Partial correlation analysis reveals abnormal retinotopically organized functional connectivity of visual areas in amblyopia
Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, pre...
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Published in | NeuroImage clinical Vol. 18; pp. 192 - 201 |
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Format | Journal Article |
Language | English |
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01.01.2018
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Abstract | Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, previous studies have used resting state measures to demonstrate altered long-range connectivity in amblyopia. This is the first study in amblyopia to analyze connectivity between regions of interest that are smaller than a single cortical area and to apply partial correlation analysis to reduce network effects. We specifically assess short-range connectivity between retinotopically defined regions of interest within the occipital lobe of 8 subjects with amblyopia and 7 subjects with normal vision (aged 19–45). The representations of visual areas V1, V2, and V3 within each of the four quadrants of visual space were further subdivided into three regions based on maps of visual field eccentricity. Connectivity between pairs of all nine regions of interest in each quadrant was tested via correlation and partial correlation for both groups. Only the tests of partial correlation, i.e., correlation between time courses of two regions following the regression of time courses from all other regions, yielded significant differences between resting state functional connectivity in amblyopic and normal subjects. Subjects with amblyopia showed significantly higher partial correlation between para-foveal and more eccentric representations within V1, and this effect associated with poor acuity of the worse eye. In addition, we observed reduced correlation in amblyopic subjects between isoeccentricity regions in V1 and V2, and separately, between such regions in V2 and V3. We conclude that partial correlation-based connectivity is altered in an eccentricity-dependent pattern in visual field maps of amblyopic patients. Moreover, results are consistent with known clinical and psychophysical vision loss. More broadly, this provides evidence that abnormal cortical adaptations to disease may be better isolated with tests of partial correlation connectivity than with the regular correlation techniques that are currently widely used.
•Cortical functional connectivity abnormalities exist in amblyopia at a scale finer than previously reported.•Connectivity changes within primary visual cortex are consistent with known loss of function.•Connectivity changes between visual areas are consistent with concept of deafferentation.•Partial correlation differentiates patients from controls, whereas correlation does not. |
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AbstractList | Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, previous studies have used resting state measures to demonstrate altered long-range connectivity in amblyopia. This is the first study in amblyopia to analyze connectivity between regions of interest that are smaller than a single cortical area and to apply partial correlation analysis to reduce network effects. We specifically assess short-range connectivity between retinotopically defined regions of interest within the occipital lobe of 8 subjects with amblyopia and 7 subjects with normal vision (aged 19–45). The representations of visual areas V1, V2, and V3 within each of the four quadrants of visual space were further subdivided into three regions based on maps of visual field eccentricity. Connectivity between pairs of all nine regions of interest in each quadrant was tested via correlation and partial correlation for both groups. Only the tests of partial correlation, i.e., correlation between time courses of two regions following the regression of time courses from all other regions, yielded significant differences between resting state functional connectivity in amblyopic and normal subjects. Subjects with amblyopia showed significantly higher partial correlation between para-foveal and more eccentric representations within V1, and this effect associated with poor acuity of the worse eye. In addition, we observed reduced correlation in amblyopic subjects between isoeccentricity regions in V1 and V2, and separately, between such regions in V2 and V3. We conclude that partial correlation-based connectivity is altered in an eccentricity-dependent pattern in visual field maps of amblyopic patients. Moreover, results are consistent with known clinical and psychophysical vision loss. More broadly, this provides evidence that abnormal cortical adaptations to disease may be better isolated with tests of partial correlation connectivity than with the regular correlation techniques that are currently widely used. Keywords: Functional MRI, Spontaneous activity, Intrinsic, Resting state functional magnetic resonance imaging, Resting state functional connectivity, Partial correlation, Regional, Strabismus, Binocular vision, Suppression AbstractAmblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, previous studies have used resting state measures to demonstrate altered long-range connectivity in amblyopia. This is the first study in amblyopia to analyze connectivity between regions of interest that are smaller than a single cortical area and to apply partial correlation analysis to reduce network effects. We specifically assess short-range connectivity between retinotopically defined regions of interest within the occipital lobe of 8 subjects with amblyopia and 7 subjects with normal vision (aged 19–45). The representations of visual areas V1, V2, and V3 within each of the four quadrants of visual space were further subdivided into three regions based on maps of visual field eccentricity. Connectivity between pairs of all nine regions of interest in each quadrant was tested via correlation and partial correlation for both groups. Only the tests of partial correlation, i.e., correlation between time courses of two regions following the regression of time courses from all other regions, yielded significant differences between resting state functional connectivity in amblyopic and normal subjects. Subjects with amblyopia showed significantly higher partial correlation between para-foveal and more eccentric representations within V1, and this effect associated with poor acuity of the worse eye. In addition, we observed reduced correlation in amblyopic subjects between isoeccentricity regions in V1 and V2, and separately, between such regions in V2 and V3. We conclude that partial correlation-based connectivity is altered in an eccentricity-dependent pattern in visual field maps of amblyopic patients. Moreover, results are consistent with known clinical and psychophysical vision loss. More broadly, this provides evidence that abnormal cortical adaptations to disease may be better isolated with tests of partial correlation connectivity than with the regular correlation techniques that are currently widely used. Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, previous studies have used resting state measures to demonstrate altered long-range connectivity in amblyopia. This is the first study in amblyopia to analyze connectivity between regions of interest that are smaller than a single cortical area and to apply partial correlation analysis to reduce network effects. We specifically assess short-range connectivity between retinotopically defined regions of interest within the occipital lobe of 8 subjects with amblyopia and 7 subjects with normal vision (aged 19–45). The representations of visual areas V1, V2, and V3 within each of the four quadrants of visual space were further subdivided into three regions based on maps of visual field eccentricity. Connectivity between pairs of all nine regions of interest in each quadrant was tested via correlation and partial correlation for both groups. Only the tests of partial correlation, i.e., correlation between time courses of two regions following the regression of time courses from all other regions, yielded significant differences between resting state functional connectivity in amblyopic and normal subjects. Subjects with amblyopia showed significantly higher partial correlation between para-foveal and more eccentric representations within V1, and this effect associated with poor acuity of the worse eye. In addition, we observed reduced correlation in amblyopic subjects between isoeccentricity regions in V1 and V2, and separately, between such regions in V2 and V3. We conclude that partial correlation-based connectivity is altered in an eccentricity-dependent pattern in visual field maps of amblyopic patients. Moreover, results are consistent with known clinical and psychophysical vision loss. More broadly, this provides evidence that abnormal cortical adaptations to disease may be better isolated with tests of partial correlation connectivity than with the regular correlation techniques that are currently widely used. •Cortical functional connectivity abnormalities exist in amblyopia at a scale finer than previously reported.•Connectivity changes within primary visual cortex are consistent with known loss of function.•Connectivity changes between visual areas are consistent with concept of deafferentation.•Partial correlation differentiates patients from controls, whereas correlation does not. Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, previous studies have used resting state measures to demonstrate altered long-range connectivity in amblyopia. This is the first study in amblyopia to analyze connectivity between regions of interest that are smaller than a single cortical area and to apply partial correlation analysis to reduce network effects. We specifically assess short-range connectivity between retinotopically defined regions of interest within the occipital lobe of 8 subjects with amblyopia and 7 subjects with normal vision (aged 19–45). The representations of visual areas V1, V2, and V3 within each of the four quadrants of visual space were further subdivided into three regions based on maps of visual field eccentricity. Connectivity between pairs of all nine regions of interest in each quadrant was tested via correlation and partial correlation for both groups. Only the tests of partial correlation, i.e., correlation between time courses of two regions following the regression of time courses from all other regions, yielded significant differences between resting state functional connectivity in amblyopic and normal subjects. Subjects with amblyopia showed significantly higher partial correlation between para-foveal and more eccentric representations within V1, and this effect associated with poor acuity of the worse eye. In addition, we observed reduced correlation in amblyopic subjects between isoeccentricity regions in V1 and V2, and separately, between such regions in V2 and V3. We conclude that partial correlation-based connectivity is altered in an eccentricity-dependent pattern in visual field maps of amblyopic patients. Moreover, results are consistent with known clinical and psychophysical vision loss. More broadly, this provides evidence that abnormal cortical adaptations to disease may be better isolated with tests of partial correlation connectivity than with the regular correlation techniques that are currently widely used. • Cortical functional connectivity abnormalities exist in amblyopia at a scale finer than previously reported. • Connectivity changes within primary visual cortex are consistent with known loss of function. • Connectivity changes between visual areas are consistent with concept of deafferentation. • Partial correlation differentiates patients from controls, whereas correlation does not. Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, previous studies have used resting state measures to demonstrate altered long-range connectivity in amblyopia. This is the first study in amblyopia to analyze connectivity between regions of interest that are smaller than a single cortical area and to apply partial correlation analysis to reduce network effects. We specifically assess short-range connectivity between retinotopically defined regions of interest within the occipital lobe of 8 subjects with amblyopia and 7 subjects with normal vision (aged 19-45). The representations of visual areas V1, V2, and V3 within each of the four quadrants of visual space were further subdivided into three regions based on maps of visual field eccentricity. Connectivity between pairs of all nine regions of interest in each quadrant was tested via correlation and partial correlation for both groups. Only the tests of partial correlation, i.e., correlation between time courses of two regions following the regression of time courses from all other regions, yielded significant differences between resting state functional connectivity in amblyopic and normal subjects. Subjects with amblyopia showed significantly higher partial correlation between para-foveal and more eccentric representations within V1, and this effect associated with poor acuity of the worse eye. In addition, we observed reduced correlation in amblyopic subjects between isoeccentricity regions in V1 and V2, and separately, between such regions in V2 and V3. We conclude that partial correlation-based connectivity is altered in an eccentricity-dependent pattern in visual field maps of amblyopic patients. Moreover, results are consistent with known clinical and psychophysical vision loss. More broadly, this provides evidence that abnormal cortical adaptations to disease may be better isolated with tests of partial correlation connectivity than with the regular correlation techniques that are currently widely used. Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, previous studies have used resting state measures to demonstrate altered long-range connectivity in amblyopia. This is the first study in amblyopia to analyze connectivity between regions of interest that are smaller than a single cortical area and to apply partial correlation analysis to reduce network effects. We specifically assess short-range connectivity between retinotopically defined regions of interest within the occipital lobe of 8 subjects with amblyopia and 7 subjects with normal vision (aged 19-45). The representations of visual areas V1, V2, and V3 within each of the four quadrants of visual space were further subdivided into three regions based on maps of visual field eccentricity. Connectivity between pairs of all nine regions of interest in each quadrant was tested via correlation and partial correlation for both groups. Only the tests of partial correlation, i.e., correlation between time courses of two regions following the regression of time courses from all other regions, yielded significant differences between resting state functional connectivity in amblyopic and normal subjects. Subjects with amblyopia showed significantly higher partial correlation between para-foveal and more eccentric representations within V1, and this effect associated with poor acuity of the worse eye. In addition, we observed reduced correlation in amblyopic subjects between isoeccentricity regions in V1 and V2, and separately, between such regions in V2 and V3. We conclude that partial correlation-based connectivity is altered in an eccentricity-dependent pattern in visual field maps of amblyopic patients. Moreover, results are consistent with known clinical and psychophysical vision loss. More broadly, this provides evidence that abnormal cortical adaptations to disease may be better isolated with tests of partial correlation connectivity than with the regular correlation techniques that are currently widely used.Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods of youth, the structure and function of adult visual cortex is abnormal. In addition to substantial deficits shown with task-based fMRI, previous studies have used resting state measures to demonstrate altered long-range connectivity in amblyopia. This is the first study in amblyopia to analyze connectivity between regions of interest that are smaller than a single cortical area and to apply partial correlation analysis to reduce network effects. We specifically assess short-range connectivity between retinotopically defined regions of interest within the occipital lobe of 8 subjects with amblyopia and 7 subjects with normal vision (aged 19-45). The representations of visual areas V1, V2, and V3 within each of the four quadrants of visual space were further subdivided into three regions based on maps of visual field eccentricity. Connectivity between pairs of all nine regions of interest in each quadrant was tested via correlation and partial correlation for both groups. Only the tests of partial correlation, i.e., correlation between time courses of two regions following the regression of time courses from all other regions, yielded significant differences between resting state functional connectivity in amblyopic and normal subjects. Subjects with amblyopia showed significantly higher partial correlation between para-foveal and more eccentric representations within V1, and this effect associated with poor acuity of the worse eye. In addition, we observed reduced correlation in amblyopic subjects between isoeccentricity regions in V1 and V2, and separately, between such regions in V2 and V3. We conclude that partial correlation-based connectivity is altered in an eccentricity-dependent pattern in visual field maps of amblyopic patients. Moreover, results are consistent with known clinical and psychophysical vision loss. More broadly, this provides evidence that abnormal cortical adaptations to disease may be better isolated with tests of partial correlation connectivity than with the regular correlation techniques that are currently widely used. |
Author | Shmuel, A. Lewis, L.B. Lam, J. Rosenstein, M. Mendola, J.D. |
AuthorAffiliation | a Department of Ophthalmology, McGill University, Montreal, QC, Canada b Departments of Neurology, Neurosurgery, Physiology and Biomedical Engineering, McGill University, Montreal, QC, Canada c Montreal Neurological Institute, McGill University, Montreal, QC, Canada |
AuthorAffiliation_xml | – name: c Montreal Neurological Institute, McGill University, Montreal, QC, Canada – name: a Department of Ophthalmology, McGill University, Montreal, QC, Canada – name: b Departments of Neurology, Neurosurgery, Physiology and Biomedical Engineering, McGill University, Montreal, QC, Canada |
Author_xml | – sequence: 1 givenname: J.D. surname: Mendola fullname: Mendola, J.D. email: janine.mendola@mcgill.ca organization: Department of Ophthalmology, McGill University, Montreal, QC, Canada – sequence: 2 givenname: J. surname: Lam fullname: Lam, J. organization: Departments of Neurology, Neurosurgery, Physiology and Biomedical Engineering, McGill University, Montreal, QC, Canada – sequence: 3 givenname: M. surname: Rosenstein fullname: Rosenstein, M. organization: Department of Ophthalmology, McGill University, Montreal, QC, Canada – sequence: 4 givenname: L.B. surname: Lewis fullname: Lewis, L.B. organization: Montreal Neurological Institute, McGill University, Montreal, QC, Canada – sequence: 5 givenname: A. surname: Shmuel fullname: Shmuel, A. organization: Departments of Neurology, Neurosurgery, Physiology and Biomedical Engineering, McGill University, Montreal, QC, Canada |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29868445$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.neuroimage.2013.12.036 10.1016/j.neuroimage.2013.10.013 10.1016/S0042-6989(02)00061-5 10.2147/NDT.S118326 10.1111/opo.12123 10.1016/j.neuron.2013.04.023 10.1089/brain.2011.0065 10.1167/16.3.16 10.1002/mrm.1910340409 10.1016/S0896-6273(03)00265-4 10.1167/iovs.12-10550 10.1002/(SICI)1522-2594(199912)42:6<1014::AID-MRM4>3.0.CO;2-F 10.1073/pnas.0811168106 10.1089/brain.2014.0331 10.1097/00006324-197710000-00006 10.3928/01913913-20101118-01 10.1002/hbm.20737 10.3389/fnhum.2015.00025 10.1111/j.1460-9568.2009.06650.x 10.1016/j.neuroimage.2007.05.020 10.3389/fpsyg.2014.00583 10.1006/nimg.1998.0395 10.1113/jphysiol.2007.136242 10.1016/0042-6989(85)90128-2 10.1002/hbm.20109 10.1016/j.neuroimage.2011.09.015 10.1016/j.neuroimage.2013.09.060 10.1167/iovs.16-20012 10.3389/fnins.2014.00339 10.1523/JNEUROSCI.22-19-08633.2002 10.1167/3.5.5 10.1523/JNEUROSCI.1657-06.2006 10.1093/cercor/7.2.181 10.1007/s10548-013-0290-1 10.1016/j.neuroimage.2016.06.030 10.1111/j.1469-7793.2001.0281b.x 10.1016/j.neuroimage.2005.08.035 10.1006/nimg.1998.0396 10.1167/4.6.10 10.1523/JNEUROSCI.4137-04.2005 10.1167/iovs.16-19986 10.1016/j.neuroimage.2016.04.056 10.1080/09273970500536243 10.1111/j.2517-6161.1995.tb02031.x 10.1016/j.neuroimage.2011.02.077 10.1016/j.neuroimage.2010.07.053 10.1167/iovs.09-3931 10.1016/j.brainres.2014.03.015 10.1523/JNEUROSCI.3228-12.2013 10.1016/j.visres.2015.04.005 10.1109/42.906426 10.1016/j.neuroimage.2016.12.063 10.1097/WNR.0000000000000767 10.1016/j.neuroimage.2017.08.077 10.1155/2013/612086 10.1016/j.neuroimage.2006.06.026 10.1167/iovs.16-20298 10.1371/journal.pone.0043373 10.1002/hbm.20829 10.1007/s00417-015-3117-9 10.1523/JNEUROSCI.1101-15.2015 10.1167/iovs.14-14543 10.1007/BF00229328 10.1016/j.neuron.2017.11.005 10.1038/nn1072 10.1523/JNEUROSCI.18-16-06411.1998 10.1098/rstb.2005.1628 10.1016/j.neuroimage.2005.11.018 10.1016/j.neuroimage.2010.01.071 10.1038/nrn2201 10.1167/iovs.12-11314 10.1523/JNEUROSCI.4715-14.2015 10.1016/j.jaapos.2007.01.119 10.7554/eLife.03952 10.1109/42.906424 10.1126/science.7754376 10.1523/JNEUROSCI.07-05-01340.1987 10.1111/j.1444-0938.2000.tb04892.x 10.1111/opo.12024 10.1016/j.visres.2009.04.009 10.1016/0042-6989(84)90150-0 10.1093/cercor/bhu277 10.1001/archopht.124.6.844 10.1111/opo.12293 10.1016/S0168-0102(01)00220-6 10.1038/nature05758 10.1002/hbm.20580 10.1073/pnas.0905267106 10.1002/cne.903340103 10.1038/eye.1996.54 10.1093/cercor/bhv175 10.1093/cercor/bhr234 10.1016/j.visres.2005.10.014 10.1167/11.14.16 10.1016/j.neuroimage.2012.11.006 |
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Keywords | Resting state functional magnetic resonance imaging Strabismus Suppression rs-fMRI Pcorr Regional Corr Resting state functional connectivity LGN Functional MRI Binocular vision Spontaneous activity Intrinsic Partial correlation partial correlation lateral geniculate nucleus resting state functional magnetic resonance imaging correlation Pcorr, partial correlation rs-fMRI, resting state functional magnetic resonance imaging LGN, lateral geniculate nucleus Corr, correlation |
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References | Buckner, Yeo (bb0085) 2014; 93 Shmuel, Leopold (bb0405) 2008; 2008 Duncan, Boynton (bb0165) 2003; 38 Amedi, Raz, Pianka, Malach, Zohary (bb0020) 2003; 6 Sireteanu, Fronius (bb0420) 1990; 79 Ding, Liu, Yan, Lin, Jiang (bb0160) 2013 Adachi, Osada, Sporns, Watanabe, Matsui, Miyamoto, Miyashita (bb0005) 2012; 22 Heinzle, Kahnt, Haynes (bb0215) 2011; 56 Hou, Kim, Lai, Verghese (bb0255) 2016; 16 Fox, Raichle (bb0190) 2007; 8 Agrawal, Conner, Odom, Schwartz (bb0015) 2006; 124 Nir, Hasson, Levy, Yeshurun, Malach (bb0375) 2006; 30 Wang, Li, Guo, Peng, Li, Qin, Yu (bb0450) 2014; 1563 Dale, Fischl, Sereno (bb0140) 1999; 9 Hess, Pointer (bb0220) 1985; 25 Benjamini, Hochberg (bb9880) 1995; 57 Yacoub, Shmuel, Logothetis, Ugurbil (bb0460) 2007; 37 Muckli, Kiess, Tonhausen, Singer, Goebel, Sireteanu (bb0360) 2006; 46 Fischl, Sereno, Dale (bb0180) 1999; 9 Wang, Mruczek, Arcaro, Kastner (bb0455) 2015; 25 Raemaekers, Schellekens, van Wezel, Petridou, Kristo, Ramsey (bb0385) 2014; 84 Sereno, Dale, Reppas, Kwong, Belliveau, Brady, Rosen, Tootell (bb0400) 1995; 268 Zhang, Brady, Smith (bb0465) 2001; 20 Hess, Thompson, Baker (bb0235) 2014; 34 Barnes, Li, Thompson, Singh, Dumoulin, Hess (bb0060) 2010; 51 Honey, Sporns, Cammoun, Gigandet, Thiran, Meuli, Hagmann (bb0245) 2009; 106 Liang, Xie, Yang, Yu, Yin, Wei, Wang (bb0335) 2016; 254 Kiorpes, Kiper, O'Keefe, Cavanaugh, Movshon (bb0285) 1998; 18 Wandell, Brewer, Dougherty (bb0435) 2005; 360 Brown, Feigl, Gole, Mullen, Hess (bb9860) 2013; 33 Crewther, Crewther (bb9855) 2015; 114 McKee, Levi, Movshon (bb0345) 2003; 3 Shmuel, Korman, Sterkin, Harel, Ullman, Malach, Grinvald (bb0410) 2005; 25 Huang, Feng, Zhou (bb0265) 2017; 28 Levi, Klein, Aitsebaomo (bb0315) 1984; 24 Niechwiej-Szwedo, Goltz, Chandrakumar, Wong (bb0370) 2014; 55 van den Heuvel, Mandl, Kahn, Hulshoff Pol (bb0240) 2009; 30 Levi (bb0305) 2006; 14 Clavagnier, Dumoulin, Hess (bb0115) 2015; 35 Jenkinson, Beckmann, Behrens, Woolrich, Smith (bb9870) 2012; 62 Chen, Tarczy-Hornoch (bb0110) 2011; 48 Movshon, Eggers, Gizzi, Hendrickson, Kiorpes, Boothe (bb0355) 1987; 7 Gravel, Harvey, Nordhjem, Haak, Dumoulin, Renken, Curčić-Blake, Cornelissen (bb0200) 2014; 8 Honey, Thivierge, Sporns (bb0250) 2010; 52 Levi, Hariharan, Klein (bb0320) 2002; 42 Mendola, Conner, Roy, Chan, Schwartz, Odom, Kwong (bb0350) 2005; 25 Engel, Glover, Wandell (bb0170) 1997; 7 Amir, Harel, Malach (bb0025) 1993; 334 Biswal, Yetkin, Haughton, Hyde (bb0070) 1995; 34 Chaimow, Yacoub, Uğurbil, Shmuel (bb0105) 2018; 164 Hamm, Black, Dai, Thompson (bb0210) 2014; 5 Dawson, Cha, Lewis, Mendola, Shmuel (bb0145) 2013; 67 Conner, Odom, Schwartz, Mendola (bb0130) 2007; 15;583 Farivar, Thompson, Mansouri, Hess (bb0175) 2011; 11 Li, Li, Chen, Liu, Yuan, Cai, Deng, Yu (bb0330) 2017; 58 Asper, Crewther, Crewther (bb0040) 2000; 83 Fischl, Liu, Dale (bb0185) 2001; 20 Brown, Woodall, Kitching, Baseler, Morland (bb0080) 2016; 36 Lee, Lee, Kim, Kim, Sohn, Choi, Gyu Choi, Hwang, Ho Park, Lee, Suk Yu, Hyun Chang (bb0295) 2001; 40 Babu, Clavagnier, Bobier, Thompson, Hess (bb0045) 2013; 54 Levi, Walters (bb0310) 1977; 54 Angelucci, Levitt, Walton, Hupe, Bullier, Lund (bb0030) 2002; 22 Arcaro, Honey, Mruczek, Kastner, Hasson (bb0035) 2015; 4 Carbonell, Bellec, Shmuel (bb0100) 2014; 86 de Zwart, van Gelderen, Liu, Duyn (bb0470) 2013; 26 Vincent, Patel, Fox, Snyder, Baker, Van Essen, Zempel, Snyder, Corbetta, Raichle (bb0430) 2007; 447 Smith, Fox, Miller, Glahn, Fox, Mackay, Filippini, Watkins, Toro, Laird, Beckmann (bb9865) 2009; 106 Sabbah, Authié, Sanda, Mohand-Saïd, Sahel, Safran, Habas, Amedi (bb0390) 2016; 136 Hess, Thompson, Gole, Mullen (bb0230) 2009; 29 Huang, Li, Zhou, Zhang, Zhong, Cai, Shao, Zeng (bb0260) 2016; 12 Sengpiel, Blakemore (bb0395) 1996; 10 Bock, Binda, Benson, Bridge, Watkins, Fine (bb0075) 2015; 35 Cox, Jesmanowicz (bb0135) 1999; 42 Dawson, Lam, Lewis, Carbonell, Mendola, Shmuel (bb0150) 2016; 6 De Luca, Beckmann, De Stefano, Matthews, Smith (bb0155) 2006; 29 Birch, Morale, Jost, De La Cruz, Kelly, Wang, Bex (bb0065) 2016; 57 Olman, Bao, Engel, Grant, Purington, Qiu, Schallmo, Tjan (bb0380) 2018; 164 Carbonell, Bellec, Shmuel (bb0095) 2011; 1 Lin, Ding, Liu, Yan, Song, Jiang (bb0340) 2012; 7 Jurcoane, Choubey, Mitsieva, Muckli, Sireteanu (bb0280) 2009; 49 Wang, Chen, Negyessy, Friedman, Mishra, Gore, Roe (bb0445) 2013; 78 Tan, Huang, Zhang, Wu, Zhong, Wu, Zhou, Shao (bb0425) 2016; 12 Conner, Sharma, Lemieux, Mendola (bb0120) 2004; 4 Genç, Schölvinck, Bergmann, Singer, Kohler (bb0195) 2016; 26 Barnes, Hess, Dumoulin, Achtman, Pike (bb0055) 2001; 15;533 Niechwiej-Szwedo, Chandrakumar, Goltz, Wong (bb0365) 2012; 53 Lerner, Hendler, Malach, Harel, Leiba, Stolovitch, Pianka (bb0300) 2006; 33 Joly, Frankó (bb0275) 2014; 6 von Noorden, Campos (bb9850) 2001 Butt, Benson, Datta, Aguirre (bb0090) 2015; 9 Wang, Cui, Zheng, Yang, Yang, Zeng (bb0440) 2012; 18 Guidi, Huber, Lampe, Gauthier, Möller (bb0205) 2016; 141 Larsson, Heeger (bb0290) 2006; 26 Babu, Clavagnier, Bobier, Thompson, Hess (bb0050) 2017; 58 Huber, Handwerker, Jangraw, Chen, Hall, Stüber, Gonzalez-Castillo, Ivanov, Marret, Guidi, Goense, Poser, Bandettini (bb0270) 2017; 96 Sireteanu (bb0415) 1982; 1 Li, Mullen, Thompson, Hess (bb0325) 2011; 54 Adams, Economides, Sincich, Horton (bb0010) 2013; 33 Conner, Odom, Schwartz, Mendola (bb0125) 2007; 11 Hess, Li, Mansouri, Thompson, Hansen (bb0225) 2009; 30 Brown (10.1016/j.nicl.2018.01.022_bb9860) 2013; 33 Conner (10.1016/j.nicl.2018.01.022_bb0130) 2007; 15;583 Hess (10.1016/j.nicl.2018.01.022_bb0235) 2014; 34 Carbonell (10.1016/j.nicl.2018.01.022_bb0095) 2011; 1 Levi (10.1016/j.nicl.2018.01.022_bb0320) 2002; 42 Sabbah (10.1016/j.nicl.2018.01.022_bb0390) 2016; 136 Angelucci (10.1016/j.nicl.2018.01.022_bb0030) 2002; 22 Movshon (10.1016/j.nicl.2018.01.022_bb0355) 1987; 7 Joly (10.1016/j.nicl.2018.01.022_bb0275) 2014; 6 Hess (10.1016/j.nicl.2018.01.022_bb0230) 2009; 29 Dale (10.1016/j.nicl.2018.01.022_bb0140) 1999; 9 Conner (10.1016/j.nicl.2018.01.022_bb0125) 2007; 11 Lin (10.1016/j.nicl.2018.01.022_bb0340) 2012; 7 Sireteanu (10.1016/j.nicl.2018.01.022_bb0415) 1982; 1 Wandell (10.1016/j.nicl.2018.01.022_bb0435) 2005; 360 Arcaro (10.1016/j.nicl.2018.01.022_bb0035) 2015; 4 Carbonell (10.1016/j.nicl.2018.01.022_bb0100) 2014; 86 Engel (10.1016/j.nicl.2018.01.022_bb0170) 1997; 7 Buckner (10.1016/j.nicl.2018.01.022_bb0085) 2014; 93 Brown (10.1016/j.nicl.2018.01.022_bb0080) 2016; 36 Olman (10.1016/j.nicl.2018.01.022_bb0380) 2018; 164 Wang (10.1016/j.nicl.2018.01.022_bb0440) 2012; 18 Birch (10.1016/j.nicl.2018.01.022_bb0065) 2016; 57 Li (10.1016/j.nicl.2018.01.022_bb0325) 2011; 54 Muckli (10.1016/j.nicl.2018.01.022_bb0360) 2006; 46 Cox (10.1016/j.nicl.2018.01.022_bb0135) 1999; 42 Tan (10.1016/j.nicl.2018.01.022_bb0425) 2016; 12 de Zwart (10.1016/j.nicl.2018.01.022_bb0470) 2013; 26 Adams (10.1016/j.nicl.2018.01.022_bb0010) 2013; 33 Conner (10.1016/j.nicl.2018.01.022_bb0120) 2004; 4 Huang (10.1016/j.nicl.2018.01.022_bb0265) 2017; 28 von Noorden (10.1016/j.nicl.2018.01.022_bb9850) 2001 Jenkinson (10.1016/j.nicl.2018.01.022_bb9870) 2012; 62 van den Heuvel (10.1016/j.nicl.2018.01.022_bb0240) 2009; 30 Biswal (10.1016/j.nicl.2018.01.022_bb0070) 1995; 34 De Luca (10.1016/j.nicl.2018.01.022_bb0155) 2006; 29 Huber (10.1016/j.nicl.2018.01.022_bb0270) 2017; 96 Hamm (10.1016/j.nicl.2018.01.022_bb0210) 2014; 5 Levi (10.1016/j.nicl.2018.01.022_bb0315) 1984; 24 Sereno (10.1016/j.nicl.2018.01.022_bb0400) 1995; 268 Agrawal (10.1016/j.nicl.2018.01.022_bb0015) 2006; 124 Sireteanu (10.1016/j.nicl.2018.01.022_bb0420) 1990; 79 Smith (10.1016/j.nicl.2018.01.022_bb9865) 2009; 106 Hess (10.1016/j.nicl.2018.01.022_bb0220) 1985; 25 Mendola (10.1016/j.nicl.2018.01.022_bb0350) 2005; 25 Hou (10.1016/j.nicl.2018.01.022_bb0255) 2016; 16 Asper (10.1016/j.nicl.2018.01.022_bb0040) 2000; 83 Yacoub (10.1016/j.nicl.2018.01.022_bb0460) 2007; 37 Barnes (10.1016/j.nicl.2018.01.022_bb0060) 2010; 51 Jurcoane (10.1016/j.nicl.2018.01.022_bb0280) 2009; 49 Bock (10.1016/j.nicl.2018.01.022_bb0075) 2015; 35 Amedi (10.1016/j.nicl.2018.01.022_bb0020) 2003; 6 Dawson (10.1016/j.nicl.2018.01.022_bb0145) 2013; 67 Larsson (10.1016/j.nicl.2018.01.022_bb0290) 2006; 26 Duncan (10.1016/j.nicl.2018.01.022_bb0165) 2003; 38 Honey (10.1016/j.nicl.2018.01.022_bb0250) 2010; 52 Kiorpes (10.1016/j.nicl.2018.01.022_bb0285) 1998; 18 Sengpiel (10.1016/j.nicl.2018.01.022_bb0395) 1996; 10 Chen (10.1016/j.nicl.2018.01.022_bb0110) 2011; 48 Wang (10.1016/j.nicl.2018.01.022_bb0450) 2014; 1563 Genç (10.1016/j.nicl.2018.01.022_bb0195) 2016; 26 Shmuel (10.1016/j.nicl.2018.01.022_bb0405) 2008; 2008 Hess (10.1016/j.nicl.2018.01.022_bb0225) 2009; 30 Niechwiej-Szwedo (10.1016/j.nicl.2018.01.022_bb0365) 2012; 53 Niechwiej-Szwedo (10.1016/j.nicl.2018.01.022_bb0370) 2014; 55 Benjamini (10.1016/j.nicl.2018.01.022_bb9880) 1995; 57 Wang (10.1016/j.nicl.2018.01.022_bb0455) 2015; 25 Gravel (10.1016/j.nicl.2018.01.022_bb0200) 2014; 8 Levi (10.1016/j.nicl.2018.01.022_bb0305) 2006; 14 Crewther (10.1016/j.nicl.2018.01.022_bb9855) 2015; 114 Huang (10.1016/j.nicl.2018.01.022_bb0260) 2016; 12 Liang (10.1016/j.nicl.2018.01.022_bb0335) 2016; 254 McKee (10.1016/j.nicl.2018.01.022_bb0345) 2003; 3 Shmuel (10.1016/j.nicl.2018.01.022_bb0410) 2005; 25 Wang (10.1016/j.nicl.2018.01.022_bb0445) 2013; 78 Fox (10.1016/j.nicl.2018.01.022_bb0190) 2007; 8 Amir (10.1016/j.nicl.2018.01.022_bb0025) 1993; 334 Zhang (10.1016/j.nicl.2018.01.022_bb0465) 2001; 20 Clavagnier (10.1016/j.nicl.2018.01.022_bb0115) 2015; 35 Levi (10.1016/j.nicl.2018.01.022_bb0310) 1977; 54 Lee (10.1016/j.nicl.2018.01.022_bb0295) 2001; 40 Nir (10.1016/j.nicl.2018.01.022_bb0375) 2006; 30 Barnes (10.1016/j.nicl.2018.01.022_bb0055) 2001; 15;533 Raemaekers (10.1016/j.nicl.2018.01.022_bb0385) 2014; 84 Babu (10.1016/j.nicl.2018.01.022_bb0050) 2017; 58 Guidi (10.1016/j.nicl.2018.01.022_bb0205) 2016; 141 Li (10.1016/j.nicl.2018.01.022_bb0330) 2017; 58 Fischl (10.1016/j.nicl.2018.01.022_bb0185) 2001; 20 Vincent (10.1016/j.nicl.2018.01.022_bb0430) 2007; 447 Adachi (10.1016/j.nicl.2018.01.022_bb0005) 2012; 22 Fischl (10.1016/j.nicl.2018.01.022_bb0180) 1999; 9 Dawson (10.1016/j.nicl.2018.01.022_bb0150) 2016; 6 Farivar (10.1016/j.nicl.2018.01.022_bb0175) 2011; 11 Lerner (10.1016/j.nicl.2018.01.022_bb0300) 2006; 33 Honey (10.1016/j.nicl.2018.01.022_bb0245) 2009; 106 Chaimow (10.1016/j.nicl.2018.01.022_bb0105) 2018; 164 Babu (10.1016/j.nicl.2018.01.022_bb0045) 2013; 54 Heinzle (10.1016/j.nicl.2018.01.022_bb0215) 2011; 56 Butt (10.1016/j.nicl.2018.01.022_bb0090) 2015; 9 Ding (10.1016/j.nicl.2018.01.022_bb0160) 2013 |
References_xml | – volume: 52 start-page: 766 year: 2010 end-page: 776 ident: bb0250 article-title: Can structure predict function in the human brain? publication-title: NeuroImage – volume: 93 start-page: 292 year: 2014 end-page: 297 ident: bb0085 article-title: Borders, map clusters, and supra-areal organization in visual cortex publication-title: NeuroImage – volume: 78 start-page: 1116 year: 2013 end-page: 1126 ident: bb0445 article-title: The relationship of anatomical and functional connectivity to resting-state connectivity in primate somatosensory cortex publication-title: Neuron – volume: 1563 start-page: 41 year: 2014 end-page: 51 ident: bb0450 article-title: Abnormal functional connectivity density in children with anisometropic amblyopia at resting-state publication-title: Brain Res. – volume: 29 start-page: 1064 year: 2009 end-page: 1070 ident: bb0230 article-title: Deficient responses from the lateral geniculate nucleus in humans with amblyopia publication-title: Eur. J. Neurosci. – volume: 57 start-page: 289 year: 1995 end-page: 300 ident: bb9880 article-title: Controlling the false discovery rate: a practical and powerful approach to multiple testing publication-title: J. R. Stat. Soc. Ser. B. – volume: 6 start-page: 62 year: 2014 ident: bb0275 article-title: Neuroimaging of amblyopia and binocular vision: a review publication-title: Front. Integr. Neurosci. – volume: 57 start-page: 5649 year: 2016 end-page: 5654 ident: bb0065 article-title: Assessing suppression in amblyopic children with a dichoptic eye chart publication-title: Invest. Ophthalmol. Vis. Sci. – volume: 164 start-page: 32 year: 2018 end-page: 47 ident: bb0105 article-title: Spatial specificity of the functional MRI blood oxygenation response relative to neuronal activity publication-title: NeuroImage – volume: 26 start-page: 525 year: 2013 end-page: 537 ident: bb0470 article-title: Independent sources of spontaneous BOLD fluctuation along the visual pathway publication-title: Brain Topogr. – volume: 9 start-page: 195 year: 1999 end-page: 207 ident: bb0180 article-title: Cortical surface-based analysis. II: inflation, flattening, and a surface-based coordinate system publication-title: NeuroImage – volume: 5 start-page: 583 year: 2014 ident: bb0210 article-title: Global processing in amblyopia: a review publication-title: Front. Psychol. – volume: 106 start-page: 13040 year: 2009 end-page: 13045 ident: bb9865 article-title: Correspondence of the brain’s functional architecture during activation and rest publication-title: Proc. Natl. Acad. Sci. U. S. A. – volume: 22 start-page: 8633 year: 2002 end-page: 8646 ident: bb0030 article-title: Circuits for local and global signal integration in primary visual cortex publication-title: J. Neurosci. – volume: 1 start-page: 496 year: 2011 end-page: 510 ident: bb0095 article-title: Global and system-specific resting-state fMRI fluctuations are uncorrelated: principal component analysis reveals anti-correlated networks publication-title: Brain Connect. – volume: 46 start-page: 506 year: 2006 end-page: 526 ident: bb0360 article-title: Cerebral correlates of impaired grating perception in individual, psychophysically assessed human amblyopes publication-title: Vis. Res. – volume: 20 start-page: 45 year: 2001 end-page: 57 ident: bb0465 article-title: Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm publication-title: IEEE Trans. Med. Imaging – volume: 26 start-page: 13128 year: 2006 end-page: 13142 ident: bb0290 article-title: Two retinotopic visual areas in human lateral occipital cortex publication-title: J. Neurosci. – volume: 54 start-page: 6585 year: 2013 end-page: 6593 ident: bb0045 article-title: The regional extent of suppression: strabismics versus nonstrabismics publication-title: Invest. Ophthalmol. Vis. Sci. – volume: 38 start-page: 659 year: 2003 end-page: 671 ident: bb0165 article-title: Cortical magnification within human primary visual cortex correlates with acuity thresholds publication-title: Neuron – volume: 24 start-page: 789 year: 1984 end-page: 800 ident: bb0315 article-title: Detection and discrimination of the direction of motion in central and peripheral vision of normal and amblyopic observers publication-title: Vis. Res. – volume: 15;583 start-page: 159 year: 2007 end-page: 173 ident: bb0130 article-title: Retinotopic maps and foveal suppression in the visual cortex of amblyopic adults publication-title: J. Physiol. – volume: 6 start-page: 758 year: 2003 end-page: 766 ident: bb0020 article-title: Early “visual” cortex activation correlates with superior verbal memory performance in the blind publication-title: Nat. Neurosci. – volume: 35 start-page: 14740 year: 2015 end-page: 14755 ident: bb0115 article-title: Is the cortical deficit in amblyopia due to reduced cortical magnification, loss of neural resolution, or neural disorganization? publication-title: J. Neurosci. – volume: 6 start-page: 57 year: 2016 end-page: 75 ident: bb0150 article-title: Partial correlation-based retinotopically organized resting-state functional connectivity within and between areas of the visual cortex reflects more than cortical distance publication-title: Brain Connect. – volume: 83 start-page: 49 year: 2000 end-page: 58 ident: bb0040 article-title: Strabismic amblyopia. Part 1. Psychophysics publication-title: Clin. Exp. Optom. – volume: 42 start-page: 1379 year: 2002 end-page: 1394 ident: bb0320 article-title: Suppressive and facilitatory spatial interactions in amblyopic vision publication-title: Vis. Res. – year: 2001 ident: bb9850 article-title: Binocular Vision and Ocular Motility: Theory and Management of Strabismus – volume: 141 start-page: 250 year: 2016 end-page: 261 ident: bb0205 article-title: Lamina-dependent calibrated BOLD response in human primary motor cortex publication-title: NeuroImage – volume: 136 start-page: 162 year: 2016 end-page: 173 ident: bb0390 article-title: Increased functional connectivity between language and visually deprived areas in late and partial blindness publication-title: NeuroImage – volume: 54 start-page: 505 year: 2011 end-page: 516 ident: bb0325 article-title: Effective connectivity anomalies in human amblyopia publication-title: NeuroImage – volume: 34 start-page: 146 year: 2014 end-page: 162 ident: bb0235 article-title: Binocular vision in amblyopia: structure, suppression and plasticity publication-title: Ophthalmic Physiol. Opt. – volume: 16 start-page: 16 year: 2016 ident: bb0255 article-title: Degraded attentional modulation of cortical neural populations in strabismic amblyopia publication-title: J. Vis. – volume: 25 start-page: 2117 year: 2005 end-page: 2131 ident: bb0410 article-title: Retinotopic axis specificity and selective clustering of feedback projections from V2 to V1 in the owl monkey publication-title: J. Neurosci. – volume: 33 start-page: 138 year: 2013 end-page: 149 ident: bb9860 article-title: Assessment of neuroretinal function in a group of functional amblyopes with documented LGN deficits publication-title: Ophthalmic Physiol. Opt. – volume: 3 start-page: 380 year: 2003 end-page: 405 ident: bb0345 article-title: The pattern of visual deficits in amblyopia publication-title: J. Vis. – start-page: 1 year: 2013 end-page: 8 ident: bb0160 article-title: Altered functional connectivity of the primary visual cortex in subjects with amblyopia publication-title: Neural Plast. – volume: 11 start-page: 341 year: 2007 end-page: 350 ident: bb0125 article-title: Monocular activation of V1 and V2 in amblyopic adults measured with functional magnetic resonance imaging publication-title: J AAPOS. – volume: 58 start-page: 2329 year: 2017 end-page: 2340 ident: bb0050 article-title: Regional extent of peripheral suppression in amblyopia publication-title: Invest. Ophthalmol. Vis. Sci. – volume: 35 start-page: 12366 year: 2015 end-page: 12382 ident: bb0075 article-title: Resting-state retinotopic organization in the absence of retinal input and visual experience publication-title: J. Neurosci. – volume: 106 start-page: 2035 year: 2009 end-page: 2040 ident: bb0245 article-title: Predicting human resting-state functional connectivity from structural connectivity publication-title: Proc. Natl. Acad. Sci. U. S. A. – volume: 30 start-page: 3127 year: 2009 end-page: 3141 ident: bb0240 article-title: Functionally linked resting-state networks reflect the underlying structural connectivity architecture of the human brain publication-title: Hum. Brain Mapp. – volume: 11 year: 2011 ident: bb0175 article-title: Interocular suppression in strabismic amblyopia results in an attenuated and delayed hemodynamic response function in early visual cortex publication-title: J. Vis. – volume: 79 start-page: 603 year: 1990 end-page: 614 ident: bb0420 article-title: Human amblyopia: structure of the visual field publication-title: Exp. Brain Res. – volume: 12 start-page: 1243 year: 2016 end-page: 1250 ident: bb0425 article-title: A functional MRI study of altered spontaneous brain activity pattern in patients with congenital comitant strabismus using amplitude of low-frequency fluctuation publication-title: Neuropsychiatr. Dis. Treat. – volume: 10 start-page: 250 year: 1996 end-page: 258 ident: bb0395 article-title: The neural basis of suppression and amblyopia in strabismus publication-title: Eye (Lond). – volume: 48 start-page: 366 year: 2011 end-page: 374 ident: bb0110 article-title: Functional magnetic resonance imaging of binocular interactions in visual cortex in strabismus publication-title: J. Pediatr. Ophthalmol. Strabismus – volume: 84 start-page: 911 year: 2014 end-page: 921 ident: bb0385 article-title: Patterns of resting state connectivity in human primary visual cortical areas: a 7T fMRI study publication-title: NeuroImage – volume: 8 start-page: 339 year: 2014 ident: bb0200 article-title: Cortical connective field estimates from resting state fMRI activity publication-title: Front. Neurosci. – volume: 7 start-page: 181 year: 1997 end-page: 192 ident: bb0170 article-title: Retinotopic organization in human visual cortex and the spatial precision of functional MRI publication-title: Cereb. Cortex – volume: 67 start-page: 331 year: 2013 end-page: 343 ident: bb0145 article-title: Evaluation and calibration of functional network modeling methods based on known anatomical connections publication-title: NeuroImage – volume: 40 start-page: 147 year: 2001 end-page: 153 ident: bb0295 article-title: Binocularity and spatial frequency dependence of calcarine activation in two types of amblyopia publication-title: Neurosci. Res. – volume: 7 year: 2012 ident: bb0340 article-title: Altered spontaneous activity in anisometropic amblyopia subjects: revealed by resting-state FMRI publication-title: PLoS One – volume: 20 start-page: 70 year: 2001 end-page: 80 ident: bb0185 article-title: Automated manifold surgery: constructing geometrically accurate and topologically correct models of the human cerebral cortex publication-title: IEEE Trans. Med. Imaging – volume: 96 start-page: 1253 year: 2017 end-page: 1263 ident: bb0270 article-title: High-resolution CBV-fMRI allows mapping of laminar activity and connectivity of cortical input and output in human M1 publication-title: Neuron – volume: 4 year: 2015 ident: bb0035 article-title: Widespread correlation patterns of fMRI signal across visual cortex reflect eccentricity organization publication-title: elife – volume: 1 start-page: 31 year: 1982 end-page: 33 ident: bb0415 article-title: Human amblyopia: consequence of chronic interocular suppression publication-title: Hum. Neurobiol. – volume: 124 start-page: 844 year: 2006 end-page: 850 ident: bb0015 article-title: Relating binocular and monocular vision in strabismic and anisometropic amblyopia publication-title: Arch. Ophthalmol. – volume: 86 start-page: 343 year: 2014 end-page: 353 ident: bb0100 article-title: Quantification of the impact of a confounding variable on functional connectivity confirms anti-correlated networks in the resting-state publication-title: NeuroImage – volume: 56 start-page: 1426 year: 2011 end-page: 1436 ident: bb0215 article-title: Topographically specific functional connectivity between visual field maps in the human brain publication-title: NeuroImage – volume: 30 start-page: 4054 year: 2009 end-page: 4069 ident: bb0225 article-title: Selectivity as well as sensitivity loss characterizes the cortical spatial frequency deficit in amblyopia publication-title: Hum. Brain Mapp. – volume: 7 start-page: 1340 year: 1987 end-page: 1351 ident: bb0355 article-title: Effects of early unilateral blur on the Macaque's visual system. III. Physiological observations publication-title: J. Neurosci. – volume: 254 start-page: 569 year: 2016 end-page: 576 ident: bb0335 article-title: Distinct patterns of spontaneous brain activity between children and adults with anisometropic amblyopia: a resting-state fMRI study publication-title: Graefes Arch. Clin. Exp. Ophthalmol. – volume: 9 start-page: 179 year: 1999 end-page: 194 ident: bb0140 article-title: Cortical surface-based analysis. I. Segmentation and surface reconstruction publication-title: Neuroimage – volume: 36 start-page: 240 year: 2016 end-page: 265 ident: bb0080 article-title: Using magnetic resonance imaging to assess visual deficits: a review publication-title: Ophthalmic Physiol. Opt. – volume: 2008 start-page: 751 year: 2008 end-page: 761 ident: bb0405 article-title: Neuronal correlates of spontaneous fluctuations in fMRI signals in monkey visual cortex: implications for functional connectivity at rest publication-title: Hum. Brain Mapp. – volume: 33 start-page: 169 year: 2006 end-page: 179 ident: bb0300 article-title: Selective fovea-related deprived activation in retinotopic and high-order visual cortex of human amblyopes publication-title: NeuroImage – volume: 18 start-page: 909 year: 2012 end-page: 919 ident: bb0440 article-title: Combination of blood oxygen level-dependent functional magnetic resonance imaging and visual evoked potential recordings for abnormal visual cortex in two types of amblyopia publication-title: Mol. Vis. – volume: 58 start-page: 481 year: 2017 end-page: 491 ident: bb0330 article-title: Spatial and global sensory suppression mapping encompassing the central 10° field in Anisometropic amblyopia publication-title: Invest. Ophthalmol. Vis. Sci. – volume: 37 start-page: 1161 year: 2007 end-page: 1177 ident: bb0460 article-title: Robust detection of ocular dominance columns in humans using Hahn spin echo BOLD functional MRI at high field publication-title: NeuroImage – volume: 14 start-page: 11 year: 2006 end-page: 19 ident: bb0305 article-title: Visual processing in amblyopia: human studies publication-title: Strabismus – volume: 360 start-page: 693 year: 2005 end-page: 707 ident: bb0435 article-title: Visual field map clusters in human cortex publication-title: Philos. Trans. R. Soc. Lond. Ser. B Biol. Sci. – volume: 25 start-page: 222 year: 2005 end-page: 236 ident: bb0350 article-title: Voxel-based analysis of MRI detects abnormal visual cortex in children and adults with amblyopia publication-title: Hum. Brain Mapp. – volume: 26 start-page: 3719 year: 2016 end-page: 3731 ident: bb0195 article-title: Functional connectivity patterns of visual cortex reflect its anatomical organization publication-title: Cereb. Cortex – volume: 62 start-page: 782 year: 2012 end-page: 790 ident: bb9870 article-title: FSL publication-title: Neuroimage – volume: 334 start-page: 9 year: 1993 end-page: 46 ident: bb0025 article-title: Cortical hierarchy reflected in the organization of intrinsic connections in macaque monkey visual cortex publication-title: J. Comp. Neurol. – volume: 8 start-page: 700 year: 2007 end-page: 711 ident: bb0190 article-title: Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging publication-title: Nat. Rev. Neurosci. – volume: 30 start-page: 1313 year: 2006 end-page: 1324 ident: bb0375 article-title: Widespread functional connectivity and fMRI fluctuations in human visual cortex in the absence of visual stimulation publication-title: NeuroImage – volume: 268 start-page: 889 year: 1995 end-page: 893 ident: bb0400 article-title: Borders of multiple visual areas in humans revealed by functional magnetic resonance imaging publication-title: Science – volume: 54 start-page: 691 year: 1977 end-page: 698 ident: bb0310 article-title: Visual evoked responses in strabismic and anisometropic amblyopia: effects of check size and retinal locus publication-title: Am. J. Optom. Physiol. Optic – volume: 55 start-page: 3857 year: 2014 end-page: 3865 ident: bb0370 article-title: Effects of strabismic amblyopia on visuomotor behavior: part II. Visually guided reaching publication-title: Invest. Ophthalmol. Vis. Sci. – volume: 15;533 start-page: 281 year: 2001 end-page: 297 ident: bb0055 article-title: The cortical deficit in humans with strabismic amblyopia publication-title: J Physiol. – volume: 34 start-page: 537 year: 1995 end-page: 541 ident: bb0070 article-title: Functional connectivity in the motor cortex of resting human brain using echo-planar MRI publication-title: Magn. Reson. Med. – volume: 53 start-page: 7458 year: 2012 end-page: 7468 ident: bb0365 article-title: Effects of strabismic amblyopia and strabismus without amblyopia on visuomotor behavior, I: saccadic eye movements publication-title: Invest. Ophthalmol. Vis. Sci. – volume: 164 start-page: 59 year: 2018 end-page: 66 ident: bb0380 article-title: Hemifield columns co-opt ocular dominance column structure in human achiasma publication-title: Neuroimage – volume: 114 start-page: 79 year: 2015 end-page: 86 ident: bb9855 article-title: A new model of strabismic amblyopia: loss of spatial acuity due to increased temporal dispersion of geniculate X-cell afferents on to cortical neurons publication-title: Vis. Res. – volume: 25 start-page: 1577 year: 1985 end-page: 1594 ident: bb0220 article-title: Differences in the neural basis of human amblyopia: the distribution of the anomaly across the visual field publication-title: Vis. Res. – volume: 447 start-page: 83 year: 2007 end-page: 86 ident: bb0430 article-title: Intrinsic functional architecture in the anaesthetized monkey brain publication-title: Nature – volume: 4 start-page: 509 year: 2004 end-page: 523 ident: bb0120 article-title: Retinotopic organization in children measured with fMRI publication-title: J. Vis. – volume: 29 start-page: 1359 year: 2006 end-page: 1367 ident: bb0155 article-title: fMRI resting state networks define distinct modes of long-distance interactions in the human brain publication-title: NeuroImage – volume: 25 start-page: 3911 year: 2015 end-page: 3931 ident: bb0455 article-title: Probabilistic maps of visual topography in human cortex publication-title: Cereb. Cortex – volume: 51 start-page: 1432 year: 2010 end-page: 1438 ident: bb0060 article-title: Decreased gray matter concentration in the lateral geniculate nuclei in human amblyopes publication-title: Invest. Ophthalmol. Vis. Sci. – volume: 49 start-page: 1681 year: 2009 end-page: 1692 ident: bb0280 article-title: Interocular transfer of orientation-specific fMRI adaptation reveals amblyopia-related deficits in humans publication-title: Vis. Res. – volume: 9 start-page: 25 year: 2015 ident: bb0090 article-title: Hierarchical and homotopic correlations of spontaneous neural activity within the visual cortex of the sighted and blind publication-title: Front. Hum. Neurosci. – volume: 28 start-page: 397 year: 2017 end-page: 403 ident: bb0265 article-title: Reduced response cluster size in early visual areas explains the acuity deficit in amblyopia publication-title: Neuroreport – volume: 42 start-page: 1014 year: 1999 end-page: 1018 ident: bb0135 article-title: Real-time 3D image registration for functional MRI publication-title: Magn. Reson. Med. – volume: 12 start-page: 1303 year: 2016 end-page: 1308 ident: bb0260 article-title: Altered intrinsic regional brain spontaneous activity in patients with comitant strabismus: a resting-state functional MRI study publication-title: Neuropsychiatr. Dis. Treat. – volume: 18 start-page: 6411 year: 1998 end-page: 6424 ident: bb0285 article-title: Neuronal correlates of amblyopia in the visual cortex of macaque monkeys with experimental strabismus and anisometropia publication-title: J. Neurosci. – volume: 33 start-page: 3752 year: 2013 end-page: 3759 ident: bb0010 article-title: Cortical metabolic activity matches the pattern of visual suppression in strabismus publication-title: J. Neurosci. – volume: 22 start-page: 1586 year: 2012 end-page: 1592 ident: bb0005 article-title: Functional connectivity between anatomically unconnected areas is shaped by collective network-level effects in the macaque cortex publication-title: Cereb. Cortex – volume: 93 start-page: 292 issue: Pt 2 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0085 article-title: Borders, map clusters, and supra-areal organization in visual cortex publication-title: NeuroImage doi: 10.1016/j.neuroimage.2013.12.036 – volume: 86 start-page: 343 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0100 article-title: Quantification of the impact of a confounding variable on functional connectivity confirms anti-correlated networks in the resting-state publication-title: NeuroImage doi: 10.1016/j.neuroimage.2013.10.013 – volume: 42 start-page: 1379 issue: 11 year: 2002 ident: 10.1016/j.nicl.2018.01.022_bb0320 article-title: Suppressive and facilitatory spatial interactions in amblyopic vision publication-title: Vis. Res. doi: 10.1016/S0042-6989(02)00061-5 – volume: 12 start-page: 1303 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0260 article-title: Altered intrinsic regional brain spontaneous activity in patients with comitant strabismus: a resting-state functional MRI study publication-title: Neuropsychiatr. Dis. Treat. doi: 10.2147/NDT.S118326 – volume: 34 start-page: 146 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0235 article-title: Binocular vision in amblyopia: structure, suppression and plasticity publication-title: Ophthalmic Physiol. Opt. doi: 10.1111/opo.12123 – volume: 78 start-page: 1116 year: 2013 ident: 10.1016/j.nicl.2018.01.022_bb0445 article-title: The relationship of anatomical and functional connectivity to resting-state connectivity in primate somatosensory cortex publication-title: Neuron doi: 10.1016/j.neuron.2013.04.023 – volume: 1 start-page: 496 issue: 6 year: 2011 ident: 10.1016/j.nicl.2018.01.022_bb0095 article-title: Global and system-specific resting-state fMRI fluctuations are uncorrelated: principal component analysis reveals anti-correlated networks publication-title: Brain Connect. doi: 10.1089/brain.2011.0065 – volume: 16 start-page: 16 issue: 3 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0255 article-title: Degraded attentional modulation of cortical neural populations in strabismic amblyopia publication-title: J. Vis. doi: 10.1167/16.3.16 – volume: 34 start-page: 537 issue: 4 year: 1995 ident: 10.1016/j.nicl.2018.01.022_bb0070 article-title: Functional connectivity in the motor cortex of resting human brain using echo-planar MRI publication-title: Magn. Reson. Med. doi: 10.1002/mrm.1910340409 – volume: 38 start-page: 659 issue: 4 year: 2003 ident: 10.1016/j.nicl.2018.01.022_bb0165 article-title: Cortical magnification within human primary visual cortex correlates with acuity thresholds publication-title: Neuron doi: 10.1016/S0896-6273(03)00265-4 – volume: 53 start-page: 7458 issue: 12 year: 2012 ident: 10.1016/j.nicl.2018.01.022_bb0365 article-title: Effects of strabismic amblyopia and strabismus without amblyopia on visuomotor behavior, I: saccadic eye movements publication-title: Invest. Ophthalmol. Vis. Sci. doi: 10.1167/iovs.12-10550 – volume: 42 start-page: 1014 year: 1999 ident: 10.1016/j.nicl.2018.01.022_bb0135 article-title: Real-time 3D image registration for functional MRI publication-title: Magn. Reson. Med. doi: 10.1002/(SICI)1522-2594(199912)42:6<1014::AID-MRM4>3.0.CO;2-F – volume: 106 start-page: 2035 year: 2009 ident: 10.1016/j.nicl.2018.01.022_bb0245 article-title: Predicting human resting-state functional connectivity from structural connectivity publication-title: Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.0811168106 – volume: 6 start-page: 57 issue: 1 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0150 article-title: Partial correlation-based retinotopically organized resting-state functional connectivity within and between areas of the visual cortex reflects more than cortical distance publication-title: Brain Connect. doi: 10.1089/brain.2014.0331 – volume: 54 start-page: 691 year: 1977 ident: 10.1016/j.nicl.2018.01.022_bb0310 article-title: Visual evoked responses in strabismic and anisometropic amblyopia: effects of check size and retinal locus publication-title: Am. J. Optom. Physiol. Optic doi: 10.1097/00006324-197710000-00006 – volume: 48 start-page: 366 issue: 6 year: 2011 ident: 10.1016/j.nicl.2018.01.022_bb0110 article-title: Functional magnetic resonance imaging of binocular interactions in visual cortex in strabismus publication-title: J. Pediatr. Ophthalmol. Strabismus doi: 10.3928/01913913-20101118-01 – volume: 30 start-page: 3127 year: 2009 ident: 10.1016/j.nicl.2018.01.022_bb0240 article-title: Functionally linked resting-state networks reflect the underlying structural connectivity architecture of the human brain publication-title: Hum. Brain Mapp. doi: 10.1002/hbm.20737 – volume: 12 start-page: 1243 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0425 article-title: A functional MRI study of altered spontaneous brain activity pattern in patients with congenital comitant strabismus using amplitude of low-frequency fluctuation publication-title: Neuropsychiatr. Dis. Treat. – volume: 9 start-page: 25 year: 2015 ident: 10.1016/j.nicl.2018.01.022_bb0090 article-title: Hierarchical and homotopic correlations of spontaneous neural activity within the visual cortex of the sighted and blind publication-title: Front. Hum. Neurosci. doi: 10.3389/fnhum.2015.00025 – volume: 29 start-page: 1064 issue: 5 year: 2009 ident: 10.1016/j.nicl.2018.01.022_bb0230 article-title: Deficient responses from the lateral geniculate nucleus in humans with amblyopia publication-title: Eur. J. Neurosci. doi: 10.1111/j.1460-9568.2009.06650.x – volume: 37 start-page: 1161 issue: 4 year: 2007 ident: 10.1016/j.nicl.2018.01.022_bb0460 article-title: Robust detection of ocular dominance columns in humans using Hahn spin echo BOLD functional MRI at high field publication-title: NeuroImage doi: 10.1016/j.neuroimage.2007.05.020 – volume: 5 start-page: 583 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0210 article-title: Global processing in amblyopia: a review publication-title: Front. Psychol. doi: 10.3389/fpsyg.2014.00583 – volume: 9 start-page: 179 year: 1999 ident: 10.1016/j.nicl.2018.01.022_bb0140 article-title: Cortical surface-based analysis. I. Segmentation and surface reconstruction publication-title: Neuroimage doi: 10.1006/nimg.1998.0395 – volume: 15;583 start-page: 159 issue: Pt 1 year: 2007 ident: 10.1016/j.nicl.2018.01.022_bb0130 article-title: Retinotopic maps and foveal suppression in the visual cortex of amblyopic adults publication-title: J. Physiol. doi: 10.1113/jphysiol.2007.136242 – volume: 25 start-page: 1577 issue: 11 year: 1985 ident: 10.1016/j.nicl.2018.01.022_bb0220 article-title: Differences in the neural basis of human amblyopia: the distribution of the anomaly across the visual field publication-title: Vis. Res. doi: 10.1016/0042-6989(85)90128-2 – volume: 25 start-page: 222 issue: 2 year: 2005 ident: 10.1016/j.nicl.2018.01.022_bb0350 article-title: Voxel-based analysis of MRI detects abnormal visual cortex in children and adults with amblyopia publication-title: Hum. Brain Mapp. doi: 10.1002/hbm.20109 – year: 2001 ident: 10.1016/j.nicl.2018.01.022_bb9850 – volume: 62 start-page: 782 year: 2012 ident: 10.1016/j.nicl.2018.01.022_bb9870 article-title: FSL publication-title: Neuroimage doi: 10.1016/j.neuroimage.2011.09.015 – volume: 84 start-page: 911 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0385 article-title: Patterns of resting state connectivity in human primary visual cortical areas: a 7T fMRI study publication-title: NeuroImage doi: 10.1016/j.neuroimage.2013.09.060 – volume: 58 start-page: 2329 issue: 4 year: 2017 ident: 10.1016/j.nicl.2018.01.022_bb0050 article-title: Regional extent of peripheral suppression in amblyopia publication-title: Invest. Ophthalmol. Vis. Sci. doi: 10.1167/iovs.16-20012 – volume: 8 start-page: 339 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0200 article-title: Cortical connective field estimates from resting state fMRI activity publication-title: Front. Neurosci. doi: 10.3389/fnins.2014.00339 – volume: 22 start-page: 8633 year: 2002 ident: 10.1016/j.nicl.2018.01.022_bb0030 article-title: Circuits for local and global signal integration in primary visual cortex publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.22-19-08633.2002 – volume: 3 start-page: 380 issue: 5 year: 2003 ident: 10.1016/j.nicl.2018.01.022_bb0345 article-title: The pattern of visual deficits in amblyopia publication-title: J. Vis. doi: 10.1167/3.5.5 – volume: 26 start-page: 13128 issue: 51 year: 2006 ident: 10.1016/j.nicl.2018.01.022_bb0290 article-title: Two retinotopic visual areas in human lateral occipital cortex publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.1657-06.2006 – volume: 7 start-page: 181 year: 1997 ident: 10.1016/j.nicl.2018.01.022_bb0170 article-title: Retinotopic organization in human visual cortex and the spatial precision of functional MRI publication-title: Cereb. Cortex doi: 10.1093/cercor/7.2.181 – volume: 26 start-page: 525 issue: 4 year: 2013 ident: 10.1016/j.nicl.2018.01.022_bb0470 article-title: Independent sources of spontaneous BOLD fluctuation along the visual pathway publication-title: Brain Topogr. doi: 10.1007/s10548-013-0290-1 – volume: 141 start-page: 250 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0205 article-title: Lamina-dependent calibrated BOLD response in human primary motor cortex publication-title: NeuroImage doi: 10.1016/j.neuroimage.2016.06.030 – volume: 15;533 start-page: 281 issue: Pt 1 year: 2001 ident: 10.1016/j.nicl.2018.01.022_bb0055 article-title: The cortical deficit in humans with strabismic amblyopia publication-title: J Physiol. doi: 10.1111/j.1469-7793.2001.0281b.x – volume: 29 start-page: 1359 year: 2006 ident: 10.1016/j.nicl.2018.01.022_bb0155 article-title: fMRI resting state networks define distinct modes of long-distance interactions in the human brain publication-title: NeuroImage doi: 10.1016/j.neuroimage.2005.08.035 – volume: 9 start-page: 195 year: 1999 ident: 10.1016/j.nicl.2018.01.022_bb0180 article-title: Cortical surface-based analysis. II: inflation, flattening, and a surface-based coordinate system publication-title: NeuroImage doi: 10.1006/nimg.1998.0396 – volume: 4 start-page: 509 year: 2004 ident: 10.1016/j.nicl.2018.01.022_bb0120 article-title: Retinotopic organization in children measured with fMRI publication-title: J. Vis. doi: 10.1167/4.6.10 – volume: 25 start-page: 2117 year: 2005 ident: 10.1016/j.nicl.2018.01.022_bb0410 article-title: Retinotopic axis specificity and selective clustering of feedback projections from V2 to V1 in the owl monkey publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.4137-04.2005 – volume: 57 start-page: 5649 issue: 13 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0065 article-title: Assessing suppression in amblyopic children with a dichoptic eye chart publication-title: Invest. Ophthalmol. Vis. Sci. doi: 10.1167/iovs.16-19986 – volume: 136 start-page: 162 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0390 article-title: Increased functional connectivity between language and visually deprived areas in late and partial blindness publication-title: NeuroImage doi: 10.1016/j.neuroimage.2016.04.056 – volume: 14 start-page: 11 year: 2006 ident: 10.1016/j.nicl.2018.01.022_bb0305 article-title: Visual processing in amblyopia: human studies publication-title: Strabismus doi: 10.1080/09273970500536243 – volume: 57 start-page: 289 year: 1995 ident: 10.1016/j.nicl.2018.01.022_bb9880 article-title: Controlling the false discovery rate: a practical and powerful approach to multiple testing publication-title: J. R. Stat. Soc. Ser. B. doi: 10.1111/j.2517-6161.1995.tb02031.x – volume: 56 start-page: 1426 issue: 3 year: 2011 ident: 10.1016/j.nicl.2018.01.022_bb0215 article-title: Topographically specific functional connectivity between visual field maps in the human brain publication-title: NeuroImage doi: 10.1016/j.neuroimage.2011.02.077 – volume: 54 start-page: 505 issue: 1 year: 2011 ident: 10.1016/j.nicl.2018.01.022_bb0325 article-title: Effective connectivity anomalies in human amblyopia publication-title: NeuroImage doi: 10.1016/j.neuroimage.2010.07.053 – volume: 51 start-page: 1432 issue: 3 year: 2010 ident: 10.1016/j.nicl.2018.01.022_bb0060 article-title: Decreased gray matter concentration in the lateral geniculate nuclei in human amblyopes publication-title: Invest. Ophthalmol. Vis. Sci. doi: 10.1167/iovs.09-3931 – volume: 18 start-page: 909 year: 2012 ident: 10.1016/j.nicl.2018.01.022_bb0440 article-title: Combination of blood oxygen level-dependent functional magnetic resonance imaging and visual evoked potential recordings for abnormal visual cortex in two types of amblyopia publication-title: Mol. Vis. – volume: 1563 start-page: 41 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0450 article-title: Abnormal functional connectivity density in children with anisometropic amblyopia at resting-state publication-title: Brain Res. doi: 10.1016/j.brainres.2014.03.015 – volume: 33 start-page: 3752 issue: 9 year: 2013 ident: 10.1016/j.nicl.2018.01.022_bb0010 article-title: Cortical metabolic activity matches the pattern of visual suppression in strabismus publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.3228-12.2013 – volume: 114 start-page: 79 year: 2015 ident: 10.1016/j.nicl.2018.01.022_bb9855 article-title: A new model of strabismic amblyopia: loss of spatial acuity due to increased temporal dispersion of geniculate X-cell afferents on to cortical neurons publication-title: Vis. Res. doi: 10.1016/j.visres.2015.04.005 – volume: 20 start-page: 70 year: 2001 ident: 10.1016/j.nicl.2018.01.022_bb0185 article-title: Automated manifold surgery: constructing geometrically accurate and topologically correct models of the human cerebral cortex publication-title: IEEE Trans. Med. Imaging doi: 10.1109/42.906426 – volume: 164 start-page: 59 year: 2018 ident: 10.1016/j.nicl.2018.01.022_bb0380 article-title: Hemifield columns co-opt ocular dominance column structure in human achiasma publication-title: Neuroimage doi: 10.1016/j.neuroimage.2016.12.063 – volume: 28 start-page: 397 issue: 7 year: 2017 ident: 10.1016/j.nicl.2018.01.022_bb0265 article-title: Reduced response cluster size in early visual areas explains the acuity deficit in amblyopia publication-title: Neuroreport doi: 10.1097/WNR.0000000000000767 – volume: 164 start-page: 32 year: 2018 ident: 10.1016/j.nicl.2018.01.022_bb0105 article-title: Spatial specificity of the functional MRI blood oxygenation response relative to neuronal activity publication-title: NeuroImage doi: 10.1016/j.neuroimage.2017.08.077 – start-page: 1 year: 2013 ident: 10.1016/j.nicl.2018.01.022_bb0160 article-title: Altered functional connectivity of the primary visual cortex in subjects with amblyopia publication-title: Neural Plast. doi: 10.1155/2013/612086 – volume: 33 start-page: 169 issue: 1 year: 2006 ident: 10.1016/j.nicl.2018.01.022_bb0300 article-title: Selective fovea-related deprived activation in retinotopic and high-order visual cortex of human amblyopes publication-title: NeuroImage doi: 10.1016/j.neuroimage.2006.06.026 – volume: 58 start-page: 481 issue: 1 year: 2017 ident: 10.1016/j.nicl.2018.01.022_bb0330 article-title: Spatial and global sensory suppression mapping encompassing the central 10° field in Anisometropic amblyopia publication-title: Invest. Ophthalmol. Vis. Sci. doi: 10.1167/iovs.16-20298 – volume: 1 start-page: 31 year: 1982 ident: 10.1016/j.nicl.2018.01.022_bb0415 article-title: Human amblyopia: consequence of chronic interocular suppression publication-title: Hum. Neurobiol. – volume: 7 issue: 8 year: 2012 ident: 10.1016/j.nicl.2018.01.022_bb0340 article-title: Altered spontaneous activity in anisometropic amblyopia subjects: revealed by resting-state FMRI publication-title: PLoS One doi: 10.1371/journal.pone.0043373 – volume: 30 start-page: 4054 issue: 12 year: 2009 ident: 10.1016/j.nicl.2018.01.022_bb0225 article-title: Selectivity as well as sensitivity loss characterizes the cortical spatial frequency deficit in amblyopia publication-title: Hum. Brain Mapp. doi: 10.1002/hbm.20829 – volume: 254 start-page: 569 issue: 3 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0335 article-title: Distinct patterns of spontaneous brain activity between children and adults with anisometropic amblyopia: a resting-state fMRI study publication-title: Graefes Arch. Clin. Exp. Ophthalmol. doi: 10.1007/s00417-015-3117-9 – volume: 35 start-page: 14740 issue: 44 year: 2015 ident: 10.1016/j.nicl.2018.01.022_bb0115 article-title: Is the cortical deficit in amblyopia due to reduced cortical magnification, loss of neural resolution, or neural disorganization? publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.1101-15.2015 – volume: 55 start-page: 3857 issue: 6 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0370 article-title: Effects of strabismic amblyopia on visuomotor behavior: part II. Visually guided reaching publication-title: Invest. Ophthalmol. Vis. Sci. doi: 10.1167/iovs.14-14543 – volume: 79 start-page: 603 issue: 3 year: 1990 ident: 10.1016/j.nicl.2018.01.022_bb0420 article-title: Human amblyopia: structure of the visual field publication-title: Exp. Brain Res. doi: 10.1007/BF00229328 – volume: 96 start-page: 1253 issue: 6 year: 2017 ident: 10.1016/j.nicl.2018.01.022_bb0270 article-title: High-resolution CBV-fMRI allows mapping of laminar activity and connectivity of cortical input and output in human M1 publication-title: Neuron doi: 10.1016/j.neuron.2017.11.005 – volume: 6 start-page: 758 year: 2003 ident: 10.1016/j.nicl.2018.01.022_bb0020 article-title: Early “visual” cortex activation correlates with superior verbal memory performance in the blind publication-title: Nat. Neurosci. doi: 10.1038/nn1072 – volume: 18 start-page: 6411 year: 1998 ident: 10.1016/j.nicl.2018.01.022_bb0285 article-title: Neuronal correlates of amblyopia in the visual cortex of macaque monkeys with experimental strabismus and anisometropia publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.18-16-06411.1998 – volume: 360 start-page: 693 issue: 1456 year: 2005 ident: 10.1016/j.nicl.2018.01.022_bb0435 article-title: Visual field map clusters in human cortex publication-title: Philos. Trans. R. Soc. Lond. Ser. B Biol. Sci. doi: 10.1098/rstb.2005.1628 – volume: 30 start-page: 1313 issue: 4 year: 2006 ident: 10.1016/j.nicl.2018.01.022_bb0375 article-title: Widespread functional connectivity and fMRI fluctuations in human visual cortex in the absence of visual stimulation publication-title: NeuroImage doi: 10.1016/j.neuroimage.2005.11.018 – volume: 52 start-page: 766 issue: 3 year: 2010 ident: 10.1016/j.nicl.2018.01.022_bb0250 article-title: Can structure predict function in the human brain? publication-title: NeuroImage doi: 10.1016/j.neuroimage.2010.01.071 – volume: 8 start-page: 700 issue: 9 year: 2007 ident: 10.1016/j.nicl.2018.01.022_bb0190 article-title: Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging publication-title: Nat. Rev. Neurosci. doi: 10.1038/nrn2201 – volume: 54 start-page: 6585 issue: 10 year: 2013 ident: 10.1016/j.nicl.2018.01.022_bb0045 article-title: The regional extent of suppression: strabismics versus nonstrabismics publication-title: Invest. Ophthalmol. Vis. Sci. doi: 10.1167/iovs.12-11314 – volume: 35 start-page: 12366 issue: 36 year: 2015 ident: 10.1016/j.nicl.2018.01.022_bb0075 article-title: Resting-state retinotopic organization in the absence of retinal input and visual experience publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.4715-14.2015 – volume: 11 start-page: 341 issue: 4 year: 2007 ident: 10.1016/j.nicl.2018.01.022_bb0125 article-title: Monocular activation of V1 and V2 in amblyopic adults measured with functional magnetic resonance imaging publication-title: J AAPOS. doi: 10.1016/j.jaapos.2007.01.119 – volume: 4 year: 2015 ident: 10.1016/j.nicl.2018.01.022_bb0035 article-title: Widespread correlation patterns of fMRI signal across visual cortex reflect eccentricity organization publication-title: elife doi: 10.7554/eLife.03952 – volume: 20 start-page: 45 issue: 1 year: 2001 ident: 10.1016/j.nicl.2018.01.022_bb0465 article-title: Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm publication-title: IEEE Trans. Med. Imaging doi: 10.1109/42.906424 – volume: 268 start-page: 889 year: 1995 ident: 10.1016/j.nicl.2018.01.022_bb0400 article-title: Borders of multiple visual areas in humans revealed by functional magnetic resonance imaging publication-title: Science doi: 10.1126/science.7754376 – volume: 7 start-page: 1340 issue: 5 year: 1987 ident: 10.1016/j.nicl.2018.01.022_bb0355 article-title: Effects of early unilateral blur on the Macaque's visual system. III. Physiological observations publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.07-05-01340.1987 – volume: 83 start-page: 49 issue: 2 year: 2000 ident: 10.1016/j.nicl.2018.01.022_bb0040 article-title: Strabismic amblyopia. Part 1. Psychophysics publication-title: Clin. Exp. Optom. doi: 10.1111/j.1444-0938.2000.tb04892.x – volume: 33 start-page: 138 issue: 20 year: 2013 ident: 10.1016/j.nicl.2018.01.022_bb9860 article-title: Assessment of neuroretinal function in a group of functional amblyopes with documented LGN deficits publication-title: Ophthalmic Physiol. Opt. doi: 10.1111/opo.12024 – volume: 49 start-page: 1681 issue: 13 year: 2009 ident: 10.1016/j.nicl.2018.01.022_bb0280 article-title: Interocular transfer of orientation-specific fMRI adaptation reveals amblyopia-related deficits in humans publication-title: Vis. Res. doi: 10.1016/j.visres.2009.04.009 – volume: 24 start-page: 789 issue: 8 year: 1984 ident: 10.1016/j.nicl.2018.01.022_bb0315 article-title: Detection and discrimination of the direction of motion in central and peripheral vision of normal and amblyopic observers publication-title: Vis. Res. doi: 10.1016/0042-6989(84)90150-0 – volume: 25 start-page: 3911 issue: 10 year: 2015 ident: 10.1016/j.nicl.2018.01.022_bb0455 article-title: Probabilistic maps of visual topography in human cortex publication-title: Cereb. Cortex doi: 10.1093/cercor/bhu277 – volume: 124 start-page: 844 issue: 6 year: 2006 ident: 10.1016/j.nicl.2018.01.022_bb0015 article-title: Relating binocular and monocular vision in strabismic and anisometropic amblyopia publication-title: Arch. Ophthalmol. doi: 10.1001/archopht.124.6.844 – volume: 36 start-page: 240 issue: 3 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0080 article-title: Using magnetic resonance imaging to assess visual deficits: a review publication-title: Ophthalmic Physiol. Opt. doi: 10.1111/opo.12293 – volume: 40 start-page: 147 issue: 2 year: 2001 ident: 10.1016/j.nicl.2018.01.022_bb0295 article-title: Binocularity and spatial frequency dependence of calcarine activation in two types of amblyopia publication-title: Neurosci. Res. doi: 10.1016/S0168-0102(01)00220-6 – volume: 447 start-page: 83 issue: 7140 year: 2007 ident: 10.1016/j.nicl.2018.01.022_bb0430 article-title: Intrinsic functional architecture in the anaesthetized monkey brain publication-title: Nature doi: 10.1038/nature05758 – volume: 2008 start-page: 751 issue: 29 year: 2008 ident: 10.1016/j.nicl.2018.01.022_bb0405 article-title: Neuronal correlates of spontaneous fluctuations in fMRI signals in monkey visual cortex: implications for functional connectivity at rest publication-title: Hum. Brain Mapp. doi: 10.1002/hbm.20580 – volume: 106 start-page: 13040 year: 2009 ident: 10.1016/j.nicl.2018.01.022_bb9865 article-title: Correspondence of the brain’s functional architecture during activation and rest publication-title: Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.0905267106 – volume: 6 start-page: 62 issue: 8 year: 2014 ident: 10.1016/j.nicl.2018.01.022_bb0275 article-title: Neuroimaging of amblyopia and binocular vision: a review publication-title: Front. Integr. Neurosci. – volume: 334 start-page: 9 year: 1993 ident: 10.1016/j.nicl.2018.01.022_bb0025 article-title: Cortical hierarchy reflected in the organization of intrinsic connections in macaque monkey visual cortex publication-title: J. Comp. Neurol. doi: 10.1002/cne.903340103 – volume: 10 start-page: 250 issue: Pt 2 year: 1996 ident: 10.1016/j.nicl.2018.01.022_bb0395 article-title: The neural basis of suppression and amblyopia in strabismus publication-title: Eye (Lond). doi: 10.1038/eye.1996.54 – volume: 26 start-page: 3719 issue: 9 year: 2016 ident: 10.1016/j.nicl.2018.01.022_bb0195 article-title: Functional connectivity patterns of visual cortex reflect its anatomical organization publication-title: Cereb. Cortex doi: 10.1093/cercor/bhv175 – volume: 22 start-page: 1586 year: 2012 ident: 10.1016/j.nicl.2018.01.022_bb0005 article-title: Functional connectivity between anatomically unconnected areas is shaped by collective network-level effects in the macaque cortex publication-title: Cereb. Cortex doi: 10.1093/cercor/bhr234 – volume: 46 start-page: 506 year: 2006 ident: 10.1016/j.nicl.2018.01.022_bb0360 article-title: Cerebral correlates of impaired grating perception in individual, psychophysically assessed human amblyopes publication-title: Vis. Res. doi: 10.1016/j.visres.2005.10.014 – volume: 11 issue: 14 year: 2011 ident: 10.1016/j.nicl.2018.01.022_bb0175 article-title: Interocular suppression in strabismic amblyopia results in an attenuated and delayed hemodynamic response function in early visual cortex publication-title: J. Vis. doi: 10.1167/11.14.16 – volume: 67 start-page: 331 year: 2013 ident: 10.1016/j.nicl.2018.01.022_bb0145 article-title: Evaluation and calibration of functional network modeling methods based on known anatomical connections publication-title: NeuroImage doi: 10.1016/j.neuroimage.2012.11.006 |
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Snippet | Amblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical periods... AbstractAmblyopia is a prevalent developmental visual disorder of childhood that typically persists in adults. Due to altered visual experience during critical... |
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SubjectTerms | Adult Amblyopia - diagnostic imaging Amblyopia - pathology Binocular vision Brain Mapping Correlation of Data Female Fourier Analysis Functional MRI Humans Image Processing, Computer-Assisted Intrinsic Magnetic Resonance Imaging Male Middle Aged Oxygen - blood Partial correlation Radiology Regional Regular Rest Resting state functional connectivity Resting state functional magnetic resonance imaging Retina - diagnostic imaging Retina - physiopathology Spontaneous activity Strabismus Suppression Visual Cortex - diagnostic imaging Visual Cortex - physiopathology Visual Pathways - diagnostic imaging Visual Pathways - physiopathology Young Adult |
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Title | Partial correlation analysis reveals abnormal retinotopically organized functional connectivity of visual areas in amblyopia |
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