2006
DOI: 10.1016/j.neuroimage.2006.01.024
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Resolution of complex tissue microarchitecture using the diffusion orientation transform (DOT)

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Cited by 340 publications
(337 citation statements)
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“…A radial truncation order n ≤ N involves (N + 1) coefficients. A low order N assumes a radial Gaussian behavior as in [26,30]; the Gaussian decay in the SPF basis arises from the normalization of the Laguerre polynomials in the spherical coordinates (more details in appendix B). On the contrary, a high order N provides a modelfree estimation.…”
Section: Spherical Polar Fourier Expansionmentioning
confidence: 99%
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“…A radial truncation order n ≤ N involves (N + 1) coefficients. A low order N assumes a radial Gaussian behavior as in [26,30]; the Gaussian decay in the SPF basis arises from the normalization of the Laguerre polynomials in the spherical coordinates (more details in appendix B). On the contrary, a high order N provides a modelfree estimation.…”
Section: Spherical Polar Fourier Expansionmentioning
confidence: 99%
“…(8) (see Appendix E for more details). Additionally, the QBI [21,40,56] and the DOT [26] methods can be expressed in our approach with respectively R n (||q||) = δ(||q|| − q )/q 2 and R n (||q||) = j n (2π||q||R 0 )δ n,l where j n is the spherical Bessel function at order n, q and R 0 are two real constants (appendix C and D for more details on this). Fig.1 points out the actual adequacy of the first R n functions to the experimental MR signal from erythrocytes (appendix A for more details).…”
Section: Spherical Polar Fourier Expansionmentioning
confidence: 99%
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“…HARDI methods attempt to recover more information about the angular structure of intravoxel diffusion by acquiring larger numbers of diffusion-encoding directional measurements at higher diffusionweighting factors (b values) than is routine for DTI [6][7][8]. There has been a growing list of proposed techniques for reconstructing fiber orientations from HARDI data, including spherical harmonic modeling of the apparent diffusion coefficient (ADC) profile [7,8], multitensor modeling [9], generalized tensor representations [10,11], persistent angular structure [12], circular spectrum mapping [13], q-ball imaging [14,15], spherical deconvolution [16], fiber orientation estimated on continuous axially symmetric tensors [17] and the diffusion orientation transform [18]. However, all of these HARDI approaches remain SNR-limited even on 3T scanners with parallel imaging capability, because of the need for both high spatial resolution and very strong diffusion-weighting, resulting in long examination times and/or suboptimal discrimination of intravoxel crossing fiber tracts.…”
Section: Introductionmentioning
confidence: 99%