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Neural and Behavioral Correlates of Aberrant Salience in Individuals at Risk for Psychosis

https://doi.org/10.1093/schbul/sbs147
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archgenpsychiatry.2008.514openalex-snapshot
Elevated Striatal Dopamine Function Linked to Prodromal Signs of Schizophrenia
inferredcites →https://doi.org/10.1001/archgenpsychiatry.2010.169openalex-snapshot
Midbrain Activation During Pavlovian Conditioning and Delusional Symptoms in Schizophrenia
inferredcites →https://doi.org/10.1002/9781118660584.ese2519openalex-snapshot
Wechsler Abbreviated Scale of Intelligence
inferredcites →https://doi.org/10.1002/hbm.10123openalex-snapshot
Three‐dimensional maximum probability atlas of the human brain, with particular reference to the temporal lobe
inferredcites →https://doi.org/10.1002/hipo.1070openalex-snapshot
Probing the human hippocampus using rCBF: Contrasts in schizophrenia
inferredcites →https://doi.org/10.1007/s00213-006-0405-4openalex-snapshot
Dysfunction of ventral striatal reward prediction in schizophrenic patients treated with typical, not atypical, neuroleptics
inferredcites →https://doi.org/10.1007/s00213-009-1561-0openalex-snapshot
From drugs to deprivation: a Bayesian framework for understanding models of psychosis
inferredcites →https://doi.org/10.1016/j.biopsych.2008.12.016openalex-snapshot
Reward Feedback Alterations in Unmedicated Schizophrenia Patients: Relevance for Delusions
inferredcites →https://doi.org/10.1016/j.biopsych.2010.08.033openalex-snapshot
Altered Medial Temporal Activation Related to Local Glutamate Levels in Subjects with Prodromal Signs of Psychosis
inferredcites →https://doi.org/10.1016/j.neuroimage.2005.07.051openalex-snapshot
Dysfunction of ventral striatal reward prediction in schizophrenia
inferredcites →https://doi.org/10.1016/j.neuroimage.2007.06.038openalex-snapshot
Anticipation of novelty recruits reward system and hippocampus while promoting recollection
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.11.075openalex-snapshot
Adaptive and aberrant reward prediction signals in the human brain
inferredcites →https://doi.org/10.1016/s0074-7742(08)60571-1openalex-snapshot
Striatal Dopamine in Reward and Attention: A System For Understanding The Symptomatology of Acute Schizophrenia and Mania
inferredcites →https://doi.org/10.1016/s0140-6736(03)12323-9openalex-snapshot
Neuroanatomical abnormalities before and after onset of psychosis: a cross-sectional and longitudinal MRI comparison
inferredcites →https://doi.org/10.1016/s0165-0173(98)00019-8openalex-snapshot
What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience?
inferredcites →https://doi.org/10.1016/s0924-9338(99)80239-9openalex-snapshot
The mini international neuropsychiatric interview
inferredcites →https://doi.org/10.1016/s1053-8119(03)00169-1openalex-snapshot
An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets
inferredcites →https://doi.org/10.1017/s0033291708003863openalex-snapshot
Do patients with schizophrenia exhibit aberrant salience?
inferredcites →https://doi.org/10.1017/s1461145711000113openalex-snapshot
Divergent activation of ventromedial and ventrolateral dopamine systems in animal models of amphetamine sensitization and schizophrenia
inferredcites →https://doi.org/10.1037/t15170-000openalex-snapshot
Wechsler Abbreviated Scale of Intelligence
inferredcites →https://doi.org/10.1038/mp.2011.20openalex-snapshot
Progressive increase in striatal dopamine synthesis capacity as patients develop psychosis: a PET study
inferredcites →https://doi.org/10.1038/mp.2012.109openalex-snapshot
Striatal dopamine release in schizophrenia comorbid with substance dependence
inferredcites →https://doi.org/10.1038/nature05051openalex-snapshot
Dopamine-dependent prediction errors underpin reward-seeking behaviour in humans
inferredcites →https://doi.org/10.1038/nn1103openalex-snapshot
Afferent modulation of dopamine neuron firing differentially regulates tonic and phasic dopamine transmission
inferredcites →https://doi.org/10.1038/npp.2008.214openalex-snapshot
Patients with Schizophrenia have a Reduced Neural Response to Both Unpredictable and Predictable Primary Reinforcers
inferredcites →https://doi.org/10.1038/npp.2009.94openalex-snapshot
Modulation of Limbic Circuitry Predicts Treatment Response to Antipsychotic Medication: A Functional Imaging Study in Schizophrenia
inferredcites →https://doi.org/10.1038/sj.mp.4002058openalex-snapshot
Substantia nigra/ventral tegmental reward prediction error disruption in psychosis
inferredcites →https://doi.org/10.1038/sj.mp.4002157openalex-snapshot
How dopamine dysregulation leads to psychotic symptoms? Abnormal mesolimbic and mesostriatal prediction error signalling in psychosis
inferredcites →https://doi.org/10.1038/sj.npp.1300963openalex-snapshot
The Hippocampus Modulates Dopamine Neuron Responsivity by Regulating the Intensity of Phasic Neuron Activation
inferredcites →https://doi.org/10.1038/sj.npp.1301437openalex-snapshot
The Formation of Abnormal Associations in Schizophrenia: Neural and Behavioral Evidence
inferredcites →https://doi.org/10.1054/mehy.1997.0656openalex-snapshot
Delusions, superstitious conditioning and chaotic dopamine neurodynamics
inferredcites →https://doi.org/10.1080/j.1440-1614.2005.01714.xopenalex-snapshot
Mapping the Onset of Psychosis: The Comprehensive Assessment of At-Risk Mental States
inferredcites →https://doi.org/10.1093/brain/awm173openalex-snapshot
Disrupted prediction-error signal in psychosis: evidence for an associative account of delusions
inferredcites →https://doi.org/10.1093/schbul/13.2.261openalex-snapshot
The Positive and Negative Syndrome Scale (PANSS) for Schizophrenia
inferredcites →https://doi.org/10.1097/00001648-199001000-00010openalex-snapshot
No Adjustments Are Needed for Multiple Comparisons
inferredcites →https://doi.org/10.1176/appi.ajp.160.1.13openalex-snapshot
Psychosis as a State of Aberrant Salience: A Framework Linking Biology, Phenomenology, and Pharmacology in Schizophrenia
inferredcites →https://doi.org/10.1176/appi.ajp.2011.11010160openalex-snapshot
Dopamine Synthesis Capacity Before Onset of Psychosis: A Prospective [ 18 F]-DOPA PET Imaging Study
inferredcites →https://doi.org/10.1186/1471-244x-8-34openalex-snapshot
Incentive motivation in first-episode psychosis: A behavioural study
inferredcites →https://doi.org/10.1523/jneurosci.2058-08.2008openalex-snapshot
Mesolimbic Functional Magnetic Resonance Imaging Activations during Reward Anticipation Correlate with Reward-Related Ventral Striatal Dopamine Release
inferredcites →https://doi.org/10.1523/jneurosci.21-13-04915.2001openalex-snapshot
Glutamatergic Afferents from the Hippocampus to the Nucleus Accumbens Regulate Activity of Ventral Tegmental Area Dopamine Neurons
inferredcites →https://doi.org/10.1523/jneurosci.2847-07.2007openalex-snapshot
Aberrant Hippocampal Activity Underlies the Dopamine Dysregulation in an Animal Model of Schizophrenia
inferredcites →https://doi.org/10.2174/138161209788957528openalex-snapshot
Mechanisms Underlying Psychosis and Antipsychotic Treatment Response in Schizophrenia: Insights from PET and SPECT Imaging

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.4046579openalex-extracted
What is Measured as Aberrant Salience?
inferred← citeshttps://doi.org/10.1001/jamapsychiatry.2015.2196openalex-snapshot
Ventral Striatal Activation During Reward Processing in Psychosis
inferred← citeshttps://doi.org/10.1001/jamapsychiatry.2018.1973openalex-snapshot
Examination of the Neural Basis of Psychoticlike Experiences in Adolescence During Reward Processing
inferred← citeshttps://doi.org/10.1001/jamapsychiatry.2020.0103openalex-snapshot
Assessment of the Role of IQ in Associations Between Population Density and Deprivation and Nonaffective Psychosis
inferred← citeshttps://doi.org/10.1002/hbm.23879openalex-snapshot
Functional dysconnectivity of the limbic loop of frontostriatal circuits in first‐episode, treatment‐naive schizophrenia
inferred← citeshttps://doi.org/10.1002/hbm.25613openalex-snapshot
Task‐related neural mechanisms of persecutory ideation in schizophrenia and community monozygotic twin‐pairs
inferred← citeshttps://doi.org/10.1002/hbm.25795openalex-snapshot
An integrated cluster‐wise significance measure for fMRI analysis
inferred← citeshttps://doi.org/10.1002/hbm.26649openalex-snapshot
Thalamic contributions to psychosis susceptibility: Evidence from co‐activation patterns accounting for intra‐seed spatial variability ( μCAPs )
inferred← citeshttps://doi.org/10.1002/mpr.1615openalex-snapshot
The relationships among aberrant salience, reward motivation, and reward sensitivity
inferred← citeshttps://doi.org/10.1002/wcs.1420openalex-snapshot
Models of neuromodulation for computational psychiatry
inferred← citeshttps://doi.org/10.1007/978-3-319-11005-9_19openalex-snapshot
Psychosis (Schizophrenia Spectrum and Other Psychotic Disorders)
inferred← citeshttps://doi.org/10.1007/978-3-319-97307-4_2openalex-snapshot
Neuroimaging and Psychopathological Domains
inferred← citeshttps://doi.org/10.1007/978-3-319-97307-4_6openalex-snapshot
Neuroimaging and the At-Risk Mental State
inferred← citeshttps://doi.org/10.1007/978-3-642-54542-9_13openalex-snapshot
Neuroimaging in Schizophrenia
inferred← citeshttps://doi.org/10.1007/s00213-017-4710-xopenalex-snapshot
Clozapine, chlorpromazine and risperidone dose-dependently reduce emotional hyperthermia, a biological marker of salience
inferred← citeshttps://doi.org/10.1007/s00406-023-01564-3openalex-snapshot
High levels of childhood trauma associated with changes in hippocampal functional activity and connectivity in young adults during novelty salience
inferred← citeshttps://doi.org/10.1007/s00406-025-02095-9openalex-snapshot
Psychotic-like experiences in adolescents enriched for high-risk for developing severe mental illness: change over two-years and associations with neural reward processing and affective symptoms
inferred← citeshttps://doi.org/10.1007/s10548-014-0418-yopenalex-snapshot
Increased Gamma Oscillations Evoked by Physically Salient Distracters are Associated with Schizotypy
inferred← citeshttps://doi.org/10.1007/s40263-014-0177-zopenalex-snapshot
Presynaptic Dopaminergic Function: Implications for Understanding Treatment Response in Psychosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-800105-9.00023-8openalex-snapshot
The Anatomy of Delusion
inferred← citeshttps://doi.org/10.1016/b978-0-12-801829-3.00024-0openalex-snapshot
Brain Computations in Schizophrenia
inferred← citeshttps://doi.org/10.1016/b978-0-12-818697-8.00089-3openalex-snapshot
Psychotic Disorders and Risk-States in Adolescence: Etiology, Developmental Considerations, and Treatment
inferred← citeshttps://doi.org/10.1016/b978-0-443-29867-7.00035-9openalex-snapshot
Dopamine dysfunction in psychosis
inferred← citeshttps://doi.org/10.1016/b978-0-443-29867-7.00041-4openalex-snapshot
Apathy and impulsivity in neurological and psychiatric disorders
inferred← citeshttps://doi.org/10.1016/j.bandc.2020.105657openalex-snapshot
Acute stress impairs reward learning in men
inferred← citeshttps://doi.org/10.1016/j.biopsych.2016.05.021openalex-snapshot
An Integrative Perspective on the Role of Dopamine in Schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2020.03.012openalex-snapshot
Aberrant Salience, Information Processing, and Dopaminergic Signaling in People at Clinical High Risk for Psychosis
inferred← citeshttps://doi.org/10.1016/j.biopsych.2022.09.029openalex-snapshot
Integrative Brain Network and Salience Models of Psychopathology and Cognitive Dysfunction in Schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2026.08.019openalex-snapshot
Dexamphetamine-induced striatal hyperdopaminergia attenuates reward-related neural activation: A11C-PHNO PET-fMRI study
inferred← citeshttps://doi.org/10.1016/j.bpsc.2016.08.001openalex-snapshot
Computational Psychiatry: From Mechanistic Insights to the Development of New Treatments
inferred← citeshttps://doi.org/10.1016/j.bpsgos.2021.12.003openalex-snapshot
Neural Circuitry of Salience and Reward Processing in Psychosis
inferred← citeshttps://doi.org/10.1016/j.bpsgos.2022.01.002openalex-snapshot
Reward Processing as an Indicator of Vulnerability or Compensatory Resilience in Psychoses? Results From a Twin Study
inferred← citeshttps://doi.org/10.1016/j.brs.2018.12.973openalex-snapshot
Delusions following deep brain stimulation of the nucleus accumbens
inferred← citeshttps://doi.org/10.1016/j.cogsys.2025.101423openalex-snapshot
Epigenetic Influences in Aberrant Salience and Reality Testing in Schizoaffective Disorder: A Multi-Level Adaptive Network Modelling Approach
inferred← citeshttps://doi.org/10.1016/j.comppsych.2022.152343openalex-snapshot
Validation of the aberrant salience inventory in a general and clinical Spanish population
inferred← citeshttps://doi.org/10.1016/j.conb.2014.11.003openalex-snapshot
The prodromal phase of psychosis
inferred← citeshttps://doi.org/10.1016/j.concog.2019.102845openalex-snapshot
The neurophenomenology of early psychosis: An integrative empirical study
inferred← citeshttps://doi.org/10.1016/j.cortex.2015.06.003openalex-snapshot
Triangles, tricks and tics: Hyper-mentalizing in response to animated shapes in Tourette syndrome
inferred← citeshttps://doi.org/10.1016/j.cpr.2016.08.003openalex-snapshot
Trauma and the psychosis spectrum: A review of symptom specificity and explanatory mechanisms
inferred← citeshttps://doi.org/10.1016/j.cpr.2017.04.006openalex-snapshot
Dopamine, cognitive biases and assessment of certainty: A neurocognitive model of delusions
inferred← citeshttps://doi.org/10.1016/j.euroneuro.2021.03.014openalex-snapshot
Reinforcement learning abnormalities in the attenuated psychosis syndrome and first episode psychosis
inferred← citeshttps://doi.org/10.1016/j.eurpsy.2013.01.001openalex-snapshot
Prediction of psychosis in clinical high-risk patients by the Schizotypal Personality Questionnaire. Results of the EPOS project
inferred← citeshttps://doi.org/10.1016/j.eurpsy.2019.04.009openalex-snapshot
Longitudinal studies of functional magnetic resonance imaging in first-episode psychosis: A systematic review
inferred← citeshttps://doi.org/10.1016/j.ijchp.2023.100405openalex-snapshot
The claustrum and consciousness: An update
inferred← citeshttps://doi.org/10.1016/j.jad.2026.121416openalex-snapshot
Aberrant salience associated with menstrual cycle, mood, and sleep alterations - A cross-sectional study in female medical students during the COVID-19 pandemic
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2015.09.005openalex-snapshot
Hyperresponsivity and impaired prefrontal control of the mesolimbic reward system in schizophrenia
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2021.01.044openalex-snapshot
“First-episode psychosis: Structural covariance deficits in salience network correlate with symptoms severity”
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2021.02.025openalex-snapshot
The prevalence and features of schizophrenia among individuals with gambling disorder
inferred← citeshttps://doi.org/10.1016/j.nbd.2019.03.002openalex-snapshot
Toward integrated understanding of salience in psychosis
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2015.09.006openalex-snapshot
Cognition in at-risk mental states for psychosis
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2017.08.022openalex-snapshot
Comprehensive review: Computational modelling of schizophrenia
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2021.06.020openalex-snapshot
Functional brain network dysfunctions in subjects at high-risk for psychosis: A meta-analysis of resting-state functional connectivity
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2026.106579openalex-snapshot
Intrinsic brain activity and multiscale mechanisms of auditory verbal hallucinations in schizophrenia: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2026.106694openalex-snapshot
Echoes of trauma: The impact of hippocampal impairments on reward and motivational dysfunction in psychosis
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2015.10.067openalex-snapshot
Neural signals encoding shifts in beliefs
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2018.09.001openalex-snapshot
Alteration of functional brain architecture in 22q11.2 deletion syndrome – Insights into susceptibility for psychosis
inferred← citeshttps://doi.org/10.1016/j.neuron.2015.07.008openalex-snapshot
Translational Perspectives for Computational Neuroimaging
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2017.06.018openalex-snapshot
Cannabis-associated psychosis: Neural substrate and clinical impact
inferred← citeshttps://doi.org/10.1016/j.neuropsychologia.2024.109006openalex-snapshot
Neuroanatomical correlates and predictors of psychotic symptoms in Alzheimer's disease: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.neuropsychologia.2025.109348openalex-snapshot
Posterior parietal cortex modulates perceptual decisions depending on psychotic phenotype
inferred← citeshttps://doi.org/10.1016/j.nicl.2016.09.006openalex-snapshot
Corticolimbic dysfunction during facial and prosodic emotional recognition in first-episode psychosis patients and individuals at ultra-high risk
inferred← citeshttps://doi.org/10.1016/j.nicl.2018.11.013openalex-snapshot
Multi-echo fMRI, resting-state connectivity, and high psychometric schizotypy
inferred← citeshttps://doi.org/10.1016/j.nicl.2020.102239openalex-snapshot
Atypical processing of uncertainty in individuals at risk for psychosis
inferred← citeshttps://doi.org/10.1016/j.nicl.2020.102277openalex-snapshot
Altered subcortical emotional salience processing differentiates Parkinson’s patients with and without psychotic symptoms
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2020.109926openalex-snapshot
From apathy to addiction: Insights from neurology and psychiatry
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2020.110128openalex-snapshot
Mesolimbic dopamine dysregulation as a signature of information processing deficits imposed by prenatal THC exposure
inferred← citeshttps://doi.org/10.1016/j.pscychresns.2015.06.008openalex-snapshot
Aberrant functioning of the putamen links delusions, antipsychotic drug dose, and compromised connectivity in first episode psychosis—Preliminary fMRI findings
inferred← citeshttps://doi.org/10.1016/j.pscychresns.2017.11.014openalex-snapshot
Dopamine in high-risk populations: A comparison of subjects with 22q11.2 deletion syndrome and subjects at ultra high-risk for psychosis
inferred← citeshttps://doi.org/10.1016/j.pscychresns.2020.111089openalex-snapshot
Psychosis risk is associated with decreased white matter integrity in limbic network corticostriatal tracts
inferred← citeshttps://doi.org/10.1016/j.pscychresns.2020.111215openalex-snapshot
High schizotypy traits are associated with reduced hippocampal resting state functional connectivity
inferred← citeshttps://doi.org/10.1016/j.pscychresns.2024.111881openalex-snapshot
Hyperactivity and altered functional connectivity of the ventral striatum in schizophrenia compared with bipolar disorder: A resting state fMRI study
inferred← citeshttps://doi.org/10.1016/j.psychres.2013.07.032openalex-snapshot
The development of delusion revisited: A transdiagnostic framework
inferred← citeshttps://doi.org/10.1016/j.psychres.2016.02.001openalex-snapshot
Prevalence and implications of Truman symptoms in subjects at ultra high risk for psychosis
inferred← citeshttps://doi.org/10.1016/j.schres.2015.04.036openalex-snapshot
Modulation of motivational salience processing during the early stages of psychosis
inferred← citeshttps://doi.org/10.1016/j.schres.2015.10.029openalex-snapshot
Baseline putamen volume as a predictor of positive symptom reduction in patients at clinical high risk for psychosis: A preliminary study
inferred← citeshttps://doi.org/10.1016/j.schres.2016.05.003openalex-snapshot
Secondary negative symptoms — A review of mechanisms, assessment and treatment
inferred← citeshttps://doi.org/10.1016/j.schres.2017.01.020openalex-snapshot
Deep dreaming, aberrant salience and psychosis: Connecting the dots by artificial neural networks
inferred← citeshttps://doi.org/10.1016/j.schres.2018.06.018openalex-snapshot
Striatal cerebral blood flow, executive functioning, and fronto-striatal functional connectivity in clinical high risk for psychosis
inferred← citeshttps://doi.org/10.1016/j.schres.2018.12.011openalex-snapshot
Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity
inferred← citeshttps://doi.org/10.1016/j.schres.2019.03.017openalex-snapshot
Evidence of reward system dysfunction in youth at clinical high-risk for psychosis from two event-related fMRI paradigms
inferred← citeshttps://doi.org/10.1016/j.schres.2020.03.016openalex-snapshot
Aberrant salience predicts psychotic-like experiences in daily life: An experience sampling study
inferred← citeshttps://doi.org/10.1016/j.schres.2020.04.017openalex-snapshot
Modeling perception and behavior in individuals at clinical high risk for psychosis: Support for the predictive processing framework
inferred← citeshttps://doi.org/10.1016/j.schres.2020.11.061openalex-snapshot
Distinguishing schizophrenia spectrum from non-spectrum disorders among young patients with first episode psychosis and at high clinical risk: The role of basic self-disturbance and neurocognition
inferred← citeshttps://doi.org/10.1016/j.schres.2021.12.025openalex-snapshot
Examining subjective experience of aberrant salience in young individuals at ultra-high risk (UHR) of psychosis: A 1-year longitudinal study
inferred← citeshttps://doi.org/10.1016/j.scog.2016.04.002openalex-snapshot
Are persistent delusions in schizophrenia associated with aberrant salience?
inferred← citeshttps://doi.org/10.1016/j.scog.2016.10.001openalex-snapshot
Validating the construct of aberrant salience in schizophrenia — Behavioral evidence for an automatic process
inferred← citeshttps://doi.org/10.1016/j.scog.2021.100235openalex-snapshot
Latent inhibition, aberrant salience, and schizotypy traits in cannabis users
inferred← citeshttps://doi.org/10.1016/j.tics.2015.09.009openalex-snapshot
How Schizophrenia Develops: Cognitive and Brain Mechanisms Underlying Onset of Psychosis
inferred← citeshttps://doi.org/10.1016/j.tins.2013.11.003openalex-snapshot
Dopaminergic basis of salience dysregulation in psychosis
inferred← citeshttps://doi.org/10.1016/j.tins.2014.12.005openalex-snapshot
Translating the MAM model of psychosis to humans
inferred← citeshttps://doi.org/10.1017/s0033291713002705openalex-snapshot
Tobacco smoking in schizophrenia: investigating the role of incentive salience
inferred← citeshttps://doi.org/10.1017/s0033291716002051openalex-snapshot
Salience attribution and its relationship to cannabis-induced psychotic symptoms
inferred← citeshttps://doi.org/10.1017/s0033291716002439openalex-snapshot
Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis
inferred← citeshttps://doi.org/10.1017/s0033291718004099openalex-snapshot
The relation between dopamine D2 receptor blockade and the brain reward system: a longitudinal study of first-episode schizophrenia patients
inferred← citeshttps://doi.org/10.1017/s0033291720000264openalex-snapshot
Aberrant salience and reward processing: a comparison of measures in schizophrenia and anxiety
inferred← citeshttps://doi.org/10.1017/s0954579418000317openalex-snapshot
Prenatal inflammation and risk for schizophrenia: A role for immune proteins in neurodevelopment
inferred← citeshttps://doi.org/10.1017/s1092852917000219openalex-snapshot
The dark side of dopaminergic therapies in Parkinson’s disease: shedding light on aberrant salience
inferred← citeshttps://doi.org/10.1037/abn0000330openalex-snapshot
Resting state connectivity dynamics in individuals at risk for psychosis.
inferred← citeshttps://doi.org/10.1037/tra0000380openalex-snapshot
Attentional biases and trauma status: Do psychotic-like experiences matter?
inferred← citeshttps://doi.org/10.1038/mp.2014.91openalex-snapshot
What causes aberrant salience in schizophrenia? A role for impaired short-term habituation and the GRIA1 (GluA1) AMPA receptor subunit
inferred← citeshttps://doi.org/10.1038/npp.2014.99openalex-snapshot
Prefrontal Cortical GABA Transmission Modulates Discrimination and Latent Inhibition of Conditioned Fear: Relevance for Schizophrenia
inferred← citeshttps://doi.org/10.1038/npp.2015.7openalex-snapshot
Abnormal Resting State fMRI Activity Predicts Processing Speed Deficits in First-Episode Psychosis
inferred← citeshttps://doi.org/10.1038/nrdp.2015.67openalex-snapshot
Schizophrenia
inferred← citeshttps://doi.org/10.1038/s41380-020-00983-1openalex-snapshot
Altered temporal, but intact spatial, features of transient network dynamics in psychosis
inferred← citeshttps://doi.org/10.1038/s41380-020-0679-7openalex-snapshot
Structural and functional imaging markers for susceptibility to psychosis
inferred← citeshttps://doi.org/10.1038/s41380-024-02495-8openalex-snapshot
Robust and replicable functional brain signatures of 22q11.2 deletion syndrome and associated psychosis: a deep neural network-based multi-cohort study
inferred← citeshttps://doi.org/10.1038/s41380-024-02607-4openalex-snapshot
A working model of neural activity and phenomenal experience in psychosis
inferred← citeshttps://doi.org/10.1038/s41386-018-0056-2openalex-snapshot
Abnormal reward prediction-error signalling in antipsychotic naive individuals with first-episode psychosis or clinical risk for psychosis
inferred← citeshttps://doi.org/10.1038/s41386-021-01019-0openalex-snapshot
Interactions between hippocampal activity and striatal dopamine in people at clinical high risk for psychosis: relationship to adverse outcomes
inferred← citeshttps://doi.org/10.1038/s41386-023-01730-0openalex-snapshot
Modulation of hippocampal activity in schizophrenia with levetiracetam: a randomized, double-blind, cross-over, placebo-controlled trial
inferred← citeshttps://doi.org/10.1038/s41398-018-0250-3openalex-snapshot
Brain responses to different types of salience in antipsychotic naïve first episode psychosis: An fMRI study
inferred← citeshttps://doi.org/10.1038/s41398-018-0347-8openalex-snapshot
Activation of the motivation-related ventral striatum during delusional experience
inferred← citeshttps://doi.org/10.1038/s41398-019-0534-2openalex-snapshot
Cannabidiol attenuates insular dysfunction during motivational salience processing in subjects at clinical high risk for psychosis
inferred← citeshttps://doi.org/10.1038/s41398-020-0862-2openalex-snapshot
A single dose of cannabidiol modulates medial temporal and striatal function during fear processing in people at clinical high risk for psychosis
inferred← citeshttps://doi.org/10.1038/s41398-021-01705-zopenalex-snapshot
Adverse clinical outcomes in people at clinical high-risk for psychosis related to altered interactions between hippocampal activity and glutamatergic function
inferred← citeshttps://doi.org/10.1038/s41398-025-03773-xopenalex-snapshot
Refining mechanistic models of hallucinations for enhanced translatability
inferred← citeshttps://doi.org/10.1038/s41537-024-00513-wopenalex-snapshot
Acute optogenetic induction of the prodromal endophenotype of CA1 hyperactivity causes schizophrenia-related deficits in cognition and salience attribution
inferred← citeshttps://doi.org/10.1038/s41598-020-62026-7openalex-snapshot
Examination of the neural basis of psychotic-like experiences in adolescence during processing of emotional faces
inferred← citeshttps://doi.org/10.1038/tp.2017.174openalex-snapshot
Altered activation and connectivity in a hippocampal–basal ganglia–midbrain circuit during salience processing in subjects at ultra high risk for psychosis
inferred← citeshttps://doi.org/10.1055/a-2389-7566openalex-snapshot
Die Entdeckung der Bedeutung von Bedeutung
inferred← citeshttps://doi.org/10.1073/pnas.1809298115openalex-snapshot
Dopaminergic basis for signaling belief updates, but not surprise, and the link to paranoia
inferred← citeshttps://doi.org/10.1080/08039488.2021.1942547openalex-snapshot
Subjective experience of aberrant salience in young people at Ultra-High Risk (UHR) for psychosis: a cross-sectional study
inferred← citeshttps://doi.org/10.1080/13546805.2019.1706465openalex-snapshot
Implicit and explicit processing of bodily emotions in schizophrenia
inferred← citeshttps://doi.org/10.1080/15622975.2016.1258491openalex-snapshot
Attentional capture by physically salient stimuli in the gamma frequency is associated with schizophrenia symptoms
inferred← citeshttps://doi.org/10.1080/15622975.2021.2014955openalex-snapshot
Relationships between global functioning and neuropsychological predictors in subjects at high risk of psychosis or with a recent onset of depression
inferred← citeshttps://doi.org/10.1080/17522439.2026.2723050openalex-snapshot
Theory of mind and context processing in individuals diagnosed with paranoid schizophrenia: a mixed-methods matched-control study
inferred← citeshttps://doi.org/10.1093/brain/awt264openalex-snapshot
Midbrain dopamine function in schizophrenia and depression: a post-mortem and positron emission tomographic imaging study
inferred← citeshttps://doi.org/10.1093/ijnp/pyad009openalex-snapshot
A Meta-Analysis of Neural Correlates of Reward Anticipation in Individuals at Clinical Risk for Schizophrenia
inferred← citeshttps://doi.org/10.1093/ijnp/pyy011openalex-snapshot
Human Striatal Response to Reward Anticipation Linked to Hippocampal Glutamate Levels
inferred← citeshttps://doi.org/10.1093/med/9780198713005.003.0060openalex-snapshot
Structural and functional neuroimaging of schizophrenia
inferred← citeshttps://doi.org/10.1093/oso/9780198872221.003.0012openalex-snapshot
The Paradox of Delusions
inferred← citeshttps://doi.org/10.1093/schbul/sbab075openalex-snapshot
Relations Among Anhedonia, Reinforcement Learning, and Global Functioning in Help-seeking Youth
inferred← citeshttps://doi.org/10.1093/schbul/sbac163openalex-snapshot
Speech Illusions in People at Clinical High Risk for Psychosis Linked to Clinical Outcome
inferred← citeshttps://doi.org/10.1093/schbul/sbv098openalex-snapshot
Aberrant Salience Is Related to Dysfunctional Self-Referential Processing in Psychosis
inferred← citeshttps://doi.org/10.1093/schbul/sbv190openalex-snapshot
Stress Sensitivity, Aberrant Salience, and Threat Anticipation in Early Psychosis: An Experience Sampling Study
inferred← citeshttps://doi.org/10.1093/schbul/sbw142openalex-snapshot
Ventral Striatal Dysfunction and Symptom Expression in Individuals With Schizotypal Personality Traits and Early Psychosis
inferred← citeshttps://doi.org/10.1093/schbul/sbw190openalex-snapshot
Studying Delusions Within Research Domain Criteria: The Challenge of Configural Traits When Building a Mechanistic Foundation for Abnormal Beliefs
inferred← citeshttps://doi.org/10.1093/schbul/sby033openalex-snapshot
Probabilistic Category Learning and Striatal Functional Activation in Psychosis Risk
inferred← citeshttps://doi.org/10.1093/schbul/sby037openalex-snapshot
Structural and Functional Neuroimaging of Polygenic Risk for Schizophrenia: A Recall-by-Genotype–Based Approach
inferred← citeshttps://doi.org/10.1093/schbul/sbz089openalex-snapshot
Neural Circuitry of Novelty Salience Processing in Psychosis Risk: Association With Clinical Outcome
inferred← citeshttps://doi.org/10.1093/schizbullopen/sgac039openalex-snapshot
Linking Salience Signaling With Early Adversity and Affective Distress in Individuals at Clinical High Risk for Psychosis: Results From an Event-Related fMRI Study
inferred← citeshttps://doi.org/10.1093/schizbullopen/sgad023openalex-snapshot
Behavioral Response to Catecholamine Depletion in Individuals With Schizophrenia and Healthy Volunteers
inferred← citeshttps://doi.org/10.1098/rstb.2017.0156openalex-snapshot
Brain neuroreceptor density and personality traits: towards dimensional biomarkers for psychiatric disorders
inferred← citeshttps://doi.org/10.1101/2021.06.02.446736openalex-snapshot
Hippocampal disinhibition reduces contextual and elemental fear conditioning while sparing the acquisition of latent inhibition
inferred← citeshttps://doi.org/10.1101/2024.11.12.623233openalex-snapshot
Midbrain dopamine D2R regulates the salience of threat-related events
inferred← citeshttps://doi.org/10.1101/263020openalex-snapshot
Brain responses to different types of salience in antipsychotic naïve first episode psychosis: An fMRI study
inferred← citeshttps://doi.org/10.1101/771162openalex-snapshot
Phasic dopamine enhances the distinct decoding and perceived salience of stimuli
inferred← citeshttps://doi.org/10.1111/cns.12973openalex-snapshot
Organic psychosis: The pathobiology and treatment of delusions
inferred← citeshttps://doi.org/10.1111/eip.13022openalex-snapshot
Aberrant salience in adolescents is related to indicators of psychopathology that are relevant in the prodromal phases of psychosis
inferred← citeshttps://doi.org/10.1111/eip.13243openalex-snapshot
Aberrant salience in first‐episode psychosis: Longitudinal stability and treatment‐response
inferred← citeshttps://doi.org/10.1111/pcn.12966openalex-snapshot
Terminology and assessment tools of psychosis: A systematic narrative review
inferred← citeshttps://doi.org/10.1111/sjop.12806openalex-snapshot
Association between psychosocial interventions and aberrant salience in adolescents with early psychosis: A follow‐up study
inferred← citeshttps://doi.org/10.1124/pharmrev.121.000514openalex-snapshot
Self-Entropic Broadening Theory: Toward a New Understanding of Self and Behavior Change Informed by Psychedelics and Psychosis
inferred← citeshttps://doi.org/10.1136/jnnp-2015-310737openalex-snapshot
Computational Psychiatry: towards a mathematically informed understanding of mental illness
inferred← citeshttps://doi.org/10.1146/annurev-pharmtox-022423-014645openalex-snapshot
Apathy and Motivation: Biological Basis and Drug Treatment
inferred← citeshttps://doi.org/10.1159/000362565openalex-snapshot
Esse est percipi: A Neurophilosophical Model of Psychosis
inferred← citeshttps://doi.org/10.1159/000440916openalex-snapshot
Structural and Functional MRI in the Prediction of Psychosis
inferred← citeshttps://doi.org/10.1176/appi.psychotherapy.2016.70.1.5openalex-snapshot
Social Adversity in the Etiology of Psychosis: A Review of the Evidence
inferred← citeshttps://doi.org/10.1177/0020764019872227openalex-snapshot
The wounds of childhood: Early trauma subtypes, salience and hyperarousal in a sample of adult psychiatric patients
inferred← citeshttps://doi.org/10.1177/0269881114563634openalex-snapshot
Glutamate and dopamine in schizophrenia: An update for the 21 st century
inferred← citeshttps://doi.org/10.1186/s11689-016-9158-5openalex-snapshot
Neural correlates of reward processing in adults with 22q11 deletion syndrome
inferred← citeshttps://doi.org/10.1186/s12888-015-0515-9openalex-snapshot
Investigating neural mechanisms of change of cognitive behavioural therapy for chronic fatigue syndrome: a randomized controlled trial
inferred← citeshttps://doi.org/10.1186/s12888-024-06176-2openalex-snapshot
The association between aberrant salience and psychotic experiences in general population twins, and genetic vulnerability as a modifier
inferred← citeshttps://doi.org/10.1186/s12991-022-00402-5openalex-snapshot
Aberrant salience correlates with psychotic dimensions in outpatients with schizophrenia spectrum disorders
inferred← citeshttps://doi.org/10.1192/j.eurpsy.2020.31openalex-snapshot
The interplay between childhood trauma, cognitive biases, and cannabis use on the risk of psychosis in nonclinical young adults in Poland
inferred← citeshttps://doi.org/10.12804/revistas.urosario.edu.co/apl/a.7475openalex-snapshot
Organismo y acción situada: mapeando el concepto de affordance
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1006319openalex-snapshot
Modeling subjective relevance in schizophrenia and its relation to aberrant salience
inferred← citeshttps://doi.org/10.14712/23366486.2021.7openalex-snapshot
„Unáhlené závěry“ u psychotických onemocnění: přehledová studie
inferred← citeshttps://doi.org/10.1503/jpn.150234openalex-snapshot
Dysfunctional insular connectivity during reward prediction in patients with first-episode psychosis
inferred← citeshttps://doi.org/10.1523/eneuro.0270-21.2021openalex-snapshot
Hippocampal Disinhibition Reduces Contextual and Elemental Fear Conditioning While Sparing the Acquisition of Latent Inhibition
inferred← citeshttps://doi.org/10.1523/jneurosci.0805-15.2015openalex-snapshot
Aberrant Salience Is Related to Reduced Reinforcement Learning Signals and Elevated Dopamine Synthesis Capacity in Healthy Adults
inferred← citeshttps://doi.org/10.1590/1415-4714.e220421openalex-snapshot
La hipótesis de la saliencia aberrante: unificando la neurobiología y la fenomenología de la esquizofrenia
inferred← citeshttps://doi.org/10.20900/jpbs.20220012openalex-snapshot
Acute and Lifetime Stress and Psychotic Illness: The Roles of Reward and Salience Networks
inferred← citeshttps://doi.org/10.2217/npy.13.89openalex-snapshot
The traumagenic neurodevelopmental model of psychosis revisited
inferred← citeshttps://doi.org/10.22365/jpsych.2020.312openalex-snapshot
inferred← citeshttps://doi.org/10.22365/jpsych.2020.312.162openalex-snapshot
Neurobiology of emotional trauma
inferred← citeshttps://doi.org/10.3109/10253890.2014.989204openalex-snapshot
“More than skin deep”: stress neurobiology and mental health consequences of racial discrimination
inferred← citeshttps://doi.org/10.31234/osf.io/m3vjyopenalex-snapshot
Apathy and Motivation: Biological Basis and Drug Treatment
inferred← citeshttps://doi.org/10.3171/2015.4.jns15120openalex-snapshot
Neurosurgery for schizophrenia: an update on pathophysiology and a novel therapeutic target
inferred← citeshttps://doi.org/10.31887/dcns.2016.18.1/ldesernoopenalex-snapshot
Striatal dopamine, reward, and decision making in schizophrenia
inferred← citeshttps://doi.org/10.3389/fnbeh.2014.00071openalex-snapshot
Gene-sex interactions in schizophrenia: focus on dopamine neurotransmission
inferred← citeshttps://doi.org/10.3389/fnbeh.2014.00382openalex-snapshot
Symptom dimensions are associated with reward processing in unmedicated persons at risk for psychosis
inferred← citeshttps://doi.org/10.3389/fnbeh.2022.963739openalex-snapshot
Dopamine activity on the perceptual salience for recognition memory
inferred← citeshttps://doi.org/10.3389/fnhum.2015.00687openalex-snapshot
Striatal Activity is Associated with Deficits of Cognitive Control and Aberrant Salience for Patients with Schizophrenia
inferred← citeshttps://doi.org/10.3389/fnmol.2022.993671openalex-snapshot
Molecular and cellular mechanisms leading to catatonia: an integrative approach from clinical and preclinical evidence
inferred← citeshttps://doi.org/10.3389/fphar.2020.486811openalex-snapshot
Hippocampal Hyperactivity as a Druggable Circuit-Level Origin of Aberrant Salience in Schizophrenia
inferred← citeshttps://doi.org/10.3389/fphar.2025.1601797openalex-snapshot
Glutamatergic mechanisms in early salience processing
inferred← citeshttps://doi.org/10.3389/fpsyg.2019.02073openalex-snapshot
Aberrant Salience Across Levels of Processing in Positive and Negative Schizotypy
inferred← citeshttps://doi.org/10.3389/fpsyt.2013.00172openalex-snapshot
Reinforcement Learning and Dopamine in Schizophrenia: Dimensions of Symptoms or Specific Features of a Disease Group?
inferred← citeshttps://doi.org/10.3389/fpsyt.2016.00189openalex-snapshot
Altered Insular Function during Aberrant Salience Processing in Relation to the Severity of Psychotic Symptoms
inferred← citeshttps://doi.org/10.3389/fpsyt.2017.00055openalex-snapshot
The Role of Trauma and Stressful Life Events among Individuals at Clinical High Risk for Psychosis: A Review
inferred← citeshttps://doi.org/10.3389/fpsyt.2019.00298openalex-snapshot
Emerging Temporal Lobe Dysfunction in People at Clinical High Risk for Psychosis
inferred← citeshttps://doi.org/10.3389/fpsyt.2020.567534openalex-snapshot
Selective Review of Neuroimaging Findings in Youth at Clinical High Risk for Psychosis: On the Path to Biomarkers for Conversion
inferred← citeshttps://doi.org/10.3389/fpsyt.2024.1309868openalex-snapshot
Exploring the relationship between frequent cannabis use, belief updating under uncertainty and psychotic-like symptoms
inferred← citeshttps://doi.org/10.3389/fpsyt.2025.1647155openalex-snapshot
The cumulative social adversity hypothesis of psychosis: Intolerance of uncertainty and aberrant salience mediate the association between humiliation and psychotic-like experiences
inferred← citeshttps://doi.org/10.3390/brainsci12010011openalex-snapshot
Early Detection and Prevention of Schizophrenic Psychosis—A Review
inferred← citeshttps://doi.org/10.3390/jcm10184126openalex-snapshot
Neural Correlates of Aberrant Salience and Source Monitoring in Schizophrenia and At-Risk Mental States—A Systematic Review of fMRI Studies
inferred← citeshttps://doi.org/10.3390/jcm8081223openalex-snapshot
Comparing the Role of Aberrant Salience and Dissociation in the Relation between Cumulative Traumatic Life Events and Psychotic-Like Experiences in a Multi-Ethnic Sample
inferred← citeshttps://doi.org/10.4103/indianjpsychiatry.indianjpsychiatry_521_24openalex-snapshot
Aberrant salience in acute versus chronic schizophrenia: Do medication and positive symptoms make a difference?
inferred← citeshttps://doi.org/10.53846/goediss-6346openalex-snapshot
Functional neuroimaging of pathophysiological mesolimbic dopamine system and aberrant motivational salience in schizophrenia
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