2020
A sensorimotor control framework for understanding emotional communication and regulation
Williams J, Huggins C, Zupan B, Willis M, Van Rheenen T, Sato W, Palermo R, Ortner C, Krippl M, Kret M, Dickson J, Li C, Lowe L. A sensorimotor control framework for understanding emotional communication and regulation. Neuroscience & Biobehavioral Reviews 2020, 112: 503-518. PMID: 32070695, PMCID: PMC7505116, DOI: 10.1016/j.neubiorev.2020.02.014.Peer-Reviewed Original ResearchConceptsEmotional communicationCommunication of emotionsContext of consciousnessGoal-directed actionsLanguage of emotionsAction wordsEmotional statesEmotionsFeeling wordsCultural learningLinguistic analysisEmbodied natureAllostatic mechanismsContextual useSensorimotor controlMotor controlLearning processWordsFeelingsCommunicationNeuroscienceLanguageMeaningSelfSenses
2019
Concurrent amygdalar and ventromedial prefrontal cortical responses during emotion processing: a meta-analysis of the effects of valence of emotion and passive exposure versus active regulation
Yang M, Tsai SJ, Li CR. Concurrent amygdalar and ventromedial prefrontal cortical responses during emotion processing: a meta-analysis of the effects of valence of emotion and passive exposure versus active regulation. Brain Structure And Function 2019, 225: 345-363. PMID: 31863185, PMCID: PMC6960357, DOI: 10.1007/s00429-019-02007-3.Peer-Reviewed Original ResearchConceptsActivation likelihood estimationPassive exposureAmygdala activityNegative emotionsRight amygdala activityEmotion processingPosterior cingulate cortexWhole-brain analysisPrefrontal cortical responsesCortical responsesLeft amygdalaCingulate cortexVentromedial prefrontal cortexBilateral amygdalaVentral striatumPrefrontal cortexConvergent activityAmygdalaVentral precuneusEffects of valenceCortexExposureVmPFCPositive emotionsVmPFC responsesA consensus guide to capturing the ability to inhibit actions and impulsive behaviors in the stop-signal task
Verbruggen F, Aron AR, Band GP, Beste C, Bissett PG, Brockett AT, Brown JW, Chamberlain SR, Chambers CD, Colonius H, Colzato LS, Corneil BD, Coxon JP, Dupuis A, Eagle DM, Garavan H, Greenhouse I, Heathcote A, Huster RJ, Jahfari S, Kenemans JL, Leunissen I, Li C, Logan G, Matzke D, Morein-Zamir S, Murthy A, Paré M, Poldrack RA, Ridderinkhof KR, Robbins TW, Roesch M, Rubia K, Schachar RJ, Schall JD, Stock AK, Swann NC, Thakkar KN, van der Molen MW, Vermeylen L, Vink M, Wessel JR, Whelan R, Zandbelt BB, Boehler CN. A consensus guide to capturing the ability to inhibit actions and impulsive behaviors in the stop-signal task. ELife 2019, 8: e46323. PMID: 31033438, PMCID: PMC6533084, DOI: 10.7554/elife.46323.Peer-Reviewed Original Research
2016
Associations of rare nicotinic cholinergic receptor gene variants to nicotine and alcohol dependence
Zuo L, Tan Y, Li C, Wang Z, Wang K, Zhang X, Lin X, Chen X, Zhong C, Wang X, Wang J, Lu L, Luo X. Associations of rare nicotinic cholinergic receptor gene variants to nicotine and alcohol dependence. American Journal Of Medical Genetics Part B Neuropsychiatric Genetics 2016, 171: 1057-1071. PMID: 27473937, PMCID: PMC5587505, DOI: 10.1002/ajmg.b.32476.Peer-Reviewed Original ResearchMeSH KeywordsAlcoholismAnimalsBlack or African AmericanCase-Control StudiesDatabases, Nucleic AcidFemaleGene FrequencyGenetic Predisposition to DiseaseGenetic VariationGenome-Wide Association StudyHumansMaleMiceNicotinePolymorphism, Single NucleotideReceptors, NicotinicTobacco Use DisorderWhite PeopleConceptsCHRN genesGenomic regionsNicotine dependenceAD risk genesAlcohol dependenceRare variantsNicotinic cholinergic receptor genesRewarding effectsDistinct subunitsMouse brainGenesMicroarray platformRisk genesNicotine's rewarding effectsCholinergic receptor genesReceptor geneSpecific brain areasDifferent neuropsychiatric disordersIndependent cohortDiscrete regionsWhole mouse brainBrain areasNeuropsychiatric disordersMRNA expressionBrain
2014
Event-Related Potentials for Post-Error and Post-Conflict Slowing
Chang A, Chen CC, Li HH, Li CS. Event-Related Potentials for Post-Error and Post-Conflict Slowing. PLOS ONE 2014, 9: e99909. PMID: 24932780, PMCID: PMC4059667, DOI: 10.1371/journal.pone.0099909.Peer-Reviewed Original ResearchConceptsPost-error slowingPost-conflict slowingError-related negativityEvent-related potentialsStop-signal taskReaction time taskYoung adult participantsAmplitude of N2Cognitive controlCognitive mechanismsNeural correlatesError trialsSignal taskTime taskNeural responsesPost errorsAdult participantsParticipants' awarenessPeak latencyTaskSlowingNegativityAwarenessParticipantsCorrelates
2013
Effects of Androgen Deprivation on Cerebral Morphometry in Prostate Cancer Patients – An Exploratory Study
Chao HH, Hu S, Ide JS, Uchio E, Zhang S, Rose M, Concato J, Li CS. Effects of Androgen Deprivation on Cerebral Morphometry in Prostate Cancer Patients – An Exploratory Study. PLOS ONE 2013, 8: e72032. PMID: 23977199, PMCID: PMC3747074, DOI: 10.1371/journal.pone.0072032.Peer-Reviewed Original ResearchConceptsAndrogen deprivation therapyProstate cancer patientsGray matter volumeMagnetic resonance imagingPrimary motor cortexCancer patientsVoxel-based morphometryMatter volumeMotor cortexProstate cancerEffects of ADTLow-risk prostate cancerCerebral gray matter volumeStatistical Parametric Mapping 8Utility of brainControl participantsHigh-resolution magnetic resonance imagingPotential side effectsQuality of lifeResolution magnetic resonance imagingSame time pointsFunctional magnetic resonance imagingHigh-resolution T1Prefrontal cortical activationDorsolateral prefrontal cortex
2007
Imaging stress‐ and cue‐induced drug and alcohol craving: association with relapse and clinical implications
SINHA R, LI C. Imaging stress‐ and cue‐induced drug and alcohol craving: association with relapse and clinical implications. Drug And Alcohol Review 2007, 26: 25-31. PMID: 17364833, DOI: 10.1080/09595230601036960.Peer-Reviewed Original ResearchConceptsRelapse outcomesDrug-related cuesPosterior insula regionsCue-induced cravingDrug cue exposureCue-induced drugBrain imaging studiesDrug cuesNeural correlatesCorticostriatal-limbic circuitryCue exposureInsula regionsBrain correlatesRelapse propensityMedial prefrontalBehavioral treatmentAddictive disordersAlcohol cravingPosterior cingulateNeural activityBrain regionsArousal responseLimbic circuitryNeural circuitsCraving