An improved Bayesian tensor regularization and sampling algorithm to track neuronal fiber pathways in the language circuit
Purpose: The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with functionally important regions in the human brain. The functional activations in the brain normally occur in the gray matter regions. Hence the...
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Published in | Medical physics (Lancaster) Vol. 37; no. 8; pp. 4274 - 4287 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Association of Physicists in Medicine
01.08.2010
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Subjects | |
Online Access | Get full text |
ISSN | 0094-2405 2473-4209 0094-2405 |
DOI | 10.1118/1.3456113 |
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Abstract | Purpose:
The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with functionally important regions in the human brain. The functional activations in the brain normally occur in the gray matter regions. Hence the fibers bordering these regions are weakly myelinated, resulting in poor performance of conventional tractography methods to trace the fiber links between them. A lower fractional anisotropy in this region makes it even difficult to track the fibers in the presence of noise. In this work, the authors focused on a stochastic approach to reconstruct these fiber pathways based on a Bayesian regularization framework.
Methods:
To estimate the true fiber direction (propagation vector), thea priori and conditional probability density functions are calculated in advance and are modeled as multivariate normal. The variance of the estimated tensor element vector is associated with the uncertainty due to noise and partial volume averaging (PVA). An adaptive and multiple sampling of the estimated tensor element vector, which is a function of the pre-estimated variance, overcomes the effect of noise and PVA in this work.
Results:
The algorithm has been rigorously tested using a variety of synthetic data sets. The quantitative comparison of the results to standard algorithms motivated the authors to implement it forin vivo DTI data analysis. The algorithm has been implemented to delineate fibers in two major language pathways (Broca’s to SMA and Broca’s to Wernicke’s) across 12 healthy subjects. Though the mean of standard deviation was marginally bigger than conventional (Euler’s) approach [P. J. Basser
et al.
, “In vivo fiber tractography using DT-MRI data,” Magn. Reson. Med.
44(4), 625–632 (2000)], the number of extracted fibers in this approach was significantly higher. The authors also compared the performance of the proposed method to Lu’s method [Y. Lu
et al.
, “Improved fiber tractography with Bayesian tensor regularization,” Neuroimage
31(3), 1061–1074 (2006)] and Friman’s stochastic approach [O. Friman
et al.
, “A Bayesian approach for stochastic white matter tractography,” IEEE Trans. Med. Imaging
25(8), 965–978 (2006)]. Overall performance of the approach is found to be superior to above two methods, particularly when the signal-to-noise ratio was low.
Conclusions:
The authors observed that an adaptive sampling of the tensor element vectors, estimated as a function of the variance in a Bayesian framework, can effectively delineate neuronal fibers to analyze the structure-function relationship in human brain. The simulated andin vivo results are in good agreement with the theoretical aspects of the algorithm. |
---|---|
AbstractList | Purpose:
The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with functionally important regions in the human brain. The functional activations in the brain normally occur in the gray matter regions. Hence the fibers bordering these regions are weakly myelinated, resulting in poor performance of conventional tractography methods to trace the fiber links between them. A lower fractional anisotropy in this region makes it even difficult to track the fibers in the presence of noise. In this work, the authors focused on a stochastic approach to reconstruct these fiber pathways based on a Bayesian regularization framework.
Methods:
To estimate the true fiber direction (propagation vector), the
a priori
and conditional probability density functions are calculated in advance and are modeled as multivariate normal. The variance of the estimated tensor element vector is associated with the uncertainty due to noise and partial volume averaging (PVA). An adaptive and multiple sampling of the estimated tensor element vector, which is a function of the pre-estimated variance, overcomes the effect of noise and PVA in this work.
Results:
The algorithm has been rigorously tested using a variety of synthetic data sets. The quantitative comparison of the results to standard algorithms motivated the authors to implement it for
in vivo
DTI data analysis. The algorithm has been implemented to delineate fibers in two major language pathways (Broca’s to SMA and Broca’s to Wernicke’s) across 12 healthy subjects. Though the mean of standard deviation was marginally bigger than conventional (Euler’s) approach [
P. J. Basser et al., “In vivo fiber tractography using DT-MRI data,” Magn. Reson. Med. 44(
4
), 625–632 (2000)
], the number of extracted fibers in this approach was significantly higher. The authors also compared the performance of the proposed method to Lu’s method [
Y. Lu et al., “Improved fiber tractography with Bayesian tensor regularization,” Neuroimage 31(
3
), 1061–1074 (2006)
] and Friman’s stochastic approach [
O. Friman et al., “A Bayesian approach for stochastic white matter tractography,” IEEE Trans. Med. Imaging 25(
8
), 965–978 (2006)
]. Overall performance of the approach is found to be superior to above two methods, particularly when the signal-to-noise ratio was low.
Conclusions:
The authors observed that an adaptive sampling of the tensor element vectors, estimated as a function of the variance in a Bayesian framework, can effectively delineate neuronal fibers to analyze the structure-function relationship in human brain. The simulated and
in vivo
results are in good agreement with the theoretical aspects of the algorithm. Purpose: The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with functionally important regions in the human brain. The functional activations in the brain normally occur in the gray matter regions. Hence the fibers bordering these regions are weakly myelinated, resulting in poor performance of conventional tractography methods to trace the fiber links between them. A lower fractional anisotropy in this region makes it even difficult to track the fibers in the presence of noise. In this work, the authors focused on a stochastic approach to reconstruct these fiber pathways based on a Bayesian regularization framework. Methods: To estimate the true fiber direction (propagation vector), thea priori and conditional probability density functions are calculated in advance and are modeled as multivariate normal. The variance of the estimated tensor element vector is associated with the uncertainty due to noise and partial volume averaging (PVA). An adaptive and multiple sampling of the estimated tensor element vector, which is a function of the pre‐estimated variance, overcomes the effect of noise and PVA in this work. Results: The algorithm has been rigorously tested using a variety of synthetic data sets. The quantitative comparison of the results to standard algorithms motivated the authors to implement it forin vivo DTI data analysis. The algorithm has been implemented to delineate fibers in two major language pathways (Broca's to SMA and Broca's to Wernicke's) across 12 healthy subjects. Though the mean of standard deviation was marginally bigger than conventional (Euler's) approach [P. J. Basser et al., “In vivo fiber tractography using DT‐MRI data,” Magn. Reson. Med. 44(4), 625–632 (2000)], the number of extracted fibers in this approach was significantly higher. The authors also compared the performance of the proposed method to Lu's method [Y. Lu et al., “Improved fiber tractography with Bayesian tensor regularization,” Neuroimage 31(3), 1061–1074 (2006)] and Friman's stochastic approach [O. Friman et al., “A Bayesian approach for stochastic white matter tractography,” IEEE Trans. Med. Imaging 25(8), 965–978 (2006)]. Overall performance of the approach is found to be superior to above two methods, particularly when the signal‐to‐noise ratio was low. Conclusions: The authors observed that an adaptive sampling of the tensor element vectors, estimated as a function of the variance in a Bayesian framework, can effectively delineate neuronal fibers to analyze the structure‐function relationship in human brain. The simulated andin vivo results are in good agreement with the theoretical aspects of the algorithm. The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with functionally important regions in the human brain. The functional activations in the brain normally occur in the gray matter regions. Hence the fibers bordering these regions are weakly myelinated, resulting in poor performance of conventional tractography methods to trace the fiber links between them. A lower fractional anisotropy in this region makes it even difficult to track the fibers in the presence of noise. In this work, the authors focused on a stochastic approach to reconstruct these fiber pathways based on a Bayesian regularization framework.PURPOSEThe purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with functionally important regions in the human brain. The functional activations in the brain normally occur in the gray matter regions. Hence the fibers bordering these regions are weakly myelinated, resulting in poor performance of conventional tractography methods to trace the fiber links between them. A lower fractional anisotropy in this region makes it even difficult to track the fibers in the presence of noise. In this work, the authors focused on a stochastic approach to reconstruct these fiber pathways based on a Bayesian regularization framework.To estimate the true fiber direction (propagation vector), the a priori and conditional probability density functions are calculated in advance and are modeled as multivariate normal. The variance of the estimated tensor element vector is associated with the uncertainty due to noise and partial volume averaging (PVA). An adaptive and multiple sampling of the estimated tensor element vector, which is a function of the pre-estimated variance, overcomes the effect of noise and PVA in this work.METHODSTo estimate the true fiber direction (propagation vector), the a priori and conditional probability density functions are calculated in advance and are modeled as multivariate normal. The variance of the estimated tensor element vector is associated with the uncertainty due to noise and partial volume averaging (PVA). An adaptive and multiple sampling of the estimated tensor element vector, which is a function of the pre-estimated variance, overcomes the effect of noise and PVA in this work.The algorithm has been rigorously tested using a variety of synthetic data sets. The quantitative comparison of the results to standard algorithms motivated the authors to implement it for in vivo DTI data analysis. The algorithm has been implemented to delineate fibers in two major language pathways (Broca's to SMA and Broca's to Wernicke's) across 12 healthy subjects. Though the mean of standard deviation was marginally bigger than conventional (Euler's) approach [P. J. Basser et al., "In vivo fiber tractography using DT-MRI data," Magn. Reson. Med. 44(4), 625-632 (2000)], the number of extracted fibers in this approach was significantly higher. The authors also compared the performance of the proposed method to Lu's method [Y. Lu et al., "Improved fiber tractography with Bayesian tensor regularization," Neuroimage 31(3), 1061-1074 (2006)] and Friman's stochastic approach [O. Friman et al., "A Bayesian approach for stochastic white matter tractography," IEEE Trans. Med. Imaging 25(8), 965-978 (2006)]. Overall performance of the approach is found to be superior to above two methods, particularly when the signal-to-noise ratio was low.RESULTSThe algorithm has been rigorously tested using a variety of synthetic data sets. The quantitative comparison of the results to standard algorithms motivated the authors to implement it for in vivo DTI data analysis. The algorithm has been implemented to delineate fibers in two major language pathways (Broca's to SMA and Broca's to Wernicke's) across 12 healthy subjects. Though the mean of standard deviation was marginally bigger than conventional (Euler's) approach [P. J. Basser et al., "In vivo fiber tractography using DT-MRI data," Magn. Reson. Med. 44(4), 625-632 (2000)], the number of extracted fibers in this approach was significantly higher. The authors also compared the performance of the proposed method to Lu's method [Y. Lu et al., "Improved fiber tractography with Bayesian tensor regularization," Neuroimage 31(3), 1061-1074 (2006)] and Friman's stochastic approach [O. Friman et al., "A Bayesian approach for stochastic white matter tractography," IEEE Trans. Med. Imaging 25(8), 965-978 (2006)]. Overall performance of the approach is found to be superior to above two methods, particularly when the signal-to-noise ratio was low.The authors observed that an adaptive sampling of the tensor element vectors, estimated as a function of the variance in a Bayesian framework, can effectively delineate neuronal fibers to analyze the structure-function relationship in human brain. The simulated and in vivo results are in good agreement with the theoretical aspects of the algorithm.CONCLUSIONSThe authors observed that an adaptive sampling of the tensor element vectors, estimated as a function of the variance in a Bayesian framework, can effectively delineate neuronal fibers to analyze the structure-function relationship in human brain. The simulated and in vivo results are in good agreement with the theoretical aspects of the algorithm. The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with functionally important regions in the human brain. The functional activations in the brain normally occur in the gray matter regions. Hence the fibers bordering these regions are weakly myelinated, resulting in poor performance of conventional tractography methods to trace the fiber links between them. A lower fractional anisotropy in this region makes it even difficult to track the fibers in the presence of noise. In this work, the authors focused on a stochastic approach to reconstruct these fiber pathways based on a Bayesian regularization framework. To estimate the true fiber direction (propagation vector), the a priori and conditional probability density functions are calculated in advance and are modeled as multivariate normal. The variance of the estimated tensor element vector is associated with the uncertainty due to noise and partial volume averaging (PVA). An adaptive and multiple sampling of the estimated tensor element vector, which is a function of the pre-estimated variance, overcomes the effect of noise and PVA in this work. The algorithm has been rigorously tested using a variety of synthetic data sets. The quantitative comparison of the results to standard algorithms motivated the authors to implement it for in vivo DTI data analysis. The algorithm has been implemented to delineate fibers in two major language pathways (Broca's to SMA and Broca's to Wernicke's) across 12 healthy subjects. Though the mean of standard deviation was marginally bigger than conventional (Euler's) approach [P. J. Basser et al., "In vivo fiber tractography using DT-MRI data," Magn. Reson. Med. 44(4), 625-632 (2000)], the number of extracted fibers in this approach was significantly higher. The authors also compared the performance of the proposed method to Lu's method [Y. Lu et al., "Improved fiber tractography with Bayesian tensor regularization," Neuroimage 31(3), 1061-1074 (2006)] and Friman's stochastic approach [O. Friman et al., "A Bayesian approach for stochastic white matter tractography," IEEE Trans. Med. Imaging 25(8), 965-978 (2006)]. Overall performance of the approach is found to be superior to above two methods, particularly when the signal-to-noise ratio was low. The authors observed that an adaptive sampling of the tensor element vectors, estimated as a function of the variance in a Bayesian framework, can effectively delineate neuronal fibers to analyze the structure-function relationship in human brain. The simulated and in vivo results are in good agreement with the theoretical aspects of the algorithm. Purpose: The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with functionally important regions in the human brain. The functional activations in the brain normally occur in the gray matter regions. Hence the fibers bordering these regions are weakly myelinated, resulting in poor performance of conventional tractography methods to trace the fiber links between them. A lower fractional anisotropy in this region makes it even difficult to track the fibers in the presence of noise. In this work, the authors focused on a stochastic approach to reconstruct these fiber pathways based on a Bayesian regularization framework. Methods: To estimate the true fiber direction (propagation vector), thea priori and conditional probability density functions are calculated in advance and are modeled as multivariate normal. The variance of the estimated tensor element vector is associated with the uncertainty due to noise and partial volume averaging (PVA). An adaptive and multiple sampling of the estimated tensor element vector, which is a function of the pre-estimated variance, overcomes the effect of noise and PVA in this work. Results: The algorithm has been rigorously tested using a variety of synthetic data sets. The quantitative comparison of the results to standard algorithms motivated the authors to implement it forin vivo DTI data analysis. The algorithm has been implemented to delineate fibers in two major language pathways (Broca’s to SMA and Broca’s to Wernicke’s) across 12 healthy subjects. Though the mean of standard deviation was marginally bigger than conventional (Euler’s) approach [P. J. Basser et al. , “In vivo fiber tractography using DT-MRI data,” Magn. Reson. Med. 44(4), 625–632 (2000)], the number of extracted fibers in this approach was significantly higher. The authors also compared the performance of the proposed method to Lu’s method [Y. Lu et al. , “Improved fiber tractography with Bayesian tensor regularization,” Neuroimage 31(3), 1061–1074 (2006)] and Friman’s stochastic approach [O. Friman et al. , “A Bayesian approach for stochastic white matter tractography,” IEEE Trans. Med. Imaging 25(8), 965–978 (2006)]. Overall performance of the approach is found to be superior to above two methods, particularly when the signal-to-noise ratio was low. Conclusions: The authors observed that an adaptive sampling of the tensor element vectors, estimated as a function of the variance in a Bayesian framework, can effectively delineate neuronal fibers to analyze the structure-function relationship in human brain. The simulated andin vivo results are in good agreement with the theoretical aspects of the algorithm. |
Author | Anderson, Adam W. Wu, Xi Mishra, Arabinda Gore, John C. Ding, Zhaohua |
Author_xml | – sequence: 1 givenname: Arabinda surname: Mishra fullname: Mishra, Arabinda email: arabinda.mishra@vanderbilt.edu organization: Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee 37232 – sequence: 2 givenname: Adam W. surname: Anderson fullname: Anderson, Adam W. organization: Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee 37232 and Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37232 – sequence: 3 givenname: Xi surname: Wu fullname: Wu, Xi organization: Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee 37232 – sequence: 4 givenname: John C. surname: Gore fullname: Gore, John C. organization: Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee 37232 and Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37232 – sequence: 5 givenname: Zhaohua surname: Ding fullname: Ding, Zhaohua organization: Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee 37232; Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37232; and Department of Electrical Engineering and Computer Science, Vanderbilt University, Nashville, Tennessee 37232 |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20879588$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_neuroimage_2022_119240 crossref_primary_10_2217_iim_11_60 crossref_primary_10_1016_j_mri_2011_12_017 crossref_primary_10_1016_j_nicl_2015_10_008 crossref_primary_10_1016_j_neuroimage_2013_11_025 crossref_primary_10_1371_journal_pone_0142860 crossref_primary_10_1007_s00429_016_1302_1 crossref_primary_10_1118_1_4811155 crossref_primary_10_1016_j_nicl_2020_102446 |
Cites_doi | 10.1073/pnas.96.18.10422 10.1002/mrm.1315 10.1016/j.neuroimage.2006.02.031 10.1038/nrn893 10.1016/j.neuroimage.2006.03.011 10.1002/mrm.20642 10.1002/mrm.10415 10.1002/mrm.20582 10.1016/j.neuroimage.2006.09.018 10.1002/mrm.20339 10.1109/TMI.2006.877093 10.1002/jmri.10350 10.1002/(SICI)1522-2594(199912)42:6<1123::AID-MRM17>3.0.CO;2-H 10.1016/j.neuroimage.2004.08.047 10.1002/mrm.20723 10.1002/hbm.10102 10.1002/(SICI)1522-2594(199907)42:1<37::AID-MRM7>3.0.CO;2-O 10.1002/nbm.779 10.1038/16056 10.1093/brain/123.12.2400 10.3406/bmsap.1865.9495 10.1016/S1361-8415(02)00053-1 10.1002/mrm.10209 10.1371/journal.pone.0004257 10.1016/S1090-7807(02)00178-7 10.1038/79892 10.1016/S1053-8119(03)00142-3 10.1016/S1053-8119(03)00277-5 10.1371/journal.pone.0006660 10.1016/j.neuroimage.2006.01.043 10.1146/annurev.neuro.22.1.49 10.1038/15967 10.1002/1522-2594(200010)44:4<625::AID-MRM17>3.0.CO;2-O |
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Copyright | American Association of Physicists in Medicine 2010 American Association of Physicists in Medicine Copyright © 2010 American Association of Physicists in Medicine 2010 American Association of Physicists in Medicine |
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Keywords | Hotelling transform Bayes decision rule diffusion tensor imaging (DTI) |
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Notes | 0094‐2405/2010/37(8)/4274/14/$30.00 Author to whom correspondence should be addressed. Electronic mail arabinda.mishra@vanderbilt.edu Telephone: (615) 322‐6213; Fax: (615) 322‐0734. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author to whom correspondence should be addressed. Electronic mail: arabinda.mishra@vanderbilt.edu; Telephone: (615) 322-6213; Fax: (615) 322-0734. |
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References | Westin, Maier, Mamata, Nabavi, Jolesz, Kikinis (c9) 2002; 6 Chen, Hsu (c10) 2005; 54 Xue, van Zijl, Crain, Solaiyappan, Mori (c4) 1999; 42 Wedeen, Hagman, Tseng, Reese, Weisskoff (c16) 2005; 54 Behrens, Berg, Jbabdi, Rushworth, Woolrich (c17) 2007; 34 Correia, Newcombe, Carpenter, Williams (c21) 2009; 17 Lazar, Alexander (c5) 2003; 20 Friman, Farneback, Westin (c20) 2006; 25 Basser, Pajevic, Pierpaoli, Duda, Aldroubi (c1) 2000; 44 Parker, Luzzi, Alexander, Claudia, Wheeler-Kingshott, Ciccarelli, Ralph (c28) 2005; 24 Romanski, Tian, Fritz, Mishkin, Goldman-Rakic, Rauschecker (c26) 1999; 2 Yarkoni, Barch, Garry, Conturo, Braver (c32) 2009; 4 Passingham, Stephan, Kotter (c23) 2002; 3 Anderson (c7) 2001; 46 Conturo, Lori, Cull, Akbudak, Snyder, Shimony, McKinstry, Burton, Raichle (c3) 1999; 96 Mishra, Lu, Meng, Anderson, Ding (c12) 2006; 31 Parker, Haroon, Wheeler-Kingshott (c14) 2003; 18 Broca (c22) 1865; 6 Jones, Simmons, Williams, Horsfield (c24) 1999; 42 Lu, Aldroubi, Gore, Anderson, Ding (c19) 2006; 31 Romanski, Tian, Fritz, Mishkin, Goldman-Rakic, Rauschecker (c27) 2000; 3 Kaas, Hackett (c25) 1999; 2 Alexander, Barker, Arridge (c30) 2002; 48 Lori, Akbudak, Shimony, Cull, Snyder, Guillory, Conturo (c8) 2002; 15 Ding, Gore, Anderson (c11) 2005; 53 Hagmann, Thiran, Jonasson, Vandergheynst, Clarke, Maeder, Meuli (c13) 2003; 19 Lazar, Weinstein, Tsuruda, Hasan, Arfanakis, Meyerand, Badie, Rowley, Haughton, Field, Alexander (c18) 2003; 18 Jones (c2) 1999; 22 Morgan, Mishra, Newton, Anderson, Gore, Ding (c33) 2009; 4 Ding, Gore, Anderson (c6) 2003; 49 Hosey, Williams, Ansorge (c15) 2005; 54 Powell, Parker, Alexzander, Symms, Boulby, Wheeler-Kingshott, Barker, Noppeney, Koepp, Duncan (c29) 2006; 32 Scott, Blank, Rosen, Wise (c34) 2000; 123 Pajevic, Basser (c31) 2003; 161 2002; 15 2006; 31 2006; 32 2000; 3 2000; 44 2002; 6 1999; 22 2002; 3 1999; 42 2003; 18 2003; 19 1999; 2 1865; 6 2001; 46 2007; 34 2005; 24 2002; 48 2006; 25 2003; 161 2005; 53 2003; 49 2005; 54 1999; 96 2009; 4 2000; 123 2003; 20 2009; 17 e_1_2_7_6_1 e_1_2_7_5_1 e_1_2_7_4_1 e_1_2_7_3_1 e_1_2_7_9_1 e_1_2_7_8_1 e_1_2_7_7_1 e_1_2_7_19_1 e_1_2_7_18_1 e_1_2_7_17_1 e_1_2_7_16_1 e_1_2_7_2_1 e_1_2_7_15_1 e_1_2_7_14_1 e_1_2_7_13_1 e_1_2_7_12_1 e_1_2_7_11_1 e_1_2_7_10_1 e_1_2_7_26_1 Correia M. M. (e_1_2_7_22_1) 2009; 17 e_1_2_7_27_1 e_1_2_7_28_1 e_1_2_7_29_1 e_1_2_7_30_1 e_1_2_7_25_1 e_1_2_7_31_1 e_1_2_7_24_1 e_1_2_7_32_1 e_1_2_7_23_1 e_1_2_7_33_1 e_1_2_7_34_1 e_1_2_7_21_1 e_1_2_7_35_1 e_1_2_7_20_1 12210942 - Magn Reson Med. 2002 Aug;48(2):331-40 15652301 - Neuroimage. 2005 Feb 1;24(3):656-66 12652543 - Magn Reson Med. 2003 Apr;49(4):716-21 16632380 - Neuroimage. 2006 Aug 1;32(1):388-99 10570492 - Nat Neurosci. 1999 Dec;2(12):1131-6 19165335 - PLoS One. 2009;4(1):e4257 10570476 - Nat Neurosci. 1999 Dec;2(12):1045-7 16265642 - Magn Reson Med. 2005 Dec;54(6):1480-9 12884338 - J Magn Reson Imaging. 2003 Aug;18(2):242-54 12880786 - Neuroimage. 2003 Jul;19(3):545-54 16624586 - Neuroimage. 2006 Jul 15;31(4):1525-35 19684850 - PLoS One. 2009;4(8):e6660 12154362 - Nat Rev Neurosci. 2002 Aug;3(8):606-16 11025519 - Magn Reson Med. 2000 Oct;44(4):625-32 12632468 - Hum Brain Mapp. 2003 Apr;18(4):306-21 16563804 - Neuroimage. 2006 Jul 1;31(3):1061-74 16247738 - Magn Reson Med. 2005 Dec;54(6):1377-86 14568483 - Neuroimage. 2003 Oct;20(2):1140-53 10202532 - Annu Rev Neurosci. 1999;22:49-103 15678537 - Magn Reson Med. 2005 Feb;53(2):485-90 12044998 - Med Image Anal. 2002 Jun;6(2):93-108 11746585 - Magn Reson Med. 2001 Dec;46(6):1174-88 17070705 - Neuroimage. 2007 Jan 1;34(1):144-55 11017162 - Nat Neurosci. 2000 Oct;3(10):966 10398948 - Magn Reson Med. 1999 Jul;42(1):37-41 12660106 - J Magn Reson. 2003 Mar;161(1):1-14 11099443 - Brain. 2000 Dec;123 Pt 12:2400-6 10571934 - Magn Reson Med. 1999 Dec;42(6):1123-7 16894991 - IEEE Trans Med Imaging. 2006 Aug;25(8):965-78 16032670 - Magn Reson Med. 2005 Aug;54(2):393-401 10468624 - Proc Natl Acad Sci U S A. 1999 Aug 31;96(18):10422-7 12489098 - NMR Biomed. 2002 Nov-Dec;15(7-8):494-515 |
References_xml | – volume: 54 start-page: 1377 issn: 0740-3194 year: 2005 ident: c16 article-title: Mapping complex tissue architecture with diffusion spectrum magnetic resonance imaging publication-title: Magn. Reson. Med. – volume: 54 start-page: 393 issn: 0740-3194 year: 2005 ident: c10 article-title: Noise removal in magnetic resonance diffusion tensor imaging publication-title: Magn. Reson. Med. – volume: 42 start-page: 37 issn: 0740-3194 year: 1999 ident: c24 article-title: Non-invasive assessment of axonal fiber connectivity in the human brain via diffusion tensor MRI publication-title: Magn. Reson. Med. – volume: 123 start-page: 2400 issn: 0006-8950 year: 2000 ident: c34 article-title: Identification of a pathway for intelligible speech in the left temporal lobe publication-title: Brain – volume: 42 start-page: 1123 issn: 0740-3194 year: 1999 ident: c4 article-title: In vivo three-dimensional reconstruction of rat brain axonal projections by diffusion tensor imaging publication-title: Magn. Reson. Med. – volume: 54 start-page: 1480 issn: 0740-3194 year: 2005 ident: c15 article-title: Inference of multiple fiber orientations in high angular resolution diffusion imaging publication-title: Magn. Reson. Med. – volume: 4 start-page: e4257 issn: 1932-6203 year: 2009 ident: c32 article-title: BOLD correlates of trial-by-trial reaction time variability in gray and white matter: A multi-study fMRI analysis publication-title: PLoS ONE – volume: 6 start-page: 337 issn: 0002-7820 year: 1865 ident: c22 article-title: Sur le siege de la faculte du langage articule publication-title: Bulletin de la Societe d’ anthropologie – volume: 32 start-page: 388 issn: 1053-8119 year: 2006 ident: c29 article-title: Hemispheric asymmetries in language-related pathways: A combined functional MRI and tractyography study publication-title: Neuroimage – volume: 44 start-page: 625 issn: 0740-3194 year: 2000 ident: c1 article-title: In vivo fiber tractography using DT-MRI data publication-title: Magn. Reson. Med. – volume: 18 start-page: 242 issn: 1053-1807 year: 2003 ident: c14 article-title: A framework for streamline-based probabilistic index of connectivity (PICo) using a structural interpretation of MRI diffusion measurements publication-title: J. Magn. Reson Imaging – volume: 24 start-page: 656 issn: 1053-8119 year: 2005 ident: c28 article-title: Lateralization of ventral and dorsal auditory-language pathways in human brain publication-title: Neuroimage – volume: 46 start-page: 1174 issn: 0740-3194 year: 2001 ident: c7 article-title: Theoretical analysis of the effects of noise on diffusion tensor imaging publication-title: Magn. Reson. Med. – volume: 19 start-page: 545 issn: 1053-8119 year: 2003 ident: c13 article-title: DTI mapping of human brain connectivity: Statistical fiber tracking and virtual dissection publication-title: Neuroimage – volume: 34 start-page: 144 issn: 1053-8119 year: 2007 ident: c17 article-title: Probabilistic diffusion tractography with multiple fiber orientations: What can we gain? publication-title: Neuroimage – volume: 4 start-page: e6660 issn: 1932-6203 year: 2009 ident: c33 article-title: An integrated fMRI and DTI analysis of structure function relationship in the human language network publication-title: PLoS ONE – volume: 6 start-page: 93 issn: 1361-8415 year: 2002 ident: c9 article-title: Processing and visualization for diffusion tensor MRI publication-title: Med. Image Anal. – volume: 53 start-page: 485 issn: 0740-3194 year: 2005 ident: c11 article-title: Reduction of noise in diffusion tensor images using anisotropic smoothing publication-title: Magn. Reson. Med. – volume: 17 start-page: 3575 year: 2009 ident: c21 article-title: Regularization of fractional anisotropy using neighborhood information publication-title: Proc. Intl. Soc. Mag. Reson. Med. – volume: 3 start-page: 956 issn: 1097-6256 year: 2000 ident: c27 article-title: Reply to ‘what’, ‘where’ and ‘how’ in auditory cortex,” Belin and Zatorre publication-title: Nat. Neurosci. – volume: 18 start-page: 306 issn: 1065-9471 year: 2003 ident: c18 article-title: White matter tractography using diffusion tensor deflection publication-title: Hum. Brain Mapp – volume: 31 start-page: 1525 issn: 1053-8119 year: 2006 ident: c12 article-title: Unified framework for anisotropic interpolation and smoothing of diffusion tensor images publication-title: Neuroimage – volume: 3 start-page: 606 issn: 1471-003X year: 2002 ident: c23 article-title: The anatomical basis of functional localization in the cortex publication-title: Nat. Rev. Neurosci. – volume: 31 start-page: 1061 issn: 1053-8119 year: 2006 ident: c19 article-title: Improved fiber tractography with Bayesian tensor regularization publication-title: Neuroimage – volume: 2 start-page: 1131 issn: 1097-6256 year: 1999 ident: c26 article-title: Dual streams of auditory afferents target multiple domains in the primate prefrontal cortex publication-title: Nat. Neurosci. – volume: 25 start-page: 965 issn: 0278-0062 year: 2006 ident: c20 article-title: A Bayesian approach for stochastic white matter tractography publication-title: IEEE Trans. Med. Imaging – volume: 161 start-page: 1 issn: 1090-7807 year: 2003 ident: c31 article-title: Parametric and non parametric statistical analysis of DT-MRI data publication-title: J. Magn. Reson. – volume: 22 start-page: 49 issn: 0147-006X year: 1999 ident: c2 article-title: Making brain connections: Neuroanatomy and the work of TPS Powell, 1923–1996 publication-title: Annu. Rev. Neurosci. – volume: 15 start-page: 494 issn: 0952-3480 year: 2002 ident: c8 article-title: Diffusion tensor fiber tracking of human brain connectivity: Acquisition methods, reliability analysis and biological results publication-title: NMR Biomed. – volume: 20 start-page: 1140 issn: 1053-8119 year: 2003 ident: c5 article-title: An error analysis of white matter tractography methods: Synthetic diffusion tensor field simulations publication-title: Neuroimage – volume: 48 start-page: 331 issn: 0740-3194 year: 2002 ident: c30 article-title: Detection and modeling of non-Gaussian apparent diffusion coefficient profiles in human brain data publication-title: Magn. Reson. Med. – volume: 49 start-page: 716 issn: 0740-3194 year: 2003 ident: c6 article-title: Classification and quantification of neuronal fiber pathways using diffusion tensor MRI publication-title: Magn. Reson. Med. – volume: 2 start-page: 1045 issn: 1097-6256 year: 1999 ident: c25 article-title: ‘What’ and ‘where’ processing in auditory cortex publication-title: Nat. Neurosci. – volume: 96 start-page: 10422 issn: 0027-8424 year: 1999 ident: c3 article-title: Tracking neuronal fiber pathways in the living human brain publication-title: Proc. Natl. Acad. Sci. U.S.A. – volume: 15 start-page: 494 issue: 7–8 year: 2002 end-page: 515 article-title: Diffusion tensor fiber tracking of human brain connectivity: Acquisition methods, reliability analysis and biological results publication-title: NMR Biomed. – volume: 6 start-page: 93 issue: 2 year: 2002 end-page: 108 article-title: Processing and visualization for diffusion tensor MRI publication-title: Med. Image Anal. – volume: 4 start-page: e4257 issue: 1 year: 2009 article-title: BOLD correlates of trial‐by‐trial reaction time variability in gray and white matter: A multi‐study fMRI analysis publication-title: PLoS ONE – volume: 48 start-page: 331 issue: 2 year: 2002 end-page: 340 article-title: Detection and modeling of non‐Gaussian apparent diffusion coefficient profiles in human brain data publication-title: Magn. Reson. Med. – volume: 22 start-page: 49 year: 1999 end-page: 103 article-title: Making brain connections: Neuroanatomy and the work of TPS Powell, 1923–1996 publication-title: Annu. Rev. Neurosci. – volume: 20 start-page: 1140 issue: 2 year: 2003 end-page: 1153 article-title: An error analysis of white matter tractography methods: Synthetic diffusion tensor field simulations publication-title: Neuroimage – volume: 49 start-page: 716 issue: 4 year: 2003 end-page: 721 article-title: Classification and quantification of neuronal fiber pathways using diffusion tensor MRI publication-title: Magn. Reson. Med. – volume: 31 start-page: 1525 issue: 4 year: 2006 end-page: 1535 article-title: Unified framework for anisotropic interpolation and smoothing of diffusion tensor images publication-title: Neuroimage – volume: 18 start-page: 242 issue: 2 year: 2003 end-page: 254 article-title: A framework for streamline‐based probabilistic index of connectivity (PICo) using a structural interpretation of MRI diffusion measurements publication-title: J. Magn. Reson Imaging – volume: 25 start-page: 965 issue: 8 year: 2006 end-page: 978 article-title: A Bayesian approach for stochastic white matter tractography publication-title: IEEE Trans. Med. Imaging – volume: 3 start-page: 606 issue: 8 year: 2002 end-page: 616 article-title: The anatomical basis of functional localization in the cortex publication-title: Nat. Rev. Neurosci. – volume: 3 start-page: 956 issue: 10 year: 2000 end-page: 966 article-title: Reply to ‘what’, ‘where’ and ‘how’ in auditory cortex,” Belin and Zatorre publication-title: Nat. Neurosci. – volume: 54 start-page: 393 issue: 2 year: 2005 end-page: 401 article-title: Noise removal in magnetic resonance diffusion tensor imaging publication-title: Magn. Reson. Med. – volume: 32 start-page: 388 issue: 1 year: 2006 end-page: 399 article-title: Hemispheric asymmetries in language‐related pathways: A combined functional MRI and tractyography study publication-title: Neuroimage – volume: 42 start-page: 37 issue: 1 year: 1999 end-page: 41 article-title: Non‐invasive assessment of axonal fiber connectivity in the human brain via diffusion tensor MRI publication-title: Magn. Reson. Med. – volume: 42 start-page: 1123 issue: 6 year: 1999 end-page: 1127 article-title: In vivo three‐dimensional reconstruction of rat brain axonal projections by diffusion tensor imaging publication-title: Magn. Reson. Med. – volume: 44 start-page: 625 issue: 4 year: 2000 end-page: 632 article-title: In vivo fiber tractography using DT‐MRI data publication-title: Magn. Reson. Med. – volume: 96 start-page: 10422 issue: 18 year: 1999 end-page: 10427 article-title: Tracking neuronal fiber pathways in the living human brain publication-title: Proc. Natl. Acad. Sci. U.S.A. – volume: 17 start-page: 3575 year: 2009 article-title: Regularization of fractional anisotropy using neighborhood information publication-title: Proc. Intl. Soc. Mag. Reson. Med. – volume: 161 start-page: 1 issue: 1 year: 2003 end-page: 14 article-title: Parametric and non parametric statistical analysis of DT‐MRI data publication-title: J. Magn. Reson. – volume: 31 start-page: 1061 issue: 3 year: 2006 end-page: 1074 article-title: Improved fiber tractography with Bayesian tensor regularization publication-title: Neuroimage – volume: 54 start-page: 1377 issue: 6 year: 2005 end-page: 1386 article-title: Mapping complex tissue architecture with diffusion spectrum magnetic resonance imaging publication-title: Magn. Reson. Med. – volume: 34 start-page: 144 issue: 1 year: 2007 end-page: 155 article-title: Probabilistic diffusion tractography with multiple fiber orientations: What can we gain? publication-title: Neuroimage – volume: 46 start-page: 1174 issue: 6 year: 2001 end-page: 1188 article-title: Theoretical analysis of the effects of noise on diffusion tensor imaging publication-title: Magn. Reson. Med. – volume: 18 start-page: 306 issue: 4 year: 2003 end-page: 321 article-title: White matter tractography using diffusion tensor deflection publication-title: Hum. Brain Mapp – volume: 4 start-page: e6660 issue: 8 year: 2009 article-title: An integrated fMRI and DTI analysis of structure function relationship in the human language network publication-title: PLoS ONE – volume: 24 start-page: 656 issue: 3 year: 2005 end-page: 666 article-title: Lateralization of ventral and dorsal auditory‐language pathways in human brain publication-title: Neuroimage – volume: 2 start-page: 1045 issue: 12 year: 1999 end-page: 1047 article-title: ‘What’ and ‘where’ processing in auditory cortex publication-title: Nat. Neurosci. – volume: 2 start-page: 1131 issue: 12 year: 1999 end-page: 1136 article-title: Dual streams of auditory afferents target multiple domains in the primate prefrontal cortex publication-title: Nat. Neurosci. – volume: 53 start-page: 485 issue: 2 year: 2005 end-page: 490 article-title: Reduction of noise in diffusion tensor images using anisotropic smoothing publication-title: Magn. Reson. Med. – volume: 54 start-page: 1480 issue: 6 year: 2005 end-page: 1489 article-title: Inference of multiple fiber orientations in high angular resolution diffusion imaging publication-title: Magn. Reson. Med. – volume: 19 start-page: 545 issue: 3 year: 2003 end-page: 554 article-title: DTI mapping of human brain connectivity: Statistical fiber tracking and virtual dissection publication-title: Neuroimage – volume: 6 start-page: 337 year: 1865 end-page: 393 article-title: Sur le siege de la faculte du langage articule publication-title: Bulletin de la Societe d’ anthropologie – volume: 123 start-page: 2400 year: 2000 end-page: 2406 article-title: Identification of a pathway for intelligible speech in the left temporal lobe publication-title: Brain – ident: e_1_2_7_4_1 doi: 10.1073/pnas.96.18.10422 – ident: e_1_2_7_8_1 doi: 10.1002/mrm.1315 – ident: e_1_2_7_13_1 doi: 10.1016/j.neuroimage.2006.02.031 – ident: e_1_2_7_24_1 doi: 10.1038/nrn893 – ident: e_1_2_7_30_1 doi: 10.1016/j.neuroimage.2006.03.011 – ident: e_1_2_7_17_1 doi: 10.1002/mrm.20642 – ident: e_1_2_7_7_1 doi: 10.1002/mrm.10415 – ident: e_1_2_7_11_1 doi: 10.1002/mrm.20582 – ident: e_1_2_7_18_1 doi: 10.1016/j.neuroimage.2006.09.018 – ident: e_1_2_7_12_1 doi: 10.1002/mrm.20339 – ident: e_1_2_7_21_1 doi: 10.1109/TMI.2006.877093 – ident: e_1_2_7_15_1 doi: 10.1002/jmri.10350 – ident: e_1_2_7_5_1 doi: 10.1002/(SICI)1522-2594(199912)42:6<1123::AID-MRM17>3.0.CO;2-H – ident: e_1_2_7_29_1 doi: 10.1016/j.neuroimage.2004.08.047 – ident: e_1_2_7_16_1 doi: 10.1002/mrm.20723 – ident: e_1_2_7_19_1 doi: 10.1002/hbm.10102 – ident: e_1_2_7_25_1 doi: 10.1002/(SICI)1522-2594(199907)42:1<37::AID-MRM7>3.0.CO;2-O – ident: e_1_2_7_9_1 doi: 10.1002/nbm.779 – ident: e_1_2_7_27_1 doi: 10.1038/16056 – ident: e_1_2_7_35_1 doi: 10.1093/brain/123.12.2400 – ident: e_1_2_7_23_1 doi: 10.3406/bmsap.1865.9495 – ident: e_1_2_7_10_1 doi: 10.1016/S1361-8415(02)00053-1 – ident: e_1_2_7_31_1 doi: 10.1002/mrm.10209 – ident: e_1_2_7_33_1 doi: 10.1371/journal.pone.0004257 – ident: e_1_2_7_32_1 doi: 10.1016/S1090-7807(02)00178-7 – ident: e_1_2_7_28_1 doi: 10.1038/79892 – ident: e_1_2_7_14_1 doi: 10.1016/S1053-8119(03)00142-3 – volume: 17 start-page: 3575 year: 2009 ident: e_1_2_7_22_1 article-title: Regularization of fractional anisotropy using neighborhood information publication-title: Proc. Intl. Soc. Mag. Reson. Med. – ident: e_1_2_7_6_1 doi: 10.1016/S1053-8119(03)00277-5 – ident: e_1_2_7_34_1 doi: 10.1371/journal.pone.0006660 – ident: e_1_2_7_20_1 doi: 10.1016/j.neuroimage.2006.01.043 – ident: e_1_2_7_3_1 doi: 10.1146/annurev.neuro.22.1.49 – ident: e_1_2_7_26_1 doi: 10.1038/15967 – ident: e_1_2_7_2_1 doi: 10.1002/1522-2594(200010)44:4<625::AID-MRM17>3.0.CO;2-O – reference: 19165335 - PLoS One. 2009;4(1):e4257 – reference: 12660106 - J Magn Reson. 2003 Mar;161(1):1-14 – reference: 16894991 - IEEE Trans Med Imaging. 2006 Aug;25(8):965-78 – reference: 12652543 - Magn Reson Med. 2003 Apr;49(4):716-21 – reference: 10202532 - Annu Rev Neurosci. 1999;22:49-103 – reference: 14568483 - Neuroimage. 2003 Oct;20(2):1140-53 – reference: 19684850 - PLoS One. 2009;4(8):e6660 – reference: 16265642 - Magn Reson Med. 2005 Dec;54(6):1480-9 – reference: 12489098 - NMR Biomed. 2002 Nov-Dec;15(7-8):494-515 – reference: 11746585 - Magn Reson Med. 2001 Dec;46(6):1174-88 – reference: 12632468 - Hum Brain Mapp. 2003 Apr;18(4):306-21 – reference: 15678537 - Magn Reson Med. 2005 Feb;53(2):485-90 – reference: 11017162 - Nat Neurosci. 2000 Oct;3(10):966 – reference: 11099443 - Brain. 2000 Dec;123 Pt 12:2400-6 – reference: 10571934 - Magn Reson Med. 1999 Dec;42(6):1123-7 – reference: 10398948 - Magn Reson Med. 1999 Jul;42(1):37-41 – reference: 10570476 - Nat Neurosci. 1999 Dec;2(12):1045-7 – reference: 12154362 - Nat Rev Neurosci. 2002 Aug;3(8):606-16 – reference: 11025519 - Magn Reson Med. 2000 Oct;44(4):625-32 – reference: 10570492 - Nat Neurosci. 1999 Dec;2(12):1131-6 – reference: 16563804 - Neuroimage. 2006 Jul 1;31(3):1061-74 – reference: 17070705 - Neuroimage. 2007 Jan 1;34(1):144-55 – reference: 16632380 - Neuroimage. 2006 Aug 1;32(1):388-99 – reference: 16032670 - Magn Reson Med. 2005 Aug;54(2):393-401 – reference: 12210942 - Magn Reson Med. 2002 Aug;48(2):331-40 – reference: 12884338 - J Magn Reson Imaging. 2003 Aug;18(2):242-54 – reference: 15652301 - Neuroimage. 2005 Feb 1;24(3):656-66 – reference: 10468624 - Proc Natl Acad Sci U S A. 1999 Aug 31;96(18):10422-7 – reference: 12880786 - Neuroimage. 2003 Jul;19(3):545-54 – reference: 12044998 - Med Image Anal. 2002 Jun;6(2):93-108 – reference: 16624586 - Neuroimage. 2006 Jul 15;31(4):1525-35 – reference: 16247738 - Magn Reson Med. 2005 Dec;54(6):1377-86 |
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The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with... The purpose of this work is to design a neuronal fiber tracking algorithm, which will be more suitable for reconstruction of fibers associated with... |
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SubjectTerms | Algorithms Anisotropy Bayes decision rule Bayes Theorem biodiffusion biomedical MRI brain Brain - anatomy & histology Computer Simulation Data analysis Diffusion diffusion tensor imaging (DTI) Diffusion Tensor Imaging - methods Eigenvalues Hotelling transform Humans Image Enhancement - methods Image Interpretation, Computer-Assisted - methods image reconstruction Imaging, Three-Dimensional - methods Interpolation Language medical image processing Models, Neurological Models, Statistical MRI: anatomic, functional, spectral, diffusion Nerve Net - anatomy & histology Neural Pathways - anatomy & histology neurophysiology Optical fiber testing Pattern Recognition, Automated - methods probability Probability density functions Probability theory Radiation Imaging Physics Reproducibility of Results Sample Size Sensitivity and Specificity smoothing methods Stochastic modeling stochastic processes Tensor methods tracking |
Title | An improved Bayesian tensor regularization and sampling algorithm to track neuronal fiber pathways in the language circuit |
URI | http://dx.doi.org/10.1118/1.3456113 https://onlinelibrary.wiley.com/doi/abs/10.1118%2F1.3456113 https://www.ncbi.nlm.nih.gov/pubmed/20879588 https://www.proquest.com/docview/756297387 https://pubmed.ncbi.nlm.nih.gov/PMC2921424 |
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