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@ARTICLE{Lotter:1018582,
      author       = {Lotter, Leon D. and Kohl, Simon H. and Gerloff, Christian
                      and Bell, Laura and Niephaus, Alexandra and Kruppa, Jana A.
                      and Dukart, Juergen and Schulte-Rüther, Martin and Reindl,
                      Vanessa and Konrad, Kerstin},
      title        = {{R}evealing the neurobiology underlying interpersonal
                      neural synchronization with multimodal data fusion},
      journal      = {Neuroscience $\&$ biobehavioral reviews},
      volume       = {146},
      issn         = {0149-7634},
      address      = {Amsterdam [u.a.]},
      publisher    = {Elsevier Science},
      reportid     = {FZJ-2023-04910},
      pages        = {105042 -},
      year         = {2023},
      note         = {Grant: DFG - CRC1451},
      abstract     = {Humans synchronize with one another to foster successful
                      interactions. Here, we use a multimodal data fusion approach
                      with the aim of elucidating the neurobiological mechanisms
                      by which interpersonal neural synchronization (INS) occurs.
                      Our meta-analysis of 22 functional magnetic resonance
                      imaging and 69 near-infrared spectroscopy hyperscanning
                      experiments (740 and 3721 subjects) revealed robust brain
                      regional correlates of INS in the right temporoparietal
                      junction and left ventral prefrontal cortex. Integrating
                      this meta-analytic information with public databases,
                      biobehavioral and brain-functional association analyses
                      suggested that INS involves sensory-integrative hubs with
                      functional connections to mentalizing and attention
                      networks. On the molecular and genetic levels, we found INS
                      to be associated with GABAergic neurotransmission and layer
                      IV/V neuronal circuits, protracted developmental gene
                      expression patterns, and disorders of neurodevelopment.
                      Although limited by the indirect nature of
                      phenotypic-molecular association analyses, our findings
                      generate new testable hypotheses on the neurobiological
                      basis of INS.},
      cin          = {INM-7},
      ddc          = {610},
      cid          = {I:(DE-Juel1)INM-7-20090406},
      pnm          = {5251 - Multilevel Brain Organization and Variability
                      (POF4-525)},
      pid          = {G:(DE-HGF)POF4-5251},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {36641012},
      UT           = {WOS:000923809300001},
      doi          = {10.1016/j.neubiorev.2023.105042},
      url          = {https://juser.fz-juelich.de/record/1018582},
}