Parkinson's disease-related pattern (PDRP) identified using resting-state functional MRI: Validation study
Spatial covariance mapping of brain activity has been used increasingly with metabolic imaging to detect and quantify abnormal disease patterns in patient populations. Metabolic topographies such as the Parkinson's disease-related pattern (PDRP), while extensively validated, require access to p...
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          | Published in | Neuroimage. Reports Vol. 1; no. 3; p. 100026 | 
|---|---|
| Main Authors | , , , , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        Netherlands
          Elsevier Inc
    
        01.09.2021
     Elsevier  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 2666-9560 2666-9560  | 
| DOI | 10.1016/j.ynirp.2021.100026 | 
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| Abstract | Spatial covariance mapping of brain activity has been used increasingly with metabolic imaging to detect and quantify abnormal disease patterns in patient populations. Metabolic topographies such as the Parkinson's disease-related pattern (PDRP), while extensively validated, require access to positron emission tomography (PET) and radiation exposure. Recently, we developed a fully non-invasive approach to identify analogous disease networks with resting-state functional MRI (rs-fMRI) using independent component analysis (ICA) and bootstrap resampling. We designated the original rs-fMRI PD topography as fPDRPNS after its site of identification at North Shore University Hospital (Manhasset, New York).
In this study, we validated fPDRPNS in rs-fMRI scans of PD patients (n = 51; 25 training and 26 testing) and age-matched healthy control subjects (n = 25) acquired in Cologne, Germany. These scans were also used to identify an independent rs-fMRI PD pattern termed fPDRPCOL. The resulting topography and expression levels (subject scores) were then compared to corresponding fPDRPNS values computed in the two populations.
We found that fPDRPNS and fPDRPCOL were topographically similar. Prominent contributions arose from the putamen, globus pallidus, pons, cerebellum, and thalamus, which have been linked to the core zone of the PDRP in prior studies. Indeed, a significant correlation was noted between core region weights on the two fPDRP topographies (r = 0.62, p < 0.005). Expression levels for fPDRPCOL and fPDRPNS were significantly correlated in the patients scanned at each site (Cologne: r = 0.39, p < 0.01; North Shore: r = 0.65, p < 0.005). Abnormal elevations in fPDRPCOL core expression were observed for both patient groups (Cologne: p = 0.01; North Shore: p = 0.05) compared to healthy controls. Correlations of fPDRP subject scores with clinical motor disability ratings were significant in each of the derivation samples (fPDRPCOL p < 0.005 for Cologne patients; fPDRPNS p < 0.05 for North Shore patients); clinical correlations were less robust on out-of-sample testing. Of note, significant clinical correlations were observed (p < 0.05) when expression values were computed for the fPDRP core in isolation as opposed to the whole network.
The findings demonstrate the reproducibility of fPDRP networks across patient populations, sites, and scanning platforms. Rs-fMRI may provide a non-invasive alternative to metabolic PET for the quantitative assessment of disease networks in the clinical setting.
•Similar rs-fMRI network topographies are expressed in independent PD populations.•A new rs-fMRI-based PD pattern (fPDRP) was derived from an independent cohort.•New and original fPDRPs show good region weight and expression level agreement.•Expression of both fPDRPs is elevated in PD patients in testing cohorts.•Pattern expression correlates with clinical ratings of motor disability. | 
    
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| AbstractList | Spatial covariance mapping of brain activity has been used increasingly with metabolic imaging to detect and quantify abnormal disease patterns in patient populations. Metabolic topographies such as the Parkinson's disease-related pattern (PDRP), while extensively validated, require access to positron emission tomography (PET) and radiation exposure. Recently, we developed a fully non-invasive approach to identify analogous disease networks with resting-state functional MRI (rs-fMRI) using independent component analysis (ICA) and bootstrap resampling. We designated the original rs-fMRI PD topography as fPDRPNS after its site of identification at North Shore University Hospital (Manhasset, New York).In this study, we validated fPDRPNS in rs-fMRI scans of PD patients (n = 51; 25 training and 26 testing) and age-matched healthy control subjects (n = 25) acquired in Cologne, Germany. These scans were also used to identify an independent rs-fMRI PD pattern termed fPDRPCOL. The resulting topography and expression levels (subject scores) were then compared to corresponding fPDRPNS values computed in the two populations.We found that fPDRPNS and fPDRPCOL were topographically similar. Prominent contributions arose from the putamen, globus pallidus, pons, cerebellum, and thalamus, which have been linked to the core zone of the PDRP in prior studies. Indeed, a significant correlation was noted between core region weights on the two fPDRP topographies (r = 0.62, p < 0.005). Expression levels for fPDRPCOL and fPDRPNS were significantly correlated in the patients scanned at each site (Cologne: r = 0.39, p < 0.01; North Shore: r = 0.65, p < 0.005). Abnormal elevations in fPDRPCOL core expression were observed for both patient groups (Cologne: p = 0.01; North Shore: p = 0.05) compared to healthy controls. Correlations of fPDRP subject scores with clinical motor disability ratings were significant in each of the derivation samples (fPDRPCOL p < 0.005 for Cologne patients; fPDRPNS p < 0.05 for North Shore patients); clinical correlations were less robust on out-of-sample testing. Of note, significant clinical correlations were observed (p < 0.05) when expression values were computed for the fPDRP core in isolation as opposed to the whole network.The findings demonstrate the reproducibility of fPDRP networks across patient populations, sites, and scanning platforms. Rs-fMRI may provide a non-invasive alternative to metabolic PET for the quantitative assessment of disease networks in the clinical setting. Spatial covariance mapping of brain activity has been used increasingly with metabolic imaging to detect and quantify abnormal disease patterns in patient populations. Metabolic topographies such as the Parkinson's disease-related pattern (PDRP), while extensively validated, require access to positron emission tomography (PET) and radiation exposure. Recently, we developed a fully non-invasive approach to identify analogous disease networks with resting-state functional MRI (rs-fMRI) using independent component analysis (ICA) and bootstrap resampling. We designated the original rs-fMRI PD topography as fPDRPNS after its site of identification at North Shore University Hospital (Manhasset, New York). In this study, we validated fPDRPNS in rs-fMRI scans of PD patients (n = 51; 25 training and 26 testing) and age-matched healthy control subjects (n = 25) acquired in Cologne, Germany. These scans were also used to identify an independent rs-fMRI PD pattern termed fPDRPCOL. The resulting topography and expression levels (subject scores) were then compared to corresponding fPDRPNS values computed in the two populations. We found that fPDRPNS and fPDRPCOL were topographically similar. Prominent contributions arose from the putamen, globus pallidus, pons, cerebellum, and thalamus, which have been linked to the core zone of the PDRP in prior studies. Indeed, a significant correlation was noted between core region weights on the two fPDRP topographies (r = 0.62, p < 0.005). Expression levels for fPDRPCOL and fPDRPNS were significantly correlated in the patients scanned at each site (Cologne: r = 0.39, p < 0.01; North Shore: r = 0.65, p < 0.005). Abnormal elevations in fPDRPCOL core expression were observed for both patient groups (Cologne: p = 0.01; North Shore: p = 0.05) compared to healthy controls. Correlations of fPDRP subject scores with clinical motor disability ratings were significant in each of the derivation samples (fPDRPCOL p < 0.005 for Cologne patients; fPDRPNS p < 0.05 for North Shore patients); clinical correlations were less robust on out-of-sample testing. Of note, significant clinical correlations were observed (p < 0.05) when expression values were computed for the fPDRP core in isolation as opposed to the whole network. The findings demonstrate the reproducibility of fPDRP networks across patient populations, sites, and scanning platforms. Rs-fMRI may provide a non-invasive alternative to metabolic PET for the quantitative assessment of disease networks in the clinical setting. •Similar rs-fMRI network topographies are expressed in independent PD populations.•A new rs-fMRI-based PD pattern (fPDRP) was derived from an independent cohort.•New and original fPDRPs show good region weight and expression level agreement.•Expression of both fPDRPs is elevated in PD patients in testing cohorts.•Pattern expression correlates with clinical ratings of motor disability. Spatial covariance mapping of brain activity has been used increasingly with metabolic imaging to detect and quantify abnormal disease patterns in patient populations. Metabolic topographies such as the Parkinson's disease-related pattern (PDRP), while extensively validated, require access to positron emission tomography (PET) and radiation exposure. Recently, we developed a fully non-invasive approach to identify analogous disease networks with resting-state functional MRI (rs-fMRI) using independent component analysis (ICA) and bootstrap resampling. We designated the original rs-fMRI PD topography as fPDRP after its site of identification at North Shore University Hospital (Manhasset, New York). In this study, we validated fPDRP in rs-fMRI scans of PD patients (n = 51; 25 training and 26 testing) and age-matched healthy control subjects (n = 25) acquired in Cologne, Germany. These scans were also used to identify an independent rs-fMRI PD pattern termed fPDRP . The resulting topography and expression levels (subject scores) were then compared to corresponding fPDRP values computed in the two populations. We found that fPDRP and fPDRP were topographically similar. Prominent contributions arose from the putamen, globus pallidus, pons, cerebellum, and thalamus, which have been linked to the core zone of the PDRP in prior studies. Indeed, a significant correlation was noted between core region weights on the two fPDRP topographies (r = 0.62, p < 0.005). Expression levels for fPDRP and fPDRP were significantly correlated in the patients scanned at each site (Cologne: r = 0.39, p < 0.01; North Shore: r = 0.65, p < 0.005). Abnormal elevations in fPDRP core expression were observed for both patient groups (Cologne: p = 0.01; North Shore: p = 0.05) compared to healthy controls. Correlations of fPDRP subject scores with clinical motor disability ratings were significant in each of the derivation samples (fPDRP p < 0.005 for Cologne patients; fPDRP p < 0.05 for North Shore patients); clinical correlations were less robust on out-of-sample testing. Of note, significant clinical correlations were observed (p < 0.05) when expression values were computed for the fPDRP core in isolation as opposed to the whole network. The findings demonstrate the reproducibility of fPDRP networks across patient populations, sites, and scanning platforms. Rs-fMRI may provide a non-invasive alternative to metabolic PET for the quantitative assessment of disease networks in the clinical setting. Spatial covariance mapping of brain activity has been used increasingly with metabolic imaging to detect and quantify abnormal disease patterns in patient populations. Metabolic topographies such as the Parkinson's disease-related pattern (PDRP), while extensively validated, require access to positron emission tomography (PET) and radiation exposure. Recently, we developed a fully non-invasive approach to identify analogous disease networks with resting-state functional MRI (rs-fMRI) using independent component analysis (ICA) and bootstrap resampling. We designated the original rs-fMRI PD topography as fPDRPNS after its site of identification at North Shore University Hospital (Manhasset, New York). In this study, we validated fPDRPNS in rs-fMRI scans of PD patients (n = 51; 25 training and 26 testing) and age-matched healthy control subjects (n = 25) acquired in Cologne, Germany. These scans were also used to identify an independent rs-fMRI PD pattern termed fPDRPCOL. The resulting topography and expression levels (subject scores) were then compared to corresponding fPDRPNS values computed in the two populations. We found that fPDRPNS and fPDRPCOL were topographically similar. Prominent contributions arose from the putamen, globus pallidus, pons, cerebellum, and thalamus, which have been linked to the core zone of the PDRP in prior studies. Indeed, a significant correlation was noted between core region weights on the two fPDRP topographies (r = 0.62, p < 0.005). Expression levels for fPDRPCOL and fPDRPNS were significantly correlated in the patients scanned at each site (Cologne: r = 0.39, p < 0.01; North Shore: r = 0.65, p < 0.005). Abnormal elevations in fPDRPCOL core expression were observed for both patient groups (Cologne: p = 0.01; North Shore: p = 0.05) compared to healthy controls. Correlations of fPDRP subject scores with clinical motor disability ratings were significant in each of the derivation samples (fPDRPCOL p < 0.005 for Cologne patients; fPDRPNS p < 0.05 for North Shore patients); clinical correlations were less robust on out-of-sample testing. Of note, significant clinical correlations were observed (p < 0.05) when expression values were computed for the fPDRP core in isolation as opposed to the whole network. The findings demonstrate the reproducibility of fPDRP networks across patient populations, sites, and scanning platforms. Rs-fMRI may provide a non-invasive alternative to metabolic PET for the quantitative assessment of disease networks in the clinical setting.Spatial covariance mapping of brain activity has been used increasingly with metabolic imaging to detect and quantify abnormal disease patterns in patient populations. Metabolic topographies such as the Parkinson's disease-related pattern (PDRP), while extensively validated, require access to positron emission tomography (PET) and radiation exposure. Recently, we developed a fully non-invasive approach to identify analogous disease networks with resting-state functional MRI (rs-fMRI) using independent component analysis (ICA) and bootstrap resampling. We designated the original rs-fMRI PD topography as fPDRPNS after its site of identification at North Shore University Hospital (Manhasset, New York). In this study, we validated fPDRPNS in rs-fMRI scans of PD patients (n = 51; 25 training and 26 testing) and age-matched healthy control subjects (n = 25) acquired in Cologne, Germany. These scans were also used to identify an independent rs-fMRI PD pattern termed fPDRPCOL. The resulting topography and expression levels (subject scores) were then compared to corresponding fPDRPNS values computed in the two populations. We found that fPDRPNS and fPDRPCOL were topographically similar. Prominent contributions arose from the putamen, globus pallidus, pons, cerebellum, and thalamus, which have been linked to the core zone of the PDRP in prior studies. Indeed, a significant correlation was noted between core region weights on the two fPDRP topographies (r = 0.62, p < 0.005). Expression levels for fPDRPCOL and fPDRPNS were significantly correlated in the patients scanned at each site (Cologne: r = 0.39, p < 0.01; North Shore: r = 0.65, p < 0.005). Abnormal elevations in fPDRPCOL core expression were observed for both patient groups (Cologne: p = 0.01; North Shore: p = 0.05) compared to healthy controls. Correlations of fPDRP subject scores with clinical motor disability ratings were significant in each of the derivation samples (fPDRPCOL p < 0.005 for Cologne patients; fPDRPNS p < 0.05 for North Shore patients); clinical correlations were less robust on out-of-sample testing. Of note, significant clinical correlations were observed (p < 0.05) when expression values were computed for the fPDRP core in isolation as opposed to the whole network. The findings demonstrate the reproducibility of fPDRP networks across patient populations, sites, and scanning platforms. Rs-fMRI may provide a non-invasive alternative to metabolic PET for the quantitative assessment of disease networks in the clinical setting. Spatial covariance mapping of brain activity has been used increasingly with metabolic imaging to detect and quantify abnormal disease patterns in patient populations. Metabolic topographies such as the Parkinson's disease-related pattern (PDRP), while extensively validated, require access to positron emission tomography (PET) and radiation exposure. Recently, we developed a fully non-invasive approach to identify analogous disease networks with resting-state functional MRI (rs-fMRI) using independent component analysis (ICA) and bootstrap resampling. We designated the original rs-fMRI PD topography as fPDRPNS after its site of identification at North Shore University Hospital (Manhasset, New York). In this study, we validated fPDRPNS in rs-fMRI scans of PD patients (n = 51; 25 training and 26 testing) and age-matched healthy control subjects (n = 25) acquired in Cologne, Germany. These scans were also used to identify an independent rs-fMRI PD pattern termed fPDRPCOL. The resulting topography and expression levels (subject scores) were then compared to corresponding fPDRPNS values computed in the two populations. We found that fPDRPNS and fPDRPCOL were topographically similar. Prominent contributions arose from the putamen, globus pallidus, pons, cerebellum, and thalamus, which have been linked to the core zone of the PDRP in prior studies. Indeed, a significant correlation was noted between core region weights on the two fPDRP topographies (r = 0.62, p < 0.005). Expression levels for fPDRPCOL and fPDRPNS were significantly correlated in the patients scanned at each site (Cologne: r = 0.39, p < 0.01; North Shore: r = 0.65, p < 0.005). Abnormal elevations in fPDRPCOL core expression were observed for both patient groups (Cologne: p = 0.01; North Shore: p = 0.05) compared to healthy controls. Correlations of fPDRP subject scores with clinical motor disability ratings were significant in each of the derivation samples (fPDRPCOL p < 0.005 for Cologne patients; fPDRPNS p < 0.05 for North Shore patients); clinical correlations were less robust on out-of-sample testing. Of note, significant clinical correlations were observed (p < 0.05) when expression values were computed for the fPDRP core in isolation as opposed to the whole network. The findings demonstrate the reproducibility of fPDRP networks across patient populations, sites, and scanning platforms. Rs-fMRI may provide a non-invasive alternative to metabolic PET for the quantitative assessment of disease networks in the clinical setting. •Similar rs-fMRI network topographies are expressed in independent PD populations.•A new rs-fMRI-based PD pattern (fPDRP) was derived from an independent cohort.•New and original fPDRPs show good region weight and expression level agreement.•Expression of both fPDRPs is elevated in PD patients in testing cohorts.•Pattern expression correlates with clinical ratings of motor disability.  | 
    
| ArticleNumber | 100026 | 
    
| Author | Ruppert, Marina C. Eggers, Carsten Eidelberg, David Rommal, Andrea Schindlbeck, Katharina A. Vo, An Greuel, Andrea  | 
    
| Author_xml | – sequence: 1 givenname: Andrea surname: Rommal fullname: Rommal, Andrea organization: Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, 11030, USA – sequence: 2 givenname: An surname: Vo fullname: Vo, An organization: Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, 11030, USA – sequence: 3 givenname: Katharina A. orcidid: 0000-0002-5643-556X surname: Schindlbeck fullname: Schindlbeck, Katharina A. organization: Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, 11030, USA – sequence: 4 givenname: Andrea orcidid: 0000-0002-0001-9225 surname: Greuel fullname: Greuel, Andrea organization: Department of Neurology, University Hospital Giessen and Marburg, Marburg, Germany – sequence: 5 givenname: Marina C. orcidid: 0000-0002-9025-7058 surname: Ruppert fullname: Ruppert, Marina C. organization: Department of Neurology, University Hospital Giessen and Marburg, Marburg, Germany – sequence: 6 givenname: Carsten surname: Eggers fullname: Eggers, Carsten organization: Department of Neurology, University Hospital Giessen and Marburg, Marburg, Germany – sequence: 7 givenname: David surname: Eidelberg fullname: Eidelberg, David email: deidelbe@northwell.edu organization: Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY, 11030, USA  | 
    
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40567285$$D View this record in MEDLINE/PubMed | 
    
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| Cites_doi | 10.1016/j.neuroimage.2016.12.036 10.1016/j.parkreldis.2018.02.013 10.2967/jnumed.117.202242 10.1073/pnas.0811879106 10.1093/brain/awm086 10.1016/j.neuroimage.2010.09.028 10.1038/npjparkd.2016.25 10.1016/j.tins.2009.06.003 10.1073/pnas.1411011112 10.1016/j.neuroimage.2016.09.008 10.1002/ana.23631 10.1007/s00259-020-04785-z 10.3389/fnhum.2019.00164 10.1093/brain/awq212 10.1016/j.neuroimage.2010.10.025 10.1007/s00234-017-1821-3 10.1136/jnnp.55.3.181 10.1371/journal.pone.0088119 10.1007/s00259-019-04570-7 10.1016/j.neuroimage.2011.07.012 10.3389/fnhum.2018.00422 10.3389/fnins.2020.00779 10.1136/jnnp-2013-306237 10.1371/journal.pone.0063691 10.1038/jcbfm.2015.118 10.1007/s12311-016-0781-1 10.1002/hbm.22863 10.1016/j.neuroimage.2019.06.012 10.3389/fnagi.2020.00125 10.3233/JPD-202117 10.1212/WNL.0000000000000130 10.1016/j.parkreldis.2013.02.013 10.3389/fneur.2017.00346 10.1006/nimg.2001.0978 10.1093/cercor/bhz280 10.1093/cercor/10.5.529 10.1523/JNEUROSCI.4188-09.2010 10.1016/j.parkreldis.2007.06.008 10.3389/fnins.2015.00395 10.3389/fnins.2019.00825 10.1093/brain/awz007 10.1093/brain/awl162 10.1002/hbm.23260 10.1038/nn.4478  | 
    
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| Keywords | Parkinson's disease DRS MRI ICA SMA Independent component analysis rs-fMRI ROI fMRI PD UPDRS-III MMSE PDRP Resting-state functional MRI HC PANDA Brain network PET  | 
    
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| References | Griffanti, Douaud, Bijsterbosch, Evangelisti, Alfaro-Almagro, Glasser, Duff, Fitzgibbon, Westphal, Carone, Beckmann, Smith (bib8) 2017; 154 Tang, Holtbernd, Ma, Spetsieris, Oh, Fink, Timmermann, Eggers, Eidelberg (bib36) 2020; 10 Liu (bib17) 2016; 143 Mure, Hirano, Tang, Isaias, Antonini, Ma, Dhawan, Eidelberg (bib24) 2011; 54 Eidelberg (bib5) 2009; 32 Spetsieris, Ko, Tang, Nazem, Sako, Peng, Ma, Dhawan, Eidelberg (bib34) 2015; 112 Tzourio-Mazoyer, Landeau, Papathanassiou, Crivello, Etard, Delcroix, Mazoyer, Joliot (bib39) 2002; 15 Hammes, Theis, Giehl, Hoenig, Greuel, Tittgemeyer, Timmermann, Fink, Drzezga, Eggers, van Eimeren (bib9) 2019; 142 Tang, Poston, Dhawan, Eidelberg (bib35) 2010; 30 Meles, Renken, Janzen, Vadasz, Pagani, Arnaldi, Morbelli, Nobili, Mayer, Leenders, Oertel (bib22) 2018; 59 Al-Zubaidi, Mertins, Heldmann, Jauch-Chara, Münte (bib1) 2019; 13 Péran, Cherubini, Assogna, Piras, Quattrocchi, Peppe, Celsis, Rascol, Démonet, Stefani, Pierantozzi, Pontieri, Caltagirone, Spalletta, Sabatini (bib27) 2010; 133 Schindlbeck, Vo, Nguyen, Tang, Niethammer, Dhawan, Brandt, Saunders-Pullman, Bressman, Eidelberg (bib30) 2020; 30 Wu, Wang, Peng, Ma, Zhang, Guan, Zuo (bib44) 2013; 19 Kalbe, Calabrese, Kohn, Hilker, Riedel, Wittchen, Dodel, Otto, Ebersbach, Kessler (bib14) 2008; 14 Liu, Jiang, Zhou, Zhang, Wang, Jiang, Wu, Ge, Wang, Ma, Zuo (bib18) 2020; 12 Wen, Wu, Liu, Li, Yao (bib42) 2013; 8 Meles, Renken, Pagani, Teune, Arnaldi, Morbelli, Nobili, van Laar, Obeso, Rodríguez-Oroz, Leenders (bib23) 2020; 47 Spetsieris, Eidelberg (bib33) 2020 Zhang, Ding, Xu, Tang, Guo (bib48) 2020 Wu, Ma, Zheng, Peng, Wu, Eidelberg, Chan (bib45) 2015; 35 Park, Pae, Friston, Jang, Razi, Zeidman, Chang, Chang (bib26) 2017; 8 Skidmore, Yang, Baxter, von Deneen, Collingwood, He, Tandon, Korenkevych, Savenkov, Heilman, Gold, Liu (bib31) 2013; 81 Holtbernd, Ma, Peng, Schwartz, Timmermann, Kracht, Fink, Tang, Eidelberg, Eggers (bib11) 2015; 36 Schindlbeck, Eidelberg (bib29) 2018; 17 Zeng, Xie, Shen, Luo, Fang, Hou, Tang, Wu, Hu (bib46) 2017; 16 Ko, Spetsieris, Ma, Dhawan, Eidelberg (bib15) 2014; 9 Mattis, Bellak, Karasu (bib21) 1976 Maknojia, Churchill, Schweizer, Graham (bib20) 2019; 13 Khosla, Jamison, Kuceyeski, Sabuncu (bib49) 2019; 199 Woo, Chang, Lindquist, Wager (bib43) 2017; 20 Wei, Chen, Li, Liu, Qiu, Wei (bib41) 2018; 12 Ko, Spetsieris, Eidelberg (bib16) 2018; 28 Holtbernd, Gagnon, Postuma, Ma, Tang, Feigin, Dhawan, Vendette, Soucy, Eidelberg, Montplaisir (bib10) 2014; 82 Tuovinen, Seppi, de Pasquale, Müller, Nocker, Schocke, Gizewski, Kremser, Wenning, Poewe, Djamshidian, Scherfler, Seki (bib38) 2018; 50 Vo, Sako, Fujita, Peng, Mattis, Skidmore, Ma, Uluğ, Eidelberg (bib40) 2017; 38 Zhang, Wang, Liu, Zhang (bib47) 2020; 14 Asanuma, Tang, Ma, Dhawan, Mattis, Edwards, Kaplitt, Feigin, Eidelberg (bib2) 2006; 129 Caligiore, Helmich, Hallett, Moustafa, Timmermann, Toni, Baldassarre (bib4) 2016; 2 Huang, Tang, Feigin, Lesser, Ma, Pourfar, Dhawan, Eidelberg (bib12) 2007; 130 Tomše, Jensterle, Grmek, Zaletel, Pirtošek, Dhawan, Peng, Eidelberg, Ma, Trošt (bib37) 2017; 59 Luo, Chen, Song, Chen, Guo, Yang, Huang, Gong, Shang (bib19) 2014; 85 Boroojerdi, Bushara, Corwell, Immisch, Battaglia, Muellbacher, Cohen (bib3) 2000; 10 Spetsieris, Eidelberg (bib32) 2011; 54 Rus, Tomše, Jensterle, Grmek, Pirtošek, Eidelberg, Tang, Trošt (bib28) 2020; 47 Filippini, MacIntosh, Hough, Goodwin, Frisoni, Smith, Matthews, Beckmann, Mackay (bib7) 2009; 106 Feis, Smith, Filippini, Douaud, Dopper, Heise, Trachtenberg, van Swieten, van Buchem, Rombouts, Mackay (bib6) 2015; 9 Hughes, Daniel, Kilford, Lees (bib13) 1992; 55 Niethammer, Eidelberg (bib25) 2012; 72 Mure (10.1016/j.ynirp.2021.100026_bib24) 2011; 54 Caligiore (10.1016/j.ynirp.2021.100026_bib4) 2016; 2 Holtbernd (10.1016/j.ynirp.2021.100026_bib11) 2015; 36 Schindlbeck (10.1016/j.ynirp.2021.100026_bib30) 2020; 30 Wu (10.1016/j.ynirp.2021.100026_bib45) 2015; 35 Tuovinen (10.1016/j.ynirp.2021.100026_bib38) 2018; 50 Wu (10.1016/j.ynirp.2021.100026_bib44) 2013; 19 Liu (10.1016/j.ynirp.2021.100026_bib17) 2016; 143 Zhang (10.1016/j.ynirp.2021.100026_bib48) 2020 Rus (10.1016/j.ynirp.2021.100026_bib28) 2020; 47 Liu (10.1016/j.ynirp.2021.100026_bib18) 2020; 12 Al-Zubaidi (10.1016/j.ynirp.2021.100026_bib1) 2019; 13 Hammes (10.1016/j.ynirp.2021.100026_bib9) 2019; 142 Filippini (10.1016/j.ynirp.2021.100026_bib7) 2009; 106 Maknojia (10.1016/j.ynirp.2021.100026_bib20) 2019; 13 Spetsieris (10.1016/j.ynirp.2021.100026_bib32) 2011; 54 Schindlbeck (10.1016/j.ynirp.2021.100026_bib29) 2018; 17 Skidmore (10.1016/j.ynirp.2021.100026_bib31) 2013; 81 Meles (10.1016/j.ynirp.2021.100026_bib23) 2020; 47 Tang (10.1016/j.ynirp.2021.100026_bib35) 2010; 30 Boroojerdi (10.1016/j.ynirp.2021.100026_bib3) 2000; 10 Tang (10.1016/j.ynirp.2021.100026_bib36) 2020; 10 Spetsieris (10.1016/j.ynirp.2021.100026_bib33) 2020 Mattis (10.1016/j.ynirp.2021.100026_bib21) 1976 Meles (10.1016/j.ynirp.2021.100026_bib22) 2018; 59 Péran (10.1016/j.ynirp.2021.100026_bib27) 2010; 133 Woo (10.1016/j.ynirp.2021.100026_bib43) 2017; 20 Zeng (10.1016/j.ynirp.2021.100026_bib46) 2017; 16 Wen (10.1016/j.ynirp.2021.100026_bib42) 2013; 8 Holtbernd (10.1016/j.ynirp.2021.100026_bib10) 2014; 82 Khosla (10.1016/j.ynirp.2021.100026_bib49) 2019; 199 Spetsieris (10.1016/j.ynirp.2021.100026_bib34) 2015; 112 Ko (10.1016/j.ynirp.2021.100026_bib15) 2014; 9 Park (10.1016/j.ynirp.2021.100026_bib26) 2017; 8 Feis (10.1016/j.ynirp.2021.100026_bib6) 2015; 9 Niethammer (10.1016/j.ynirp.2021.100026_bib25) 2012; 72 Tomše (10.1016/j.ynirp.2021.100026_bib37) 2017; 59 Huang (10.1016/j.ynirp.2021.100026_bib12) 2007; 130 Kalbe (10.1016/j.ynirp.2021.100026_bib14) 2008; 14 Ko (10.1016/j.ynirp.2021.100026_bib16) 2018; 28 Griffanti (10.1016/j.ynirp.2021.100026_bib8) 2017; 154 Zhang (10.1016/j.ynirp.2021.100026_bib47) 2020; 14 Eidelberg (10.1016/j.ynirp.2021.100026_bib5) 2009; 32 Asanuma (10.1016/j.ynirp.2021.100026_bib2) 2006; 129 Vo (10.1016/j.ynirp.2021.100026_bib40) 2017; 38 Luo (10.1016/j.ynirp.2021.100026_bib19) 2014; 85 Tzourio-Mazoyer (10.1016/j.ynirp.2021.100026_bib39) 2002; 15 Wei (10.1016/j.ynirp.2021.100026_bib41) 2018; 12 Hughes (10.1016/j.ynirp.2021.100026_bib13) 1992; 55  | 
    
| References_xml | – volume: 9 year: 2014 ident: bib15 article-title: Quantifying significance of topographical similarities of disease-related brain metabolic patterns publication-title: PloS One – volume: 8 year: 2013 ident: bib42 article-title: Abnormal baseline brain activity in non-depressed Parkinson's disease and depressed Parkinson's disease: a resting-state functional magnetic resonance imaging study publication-title: PloS One – volume: 81 start-page: 484 year: 2013 end-page: 495 ident: bib31 article-title: Apathy, depression, and motor symptoms have distinct and separable resting activity patterns in idiopathic Parkinson disease publication-title: Neuroimage – volume: 14 year: 2020 ident: bib47 article-title: A survey on deep learning for neuroimaging-based brain disorder analysis publication-title: Front. Neurosci. – volume: 154 start-page: 188 year: 2017 end-page: 205 ident: bib8 article-title: Hand classification of fMRI ICA noise components publication-title: Neuroimage – volume: 47 start-page: 437 year: 2020 end-page: 450 ident: bib23 article-title: Abnormal pattern of brain glucose metabolism in Parkinson's disease: replication in three European cohorts publication-title: Eur. J. Nucl. Med. Mol. Imag. – volume: 50 start-page: 61 year: 2018 end-page: 68 ident: bib38 article-title: The reorganization of functional architecture in the early-stages of Parkinson's disease publication-title: Park. Relat. Disord. – volume: 106 start-page: 7209 year: 2009 end-page: 7214 ident: bib7 article-title: Distinct patterns of brain activity in young carriers of the APOE-epsilon4 allele publication-title: Proc. Natl. Acad. Sci. U.S.A. – volume: 8 start-page: 346 year: 2017 ident: bib26 article-title: Hierarchical dynamic causal modeling of resting-state fMRI reveals longitudinal changes in effective connectivity in the motor system after thalamotomy for essential tremor publication-title: Front. Neurol. – volume: 59 start-page: 1437 year: 2018 end-page: 1444 ident: bib22 article-title: The metabolic pattern of idiopathic REM sleep behavior disorder reflects early-stage Parkinson disease publication-title: J. Nucl. Med. : Off. Publ. Soc. Nucl. Med. – volume: 19 start-page: 622 year: 2013 end-page: 627 ident: bib44 article-title: Metabolic brain network in the Chinese patients with Parkinson's disease based on 18F-FDG PET imaging publication-title: Park. Relat. Disord. – volume: 133 start-page: 3423 year: 2010 end-page: 3433 ident: bib27 article-title: Magnetic resonance imaging markers of Parkinson's disease nigrostriatal signature publication-title: Brain – volume: 12 start-page: 422 year: 2018 ident: bib41 article-title: Eyes-open and eyes-closed resting states with opposite brain activity in sensorimotor and occipital regions: multidimensional evidences from machine learning perspective publication-title: Front. Hum. Neurosci. – volume: 20 start-page: 365 year: 2017 end-page: 377 ident: bib43 article-title: Building better biomarkers: brain models in translational neuroimaging publication-title: Nat. Neurosci. – volume: 16 start-page: 151 year: 2017 end-page: 157 ident: bib46 article-title: Differentiating patients with Parkinson's disease from normal controls using gray matter in the cerebellum publication-title: Cerebellum – volume: 17 start-page: 629 year: 2018 end-page: 640 ident: bib29 article-title: Network imaging biomarkers: insights and clinical applications in Parkinson's disease. The Lancet publication-title: Neurology – volume: 142 start-page: 733 year: 2019 end-page: 743 ident: bib9 article-title: Dopamine metabolism of the nucleus accumbens and fronto-striatal connectivity modulate impulse control publication-title: Brain : J. Neurol. – volume: 13 start-page: 164 year: 2019 ident: bib1 article-title: Machine learning based classification of resting-state fMRI features exemplified by metabolic state (Hunger/Satiety) publication-title: Front. Hum. Neurosci. – volume: 129 start-page: 2667 year: 2006 end-page: 2678 ident: bib2 article-title: Network modulation in the treatment of Parkinson's disease publication-title: Brain : J. Neurol. – volume: 14 start-page: 93 year: 2008 end-page: 101 ident: bib14 article-title: Screening for cognitive deficits in Parkinson's disease with the Parkinson neuropsychometric dementia assessment (PANDA) instrument publication-title: Park. Relat. Disord. – volume: 199 start-page: 651 year: 2019 end-page: 662 ident: bib49 article-title: Ensemble learning with 3D convolutional neural networks for functional connectome-based prediction publication-title: Neuroimage – volume: 38 start-page: 617 year: 2017 end-page: 630 ident: bib40 article-title: Parkinson's disease-related network topographies characterized with resting state functional MRI publication-title: Hum. Brain Mapp. – volume: 130 start-page: 1834 year: 2007 end-page: 1846 ident: bib12 article-title: Changes in network activity with the progression of Parkinson's disease publication-title: Brain : J. Neurol. – volume: 59 start-page: 507 year: 2017 end-page: 515 ident: bib37 article-title: Abnormal metabolic brain network associated with Parkinson's disease: replication on a new European sample publication-title: Neuroradiology – volume: 72 start-page: 635 year: 2012 end-page: 647 ident: bib25 article-title: Metabolic brain networks in translational neurology: concepts and applications publication-title: Ann. Neurol. – volume: 30 start-page: 1049 year: 2010 end-page: 1056 ident: bib35 article-title: Abnormalities in metabolic network activity precede the onset of motor symptoms in Parkinson's disease publication-title: J. Neurosci. : Off. J. Soc. Neurosci. – volume: 143 start-page: 141 year: 2016 end-page: 151 ident: bib17 article-title: Noise contributions to the fMRI signal: an overview publication-title: Neuroimage – volume: 32 start-page: 548 year: 2009 end-page: 557 ident: bib5 article-title: Metabolic brain networks in neurodegenerative disorders: a functional imaging approach publication-title: Trends Neurosci. – volume: 15 start-page: 273 year: 2002 end-page: 289 ident: bib39 article-title: Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain publication-title: Neuroimage – year: 2020 ident: bib48 article-title: Multi-scale time-series kernel-based learning method for brain disease diagnosis publication-title: IEEE J. Biomed. Health Inform. – volume: 82 start-page: 620 year: 2014 end-page: 627 ident: bib10 article-title: Abnormal metabolic network activity in REM sleep behavior disorder publication-title: Neurology – volume: 30 start-page: 2867 year: 2020 end-page: 2878 ident: bib30 article-title: LRRK2 and GBA variants exert distinct influences on Parkinson's disease-specific metabolic networks publication-title: Cerebr. Cortex – volume: 36 start-page: 3575 year: 2015 end-page: 3585 ident: bib11 article-title: Dopaminergic correlates of metabolic network activity in Parkinson's disease publication-title: Hum. Brain Mapp. – volume: 35 start-page: 1764 year: 2015 end-page: 1770 ident: bib45 article-title: Parkinson's disease-related spatial covariance pattern identified with resting-state functional MRI publication-title: J. Cerebr. Blood Flow Metabol. : Off. J. Int. Soc. Cerebr. Blood Flow Metabol. – volume: 2 start-page: 16025 year: 2016 ident: bib4 article-title: Parkinson's disease as a system-level disorder publication-title: NPJ Parkinson's disease – volume: 13 start-page: 825 year: 2019 ident: bib20 article-title: Resting state fMRI: going through the motions publication-title: Front. Neurosci. – volume: 28 start-page: 4121 year: 2018 end-page: 4135 ident: bib16 article-title: Network structure and function in Parkinson's disease publication-title: Cerebr. Cortex – start-page: 117568 year: 2020 ident: bib33 article-title: Spectral Guided Sparse Inverse Covariance Estimation of Metabolic Networks in Parkinson's Disease. NeuroImage – volume: 85 start-page: 675 year: 2014 end-page: 683 ident: bib19 article-title: Resting-state fMRI study on drug-naive patients with Parkinson's disease and with depression publication-title: J. Neurol. Neurosurg. Psychiatr. – volume: 112 start-page: 2563 year: 2015 end-page: 2568 ident: bib34 article-title: Metabolic resting-state brain networks in health and disease publication-title: Proc. Natl. Acad. Sci. U.S.A. – volume: 12 start-page: 125 year: 2020 ident: bib18 article-title: Brain functional and structural signatures in Parkinson's disease publication-title: Front. Aging Neurosci. – volume: 10 start-page: 529 year: 2000 end-page: 534 ident: bib3 article-title: Enhanced excitability of the human visual cortex induced by short-term light deprivation publication-title: Cerebr. Cortex – volume: 9 start-page: 395 year: 2015 ident: bib6 article-title: ICA-based artifact removal diminishes scan site differences in multi-center resting-state fMRI publication-title: Front. Neurosci. – start-page: 77 year: 1976 end-page: 121 ident: bib21 article-title: Mental status examination for organic mental syndrome in the elderly patient publication-title: Geriatric Psychiatry. A Handbook for Psychiatrists and Primary Care Physicians – volume: 54 start-page: 1244 year: 2011 end-page: 1253 ident: bib24 article-title: Parkinson's disease tremor-related metabolic network: characterization, progression, and treatment effects publication-title: Neuroimage – volume: 54 start-page: 2899 year: 2011 end-page: 2914 ident: bib32 article-title: Scaled subprofile modeling of resting state imaging data in Parkinson's disease: methodological issues publication-title: Neuroimage – volume: 47 start-page: 2901 year: 2020 end-page: 2910 ident: bib28 article-title: Differential diagnosis of parkinsonian syndromes: a comparison of clinical and automated - metabolic brain patterns' based approach publication-title: Eur. J. Nucl. Med. Mol. Imag. – volume: 55 start-page: 181 year: 1992 end-page: 184 ident: bib13 article-title: Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases publication-title: J. Neurol. Neurosurg. Psychiatr. – volume: 10 start-page: 1737 year: 2020 end-page: 1749 ident: bib36 article-title: Hemispheric network expression in Parkinson's disease: relationship to dopaminergic asymmetries publication-title: J. Parkinsons Dis. – volume: 154 start-page: 188 year: 2017 ident: 10.1016/j.ynirp.2021.100026_bib8 article-title: Hand classification of fMRI ICA noise components publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.12.036 – volume: 50 start-page: 61 year: 2018 ident: 10.1016/j.ynirp.2021.100026_bib38 article-title: The reorganization of functional architecture in the early-stages of Parkinson's disease publication-title: Park. Relat. Disord. doi: 10.1016/j.parkreldis.2018.02.013 – volume: 59 start-page: 1437 issue: 9 year: 2018 ident: 10.1016/j.ynirp.2021.100026_bib22 article-title: The metabolic pattern of idiopathic REM sleep behavior disorder reflects early-stage Parkinson disease publication-title: J. Nucl. Med. : Off. Publ. Soc. Nucl. Med. doi: 10.2967/jnumed.117.202242 – volume: 106 start-page: 7209 issue: 17 year: 2009 ident: 10.1016/j.ynirp.2021.100026_bib7 article-title: Distinct patterns of brain activity in young carriers of the APOE-epsilon4 allele publication-title: Proc. Natl. Acad. Sci. U.S.A. doi: 10.1073/pnas.0811879106 – volume: 130 start-page: 1834 issue: Pt 7 year: 2007 ident: 10.1016/j.ynirp.2021.100026_bib12 article-title: Changes in network activity with the progression of Parkinson's disease publication-title: Brain : J. Neurol. doi: 10.1093/brain/awm086 – volume: 54 start-page: 1244 issue: 2 year: 2011 ident: 10.1016/j.ynirp.2021.100026_bib24 article-title: Parkinson's disease tremor-related metabolic network: characterization, progression, and treatment effects publication-title: Neuroimage doi: 10.1016/j.neuroimage.2010.09.028 – volume: 2 start-page: 16025 year: 2016 ident: 10.1016/j.ynirp.2021.100026_bib4 article-title: Parkinson's disease as a system-level disorder publication-title: NPJ Parkinson's disease doi: 10.1038/npjparkd.2016.25 – volume: 32 start-page: 548 issue: 10 year: 2009 ident: 10.1016/j.ynirp.2021.100026_bib5 article-title: Metabolic brain networks in neurodegenerative disorders: a functional imaging approach publication-title: Trends Neurosci. doi: 10.1016/j.tins.2009.06.003 – volume: 112 start-page: 2563 issue: 8 year: 2015 ident: 10.1016/j.ynirp.2021.100026_bib34 article-title: Metabolic resting-state brain networks in health and disease publication-title: Proc. Natl. Acad. Sci. U.S.A. doi: 10.1073/pnas.1411011112 – volume: 143 start-page: 141 year: 2016 ident: 10.1016/j.ynirp.2021.100026_bib17 article-title: Noise contributions to the fMRI signal: an overview publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.09.008 – volume: 72 start-page: 635 issue: 5 year: 2012 ident: 10.1016/j.ynirp.2021.100026_bib25 article-title: Metabolic brain networks in translational neurology: concepts and applications publication-title: Ann. Neurol. doi: 10.1002/ana.23631 – volume: 47 start-page: 2901 issue: 12 year: 2020 ident: 10.1016/j.ynirp.2021.100026_bib28 article-title: Differential diagnosis of parkinsonian syndromes: a comparison of clinical and automated - metabolic brain patterns' based approach publication-title: Eur. J. Nucl. Med. Mol. Imag. doi: 10.1007/s00259-020-04785-z – year: 2020 ident: 10.1016/j.ynirp.2021.100026_bib48 article-title: Multi-scale time-series kernel-based learning method for brain disease diagnosis publication-title: IEEE J. Biomed. Health Inform. – volume: 13 start-page: 164 year: 2019 ident: 10.1016/j.ynirp.2021.100026_bib1 article-title: Machine learning based classification of resting-state fMRI features exemplified by metabolic state (Hunger/Satiety) publication-title: Front. Hum. Neurosci. doi: 10.3389/fnhum.2019.00164 – volume: 28 start-page: 4121 issue: 12 year: 2018 ident: 10.1016/j.ynirp.2021.100026_bib16 article-title: Network structure and function in Parkinson's disease publication-title: Cerebr. Cortex – volume: 133 start-page: 3423 issue: 11 year: 2010 ident: 10.1016/j.ynirp.2021.100026_bib27 article-title: Magnetic resonance imaging markers of Parkinson's disease nigrostriatal signature publication-title: Brain doi: 10.1093/brain/awq212 – volume: 17 start-page: 629 issue: 7 year: 2018 ident: 10.1016/j.ynirp.2021.100026_bib29 article-title: Network imaging biomarkers: insights and clinical applications in Parkinson's disease. The Lancet publication-title: Neurology – start-page: 117568 year: 2020 ident: 10.1016/j.ynirp.2021.100026_bib33 – volume: 54 start-page: 2899 issue: 4 year: 2011 ident: 10.1016/j.ynirp.2021.100026_bib32 article-title: Scaled subprofile modeling of resting state imaging data in Parkinson's disease: methodological issues publication-title: Neuroimage doi: 10.1016/j.neuroimage.2010.10.025 – volume: 59 start-page: 507 issue: 5 year: 2017 ident: 10.1016/j.ynirp.2021.100026_bib37 article-title: Abnormal metabolic brain network associated with Parkinson's disease: replication on a new European sample publication-title: Neuroradiology doi: 10.1007/s00234-017-1821-3 – volume: 55 start-page: 181 issue: 3 year: 1992 ident: 10.1016/j.ynirp.2021.100026_bib13 article-title: Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases publication-title: J. Neurol. Neurosurg. Psychiatr. doi: 10.1136/jnnp.55.3.181 – volume: 9 issue: 1 year: 2014 ident: 10.1016/j.ynirp.2021.100026_bib15 article-title: Quantifying significance of topographical similarities of disease-related brain metabolic patterns publication-title: PloS One doi: 10.1371/journal.pone.0088119 – volume: 47 start-page: 437 issue: 2 year: 2020 ident: 10.1016/j.ynirp.2021.100026_bib23 article-title: Abnormal pattern of brain glucose metabolism in Parkinson's disease: replication in three European cohorts publication-title: Eur. J. Nucl. Med. Mol. Imag. doi: 10.1007/s00259-019-04570-7 – volume: 81 start-page: 484 year: 2013 ident: 10.1016/j.ynirp.2021.100026_bib31 article-title: Apathy, depression, and motor symptoms have distinct and separable resting activity patterns in idiopathic Parkinson disease publication-title: Neuroimage doi: 10.1016/j.neuroimage.2011.07.012 – volume: 12 start-page: 422 year: 2018 ident: 10.1016/j.ynirp.2021.100026_bib41 article-title: Eyes-open and eyes-closed resting states with opposite brain activity in sensorimotor and occipital regions: multidimensional evidences from machine learning perspective publication-title: Front. Hum. Neurosci. doi: 10.3389/fnhum.2018.00422 – volume: 14 year: 2020 ident: 10.1016/j.ynirp.2021.100026_bib47 article-title: A survey on deep learning for neuroimaging-based brain disorder analysis publication-title: Front. Neurosci. doi: 10.3389/fnins.2020.00779 – volume: 85 start-page: 675 issue: 6 year: 2014 ident: 10.1016/j.ynirp.2021.100026_bib19 article-title: Resting-state fMRI study on drug-naive patients with Parkinson's disease and with depression publication-title: J. Neurol. Neurosurg. Psychiatr. doi: 10.1136/jnnp-2013-306237 – volume: 8 issue: 5 year: 2013 ident: 10.1016/j.ynirp.2021.100026_bib42 article-title: Abnormal baseline brain activity in non-depressed Parkinson's disease and depressed Parkinson's disease: a resting-state functional magnetic resonance imaging study publication-title: PloS One doi: 10.1371/journal.pone.0063691 – volume: 35 start-page: 1764 issue: 11 year: 2015 ident: 10.1016/j.ynirp.2021.100026_bib45 article-title: Parkinson's disease-related spatial covariance pattern identified with resting-state functional MRI publication-title: J. Cerebr. Blood Flow Metabol. : Off. J. Int. Soc. Cerebr. Blood Flow Metabol. doi: 10.1038/jcbfm.2015.118 – volume: 16 start-page: 151 issue: 1 year: 2017 ident: 10.1016/j.ynirp.2021.100026_bib46 article-title: Differentiating patients with Parkinson's disease from normal controls using gray matter in the cerebellum publication-title: Cerebellum doi: 10.1007/s12311-016-0781-1 – volume: 36 start-page: 3575 issue: 9 year: 2015 ident: 10.1016/j.ynirp.2021.100026_bib11 article-title: Dopaminergic correlates of metabolic network activity in Parkinson's disease publication-title: Hum. Brain Mapp. doi: 10.1002/hbm.22863 – volume: 199 start-page: 651 year: 2019 ident: 10.1016/j.ynirp.2021.100026_bib49 article-title: Ensemble learning with 3D convolutional neural networks for functional connectome-based prediction publication-title: Neuroimage doi: 10.1016/j.neuroimage.2019.06.012 – volume: 12 start-page: 125 year: 2020 ident: 10.1016/j.ynirp.2021.100026_bib18 article-title: Brain functional and structural signatures in Parkinson's disease publication-title: Front. Aging Neurosci. doi: 10.3389/fnagi.2020.00125 – volume: 10 start-page: 1737 issue: 4 year: 2020 ident: 10.1016/j.ynirp.2021.100026_bib36 article-title: Hemispheric network expression in Parkinson's disease: relationship to dopaminergic asymmetries publication-title: J. Parkinsons Dis. doi: 10.3233/JPD-202117 – volume: 82 start-page: 620 issue: 7 year: 2014 ident: 10.1016/j.ynirp.2021.100026_bib10 article-title: Abnormal metabolic network activity in REM sleep behavior disorder publication-title: Neurology doi: 10.1212/WNL.0000000000000130 – volume: 19 start-page: 622 issue: 6 year: 2013 ident: 10.1016/j.ynirp.2021.100026_bib44 article-title: Metabolic brain network in the Chinese patients with Parkinson's disease based on 18F-FDG PET imaging publication-title: Park. Relat. Disord. doi: 10.1016/j.parkreldis.2013.02.013 – volume: 8 start-page: 346 year: 2017 ident: 10.1016/j.ynirp.2021.100026_bib26 article-title: Hierarchical dynamic causal modeling of resting-state fMRI reveals longitudinal changes in effective connectivity in the motor system after thalamotomy for essential tremor publication-title: Front. Neurol. doi: 10.3389/fneur.2017.00346 – volume: 15 start-page: 273 issue: 1 year: 2002 ident: 10.1016/j.ynirp.2021.100026_bib39 article-title: Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain publication-title: Neuroimage doi: 10.1006/nimg.2001.0978 – volume: 30 start-page: 2867 issue: 5 year: 2020 ident: 10.1016/j.ynirp.2021.100026_bib30 article-title: LRRK2 and GBA variants exert distinct influences on Parkinson's disease-specific metabolic networks publication-title: Cerebr. Cortex doi: 10.1093/cercor/bhz280 – volume: 10 start-page: 529 issue: 5 year: 2000 ident: 10.1016/j.ynirp.2021.100026_bib3 article-title: Enhanced excitability of the human visual cortex induced by short-term light deprivation publication-title: Cerebr. Cortex doi: 10.1093/cercor/10.5.529 – start-page: 77 year: 1976 ident: 10.1016/j.ynirp.2021.100026_bib21 article-title: Mental status examination for organic mental syndrome in the elderly patient – volume: 30 start-page: 1049 issue: 3 year: 2010 ident: 10.1016/j.ynirp.2021.100026_bib35 article-title: Abnormalities in metabolic network activity precede the onset of motor symptoms in Parkinson's disease publication-title: J. Neurosci. : Off. J. Soc. Neurosci. doi: 10.1523/JNEUROSCI.4188-09.2010 – volume: 14 start-page: 93 issue: 2 year: 2008 ident: 10.1016/j.ynirp.2021.100026_bib14 article-title: Screening for cognitive deficits in Parkinson's disease with the Parkinson neuropsychometric dementia assessment (PANDA) instrument publication-title: Park. Relat. Disord. doi: 10.1016/j.parkreldis.2007.06.008 – volume: 9 start-page: 395 year: 2015 ident: 10.1016/j.ynirp.2021.100026_bib6 article-title: ICA-based artifact removal diminishes scan site differences in multi-center resting-state fMRI publication-title: Front. Neurosci. doi: 10.3389/fnins.2015.00395 – volume: 13 start-page: 825 year: 2019 ident: 10.1016/j.ynirp.2021.100026_bib20 article-title: Resting state fMRI: going through the motions publication-title: Front. Neurosci. doi: 10.3389/fnins.2019.00825 – volume: 142 start-page: 733 issue: 3 year: 2019 ident: 10.1016/j.ynirp.2021.100026_bib9 article-title: Dopamine metabolism of the nucleus accumbens and fronto-striatal connectivity modulate impulse control publication-title: Brain : J. Neurol. doi: 10.1093/brain/awz007 – volume: 129 start-page: 2667 issue: Pt 10 year: 2006 ident: 10.1016/j.ynirp.2021.100026_bib2 article-title: Network modulation in the treatment of Parkinson's disease publication-title: Brain : J. Neurol. doi: 10.1093/brain/awl162 – volume: 38 start-page: 617 issue: 2 year: 2017 ident: 10.1016/j.ynirp.2021.100026_bib40 article-title: Parkinson's disease-related network topographies characterized with resting state functional MRI publication-title: Hum. Brain Mapp. doi: 10.1002/hbm.23260 – volume: 20 start-page: 365 issue: 3 year: 2017 ident: 10.1016/j.ynirp.2021.100026_bib43 article-title: Building better biomarkers: brain models in translational neuroimaging publication-title: Nat. Neurosci. doi: 10.1038/nn.4478  | 
    
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