An fMRI study
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2008.05.030openalex-snapshot
Volunteer studies in pain research — Opportunities and challenges to replace animal experiments
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2008.08.001openalex-snapshot
The pain of a model in the personality of an onlooker: Influence of state-reactivity and personality traits on embodied empathy for pain
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2010.05.037openalex-snapshot
Brain responses to facial expressions of pain: Emotional or motor mirroring?
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2011.08.083openalex-snapshot
Turning on the alarm: The neural mechanisms of the transition from innocuous to painful sensation
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.04.049openalex-snapshot
Real-time imaging of cortical areas involved in the generation of increases in skin sympathetic nerve activity when viewing emotionally charged images
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.09.038openalex-snapshot
The ‘where’ and the ‘when’ of the BOLD response to pain in the insular cortex. Discussion on amplitudes and latencies
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.02.028openalex-snapshot
Intrinsic variability in the human response to pain is assembled from multiple, dynamic brain processes
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.01.001openalex-snapshot
Ranking brain areas encoding the perceived level of pain from fMRI data
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2015.06.059openalex-snapshot
Psychosocial versus physiological stress — Meta-analyses on deactivations and activations of the neural correlates of stress reactions
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.04.064openalex-snapshot
Serotonin transporter polymorphism alters citalopram effects on human pain responses to physical pain
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2019.01.039openalex-snapshot
Brain regions preferentially responding to transient and iso-intense painful or tactile stimuli
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2019.116049openalex-snapshot
Identifying inter-individual differences in pain threshold using brain connectome: a test-retest reproducible study
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.116885openalex-snapshot
Keeping an eye on pain expression in primary somatosensory cortex
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.117506openalex-snapshot
Designing individual-specific and trial-specific models to accurately predict the intensity of nociceptive pain from single-trial fMRI responses
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.117548openalex-snapshot
Parallel cortical-brainstem pathways to attentional analgesia
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2022.119436openalex-snapshot
Brain-activation-based individual identification reveals individually unique activation patterns elicited by pain and touch
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2022.119710openalex-snapshot
Imitation encourages empathic capacity toward other individuals with physical disabilities
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2023.120432openalex-snapshot
Longitudinal changes in human supraspinal processing after RIII-feedback training to improve descending pain inhibition
inferred← citeshttps://doi.org/10.1016/j.neuron.2007.07.012openalex-snapshot
The Cerebral Signature for Pain Perception and Its Modulation
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