UHF-MRI; brain segmentation; contrast and resolution agnosticity; deep learning; domain randomization; neuroimaging; Neuroscience (miscellaneous); Medicine (miscellaneous); Radiology, Nuclear Medicine and Imaging; Neurology (clinical)
Abstract :
[en] Recently, ultra-high-field MRI (UHF-MRI) has become more available and one of the best tools to study the brain for neuroscientists. One common step in quantitative neuroimaging is to segment the brain into several regions, which has been done using software packages such as FreeSurfer, FastSurferVINN, or SynthSeg. However, the differences between UHF-MRI and 1.5T or 3T images are such that the automatic segmentation techniques optimized at these field strengths usually produce unsatisfactory segmentation results for UHF images. Thus, it has been particularly challenging to perform region-based quantitative analyses as typically done with 1.5-3T data, considerably limiting the potential of UHF-MRI until now. Ultimately, this underscores the crucial need for developing new automatic segmentation techniques designed to handle UHF images. Hence, we propose a novel Deep Learning (DL)-based segmentation technique called GOUHFI: Generalized and Optimized segmentation tool for ultra-high-field images, designed to segment UHF images of various contrasts and resolutions. For training, we used a total of 206 label maps from four datasets acquired at 3T, 7T, and 9.4T. In contrast to most DL strategies, we used a previously proposed domain randomization approach, where synthetic images generated from the 206 label maps were used for training a 3D U-Net. This approach enables the DL model to become contrast agnostic. GOUHFI was tested on seven different datasets and compared with existing techniques such as FastSurferVINN, SynthSeg, and CEREBRUM-7T. GOUHFI was able to segment the six contrasts and seven resolutions tested at 3T, 7T, and 9.4T. Average Dice-Sørensen Similarity Coefficient (DSC) scores of 0.90, 0.90, and 0.93 were computed against the ground truth segmentations at 3T, 7T, and 9.4T, respectively. These results demonstrated GOUHFI's superior performance to competing approaches at each resolution and contrast level tested. Moreover, GOUHFI demonstrated impressive resistance to the typical inhomogeneities observed at UHF-MRI, making it a new powerful segmentation tool allowing the usual quantitative analysis pipelines performed at lower fields to be applied also at UHF. Ultimately, GOUHFI is a promising new segmentation tool, being the first of its kind proposing a contrast- and resolution-agnostic alternative for UHF-MRI without requiring fine tuning or retraining, making it the forthcoming alternative for neuroscientists working with UHF-MRI or even lower field strengths.
Disciplines :
Neurology
Author, co-author :
Fortin, Marc-Antoine ; Department of Physics, Norwegian University of Science and Technology, Trondheim, Norway
Kristoffersen, Anne Louise; Department of Physics, Norwegian University of Science and Technology, Trondheim, Norway
Larsen, Michael Staff; Department of Computer Science, Norwegian University of Science and Technology, Trondheim, Norway
Lamalle, Laurent ; Université de Liège - ULiège > Département de physique
Stirnberg, Rüdiger; German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany
Goa, Pål Erik; Department of Physics, Norwegian University of Science and Technology, Trondheim, Norway ; Department of Radiology and Nuclear Medicine, St. Olavs Hospital HF, Trondheim, Norway
Language :
English
Title :
GOUHFI: A novel contrast- and resolution-agnostic segmentation tool for ultra-high-field MRI.
F.R.S.-FNRS - Fonds de la Recherche Scientifique BMBF - Federal Ministry of Education and Research RCN - Research Council of Norway
Funding text :
This project and SCAIFIELD data acquisition were supported through the following funding organizations under the aegis of JPND: Belgium, The Fund for Scientific Research (F.R.S.-FNRS; funding code PINT-MULTI/BEJR.8006.20); Germany, Federal Ministry of Education and Research (BMBF; funding codes 01ED2109A/B); and Norway, The Research Council of Norway (RCN; funding code 322980).We would also like to thank all the publicly available datasets used in this work. First, data provided as part as the Human Connectome Project, WU-Minn Consortium (principal investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University were used in this publication. Finally, we would also like to thank individually all these following projects/initiatives for sharing their dataset and making this article possible: (1) the UltraCortex: Submillimeter Ultra-High Field 9.4 T1 Brain MR Image Collection and Manual Cortical Segmentations dataset (DOI: https://doi.org/10.18112/openneuro.ds005216.v1.1.0 ), (2) Autism Brain Imaging Data Exchange II (ABIDE-II) initiative (DOI: https://dx.doi.org/10.21227/y3v9-b041 ), (3) Open Science CBS Neuroimaging Repository ( https://www.nitrc.org/frs/?group_id=606 ), (4) CEREBRUM-7T: Fast and Fully-volumetric Brain Segmentation of 7 Tesla MR Volumes (DOI: https://doi.org/10.25493/RF12-09N ), and (5) Human Brain Atlas ( https://osf.io/ckh5t/ ).
Arruda, W. O., Meira, A. T., Ono, S. E., de Carvalho Neto, A., Betting, L. E. G. G., Raskin, S., Camargo, C. H. F., & Teive, H. A. G. (2020). Volumetric MRI changes in spinocerebellar ataxia (SCA3 and SCA10) patients. The Cerebellum, 19, 536–543. https://doi.org/10.1007/s12311-020-01137-3
Ashburner, J. (2012). SPM: A history. Neuroimage, 62(2), 791–800. https://doi.org/10.1016/j.neuroimage.2011.10.025
Beisteiner, R., Robinson, S., Wurnig, M., Hilbert, M., Merksa, K., Rath, J., Höllinger, I., Klinger, N., Marosi, C., & Trattnig, S. (2011). Clinical fMRI: Evidence for a 7 T benefit over 3 T. NeuroImage, 57(3), 1015–1021. https://doi.org/10.1016/j.neuroimage.2011.03.078
Billot, B., Greve, D. N., Puonti, O., Thielscher, A., Van Leemput, K., Fischl, B., Dalca, A. V., & Iglesias, J. E. (2023). Synthseg: Segmentation of brain MRI scans of any contrast and resolution without retraining. Medical Image Analysis, 83, 102687. https://doi.org/10.1016/j.media.2022.102687
Bonferroni, C. (1936). Teoria statistica delle classi e calcolo delle probabilita. Pubblicazioni del R Istituto Superiore di Scienze Economiche e Commericiali di Firenze, 8, 3–62. https://doi.org/10.4135/9781412961288.n455
Cabalo, D. G., Leppert, I. R., Thevakumaran, R., DeKraker, J., Hwang, Y., Royer, J., Kebets, V., Tavakol, S., Wang, Y., & Zhou, Y. (2025). Multimodal precision neuroimaging of the individual human brain at ultra-high fields. Scientific Data, 12(1), 123. https://doi.org/10.1038/s41597-025-04863-7
Casamitjana, A., Mancini, M., Robinson, E., Peter, L., Annunziata, R., Althonayan, J., Crampsie, S., Blackburn, E., Billot, B., Atzeni, A., Puonti, O., Balbastre, Y., Schmidt, P., Hughes, J., Augustinack, J. C., Edlow, B. L., Zöllei, L., Thomas, D. L., Kliemann, D., … Iglesias, J. E. (2024). A next-generation, histological atlas of the human brain and its application to automated brain MRI segmentation. bioRxiv. https://doi.org/10.1101/2024.02.05.579016
Coupé, P., Mansencal, B., Clément, M., Giraud, R., Denis De Senneville, B., Ta, V.-T., Lepetit, V., & Manjon, J. V. (2020). AssemblyNet: A large ensemble of CNNs for 3D whole brain MRI segmentation. NeuroImage, 219, 117026. https://doi.org/10.1016/j.neuroimage.2020.117026
Cox, R. W. (1996). AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages. Computers and Biomedical research, 29(3), 162–173. https://doi.org/10.1006/cbmr.1996.0014
Deeley, M. A., Chen, A., Datteri, R., Noble, J. H., Cmelak, A. J., Donnelly, E. F., Malcolm, A. W., Moretti, L., Jaboin, J., Niermann, K., Yang, E. S., Yu, D. S., Yei, F., Koyama, T., Ding, G. X., & Dawant, B. M. (2011). Comparison of manual and automatic segmentation methods for brain structures in the presence of space-occupying lesions: A multi-expert study. Physics in Medicine Biology, 56(14), 4557–4577. https://doi.org/10.1088/0031-9155/56/14/021
Despotović, I., Goossens, B., & Philips, W. (2015). MRI segmentation of the human brain: Challenges, methods, and applications. Computational and Mathematical Methods in Medicine, 2015(1), 450341. https://doi.org/10.1155/2015/450341
Di Martino, A., O’Connor, D., Chen, B., Alaerts, K., Anderson, J. S., Assaf, M., Balsters, J. H., Baxter, L., Beggiato, A., Bernaerts, S., Blanken, L. M. E., Bookheimer, S. Y., Braden, B. B., Byrge, L., Castellanos, F. X., Dapretto, M., Delorme, R., Fair, D. A., Fishman, I., … Milham, M. P. (2017). Enhancing studies of the connectome in autism using the autism brain imaging data exchange ii. Scientific Data, 4, 170010. https://doi.org/10.1038/sdata.2017.10
Dice, L. R. (1945). Measures of the amount of ecologic association between species. Ecology, 26(3), 297–302. https://doi.org/10.2307/1932409
Drozdzal, M., Vorontsov, E., Chartrand, G., Kadoury, S., & Pal, C. (2016). The importance of skip connections in biomedical image segmentation. InInternational workshop on deep learning in medical image analysis, international workshop on large-scale annotation of biomedical data and expert label synthesis (pp. 179–187). Springer. https://doi.org/10.1007/978-3-319-46976-8_19
Faber, J., Kügler, D., Bahrami, E., Heinz, L.-S., Timmann, D., Ernst, T. M., Deike-Hofmann, K., Klockgether, T., Van De Warrenburg, B., Van Gaalen, J., Reetz, K., Romanzetti, S., Oz, G., Joers, J. M., Diedrichsen, J., Reuter, M., Giunti, P., Garcia-Moreno, H., Jacobi, H., … Krahe, J. (2022). CerebNet: A fast and reliable deep-learning pipeline for detailed cerebellum sub-segmentation. NeuroImage, 264, 119703. https://doi.org/10.1016/j.neuroimage.2022.119703
Feldman, R. E., Rutland, J. W., Fields, M. C., Marcuse, L. V., Pawha, P. S., Delman, B. N., & Balchandani, P. (2018). Quantification of perivascular spaces at 7 T: A potential MRI biomarker for epilepsy. Seizure, 54, 11–18. https://doi.org/10.1016/j.seizure.2017.11.004
Ferreira, M., Schaprian, T., Kügler, D., Reuter, M., Deike-Hoffmann, K., Timmann, D., Ernst, T. M., Giunti, P., Garcia-Moreno, H., & van de Warrenburg, B. (2024). Cerebellar volumetry in ataxias: Relation to ataxia severity and duration. The Cerebellum, 23(4), 1521–1529. https://doi.org/10.1007/s12311-024-01659-0
Fischl, B., Salat, D. H., Busa, E., Albert, M., Dieterich, M., Haselgrove, C., Van Der Kouwe, A., Killiany, R., Kennedy, D., Klaveness, S., Montillo, A., Makris, N., Rosen, B., & Dale, A. M. (2002). Whole brain segmentation: Automated labeling of neuroanatomical structures in the human brain. Neuron, 33(3), 341–355. https://doi.org/10.1016/S0896-6273(02)00569-X
Fortin, M.-A., Stirnberg, R., Völzke, Y., Lamalle, L., Pracht, E., Löwen, D., Stöcker, T., & Goa, P. E. (2025). MPRAGElike: A novel approach to generate t1w images from multi-contrast gradient echo images for brain segmentation. Magnetic Resonance in Medicine, 94(1), 134–149. https://doi.org/10.1002/mrm.30453
Fracasso, A., van Veluw, S. J., Visser, F., Luijten, P. R., Spliet, W., Zwanenburg, J. J., Dumoulin, S. O., & Petridou, N. (2016). Lines of baillarger in vivo and ex vivo: Myelin contrast across lamina at 7 T MRI and histology. NeuroImage, 133, 163–175. https://doi.org/10.1016/j.neuroimage.2016.02.072
Geng, D.-y., Li, Y.-X., & Zee, C.-S. (2006). Magnetic resonance imaging-based volumetric analysis of basal ganglia nuclei and substantia nigra in patients with Parkinson’s disease. Neurosurgery, 58(2), 256–262. https://doi.org/10.1227/01.neu.0000194845.19462.7b
George, I., Arrighi-Allisan, A., Delman, B., Balchandani, P., Horng, S., & Feldman, R. (2021). A novel method to measure venular perivascular spaces in patients with MS on 7T MRI. American Journal of Neuroradiology, 42(6), 1069–1072. https://doi.org/10.3174/ajnr.a7144
Ghafoorian, M., Mehrtash, A., Kapur, T., Karssemeijer, N., Marchiori, E., Pesteie, M., Guttmann, C. R., de Leeuw, F.-E., Tempany, C. M., & Van Ginneken, B. (2017). Transfer learning for domain adaptation in MRI: Application in brain lesion segmentation. Medical Image Analysis, 37, 43–58. https://doi.org/10.1016/j.media.2017.01.004
Gibson, E., Ramirez, J., Woods, L. A., Ottoy, J., Berberian, S., Scott, C. J. M., Yhap, V., Gao, F., Coello, R. D., Valdes Hernandez, M., Lang, A. E., Tartaglia, C. M., Kumar, S., Binns, M. A., Bartha, R., Symons, S., Swartz, R. H., Masellis, M., Singh, N., … Goubran, M. (2024). segcsvdwmh: A convolutional neural network-based tool for quantifying white matter hyperintensities in heterogeneous patient cohorts (tech. rep. No. 18). Wiley. https://doi.org/10.1002/hbm.70104
González-Villà, S., Oliver, A., Valverde, S., Wang, L., Zwiggelaar, R., & Lladó, X. (2016). A review on brain structures segmentation in magnetic resonance imaging. Artificial Intelligence in Medicine, 73, 45–69. https://doi.org/10.1016/j.artmed.2016.09.001
Gras, V., Vignaud, A., Amadon, A., Le Bihan, D., & Boulant, N. (2017). Universal pulses: A new concept for calibration-free parallel transmission. Magnetic Resonance in Medicine, 77(2), 635–643. https://doi.org/10.1002/mrm.26148
Haast, R. A., Kashyap, S., Ivanov, D., Yousif, M. D., DeKraker, J., Poser, B. A., & Khan, A. R. (2024). Insights into hippocampal perfusion using high-resolution, multi-modal 7T MRI. Proceedings of the National Academy of Sciences of the United States, 121(11), e2310044121. https://doi.org/10.1101/2023.07.19.549533
Havaei, M., Guizard, N., Chapados, N., & Bengio, Y. (2016). Hemis: Hetero-modal image segmentation. In Medical Image Computing and Computer-Assisted Intervention–MICCAI 2016: 19th International Conference, Athens, Greece, October 17–21, 2016, Proceedings, Part II 19 (pp. 469–477). Springer. https://doi.org/10.1007/978-3-319-46723-8_54
Henschel, L., Conjeti, S., Estrada, S., Diers, K., Fischl, B., & Reuter, M. (2020). FastSurfer—A fast and accurate deep learning based neuroimaging pipeline. NeuroImage, 219, 117012. https://doi.org/10.1016/j.neuroimage.2020.117012
Henschel, L., Kügler, D., & Reuter, M. (2022). FastSurferVINN: Building resolution-independence into deep learning segmentation methods—A solution for HighRes brain MRI. NeuroImage, 251, 118933. https://doi.org/10.1016/j.neuroimage.2022.118933
Hoopes, A., Mora, J. S., Dalca, A. V., Fischl, B., & Hoffmann, M. (2022). Synthstrip: Skull-stripping for any brain image. NeuroImage, 260, 119474. https://doi.org/10.1016/j.neuroimage.2022.119474
Huo, Y., Xu, Z., Xiong, Y., Aboud, K., Parvathaneni, P., Bao, S., Bermudez, C., Resnick, S. M., Cutting, L. E., & Landman, B. A. (2019). 3D whole brain segmentation using spatially localized atlas network tiles. NeuroImage, 194, 105–119. https://doi.org/10.1016/j.neuroimage.2019.03.041
Iglesias, J. E., Liu, C.-Y., Thompson, P. M., & Tu, Z. (2011). Robust brain extraction across datasets and comparison with publicly available methods. IEEE Transactions on Medical Imaging, 30(9), 1617–1634. https://doi.org/10.1109/tmi.2011.2138152
Isensee, F., Jaeger, P. F., Kohl, S. A., Petersen, J., & Maier-Hein, K. H. (2021). Nnu-net: A self-configuring method for deep learning-based biomedical image segmentation. Nature Methods, 18(2), 203–211. https://doi.org/10.1038/s41592-020-01008-z
Isensee, F., Schell, M., Pflueger, I., Brugnara, G., Bonekamp, D., Neuberger, U., Wick, A., Schlemmer, H.-P., Heiland, S., Wick, W., Bendszus, M., & Maier-Hein, K. H. (2019). Automated brain extraction of multisequence MRI using artificial neural networks. Human Brain Mapping, 40(17), 4952–4964. https://doi.org/10.1002/hbm.24750
Isensee, F., Wald, T., Ulrich, C., Baumgartner, M., Roy, S., Maier-Hein, K., & Jaeger, P. F. (2024). nnU-net revisited: A call for rigorous validation in 3D medical image segmentation. In International Conference on Medical Image Computing and Computer-Assisted Intervention (pp. 488–498). Springer. https://doi.org/10.1007/978-3-031-72114-4_47
Jack Jr, C. R., Bernstein, M. A., Fox, N. C., Thompson, P., Alexander, G., Harvey, D., Borowski, B., Britson, P. J., Whitwell, J. L., Ward, C., Dale, A. M., Felmlee, J. P., Gunter, J. L., Hill, D. L. G., Killiany, R., Schuff, N., Fox-Bosetti, S., Lin, C., Studholme, C., … Weiner, M. W. (2008). The Alzheimer’s disease neuroimaging initiative (ADNI): MRI methods. Journal of Magnetic Resonance Imaging, 27(4), 685–691. https://doi.org/10.1002/jmri.21049
Jia, H., Yap, P.-T., & Shen, D. (2012). Iterative multi-atlas-based multi-image segmentation with tree-based registration. NeuroImage, 59(1), 422–430. https://doi.org/10.1016/j.neuroimage.2011.07.036
Junqué, C., Ramırez-Ruiz, B., Tolosa, E., Summerfield, C., Martı, M.-J., Pastor, P., Gómez-Ansón, B., & Mercader, J. M. (2005). Amygdalar and hippocampal MRI volumetric reductions in Parkinson’s disease with dementia. Movement Disorders: Official Journal of the Movement Disorder Society, 20(5), 540–544. https://doi.org/10.1002/mds.20371
Karani, N., Chaitanya, K., Baumgartner, C., & Konukoglu, E. (2018). A lifelong learning approach to brain MR segmentation across scanners and protocols. In International Conference on Medical Image Computing and Computer-Assisted Intervention (pp. 476–484). Springer. https://doi.org/10.1007/978-3-030-00928-1_54
Karani, N., Erdil, E., Chaitanya, K., & Konukoglu, E. (2021). Test-time adaptable neural networks for robust medical image segmentation. Medical Image Analysis, 68, 101907. https://doi.org/10.1016/j.media.2020.101907
Keuken, M. C., Bazin, P.-L., Schäfer, A., Neumann, J., Turner, R., & Forstmann, B. U. (2013). Ultra-high 7T MRI of structural age-related changes of the subthalamic nucleus. Journal of Neuroscience, 33(11), 4896–4900. https://doi.org/10.1523/jneurosci.3241-12.2013
Kilsdonk, I. D., Steenwijk, M. D., Pouwels, P., Zwanenburg, J. J., Visser, F., Luijten, P., Geurts, J., Barkhof, F., & Wattjes, M. (2015). Perivascular spaces in MS patients at 7 Tesla MRI: A marker of neurodegeneration?Multiple Sclerosis Journal, 21(2), 155–162. https://doi.org/10.1177/1352458514540358
Kleesiek, J., Urban, G., Hubert, A., Schwarz, D., Maier-Hein, K., Bendszus, M., & Biller, A. (2016). Deep MRI brain extraction: A 3D convolutional neural network for skull stripping. NeuroImage, 129, 460–469. https://doi.org/10.1016/j.neuroimage.2016.01.024
Klinger, J. H., Leithner, D., Woo, S., Weber, M., Vargas, H. A., & Mayerhoefer, M. E. (2024). Reproducibility of radiomic features of the brain on ultrahigh-resolution MRI at 7 Tesla: A comparison of different segmentation techniques. medRxiv. https://doi.org/10.1101/2024.06.24.24308597
Maas, A. L., Hannun, A. Y., & Ng, A. Y. (2013). Rectifier nonlinearities improve neural network acoustic models. Proceedings of ICML, 30(1), 3. https://doi.org/10.1016/j.csl.2016.06.007
Mahler, L., Steiglechner, J., Bender, B., Lindig, T., Ramadan, D., Bause, J., Birk, F., Heule, R., Charyasz, E., Erb, M., Kumar, V. J., Hagberg, G. E., Martin, P., Lohmann, G., & Scheffler, K. (2025). Submillimeter ultra-high field 9.4 t brain MR image collection and manual cortical segmentations. Scientific Data, 12(1), 635. https://doi.org/10.1038/s41597-025-04779-2
Mann, H. B., & Whitney, D. R. (1947). On a test of whether one of two random variables is stochastically larger than the other. The Annals of Mathematical Statistics, 18(1), 50–60. https://doi.org/10.1214/aoms/1177730491
Marcus, D. S., Wang, T. H., Parker, J., Csernansky, J. G., Morris, J. C., & Buckner, R. L. (2007). Open access series of imaging studies (OASIS): Cross-sectional MRI data in young, middle aged, nondemented, and demented older adults. Journal of Cognitive Neuroscience, 19(9), 1498–1507. https://doi.org/10.1162/jocn.2007.19.9.1498
Morell-Ortega, S., Ruiz-Perez, M., Gadea, M., Vivo-Hernando, R., Rubio, G., Aparici, F., de la Iglesia-Vaya, M., Catheline, G., Coupé, P., & Manjón, J. V. (2024). Deepceres: A deep learning method for cerebellar lobule segmentation using ultra-high resolution multimodal MRI. arXiv preprint arXiv:2401.12074. https://doi.org/10.1016/j.neuroimage.2025.121063
O’Brien, K. R., Kober, T., Hagmann, P., Maeder, P., Marques, J., Lazeyras, F., Krueger, G., & Roche, A. (2014). Robust T1-weighted structural brain imaging and morphometry at 7T using mp2rage. PLoS One, 9(6), e99676. https://doi.org/10.1371/journal.pone.0099676
Pan, S. J., & Yang, Q. (2009). A survey on transfer learning. IEEE Transactions on Knowledge and Data Engineering, 22(10), 1345–1359. https://doi.org/10.1109/tkde.2009.191
Patenaude, B., Smith, S. M., Kennedy, D. N., & Jenkinson, M. (2011). A Bayesian model of shape and appearance for subcortical brain segmentation. NeuroImage, 56(3), 907–922. https://doi.org/10.1016/j.neuroimage.2011.02.046
Pei, L., Murat, A., Tahon, N., Zenkin, S., Karawi, S., Kamal, A., Yilmaz, M., Chen, L., Er, M., & Colen, R. (2022). A generative skull stripping of multiparametric brain MRIs using 3D convolutional neural network. https://doi.org/10.21203/rs.3.rs-1251147/v1
Pieperhoff, P., Südmeyer, M., Dinkelbach, L., Hartmann, C. J., Ferrea, S., Moldovan, A. S., Minnerop, M., Diaz-Pier, S., Schnitzler, A., & Amunts, K. (2022). Regional changes of brain structure during progression of idiopathic Parkinson’s disease—A longitudinal study using deformation based morphometry. Cortex, 151, 188–210. https://doi.org/10.1016/j.cortex.2022.03.009
Plantinga, B. R., Temel, Y., Duchin, Y., Uludağ, K., Patriat, R., Roebroeck, A., Kuijf, M., Jahanshahi, A., ter Haar Romenij, B., Vitek, J., & Harel, N. (2018). Individualized parcellation of the subthalamic nucleus in patients with Parkinson’s disease with 7T MRI. NeuroImage, 168, 403–411. https://doi.org/10.1016/j.neuroimage.2016.09.023
Puonti, O., Iglesias, J. E., & Van Leemput, K. (2016). Fast and sequence-adaptive whole-brain segmentation using parametric Bayesian modeling. NeuroImage, 143, 235–249. https://doi.org/10.1016/j.neuroimage.2016.09.011
Reinke, A., Tizabi, M. D., Baumgartner, M., Eisenmann, M., Heckmann-Nötzel, D., Kavur, A. E., Rädsch, T., Sudre, C. H., Acion, L., Antonelli, M., Arbel, T., Bakas, S., Benis, A., Buettner, F., Cardoso, M. J., Cheplygina, V., Chen, J., Christodoulou, E., Cimini, B. A., … Maier-Hein, L. (2024). Understanding metric-related pitfalls in image analysis validation. Nature Methods, 21(2), 182–194. https://doi.org/10.1038/s41592-023-02150-0
Ronneberger, O., Fischer, P., & Brox, T. (2015). U-net: Convolutional networks for biomedical image segmentation. In Medical image computing and computer-assisted intervention–MICCAI 2015: 18th international conference, Munich, Germany, October 5–9, 2015, proceedings, part III 18 (pp. 234–241). Springer. https://doi.org/10.1007/978-3-319-24574-4_28
Roy, A. G., Conjeti, S., Navab, N., & Wachinger, C. (2019). Quicknat: A fully convolutional network for quick and accurate segmentation of neuroanatomy. NeuroImage, 186, 713–727. https://doi.org/10.1016/j.neuroimage.2018.11.042
Roy, S., Butman, J. A., & Pham, D. L. (2017). Robust skull stripping using multiple MR image contrasts insensitive to pathology. NeuroImage, 146, 132–147. https://doi.org/10.1016/j.neuroimage.2016.11.017
Rua, C., Clarke, W. T., Driver, I. D., Mougin, O., Morgan, A. T., Clare, S., Francis, S., Muir, K. W., Wise, R. G., Carpenter, T. A., Williams, G. B., Rowe, J. B., Bowtell, R., & Rodgers, C. T. (2020). Multi-centre, multi-vendor reproducibility of 7T QSM and R2* in the human brain: Results from the UK7T study. NeuroImage, 223, 117358. https://doi.org/10.1016/j.neuroimage.2020.117358
Schick, F. (2005). Whole-body MRI at high field: Technical limits and clinical potential. European Radiology, 15(5), 946–959. https://doi.org/10.1007/s00330-005-2678-0
Schira, M. M., Isherwood, Z. J., Kassem, M. S., Barth, M., Shaw, T. B., Roberts, M. M., & Paxinos, G. (2023). Humanbrainatlas: An in vivo MRI dataset for detailed segmentations. Brain Structure and Function, 228(8), 1849–1863. https://doi.org/10.1007/s00429-023-02653-8
Singh, M. K., & Singh, K. K. (2021). A review of publicly available automatic brain segmentation methodologies, machine learning models, recent advancements, and their comparison. Annals of Neurosciences, 28(1–2), 82–93. https://doi.org/10.1177/0972753121990175
Smith, S. M. (2002). Fast robust automated brain extraction. Human Brain Mapping, 17(3), 143–155. https://doi.org/10.1002/hbm.10062
Solomon, A. J., Watts, R., Dewey, B. E., & Reich, D. S. (2017). MRI evaluation of thalamic volume differentiates MS from common mimics. Neurology: Neuroimmunology & Neuroinflammation, 4(5), e387. https://doi.org/10.1212/nxi.0000000000000387
Sorensen, T. (1948). A method of establishing groups of equal amplitude in plant sociology based on similarity of species content and its application to analyses of the vegetation on Danish commons. Biologiske skrifter, 5, 1–34.
Stige, K. E., Kverneng, S. U., Sharma, S., Skeie, G.-O., Sheard, E., Søgnen, M., Geijerstam, S. A., Vetås, T., Wahlvåg, A. G., Berven, H., Buch, S., Reese, D., Babiker, D., Mahdi, Y., Wade, T., Miranda, G. P., Ganguly, J., Tamilselvam, Y. K., Chai, J. R., … Tzoulis, C. (2024). The strat-park cohort: A personalized initiative to stratify Parkinson’s disease. Progress in Neurobiology, 236, 102603. https://doi.org/10.1016/j.pneurobio.2024.102603
Svanera, M., Benini, S., Bontempi, D., & Muckli, L. (2021). CEREBRUM-7T: Fast and fully volumetric brain segmentation of 7 Tesla MR volumes. Human Brain Mapping, 42(17), 5563–5580. https://doi.org/10.1002/hbm.25636
Tardif, C. L., Schäfer, A., Trampel, R., Villringer, A., Turner, R., & Bazin, P.-L. (2016). Open science CBS neuroimaging repository: Sharing ultra-high-field MR images of the brain. NeuroImage, 124, 1143–1148. https://doi.org/10.1016/j.neuroimage.2015.08.042
Trattnig, S., Springer, E., Bogner, W., Hangel, G., Strasser, B., Dymerska, B., Cardoso, P. L., & Robinson, S. D. (2018). Key clinical benefits of neuroimaging at 7 T. NeuroImage, 168, 477–489. https://doi.org/10.1016/j.neuroimage.2016.11.031
Tustison, N. J., Avants, B. B., Cook, P. A., Zheng, Y., Egan, A., Yushkevich, P. A., & Gee, J. C. (2010). N4itk: Improved n3 bias correction. IEEE Transactions on Medical Imaging, 29(6), 1310–1320. https://doi.org/10.1109/tmi.2010.2046908
Tustison, N. J., Cook, P. A., Holbrook, A. J., Johnson, H. J., Muschelli, J., Devenyi, G. A., Duda, J. T., Das, S. R., Cullen, N. C., Gillen, D. L., Yassa, M. A., Stone, J. R., Gee, J. C., & Avants, B. B. (2021). The ANTsX ecosystem for quantitative biological and medical imaging. Scientific Reports, 11(1), 9068. https://doi.org/10.1038/s41598-021-87564-6
Valabregue, R., Girka, F., Pron, A., Rousseau, F., & Auzias, G. (2024). Comprehensive analysis of synthetic learning applied to neonatal brain MRI segmentation. Human Brain Mapping, 45(6), e26674. https://doi.org/10.1002/hbm.26674
Van Essen, D. C., Ugurbil, K., Auerbach, E., Barch, D., Behrens, T. E. J., Bucholz, R., Chang, A., Chen, L., Corbetta, M., Curtiss, S. W., Della Penna, S., Feinberg, D., Glasser, M. F., Harel, N., Heath, A. C., Larson-Prior, L., Marcus, D., Michalareas, G., Moeller, S., … Yacoub, E. (2012). The human connectome project: A data acquisition perspective. NeuroImage, 62(4), 2222–2231. https://doi.org/10.1016/j.neuroimage.2012.02.018
Van Leemput, K., Maes, F., Vandermeulen, D., & Suetens, P. (1999). Automated model-based tissue classification of MR images of the brain, IEEE Transactions on Medical Imaging, 18(10), 897–908. https://doi.org/10.1109/42.811270
Wardlaw, J. M., Benveniste, H., Nedergaard, M., Zlokovic, B. V., Mestre, H., Lee, H., Doubal, F. N., Brown, R., Ramirez, J., MacIntosh, B. J., Tannenbaum, A., Ballerini, L., Rungta, R. L., Boido, D., Sweeney, M., Montagne, A., Charpak, S., Joutel, A., Smith, K. J., & Black, S. E. (2020). Perivascular spaces in the brain: Anatomy, physiology and pathology. Nature Reviews Neurology, 16(3), 137–153. https://doi.org/10.1038/s41582-020-0312-z
Webb, A. G., & Collins, C. M. (2010). Parallel transmit and receive technology in high-field magnetic resonance neuroimaging. International Journal of Imaging Systems and Technology, 20(1), 2–13. https://doi.org/10.1002/ima.20219
Zaretskaya, N., Fischl, B., Reuter, M., Renvall, V., & Polimeni, J. R. (2018). Advantages of cortical surface reconstruction using submillimeter 7 T memprage. NeuroImage, 165, 11–26. https://doi.org/10.1016/j.neuroimage.2017.09.060
Zong, X., Park, S. H., Shen, D., & Lin, W. (2016). Visualization of perivascular spaces in the human brain at 7 T: Sequence optimization and morphology characterization. NeuroImage, 125, 895–902. https://doi.org/10.1016/j.neuroimage.2015.10.078