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@ARTICLE{Bijsterbosch:904401,
author = {Bijsterbosch, Janine D. and Valk, Sofie L. and Wang,
Danhong and Glasser, Matthew F.},
title = {{R}ecent developments in representations of the connectome},
journal = {NeuroImage},
volume = {243},
issn = {1053-8119},
address = {Orlando, Fla.},
publisher = {Academic Press},
reportid = {FZJ-2021-05971},
pages = {118533 -},
year = {2021},
abstract = {Research into the human connectome (i.e., all connections
in the human brain) with the use of resting state functional
MRI has rapidly increased in popularity in recent years,
especially with the growing availability of large-scale
neuroimaging datasets. The goal of this review article is to
describe innovations in functional connectome
representations that have come about in the past 8 years,
since the 2013 NeuroImage special issue on ‘Mapping the
Connectome’. In the period, research has shifted from
group-level brain parcellations towards the characterization
of the individualized connectome and of relationships
between individual connectomic differences and
behavioral/clinical variation. Achieving subject-specific
accuracy in parcel boundaries while retaining cross-subject
correspondence is challenging, and a variety of different
approaches are being developed to meet this challenge,
including improved alignment, improved noise reduction, and
robust group-to-subject mapping approaches. Beyond the
interest in the individualized connectome, new
representations of the data are being studied to complement
the traditional parcellated connectome representation (i.e.,
pairwise connections between distinct brain regions), such
as methods that capture overlapping and smoothly varying
patterns of connectivity (‘gradients’). These different
connectome representations offer complimentary insights into
the inherent functional organization of the brain, but
challenges for functional connectome research remain.
Interpretability will be improved by future research towards
gaining insights into the neural mechanisms underlying
connectome observations obtained from functional MRI.
Validation studies comparing different connectome
representations are also needed to build consensus and
confidence to proceed with clinical trials that may produce
meaningful clinical translation of connectome insights.},
cin = {INM-7},
ddc = {610},
cid = {I:(DE-Juel1)INM-7-20090406},
pnm = {5252 - Brain Dysfunction and Plasticity (POF4-525)},
pid = {G:(DE-HGF)POF4-5252},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:34469814},
UT = {WOS:000697098400004},
doi = {10.1016/j.neuroimage.2021.118533},
url = {https://juser.fz-juelich.de/record/904401},
}