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Susceptibility induced gray–white matter MRI contrast in the human brain
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ana.20202openalex-snapshot
Magnetization transfer ratio and myelin in postmortem multiple sclerosis brain
inferredcites →https://doi.org/10.1002/mrm.1204openalex-snapshot
Inverse T2 contrast at 1.5 Tesla between gray matter and white matter in the occipital lobe of normal adult human brain
inferredcites →https://doi.org/10.1002/mrm.1910320610openalex-snapshot
Theory of NMR signal behavior in magnetically inhomogeneous tissues: The static dephasing regime
inferredcites →https://doi.org/10.1002/mrm.20198openalex-snapshot
Susceptibility weighted imaging (SWI)
inferredcites →https://doi.org/10.1002/mrm.20536openalex-snapshot
Quantitative T1ρ and adiabatic Carr–Purcell T2 magnetic resonance imaging of human occipital lobe at 4 T
inferredcites →https://doi.org/10.1002/mrm.20578openalex-snapshot
Magnetic resonance imaging and mathematical modeling of progressive formalin fixation of the human brain
inferredcites →https://doi.org/10.1002/mrm.20605openalex-snapshot
T1, T2 relaxation and magnetization transfer in tissue at 3T
inferredcites →https://doi.org/10.1002/mrm.21754openalex-snapshot
Susceptibility weighted imaging at ultra high magnetic field strengths: Theoretical considerations and experimental results
inferredcites →https://doi.org/10.1002/mrm.21909openalex-snapshot
Postmortem MRI of human brain hemispheres: T 2 relaxation times during formaldehyde fixation
inferredcites →https://doi.org/10.1002/mrm.22097openalex-snapshot
Estimation of brain iron concentration in vivo using a linear relationship between regional iron and apparent transverse relaxation rate of the tissue water at 4.7T
inferredcites →https://doi.org/10.1002/mrm.22604openalex-snapshot
The contribution of chemical exchange to MRI frequency shifts in brain tissue
inferredcites →https://doi.org/10.1002/mrm.22816openalex-snapshot
Morphology enabled dipole inversion (MEDI) from a single‐angle acquisition: Comparison with COSMOS in human brain imaging
inferredcites →https://doi.org/10.1002/nbm.1581openalex-snapshot
The influence of white matter fibre orientation on MR signal phase and decay
inferredcites →https://doi.org/10.1002/nbm.683openalex-snapshot
Magnetization transfer in MRI: a review
inferredcites →https://doi.org/10.1002/nbm.922openalex-snapshot
High‐field magnetic resonance imaging of brain iron: birth of a biomarker?
inferredcites →https://doi.org/10.1016/j.jmr.2009.10.005openalex-snapshot
Protein-induced water 1H MR frequency shifts: Contributions from magnetic susceptibility and exchange effects
inferredcites →https://doi.org/10.1016/j.mri.2005.10.016openalex-snapshot
Measurement of in vivo multi-component T2 relaxation times for brain tissue using multi-slice T2 prep at 1.5 and 3 T
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2004.09.017openalex-snapshot
Age-related alterations in white matter microstructure measured by diffusion tensor imaging
inferredcites →https://doi.org/10.1016/j.neuroimage.2004.07.051openalex-snapshot
Advances in functional and structural MR image analysis and implementation as FSL
inferredcites →https://doi.org/10.1016/j.neuroimage.2008.01.061openalex-snapshot
The molecular basis for gray and white matter contrast in phase imaging
inferredcites →https://doi.org/10.1016/j.neuroimage.2008.07.008openalex-snapshot
Investigation of the influence of carbon dioxide concentrations on cerebral physiology by susceptibility-weighted magnetic resonance imaging (SWI)
inferredcites →https://doi.org/10.1016/j.neuroimage.2008.10.029openalex-snapshot
Susceptibility contrast in high field MRI of human brain as a function of tissue iron content
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.02.023openalex-snapshot
On the origin of the MR image phase contrast: An in vivo MR microscopy study of the rat brain at 14.1 T
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.07.017openalex-snapshot
On the contribution of deoxy-hemoglobin to MRI gray–white matter phase contrast at high field
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.12.052openalex-snapshot
Investigating the effect of blood susceptibility on phase contrast in the human brain
inferredcites →https://doi.org/10.1016/j.neuroimage.2010.08.033openalex-snapshot
Regional differences in MRI detection of amyloid plaques in AD transgenic mouse brain
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.2010.11.086openalex-snapshot
Phase contrast imaging in neonates
inferredcites →https://doi.org/10.1016/j.neuroimage.2011.02.024openalex-snapshot
High-field (9.4T) MRI of brain dysmyelination by quantitative mapping of magnetic susceptibility
inferredcites →https://doi.org/10.1016/s0730-725x(99)00017-xopenalex-snapshot
The correlation between phase shifts in gradient-echo MR images and regional brain iron concentration
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/10.1073/pnas.0911177107openalex-snapshot
Layer-specific variation of iron content in cerebral cortex as a source of MRI contrast
inferredcites →https://doi.org/10.1093/brain/awp335openalex-snapshot
High field (9.4 Tesla) magnetic resonance imaging of cortical grey matter lesions in multiple sclerosis
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/10.1148/radiol.10100495openalex-snapshot
Quantitative MR Imaging of Brain Iron: A Postmortem Validation Study
inferredcites →https://doi.org/10.1148/radiology.198.1.8539373openalex-snapshot
Intracranial calcification on gradient-echo phase image: depiction of diamagnetic susceptibility.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Differentiation of calcified regions and iron deposits in the ageing brain on conventional structural MR images
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Multicenter mapping in the healthy brain
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Microstructural origins of gadolinium‐enhanced susceptibility contrast and anisotropy
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An automated tool for cortical feature analysis: Application to differences on 7 T esla T 2*‐weighted images between young and older healthy subjects
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Contribution of iron and protein contents from rat brain subcellular fractions to MR phase imaging
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Cerebral metabolic rate of oxygen (CMRO2) mapping by combining quantitative susceptibility mapping (QSM) and quantitative blood oxygenation level‐dependent imaging (qBOLD)
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Rapid brain MRI acquisition techniques at ultra‐high fields
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Mechanisms of T2* anisotropy and gradient echo myelin water imaging
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Iron quantification with susceptibility
inferred← citeshttps://doi.org/10.1002/nbm.3655openalex-snapshot
Effects of biological tissue structural anisotropy and anisotropy of magnetic susceptibility on the gradient echo MRI signal phase: theoretical background
inferred← citeshttps://doi.org/10.1002/nbm.3727openalex-snapshot
Susceptibility‐sensitive MRI of multiple sclerosis lesions and the impact of normal‐appearing white matter changes
inferred← citeshttps://doi.org/10.1002/nbm.3766openalex-snapshot
Simultaneous MR quantification of hepatic fat content, fatty acid composition, transverse relaxation time and magnetic susceptibility for the diagnosis of non‐alcoholic steatohepatitis
inferred← citeshttps://doi.org/10.1002/nbm.4222openalex-snapshot
Myelin water imaging and R2* mapping in neonates: Investigating R2* dependence on myelin and fibre orientation in whole brain white matter
inferred← citeshttps://doi.org/10.1002/nbm.4438openalex-snapshot
Quantitative susceptibility mapping of the rat brain after traumatic brain injury
inferred← citeshttps://doi.org/10.1002/nbm.4750openalex-snapshot
Developmental trajectory of magnetic susceptibility in the healthy rhesus macaque brain
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Reducing Variability in Deep Gray Matter QSM Using Differential ROI Referencing: A Phantom and In Vivo Evaluation
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Assessment of Melanin Content and its Influence on Susceptibility Contrast in Melanoma Metastases
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MR imaging differentiation of Fe2+ and Fe3+ based on relaxation and magnetic susceptibility properties
inferred← citeshttps://doi.org/10.1007/s00330-014-3480-7openalex-snapshot
Characterizing the contrast of white matter and grey matter in high-resolution phase difference enhanced imaging of human brain at 3.0 T
inferred← citeshttps://doi.org/10.1007/s11065-015-9292-yopenalex-snapshot
Appraising the Role of Iron in Brain Aging and Cognition: Promises and Limitations of MRI Methods
inferred← citeshttps://doi.org/10.1007/s11357-015-9837-2openalex-snapshot
Brain iron deposits and lifespan cognitive ability
inferred← citeshttps://doi.org/10.1007/s11682-013-9284-6openalex-snapshot
Grasp force matching and brain iron content estimated in vivo in older women
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/b978-0-323-95739-7.00027-7openalex-snapshot
Quantitative susceptibility mapping in multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.acra.2015.08.003openalex-snapshot
Improved Detection of Cortical Gray Matter Involvement in Multiple Sclerosis with Quantitative Susceptibility Mapping
inferred← citeshttps://doi.org/10.1016/j.autrev.2021.102924openalex-snapshot
A proposal: How to study pro-myelinating proteins in MS
inferred← citeshttps://doi.org/10.1016/j.brain.2023.100063openalex-snapshot
Iron level changes in the brain with neurodegenerative disease
inferred← citeshttps://doi.org/10.1016/j.dcn.2014.12.003openalex-snapshot
In vivo evidence of neurophysiological maturation of the human adolescent striatum
inferred← citeshttps://doi.org/10.1016/j.dcn.2023.101326openalex-snapshot
Developmental coupling of brain iron and intrinsic activity in infants during the first 150 days
inferred← citeshttps://doi.org/10.1016/j.mri.2012.04.011openalex-snapshot
Imaging of stroke: a comparison between X-ray fluorescence and magnetic resonance imaging methods
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.2015.09.002openalex-snapshot
Value of transverse relaxometry difference methods for iron in human brain
inferred← citeshttps://doi.org/10.1016/j.mri.2019.02.012openalex-snapshot
SWI processing using a local phase difference modulated venous enhancement filter with noise compensation
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2020.01.006openalex-snapshot
Converging patterns of aging-associated brain volume loss and tissue microstructure differences
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2011.10.065openalex-snapshot
The future of ultra-high field MRI and fMRI for study of the human brain
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.2012.08.071openalex-snapshot
Predicting the location of human perirhinal cortex, Brodmann's area 35, from MRI
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.2012.12.040openalex-snapshot
Age-related differences in iron content of subcortical nuclei observed in vivo: A meta-analysis
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.01.051openalex-snapshot
Origin of B0 orientation dependent R2* (=1/T2*) in white matter
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.03.044openalex-snapshot
Regional structural differences across functionally parcellated Brodmann areas of human primary somatosensory cortex
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.04.022openalex-snapshot
Measuring iron in the brain using quantitative susceptibility mapping and X-ray fluorescence imaging
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.05.053openalex-snapshot
MRI parcellation of ex vivo medial temporal lobe
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2014.02.026openalex-snapshot
Myelin and iron concentration in the human brain: A quantitative study of MRI contrast
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2015.08.042openalex-snapshot
Open Science CBS Neuroimaging Repository: Sharing ultra-high-field MR images of the brain
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2015.08.047openalex-snapshot
Advanced MRI techniques to improve our understanding of experience-induced neuroplasticity
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.05.057openalex-snapshot
Laser ablation-inductively coupled plasma-mass spectrometry imaging of white and gray matter iron distribution in Alzheimer's disease frontal cortex
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.09.044openalex-snapshot
A virtual water maze revisited: Two-year changes in navigation performance and their neural correlates in healthy adults
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.09.062openalex-snapshot
Effects of tissue susceptibility on brain temperature mapping
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.12.033openalex-snapshot
Changes in brain iron concentration after exposure to high-altitude hypoxia measured by quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.12.051openalex-snapshot
The γ-parameter of anomalous diffusion quantified in human brain by MRI depends on local magnetic susceptibility differences
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.08.050openalex-snapshot
An R2* model of white matter for fiber orientation and myelin concentration
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2018.04.047openalex-snapshot
Quantifying iron content in magnetic resonance imaging
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2018.06.007openalex-snapshot
The influence of brain iron and myelin on magnetic susceptibility and effective transverse relaxation - A biochemical and histological validation study
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2018.10.031openalex-snapshot
Neonate and infant brain development from birth to 2 years assessed using MRI-based quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2019.05.042openalex-snapshot
The influence of brain iron on myelin water imaging
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.117080openalex-snapshot
The influence of iron oxidation state on quantitative MRI parameters in post mortem human brain
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.117216openalex-snapshot
Methods for quantitative susceptibility and R2* mapping in whole post-mortem brains at 7T applied to amyotrophic lateral sclerosis
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2023.120058openalex-snapshot
Depth-wise profiles of iron and myelin in the cortex and white matter using χ-separation: A preliminary study
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2024.120547openalex-snapshot
Neuroimaging of Parkinson's disease by quantitative susceptibility mapping
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Synthesized myelin and iron stainings from 7T multi-contrast MRI via deep learning
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Thalamic iron in multiple sclerosis: Waning support for the early-rise late-decline hypothesis
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Effects of Alzheimer’s disease and formalin fixation on the different mineralised-iron forms in the human brain
inferred← citeshttps://doi.org/10.1038/s41598-020-80212-5openalex-snapshot
Magnetic domains oscillation in the brain with neurodegenerative disease
inferred← citeshttps://doi.org/10.1038/s41598-021-88840-1openalex-snapshot
Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning
inferred← citeshttps://doi.org/10.1038/s41598-025-07808-7openalex-snapshot
Quantum magnetization exchange through transient hydrogen bond matrix defines magnetic resonance signal relaxation and anisotropy in central nervous system
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Biophysical mechanisms of MRI signal frequency contrast in multiple sclerosis
inferred← citeshttps://doi.org/10.1093/brain/awac436openalex-snapshot
Quantitative myelin imaging with MRI and PET: an overview of techniques and their validation status
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Methods for quantitative susceptibility and R2* mapping in whole post-mortem brains at 7T
inferred← citeshttps://doi.org/10.1101/2022.08.01.22271457openalex-snapshot
Quantitative MRI and histopathology detect remyelination in inactive multiple sclerosis lesions
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inferred← citeshttps://doi.org/10.1111/bpa.13150openalex-snapshot
Quantitative magnetic resonance imaging reflects different levels of histologically determined myelin densities in multiple sclerosis, including remyelination in inactive multiple sclerosis lesions
inferred← citeshttps://doi.org/10.1111/jon.12364openalex-snapshot
White Matter Tract Injury is Associated with Deep Gray Matter Iron Deposition in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1111/vru.13395openalex-snapshot
Effect of gadolinium contrast medium administration on susceptibility‐weighted imaging of the canine brain
inferred← citeshttps://doi.org/10.1136/jnnp-2014-310183openalex-snapshot
Iron accumulation in the basal ganglia in Huntington's disease: cross-sectional data from the IMAGE-HD study
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Quantitative Susceptibility Mapping in Multiple Sclerosis
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inferred← citeshttps://doi.org/10.1148/radiol.2020192541openalex-snapshot
Cross-sectional and Longitudinal Assessment of Brain Iron Level in Alzheimer Disease Using 3-T MRI
inferred← citeshttps://doi.org/10.1148/rg.210054openalex-snapshot
Quantitative Susceptibility Mapping: Basic Methods and Clinical Applications
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Brain oxygen extraction fraction mapping in patients with multiple sclerosis
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A pilot, longitudinal, 24-week study to evaluate the effect of interferon beta-1a subcutaneous on changes in susceptibility-weighted imaging-filtered phase assessment of lesions and subcortical deep-gray matter in relapsing–remitting multiple sclerosis
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Association between changes in brain microstructure and cognition in older subjects at increased risk for vascular disease
inferred← citeshttps://doi.org/10.1212/nxi.0000000000200271openalex-snapshot
Cerebrospinal Fluid-In Gradient of Cortical and Deep Gray Matter Damage in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1259/bjr.20181016openalex-snapshot
Introduction to Quantitative Susceptibility Mapping and Susceptibility Weighted Imaging
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Assessment of Iron Deposition and White Matter Maturation in Infant Brains by Using Enhanced T2 Star Weighted Angiography (ESWAN): R2* versus Phase Values
inferred← citeshttps://doi.org/10.1371/journal.pone.0108863openalex-snapshot
7 Tesla Magnetic Resonance Imaging to Detect Cortical Pathology in Multiple Sclerosis
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Susceptibility-Weighted Imaging Provides Insight into White Matter Damage in Amyotrophic Lateral Sclerosis
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Multistage Background Field Removal (MUBAFIRE)—Compensating for B0 Distortions at Ultra-High Field
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Ex-vivo quantitative susceptibility mapping of human brain hemispheres
inferred← citeshttps://doi.org/10.1371/journal.pone.0193839openalex-snapshot
Untangling the R2* contrast in multiple sclerosis: A combined MRI-histology study at 7.0 Tesla
inferred← citeshttps://doi.org/10.1371/journal.pone.0219705openalex-snapshot
MR susceptibility contrast imaging using a 2D simultaneous multi-slice gradient-echo sequence at 7T
inferred← citeshttps://doi.org/10.1371/journal.pone.0306006openalex-snapshot
The Advanced BRain Imaging on ageing and Memory (ABRIM) data collection: Study design, data processing, and rationale
inferred← citeshttps://doi.org/10.1523/jneurosci.4717-14.2015openalex-snapshot
Striatal Iron Content Predicts Its Shrinkage and Changes in Verbal Working Memory after Two Years in Healthy Adults
inferred← citeshttps://doi.org/10.21037/qims-19-1014openalex-snapshot
The association of myelination in the internal capsule with iron deposition in the basal ganglia in macaques: a magnetic resonance imaging study
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2934494/v1openalex-snapshot
Altered brain tissue composition and microstructure during migraine attacks
inferred← citeshttps://doi.org/10.2463/mrms.2013-0108openalex-snapshot
Analysis of Susceptibility-Weighted Images of Cortico-Medullary Junction
inferred← citeshttps://doi.org/10.3174/ajnr.a3569openalex-snapshot
Effect of Age on MRI Phase Behavior in the Subcortical Deep Gray Matter of Healthy Individuals
inferred← citeshttps://doi.org/10.3174/ajnr.a3969openalex-snapshot
Phase White Matter Signal Abnormalities in Patients with Clinically Isolated Syndrome and Other Neurologic Disorders
inferred← citeshttps://doi.org/10.3174/ajnr.a4726openalex-snapshot
Lesion Heterogeneity on High-Field Susceptibility MRI Is Associated with Multiple Sclerosis Severity
inferred← citeshttps://doi.org/10.3174/ajnr.a4830openalex-snapshot
In Vivo 7T MR Quantitative Susceptibility Mapping Reveals Opposite Susceptibility Contrast between Cortical and White Matter Lesions in Multiple Sclerosis
inferred← citeshttps://doi.org/10.3389/fnana.2019.00068openalex-snapshot
Matching ex vivo MRI With Iron Histology: Pearls and Pitfalls
inferred← citeshttps://doi.org/10.3389/fneur.2024.1422313openalex-snapshot
Dynamic fluctuations in brain iron content during migraine attacks: insights from relaxometry and diffusion tensor imaging
inferred← citeshttps://doi.org/10.3389/fnhum.2013.00710openalex-snapshot
High-Resolution MR Imaging of the Human Brainstem In vivo at 7 Tesla
inferred← citeshttps://doi.org/10.3389/fnhum.2021.641616openalex-snapshot
Stable Anatomy Detection in Multimodal Imaging Through Sparse Group Regularization: A Comparative Study of Iron Accumulation in the Aging Brain
inferred← citeshttps://doi.org/10.3389/fnimg.2026.1728970openalex-snapshot
Study protocol for the Champaign-Urbana population study
inferred← citeshttps://doi.org/10.3389/fnins.2022.938092openalex-snapshot
Quantitative susceptibility mapping as an imaging biomarker for Alzheimer’s disease: The expectations and limitations
inferred← citeshttps://doi.org/10.3390/ijms17010100openalex-snapshot
Iron in Multiple Sclerosis and Its Noninvasive Imaging with Quantitative Susceptibility Mapping
inferred← citeshttps://doi.org/10.7936/k76971mbopenalex-snapshot
On Nature of the Gradient Echo MR Signal and Its Application to Monitoring Multiple Sclerosis
inferred← citeshttps://doi.org/10.7939/r35x25m6hopenalex-snapshot
Quantitative Transverse Relaxometry in Multiple Sclerosis
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