2022
The thalamus and its subnuclei—a gateway to obsessive-compulsive disorder
Weeland CJ, Kasprzak S, de Joode NT, Abe Y, Alonso P, Ameis SH, Anticevic A, Arnold PD, Balachander S, Banaj N, Bargallo N, Batistuzzo MC, Benedetti F, Beucke JC, Bollettini I, Brecke V, Brem S, Cappi C, Cheng Y, Cho KIK, Costa DLC, Dallaspezia S, Denys D, Eng GK, Ferreira S, Feusner JD, Fontaine M, Fouche JP, Grazioplene RG, Gruner P, He M, Hirano Y, Hoexter MQ, Huyser C, Hu H, Jaspers-Fayer F, Kathmann N, Kaufmann C, Kim M, Koch K, Bin Kwak Y, Kwon JS, Lazaro L, Li CR, Lochner C, Marsh R, Martínez-Zalacaín I, Mataix-Cols D, Menchón JM, Minnuzi L, Moreira PS, Morgado P, Nakagawa A, Nakamae T, Narayanaswamy JC, Nurmi EL, Ortiz AE, Pariente JC, Piacentini J, Picó-Pérez M, Piras F, Piras F, Pittenger C, Reddy YCJ, Rodriguez-Manrique D, Sakai Y, Shimizu E, Shivakumar V, Simpson HB, Soreni N, Soriano-Mas C, Sousa N, Spalletta G, Stern ER, Stevens MC, Stewart SE, Szeszko PR, Takahashi J, Tanamatis T, Tang J, Thorsen AL, Tolin D, van der Werf YD, van Marle H, van Wingen GA, Vecchio D, Venkatasubramanian G, Walitza S, Wang J, Wang Z, Watanabe A, Wolters LH, Xu X, Yun JY, Zhao Q, White T, Thompson P, Stein D, van den Heuvel O, Vriend C. The thalamus and its subnuclei—a gateway to obsessive-compulsive disorder. Translational Psychiatry 2022, 12: 70. PMID: 35190533, PMCID: PMC8861046, DOI: 10.1038/s41398-022-01823-2.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAdultBrainChildHumansMagnetic Resonance ImagingObsessive-Compulsive DisorderThalamusConceptsObsessive-compulsive disorderMagnetic resonance imagingThalamic volumeOCD patientsThalamic subregionsT1-weighted brain magnetic resonance imagingBrain magnetic resonance imagingClinical-level symptomsLarger thalamic volumesPediatric OCD patientsAdult OCD patientsSeparate multiple linear regression modelsVolumetric group differencesThalamus sizeMedicated patientsAdolescent patientsAnterior thalamusHealthy controlsSubregional volumesGeneral populationMedication statusMultiple comparison correctionPatientsResonance imagingIntracranial volume
2019
Toward a Neural Model of the Openness-Psychoticism Dimension: Functional Connectivity in the Default and Frontoparietal Control Networks
Blain S, Grazioplene R, Ma Y, DeYoung C. Toward a Neural Model of the Openness-Psychoticism Dimension: Functional Connectivity in the Default and Frontoparietal Control Networks. Schizophrenia Bulletin 2019, 46: 540-551. PMID: 31603227, PMCID: PMC7147581, DOI: 10.1093/schbul/sbz103.Peer-Reviewed Original ResearchConceptsFrontoparietal networkFunctional connectivityFunctional magnetic resonance imagingFrontoparietal control networkState functional magnetic resonance imagingIntelligenceNeural modelIntrinsic connectivity networksMeasures of psychoticismHuman Connectome ProjectStructural equation modelingNetworkCognitive controlNeural correlatesPsychosis pronenessLatter networkCognitive deficitsNetwork coherenceConnectome ProjectControl networkEquation modelingPsychosis riskConnectivityStructural correlates of the orbitofrontal cortex and amygdala and personality in female adolescents
Delaparte L, Bartlett E, Grazioplene R, Perlman G, Gardus J, DeLorenzo C, Klein D, Kotov R. Structural correlates of the orbitofrontal cortex and amygdala and personality in female adolescents. Psychophysiology 2019, 56: e13376. PMID: 30942481, PMCID: PMC6650330, DOI: 10.1111/psyp.13376.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAmygdalaDiffusion Tensor ImagingFemaleGray MatterHumansMagnetic Resonance ImagingPersonalityPersonality InventoryPrefrontal CortexWhite MatterConceptsMedial orbitofrontal cortexOrbitofrontal cortexT1-weighted structural MRIHigher white matter integrityCritical neurodevelopmental periodMultimodal neuroimaging techniquesWhite matter integrityNeurodevelopmental periodAmygdala volumeCortical thicknessBrain regionsStructural MRIUncinate fasciculusFractional anisotropyNeuroimaging techniquesCortexAdolescent girlsStructural correlatesFemale adolescentsDiffusion tensorAmygdalaAdolescenceAssociationAdult samplesHigh neuroticism
2015
Functional Coherence of Insula Networks Is Associated With Externalizing Behavior
Abram S, Wisner K, Grazioplene R, Krueger R, MacDonald A, DeYoung C. Functional Coherence of Insula Networks Is Associated With Externalizing Behavior. Journal Of Psychopathology And Clinical Science 2015, 124: 1079-1091. PMID: 26301974, PMCID: PMC4658249, DOI: 10.1037/abn0000078.Peer-Reviewed Original ResearchMeSH KeywordsAdultAggressionBrain MappingCerebral CortexFemaleFunctional NeuroimagingHumansMagnetic Resonance ImagingMaleNerve NetSex FactorsYoung AdultConceptsIntrinsic connectivity networksGeneral disinhibitionSubstance abuseInsula networksFunctional MRI scansSubstance use problemsInsular cortexMRI scansAmygdala abnormalitiesLarge community sampleNeural synchronyDisinhibitionExternalizing behaviorsCommunity sampleAggression domainExternalizing psychopathologyRegression modelsConnectivity networksRecent studiesAbuseCommunity participantsMaladaptive behaviorsExternalizing Spectrum Inventory
2014
Subcortical intelligence: Caudate volume predicts IQ in healthy adults
Grazioplene R, Ryman S, Gray J, Rustichini A, Jung R, DeYoung C. Subcortical intelligence: Caudate volume predicts IQ in healthy adults. Human Brain Mapping 2014, 36: 1407-1416. PMID: 25491047, PMCID: PMC6869035, DOI: 10.1002/hbm.22710.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAdultAgingCaudate NucleusFemaleHumansIntelligenceIntelligence TestsMagnetic Resonance ImagingMaleOrgan SizeRegression AnalysisSex CharacteristicsYoung AdultConceptsCaudate volumeDopamine receptor availabilityHealthy adultsAttentional functionsVerbal abilityLarge independent samplesIQTotal brain volumeSubcortical structuresIndependent samplesIntelligenceBilateral caudate volumesCaudate morphologyBrain volumeReceptor availabilityPositive associationCaudate nucleusAdultsSignificant positive correlationLearningCaudatePositive correlationAssociation
2010
Cortical Thickness and Subcortical Gray Matter Reductions in Neuropsychiatric Systemic Lupus Erythematosus
Jung R, Segall J, Grazioplene R, Qualls C, Sibbitt W, Roldan C. Cortical Thickness and Subcortical Gray Matter Reductions in Neuropsychiatric Systemic Lupus Erythematosus. PLOS ONE 2010, 5: e9302. PMID: 20352085, PMCID: PMC2844408, DOI: 10.1371/journal.pone.0009302.Peer-Reviewed Original ResearchConceptsNeuropsychiatric systemic lupus erythematosusSystemic lupus erythematosusNPSLE groupSLE patientsGray matter volumeCortical thicknessLupus erythematosusNeuropsychiatric symptomsMatter volumeCentral nervous system involvementSystemic lupus erythematosus patientsFreeSurfer image analysis suiteLupus erythematosus patientsNervous system involvementSubcortical gray matter volumesGray matter reductionsGroup differencesSubcortical gray matter structuresSubcortical structure volumesRegional gray matter volumeGray matter structuresSLE groupCortical atrophyCortical thinningControl subjects