Graph‐matching distance between individuals' functional connectomes varies with relatedness, age, and cognitive score

Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences...

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Published inHuman brain mapping Vol. 44; no. 9; pp. 3541 - 3554
Main Authors Bukhari, Hussain, Su, Chang, Dhamala, Elvisha, Gu, Zijin, Jamison, Keith, Kuceyeski, Amy
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 15.06.2023
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Abstract Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences between individuals also provides a rich source of information with which to map to differences in those individuals' biology, experience, genetics or behavior. In this study, graph matching is used to create a novel inter‐individual FC metric, called swap distance, that quantifies the distance between pairs of individuals' partial FCs, with a smaller swap distance indicating the individuals have more similar FC. We apply graph matching to align FCs between individuals from the the Human Connectome Project N=997 and find that swap distance (i) increases with increasing familial distance, (ii) increases with subjects' ages, (iii) is smaller for pairs of females compared to pairs of males, and (iv) is larger for females with lower cognitive scores compared to females with larger cognitive scores. Regions that contributed most to individuals' swap distances were in higher‐order networks, that is, default‐mode and fronto‐parietal, that underlie executive function and memory. These higher‐order networks' regions also had swap frequencies that varied monotonically with familial relatedness of the individuals in question. We posit that the proposed graph matching technique provides a novel way to study inter‐subject differences in FC and enables quantification of how FC may vary with age, relatedness, sex, and behavior. We use a novel graph‐matching metric, swap distance, to quantify differences between FCs of pairs of individuals and look at how this pairwise metric varies with age, sex, cognitive scores, and familial relationships. This metric highlights similarity of FCs between pairs of individuals, increases monotonically along with familial distance, increases with subjects' ages, is smaller for pairs of females compared to pairs of males, and is larger for females with lower cognitive scores compared to females with higher cognitive scores. Furthermore, higher‐order association regions like those in the frontoparietal and default mode network show more variability across individuals compared to lower regions belong to lower order networks.
AbstractList Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences between individuals also provides a rich source of information with which to map to differences in those individuals' biology, experience, genetics or behavior. In this study, graph matching is used to create a novel inter‐individual FC metric, called swap distance, that quantifies the distance between pairs of individuals' partial FCs, with a smaller swap distance indicating the individuals have more similar FC. We apply graph matching to align FCs between individuals from the the Human Connectome Project N = 997 and find that swap distance (i) increases with increasing familial distance, (ii) increases with subjects' ages, (iii) is smaller for pairs of females compared to pairs of males, and (iv) is larger for females with lower cognitive scores compared to females with larger cognitive scores. Regions that contributed most to individuals' swap distances were in higher‐order networks, that is, default‐mode and fronto‐parietal, that underlie executive function and memory. These higher‐order networks' regions also had swap frequencies that varied monotonically with familial relatedness of the individuals in question. We posit that the proposed graph matching technique provides a novel way to study inter‐subject differences in FC and enables quantification of how FC may vary with age, relatedness, sex, and behavior. We use a novel graph‐matching metric, swap distance, to quantify differences between FCs of pairs of individuals and look at how this pairwise metric varies with age, sex, cognitive scores, and familial relationships. This metric highlights similarity of FCs between pairs of individuals, increases monotonically along with familial distance, increases with subjects' ages, is smaller for pairs of females compared to pairs of males, and is larger for females with lower cognitive scores compared to females with higher cognitive scores. Furthermore, higher‐order association regions like those in the frontoparietal and default mode network show more variability across individuals compared to lower regions belong to lower order networks.
Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences between individuals also provides a rich source of information with which to map to differences in those individuals' biology, experience, genetics or behavior. In this study, graph matching is used to create a novel inter-individual FC metric, called swap distance, that quantifies the distance between pairs of individuals' partial FCs, with a smaller swap distance indicating the individuals have more similar FC. We apply graph matching to align FCs between individuals from the the Human Connectome Project N = 997 and find that swap distance (i) increases with increasing familial distance, (ii) increases with subjects' ages, (iii) is smaller for pairs of females compared to pairs of males, and (iv) is larger for females with lower cognitive scores compared to females with larger cognitive scores. Regions that contributed most to individuals' swap distances were in higher-order networks, that is, default-mode and fronto-parietal, that underlie executive function and memory. These higher-order networks' regions also had swap frequencies that varied monotonically with familial relatedness of the individuals in question. We posit that the proposed graph matching technique provides a novel way to study inter-subject differences in FC and enables quantification of how FC may vary with age, relatedness, sex, and behavior.Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences between individuals also provides a rich source of information with which to map to differences in those individuals' biology, experience, genetics or behavior. In this study, graph matching is used to create a novel inter-individual FC metric, called swap distance, that quantifies the distance between pairs of individuals' partial FCs, with a smaller swap distance indicating the individuals have more similar FC. We apply graph matching to align FCs between individuals from the the Human Connectome Project N = 997 and find that swap distance (i) increases with increasing familial distance, (ii) increases with subjects' ages, (iii) is smaller for pairs of females compared to pairs of males, and (iv) is larger for females with lower cognitive scores compared to females with larger cognitive scores. Regions that contributed most to individuals' swap distances were in higher-order networks, that is, default-mode and fronto-parietal, that underlie executive function and memory. These higher-order networks' regions also had swap frequencies that varied monotonically with familial relatedness of the individuals in question. We posit that the proposed graph matching technique provides a novel way to study inter-subject differences in FC and enables quantification of how FC may vary with age, relatedness, sex, and behavior.
Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences between individuals also provides a rich source of information with which to map to differences in those individuals' biology, experience, genetics or behavior. In this study, graph matching is used to create a novel inter‐individual FC metric, called swap distance, that quantifies the distance between pairs of individuals' partial FCs, with a smaller swap distance indicating the individuals have more similar FC. We apply graph matching to align FCs between individuals from the the Human Connectome Project N=997 and find that swap distance (i) increases with increasing familial distance, (ii) increases with subjects' ages, (iii) is smaller for pairs of females compared to pairs of males, and (iv) is larger for females with lower cognitive scores compared to females with larger cognitive scores. Regions that contributed most to individuals' swap distances were in higher‐order networks, that is, default‐mode and fronto‐parietal, that underlie executive function and memory. These higher‐order networks' regions also had swap frequencies that varied monotonically with familial relatedness of the individuals in question. We posit that the proposed graph matching technique provides a novel way to study inter‐subject differences in FC and enables quantification of how FC may vary with age, relatedness, sex, and behavior.
Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences between individuals also provides a rich source of information with which to map to differences in those individuals' biology, experience, genetics or behavior. In this study, graph matching is used to create a novel inter‐individual FC metric, called swap distance, that quantifies the distance between pairs of individuals' partial FCs, with a smaller swap distance indicating the individuals have more similar FC. We apply graph matching to align FCs between individuals from the the Human Connectome Project and find that swap distance (i) increases with increasing familial distance, (ii) increases with subjects' ages, (iii) is smaller for pairs of females compared to pairs of males, and (iv) is larger for females with lower cognitive scores compared to females with larger cognitive scores. Regions that contributed most to individuals' swap distances were in higher‐order networks, that is, default‐mode and fronto‐parietal, that underlie executive function and memory. These higher‐order networks' regions also had swap frequencies that varied monotonically with familial relatedness of the individuals in question. We posit that the proposed graph matching technique provides a novel way to study inter‐subject differences in FC and enables quantification of how FC may vary with age, relatedness, sex, and behavior.
Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences between individuals also provides a rich source of information with which to map to differences in those individuals' biology, experience, genetics or behavior. In this study, graph matching is used to create a novel inter‐individual FC metric, called swap distance, that quantifies the distance between pairs of individuals' partial FCs, with a smaller swap distance indicating the individuals have more similar FC. We apply graph matching to align FCs between individuals from the the Human Connectome Project N=997 and find that swap distance (i) increases with increasing familial distance, (ii) increases with subjects' ages, (iii) is smaller for pairs of females compared to pairs of males, and (iv) is larger for females with lower cognitive scores compared to females with larger cognitive scores. Regions that contributed most to individuals' swap distances were in higher‐order networks, that is, default‐mode and fronto‐parietal, that underlie executive function and memory. These higher‐order networks' regions also had swap frequencies that varied monotonically with familial relatedness of the individuals in question. We posit that the proposed graph matching technique provides a novel way to study inter‐subject differences in FC and enables quantification of how FC may vary with age, relatedness, sex, and behavior. We use a novel graph‐matching metric, swap distance, to quantify differences between FCs of pairs of individuals and look at how this pairwise metric varies with age, sex, cognitive scores, and familial relationships. This metric highlights similarity of FCs between pairs of individuals, increases monotonically along with familial distance, increases with subjects' ages, is smaller for pairs of females compared to pairs of males, and is larger for females with lower cognitive scores compared to females with higher cognitive scores. Furthermore, higher‐order association regions like those in the frontoparietal and default mode network show more variability across individuals compared to lower regions belong to lower order networks.
Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a population level to age, sex, cognitive/behavioral scores, life experience, genetics, and disease/disorders. However, quantifying FC differences between individuals also provides a rich source of information with which to map to differences in those individuals' biology, experience, genetics or behavior. In this study, graph matching is used to create a novel inter-individual FC metric, called swap distance, that quantifies the distance between pairs of individuals' partial FCs, with a smaller swap distance indicating the individuals have more similar FC. We apply graph matching to align FCs between individuals from the the Human Connectome Project and find that swap distance (i) increases with increasing familial distance, (ii) increases with subjects' ages, (iii) is smaller for pairs of females compared to pairs of males, and (iv) is larger for females with lower cognitive scores compared to females with larger cognitive scores. Regions that contributed most to individuals' swap distances were in higher-order networks, that is, default-mode and fronto-parietal, that underlie executive function and memory. These higher-order networks' regions also had swap frequencies that varied monotonically with familial relatedness of the individuals in question. We posit that the proposed graph matching technique provides a novel way to study inter-subject differences in FC and enables quantification of how FC may vary with age, relatedness, sex, and behavior.
Author Su, Chang
Gu, Zijin
Kuceyeski, Amy
Jamison, Keith
Bukhari, Hussain
Dhamala, Elvisha
AuthorAffiliation 1 Department of Neuroscience Weill Cornell Medicine New York New York USA
4 Department of Electrical and Computer Engineering Cornell University Ithaca New York USA
3 Department of Psychology Yale University New Haven Connecticut USA
5 Department of Radiology Weill Cornell Medicine New York New York USA
2 Department of Biostatistics Yale University New Haven Connecticut USA
AuthorAffiliation_xml – name: 3 Department of Psychology Yale University New Haven Connecticut USA
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Cites_doi 10.1093/cercor/bhw332
10.1016/j.neuron.2017.07.011
10.1037/rep0000195
10.1073/pnas.1700765114
10.1002/hbm.25204
10.1073/pnas.1401651112
10.1016/j.imavis.2006.08.005
10.1002/hbm.25420
10.1111/mono.12031
10.1007/978-3-030-60365-6_13
10.1093/cercor/bht056
10.1093/cercor/bhaa391
10.1038/nn.4393
10.1017/S1355617714000472
10.1097/WCO.0b013e32832d93dd
10.1037/rep0000183
10.1523/JNEUROSCI.1443-09.2009
10.1017/S1355617714000241
10.1038/s41467-020-18974-9
10.1371/journal.pone.0111048
10.1523/JNEUROSCI.19-10-04065.1999
10.1016/j.neuroimage.2014.03.034
10.1038/s41467-021-25184-4
10.1016/j.neuroimage.2017.03.064
10.1016/j.neuroscience.2010.11.039
10.1016/j.neuroimage.2019.02.002
10.1038/s41598-019-42090-4
10.1088/1741-2552/ab947b
10.1073/pnas.1415122111
10.1038/nn.4135
10.1002/hbm.25709
10.1371/journal.pone.0249502
10.1016/j.neuroimage.2013.05.039
10.1016/j.neuroimage.2019.06.045
10.1093/cercor/bhaa123
10.1016/j.neuroimage.2019.116041
10.1016/j.neuron.2014.05.014
10.1016/j.neuroimage.2016.09.038
10.1016/j.tics.2013.09.016
10.1016/j.neuroimage.2013.04.007
10.1002/nav.3800020109
10.1016/j.neuroimage.2018.01.058
10.1017/pen.2018.4
10.1016/j.neuroimage.2021.118642
10.1146/annurev-clinpsy-040510-143934
10.1089/brain.2016.0429
10.1016/j.ymeth.2021.06.008
10.1371/journal.pcbi.0010042
10.1016/j.neuron.2019.11.012
10.1016/j.neuroimage.2013.04.127
10.1093/cercor/bhu012
10.1038/s41598-017-06389-4
10.1016/j.isci.2019.100801
10.1371/journal.pone.0222914
10.1073/pnas.0909969107
10.1152/jn.00338.2011
10.1016/j.neuroimage.2013.05.041
10.1017/S1355617714000320
10.1109/TPAMI.2008.245
10.1016/j.neuroimage.2021.118543
10.1016/j.neuroimage.2019.116157
10.1002/hbm.25894
10.1016/j.neuroimage.2014.07.067
10.1016/j.neuroimage.2020.116604
10.1162/netn_a_00166
10.1002/hbm.25118
10.1098/rstb.2017.0284
10.1002/hbm.21333
10.1371/journal.pone.0130045
10.1109/TMI.2021.3051604
10.1016/j.neuroimage.2019.05.064
10.1117/12.2580980
10.1038/nrn2575
10.1073/pnas.1906144117
10.1177/1073858404263960
10.1016/j.neuroimage.2012.11.039
10.1162/netn_a_00029
10.1016/j.neuroimage.2013.11.046
10.1212/WNL.0b013e3182872e5f
10.1093/cercor/bhy123
10.1016/j.neuroimage.2019.01.068
10.1017/S1355617714000307
10.1016/j.biopsych.2007.03.001
10.3389/fnhum.2017.00189
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Issue 9
Keywords functional MRI
functional connectome
inter-individual variability
graph-matching
Language English
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2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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Notes Hussain Bukhari and Chang Su contributed equally to this study.
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PublicationDate June 15, 2023
PublicationDateYYYYMMDD 2023-06-15
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  text: June 15, 2023
  day: 15
PublicationDecade 2020
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PublicationTitle Human brain mapping
PublicationTitleAlternate Hum Brain Mapp
PublicationYear 2023
Publisher John Wiley & Sons, Inc
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References 2017; 7
2010; 107
2021; 245
2021; 244
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2020; 17
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2008; 31
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2018; 172
1999; 19
2018; 1
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2019; 29
2020; 211
2007; 62
2014; 9
2014; 95
2021; 40
2019; 199
2007; 25
2022; 202
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2009; 22
2019; 9
2021; 42
2014; 90
2015; 18
2016; 19
2020; 41
2017; 27
2015; 10
2020; 105
2004
2022; 43
2014; 111
2014; 83
2012; 33
2011; 7
2019; 189
2009; 29
2011; 175
2017; 95
2004; 10
2016; 6
2015; 25
2021; 12
2011; 106
2020; 30
2021; 11596
2020
2013; 78
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References_xml – volume: 112
  start-page: 2942
  year: 2015
  end-page: 2947
  article-title: On convex relaxation of graph isomorphism
  publication-title: Proceedings of the National Academic Sciences of the United States of America
– volume: 106
  start-page: 1125
  year: 2011
  end-page: 1165
  article-title: The organization of the human cerebral cortex estimated by intrinsic functional connectivity
  publication-title: Journal of Neurophysiology
– volume: 27
  start-page: 5626
  year: 2017
  end-page: 5634
  article-title: Heritability of the effective connectivity in the resting‐state default mode network
  publication-title: Cerebral Cortex
– volume: 9
  start-page: 1
  year: 2019
  end-page: 11
  article-title: A comparison of static and dynamic functional connectivities for identifying subjects and biological sex using intrinsic individual brain connectivity
  publication-title: Scientific Reports
– volume: 1
  year: 2005
  article-title: The human connectome: A structural description of the human brain
  publication-title: PLoS Computational Biology
– volume: 83
  start-page: 238
  year: 2014
  end-page: 251
  article-title: Intrinsic and task‐evoked network architectures of the human brain
  publication-title: Neuron
– volume: 18
  start-page: 1664
  year: 2015
  end-page: 1671
  article-title: Functional connectome fingerprinting: Identifying individuals using patterns of brain connectivity
  publication-title: Nature Neuroscience
– volume: 17
  start-page: 666
  year: 2013
  end-page: 682
  article-title: Functional connectomics from resting‐state fMRI
  publication-title: Trends Cognitive Sciences
– volume: 42
  start-page: 3102
  year: 2021
  end-page: 3118
  article-title: Distinct functional and structural connections predict crystallised and fluid cognition in healthy adults
  publication-title: Human Brain Mapping
– volume: 172
  start-page: 740
  year: 2018
  end-page: 752
  article-title: Are you thinking what I'm thinking? Synchronization of resting fmri time‐series across subjects
  publication-title: NeuroImage
– volume: 25
  start-page: 1987
  year: 2015
  end-page: 1999
  article-title: A brain‐wide study of age‐related changes in functional connectivity
  publication-title: Cerebral Cortex
– volume: 11
  start-page: 1
  year: 2020
  end-page: 14
  article-title: Prevalent and sex‐biased breathing patterns modify functional connectivity mri in young adults
  publication-title: Nature Communications
– volume: 245
  year: 2021
  article-title: Functional connectome reorganization relates to post‐stroke motor recovery and structural and functional disconnection
  publication-title: NeuroImage
– volume: 160
  start-page: 140
  year: 2017
  end-page: 151
  article-title: Can brain state be manipulated to emphasize individual differences in functional connectivity?
  publication-title: NeuroImage
– volume: 11
  start-page: 189
  year: 2017
  article-title: Resting‐state functional connectivity and network analysis of cerebellum with respect to iq and gender
  publication-title: Frontiers Human Neuroscience
– volume: 175
  start-page: 169
  year: 2011
  end-page: 177
  article-title: Cognition is related to resting‐state small‐world network topology: An magnetoencephalographic study
  publication-title: Neuroscience
– volume: 30
  start-page: 5420
  year: 2020
  end-page: 5430
  article-title: Sex differences in variability of brain structure across the lifespan
  publication-title: Cerebral Cortex
– volume: 6
  start-page: 700
  year: 2016
  end-page: 713
  article-title: Sex and age effects of functional connectivity in early adulthood
  publication-title: Brain Connectivity
– volume: 373
  year: 2018
  article-title: A distributed brain network predicts general intelligence from resting‐state human neuroimaging data
  publication-title: Philosophical Transactions Royal Society B: Biological Sciences
– volume: 90
  start-page: 449
  year: 2014
  end-page: 468
  article-title: Automatic denoising of functional mri data: Combining independent component analysis and hierarchical fusion of classifiers
  publication-title: NeuroImage
– volume: 80
  start-page: 62
  year: 2013
  end-page: 79
  article-title: The wu‐minn human connectome project: An overview
  publication-title: NeuroImage
– volume: 17
  year: 2022
  article-title: Individualized spatial network predictions using siamese convolutional neural networks: A resting‐state fmri study of over 11,000 unaffected individuals
  publication-title: PLoS One
– volume: 9
  year: 2014
  article-title: Connectotyping: Model based fingerprinting of the functional connectome
  publication-title: PLoS One
– volume: 244
  year: 2021
  article-title: The human connectome project: A retrospective
  publication-title: NeuroImage
– volume: 78
  start-page: 1
  year: 2013
  end-page: 15
  article-title: I. Nih toolbox cognition battery (cb): Introduction and pediatric data
  publication-title: Monographs Society for Research Child Development
– volume: 62
  start-page: 443
  year: 2017
  end-page: 454
  article-title: Construct validity of the nih toolbox cognition battery in individuals with stroke
  publication-title: Rehabilitation Psychology
– volume: 95
  start-page: 232
  year: 2014
  end-page: 247
  article-title: Ica‐based artefact removal and accelerated fmri acquisition for improved resting state network imaging
  publication-title: NeuroImage
– volume: 19
  start-page: 4065
  year: 1999
  end-page: 4072
  article-title: Sex differences in brain gray and white matter in healthy young adults: Correlations with cognitive performance
  publication-title: Journal of Neuroscience
– volume: 203
  year: 2019
  article-title: A decade of test‐retest reliability of functional connectivity: A systematic review and meta‐analysis
  publication-title: NeuroImage
– volume: 31
  start-page: 2834
  year: 2021
  end-page: 2844
  article-title: Heritability of functional connectivity in resting state: Assessment of the dynamic mean, dynamic variance, and static connectivity across networks
  publication-title: Cerebral Cortex
– volume: 23
  year: 2020
  article-title: Functional connectivity fingerprints at rest are similar across youths and adults and vary with genetic similarity
  publication-title: iScience
– volume: 10
  year: 2015
  article-title: Graph theoretical analysis reveals: Women's brains are better connected than men's
  publication-title: PLoS One
– volume: 12
  start-page: 1
  year: 2021
  end-page: 12
  article-title: Heritability and interindividual variability of regional structurefunction coupling
  publication-title: Nature Communications
– volume: 20
  start-page: 620
  year: 2014
  end-page: 629
  article-title: Nih toolbox cognition battery (cb): Validation of executive function measures in adults
  publication-title: Journal International Neuropsychological Society
– volume: 24
  start-page: 2036
  year: 2014
  end-page: 2054
  article-title: Parcellating an individual subject's cortical and subcortical brain structures using snowball sampling of resting‐state correlations
  publication-title: Cerebral Cortex
– volume: 22
  start-page: 340
  year: 2009
  end-page: 347
  article-title: Human brain networks in health and disease
  publication-title: Current Opinion in Neurology
– year: 2004
– volume: 7
  start-page: 1
  year: 2017
  end-page: 13
  article-title: On wakefulness fluctuations as a source of bold functional connectivity dynamics
  publication-title: Scientific Reports
– volume: 17
  year: 2020
  article-title: Connectomic consistency: A systematic stability analysis of structural and functional connectivity
  publication-title: Journal of Neural Engineering
– volume: 10
  start-page: 186
  year: 2009
  end-page: 198
  article-title: Complex brain networks: Graph theoretical analysis of structural and functional systems
  publication-title: Nature Reviews Neuroscience
– volume: 20
  start-page: 588
  year: 2014
  end-page: 598
  article-title: Reliability and validity of composite scores from the nih toolbox cognition battery in adults
  publication-title: Journal International Neuropsychological Society
– volume: 62
  start-page: 435
  year: 2017
  end-page: 442
  article-title: Factor structure of the nih toolbox cognition battery in individuals with acquired brain injury
  publication-title: Rehabilitation Psychology
– volume: 80
  start-page: S2
  year: 2013
  end-page: S6
  article-title: Nih toolbox for assessment of neurological and behavioral function
  publication-title: Neurology
– volume: 114
  start-page: 5521
  year: 2017
  end-page: 5526
  article-title: Heritability analysis with repeat measurements and its application to resting‐state functional connectivity
  publication-title: Proceedings of the National Academic Sciences of the United States of America
– volume: 80
  start-page: 405
  year: 2013
  end-page: 415
  article-title: Learning and comparing functional connectomes across subjects
  publication-title: NeuroImage
– volume: 199
  start-page: 93
  year: 2019
  end-page: 104
  article-title: System‐level matching of structural and functional connectomes in the human brain
  publication-title: NeuroImage
– volume: 95
  start-page: 791
  year: 2017
  end-page: 807
  article-title: Precision functional mapping of individual human brains
  publication-title: Neuron
– volume: 7
  start-page: 113
  year: 2011
  end-page: 140
  article-title: Brain graphs: Graphical models of the human brain connectome
  publication-title: Annual Review Clinical Psychology
– volume: 29
  start-page: 2533
  year: 2019
  end-page: 2551
  article-title: Spatial topography of individual‐specific cortical networks predicts human cognition, personality, and emotion
  publication-title: Cerebral Cortex
– volume: 40
  start-page: 1279
  year: 2021
  end-page: 1289
  article-title: A mutual multi‐scale triplet graph convolutional network for classification of brain disorders using functional or structural connectivity
  publication-title: IEEE Transactions on Medical Imaging
– volume: 102
  start-page: 345
  year: 2014
  end-page: 357
  article-title: Changes in structural and functional connectivity among resting‐state networks across the human lifespan
  publication-title: NeuroImage
– volume: 10
  start-page: 372
  year: 2004
  end-page: 392
  article-title: Mapping changes in the human cortex throughout the span of life
  publication-title: The Neuroscientist
– volume: 211
  year: 2020
  article-title: Optimising network modelling methods for fmri
  publication-title: NeuroImage
– volume: 1
  year: 2018
  article-title: Network approaches to understand individual differences in brain connectivity: Opportunities for personality neuroscience
  publication-title: Personality Neuroscience
– volume: 80
  start-page: 144
  year: 2013
  end-page: 168
  article-title: Resting‐state fmri in the human connectome project
  publication-title: NeuroImage
– volume: 80
  start-page: 105
  year: 2013
  end-page: 124
  article-title: The minimal preprocessing pipelines for the human connectome project
  publication-title: NeuroImage
– volume: 11596
  start-page: 96
  year: 2021
  end-page: 102
– volume: 4
  start-page: 1235
  year: 2020
  end-page: 1251
  article-title: Revisiting correlation‐based functional connectivity and its relationship with structural connectivity
  publication-title: Network Neuroscience
– volume: 43
  start-page: 3944
  year: 2022
  end-page: 3957
  article-title: Connectomic assessment of injury burden and longitudinal structural network alterations in moderate‐to‐severe traumatic brain injury
  publication-title: Human Brain Mapping
– volume: 20
  start-page: 579
  year: 2014
  end-page: 587
  article-title: Factor structure, convergent validity, and discriminant validity of the nih toolbox cognitive health battery (nihtb‐chb) in adults
  publication-title: Journal International Neuropsychological Society
– volume: 31
  start-page: 2227
  year: 2008
  end-page: 2242
  article-title: A path following algorithm for the graph matching problem
  publication-title: IEEE Transactions on Pattern Analysis Machine Intelligence
– volume: 107
  start-page: 1223
  year: 2010
  end-page: 1228
  article-title: Genetic control over the resting brain
  publication-title: Proceedings of the National Academic Sciences of the United States of America
– volume: 14
  year: 2019
  article-title: Intersubject mvpd: Empirical comparison of fmri denoising methods for connectivity analysis
  publication-title: PLoS One
– volume: 62
  start-page: 847
  year: 2007
  end-page: 855
  article-title: Evolving knowledge of sex differences in brain structure, function, and chemistry
  publication-title: Biological Psychiatry
– volume: 29
  start-page: 7619
  year: 2009
  end-page: 7624
  article-title: Efficiency of functional brain networks and intellectual performance
  publication-title: Journal of Neuroscience
– volume: 43
  start-page: 470
  year: 2022
  end-page: 499
  article-title: Greater male than female variability in regional brain structure across the lifespan
  publication-title: Human Brain Mapping
– volume: 19
  start-page: 1523
  year: 2016
  end-page: 1536
  article-title: Multimodal population brain imaging in the UK biobank prospective epidemiological study
  publication-title: Nature Neuroscience
– volume: 33
  start-page: 1914
  year: 2012
  end-page: 1928
  article-title: A whole brain fmri atlas generated via spatially constrained spectral clustering
  publication-title: Human Brain Mapping
– volume: 2
  start-page: 83
  year: 1955
  end-page: 97
  article-title: The Hungarian method for the assignment problem
  publication-title: Naval Research Logistics Quarterly
– volume: 43
  start-page: 1087
  year: 2022
  end-page: 1102
  article-title: Shared functional connections within and between cortical networks predict cognitive abilities in adult males and females
  publication-title: Human Brain Mapping
– volume: 189
  start-page: 676
  year: 2019
  end-page: 687
  article-title: The individual functional connectome is unique and stable over months to years
  publication-title: NeuroImage
– volume: 202
  start-page: 3
  year: 2022
  end-page: 13
  article-title: Graph matching survey for medical imaging: On the way to deep learning
  publication-title: Methods
– volume: 189
  start-page: 516
  year: 2019
  end-page: 532
  article-title: General functional connectivity: Shared features of resting‐state and task fmri drive reliable and heritable individual differences in functional brain networks
  publication-title: NeuroImage
– volume: 105
  start-page: 742
  year: 2020
  end-page: 758
  article-title: Integrative and network‐specific connectivity of the basal ganglia and thalamus defined in individuals
  publication-title: Neuron
– volume: 146
  start-page: 609
  year: 2017
  end-page: 625
  article-title: Sources and implications of whole‐brain fmri signals in humans
  publication-title: NeuroImage
– start-page: 131
  year: 2020
  end-page: 141
– volume: 68
  start-page: 63
  year: 2013
  end-page: 74
  article-title: Alzheimer's disease neuroimaging initiative brain development and aging: Overlapping and unique patterns of change
  publication-title: NeuroImage
– volume: 201
  year: 2019
  article-title: Distinctions among real and apparent respiratory motions in human fmri data
  publication-title: NeuroImage
– volume: 117
  start-page: 3248
  year: 2020
  end-page: 3253
  article-title: Conservative and disruptive modes of adolescent change in human brain functional connectivity
  publication-title: Proceedings of the National Academic Sciences of the United States of America
– volume: 20
  start-page: 567
  year: 2014
  end-page: 578
  article-title: The cognition battery of the nih toolbox for assessment of neurological and behavioral function: Validation in an adult sample
  publication-title: Journal International Neuropsychological Society
– volume: 2
  start-page: 175
  year: 2018
  end-page: 199
  article-title: Heritability of the human connectome: A connectotyping study
  publication-title: Network Neuroscience
– volume: 202
  year: 2019
  article-title: Uncovering multi‐site identifiability based on resting‐state functional connectomes
  publication-title: NeuroImage
– volume: 41
  start-page: 4187
  year: 2020
  end-page: 4199
  article-title: Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart
  publication-title: Human Brain Mapping
– volume: 111
  start-page: E4997
  year: 2014
  end-page: E5006
  article-title: Decreased segregation of brain systems across the healthy adult lifespan
  publication-title: Proceedings of the National Academic Sciences of the United States of America
– volume: 25
  start-page: 1301
  year: 2007
  end-page: 1314
  article-title: Evaluation of a convex relaxation to a quadratic assignment matching approach for relational object views
  publication-title: Image Vision Computing
– ident: e_1_2_7_82_1
  doi: 10.1093/cercor/bhw332
– ident: e_1_2_7_79_1
– ident: e_1_2_7_29_1
  doi: 10.1016/j.neuron.2017.07.011
– ident: e_1_2_7_9_1
  doi: 10.1037/rep0000195
– ident: e_1_2_7_24_1
  doi: 10.1073/pnas.1700765114
– ident: e_1_2_7_80_1
  doi: 10.1002/hbm.25204
– ident: e_1_2_7_2_1
  doi: 10.1073/pnas.1401651112
– ident: e_1_2_7_62_1
  doi: 10.1016/j.imavis.2006.08.005
– ident: e_1_2_7_15_1
  doi: 10.1002/hbm.25420
– ident: e_1_2_7_77_1
  doi: 10.1111/mono.12031
– ident: e_1_2_7_63_1
  doi: 10.1007/978-3-030-60365-6_13
– ident: e_1_2_7_81_1
  doi: 10.1093/cercor/bht056
– ident: e_1_2_7_3_1
  doi: 10.1093/cercor/bhaa391
– ident: e_1_2_7_48_1
  doi: 10.1038/nn.4393
– ident: e_1_2_7_85_1
  doi: 10.1017/S1355617714000472
– ident: e_1_2_7_5_1
  doi: 10.1097/WCO.0b013e32832d93dd
– ident: e_1_2_7_72_1
  doi: 10.1037/rep0000183
– ident: e_1_2_7_73_1
  doi: 10.1523/JNEUROSCI.1443-09.2009
– ident: e_1_2_7_36_1
  doi: 10.1017/S1355617714000241
– ident: e_1_2_7_46_1
  doi: 10.1038/s41467-020-18974-9
– ident: e_1_2_7_50_1
  doi: 10.1371/journal.pone.0111048
– ident: e_1_2_7_33_1
  doi: 10.1523/JNEUROSCI.19-10-04065.1999
– ident: e_1_2_7_31_1
  doi: 10.1016/j.neuroimage.2014.03.034
– ident: e_1_2_7_32_1
  doi: 10.1038/s41467-021-25184-4
– ident: e_1_2_7_21_1
  doi: 10.1016/j.neuroimage.2017.03.064
– ident: e_1_2_7_17_1
  doi: 10.1016/j.neuroscience.2010.11.039
– ident: e_1_2_7_37_1
  doi: 10.1016/j.neuroimage.2019.02.002
– ident: e_1_2_7_47_1
  doi: 10.1038/s41598-019-42090-4
– ident: e_1_2_7_54_1
  doi: 10.1088/1741-2552/ab947b
– ident: e_1_2_7_10_1
  doi: 10.1073/pnas.1415122111
– ident: e_1_2_7_22_1
  doi: 10.1038/nn.4135
– ident: e_1_2_7_16_1
  doi: 10.1002/hbm.25709
– ident: e_1_2_7_35_1
  doi: 10.1371/journal.pone.0249502
– ident: e_1_2_7_64_1
  doi: 10.1016/j.neuroimage.2013.05.039
– ident: e_1_2_7_4_1
  doi: 10.1016/j.neuroimage.2019.06.045
– ident: e_1_2_7_23_1
  doi: 10.1093/cercor/bhaa123
– ident: e_1_2_7_59_1
  doi: 10.1016/j.neuroimage.2019.116041
– ident: e_1_2_7_11_1
  doi: 10.1016/j.neuron.2014.05.014
– ident: e_1_2_7_60_1
  doi: 10.1016/j.neuroimage.2016.09.038
– ident: e_1_2_7_65_1
  doi: 10.1016/j.tics.2013.09.016
– ident: e_1_2_7_75_1
  doi: 10.1016/j.neuroimage.2013.04.007
– ident: e_1_2_7_42_1
  doi: 10.1002/nav.3800020109
– ident: e_1_2_7_40_1
  doi: 10.1016/j.neuroimage.2018.01.058
– ident: e_1_2_7_71_1
  doi: 10.1017/pen.2018.4
– ident: e_1_2_7_53_1
  doi: 10.1016/j.neuroimage.2021.118642
– ident: e_1_2_7_8_1
  doi: 10.1146/annurev-clinpsy-040510-143934
– ident: e_1_2_7_86_1
  doi: 10.1089/brain.2016.0429
– ident: e_1_2_7_43_1
  doi: 10.1016/j.ymeth.2021.06.008
– ident: e_1_2_7_67_1
  doi: 10.1371/journal.pcbi.0010042
– ident: e_1_2_7_30_1
  doi: 10.1016/j.neuron.2019.11.012
– ident: e_1_2_7_28_1
  doi: 10.1016/j.neuroimage.2013.04.127
– ident: e_1_2_7_25_1
  doi: 10.1093/cercor/bhu012
– ident: e_1_2_7_34_1
  doi: 10.1038/s41598-017-06389-4
– ident: e_1_2_7_14_1
  doi: 10.1016/j.isci.2019.100801
– ident: e_1_2_7_44_1
  doi: 10.1371/journal.pone.0222914
– ident: e_1_2_7_27_1
  doi: 10.1073/pnas.0909969107
– ident: e_1_2_7_70_1
  doi: 10.1152/jn.00338.2011
– ident: e_1_2_7_74_1
  doi: 10.1016/j.neuroimage.2013.05.041
– ident: e_1_2_7_78_1
  doi: 10.1017/S1355617714000320
– ident: e_1_2_7_84_1
  doi: 10.1109/TPAMI.2008.245
– ident: e_1_2_7_19_1
  doi: 10.1016/j.neuroimage.2021.118543
– ident: e_1_2_7_52_1
  doi: 10.1016/j.neuroimage.2019.116157
– ident: e_1_2_7_56_1
  doi: 10.1002/hbm.25894
– ident: e_1_2_7_6_1
  doi: 10.1016/j.neuroimage.2014.07.067
– ident: e_1_2_7_57_1
  doi: 10.1016/j.neuroimage.2020.116604
– ident: e_1_2_7_45_1
  doi: 10.1162/netn_a_00166
– ident: e_1_2_7_38_1
  doi: 10.1002/hbm.25118
– ident: e_1_2_7_18_1
  doi: 10.1098/rstb.2017.0284
– ident: e_1_2_7_13_1
  doi: 10.1002/hbm.21333
– ident: e_1_2_7_68_1
  doi: 10.1371/journal.pone.0130045
– ident: e_1_2_7_83_1
  doi: 10.1109/TMI.2021.3051604
– ident: e_1_2_7_55_1
  doi: 10.1016/j.neuroimage.2019.05.064
– ident: e_1_2_7_39_1
  doi: 10.1117/12.2580980
– ident: e_1_2_7_7_1
  doi: 10.1038/nrn2575
– ident: e_1_2_7_76_1
  doi: 10.1073/pnas.1906144117
– ident: e_1_2_7_66_1
  doi: 10.1177/1073858404263960
– ident: e_1_2_7_69_1
  doi: 10.1016/j.neuroimage.2012.11.039
– ident: e_1_2_7_49_1
  doi: 10.1162/netn_a_00029
– ident: e_1_2_7_61_1
  doi: 10.1016/j.neuroimage.2013.11.046
– ident: e_1_2_7_26_1
  doi: 10.1212/WNL.0b013e3182872e5f
– ident: e_1_2_7_41_1
  doi: 10.1093/cercor/bhy123
– ident: e_1_2_7_20_1
  doi: 10.1016/j.neuroimage.2019.01.068
– ident: e_1_2_7_51_1
  doi: 10.1017/S1355617714000307
– ident: e_1_2_7_12_1
  doi: 10.1016/j.biopsych.2007.03.001
– ident: e_1_2_7_58_1
  doi: 10.3389/fnhum.2017.00189
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Snippet Functional connectomes (FCs), represented by networks or graphs that summarize coactivation patterns between pairs of brain regions, have been related at a...
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SubjectTerms Age
Anatomy & physiology
Brain
Brain - physiology
Cognition - physiology
Cognitive ability
Connectome - methods
Executive Function
Female
Females
functional connectome
functional MRI
Genetics
Graph matching
Graphical representations
Humans
inter‐individual variability
Magnetic Resonance Imaging - methods
Male
Networks
Physiology
Sex
Sexual behavior
Time series
Young adults
Title Graph‐matching distance between individuals' functional connectomes varies with relatedness, age, and cognitive score
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhbm.26296
https://www.ncbi.nlm.nih.gov/pubmed/37042411
https://www.proquest.com/docview/2817261739
https://www.proquest.com/docview/2800147759
https://pubmed.ncbi.nlm.nih.gov/PMC10203814
Volume 44
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