Comparison of manual and automated fiber quantification tractography in patients with temporal lobe epilepsy
Open accessAbstract
OBJECTIVE: To investigate the agreement between manually and automatically generated tracts from diffusion tensor imaging (DTI) in patients with temporal lobe epilepsy (TLE). Whole and along-the-tract diffusivity metrics and correlations with patient clinical characteristics were analyzed with respect to tractography approach. METHODS: We recruited 40 healthy controls and 24 patients with TLE who underwent conventional T1-weighted imaging and 60-direction DTI. An automated (Automated Fiber Quantification, AFQ) and manual (TrackVis) deterministic tractography approach was used to identify the uncinate fasciculus (UF) and parahippocampal white matter bundle (PHWM). Tract diffusion scalar metrics were analyzed with respect to agreement across automated and manual approaches (Dice Coefficient and Spearman correlations), to side of onset of epilepsy and patient clinical characteristics, including duration of epilepsy, age of onset and presence of hippocampal sclerosis. RESULTS: Across approaches the analysis of tract morphology similarity revealed Dice coefficients at moderate to good agreement (0.54 - 0.6) and significant correlations between diffusion values (Spearman's Rho=0.4-0.9). However, within bilateral PHWM, AFQ yielded significantly lower FA (left: Z = 4.4, p<0.001; right: Z = 5.1, p<0.001) and higher MD values (left: Z=-4.7, p<0.001; right: Z=-3.7, p<0.001) compared to the manual approach. Whole tract DTI metrics determined using AFQ were significantly correlated with patient characteristics, including age of epilepsy onset in FA (R = 0.6, p = 0.02) and MD of the ipsilateral PHWM (R=-0.6, p = 0.02), while duration of epilepsy corrected for age correlated with MD in ipsilateral PHWM (R = 0.7, p<0.01). Correlations between clinical metrics and diffusion values extracted using the manual whole tract technique did not survive correction for multiple comparisons. Both manual and automated along-the-tract analyses demonstrated significant correlations with patient clinical characteristics such as age of onset and epilepsy duration. The strongest and most widespread localized ipsi- and contralateral diffusivity alterations were observed in patients with left TLE and patients with HS compared to controls, while patients with right TLE and patients without HS did not show these strong effects. CONCLUSIONS: Manual and AFQ tractography approaches revealed significant correlations in the reconstruction of tract morphology and extracted whole and along-tract diffusivity values. However, as non-identical methods they differed in the respective yield of significant results across clinical correlations and group-wise statistics. Given the absence of excellent agreement between manual and AFQ techniques as demonstrated in the present study, caution should be considered when using AFQ particularly when used without reference to benchmark manual measures.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Manual streamline selection is considered the gold standard for delineating anatomical fiber tracts in tractography, for validating other tract identification techniques, and for benchmarked comparisons and algorithm training.
“Manual streamline selection is considered to be the gold standard to delineate anatomical fiber tracts in tractography and has been widely used to validate other anatomical tract identification techniques (Poulin et al., 2019; Pujol et al., 2015; Xie et al., 2020).”
From Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review (2022) · cites this paper as Kreilkamp et al., 2019
The Introduction (page unavailable) describes manual techniques as closest to ground truth in the absence of histological data and as a benchmark for comparing automated tractography, supporting the core of the claim. It does not establish that manual selection has been widely used to validate other tract-identification techniques; it says recent automated methods have not been extensively validated. It also does not describe using manual selections for algorithm training. (LLM, conf=0.86)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Advances in functional and structural MR image analysis and implementation as FSL
Smith, S. M., Jenkinson, M., Woolrich, M. W., Beckmann, C. F., Behrens, T. E. J., Johansen-Berg, H., Bannister, P. R., De Luca, M., Drobnjak, I., Flitney, D. E., et al. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.07.051 · Cited by 13,630 · see citing works
Measures of the Amount of Ecologic Association Between Species
Dice, L. R. (1945) · Ecology · doi:10.2307/1932409 · Cited by 12,153 · see citing works
Fast robust automated brain extraction
Smith, S. M. (2002) · Human Brain Mapping · doi:10.1002/hbm.10062 · Cited by 10,496 · see citing works
Early Identification of Refractory Epilepsy
Kwan, P., & Brodie, M. J. (2000) · New England Journal of Medicine · doi:10.1056/nejm200002033420503 · Cited by 5,204 · see citing works
Andersson, J. L. R., Skare, S., & Ashburner, J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00336-7 · Cited by 3,469 · see citing works
Andersson, J., & Sotiropoulos, S. N. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.019 · Cited by 3,439 · see citing works
Reproducibility of quantitative tractography methods applied to cerebral white matter
Wakana, S., Caprihan, A., Panzenboeck, M. M., Fallon, J. H., Perry, M., Gollub, R. L., Hua, K., Zhang, J., Jiang, H., Dubey, P., et al. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.049 · Cited by 1,686 · see citing works
Hua, K., Zhang, J., Wakana, S., Jiang, H., Li, X., Reich, D. S., Calabresi, P. A., Pekar, J. J., van Zijl, P. C. M., & Mori, S. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.053 · Cited by 1,507 · see citing works
Morphometric analysis of white matter lesions in MR images: method and validation
Zijdenbos, A. P., Dawant, B. M., Margolin, R. A., & Palmer, A. C. (1994) · IEEE Transactions on Medical Imaging · doi:10.1109/42.363096 · Cited by 1,268 · see citing works
The B‐matrix must be rotated when correcting for subject motion in DTI data
Leemans, A., & Jones, D. K. (2009) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21890 · Cited by 1,266 · see citing works
Tract profiles of white matter properties: automating fiber-tract quantification
Yeatman, J. D., Dougherty, R. F., Myall, N. J., Wandell, B. A., & Feldman, H. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049790 · Cited by 840 · see citing works
Chronic epilepsy and cognition
Elger, C. E., Helmstaedter, C., & Kurthen, M. (2004) · The Lancet Neurology · doi:10.1016/s1474-4422(04)00906-8 · Cited by 766 · see citing works
Yendiki, A. (2011) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2011.00023 · Cited by 590 · see citing works
Spurious group differences due to head motion in a diffusion MRI study
Yendiki, A., Koldewyn, K., Kakunoori, S., Kanwisher, N., & Fischl, B. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.027 · Cited by 508 · see citing works
Voxel‐based morphometry of temporal lobe epilepsy: An introduction and review of the literature
Keller, S. S., & Roberts, N. (2008) · Epilepsia · doi:10.1111/j.1528-1167.2007.01485.x · Cited by 443 · see citing works
Self-citationOn the biological basis of human laterality: I. Evidence for a maturational left–right gradient
Corballis, M. C., & Morgan, M. J. (1978) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00074471 · Cited by 415 · see citing works
Farrell, J. A. D., Landman, B. A., Jones, C. K., Smith, S. A., Prince, J. L., van Zijl, P. C. M., & Mori, S. (2007) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.21053 · Cited by 353 · see citing works
New concepts in classification of the epilepsies: Entering the 21st century
Berg, A. T., & Scheffer, I. E. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2011.03101.x · Cited by 310 · see citing works
Large scale brain models of epilepsy: dynamics meets connectomics
Richardson, M. P. (2012) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2011-301944 · Cited by 303 · see citing works
Hagler, D. J., Ahmadi, M. E., Kuperman, J. M., Holland, D., McDonald, C. R., Halgren, E., & Dale, A. M. (2008) · Human Brain Mapping · doi:10.1002/hbm.20619 · Cited by 286 · see citing works
Frontotemporal connections in episodic memory and aging: a diffusion MRI tractography study
Metzler-Baddeley, C., Jones, D. K., Belaroussi, B., Aggleton, J. P., & O'Sullivan, M. J. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2317-11.2011 · Cited by 247 · see citing works
Along-tract statistics allow for enhanced tractography analysis
Colby, J. B., Soderberg, L., Lebel, C. A., Dinov, I. D., Thompson, P. M., & Sowell, E. R. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.004 · Cited by 233 · see citing works
Imaging structural and functional brain networks in temporal lobe epilepsy
Bernhardt, B. C., Hong, S., Bernasconi, A., & Bernasconi, N. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00624 · Cited by 232 · see citing works
In VivoDiffusion Tensor Imaging and Histopathology of the Fimbria-Fornix in Temporal Lobe Epilepsy
Concha, L., Livy, D. J., Beaulieu, C., Wheatley, B. M., & Gross, D. W. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1619-09.2010 · Cited by 212 · see citing works
Side Matters: Diffusion Tensor Imaging Tractography in Left and Right Temporal Lobe Epilepsy
Ahmadi, M. E., Hagler, D. J., McDonald, C. R., Tecoma, E. S., Iragui, V. J., Dale, A. M., & Halgren, E. (2009) · American Journal of Neuroradiology · doi:10.3174/ajnr.a1650 · Cited by 205 · see citing works
Diffusion tensor imaging in medial temporal lobe epilepsy with hippocampal sclerosis
Thivard, L., Lehéricy, S., Krainik, A., Adam, C., Dormont, D., Jacques Chiras, C., Baulac, M., & Dupont, S. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.045 · Cited by 193 · see citing works
Keller, S. S. (2002) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.73.6.648 · Cited by 193 · see citing works
Self-citationConcha, L., Beaulieu, C., Collins, D. L., & Gross, D. W. (2008) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2007.139287 · Cited by 193 · see citing works
Mueller, S. G., Laxer, K. D., Cashdollar, N. M., Buckley, S. T., Paul, C., & Weiner, M. W. (2006) · Epilepsia · doi:10.1111/j.1528-1167.2006.00512.x · Cited by 150 · see citing works
Kemmotsu, N., Girard, H. M., Bernhardt, B. C., Bonilha, L., Lin, J. J., Tecoma, E. S., Iragui, V. J., Hagler, D. J., Halgren, E., & McDonald, C. R. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2011.03278.x · Cited by 148 · see citing works
Diffusion tensor imaging in temporal lobe epilepsy
Gross, D. W. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2011.03149.x · Cited by 141 · see citing works
Libero, L. E., DeRamus, T. P., Lahti, A. C., Deshpande, G., & Kana, R. K. (2015) · Cortex · doi:10.1016/j.cortex.2015.02.008 · Cited by 139 · see citing works
Spatial patterns of water diffusion along white matter tracts in temporal lobe epilepsy
Concha, L., Kim, H., Bernasconi, A., Bernhardt, B. C., & Bernasconi, N. (2012) · Neurology · doi:10.1212/wnl.0b013e31826170b6 · Cited by 127 · see citing works
Bonilha, L., Rorden, C., Halford, J. J., Eckert, M. A., Appenzeller, S., Cendes, F., & Li, L. M. (2006) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2006.103994 · Cited by 118 · see citing works
Keller, S. S., Glenn, G. R., Weber, B., Kreilkamp, B. A. K., Jensen, J. H., Helpern, J. A., Wagner, J., Barker, G. J., Richardson, M. P., & Bonilha, L. (2016) · Brain · doi:10.1093/brain/aww280 · Cited by 112 · see citing works
Self-citationRelation of sorting impairment to hippocampal damage in temporal lobe epilepsy
Gıovagnolı, A. R. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(00)00104-4 · Cited by 97 · see citing works
Keller, S. S., Schoene‐Bake, J., Gerdes, J. S., Weber, B., & Deppe, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046791 · Cited by 94 · see citing works
Self-citationDiffusion properties of major white matter tracts in young, typically developing children
Johnson, R. T., Yeatman, J. D., Wandell, B. A., Buonocore, M. H., Amaral, D. G., & Nordahl, C. W. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.025 · Cited by 90 · see citing works
Vulnerability of the frontal-temporal connections in temporal lobe epilepsy
Lin, J. J., Riley, J. D., Juranek, J. J., & Cramer, S. C. (2008) · Epilepsy Research · doi:10.1016/j.eplepsyres.2008.07.020 · Cited by 90 · see citing works
Volume estimation of the thalamus using freesurfer and stereology: consistency between methods
Keller, S. S., Gerdes, J. S., Mohammadi, S., Kellinghaus, C., Kugel, H., Deppe, K., Ringelstein, E. B., Evers, S., Schwindt, W., & Deppe, M. (2012) · Neuroinformatics · doi:10.1007/s12021-012-9147-0 · Cited by 84 · see citing works
Self-citationCoan, A. C., de Campos, B. M., Yasuda, C. L., Kubota, B. Y., Bergo, F. P. G., Guerreiro, C. A. M., & Cendes, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085843 · Cited by 79 · see citing works
Pail, M., Brázdil, M., Mareček, R., & Mikl, M. (2009) · Epilepsia · doi:10.1111/j.1528-1167.2009.02324.x · Cited by 77 · see citing works
White matter abnormalities associate with type and localization of focal epileptogenic lesions
de Campos, B. M., Coan, A. C., Beltramini, G. C., Liu, M., Yasuda, C. L., Ghizoni, E., Beaulieu, C., Gross, D. W., & Cendes, F. (2014) · Epilepsia · doi:10.1111/epi.12871 · Cited by 76 · see citing works
Rodríguez‐Cruces, R., & Concha, L. (2015) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.2223-4292.2015.02.06 · Cited by 73 · see citing works
Quantitative MRI in refractory temporal lobe epilepsy: relationship with surgical outcomes.
Bonilha, L., & Keller, S. S. (2015) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.2223-4292.2015.01.01 · Cited by 69 · see citing works
Self-citationLiu, M., Concha, L., Lebel, C. A., Beaulieu, C., & Gross, D. W. (2012) · NeuroImage Clinical · doi:10.1016/j.nicl.2012.09.010 · Cited by 69 · see citing works
Morphometric MRI alterations and postoperative seizure control in refractory temporal lobe epilepsy
Keller, S. S., Richardson, M. P., O’Muircheartaigh, J., Schoene‐Bake, J., Elger, C. E., & Weber, B. (2015) · Human Brain Mapping · doi:10.1002/hbm.22722 · Cited by 68 · see citing works
Self-citationAbnormal white matter properties in adolescent girls with anorexia nervosa
Travis, K. E., Golden, N. H., Feldman, H. M., Solomon, M. A., Nguyen, J., Mezer, A., Yeatman, J. D., & Dougherty, R. F. (2015) · NeuroImage Clinical · doi:10.1016/j.nicl.2015.10.008 · Cited by 55 · see citing works
Fonseca, V. D. C., Yasuda, C. L., Tedeschi, G. G., Betting, L. E., & Cendes, F. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00121 · Cited by 54 · see citing works
Travis, K. E., Adams, J. N., Ben‐Shachar, M., & Feldman, H. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0142860 · Cited by 46 · see citing works
Structural abnormality of the corticospinal tract in major depressive disorder
Sacchet, M. D., Prasad, G., Foland‐Ross, L. C., Joshi, S. H., Hamilton, J. P., Thompson, P. M., & Gotlib, I. H. (2014) · Biology of Mood & Anxiety Disorders · doi:10.1186/2045-5380-4-8 · Cited by 44 · see citing works
Variations in the neurobiology of reading in children and adolescents born full term and preterm
Travis, K. E., Ben‐Shachar, M., Myall, N. J., & Feldman, H. M. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.04.003 · Cited by 41 · see citing works
Kreilkamp, B. A. K., Weber, B., Richardson, M. P., & Keller, S. S. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.01.003 · Cited by 40 · see citing works
Self-citationDegree of hippocampal atrophy is related to side of seizure onset in temporal lobe epilepsy.
García‐Fiñana, M., Denby, C. E., Keller, S. S., Wieshmann, U. C., & Roberts, N. (2006) · PubMed Central · Cited by 39 · see citing works
Self-citationInterhemispheric microstructural connectivity in bitemporal lobe epilepsy with hippocampal sclerosis
Miró, J., Gurtubay-Antolín, A., Ripollés, P., Sierpowska, J., Juncadella, M., Fuentemilla, L., Sánchez, V., Falip, M., & Rodríguez‐Fornells, A. (2015) · Cortex · doi:10.1016/j.cortex.2015.03.018 · Cited by 36 · see citing works
Epilepsy-related cytoarchitectonic abnormalities along white matter pathways
Glenn, G. R., Jensen, J. H., Helpern, J. A., Spampinato, M. V., Kuzniecky, R., Keller, S. S., & Bonilha, L. (2016) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2015-312980 · Cited by 28 · see citing works
Self-citationNetwork specific change in white matter integrity in mesial temporal lobe epilepsy
Imamura, H., Matsumoto, R., Takaya, S., Nakagawa, T., Shimotake, A., Kikuchi, T., Sawamoto, N., Kunieda, T., Mikuni, N., Miyamoto, S., et al. (2015) · Epilepsy Research · doi:10.1016/j.eplepsyres.2015.12.003 · Cited by 26 · see citing works
Differences in vulnerability between the hemispheres in early childhood and adulthood
Njiokiktjien, C. (2006) · Human Physiology · doi:10.1134/s0362119706010051 · Cited by 22 · see citing works
Abnormal White Matter Properties in Adolescent Girls With Anorexia Nervosa
Golden, N. H., Travis, K. E., Feldman, H. M., Solomon, M. A., Nguyen, J., Mezer, A., Yeatman, J. D., & Dougherty, R. F. (2016) · Journal of Adolescent Health · doi:10.1016/j.jadohealth.2015.10.062 · Cited by 17 · see citing works
Sacchet, M. D., Prasad, G., Foland‐Ross, L. C., Joshi, S. H., Hamilton, J. P., Thompson, P. M., & Gotlib, I. H. (2014) · IEEE International Symposium on Biomedical Imaging (ISBI) · doi:10.1109/isbi.2014.6867940 · Cited by 17 · see citing works
Kreilkamp, B. A. K., Zacà, D., Papinutto, N., & Jovicich, J. (2015) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.24965 · Cited by 14 · see citing works
Self-citationGil, E. M., Gómez, C. M., Vaquero, E., & Rodríguez‐Martínez, E. I. (2002) · Journal of Child Neurology · doi:10.1177/088307380201700706 · Cited by 6 · see citing works
Basser (2000) · doi:10.1002/1522-2594(200010)44:4
Flagged first, then by citations
Cited by
Sorted by citations
Zhang, F., Daducci, A., He, Y., Schiavi, S., Seguin, C., Smith, R. E., Yeh, C.-H., Zhao, T., & O’Donnell, L. J. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2021.118870 · Cited by 302 · see citing works
“the gold standard for benchmarked comparisons and algorithm training [268, 526, 593].”
BackgroundRadwan, A., Sunaert, S. G., Schilling, K. G., Descoteaux, M., Landman, B. A., Vandenbulcke, M., Theys, T., Dupont, P. J., & Emsell, L. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119029 · Cited by 98 · see citing works
Tractostorm: The what, why, and how of tractography dissection reproducibility
Rheault, F., BENEDICTIS, A. D., Daducci, A., Maffei, C., Tax, C. M. W., Romascano, D., Caverzasi, E., Morency, F. C., Corrivetti, F., Pestilli, F., et al. (2020) · Human Brain Mapping · doi:10.1002/hbm.24917 · Cited by 87 · see citing works
Ji, G., Sun, J., Hua, Q., Zhang, L., Zhang, T., Bai, T., Wei, L., Wang, X., Qiu, B., Wang, K., et al. (2023) · Nature Mental Health · doi:10.1038/s44220-023-00111-2 · Cited by 89 · see citing works
Kreilkamp, B. A. K., McKavanagh, A., Alonazi, B., Bryant, L., Das, K., Wieshmann, U. C., Marson, A. G., Taylor, P. N., & Keller, S. S. (2021) · NeuroImage Clinical · doi:10.1016/j.nicl.2021.102564 · Cited by 27 · see citing works
Self-citationLiu, Y., Jiang, Y., Du, W., Gao, B., Gao, J., Hu, S., Song, Q., Wang, W., & Miao, Y. (2024) · Scientific Reports · doi:10.1038/s41598-023-50768-z · Cited by 20 · see citing works
Muncy, N. M., Kimbler, A., Hedges‐Muncy, A., McMakin, D. L., & Mattfeld, A. T. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.102937 · Cited by 17 · see citing works
Thalamohippocampal atrophy in focal epilepsy of unknown cause at the time of diagnosis
Leek, N., Kreilkamp, B. A. K., Neason, M. R., de Bézenac, C. E., Ziso, B., Elkommos, S., Das, K., Marson, A. G., & Keller, S. S. (2020) · European Journal of Neurology · doi:10.1111/ene.14565 · Cited by 19 · see citing works
Self-citationFiber ball white matter modeling in focal epilepsy
Bryant, L., McKinnon, E. T., Taylor, J. A., Jensen, J. H., Bonilha, L., de Bézenac, C. E., Kreilkamp, B. A. K., Adan, G., Wieshmann, U. C., Biswas, S., et al. (2021) · Human Brain Mapping · doi:10.1002/hbm.25382 · Cited by 16 · see citing works
Self-citationMapping the subcortical connectome using in vivo diffusion MRI: Feasibility and reliability
Kai, J., KHAN, A. R., Haast, R. A. M., & Lau, J. C. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119553 · Cited by 15 · see citing works
Andica, C., Kamagata, K., & Aoki, S. (2023) · Anatomical Science International · doi:10.1007/s12565-023-00715-9 · Cited by 12 · see citing works
Lateralized brunt of sleep deprivation on white matter injury in a rat model of Alzheimer’s disease
Mao, X., Han, D., Guo, W., Zhang, W., Wang, H., Zhang, G., Zhang, N., Jin, L.-Y., Nie, B., Li, H., et al. (2023) · GeroScience · doi:10.1007/s11357-023-01000-3 · Cited by 12 · see citing works
Wendt, J., Neubauer, A., Hedderich, D. M., Schmitz‐Koep, B., Ayyıldız, S., Schinz, D., Hippen, R., Daamen, M., Boecker, H., Zimmer, C., et al. (2024) · Human Brain Mapping · doi:10.1002/hbm.70042 · Cited by 11 · see citing works
Seto, T., Suzuki, H., Okazaki, T., Imajo, Y., Nishida, N., Funaba, M., Kanchiku, T., Taguchi, T., & Sakai, T. (2021) · BioMedical Engineering OnLine · doi:10.1186/s12938-021-00892-6 · Cited by 10 · see citing works
Safri, A. A., Nassir, C. M. N. C. M., Iman, I. N., Taib, N. H. M., Achuthan, A., & Mustapha, M. (2022) · World Journal of Clinical Cases · doi:10.12998/wjcc.v10.i24.8450 · Cited by 9 · see citing works
Multivariate white matter alterations are associated with epilepsy duration
Owen, T. W., de Tisi, J., Vos, S. B., Winston, G. P., Duncan, J. S., Wang, Y., & Taylor, P. N. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15055 · Cited by 4 · see citing works
Nichols, N., Seenarine, N., Le, C., Liu, X., & Yong, R. L. M. (2025) · Neurosurgery · doi:10.1227/neu.0000000000003668 · Cited by 3 · see citing works
Amandola, M., Farber, K., Kidambi, R., & Leung, H. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0821-24.2025 · Cited by 3 · see citing works
Luo, S., Xia, Y., Lu, C., Wang, Y., & Qiao, Z. (2024) · Seizure · doi:10.1016/j.seizure.2024.12.017 · Cited by 2 · see citing works
Mapping the topographic organization of the human zona incerta using diffusion MRI
Haast, R. A. M., Kai, J., Taha, A., Liu, V. M., Kasa, L. W., Gilmore, G., Guye, M., KHAN, A. R., & Lau, J. C. (2026) · eLife · doi:10.1101/2024.09.05.610266 · Cited by 1 · see citing works
Mapping the topographic organization of the human zona incerta using diffusion MRIPreprint
Haast, R. A. M., Kai, J., Taha, A., Liu, V. M., Gilmore, G., Guye, M., KHAN, A. R., & Lau, J. C. (2025) · eLife · doi:10.7554/elife.103530.1
Mapping the topographic organization of the human zona incerta using diffusion MRIPreprint
Haast, R. A. M., Kai, J., Taha, A., Liu, V. M., Kasa, L. W., Gilmore, G., Guye, M., KHAN, A. R., & Lau, J. C. (2025) · eLife · doi:10.7554/elife.103530
Mazzucchi, E., Hiepe, P., Pignotti, F., Rocca, G. L., Rinaldi, P., Olivi, A., & Sabatino, G. (2025) · Neurosurgical Review · doi:10.1007/s10143-025-03488-z
Mapping the topographic organization of the human zona incerta using diffusion MRIPreprint
Haast, R. A. M., Kai, J., Taha, A., Liu, V., Kasa, L. W., Gilmore, G., Guye, M., KHAN, A. R., & Lau, J. C. (2026) · eLife · doi:10.7554/elife.103530.2
- Authors
- Kreilkamp, B. A. K., Lisanti, L., Glenn, G. R., Wieshmann, U. C., Das, K., Marson, A. G., & Keller, S. S.
- Affiliations
- University of Liverpool (GB)
- Royal Society (GB)
- Emory University (US)
- Walton Centre (GB)
- Corresponding author
- Kreilkamp, Barbara A.K.
- Venue
- NeuroImage: Clinical
- Publisher
- Elsevier BV
- Published
- 2019
- Volume
- 24
- Pages
- 102024
- ISSN
- 2213-1582 (ISSN-L)
- PMC
- PMC6831895
- OpenAlex
- W2980870414
- Semantic Scholar
- 4bc0e162399b816ec539cb948350fa42474618f6
- Cited by
- 27
- References
- 63
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 3 · 2023: 3 · 2022: 5 · 2021: 3 · 2020: 3
- FWCI
- 1.78
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- NeuroImage Clinical (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Epilepsy Action
- Medical Research Council
- Epilepsy Research UK
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Health Sciences › Medicine › Psychiatry and Mental health › Epilepsy research and treatment
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Keywords
- temporal lobe epilepsy, automated fiber quantification, uncinate fasciculus, hippocampal sclerosis, fractional anisotropy, mean diffusivity, epilepsy onset age, epilepsy duration, white matter microstructure, diffusion tensor imaging, left temporal lobe epilepsy, right temporal lobe epilepsy
- MeSH terms
- Adolescent, Adult, Automation, Brain Mapping, Cell Count, Electroencephalography, Epilepsy, Temporal Lobe, Female, Hippocampus, Humans, Image Processing, Computer-Assisted, Functional Laterality, Male, Middle Aged, Nerve Fibers, Sclerosis, Young Adult, Diffusion Tensor Imaging, White Matter
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review