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@ARTICLE{Eickhoff:171837,
author = {Eickhoff, Simon and Laird, Angela R and Fox, Peter T and
Bzdok, Danilo and Hensel, Lukas},
title = {{F}unctional {S}egregation of the {H}uman {D}orsomedial
{P}refrontal {C}ortex.},
journal = {Cerebral cortex},
volume = {26},
number = {1},
issn = {1460-2199},
address = {Oxford},
publisher = {Oxford Univ. Press},
reportid = {FZJ-2014-05394},
pages = {304-321},
year = {2016},
abstract = {The human dorsomedial prefrontal cortex (dmPFC) has been
implicated in various complex cognitive processes, including
social cognition. To unravel its functional organization, we
assessed the dmPFC's regional heterogeneity, connectivity
patterns, and functional profiles. First, the heterogeneity
of a dmPFC seed, engaged during social processing, was
investigated by assessing local differences in whole-brain
coactivation profiles. Second, functional connectivity of
the ensuing dmPFC clusters was compared by task-constrained
meta-analytic coactivation mapping and task-unconstrained
resting-state correlations. Third, dmPFC clusters were
functionally profiled by forward/reverse inference. The
dmPFC seed was thus segregated into 4 clusters
(rostroventral, rostrodorsal, caudal-right, and
caudal-left). Both rostral clusters were connected to the
amygdala and hippocampus and associated with memory and
social cognitive tasks in functional decoding. The
rostroventral cluster exhibited strongest connectivity to
the default mode network. Unlike the rostral segregation,
the caudal dmPFC was divided by hemispheres. The
caudal-right cluster was strongly connected to a
frontoparietal network (dorsal attention network), whereas
the caudal-left cluster was strongly connected to the
anterior midcingulate cortex and bilateral anterior insula
(salience network). In conclusion, we demonstrate that a
dmPFC seed reflecting social processing can be divided into
4 separate functional modules that contribute to distinct
facets of advanced human cognition.},
cin = {INM-1},
ddc = {610},
cid = {I:(DE-Juel1)INM-1-20090406},
pnm = {333 - Pathophysiological Mechanisms of Neurological and
Psychiatric Diseases (POF2-333)},
pid = {G:(DE-HGF)POF2-333},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:25331597},
UT = {WOS:000370972500029},
doi = {10.1093/cercor/bhu250},
url = {https://juser.fz-juelich.de/record/171837},
}