Publication

CONNECTOME-SCALE FUNCTIONAL INTRINSIC CONNECTIVITY NETWORKS IN MACAQUES

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Last modified
  • 05/21/2025
Type of Material
Authors
    Wei Zhang, University of GeorgiaXi Jiang, University of GeorgiaShu Zhang, University of GeorgiaBrittany R Howell, Emory UniversityYu Zhao, University of GeorgiaTuo Zhang, University of GeorgiaLei Guo, Northwestern Polytechnical UniversityMaria Sanchez, Emory UniversityXiaoping Hu, Emory UniversityTianming Liu, University of Georgia
Language
  • English
Date
  • 2017-11-19
Publisher
  • Elsevier: 12 months
Publication Version
Copyright Statement
  • © 2017 IBRO
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0306-4522
Volume
  • 364
Start Page
  • 1
End Page
  • 14
Grant/Funding Information
  • This work was partially supported by National Institutes of Health (DA033393, AG042599, MH078105, MH078105-04S1, HD055255), National Science Foundation (IIS-1149260, CBET-1302089, BCS-1439051, and DBI-1564736), and Office of Research Infrastructure Programs/OD grant OD11132 (YNPRC Base grant, formerly RR000165).
Abstract
  • There have been extensive studies of intrinsic connectivity networks (ICNs) in the human brains using resting-state functional magnetic resonance imaging (fMRI) in the literature. However, the functional organization of ICNs in macaque brains has been less explored so far, despite growing interests in the field. In this work, we propose a computational framework to identify connectome-scale group-wise consistent ICNs in macaques via sparse representation of whole-brain resting-state fMRI data. Experimental results demonstrate that 70 group-wise consistent ICNs are successfully identified in macaque brains via the proposed framework. These 70 ICNs are interpreted based on two publicly available parcellation maps of macaque brains and our work significantly expand currently known macaque ICNs already reported in the literature. In general, this set of connectome-scale group-wise consistent ICNs can potentially benefit a variety of studies in the neuroscience and brain-mapping fields, and they provide a foundation to better understand brain evolution in the future.
Author Notes
  • Correspondence to: Mar M. Sanchez; Xiaoping Hu; Tianming Liu. Address: Boyd GSRC 420, Athens, GA, 30602; telephone: 1-706-542-3478; Fax: 1-706-542-2996; tliu@cs.uga.edu
Keywords
Research Categories
  • Biology, Neuroscience

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