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Whole brain susceptibility mapping using compressed sensing
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archpsyc.57.1.47openalex-snapshot
In Vivo Evaluation of Brain Iron in Alzheimer Disease Using Magnetic Resonance Imaging
inferredcites →https://doi.org/10.1002/cmr.b.10083openalex-snapshot
A fast calculation method for magnetic field inhomogeneity due to an arbitrary distribution of bulk susceptibility
inferredcites →https://doi.org/10.1002/cmr.b.20034openalex-snapshot
Application of a Fourier-based method for rapid calculation of field inhomogeneity due to spatial variation of magnetic susceptibility
inferredcites →https://doi.org/10.1002/jmri.21230openalex-snapshot
A modified fourier‐based phase unwrapping algorithm with an application to MRI venography
inferredcites →https://doi.org/10.1002/mrm.10718openalex-snapshot
Parallel imaging reconstruction using automatic regularization
inferredcites →https://doi.org/10.1002/mrm.20054openalex-snapshot
Quantifying arbitrary magnetic susceptibility distributions with MR
inferredcites →https://doi.org/10.1002/mrm.20198openalex-snapshot
Susceptibility weighted imaging (SWI)
inferredcites →https://doi.org/10.1002/mrm.21391openalex-snapshot
Sparse MRI: The application of compressed sensing for rapid MR imaging
inferredcites →https://doi.org/10.1002/mrm.21828openalex-snapshot
Calculation of susceptibility through multiple orientation sampling (COSMOS): A method for conditioning the inverse problem from measured magnetic field map to susceptibility source image in MRI
inferredcites →https://doi.org/10.1002/mrm.21907openalex-snapshot
Improving non‐contrast‐enhanced steady‐state free precession angiography with compressed sensing
inferredcites →https://doi.org/10.1002/mrm.22135openalex-snapshot
Magnetic susceptibility mapping of brain tissue in vivo using MRI phase data
inferredcites →https://doi.org/10.1002/mrm.22187openalex-snapshot
Quantitative susceptibility map reconstruction from MR phase data using bayesian regularization: Validation and application to brain imaging
inferredcites →https://doi.org/10.1002/mrm.22334openalex-snapshot
Susceptibility mapping in the human brain using threshold‐based k‐space division
inferredcites →https://doi.org/10.1002/mrm.22481openalex-snapshot
Compressed sensing MRI with multichannel data using multicore processors
inferredcites →https://doi.org/10.1016/0167-2789(92)90242-fopenalex-snapshot
Nonlinear total variation based noise removal algorithms
inferredcites →https://doi.org/10.1016/j.jmr.2008.03.003openalex-snapshot
Compressed sensing for resolution enhancement of hyperpolarized 13C flyback 3D-MRSI
inferredcites →https://doi.org/10.1016/j.mri.2004.10.001openalex-snapshot
Imaging iron stores in the brain using magnetic resonance imaging
inferredcites →https://doi.org/10.1016/j.mri.2010.06.011openalex-snapshot
Unambiguous identification of superparamagnetic iron oxide particles through quantitative susceptibility mapping of the nonlinear response to magnetic fields
inferredcites →https://doi.org/10.1016/j.neuroimage.2010.06.070openalex-snapshot
Whole-brain susceptibility mapping at high field: A comparison of multiple- and single-orientation methods
inferredcites →https://doi.org/10.1016/j.neuroimage.2010.10.070openalex-snapshot
Quantitative imaging of intrinsic magnetic tissue properties using MRI signal phase: An approach to in vivo brain iron metabolism?
inferredcites →https://doi.org/10.1016/j.neuroimage.2010.11.088openalex-snapshot
Quantitative susceptibility mapping of human brain reflects spatial variation in tissue composition
inferredcites →https://doi.org/10.1073/pnas.0610821104openalex-snapshot
High-field MRI of brain cortical substructure based on signal phase
inferredcites →https://doi.org/10.1073/pnas.0904899106openalex-snapshot
Biophysical mechanisms of phase contrast in gradient echo MRI
inferredcites →https://doi.org/10.1073/pnas.0910222107openalex-snapshot
Sensitivity of MRI resonance frequency to the orientation of brain tissue microstructure
inferredcites →https://doi.org/10.1088/0031-9155/53/17/021openalex-snapshot
Image reconstruction in circular cone-beam computed tomography by constrained, total-variation minimization
inferredcites →https://doi.org/10.1088/0266-5611/23/3/008openalex-snapshot
Sparsity and incoherence in compressive sampling
inferredcites →https://doi.org/10.1093/brain/114.4.1953openalex-snapshot
ALTERATIONS IN THE LEVELS OF IRON, FERRITIN AND OTHER TRACE METALS IN PARKINSON'S DISEASE AND OTHER NEURODEGENERATIVE DISEASES AFFECTING THE BASAL GANGLIA
inferredcites →https://doi.org/10.1109/tmi.2009.2023787openalex-snapshot
Nonlinear Regularization for Per Voxel Estimation of Magnetic Susceptibility Distributions From MRI Field Maps
inferredcites →https://doi.org/10.1111/j.1471-4159.1958.tb12607.xopenalex-snapshot
THE EFFECT OF AGE ON THE NON‐HAEMIN IRON IN THE HUMAN BRAIN
inferredcites →https://doi.org/10.1159/000107298openalex-snapshot
Distribution of Iron in the Basal Ganglia and Neocortex in Postmortem Tissue in Parkinson's Disease and Alzheimer's Disease
inferredcites →https://doi.org/10.1364/ol.28.002156openalex-snapshot
Deterministic phase unwrapping in the presence of noise
inferredcites →https://doi.org/10.3174/ajnr.a1400openalex-snapshot
Susceptibility-Weighted Imaging: Technical Aspects and Clinical Applications, Part 1
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/acn3.51418openalex-snapshot
Combining structural and metabolic markers in a quantitative MRI study of motor neuron diseases
inferred← citeshttps://doi.org/10.1002/acn3.70161openalex-snapshot
Quantitative Iron Measurements in the Basal Ganglia of NBIA Patients Using QSM : Insights From a Tertiary Center
inferred← citeshttps://doi.org/10.1002/alz.14459openalex-snapshot
Regional brain iron correlates with transcriptional and cellular signatures in Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/brb3.70096openalex-snapshot
Iron Deposition and Functional Connectivity Differences in Females With Migraine Without Aura: A Comparative Study of Headache Sides
inferred← citeshttps://doi.org/10.1002/cns.70677openalex-snapshot
Neuroimaging and Transcriptomic Insights Into Iron Accumulation and Glymphatic Dysfunction in Olfactory Dysfunction
inferred← citeshttps://doi.org/10.1002/dad2.12002openalex-snapshot
APOE4 moderates effects of cortical iron on synchronized default mode network activity in cognitively healthy old‐aged adults
inferred← citeshttps://doi.org/10.1002/hbm.22360openalex-snapshot
Differential developmental trajectories of magnetic susceptibility in human brain gray and white matter over the lifespan
inferred← citeshttps://doi.org/10.1002/hbm.22928openalex-snapshot
Region‐specific disturbed iron distribution in early idiopathic P arkinson's disease measured by quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/hbm.24227openalex-snapshot
Thalamic white matter in multiple sclerosis: A combined diffusion‐tensor imaging and quantitative susceptibility mapping study
inferred← citeshttps://doi.org/10.1002/hbm.25556openalex-snapshot
HybraPD atlas: Towards precise subcortical nuclei segmentation using multimodality medical images in patients with Parkinson disease
inferred← citeshttps://doi.org/10.1002/hbm.26487openalex-snapshot
Sub‐voxel quantitative susceptibility mapping for assessing whole‐brain magnetic susceptibility from ages 4 to 80
inferred← citeshttps://doi.org/10.1002/hbm.26688openalex-snapshot
Quantitative susceptibility mapping in the brain reflects spatial expression of genes involved in iron homeostasis and myelination
inferred← citeshttps://doi.org/10.1002/hbm.70136openalex-snapshot
χ ‐sepnet: Deep Neural Network for Magnetic Susceptibility Source Separation
inferred← citeshttps://doi.org/10.1002/hbm.70325openalex-snapshot
Imaging Developmental Trajectories of Laminar Magnetic Susceptibility Throughout Adulthood in Human Brain Cortex
inferred← citeshttps://doi.org/10.1002/jmri.24128openalex-snapshot
Noncontrast‐enhanced magnetic resonance angiography and venography imaging with enhanced angiography
inferred← citeshttps://doi.org/10.1002/jmri.24768openalex-snapshot
Susceptibility-weighted imaging and quantitative susceptibility mapping in the brain
inferred← citeshttps://doi.org/10.1002/jmri.24951openalex-snapshot
Subcortical gray matter segmentation and voxel‐based analysis using transverse relaxation and quantitative susceptibility mapping with application to multiple sclerosis
inferred← citeshttps://doi.org/10.1002/jmri.24976openalex-snapshot
Magnetic susceptibility contrast variations in multiple sclerosis lesions
inferred← citeshttps://doi.org/10.1002/jmri.25385openalex-snapshot
Potential of quantitative susceptibility mapping for detection of prostatic calcifications
inferred← citeshttps://doi.org/10.1002/jmri.25434openalex-snapshot
Influence of regional iron on the motor impairments of Parkinson's disease: A quantitative susceptibility mapping study
inferred← citeshttps://doi.org/10.1002/jmri.25490openalex-snapshot
Quantitative assessment of gadolinium deposition in dentate nucleus using quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/jmri.25671openalex-snapshot
Methods for the computation of templates from quantitative magnetic susceptibility maps (QSM): Toward improved atlas‐ and voxel‐based analyses (VBA)
inferred← citeshttps://doi.org/10.1002/jmri.25693openalex-snapshot
Clinical quantitative susceptibility mapping (QSM): Biometal imaging and its emerging roles in patient care
inferred← citeshttps://doi.org/10.1002/jmri.25777openalex-snapshot
Nuclei‐specific deposits of iron and calcium in the rat thalamus after status epilepticus revealed with quantitative susceptibility mapping (QSM)
inferred← citeshttps://doi.org/10.1002/jmri.25957openalex-snapshot
Quantitative susceptibility mapping (QSM) as a means to monitor cerebral hematoma treatment
inferred← citeshttps://doi.org/10.1002/jmri.26535openalex-snapshot
Quantitative susceptibility mapping of articular cartilage in patients with osteoarthritis at 3T
inferred← citeshttps://doi.org/10.1002/jmri.26579openalex-snapshot
Spatiotemporal variations of magnetic susceptibility in the deep gray matter nuclei from 1 month to 6 years: A quantitative susceptibility mapping study
inferred← citeshttps://doi.org/10.1002/jmri.26606openalex-snapshot
Seed prioritized unwrapping (SPUN) for MR phase imaging
inferred← citeshttps://doi.org/10.1002/jmri.27680openalex-snapshot
Serum Ceruloplasmin Depletion is Associated With Magnetic Resonance Evidence of Widespread Accumulation of Brain Iron in Parkinson's Disease
inferred← citeshttps://doi.org/10.1002/jmri.70110openalex-snapshot
Hemispheric Asymmetry of Neuromelanin‐Iron Dysfunction in the Substantia Nigra: MRI ‐Based Evidence for Lateralized Motor Onset in Early‐Stage Parkinson's Disease
inferred← citeshttps://doi.org/10.1002/jmri.70194openalex-snapshot
Mapping Intracellular Volume Fraction With Susceptibility Source Decomposition as a Marker for Tissue Cellularity
inferred← citeshttps://doi.org/10.1002/jnr.24358openalex-snapshot
Altered brain iron content and deposition rate in Huntington’s disease as indicated by quantitative susceptibility MRI
inferred← citeshttps://doi.org/10.1002/jnr.24701openalex-snapshot
Toward quantitative neuroimaging biomarkers for Friedreich's ataxia at 7 Tesla: Susceptibility mapping, diffusion imaging, R 2 and R 1 relaxometry
inferred← citeshttps://doi.org/10.1002/jor.24353openalex-snapshot
Evaluation of the Suitability of Miniature Pigs as an Animal Model of Juvenile Osteochondritis Dissecans
inferred← citeshttps://doi.org/10.1002/jor.25732openalex-snapshot
Epiphyseal cartilage vascular architecture at the distal humeral osteochondritis dissecans predilection site in juvenile pigs
inferred← citeshttps://doi.org/10.1002/mdc3.70357openalex-snapshot
Quantitative Susceptibility Mapping and Iron Deposition in Autopsy‐Confirmed Progressive Supranuclear Palsy
inferred← citeshttps://doi.org/10.1002/mds.27606openalex-snapshot
Longitudinal evaluation of iron concentration and atrophy in the dentate nuclei in friedreich ataxia
inferred← citeshttps://doi.org/10.1002/mds.27730openalex-snapshot
Ventral posterior substantia nigra iron increases over 3 years in Parkinson's disease
inferred← citeshttps://doi.org/10.1002/mds.27929openalex-snapshot
Quantitative Evaluation of Iron Content in Idiopathic Rapid Eye Movement Sleep Behavior Disorder
inferred← citeshttps://doi.org/10.1002/mds.29613openalex-snapshot
Magnetic Susceptibility in Progressive Supranuclear Palsy Variants, Parkinson's Disease, and Corticobasal Syndrome
inferred← citeshttps://doi.org/10.1002/mds.29816openalex-snapshot
Localized Changes in Dentate Nucleus Shape and Magnetic Susceptibility in Friedreich Ataxia
inferred← citeshttps://doi.org/10.1002/mds.70204openalex-snapshot
Localized Iron Deposition and Shape Changes of Cerebellar Dentate in Progressive Supranuclear Palsy Clinical Variants
inferred← citeshttps://doi.org/10.1002/mrm.24272openalex-snapshot
Nonlinear formulation of the magnetic field to source relationship for robust quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.24343openalex-snapshot
Alias subtraction more efficient than conventional zero‐padding in the Fourier‐based calculation of the susceptibility induced perturbation of the magnetic field in MR
inferred← citeshttps://doi.org/10.1002/mrm.24405openalex-snapshot
Toward online reconstruction of quantitative susceptibility maps: Superfast dipole inversion
inferred← citeshttps://doi.org/10.1002/mrm.24765openalex-snapshot
Background field removal using spherical mean value filtering and Tikhonov regularization
inferred← citeshttps://doi.org/10.1002/mrm.24918openalex-snapshot
Quantitative oxygenation venography from MRI phase
inferred← citeshttps://doi.org/10.1002/mrm.25029openalex-snapshot
Fast quantitative susceptibility mapping with L1‐regularization and automatic parameter selection
inferred← citeshttps://doi.org/10.1002/mrm.25082openalex-snapshot
Microstructural origins of gadolinium‐enhanced susceptibility contrast and anisotropy
inferred← citeshttps://doi.org/10.1002/mrm.25148openalex-snapshot
SHARP edges: Recovering cortical phase contrast through harmonic extension
inferred← citeshttps://doi.org/10.1002/mrm.25219openalex-snapshot
Susceptibility tensor imaging of the kidney and its microstructural underpinnings
inferred← citeshttps://doi.org/10.1002/mrm.25316openalex-snapshot
Quantitative susceptibility mapping using single-shot echo-planar imaging
inferred← citeshttps://doi.org/10.1002/mrm.25322openalex-snapshot
Mean magnetic susceptibility regularized susceptibility tensor imaging ( MMSR ‐ STI ) for estimating orientations of white matter fibers in human brain
inferred← citeshttps://doi.org/10.1002/mrm.25347openalex-snapshot
Wave‐CAIPI for highly accelerated 3D imaging
inferred← citeshttps://doi.org/10.1002/mrm.25358openalex-snapshot
Quantitative susceptibility mapping (QSM): Decoding MRI data for a tissue magnetic biomarker
inferred← citeshttps://doi.org/10.1002/mrm.25448openalex-snapshot
Quantitative susceptibility mapping in the abdomen as an imaging biomarker of hepatic iron overload
inferred← citeshttps://doi.org/10.1002/mrm.25453openalex-snapshot
Susceptibility‐based positive contrast MRI of brachytherapy seeds
inferred← citeshttps://doi.org/10.1002/mrm.25463openalex-snapshot
Quantitative mapping of cerebral metabolic rate of oxygen (CMRO2) using quantitative susceptibility mapping (QSM)
inferred← citeshttps://doi.org/10.1002/mrm.25652openalex-snapshot
Enhancing k‐space quantitative susceptibility mapping by enforcing consistency on the cone data (CCD) with structural priors
inferred← citeshttps://doi.org/10.1002/mrm.25735openalex-snapshot
Quantitative susceptibility mapping using single-shot echo-planar imaging
inferred← citeshttps://doi.org/10.1002/mrm.25919openalex-snapshot
Quantitative susceptibility mapping using a superposed dipole inversion method: Application to intracranial hemorrhage
inferred← citeshttps://doi.org/10.1002/mrm.26208openalex-snapshot
B0‐orientation dependent magnetic susceptibility‐induced white matter contrast in the human brainstem at 11.7T
inferred← citeshttps://doi.org/10.1002/mrm.26281openalex-snapshot
Echo time‐dependent quantitative susceptibility mapping contains information on tissue properties
inferred← citeshttps://doi.org/10.1002/mrm.26331openalex-snapshot
Preconditioned total field inversion (TFI) method for quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.26369openalex-snapshot
Suitable reference tissues for quantitative susceptibility mapping of the brain
inferred← citeshttps://doi.org/10.1002/mrm.26475openalex-snapshot
Susceptibility underestimation in a high‐susceptibility phantom: Dependence on imaging resolution, magnitude contrast, and other parameters
inferred← citeshttps://doi.org/10.1002/mrm.26627openalex-snapshot
Primal‐dual and forward gradient implementation for quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.26748openalex-snapshot
Coherence enhancement in quantitative susceptibility mapping by means of anisotropic weighting in morphology enabled dipole inversion
inferred← citeshttps://doi.org/10.1002/mrm.26830openalex-snapshot
Quantitative susceptibility mapping: Report from the 2016 reconstruction challenge
inferred← citeshttps://doi.org/10.1002/mrm.26882openalex-snapshot
Susceptibility tensor imaging and tractography of collagen fibrils in the articular cartilage
inferred← citeshttps://doi.org/10.1002/mrm.26989openalex-snapshot
Phase processing for quantitative susceptibility mapping of regions with large susceptibility and lack of signal
inferred← citeshttps://doi.org/10.1002/mrm.27073openalex-snapshot
Fast nonlinear susceptibility inversion with variational regularization
inferred← citeshttps://doi.org/10.1002/mrm.27216openalex-snapshot
Quantitative susceptibility mapping of articular cartilage: Ex vivo findings at multiple orientations and following different degradation treatments
inferred← citeshttps://doi.org/10.1002/mrm.27483openalex-snapshot
Weak‐harmonic regularization for quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.27492openalex-snapshot
Background field removal for susceptibility mapping of human brain with large susceptibility variations
inferred← citeshttps://doi.org/10.1002/mrm.27516openalex-snapshot
Correction of magnetic field inhomogeneity effects for fast quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.27891openalex-snapshot
Analysis of different phase unwrapping methods to optimize quantitative susceptibility mapping in the abdomen
inferred← citeshttps://doi.org/10.1002/mrm.27900openalex-snapshot
Automated adaptive preconditioner for quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.27975openalex-snapshot
Extracting more for less: multi‐echo MP2RAGE for simultaneous T1‐weighted imaging, T1 mapping, mapping, SWI, and QSM from a single acquisition
inferred← citeshttps://doi.org/10.1002/mrm.27976openalex-snapshot
Quantitative susceptibility map reconstruction using annihilating filter‐based low‐rank Hankel matrix approach
inferred← citeshttps://doi.org/10.1002/mrm.27995openalex-snapshot
Imaging diamagnetic susceptibility of collagen in hepatic fibrosis using susceptibility tensor imaging
inferred← citeshttps://doi.org/10.1002/mrm.28957openalex-snapshot
Streaking artifact suppression of quantitative susceptibility mapping reconstructions via L1‐norm data fidelity optimization (L1‐QSM)
inferred← citeshttps://doi.org/10.1002/mrm.29219openalex-snapshot
Blip up‐down acquisition for spin‐ and gradient‐echo imaging ( BUDA‐SAGE ) with self‐supervised denoising enables efficient T 2 , T 2 *, para‐ and dia‐magnetic susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.29265openalex-snapshot
Deep learning–based quantitative susceptibility mapping (QSM) in the presence of fat using synthetically generated multi‐echo phase training data
inferred← citeshttps://doi.org/10.1002/mrm.29494openalex-snapshot
An improved asymmetric susceptibility tensor imaging model with frequency offset correction
inferred← citeshttps://doi.org/10.1002/mrm.29588openalex-snapshot
Multi‐echo dipole inversion for magnetic susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.29644openalex-snapshot
Data adaptive regularization with reference tissue constraints for liver quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.29992openalex-snapshot
Improved test–retest reliability of R2*$$ {\mathrm{R}}_2^{\ast } $$ and susceptibility quantification using multishot multi‐echo 3D EPI
inferred← citeshttps://doi.org/10.1002/mrm.30006openalex-snapshot
Recommended implementation of quantitative susceptibility mapping for clinical research in the brain: A consensus of the ISMRM electro‐magnetic tissue properties study group
inferred← citeshttps://doi.org/10.1002/mrm.30216openalex-snapshot
Rapid submillimeter QSM and R2* mapping using interleaved multishot 3D‐EPI at 7 and 3 Tesla
inferred← citeshttps://doi.org/10.1002/mrm.30288openalex-snapshot
Quantitative mapping of renal oxygen consumption using pseudo‐continuous arterial spin labeling and quantitative susceptibility mapping in humans
inferred← citeshttps://doi.org/10.1002/mrm.70054openalex-snapshot
Vessel segmentation for χ$$ \chi $$‐separation in quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/mrm.70108openalex-snapshot
Rapid whole‐brain T 2 * and susceptibility mapping using 3D multiple overlapping‐echo detachment acquisition and missing modality synthesis embedded simulation
inferred← citeshttps://doi.org/10.1002/mrm.70193openalex-snapshot
Quantitative Susceptibility Mapping in Skull Base Chordoma: In Silico Analysis and In Vivo Application Towards Indirect Hypoxia Assessment
inferred← citeshttps://doi.org/10.1002/mrm.70366openalex-snapshot
Mesoscale Whole‐Brain T 2 *‐Weighted and Associated Quantitative MRI in Humans at 10.5 T
inferred← citeshttps://doi.org/10.1002/nbm.3056openalex-snapshot
Integrated Laplacian‐based phase unwrapping and background phase removal for quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/nbm.3383openalex-snapshot
Streaking artifact reduction for quantitative susceptibility mapping of sources with large dynamic range
inferred← citeshttps://doi.org/10.1002/nbm.3489openalex-snapshot
Regionally progressive accumulation of iron in Parkinson's disease as measured by quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/nbm.3501openalex-snapshot
Joint 2D and 3D phase processing for quantitative susceptibility mapping: application to 2D echo‐planar imaging
inferred← citeshttps://doi.org/10.1002/nbm.3536openalex-snapshot
Spatiotemporal changes in diffusion, T2 and susceptibility of white matter following mild traumatic brain injury
inferred← citeshttps://doi.org/10.1002/nbm.3540openalex-snapshot
Susceptibility tensor imaging (STI) of the brain
inferred← citeshttps://doi.org/10.1002/nbm.3545openalex-snapshot
Computational methods for image reconstruction
inferred← citeshttps://doi.org/10.1002/nbm.3569openalex-snapshot
Overview of quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/nbm.3570openalex-snapshot
Single‐step quantitative susceptibility mapping with variational penalties
inferred← citeshttps://doi.org/10.1002/nbm.3604openalex-snapshot
An illustrated comparison of processing methods for phase MRI and QSM: removal of background field contributions from sources outside the region of interest
inferred← citeshttps://doi.org/10.1002/nbm.3619openalex-snapshot
Structural and functional quantitative susceptibility mapping from standard fMRI studies
inferred← citeshttps://doi.org/10.1002/nbm.3999openalex-snapshot
Quantitative susceptibility mapping (QSM) with an extended physical model for MRI frequency contrast in the brain: a proof‐of‐concept of quantitative susceptibility and residual (QUASAR) mapping
inferred← citeshttps://doi.org/10.1002/nbm.4067openalex-snapshot
Fast quantitative susceptibility reconstruction via total field inversion with improved weighted L0 norm approximation
inferred← citeshttps://doi.org/10.1002/nbm.4118openalex-snapshot
Mapping the human brainstem: Brain nuclei and fiber tracts at 3 T and 7 T
inferred← citeshttps://doi.org/10.1002/nbm.4271openalex-snapshot
Nonlinear dipole inversion (NDI) enables robust quantitative susceptibility mapping (QSM)
inferred← citeshttps://doi.org/10.1002/nbm.4517openalex-snapshot
Single‐step calculation of susceptibility through multiple orientation sampling
inferred← citeshttps://doi.org/10.1002/nbm.4666openalex-snapshot
Comparison of quantitative susceptibility mapping methods on evaluating radiation‐induced cerebral microbleeds and basal ganglia at 3T and 7T
inferred← citeshttps://doi.org/10.1002/nbm.4750openalex-snapshot
Developmental trajectory of magnetic susceptibility in the healthy rhesus macaque brain
inferred← citeshttps://doi.org/10.1002/nbm.4847openalex-snapshot
Quantitative magnetic resonance imaging biomarkers for cortical pathology in multiple sclerosis at 7 T
inferred← citeshttps://doi.org/10.1002/nbm.5055openalex-snapshot
Model resolution‐based deconvolution for improved quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1002/nbm.5167openalex-snapshot
Comparison between R2′‐based and R2*‐based χ‐separation methods: A clinical evaluation in individuals with multiple sclerosis
inferred← citeshttps://doi.org/10.1002/nbm.5226openalex-snapshot
A human brain atlas of χ ‐separation for normative iron and myelin distributions
inferred← citeshttps://doi.org/10.1002/nbm.70057openalex-snapshot
An Optimized Framework of QSM Mask Generation Using Deep Learning: QSMmask‐Net
inferred← citeshttps://doi.org/10.1002/nbm.70262openalex-snapshot
Multimodal MRI Reveals Cerebral and Vascular Amyloid‐Driven Myeloarchitectural Disorganization in a Mouse Model of Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/viw2.70210openalex-snapshot
Retinal neurovascular alterations are associated with optic radiation microstructure in adrenomyeloneuropathy: A susceptibility separation MRI study
inferred← citeshttps://doi.org/10.1007/978-1-4939-3816-2_35openalex-snapshot
Magnetic Resonance Imaging in Experimental Traumatic Brain Injury
inferred← citeshttps://doi.org/10.1007/978-3-030-61598-7_5openalex-snapshot
Model-Based Learning for Quantitative Susceptibility Mapping
inferred← citeshttps://doi.org/10.1007/978-3-030-61598-7_7openalex-snapshot
Weakly-Supervised Learning for Single-Step Quantitative Susceptibility Mapping
inferred← citeshttps://doi.org/10.1007/978-3-642-38868-2_30openalex-snapshot
Retrospective Estimation of the Susceptibility Driven Field Map for Distortion Correction in Echo Planar Imaging
inferred← citeshttps://doi.org/10.1007/s00062-019-00816-xopenalex-snapshot
Assessment of Melanin Content and its Influence on Susceptibility Contrast in Melanoma Metastases
inferred← citeshttps://doi.org/10.1007/s00234-018-2137-7openalex-snapshot
Characterization of normal-appearing white matter in multiple sclerosis using quantitative susceptibility mapping in conjunction with diffusion tensor imaging
inferred← citeshttps://doi.org/10.1007/s00330-017-5263-4openalex-snapshot
Quantitative susceptibility mapping in combination with water-fat separation for simultaneous liver iron and fat fraction quantification
inferred← citeshttps://doi.org/10.1007/s00330-023-10283-1openalex-snapshot
Spatiotemporal patterns of brain iron-oxygen metabolism in patients with Parkinson’s disease
inferred← citeshttps://doi.org/10.1007/s00429-022-02547-1openalex-snapshot
Quantitative susceptibility atlas construction in Montreal Neurological Institute space: towards histological-consistent iron-rich deep brain nucleus subregion identification
inferred← citeshttps://doi.org/10.1007/s10334-025-01226-6openalex-snapshot
The statistical impact of ROI referencing on quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1007/s10334-025-01229-3openalex-snapshot
Comparing repeatability metrics for quantitative susceptibility mapping in the head and neck
inferred← citeshttps://doi.org/10.1007/s11604-026-01956-0openalex-snapshot
Low-intensity rim on T2-weighted brainstem imaging: a universally observed structure exhibiting a negative magnetic susceptibility effect
inferred← citeshttps://doi.org/10.1007/s11682-018-9842-zopenalex-snapshot
Quantitative susceptibility mapping as a biomarker for evaluating white matter alterations in Parkinson’s disease
inferred← citeshttps://doi.org/10.1007/s12264-017-0138-xopenalex-snapshot
Region-Specific Iron Measured by MRI as a Biomarker for Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/s12311-025-01870-7openalex-snapshot
Detailed Mapping of the Cerebellar Dentate Nucleus Using Ultra-High Field (7T) Susceptibility-Weighted Imaging
inferred← citeshttps://doi.org/10.1007/s40134-017-0204-1openalex-snapshot
Susceptibility-Based Neuroimaging: Standard Methods, Clinical Applications, and Future Directions
inferred← citeshttps://doi.org/10.1016/b978-0-12-397025-1.00019-1openalex-snapshot
Susceptibility-Weighted Imaging and Quantitative Susceptibility Mapping
inferred← citeshttps://doi.org/10.1016/b978-0-12-817057-1.00031-7openalex-snapshot
Iron Mapping Techniques and Applications
inferred← citeshttps://doi.org/10.1016/b978-0-12-817057-1.00033-0openalex-snapshot
Quantitative Susceptibility Mapping
inferred← citeshttps://doi.org/10.1016/b978-0-12-819361-7.00004-xopenalex-snapshot
Compressive sensing in medical signal processing and imaging systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-822726-8.00027-0openalex-snapshot
Quantitative Susceptibility-Mapping Reconstruction
inferred← citeshttps://doi.org/10.1016/b978-0-323-91771-1.00013-7openalex-snapshot
Iron imaging in neuroinflammation
inferred← citeshttps://doi.org/10.1016/j.bspc.2024.107451openalex-snapshot
Self-supervised denoising for high-dimensional magnetic resonance image
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2016.10.002openalex-snapshot
Rapid reconstruction of quantitative susceptibility mapping via improved ℓ0 norm approximation
inferred← citeshttps://doi.org/10.1016/j.crad.2017.04.008openalex-snapshot
The utility of susceptibility-weighted imaging to evaluate the extent of iron accumulation in the choroid plexus of patients with β-thalassaemia major
inferred← citeshttps://doi.org/10.1016/j.ebiom.2025.106040openalex-snapshot
Quantitative susceptibility mapping at 7T as a biomarker of post- and interictal extravascular iron in patients with focal epilepsy
inferred← citeshttps://doi.org/10.1016/j.ejmp.2021.03.039openalex-snapshot
An interictal measurement of cerebral oxygen extraction fraction in MRI-negative refractory epilepsy using quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1016/j.ejmp.2021.07.015openalex-snapshot
A novel phantom with dia- and paramagnetic substructure for quantitative susceptibility mapping and relaxometry
inferred← citeshttps://doi.org/10.1016/j.ejrad.2023.111030openalex-snapshot
Free water and iron content in the substantia nigra at different stages of Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.expneurol.2020.113314openalex-snapshot
Quantitative susceptibility mapping depicts severe myelin deficit and iron deposition in a transgenic model of multiple system atrophy
inferred← citeshttps://doi.org/10.1016/j.jare.2025.05.047openalex-snapshot
In newly diagnosed diabetes, hyperglycemia is associated with increased brain iron deposition, measured by MRI-based Quantitative Susceptibility Mapping (QSM)
inferred← citeshttps://doi.org/10.1016/j.jmr.2016.11.004openalex-snapshot
Optimization of sparse phase encodings for variable repetition-delay turbo-spin echo (TSE) T1 measurements for preclinical applications
inferred← citeshttps://doi.org/10.1016/j.jmr.2017.05.004openalex-snapshot
Background field removal using a region adaptive kernel for quantitative susceptibility mapping of human brain
inferred← citeshttps://doi.org/10.1016/j.jmr.2021.107033openalex-snapshot
On the separation of susceptibility sources in quantitative susceptibility mapping: Theory and phantom validation with an in vivo application to multiple sclerosis lesions of different age
inferred← citeshttps://doi.org/10.1016/j.media.2020.101827openalex-snapshot
Diffusion-regularized susceptibility tensor imaging (DRSTI) of tissue microstructures in the human brain
inferred← citeshttps://doi.org/10.1016/j.media.2022.102477openalex-snapshot
Unsupervised resolution-agnostic quantitative susceptibility mapping using adaptive instance normalization
inferred← citeshttps://doi.org/10.1016/j.media.2023.102829openalex-snapshot
DeepSTI: Towards tensor reconstruction using fewer orientations in susceptibility tensor imaging
inferred← citeshttps://doi.org/10.1016/j.media.2024.103173openalex-snapshot
A subject-specific unsupervised deep learning method for quantitative susceptibility mapping using implicit neural representation
inferred← citeshttps://doi.org/10.1016/j.media.2025.103530openalex-snapshot
Coordinate-based neural representation enabling zero-shot learning for fast 3D multiparametric quantitative MRI
inferred← citeshttps://doi.org/10.1016/j.mri.2014.09.004openalex-snapshot
Quantitative susceptibility mapping: current status and future directions
inferred← citeshttps://doi.org/10.1016/j.mri.2015.12.032openalex-snapshot
Importance of extended spatial coverage for quantitative susceptibility mapping of iron-rich deep gray matter
inferred← citeshttps://doi.org/10.1016/j.mri.2016.04.019openalex-snapshot
Background field removal technique using regularization enabled sophisticated harmonic artifact reduction for phase data with varying kernel sizes
inferred← citeshttps://doi.org/10.1016/j.mri.2017.02.002openalex-snapshot
An improved FSL-FIRST pipeline for subcortical gray matter segmentation to study abnormal brain anatomy using quantitative susceptibility mapping (QSM)
inferred← citeshttps://doi.org/10.1016/j.mri.2017.05.002openalex-snapshot
Quantitative susceptibility mapping using principles of echo shifting with a train of observations sequence on 1.5 T MRI
inferred← citeshttps://doi.org/10.1016/j.mri.2018.06.006openalex-snapshot
Background field removal technique based on non-regularized variable kernels sophisticated harmonic artifact reduction for phase data for quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1016/j.mri.2018.07.009openalex-snapshot
Removing unwanted background phase with a reference phantom for applications in susceptibility quantification
inferred← citeshttps://doi.org/10.1016/j.mri.2019.03.022openalex-snapshot
Multivariate MR biomarkers better predict cognitive dysfunction in mouse models of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.mri.2020.04.018openalex-snapshot
Field strength influences on gradient recalled echo MRI signal compartment frequency shifts
inferred← citeshttps://doi.org/10.1016/j.mri.2022.01.018openalex-snapshot
A data-driven deep learning pipeline for quantitative susceptibility mapping (QSM)
inferred← citeshttps://doi.org/10.1016/j.mri.2026.110623openalex-snapshot
Paramagnetic susceptibility versus QSM for estimating OEF: A comparative study in cerebral small vessel disease
inferred← citeshttps://doi.org/10.1016/j.nbd.2025.107076openalex-snapshot
Multimodal MRI biomarkers optimize differentiation between progressive supranuclear palsy and Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.neulet.2023.137249openalex-snapshot
Distribution pattern of iron deposition in the basal ganglia of different motor subtypes of Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2017.12.014openalex-snapshot
Low cortical iron and high entorhinal cortex volume promote cognitive functioning in the oldest-old
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2018.11.013openalex-snapshot
Iron-related nigral degeneration influences functional topology mediated by striatal dysfunction in Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2011.07.019openalex-snapshot
Fast and tissue-optimized mapping of magnetic susceptibility and T2* with multi-echo and multi-shot spirals
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2011.10.038openalex-snapshot
Magnetic susceptibility anisotropy of human brain in vivo and its molecular underpinnings
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.01.004openalex-snapshot
The future of susceptibility contrast for assessment of anatomy and function
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.04.042openalex-snapshot
Mapping magnetic susceptibility anisotropies of white matter in vivo in the human brain at 7T
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.05.049openalex-snapshot
Quantitative susceptibility mapping (QSM) as a means to measure brain iron? A post mortem validation study
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.05.067openalex-snapshot
Quantitative susceptibility mapping for investigating subtle susceptibility variations in the human brain
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.09.055openalex-snapshot
Toward in vivo histology: A comparison of quantitative susceptibility mapping (QSM) with magnitude-, phase-, and R2⁎-imaging at ultra-high magnetic field strength
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.06.011openalex-snapshot
Functional quantitative susceptibility mapping (fQSM)
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.08.035openalex-snapshot
Prenatal alcohol exposure reduces magnetic susceptibility contrast and anisotropy in the white matter of mouse brains
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.10.009openalex-snapshot
Association between increased magnetic susceptibility of deep gray matter nuclei and decreased motor function in healthy adults
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.11.010openalex-snapshot
Validation of quantitative susceptibility mapping with Perls' iron staining for subcortical gray matter
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.11.038openalex-snapshot
A modulated closed form solution for quantitative susceptibility mapping — A thorough evaluation and comparison to iterative methods based on edge prior knowledge
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.12.043openalex-snapshot
A method for estimating and removing streaking artifacts in quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2015.08.015openalex-snapshot
Rapid multi-orientation quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.02.028openalex-snapshot
Magnetic susceptibility of brain iron is associated with childhood spatial IQ
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