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Cues

Psychiatry and Psychology · NLM MeSH · updated 2026-11-04 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 5 min read

Signals for an action; that specific portion of a perceptual field or pattern of stimuli to which a subject has learned to respond.

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (942 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

Signals for an action; that specific portion of a perceptual field or pattern of stimuli to which a subject has learned to respond.

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Cue.

Where it fits in the MeSH classification

Broader topics
Learning

Research landscape

PubMed indexes 47,191 records tagged with the MeSH heading “Cues” (counts retrieved 2026-10-31). 9,922 of them (21.0%) were published from 2020 onward, and the busiest period so far is 2010-2019 with 18,330 records.

Reviews account for 2,102 records (4.5%) and meta-analyses for 207. Randomized controlled trials number 2,011 (4.3%) as a share of all records on the topic.

PubMed records by publication periodthrough 1999: 7,663 records; 2000-2009: 11,276 records; 2010-2019: 18,330 records; 2020 onward: 9,922 records7,663through 199911,2762000-200918,3302010-20199,9222020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 19997,663
2000-200911,276
2010-201918,330
2020 onward9,922
Share of records by publication typeReviews: 4.5 percent; Meta-analyses: 0.4 percent; Randomized controlled trials: 4.3 percentReviews4.5% (2,102)Meta-analyses0.4% (207)Randomized controlled trials4.3% (2,011)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 47,191 PubMed records
TypeRecordsShare
Reviews2,1024.5%
Meta-analyses2070.4%
Randomized controlled trials2,0114.3%

Method: PubMed query "Cues"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in psychiatry and psychology

Research on mental health and behaviour relies on questionnaires, interviews and rating scales rather than physical measurements, so how a condition was defined and measured shapes every result. Many studies are observational or small, placebo responses can be large, and findings in one group or culture may not carry over to another. Nothing on this page is advice about diagnosis or treatment; anyone worried about their mental health should talk to a qualified clinician. Check how outcomes were measured, who took part and how long they were followed.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Multimodal cue integration and learning in a neural representation of head direction
Basnak MA, Kutschireiter A, Okubo TS, Chen A, Gorelik P, Drugowitsch J, et al.
2025Research article
Design not recorded in structured metadata
17cc by
PMID 40702322 · DOI · PMC12321575
Robust encoding of stimulus-response mapping by neurons in visual cortex
Jonikaitis D, Xia R, Moore T
2025Research article
Design not recorded in structured metadata
15cc by
PMID 39993188 · DOI · PMC11892596
Neural Response to Food Cues in Avoidant/Restrictive Food Intake Disorder
Thomas JJ, Holsen L, Van De Water AL, Becker KR, Breithaupt L, Burton-Murray H, et al.
2025Research article
Design not recorded in structured metadata
13cc by
PMID 39964683 · DOI · PMC11836757
Wolves respond differently to human cues as they expand into urban landscapes
Lazzaroni M, Brogi R, Brivio F, Bassi E, Boromello A, Teichmann T, et al.
2026Research article
Design not recorded in structured metadata
3cc by
PMID 41701816 · DOI · PMC12933097

Multimodal cue integration and learning in a neural representation of head direction [1]

Research article Basnak MA, Kutschireiter A, Okubo TS, Chen A, Gorelik P, Drugowitsch J, et al. · · 2025 · cited 17 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Navigation requires us to take account of multiple spatial cues with varying levels of informativeness and learn their spatial relationships.
Closing excerpt
Our findings provide a mechanistic explanation for how the brain assembles spatial representations through inference and learning.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (146 words)

Navigation requires us to take account of multiple spatial cues with varying levels of informativeness and learn their spatial relationships. Here we investigate this process in the Drosophila head direction system, which functions as a ring attractor and a topographic map of head direction. Using population calcium imaging and multimodal virtual reality environments, we show that increasing cue informativeness improves encoding accuracy and produces a narrower and higher bump of activity. When cues conflict, the more informative cue exerts more weight. A familiar cue is weighted more heavily and used to guide the remapping of a less familiar cue. When a cue is less informative, it is remapped more readily in response to cue conflict. All these results can be explained by an attractor model with plastic sensory synapses. Our findings provide a mechanistic explanation for how the brain assembles spatial representations through inference and learning.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 40702322 · DOI · PMC12321575

Robust encoding of stimulus-response mapping by neurons in visual cortex [2]

Research article Jonikaitis D, Xia R, Moore T · · 2025 · cited 15 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Neural activity in sensory cortex is modulated by behavioral and cognitive factors, and this modulation is thought to contribute to the selection of specific sensory information needed to achieve behavioral goals.
Closing excerpt
The results demonstrate that behavioral modulation of visual cortical activity is not solely related to the selection of sensory stimuli but instead reflects a distinct mechanism for sensory-guided motor output.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (216 words)

Neural activity in sensory cortex is modulated by behavioral and cognitive factors, and this modulation is thought to contribute to the selection of specific sensory information needed to achieve behavioral goals. In contrast, more abstract behavioral variables that are independent of stimulus selection, such as stimulus-response mapping, are thought to be encoded by neurons outside of sensory cortex. We show that information about such mapping is robustly encoded in the responses of neurons in primate visual cortex. Monkeys were trained to alternate between two tasks that differed in the rule governing the mapping of a remembered visual cue onto an eye movement response. During the memory-delay period, neurons in area V4 reliably signaled the remembered cue location in both tasks. However, the encoding of cue location depended critically on the stimulus-response mapping rule. Thus, V4 delay activity encoded the mapping rule and signaled the preparation of the appropriate motor response rather than spatial working memory per se, contrary to previous assumptions. In addition, we probed the origins of motor-related delay activity and found that it was reduced during local inactivation of the frontal eye field (FEF). The results demonstrate that behavioral modulation of visual cortical activity is not solely related to the selection of sensory stimuli but instead reflects a distinct mechanism for sensory-guided motor output.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 39993188 · DOI · PMC11892596

Neural Response to Food Cues in Avoidant/Restrictive Food Intake Disorder [3]

Research article Thomas JJ, Holsen L, Van De Water AL, Becker KR, Breithaupt L, Burton-Murray H, et al. · · 2025 · cited 13 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
ImportanceThe neurobiology of avoidant/restrictive food intake disorder (ARFID) is poorly understood.
Closing excerpt
Activation appears consistent with ARFID phenotypic rationales for food avoidance, with hyperactivation of fear regions in ARFID-fear and hypoactivation of appetite regions with increasing ARFID-lack of interest severity.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (422 words)

ImportanceThe neurobiology of avoidant/restrictive food intake disorder (ARFID) is poorly understood.ObjectiveTo evaluate whether individuals with ARFID exhibit disruptions in fear, appetite, and disgust brain regions compared with healthy control (HC) participants when shown images of food and objects.Design, setting, and participantsIn this case-control study conducted from July 2016 to January 2021, children, adolescents, and young adults completed structured interviews and a validated functional magnetic resonance imaging (fMRI) food cue paradigm. The study was conducted at a single academic medical center. Data analysis was conducted from April 2023 to August 2024.ExposuresPresence vs absence of ARFID and its phenotypes (ARFID-fear, ARFID-lack of interest in eating, ARFID-sensory sensitivity); pictures of food vs objects during fMRI food cue paradigm.Main outcomes and measuresBlood oxygenation level-dependent activation in regions of interest (ROIs; amygdala, hypothalamus, insula, anterior cingulate cortex [ACC]) and the whole brain.ResultsParticipants were 110 children, adolescents, and young adults with full or subthreshold ARFID (75 participants; mean [SD] age, 16.2 [3.8] years; 41 [55%] female) and age-matched HC participants (35 participants; mean [SD] age, 17.3 [4.0] years; 27 [69%] female) recruited for studies of the neurobiology of ARFID and restrictive eating disorders. Participants with ARFID demonstrated greater activation than HC participants of the ACC (mean difference, 0.48 [95% CI, 0.19 to 0.77]; P = .009), sensory association cortex (mean difference on left side, 0.54 [95% CI, 0.29 to 0.79]; P = .005; right side, 0.52 [95% CI, 0.28 to 0.76]; P = .02), and supplementary motor cortex (mean difference, 0.81 [95% CI, 0.47 to 1.15]; P = .04). The ARFID-fear group showed greater amygdala activation vs HC (mean difference, 0.49 [95% CI, 0.16 to 0.82]; P = .04), and greater lack of interest was associated with lower hypothalamus activation in the ARFID-lack of interest group (r = -0.38 [95% CI, -0.69 to -0.11]; P = .03). The ARFID-sensory sensitivity group did not show greater insula activation vs HC but showed greater activation of the ACC (mean difference, 0.48 [95% CI, 0.22 to 0.74]; P = .005) and somatosensory cortex (mean difference on left side, 0.60 [95% CI, 0.33-0.87]; P = .001; right side, 0.54 [95% CI, 0.29 to 0.80]; P = .03).Conclusions and relevanceResults indicate generalized hyperactivation of ACC, sensory association cortex, and supplementary motor cortex in response to visual food stimuli in children, adolescents, and young adults with ARFID, suggesting a novel neurobiological circuit associated with this disorder. Activation appears consistent with ARFID phenotypic rationales for food avoidance, with hyperactivation of fear regions in ARFID-fear and hypoactivation of appetite regions with increasing ARFID-lack of interest severity.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 39964683 · DOI · PMC11836757

Wolves respond differently to human cues as they expand into urban landscapes [4]

Research article Lazzaroni M, Brogi R, Brivio F, Bassi E, Boromello A, Teichmann T, et al. · · 2026 · cited 3 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Wolves (Canis lupus) recolonizing human-dominated landscapes encounter anthropogenic risks and opportunities, but how this shapes their fear of humans is unknown.
Closing excerpt
Results show that wolves are capable of flexibly modulating their behavioral responses to both the risks and opportunities of human-dominated landscapes, which likely underpins their urban success and requires us to rise to the challenge of peaceful coexistence.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (158 words)

Wolves (Canis lupus) recolonizing human-dominated landscapes encounter anthropogenic risks and opportunities, but how this shapes their fear of humans is unknown. We tested 185 individually identified wild wolves across 44 locations covering a wide urbanization gradient, exposing them to novel objects and human playbacks. Wolves from more urbanized areas showed reduced fear at first exposure to an object but heightened caution when the object changed, indicating increased attention to environmental changes, rather than uniform fear reduction. By contrast, playbacks of human voices elicited strong fear responses (>80%), regardless of urbanization. However, individuals habituated to both stimuli quickly and at a similar pace, highlighting their rapid learning abilities. Sociality buffered fear, with wolves in groups reacting less fearfully than wolves alone. Results show that wolves are capable of flexibly modulating their behavioral responses to both the risks and opportunities of human-dominated landscapes, which likely underpins their urban success and requires us to rise to the challenge of peaceful coexistence.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41701816 · DOI · PMC12933097

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article Food cue reactivity and craving predict eating and weight gain: a meta-analytic review [5]
    Boswell RG, Kober H · Obes Rev · 2016 · cited 498 times (Europe PMC)
  • Research article Psychology of Habit [6]
    Wood W, Rünger D · Annu Rev Psychol · 2016 · cited 480 times (Europe PMC)
  • Research article Functional neuroimaging studies of alcohol cue reactivity: a quantitative meta-analysis and systematic review [7]
    Schacht JP, Anton RF, Myrick H · Addict Biol · 2013 · cited 432 times (Europe PMC)
  • Research article Cues to deception [8]
    DePaulo BM, Lindsay JJ, Malone BE, Muhlenbruck L, Charlton K, Cooper H · Psychol Bull · 2003 · cited 389 times (Europe PMC)
  • Research article Food and drug cues activate similar brain regions: a meta-analysis of functional MRI studies [9]
    Tang DW, Fellows LK, Small DM, Dagher A · Physiol Behav · 2012 · cited 313 times (Europe PMC)
  • Research article In search of the focus of attention in working memory: 13 years of the retro-cue effect [10]
    Souza AS, Oberauer K · Atten Percept Psychophys · 2016 · cited 279 times (Europe PMC)

References

  1. Basnak MA, Kutschireiter A, Okubo TS, Chen A, Gorelik P, Drugowitsch J, et al.. Multimodal cue integration and learning in a neural representation of head direction. . 2025. PMID 40702322 · DOI · PMC12321575
  2. Jonikaitis D, Xia R, Moore T. Robust encoding of stimulus-response mapping by neurons in visual cortex. . 2025. PMID 39993188 · DOI · PMC11892596
  3. Thomas JJ, Holsen L, Van De Water AL, Becker KR, Breithaupt L, Burton-Murray H, et al.. Neural Response to Food Cues in Avoidant/Restrictive Food Intake Disorder. . 2025. PMID 39964683 · DOI · PMC11836757
  4. Lazzaroni M, Brogi R, Brivio F, Bassi E, Boromello A, Teichmann T, et al.. Wolves respond differently to human cues as they expand into urban landscapes. . 2026. PMID 41701816 · DOI · PMC12933097
  5. Boswell RG, Kober H. Food cue reactivity and craving predict eating and weight gain: a meta-analytic review. Obes Rev. 2016. PMID 26644270 · DOI · PMC6042864
  6. Wood W, Rünger D. Psychology of Habit. Annu Rev Psychol. 2016. PMID 26361052 · DOI
  7. Schacht JP, Anton RF, Myrick H. Functional neuroimaging studies of alcohol cue reactivity: a quantitative meta-analysis and systematic review. Addict Biol. 2013. PMID 22574861 · DOI · PMC3419322
  8. DePaulo BM, Lindsay JJ, Malone BE, Muhlenbruck L, Charlton K, Cooper H. Cues to deception. Psychol Bull. 2003. PMID 12555795 · DOI
  9. Tang DW, Fellows LK, Small DM, Dagher A. Food and drug cues activate similar brain regions: a meta-analysis of functional MRI studies. Physiol Behav. 2012. PMID 22450260 · DOI
  10. Souza AS, Oberauer K. In search of the focus of attention in working memory: 13 years of the retro-cue effect. Atten Percept Psychophys. 2016. PMID 27098647 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-11-04; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-11-04.

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At a glance

47,191
PubMed records on this heading
21%
published since 2020
2,102
review articles
2,011
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

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