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Dynamic functional connectivity

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279:. Because of the newness of the field, DFC has only recently been used to investigate disease states, but since 2012 each of these three diseases has been shown to be correlated to dynamic temporal characteristics in functional connectivity. Most of these differences are related to the amount of time that is spent in different transient states. Patients with Schizophrenia have less frequent state changes than healthy patients, and this result has led to the suggestion that the disease is related to patients being stuck in certain brain states where the brain is unable to respond quickly to different queues. Also, a study in the visual sensory network showed that schizophrenia subjects spent more time than the healthy subjects in a state in which the connectivity between the middle temporal gyrus and other regions of the visual sensory network is highly negative. Studies with Alzheimer's disease have shown that patients with this ailment have altered network connectivity as well as altered time spent in the networks that are present. The observed correlation between DFC and disease does not imply that the changes in DFC are the cause of any of these diseases, but information from DFC analysis may be used to better understand the effects of the disease and to more quickly and accurately diagnose them. 119:
scans is the length of the sliding window. The defined window is then moved a certain number of scans forward in time and additional analysis is performed. The movement of the window is usually referenced in terms of the degree of overlap between adjacent windows. One of the principle benefits of sliding window analysis is that almost any steady state analysis can also be performed using sliding window if the window length is sufficiently large. Sliding window analysis also has a benefit of being easy to understand and in some ways easier to interpret. As the most common method of analysis, sliding window analysis has been used in many different ways to investigate a variety of different characteristics and implications of DFC. In order to be accurately interpreted, data from sliding window analysis generally must be compared between two different groups. Researchers have used this type of analysis to show different DFC characteristics in diseased and healthy patients, high and low performers on cognitive tasks, and between large scale brain states.
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dynamic functional connectivity has shown that far from being completely static, the functional networks of the brain fluctuate on the scale of seconds to minutes. These changes are generally seen as movements from one short term state to another, rather than continuous shifts. Many studies have shown reproducible patterns of network activity that move throughout the brain. These patterns have been seen in both animals and humans, and are present at only certain points during a scanner session. In addition to showing transient brain states, DFC analysis has shown a distinct hierarchical organization of the networks of the brain. Connectivity between bilaterally symmetric regions is the most stable form of connectivity in the brain, followed by other regions with direct anatomical connections. Steady state functional connectivity networks exist and have
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is heavily influenced by the ratio of oxygenated and deoxygenated blood. Since active neurons require more energy than resting neurons, changes in this contrast is traditionally interpreted an indirect measure of neural activity. Because of its indirect nature, fMRI data in DFC studies could be criticized as potentially being a reflection of non neural information. This concern has been alleviated recently by the observed correlation between fMRI DFC and simultaneously acquired electrophysiology data. Battaglia and colleagues have tried to address those controversies, linking dynamic functional connectivity to causality or effective connectivity. The scientists claim indeed that dynamic effective connectivity can emerge from transitions in the collective organization of coherent neural activity.
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on the magnitude of activation in brain regions as a predictor of performance, but recent research has shown that correlation between networks as measured with sliding window analysis is an even stronger predictor of performance. Individual differences in functional connectivity variability (FCV) across sliding windows within fMRI scans have been shown to correlate with the tendency to attend to pain. The degree to which a subject is mind wandering away from a sensory stimulus has also been related to FCV.
74: 236:(MEG) can be used to measure the magnetic fields produced by electrical activity in the brain. MEG has high temporal resolution and has generally higher spatial resolution than EEG. Resting state studies with MEG are still limited by spatial resolution, but the modality has been used to show that resting state networks move through periods of low and high levels of correlation. This observation is consistent with the results seen in other DFC studies such as DFC activation pattern analysis. 225:(EEG) has also been used in humans to both validate and interpret observations made in DFC. EEG has poor spatial resolution because it is only able to acquire data on the surface of the scalp, but it is reflective of broad electrical activity from many neurons. EEG has been used simultaneously with fMRI to account for some of the inter scan variance in FC. EEG has also been used to show that changes in FC are related to broad brain states observed in EEG. 245:
coefficients were typically < 0.05. These functional connections were found to be plastic – changing the correlation for a conditioning period of Ts (typically a few minutes), by means of spike-triggered sensory stimulations, induced short-term (typically < Ts) lasting changes of the connections. The pre-post conditioning strengthening of a functional connection was typically equal to the square root of its pre-during conditioning strengthening.
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probably reflects some of the constant processes of the brain. Repeating patterns of network information have been suggested to account for 25–50% of the variance in fMRI BOLD data. These patterns of activity have primarily been seen in rats as a propagating wave of synchronized activity along the cortex. These waves have also been shown to be related to underlying neural activity, and has been shown to be present in humans as well as rats.
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analysis. Some researchers have proposed that the variability in functional connectivity in fMRI studies is consistent with the variability that one would expect from simply analyzing random data. This complaint that DFC may reflect only noise has been recently lessened by the observation of electrical basis to fMRI DFC data and behavioral relevance of DFC characteristics.
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tasks, sleep, and learning. These changes often occur within the same individual and are clearly relevant to behavior. DFC has now been investigated in a variety of different contexts with many analysis tools. It has been shown to be related to both behavior and neural activity. Some researchers believe that it may be heavily related to high level thought or consciousness.
70:, and spatial grouping based on temporal similarities. These methods have been used to show that functional connectivity is related to behavior in a variety of different tasks, and that it has a neural basis. These methods assume the functional connections in the brain remain constant in a short time over a task or period of data collection. 137:
the peaks). These few points contain a great portion of the information pertaining functional connectivity, because it has been demonstrated, that despite the tremendous reduction on the data size (> 95%), it compares very well with inferences of functional connectivity obtained with standard methods which uses the full signal.
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potassium channels on spines, thus weakening or strengthening connectivity, respectively . For example, dopamine D1 receptor and/or noradrenergic beta-1 receptor stimulation on spines can increase cAMP-PKA-calcium signaling to open HCN, KCNQ2, and/or SK channels to rapidly weaken a connection, e.g. as occurs during stress .
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DFC has been shown to be significantly related to human performance, including vigilance and aspects of attention. It has been proposed and supported that the network behavior immediately prior to a task onset is a strong predictor of performance on that task. Traditionally, fMRI studies have focused
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Dynamic Functional Connectivity studied using fMRI may be related to a phenomenon previously discovered in macaque prefrontal cortex termed Dynamic Network Connectivity, whereby arousal mechanisms rapidly alter the strength of glutamate synaptic connections onto dendritic spines by opening or closing
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In addition to complaints that DFC may be a product of scanner noise, observed DFC could be criticized based on the indirect nature of fMRI which is used to observe it. fMRI data is collected by quickly acquiring a sequence of MRI images in time using echo planar imaging. The contrast in these images
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has become one of the most common methods of network generation in steady state functional connectivity. ICA divides fMRI signal into several spatial components that have similar temporal patterns. More recently, ICA has been used to divide fMRI data into different temporal components. This has been
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The large information content of these few points is consistent with the results of Petridou et al. who demonstrated he contribution of these "spontaneous events" to the correlation strength and power spectra of the slow spontaneous fluctuations by deconvolving the task hemodynamic response function
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Departing from the traditional approaches, recently an efficient method was introduced to analyze rapidly changing functional activations patterns which transforms the fMRI BOLD data into a point process. This is achieved by selecting for each voxel the points of inflection of the BOLD signal (i.e.,
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Studies that showed brain state dependent changes in functional connectivity were the first indicators that temporal variation in functional connectivity may be significant. Several studies in the mid-2000s examined the changes in FC that were related to a variety of different causes such as mental
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Correlation between DFC and electrophysiology has led some scientists to suggest that DFC could reflect hemodynamic results of dynamic network behavior that has been seen in single cell analysis of neuron populations. Although hemodynamic response is too slow to reflect a one-to-one correspondence
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Several researchers have argued that DFC may be a simple reflection of analysis, scanner, or physiological noise. Noise in fMRI can arise from a variety of different factors including heart beat, changes in the blood brain barrier, characteristics of the acquiring scanner, or unintended effects of
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which looks for physical connections in the brain, functional connectivity is related to similar patterns of activation in different brain regions regardless of the apparent physical connectedness of the regions. This type of connectivity was discovered in the mid-1990s and has been seen primarily
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changes over a short time. Dynamic functional connectivity is a recent expansion on traditional functional connectivity analysis which typically assumes that functional networks are static in time. DFC is related to a variety of different neurological disorders, and has been suggested to be a more
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fMRI is the primary means of investigating DFC. This presents unique challenges because fMRI has fairly low temporal resolution, typically 0.5 Hz, and is only an indirect measure of neural activity. The indirect nature of fMRI analysis suggests that validation is needed to show that findings
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Sliding window analysis is the most common method used in the analysis of functional connectivity, first introduced by Sakoglu and Calhoun in 2009, and applied to schizophrenia. Sliding window analysis is performed by conducting analysis on a set number of scans in an fMRI session. The number of
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Single-unit recording were used in order to explore the extent, strength and plasticity of functional connectivity between individual cortical neurons in cats and monkeys. Such studies revealed correlated activity at various time scales. At the fastest time scale, that of 1 – 20 ms, correlation
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One of the first methods ever used to analyze DFC was pattern analysis of fMRI images to show that there are patterns of activation in spatially separated brain regions that tend to have synchronous activity. It has become clear that there is a spatial and temporal periodicity in the brain that
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Because DFC is such a new field, much of the research related to it is conducted to validate the relevance of these dynamic changes rather than explore their implications; however, many critical findings have been made that help the scientific community better understand the brain. Analysis of
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has been used to conduct DFC analysis that has validated the existence of DFC by showing its significant changes in time. This same method has recently been used to investigate some of the dynamic characteristics of accepted networks. For example, time frequency analysis has shown that the
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Hutchison, R. M.; Womelsdorf, T.; Allen, E. A.; Bandettini, P. A.; Calhoun, V. D.; Corbetta, M.; Della Penna, S.; Duyn, J. H.; Glover, G. H.; Gonzalez-Castillo, J.; Handwerker, D. A.; Keilholz, S.; Kiviniemi, V.; Leopold, D. A.; De Pasquale, F.; Sporns, O.; Walter, M.; Chang, C. (2013).
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has been proposed as an analysis method that is capable of overcoming many of the challenges associated with sliding windows. Unlike sliding window analysis, time frequency analysis allows the researcher to investigate both frequency and amplitude information simultaneously. The
105:, but have less temporal stability than the anatomical networks. Finally, some functional networks are fleeting enough to only be seen with DFC analysis. These networks also possess physiological relevance but are much less temporally stable than the other networks in the brain. 454:
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above is one example of a brain network seen using steady state connectivity. This network is fairly stable in time, but it has been shown to have a variable relationship with other networks, and to vary slightly in its own characteristics in time.
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One of the principal motivations of DFC analysis is to better understand, detect and treat neurological diseases. Static functional connectivity has been shown to be significantly related to a variety of diseases such as
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Sakoglu, U.; Michael, A. M.; Calhoun, V. D. (2009). "Classification of schizophrenia patients vs healthy controls with dynamic functional network connectivity".
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Sakoglu, U.; Calhoun, V. D. (2009). "Temporal Dynamics of Functional Network Connectivity at Rest: A Comparison of Schizophrenia Patients and Healthy Controls".
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caps like the one above are often used simultaneously with fMRI in order to capture information about the electrical signals underlying the BOLD signal.
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termed temporal ICA and it has been used to plot network behavior that accounts for 25% of variability in the correlation of anatomical nodes in fMRI.
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Thompson, G. J.; Magnuson, M. E.; Merritt, M. D.; Schwarb, H.; Pan, W. J.; McKinley, A.; Tripp, L. D.; Schumacher, E. H.; Keilholz, S. D. (2013).
1436:"Short-time windows of correlation between large-scale functional brain networks predict vigilance intraindividually and interindividually" 1730:
Arnsten, A.F.T., Wang, M., D'Esposito. Dynamic Network Connectivity: from monkeys to humans. Front Hum Neurosci. 18, 1353043 (2024)
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whose discovery was motivated by the observation of temporal variability in the rising field of steady state connectivity research.
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Battaglia, Demian; Witt, Annette; Wolf, Fred; Geisel, Theo (2012). "Dynamic effective connectivity of inter-areal brain circuits".
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with neural network dynamics, it is plausible that DFC is a reflection of the power of some frequencies of electrophysiology data.
1056:"The voxel-wise functional connectome can be efficiently derived from co-activations in a sparse spatio-temporal point-process" 141:
from the rest data. Subsequently, similar principles were successfully applied under the name of co-activation patterns (CAP).
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Functional connectivity refers to the functionally integrated relationship between spatially separated brain regions. Unlike
1107:"Periods of rest in fMRI contain individual spontaneous events which are related to slowly fluctuating spontaneous activity" 1867: 1651:
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687:"Dynamic windowing reveals task-modulation of functional connectivity in schizophrenia patients vs healthy controls" 498:
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67: 32:, but DFC has also been observed with several other mediums. DFC is a recent development within the field of 500:"Low frequency BOLD fluctuations during resting wakefulness and light sleep: A simultaneous EEG-fMRI study" 59: 1164:"Time-varying functional network information extracted from brief instances of spontaneous brain activity" 879:
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Detection of task transitions on 45mins long continuous muli task runs using whole brain connectivity
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accurate representation of functional brain networks. The primary tool for analyzing DFC is
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from fMRI are actually relevant and reflective of neural activity.
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is not constant in time but rather is a temporary state.
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Mapping 1007:2014arXiv1405.6466T 985:Human Brain Mapping 575:2011PNAS..108.7641B 504:Human Brain Mapping 277:Alzheimer's disease 240:Neuronal mechanisms 123:Activation patterns 109:Methods of analysis 45:Static connectivity 719:(Suppl. 1): S169. 639:10.1002/jmri.21848 297:Brain Connectivity 262:Clinical relevance 220: 84: 64:resting state fMRI 1452:10.1002/hbm.22140 1446:(12): 3280–3298. 1400:10.1002/hbm.20968 1394:(11): 1713–1726. 1174:(11): 4392–4397. 1123:10.1002/hbm.21513 1015:10.1002/hbm.22562 991:(11): 5442–5456. 754:(Suppl. 1): S57. 559:(18): 7641–7646. 516:10.1002/hbm.20428 202:Electrophysiology 155:wavelet transform 1989: 1967: 1966: 1956: 1946: 1913: 1907: 1906: 1872: 1863: 1857: 1856: 1848: 1842: 1841: 1805: 1799: 1798: 1788: 1778: 1746: 1740: 1737: 1731: 1728: 1722: 1719: 1713: 1710: 1704: 1701: 1695: 1691: 1685: 1684: 1653:Brain Topography 1648: 1642: 1641: 1631: 1599: 1593: 1592: 1582: 1572: 1548: 1542: 1541: 1531: 1499: 1493: 1492: 1480: 1474: 1473: 1463: 1431: 1422: 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779: 775: 744: 740: 709: 705: 689: 683: 679: 668: 664: 619: 610: 545: 541: 496: 492: 452: 448: 402: 385: 346: 342: 310:10.1.1.222.9471 293: 289: 285: 264: 255: 242: 231: 204: 199: 190: 177: 147: 134: 125: 116: 111: 98: 89: 47: 42: 12: 11: 5: 1995: 1985: 1984: 1969: 1968: 1908: 1858: 1843: 1800: 1741: 1732: 1723: 1714: 1705: 1696: 1686: 1643: 1594: 1543: 1494: 1491:(3): e1002438. 1475: 1423: 1374: 1321: 1272: 1221: 1154: 1097: 1046: 971: 920: 891:(2): 158–163. 871: 822: 793:(6): 351–366. 773: 738: 703: 677: 662: 633:(2): 384–393. 608: 539: 510:(6): 671–682. 490: 446: 383: 356:(4): 537–541. 340: 286: 284: 281: 263: 260: 254: 251: 241: 238: 230: 227: 203: 200: 198: 195: 189: 186: 176: 173: 146: 143: 133: 130: 124: 121: 115: 114:Sliding window 112: 110: 107: 97: 94: 88: 85: 46: 43: 41: 38: 9: 6: 4: 3: 2: 1994: 1983: 1980: 1979: 1977: 1964: 1960: 1955: 1950: 1945: 1940: 1936: 1932: 1929:(6): e39731. 1928: 1924: 1920: 1912: 1904: 1900: 1896: 1892: 1888: 1884: 1880: 1876: 1869: 1862: 1854: 1847: 1839: 1835: 1831: 1827: 1823: 1819: 1815: 1811: 1804: 1796: 1792: 1787: 1782: 1777: 1772: 1768: 1764: 1760: 1756: 1752: 1745: 1736: 1727: 1718: 1709: 1700: 1690: 1682: 1678: 1674: 1670: 1666: 1662: 1659:(3): 338–52. 1658: 1654: 1647: 1639: 1635: 1630: 1625: 1621: 1617: 1613: 1609: 1605: 1598: 1590: 1586: 1581: 1576: 1571: 1566: 1562: 1558: 1554: 1547: 1539: 1535: 1530: 1525: 1521: 1517: 1513: 1509: 1505: 1498: 1490: 1486: 1479: 1471: 1467: 1462: 1457: 1453: 1449: 1445: 1441: 1437: 1430: 1428: 1419: 1415: 1410: 1405: 1401: 1397: 1393: 1389: 1385: 1378: 1370: 1366: 1361: 1356: 1352: 1348: 1344: 1340: 1336: 1332: 1331:Glover, G. H. 1325: 1317: 1313: 1308: 1303: 1299: 1295: 1291: 1287: 1283: 1276: 1268: 1264: 1259: 1254: 1249: 1244: 1240: 1236: 1232: 1225: 1217: 1213: 1208: 1203: 1199: 1195: 1190: 1185: 1181: 1177: 1173: 1169: 1165: 1158: 1150: 1146: 1141: 1136: 1132: 1128: 1124: 1120: 1116: 1112: 1108: 1101: 1093: 1089: 1084: 1079: 1074: 1069: 1065: 1061: 1057: 1050: 1042: 1038: 1033: 1028: 1024: 1020: 1016: 1012: 1008: 1004: 999: 994: 990: 986: 982: 975: 967: 963: 958: 953: 948: 943: 939: 935: 931: 924: 916: 912: 907: 902: 898: 894: 890: 886: 882: 875: 867: 863: 858: 853: 849: 845: 841: 837: 833: 826: 818: 814: 809: 804: 800: 796: 792: 788: 784: 777: 769: 765: 761: 757: 753: 749: 742: 734: 730: 726: 722: 718: 714: 707: 699: 695: 688: 681: 673: 666: 658: 654: 649: 644: 640: 636: 632: 628: 624: 617: 615: 613: 604: 600: 595: 590: 585: 580: 576: 572: 567: 562: 558: 554: 550: 543: 535: 531: 526: 521: 517: 513: 509: 505: 501: 494: 486: 482: 478: 474: 470: 466: 462: 458: 450: 442: 438: 433: 428: 424: 420: 416: 412: 408: 400: 398: 396: 394: 392: 390: 388: 379: 375: 371: 367: 363: 359: 355: 351: 344: 336: 332: 328: 324: 320: 316: 311: 306: 302: 298: 291: 287: 280: 278: 274: 273:schizophrenia 270: 259: 250: 246: 237: 235: 226: 224: 217: 212: 208: 194: 185: 181: 172: 169: 165: 161: 156: 151: 145:Other methods 142: 138: 129: 120: 106: 104: 93: 80: 75: 71: 69: 65: 61: 57: 52: 37: 35: 31: 26: 22: 18: 1982:Neuroimaging 1926: 1922: 1911: 1878: 1874: 1861: 1852: 1846: 1813: 1809: 1803: 1758: 1754: 1744: 1735: 1726: 1717: 1708: 1699: 1689: 1656: 1652: 1646: 1611: 1607: 1597: 1560: 1556: 1546: 1511: 1507: 1497: 1488: 1484: 1478: 1443: 1439: 1391: 1387: 1377: 1345:(1): 81–98. 1342: 1338: 1324: 1289: 1285: 1275: 1238: 1234: 1224: 1171: 1167: 1157: 1114: 1110: 1100: 1063: 1059: 1049: 988: 984: 974: 937: 933: 923: 888: 884: 874: 839: 835: 825: 790: 786: 776: 751: 747: 741: 716: 712: 706: 697: 693: 680: 671: 665: 630: 626: 556: 552: 542: 507: 503: 493: 460: 456: 449: 414: 410: 353: 349: 343: 303:(1): 13–36. 300: 296: 290: 265: 256: 247: 243: 232: 221: 205: 191: 182: 178: 148: 139: 135: 126: 117: 99: 90: 48: 20: 16: 15: 1881:: 103–111. 1514:: 826–836. 1329:Chang, C.; 1292:: 476–488. 694:Proc. ISMRM 417:: 360–378. 1816:: 471–80. 1810:NeuroImage 1614:: 227–36. 1608:NeuroImage 1508:NeuroImage 1339:NeuroImage 1286:NeuroImage 836:NeuroImage 748:NeuroImage 713:NeuroImage 411:NeuroImage 283:References 269:depression 1903:231391460 1198:0027-8424 1131:1097-0193 1023:1097-0193 998:1405.6466 566:1010.3775 305:CiteSeerX 68:coherence 1976:Category 1963:22761880 1923:PLOS ONE 1895:33434723 1838:13082197 1830:24973603 1795:24167282 1681:16494240 1673:24104726 1638:23376790 1589:23293596 1538:23876248 1470:22736565 1418:20725910 1369:20006716 1333:(2010). 1316:25662866 1267:24550788 1216:23440216 1149:22331588 1092:27601975 1041:24989126 966:22347863 915:21078369 866:20728554 817:20162320 768:54432053 733:54291742 657:19629982 603:21502525 534:17598166 485:23195652 477:17027761 441:23707587 327:22432952 162:and the 1954:3386248 1931:Bibcode 1786:3832014 1763:Bibcode 1629:3602157 1580:3531919 1563:: 339. 1529:3815981 1461:6870033 1409:6870948 1360:2827259 1307:4386757 1258:3913885 1241:: 101. 1207:3600481 1176:Bibcode 1140:6869909 1083:4994538 1066:: 381. 1032:6869695 1003:Bibcode 957:3274757 906:3014405 857:2997178 808:2891285 700:: 3675. 648:2758521 594:3088578 571:Bibcode 525:6871022 432:3807588 370:8524021 335:6116761 1961:  1951:  1901:  1893:  1836:  1828:  1793:  1783:  1679:  1671:  1636:  1626:  1587:  1577:  1536:  1526:  1468:  1458:  1416:  1406:  1367:  1357:  1314:  1304:  1265:  1255:  1214:  1204:  1196:  1147:  1137:  1129:  1090:  1080:  1039:  1029:  1021:  964:  954:  940:: 15. 913:  903:  864:  854:  815:  805:  766:  731:  655:  645:  601:  591:  532:  522:  483:  475:  439:  429:  378:775793 376:  368:  333:  325:  307:  275:, and 54:using 1899:S2CID 1871:(PDF) 1834:S2CID 1677:S2CID 993:arXiv 764:S2CID 729:S2CID 690:(PDF) 561:arXiv 481:S2CID 374:S2CID 331:S2CID 214:Full 1959:PMID 1891:PMID 1826:PMID 1791:PMID 1669:PMID 1634:PMID 1585:PMID 1534:PMID 1466:PMID 1414:PMID 1365:PMID 1312:PMID 1263:PMID 1212:PMID 1194:ISSN 1145:PMID 1127:ISSN 1088:PMID 1037:PMID 1019:ISSN 962:PMID 911:PMID 862:PMID 813:PMID 653:PMID 599:PMID 530:PMID 473:PMID 437:PMID 366:PMID 323:PMID 77:The 58:and 56:fMRI 30:fMRI 1949:PMC 1939:doi 1883:doi 1879:228 1818:doi 1814:100 1781:PMC 1771:doi 1759:110 1661:doi 1624:PMC 1616:doi 1575:PMC 1565:doi 1524:PMC 1516:doi 1456:PMC 1448:doi 1404:PMC 1396:doi 1355:PMC 1347:doi 1302:PMC 1294:doi 1290:111 1253:PMC 1243:doi 1202:PMC 1184:doi 1172:110 1135:PMC 1119:doi 1078:PMC 1068:doi 1027:PMC 1011:doi 952:PMC 942:doi 901:PMC 893:doi 889:488 852:PMC 844:doi 803:PMC 795:doi 756:doi 721:doi 643:PMC 635:doi 589:PMC 579:doi 557:108 520:PMC 512:doi 465:doi 427:PMC 419:doi 358:doi 315:doi 229:MEG 216:EEG 21:DFC 1978:: 1957:. 1947:. 1937:. 1925:. 1921:. 1897:. 1889:. 1877:. 1873:. 1832:. 1824:. 1812:. 1789:. 1779:. 1769:. 1757:. 1753:. 1675:. 1667:. 1657:27 1655:. 1632:. 1622:. 1612:72 1610:. 1606:. 1583:. 1573:. 1559:. 1555:. 1532:. 1522:. 1512:83 1510:. 1506:. 1487:. 1464:. 1454:. 1444:34 1442:. 1438:. 1426:^ 1412:. 1402:. 1392:31 1390:. 1386:. 1363:. 1353:. 1343:50 1341:. 1337:. 1310:. 1300:. 1288:. 1284:. 1261:. 1251:. 1237:. 1233:. 1210:. 1200:. 1192:. 1182:. 1170:. 1166:. 1143:. 1133:. 1125:. 1115:34 1113:. 1109:. 1086:. 1076:. 1064:10 1062:. 1058:. 1035:. 1025:. 1017:. 1009:. 1001:. 989:35 987:. 983:. 960:. 950:. 936:. 932:. 909:. 899:. 887:. 883:. 860:. 850:. 840:54 838:. 834:. 811:. 801:. 791:23 789:. 785:. 762:. 752:47 750:. 727:. 717:47 715:. 698:17 696:. 692:. 651:. 641:. 631:30 629:. 625:. 611:^ 597:. 587:. 577:. 569:. 555:. 551:. 528:. 518:. 508:29 506:. 502:. 479:. 471:. 461:70 459:. 435:. 425:. 415:80 413:. 409:. 386:^ 372:. 364:. 354:34 352:. 329:. 321:. 313:. 299:. 271:, 1965:. 1941:: 1933:: 1927:7 1905:. 1885:: 1855:. 1840:. 1820:: 1797:. 1773:: 1765:: 1683:. 1663:: 1640:. 1618:: 1591:. 1567:: 1561:6 1540:. 1518:: 1489:8 1472:. 1450:: 1420:. 1398:: 1371:. 1349:: 1318:. 1296:: 1269:. 1245:: 1239:7 1218:. 1186:: 1178:: 1151:. 1121:: 1094:. 1070:: 1043:. 1013:: 1005:: 995:: 968:. 944:: 938:3 917:. 895:: 868:. 846:: 819:. 797:: 770:. 758:: 735:. 723:: 659:. 637:: 605:. 581:: 573:: 563:: 536:. 514:: 487:. 467:: 443:. 421:: 380:. 360:: 337:. 317:: 301:1 19:(

Index

functional connectivity
fMRI
functional neuroimaging
structural connectivity
fMRI
Positron emission tomography
resting state fMRI
coherence

default mode network
physiological relevance
Time-frequency analysis
wavelet transform
default mode network
task-positive network
Independent component analysis

EEG
Electroencephalography
Magnetoencephalography
depression
schizophrenia
Alzheimer's disease
CiteSeerX
10.1.1.222.9471
doi
10.1089/brain.2011.0008
PMID
22432952
S2CID

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