I graduated from the University of Cagliari (BEng Biomedical engineering, 2009) and University of Genoa (MEng Bioengineering, 2012), Italy. I then obtained a PhD from University College London (UCL, UK) in Magnetic Resonance Physics (2016). I worked as a post-doc at UCL from 2016 to 2020, where I investigated new ways of acquiring and analysing spinal cord diffusion MRI scans in multiple sclerosis. During my post-doc, I visited New York University (NY, USA) in 2017 (Sept-Nov), and I was elected Trainee representative (2018-2020) of the International Society for Magnetic Resonance in Medicine (ISMRM) White Matter Study Group. From October 2020 I have been a post-doctoral researcher at the Vall d’Hebron Institute of Oncology, where I work on MRI for precision medicine in oncology. In September 2021 he was awarded a Beatriu de Pinós Fellowship, and from September 2022 I am a “la Caixa” Foundation Junior Leader Fellow. From January 1st 2025, I am Senior Investigator at VHIO.
EDUCATION
- BEng Biomedical Engineering, University of Cagliari, Italy (2006)
- MEng Bioengineering, University of Genova, Italy (2012)
- PhD MRI Physics, University College London (UCL), UK (2016)
RESEARCH, TEACHING, or OTHER INTERESTS
Radiology, Nuclear Medicine and imaging, Biomedical Engineering, Oncology, Computational Theory and Mathematics
70
Scopus Publications
2711
Scholar Citations
26
Scholar h-index
45
Scholar i10-index
Scopus Publications
Simulation-Informed Evaluation of Microvascular Parameter Mapping for Diffusion MR Imaging of Solid Tumours Anna Kira Voronova, Olivia Prior, Athanasios Grigoriou, Francesc Salvà, Elena Elez, et al. Magnetic Resonance in Medicine, 2026 Purpose We aim to inform the design of new diffusion MRI (dMRI) approaches for microvasculature quantification that enhance the biological specificity of imaging towards cancer. Methods We adopted simulation‐informed modelling of the vascular dMRI signal. We synthesised signals from 1500 synthetic vascular networks, for a variety of protocols (flow‐compensated [FC], non‐compensated [NC], hybrid), featuring different samplings and diffusion times. We estimated the number of independent, recoverable signal degrees of freedom in presence of noise (signal‐to‐noise ratio of 5), and ranked 12 microvascular metrics depending on the quality of their estimation. Lastly, we demonstrated the feasibility of estimating the top‐ranking metrics on 3T dMRI of a healthy volunteer and of a metastatic colorectal cancer (CRC) patient. Results Both NC and FC synthetic vascular signals exhibited complex behaviour as, for example, non‐zero kurtosis and diffusion time dependence. Two independent degrees of freedom appeared recoverable from directionally‐averaged vascular signals (SNR of 5). Mean volumetric flow rate and an Apparent Network Branching (ANB) index maximised correlations between ground truth and estimated values in silico. In the patient, both and detected re‐vascularisation after 3 months of targeted therapy against liver metastases, consistently with Intra‐Voxel Incoherent Motion (IVIM) metrics. Conclusions Simulation‐based modelling of the vascular dMRI signal suggests and as the most promising metrics for tissue microvasculature characterisation. Their estimation in vivo appears feasible to capture general trends, and demonstrates contrasts that are biologically plausible, encouraging their usage in future studies.
ESR Essentials: diffusion-weighted MRI—practice recommendations by the European Society for Magnetic Resonance in Medicine and Biology Marco Palombo, Benedetta Bodini, Francesco Grussu, Denis Le Bihan, Markus Nilsson, et al. European Radiology, 2026 Diffusion-weighted imaging (DWI) offers critical insights into tissue microstructure through the assessment of water molecule random displacements and plays a central role in the assessment of neoplastic and non-neoplastic diseases. To successfully implement and use DWI in clinical practice, guidelines for acquisition, interpretation of image contrast and of artefacts should be followed, taking the disease process and body part into account. We recommend covering a b-value range of 0–1000 s/mm2 in the brain (along at least six directions for white matter), and 50–800 s/mm2 in the body. Available acquisition acceleration options should be used to reduce repetition time (TR), echo time (TE), and echo-planar imaging (EPI) distortions, while considering the penalty in signal-to-noise ratio (SNR) and image sharpness. DW images and the apparent diffusion coefficient (ADC) map should be read jointly for the clinical interpretation. Areas of slower diffusion are hyperintense on DW images and hypointense on the ADC map, and vice versa. Magnetic susceptibility distortions and signal drop-outs or pile-ups are particularly pronounced at air-tissue or metal-tissue interfaces and may obscure areas of interest or hinder the co-localisation with structural scans. By following these guidelines and recommendations, radiologists and imaging professionals can enhance diagnostic accuracy, reduce variability, and maximise the clinical value of DWI across diverse applications. Key Points This article provides an overview of DWI principles, clinical applications, potential pitfalls, and emerging advances, alongside expert recommendations for optimal implementation. We provide key considerations tailored to specific applications (neuro and whole-body imaging), including protocol optimisation, adherence to established guidelines, and quality assurance measures to minimise artefacts and ensure reproducibility. By following the guidelines and recommendations summarised in this work, radiologists and imaging professionals can enhance diagnostic accuracy, reduce variability, and maximise the clinical value of DWI across diverse applications.
The Sense of Smell (SoS) Atlas: Its Creation and First Application to Investigate COVID-19 Related Anosmia With a Comprehensive Quantitative MRI Protocol Marta Gaviraghi, Eleonora Lupi, Elena Grosso, Andrea Fusari, Mattia Baiguera, et al. Journal of Magnetic Resonance Imaging, 2026 BackgroundThe loss of smell (anosmia) has been noted in numerous diseases, including COVID‐19. Inflammatory and microstructural alterations are possible underlying mechanisms of anosmia in COVID‐19. However, no atlas exists to study olfaction and the associated tissue property changes.PurposeTo develop the sense of smell (SoS) atlas, including gray matter regions and white matter tracts of the olfactory circuit, to investigate the underpinnings of COVID‐19 related anosmia.Study TypeRetrospective.SubjectsFor the SoS atlas, high‐resolution tractograms of 10 healthy controls (HC) of the Human Connectome Project (7 females, 22–35 years) were used. The SoS atlas was applied to 8 subjects with persistent anosmia following COVID‐19 (COVID‐P, 7 females, 52 ± 12 years), 19 subjects that recovered from COVID‐19 anosmia (COVID‐R, 14 females, 38 ± 13 years), and 17 HC (8 females, 39 ± 12 years).Field Strength/Sequence3 T, 3D inversion recovery, 3D fast field echo, and spin‐echo echo‐planar imaging sequences.AssessmentTo create the SoS atlas, regions were identified and tracts were extracted via tractography following biological constraints. MRI metrics sensitive to alterations in neuroinflammation, axonal degeneration, myelin and macromolecular density, and iron were analyzed.Statistical TestsRegion‐based analysis (p‐value < 0.05, false discovery rate (FDR) corrected) and voxel‐based analysis (p‐value < 0.001 uncorrected, FDR‐corrected cluster extent = 5 voxels) were performed on 15 multisequence‐MRI metrics between the three groups.ResultsThe SoS atlas consisted of 35 regions and, after anatomical curation, the initial 506 tracts were refined to 78. Compared to HC, COVID‐P presented alterations in neuroinflammation‐related (mean: 41% of total alterations) and axonal degeneration‐related (31%) MRI metrics, while COVID‐R presented alterations of myelin‐related metrics (68%). COVID‐P alterations mainly affected the hindbrain (56%), while COVID‐R the hindbrain (39%).Data ConclusionA novel tool, the SoS atlas, was developed to study the olfactory system and applied in combination with multisequence‐MRI metrics to investigate the mechanisms of COVID‐19 related anosmia.Evidence Level3.Technical EfficacyStage 1.
Broad Utility of Ultrasensitive Analysis of ctDNA Dynamics across Solid Tumors Treated with Immunotherapy Elena Garralda, Charles Abbott, Alma Calahorro, Oriol Mirallas, Jason Pugh, et al. Clinical Cancer Research, 2026 Purpose: Prior studies have suggested the biomarker potential of plasma-derived ctDNA in patients with cancer treated with immune checkpoint inhibitors. This study investigated the ability of ctDNA to predict progression-free and overall survival in a cohort of patients with advanced cancer treated with immunotherapies. Experimental Design: In order to characterize the potential role of ultrasensitive ctDNA detection in the management of these patients, we have performed tumor whole-genome sequencing–informed, ultrasensitive ctDNA analysis—tracking approximately 1,800 tumor-specific mutations per patient—in a retrospective cohort (n = 136) and a prospective validation cohort (n = 66) across 24 cancer types treated with immune checkpoint inhibitors alone or in combination with bispecific antibodies or immune cell engagers. Results: Analyzing 1,455 longitudinal samples, we found that ctDNA molecular response measured as early as 3 weeks after treatment initiation correlated with improved progression-free and overall survival, whereas ctDNA clearance at any time strongly correlated with radiologic response and prolonged survival. Additionally, ctDNA dynamics distinguished true progression from pseudoprogression and predicted outcomes in patients receiving continued immunotherapy beyond initial progression. Conclusions: This study highlights the broader applicability of ultrasensitive ctDNA as a biomarker across cancer types and immunotherapy modalities.
Integrating C-reactive protein flare and early MRI dynamics for enhanced prediction of immunotherapy response Daniel Navarro-Garcia, Francesco Grussu, Christina Zatse, Niklas Klümper, Carlos Macarro, et al. Journal for Immunotherapy of Cancer, 2025 Background The C-reactive protein (CRP) flare response, an indicator of early immune activation, has emerged as a promising and cost-effective biomarker for predicting response to immune checkpoint inhibitors (ICIs) across various tumor types. This study evaluates the utility of CRP dynamics as a tumor-agnostic biomarker and integrates systemic inflammatory markers with advanced multiparametric MRI metrics to uncover the biological mechanisms underlying the CRP flare phenomenon and its relationship with treatment response. Methods Patients were stratified into three groups based on CRP kinetics: (1) flare-responders, characterized by an initial doubling of baseline CRP followed by a decrease below baseline; (2) CRP responders, defined as patients with no flare increase but a CRP reduction of at least 30% below baseline and (3) CRP non-responders. Multiparametric MRI was performed at baseline, early (1–3 weeks), and intermediate (6–8 weeks) time points to assess tumor size and microstructural features, including cell density and vascularization. Clinical benefit and survival outcomes, including progression-free survival (PFS) and overall survival (OS), were analyzed using Kaplan-Meier curves and log-rank tests. Cox regression analyses were performed to identify independent predictors of clinical outcomes, while intergroup differences in MRI metrics were assessed using Wilcoxon rank-sum and Kruskal-Wallis tests. Results Among the 121 evaluable patients with solid tumors enrolled in the PREDICT trial, CRP flare-responders demonstrated significantly longer PFS (5.6 months) and OS (12.1 months) compared with responders (PFS: 3.4 months, OS: 8.0 months) and non-responders (PFS: 3.2 months, OS: 6.7 months; p=0.01 and p<0.01, respectively). Additionally, clinical benefit was achieved in 50% of flare-responders, compared with 13% of responders (p=0.05) and 23% of non-responders (p<0.01). Tumor growth was interrupted early after treatment initiation in CRP flare-responders, whereas non-responders exhibited marked increases in tumor size. In the pilot subset of 33 patients with MRI data, diffusion MRI revealed stable or increased apparent diffusion coefficient values in CRP flare-responders, indicative of reduced tumor cellularity just after 1–3 weeks of treatment. Conclusions This study highlights the potential of combining early CRP dynamics with non-invasive imaging metrics to identify ICI responders as early as 2 weeks after treatment initiation. By integrating systemic inflammatory biomarkers with MRI-derived insights into tumor size and microstructural changes, these findings optimize therapeutic strategies and advance understanding of immunotherapy-driven tumor dynamics.
Evaluation of magnetic resonance spectroscopy total sodium concentration measures, and associations with microstructure and physical impairment in cervical myelopathy Bhavana S. Solanky, Ferran Prados, Carmen Tur, Francesco Grussu, Selma Al-Ahmad, et al. Scientific Reports, 2025 Spinal cord injury causes a cascade of physiological responses, which may trigger a subsequent neurotoxic increase in intracellular sodium. This can lead to neurodegeneration, both at and beyond the site of injury, causing clinical symptoms and loss of function. However, in vivo measurements of tissue sodium remain challenging. Here we utilise sodium magnetic resonance spectroscopy (23Na-MRS) at 3T to measure tissue sodium concentration (TSC) and its association with microstructural measures and macromolecular MRI metrics in the cervical spinal cord, distal to the site of injury. Twenty people with cervical myelopathy and twenty healthy controls, were studied. Associations with motor and sensory impairments were explored using ASIA and jOAMEQ scores. No significant difference in TSC in the cervical myelopathy group (39 ± 10 mM) relative to healthy controls (35 ± 13 mM) was found. However, patients had a significantly lower cord-cross-sectional area than controls (70 ± 9 mm2 vs. 82 ± 9 mm2, p < 0.001). Lower-extremity function positively correlated with intracellular volume fraction (p = 0.031). In conclusion, using 23Na-MRS, TSC in cervical myelopathy patients was successfully measured. Differences in TSC relative to healthy controls did not reach significance, despite a significant reduction in cord-cross-sectional area. However, lower intracellular volume fraction, indicating reduced neurite density distal to the site of injury, was associated with physical impairment.
Considerations and recommendations from the ISMRM Diffusion Study Group for preclinical diffusion MRI: Part 3—Ex vivo imaging: Data processing, comparisons with microscopy, and tractography Kurt G. Schilling, Amy F. D. Howard, Francesco Grussu, Andrada Ianus, Brian Hansen, et al. Magnetic Resonance in Medicine, 2025 Preclinical diffusion MRI (dMRI) has proven value in methods development and validation, characterizing the biological basis of diffusion phenomena, and comparative anatomy. While dMRI enables in vivo non‐invasive characterization of tissue, ex vivo dMRI is increasingly being used to probe tissue microstructure and brain connectivity. Ex vivo dMRI has several experimental advantages that facilitate high spatial resolution and high SNR images, cutting‐edge diffusion contrasts, and direct comparison with histological data as a methodological validation. However, there are a number of considerations that must be made when performing ex vivo experiments. The steps from tissue preparation, image acquisition and processing, and interpretation of results are complex, with many decisions that not only differ dramatically from in vivo imaging of small animals, but ultimately affect what questions can be answered using the data. This work concludes a three‐part series of recommendations and considerations for preclinical dMRI. Herein, we describe best practices for dMRI of ex vivo tissue, with a focus on image pre‐processing, data processing, and comparisons with microscopy. In each section, we attempt to provide guidelines and recommendations but also highlight areas for which no guidelines exist (and why), and where future work should lie. We end by providing guidelines on code sharing and data sharing and point toward open‐source software and databases specific to small animal and ex vivo imaging.
Considerations and recommendations from the ISMRM diffusion study group for preclinical diffusion MRI: Part 1: In vivo small-animal imaging Ileana O. Jelescu, Francesco Grussu, Andrada Ianus, Brian Hansen, Rachel L. C. Barrett, et al. Magnetic Resonance in Medicine, 2025 Small‐animal diffusion MRI (dMRI) has been used for methodological development and validation, characterizing the biological basis of diffusion phenomena, and comparative anatomy. The steps from animal setup and monitoring, to acquisition, analysis, and interpretation are complex, with many decisions that may ultimately affect what questions can be answered using the resultant data. This work aims to present selected considerations and recommendations from the diffusion community on best practices for preclinical dMRI of in vivo animals. We describe the general considerations and foundational knowledge that must be considered when designing experiments. We briefly describe differences in animal species and disease models and discuss why some may be more or less appropriate for different studies. We, then, give recommendations for in vivo acquisition protocols, including decisions on hardware, animal preparation, and imaging sequences, followed by advice for data processing including preprocessing, model‐fitting, and tractography. Finally, we provide an online resource that lists publicly available preclinical dMRI datasets and software packages to promote responsible and reproducible research. In each section, we attempt to provide guides and recommendations, but also highlight areas for which no guidelines exist (and why), and where future work should focus. Although we mainly cover the central nervous system (on which most preclinical dMRI studies are focused), we also provide, where possible and applicable, recommendations for other organs of interest. An overarching goal is to enhance the rigor and reproducibility of small animal dMRI acquisitions and analyses, and thereby advance biomedical knowledge.
Bayesian image quality transfer Ryutaro Tanno, Aurobrata Ghosh, Francesco Grussu, Enrico Kaden, Antonio Criminisi, et al. Lecture Notes in Computer Science Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics, 2016
Simulation‐informed evaluation of microvascular parameter mapping for diffusion MR imaging of solid tumours AK Voronova, O Prior, A Grigoriou, F Salvà, E Elez, LM Atlagich, ... Magnetic Resonance in Medicine 96 (1), 387-402 , 2026 2026
ESR Essentials: diffusion-weighted MRI—practice recommendations by the European Society for Magnetic Resonance in Medicine and Biology M Palombo, B Bodini, F Grussu, D Le Bihan, M Nilsson, R Perez-Lopez, ... European Radiology 36, 2198–2208 , 2026 2026 Citations: 2
The Sense of Smell (SoS) atlas: its creation and first application to investigate COVID‐19 related anosmia with a comprehensive quantitative MRI protocol M Gaviraghi, E Lupi, E Grosso, A Fusari, M Baiguera, A Monteverdi, ... Journal of Magnetic Resonance Imaging 63 (2), 574-593 , 2026 2026 Citations: 2
Broad utility of ultrasensitive analysis of ctDNA dynamics across solid tumors treated with immunotherapy E Garralda, C Abbott, A Calahorro, O Mirallas, J Pugh, ... Clinical Cancer Research 32 (2), 333–349 , 2026 2026 Citations: 2
Integrating C-reactive protein flare and early MRI dynamics for enhanced prediction of immunotherapy response D Navarro-Garcia*, F Grussu*, C Zatse, N Klümper, C Macarro, ... Journal for Immunotherapy of Cancer 13, e012143 , 2025 2025
Histology-informed microstructural diffusion simulations for MRI cancer characterisation—the Histo-μSim framework A Grigoriou, C Macarro, M Palombo, D Navarro-Garcia, AK Voronova, ... Communications Biology 8, 1695 , 2025 2025
Clinically feasible liver tumour cell size measurement through histology-informed in vivo diffusion MRI F Grussu, A Grigoriou, K Bernatowicz, M Palombo, I Casanova-Salas, ... Communications Medicine 5, 535 , 2025 2025 Citations: 1
Considerations and recommendations from the ISMRM Diffusion Study Group for preclinical diffusion MRI: Part 3—Ex vivo imaging: Data processing, comparisons with microscopy … KG Schilling, AFD Howard, F Grussu, A Ianus, B Hansen, RLC Barrett, ... Magnetic Resonance in Medicine 93 (6), 2561-2582 , 2025 2025 Citations: 8
Considerations and recommendations from the ISMRM diffusion study group for preclinical diffusion MRI: Part 1: In vivo small‐animal imaging IO Jelescu, F Grussu, A Ianus, B Hansen, RLC Barrett, M Aggarwal, ... Magnetic Resonance in Medicine 93 (6), 2507-2534 , 2025 2025 Citations: 13
Considerations and recommendations from the ISMRM diffusion study group for preclinical diffusion MRI: Part 2—Ex vivo imaging: Added value and acquisition KG Schilling, F Grussu, A Ianus, B Hansen, AFD Howard, RLC Barrett, ... Magnetic Resonance in Medicine 93 (6), 2535-2560 , 2025 2025 Citations: 9
Body size and intracranial volume interact with the structure of the central nervous system: A multi-center in vivo neuroimaging study R Labounek, MT Bondy, AL Paulson, S Bédard, M Abramovic, ... Imaging Neuroscience 3, 00559 , 2025 2025 Citations: 6
SpinFlowSim: a blood flow simulation framework for histology-informed diffusion MRI microvasculature mapping in cancer AK Voronova, A Grigoriou, K Bernatowicz, S Simonetti, G Serna, N Roson, ... Medical Image Analysis 102, 103531 , 2025 2025 Citations: 6
Evaluation of magnetic resonance spectroscopy total sodium concentration measures, and associations with microstructure and physical impairment in cervical myelopathy BS Solanky, F Prados, C Tur, F Grussu, S Al-Ahmad, X Yang, A Bianchi, ... Scientific Reports 15 (1), 7014 , 2025 2025
Enhancing tumor microstructural quantification with machine learning and diffusion-relaxation MRI C Macarro, K Bernatowicz, A Garcia-Ruiz, G Serna, C Monreal-Agüero, ... Journal of Magnetic Resonance Imaging 61 (2), 1018-1021 , 2025 2025 Citations: 1
Radiomics signature for dynamic monitoring of tumor inflamed microenvironment and immunotherapy response prediction K Bernatowicz, R Amat, O Prior, J Frigola, M Ligero, F Grussu, C Zatse, ... Journal for ImmunoTherapy of Cancer 13 (1), e009140 , 2025 2025 Citations: 28
Advanced diffusion‐weighted MRI for cancer microstructure assessment in body imaging, and its relationship with histology E Fokkinga, JA Hernandez‐Tamames, A Ianus, M Nilsson, CMW Tax, ... Journal of Magnetic Resonance Imaging 60 (4), 1278-1304 , 2024 2024 Citations: 40
Whole-body Magnetic Resonance Imaging as a treatment response biomarker in castration-resistant prostate cancer with bone metastases: the iPROMET clinical trial A Garcia-Ruiz, C Macarro, F Zacchi, R Morales-Barrera, F Grussu, ... European urology 86 (3), 272-274 , 2024 2024 Citations: 15
Investigating the relationship between thalamic iron concentration and disease severity in secondary progressive multiple sclerosis using quantitative susceptibility mapping … T Williams, N John, A Calvi, A Bianchi, F De Angelis, A Doshi, S Wright, ... NeuroImage: Reports 4 (3), 100216 , 2024 2024 Citations: 3
What contributes to disability in progressive MS? A brain and cervical cord–matched quantitative MRI study C Tur, M Battiston, MC Yiannakas, S Collorone, A Calvi, F Prados, ... Multiple Sclerosis Journal 30 (4-5), 516-534 , 2024 2024 Citations: 9
An accessible deep learning tool for voxel-wise classification of brain malignancies from perfusion MRI A Garcia-Ruiz*, A Pons-Escoda*, F Grussu*, P Naval-Baudin, ... Cell Reports Medicine 5 (3), 101464 , 2024 2024 Citations: 18
MOST CITED SCHOLAR PUBLICATIONS
Neurite dispersion: a new marker of multiple sclerosis spinal cord pathology? F Grussu, T Schneider, C Tur, RL Yates, M Tachrount, A Ianuş, ... Annals of clinical and translational neurology 4 (9), 663-679 , 2017 2017 Citations: 377
Spinal cord grey matter segmentation challenge F Prados, J Ashburner, C Blaiotta, T Brosch, J Carballido-Gamio, ... NeuroImage 152, 312-329 , 2017 2017 Citations: 199
Neurite orientation dispersion and density imaging of the healthy cervical spinal cord in vivo F Grussu, T Schneider, H Zhang, DC Alexander, CAM Wheeler–Kingshott NeuroImage 111, 590-601 , 2015 2015 Citations: 168
Generic acquisition protocol for quantitative MRI of the spinal cord J Cohen-Adad, E Alonso-Ortiz, M Abramovic, C Arneitz, N Atcheson, ... Nature protocols 16, 4611–4632 , 2021 2021 Citations: 167
Uncertainty modelling in deep learning for safer neuroimage enhancement: Demonstration in diffusion MRI R Tanno, DE Worrall, E Kaden, A Ghosh, F Grussu, A Bizzi, ... NeuroImage 225, 117366 , 2021 2021 Citations: 145
Cross-scanner and cross-protocol diffusion MRI data harmonisation: A benchmark database and evaluation of algorithms CMW Tax, F Grussu, E Kaden, L Ning, U Rudrapatna, CJ Evans, ... NeuroImage 195, 285-299 , 2019 2019 Citations: 141
Differentiating multiple sclerosis from AQP4-neuromyelitis optica spectrum disorder and MOG-antibody disease with imaging R Cortese, FP Carrasco, C Tur, A Bianchi, W Brownlee, F De Angelis, ... Neurology 100 (3), e308-e323 , 2023 2023 Citations: 140
Diffusion-Weighted Imaging: recent advances and applications E Martinez-Heras, F Grussu, F Prados, E Solana, S Llufriu Seminars in Ultrasound, CT and MRI 42 (5), 490-506 , 2021 2021 Citations: 125
Open-access quantitative MRI data of the spinal cord and reproducibility across participants, sites and manufacturers J Cohen-Adad, E Alonso-Ortiz, M Abramovic, C Arneitz, N Atcheson, ... Scientific data 8, 219 , 2021 2021 Citations: 109
Cross-scanner and cross-protocol multi-shell diffusion MRI data harmonization: Algorithms and results L Ning, E Bonet-Carne, F Grussu, F Sepehrband, E Kaden, J Veraart, ... NeuroImage 221, 117128 , 2020 2020 Citations: 96
Reduced neurite density in the brain and cervical spinal cord in relapsing–remitting multiple sclerosis: A NODDI study S Collorone, N Cawley, F Grussu, F Prados, F Tona, A Calvi, B Kanber, ... Multiple Sclerosis Journal 26 (13), 1647-1657 , 2020 2020 Citations: 83
Multi-parametric quantitative in vivo spinal cord MRI with unified signal readout and image denoising F Grussu, M Battiston, J Veraart, T Schneider, J Cohen-Adad, ... NeuroImage 217, 116884 , 2020 2020 Citations: 58
Brain microstructural and metabolic alterations detected in vivo at onset of the first demyelinating event S Collorone, F Prados, B Kanber, NM Cawley, C Tur, F Grussu, ... Brain 144 (5), 1409-1421 , 2021 2021 Citations: 49
Identification of precise 3D CT radiomics for habitat computation by machine learning in cancer O Prior, C Macarro, V Navarro, C Monreal, M Ligero, A Garcia-Ruiz, ... Radiology: Artificial Intelligence 6 (2), e230118 , 2024 2024 Citations: 44
Relevance of time‐dependence for clinically viable diffusion imaging of the spinal cord F Grussu, A Ianuş, C Tur, F Prados, T Schneider, E Kaden, S Ourselin, ... Magnetic resonance in medicine 81 (2), 1247-1264 , 2019 2019 Citations: 44
Robust imaging habitat computation using voxel-wise radiomics features K Bernatowicz, F Grussu, M Ligero, A Garcia, E Delgado, R Perez-Lopez Scientific Reports 11, 20133 , 2021 2021 Citations: 43
Advanced diffusion‐weighted MRI for cancer microstructure assessment in body imaging, and its relationship with histology E Fokkinga, JA Hernandez‐Tamames, A Ianus, M Nilsson, CMW Tax, ... Journal of Magnetic Resonance Imaging 60 (4), 1278-1304 , 2024 2024 Citations: 40
A framework for optimal whole-sample histological quantification of neurite orientation dispersion in the human spinal cord F Grussu, T Schneider, RL Yates, H Zhang, CAMG Wheeler-Kingshott, ... Journal of neuroscience methods 273, 20-32 , 2016 2016 Citations: 40
Deep learning model fitting for diffusion-relaxometry: a comparative study F Grussu, M Battiston, M Palombo, T Schneider, CAM Wheeler-Kingshott, ... Proceedings of Computational Diffusion MRI 2020 (MICCAI workshop), 159-172 , 2021 2021 Citations: 37
Fast and reproducible in vivo T 1 mapping of the human cervical spinal cord M Battiston, T Schneider, F Prados, F Grussu, MC Yiannakas, S Ourselin, ... Magnetic resonance in medicine 79 (4), 2142-2148 , 2018 2018 Citations: 34