about
Prefrontal Activity and Connectivity with the Basal Ganglia during Performance of Complex Cognitive Tasks Is Associated with Apathy in Healthy SubjectsRasd2 Modulates Prefronto-Striatal Phenotypes in Humans and 'Schizophrenia-Like Behaviors' in Mice.Interaction between DRD2 variation and sound environment on mood and emotion-related brain activity.Preferential amygdala reactivity to the negative assessment of neutral facesGenetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance.DRD2/CHRNA5 interaction on prefrontal biology and physiology during working memory.Functional variation of the dopamine D2 receptor gene is associated with emotional control as well as brain activity and connectivity during emotion processing in humans.Expression of DISC1-interactome members correlates with cognitive phenotypes related to schizophrenia.DRD2/AKT1 interaction on D2 c-AMP independent signaling, attentional processing, and response to olanzapine treatment in schizophrenia.Association between Ability Emotional Intelligence and Left Insula during Social Judgment of Facial Emotions.Treatment with olanzapine is associated with modulation of the default mode network in patients with SchizophreniaInteraction Between Functional Genetic Variation of DRD2 and Cannabis Use on Risk of Psychosis.DRD2 genotype-based variation of default mode network activity and of its relationship with striatal DAT binding.BDNF rs6265 methylation and genotype interact on risk for schizophreniaVariation in Dopamine D2 and Serotonin 5-HT2A Receptor Genes is Associated with Working Memory Processing and Response to Treatment with Antipsychotics.Functional variants of the dopamine receptor D2 gene modulate prefronto-striatal phenotypes in schizophrenia.Genetically determined interaction between the dopamine transporter and the D2 receptor on prefronto-striatal activity and volume in humans.DAT by perceived MC interaction on human prefrontal activity and connectivity during emotion processing.Changes in prefrontal and amygdala activity during olanzapine treatment in schizophrenia.Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia.Aversive emotional interference impacts behavior and prefronto-striatal activity during increasing attentional control.Prefronto-striatal physiology is associated with schizotypy and is modulated by a functional variant of DRD2Load-dependent dysfunction of the putamen during attentional processing in patients with clinically isolated syndrome suggestive of multiple sclerosis.Nonlinear response of the anterior cingulate and prefrontal cortex in schizophrenia as a function of variable attentional control.Converging evidence for the association of functional genetic variation in the serotonin receptor 2a gene with prefrontal function and olanzapine treatment.Epistasis between dopamine regulating genes identifies a nonlinear response of the human hippocampus during memory tasks.Familial Risk and a Genome-Wide Supported DRD2 Variant for Schizophrenia Predict Lateral Prefrontal-Amygdala Effective Connectivity During Emotion Processing.A Polygenic Risk Score of glutamatergic SNPs associated with schizophrenia predicts attentional behavior and related brain activity in healthy humans.Evidence that hippocampal-parahippocampal dysfunction is related to genetic risk for schizophrenia.Preferential responses in amygdala and insula during presentation of facial contempt and disgust.Abnormal functional motor lateralization in healthy siblings of patients with schizophrenia.Grey matter volume patterns in thalamic nuclei are associated with familial risk for schizophrenia.Prefrontal activity during working memory is modulated by the interaction of variation in CB1 and COX2 coding genes and correlates with frequency of cannabis use.Association of familial risk for schizophrenia with thalamic and medial prefrontal functional connectivity during attentional control.DRD2 genotype predicts prefrontal activity during working memory after stimulation of D2 receptors with bromocriptine.Stress-related methylation of the catechol-O-methyltransferase Val 158 allele predicts human prefrontal cognition and activity.Catechol-O-methyltransferase Val(158)Met association with parahippocampal physiology during memory encoding in schizophrenia.Association of GSK-3β genetic variation with GSK-3β expression, prefrontal cortical thickness, prefrontal physiology, and schizophrenia.D2 receptor genotype and striatal dopamine signaling predict motor cortical activity and behavior in humans.Cerebrospinal fluid neurofilament tracks fMRI correlates of attention at the first attack of multiple sclerosis
P50
Q28109662-62B041F5-2EB2-4F5A-86B6-D803D57F7757Q30364690-1EEA2871-52AA-4338-9669-FF32E7B48D47Q30395423-5650DA7E-4BE3-4218-BBDC-1A22775D354CQ30497781-72CD10E9-EC1D-49D2-859E-F9B147A1DFEEQ33533750-E04F39DB-22DF-4AA7-9379-67BF1160D53EQ33599626-1581E5C8-A85F-441F-8D2E-6D79F5D7D55BQ33599626-B8AC6E09-DEF5-42F7-80BC-F579727B7868Q33711011-43444E11-9F14-4568-9B3A-AB7FD8CD12BDQ33773726-78E0C236-AF96-4235-B251-C512B3C222AEQ34508840-69EE48D9-DDE5-4057-8623-8378AC210BE9Q34513140-04298F33-0309-4732-A8D5-FCD5B8201C56Q34660641-B66FB559-8A00-4889-B187-DBBE9C0C526FQ35950814-F9B73048-F5DA-4405-86E6-9B5D050DE806Q36471450-716D08C1-480B-4041-B54E-E26FEFBDDB15Q36838967-674E00B2-530B-4109-A0FA-E7CF6EFF1C0AQ37024867-027847D8-C782-4176-B22A-1723F781F8BFQ37092462-29D2A40D-3400-4DE5-BB7A-3B56C89C9F29Q37201805-97EA6613-981D-4BEA-B01C-E871F10E8EFDQ37318439-DA26579A-4911-4D1B-912B-9ABEE25AE10FQ37329216-7DF7F140-A44F-425A-9651-51E3661C3BF9Q39795321-26B9FF5B-6237-4506-8691-9D4053B1C4A7Q39836000-6DF69D78-FF34-4A1A-8193-D6AB63266CB0Q41867856-5C381D6C-88F9-4EAC-BC0E-9B08502121B4Q43514569-96C77057-6801-4415-B32C-4E0ADB389DFAQ44959646-80C77487-C0B8-4933-99A7-E7F229443703Q46431487-AAFC8609-7EB7-4807-86EB-5F240D0EFF98Q46675306-5989723F-1B76-460E-A1AF-73EB7BA07072Q48032539-213D9330-1CC1-446D-A7F9-31F908E4D288Q48223469-4C473653-71A9-4B75-B898-4A2E49F12B26Q48314987-9072EDAC-7BEB-4F33-8B50-E43FA98586FFQ48396607-1B94A47A-DF72-4D24-BA4F-D054A438CA9FQ48406000-5C32426E-DB56-48D2-9931-2C92D12385BFQ48608060-4CAB86FB-A19E-49A1-8CEA-34FDCA2EDCFBQ48694806-10AD51D3-D6B1-48BB-8BC6-D46FD200BA03Q48805552-973524E8-0258-4357-A3FE-18C7D001CC46Q50695782-CB5634A0-7227-496C-8F91-F2C81557DF22Q51010260-39F5F6D8-DD62-4A83-BC63-B954B678380CQ51027863-9AADD1AC-7FC7-4CC9-9374-914A603EEC66Q51061597-48A24749-A626-4DC5-A98E-F4E2DC524604Q53260429-1C6C15DD-99EF-4413-A179-1DFD4E412443
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Paolo Taurisano
@ast
Paolo Taurisano
@en
Paolo Taurisano
@es
Paolo Taurisano
@nl
Paolo Taurisano
@sl
type
label
Paolo Taurisano
@ast
Paolo Taurisano
@en
Paolo Taurisano
@es
Paolo Taurisano
@nl
Paolo Taurisano
@sl
prefLabel
Paolo Taurisano
@ast
Paolo Taurisano
@en
Paolo Taurisano
@es
Paolo Taurisano
@nl
Paolo Taurisano
@sl
P1053
U-1828-2017
P106
P21
P31
P3829
P496
0000-0001-6140-9326