Identification of early mild cognitive impairment using multi-modal data and graph convolutional networks

Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer’s disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identific...

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Published inBMC bioinformatics Vol. 21; no. Suppl 6; pp. 123 - 12
Main Authors Liu, Jin, Tan, Guanxin, Lan, Wei, Wang, Jianxin
Format Journal Article
LanguageEnglish
Published London BioMed Central 18.11.2020
BioMed Central Ltd
BMC
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ISSN1471-2105
1471-2105
DOI10.1186/s12859-020-3437-6

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Abstract Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer’s disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task. Results Our proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification. Conclusion Our proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice.
AbstractList Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer’s disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task. Results Our proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification. Conclusion Our proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice.
The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer's disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task. Our proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification. Our proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice.
Abstract Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer’s disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task. Results Our proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification. Conclusion Our proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice.
Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer's disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task. Results Our proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification. Conclusion Our proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice. Keywords: Early mild cognitive impairment, Multi-modal MRI data, Graph convolutional networks, Identification
The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer's disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task.BACKGROUNDThe identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer's disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task.Our proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification.RESULTSOur proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification.Our proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice.CONCLUSIONOur proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice.
Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer’s disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task. Results Our proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification. Conclusion Our proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice.
The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer's disease (AD) and is associated with brain structural and functional changes, is still a challenging task. Recent studies show great promises for improving the performance of EMCI identification by combining multiple structural and functional features, such as grey matter volume and shortest path length. However, extracting which features and how to combine multiple features to improve the performance of EMCI identification have always been a challenging problem. To address this problem, in this study we propose a new EMCI identification framework using multi-modal data and graph convolutional networks (GCNs). Firstly, we extract grey matter volume and shortest path length of each brain region based on automated anatomical labeling (AAL) atlas as feature representation from T1w MRI and rs-fMRI data of each subject, respectively. Then, in order to obtain features that are more helpful in identifying EMCI, a common multi-task feature selection method is applied. Afterwards, we construct a non-fully labelled subject graph using imaging and non-imaging phenotypic measures of each subject. Finally, a GCN model is adopted to perform the EMCI identification task. Our proposed EMCI identification method is evaluated on 210 subjects, including 105 subjects with EMCI and 105 normal controls (NCs), with both T1w MRI and rs-fMRI data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Experimental results show that our proposed framework achieves an accuracy of 84.1% and an area under the receiver operating characteristic (ROC) curve (AUC) of 0.856 for EMCI/NC classification. In addition, by comparison, the accuracy and AUC values of our proposed framework are better than those of some existing methods in EMCI identification. Our proposed EMCI identification framework is effective and promising for automatic diagnosis of EMCI in clinical practice.
ArticleNumber 123
Audience Academic
Author Tan, Guanxin
Lan, Wei
Liu, Jin
Wang, Jianxin
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  email: jxwang@mail.csu.edu.cn
  organization: Hunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33203351$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1109/TCBB.2016.2635144
10.1109/isbi.2017.7950682
10.1016/j.neucom.2019.03.049
10.1109/TNB.2017.2751074
10.1109/ICIP.2017.8296892
10.1006/nimg.2001.0978
10.3389/fbioe.2019.00479
10.1016/j.neuroimage.2004.07.006
10.1016/j.jalz.2012.04.007
10.1016/j.neuroimage.2012.01.021
10.1212/WNL.0b013e3181a2e864
10.1038/nrg1916
10.1002/hbm.22531
10.1016/j.mri.2012.01.003
10.1148/radiol.10100734
10.26599/BDMA.2018.9020001
10.1016/j.neuroimage.2008.07.003
10.1097/WAD.0000000000000208
10.1016/j.jbi.2019.103114
10.1111/j.1467-9868.2005.00532.x
10.1148/radiology.143.1.7063747
10.1016/j.neuroimage.2011.10.015
10.1109/TCBB.2016.2586190
10.1109/TNB.2017.2707139
10.1016/j.biopsych.2012.03.026
10.1007/s11042-017-5470-7
10.1016/j.neuroimage.2017.12.052
10.1111/j.2517-6161.1996.tb02080.x
10.1038/nn.4502
10.1109/TNB.2015.2403274
10.1155/2017/8362741
10.1109/TCBB.2017.2731849
10.1016/j.jalz.2016.03.001
10.1109/TCBB.2018.2847690
10.1006/cbmr.1996.0014
10.1016/j.media.2018.06.001
10.1093/bioinformatics/bty1001
10.1016/j.neurobiolaging.2013.10.081
10.26599/BDMA.2019.9020007
10.1016/j.neucom.2018.04.080
10.1016/j.neucom.2019.12.050
10.1016/j.neuroimage.2009.10.003
10.1016/j.media.2018.03.013
10.1038/s41592-020-0772-5
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Issue Suppl 6
Keywords Multi-modal MRI data
Identification
Graph convolutional networks
Early mild cognitive impairment
Language English
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References J Liu (3437_CR4) 2018; 15
3437_CR29
A Association (3437_CR1) 2016; 12
JA Hanley (3437_CR44) 1982; 143
S Parisot (3437_CR31) 2018; 48
F Pedregosa (3437_CR49) 2011; 12
MR Brier (3437_CR16) 2014; 35
3437_CR20
B Fischl (3437_CR36) 2012; 62
N Tzourio-Mazoyer (3437_CR33) 2002; 15
MC Carrillo (3437_CR34) 2012; 8
RW Cox (3437_CR39) 1996; 29
3437_CR26
3437_CR28
3437_CR27
Y Yu (3437_CR32) 2019; 2
B Jie (3437_CR21) 2018; 47
X Zhang (3437_CR17) 2015; 14
Y An (3437_CR24) 2019; PP
Y Kong (3437_CR8) 2019; 324
C-Y Wee (3437_CR18) 2012; 59
L Liu (3437_CR22) 2019; 350
J Liu (3437_CR3) 2018; 1
M Rubinov (3437_CR40) 2010; 52
DJ Balding (3437_CR35) 2006; 7
J Liu (3437_CR12) 2017; 16
SI Ktena (3437_CR30) 2018; 169
J Liu (3437_CR6) 2017; 16
H-D Li (3437_CR5) 2018; 35
DS Bassett (3437_CR41) 2017; 20
G Karas (3437_CR9) 2004; 23
3437_CR42
JH Morra (3437_CR10) 2008; 43
R Tibshirani (3437_CR47) 1996; 58
R Min (3437_CR37) 2014; 35
J Liu (3437_CR38) 2018; 15
3437_CR48
G Chen (3437_CR13) 2011; 259
K Kantarci (3437_CR2) 2009; 72
L Liu (3437_CR25) 2020; 384
Y Xiang (3437_CR7) 2020; 7
M Yuan (3437_CR43) 2006; 68
J Liu (3437_CR11) 2018; 77
J Wang (3437_CR15) 2013; 73
Y Feng (3437_CR14) 2012; 30
Q Chen (3437_CR46) 2019; PP
M De Marco (3437_CR19) 2017; 31
Y Yu (3437_CR23) 2019; 91
W Lan (3437_CR45) 2018; 15
References_xml – volume: 15
  start-page: 624
  issue: 2
  year: 2018
  ident: 3437_CR4
  publication-title: IEEE/ACM Trans Comput Biol Bioinforma
  doi: 10.1109/TCBB.2016.2635144
– ident: 3437_CR20
  doi: 10.1109/isbi.2017.7950682
– volume: 350
  start-page: 117
  year: 2019
  ident: 3437_CR22
  publication-title: Neurocomputing
  doi: 10.1016/j.neucom.2019.03.049
– volume: 16
  start-page: 600
  issue: 7
  year: 2017
  ident: 3437_CR6
  publication-title: IEEE Trans NanoBioscience
  doi: 10.1109/TNB.2017.2751074
– ident: 3437_CR29
  doi: 10.1109/ICIP.2017.8296892
– ident: 3437_CR27
– volume: 15
  start-page: 273
  issue: 1
  year: 2002
  ident: 3437_CR33
  publication-title: Neuroimage
  doi: 10.1006/nimg.2001.0978
– volume: 7
  start-page: 479
  year: 2020
  ident: 3437_CR7
  publication-title: Front Bioeng Biotechnol
  doi: 10.3389/fbioe.2019.00479
– volume: 23
  start-page: 708
  issue: 2
  year: 2004
  ident: 3437_CR9
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2004.07.006
– volume: 8
  start-page: 337
  issue: 4
  year: 2012
  ident: 3437_CR34
  publication-title: Alzheimer’s Dement
  doi: 10.1016/j.jalz.2012.04.007
– volume: 62
  start-page: 774
  issue: 2
  year: 2012
  ident: 3437_CR36
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2012.01.021
– volume: 72
  start-page: 1519
  issue: 17
  year: 2009
  ident: 3437_CR2
  publication-title: Neurology
  doi: 10.1212/WNL.0b013e3181a2e864
– volume: 7
  start-page: 781
  issue: 10
  year: 2006
  ident: 3437_CR35
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg1916
– volume: 35
  start-page: 5052
  issue: 10
  year: 2014
  ident: 3437_CR37
  publication-title: Hum Brain Mapp
  doi: 10.1002/hbm.22531
– ident: 3437_CR26
– volume: 30
  start-page: 672
  issue: 5
  year: 2012
  ident: 3437_CR14
  publication-title: Magn Reson Imaging
  doi: 10.1016/j.mri.2012.01.003
– volume: 259
  start-page: 213
  issue: 1
  year: 2011
  ident: 3437_CR13
  publication-title: Radiology
  doi: 10.1148/radiol.10100734
– volume: 1
  start-page: 1
  issue: 1
  year: 2018
  ident: 3437_CR3
  publication-title: Big Data Min Analytics
  doi: 10.26599/BDMA.2018.9020001
– volume: 43
  start-page: 59
  issue: 1
  year: 2008
  ident: 3437_CR10
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2008.07.003
– volume: 31
  start-page: 278
  issue: 4
  year: 2017
  ident: 3437_CR19
  publication-title: Alzheimer Dis Assoc Disord
  doi: 10.1097/WAD.0000000000000208
– volume: 91
  start-page: 103114
  year: 2019
  ident: 3437_CR23
  publication-title: J Biomed Inform
  doi: 10.1016/j.jbi.2019.103114
– volume: 68
  start-page: 49
  issue: 1
  year: 2006
  ident: 3437_CR43
  publication-title: J R Stat Soc
  doi: 10.1111/j.1467-9868.2005.00532.x
– volume: 143
  start-page: 29
  issue: 1
  year: 1982
  ident: 3437_CR44
  publication-title: Radiology
  doi: 10.1148/radiology.143.1.7063747
– volume: 59
  start-page: 2045
  issue: 3
  year: 2012
  ident: 3437_CR18
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2011.10.015
– volume: 15
  start-page: 1774
  issue: 6
  year: 2018
  ident: 3437_CR45
  publication-title: IEEE/ACM Trans Comput Biol Bioinforma
  doi: 10.1109/TCBB.2016.2586190
– volume: 16
  start-page: 428
  issue: 6
  year: 2017
  ident: 3437_CR12
  publication-title: IEEE Trans NanoBioscience
  doi: 10.1109/TNB.2017.2707139
– volume: 73
  start-page: 472
  issue: 5
  year: 2013
  ident: 3437_CR15
  publication-title: Biol Psychiatry
  doi: 10.1016/j.biopsych.2012.03.026
– volume: 77
  start-page: 29651
  issue: 22
  year: 2018
  ident: 3437_CR11
  publication-title: Multimed Tools Appl
  doi: 10.1007/s11042-017-5470-7
– volume: 169
  start-page: 431
  year: 2018
  ident: 3437_CR30
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2017.12.052
– volume: 58
  start-page: 267
  issue: 1
  year: 1996
  ident: 3437_CR47
  publication-title: J R Stat Soc Ser B Methodol
  doi: 10.1111/j.2517-6161.1996.tb02080.x
– volume: 20
  start-page: 353
  issue: 3
  year: 2017
  ident: 3437_CR41
  publication-title: Nat Neurosci
  doi: 10.1038/nn.4502
– volume: 14
  start-page: 237
  issue: 2
  year: 2015
  ident: 3437_CR17
  publication-title: IEEE Trans NanoBioscience
  doi: 10.1109/TNB.2015.2403274
– volume: 12
  start-page: 2825
  issue: Oct
  year: 2011
  ident: 3437_CR49
  publication-title: J Mach Learn Res
– ident: 3437_CR42
  doi: 10.1155/2017/8362741
– volume: 15
  start-page: 1649
  issue: 5
  year: 2018
  ident: 3437_CR38
  publication-title: IEEE/ACM Trans Comput Biol Bioinforma
  doi: 10.1109/TCBB.2017.2731849
– volume: 12
  start-page: 459
  issue: 4
  year: 2016
  ident: 3437_CR1
  publication-title: Alzheimers Dement
  doi: 10.1016/j.jalz.2016.03.001
– volume: PP
  start-page: 1
  issue: 99
  year: 2019
  ident: 3437_CR46
  publication-title: IEEE/ACM Trans Comput Biol Bioinforma
  doi: 10.1109/TCBB.2018.2847690
– volume: 29
  start-page: 162
  issue: 3
  year: 1996
  ident: 3437_CR39
  publication-title: Comput Biomed Res
  doi: 10.1006/cbmr.1996.0014
– volume: 48
  start-page: 117
  year: 2018
  ident: 3437_CR31
  publication-title: Med Image Anal
  doi: 10.1016/j.media.2018.06.001
– volume: 35
  start-page: 2486
  issue: 14
  year: 2018
  ident: 3437_CR5
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/bty1001
– ident: 3437_CR28
– volume: 35
  start-page: 757
  issue: 4
  year: 2014
  ident: 3437_CR16
  publication-title: Neurobiol Aging
  doi: 10.1016/j.neurobiolaging.2013.10.081
– volume: 2
  start-page: 288
  issue: 4
  year: 2019
  ident: 3437_CR32
  publication-title: Big Data Min Analytics
  doi: 10.26599/BDMA.2019.9020007
– volume: 324
  start-page: 63
  issue: 9
  year: 2019
  ident: 3437_CR8
  publication-title: Neurocomputing
  doi: 10.1016/j.neucom.2018.04.080
– volume: PP
  start-page: 1
  issue: 99
  year: 2019
  ident: 3437_CR24
  publication-title: IEEE/ACM Trans Comput Biol Bioinforma
– volume: 384
  start-page: 231
  year: 2020
  ident: 3437_CR25
  publication-title: Neurocomputing
  doi: 10.1016/j.neucom.2019.12.050
– volume: 52
  start-page: 1059
  issue: 3
  year: 2010
  ident: 3437_CR40
  publication-title: NeuroImage
  doi: 10.1016/j.neuroimage.2009.10.003
– volume: 47
  start-page: 81
  year: 2018
  ident: 3437_CR21
  publication-title: Med Image Anal
  doi: 10.1016/j.media.2018.03.013
– ident: 3437_CR48
  doi: 10.1038/s41592-020-0772-5
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Snippet Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer’s disease (AD) and is associated with brain...
The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer's disease (AD) and is associated with brain structural and...
Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer's disease (AD) and is associated with brain...
Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer’s disease (AD) and is associated with brain...
Abstract Background The identification of early mild cognitive impairment (EMCI), which is an early stage of Alzheimer’s disease (AD) and is associated with...
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SubjectTerms Algorithms
Alzheimer Disease - diagnostic imaging
Alzheimer's disease
Artificial neural networks
Autism
Automation
Bioinformatics
Biomedical and Life Sciences
Brain
Brain - diagnostic imaging
Brain mapping
Classification
Cognition disorders
Cognitive ability
Cognitive Dysfunction - diagnostic imaging
Computational Biology/Bioinformatics
Computer Appl. in Life Sciences
Computer-aided medical diagnosis
Diagnosis
Early mild cognitive impairment
Feature extraction
Female
Functional magnetic resonance imaging
Graph convolutional networks
Graphic methods
Humans
Identification
Identification methods
Impairment
Life Sciences
Machine Learning
Magnetic Resonance Imaging
Male
Medical imaging
Methodology
Methods
Microarrays
Modal data
Multi-modal MRI data
Neural networks
Neurodegenerative diseases
Neuroimaging
Performance enhancement
Structure-function relationships
Substantia grisea
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Title Identification of early mild cognitive impairment using multi-modal data and graph convolutional networks
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