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Longitudinal Associations of Magnetic Susceptibility with Clinical Severity in Parkinson's Disease

https://doi.org/10.1002/mds.29702
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.902140206openalex-snapshot
Cholinergic innervation of cortex by the basal forebrain: Cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (Substantia innominata), and hypothalamus in the rhesus monkey
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Fast robust automated brain extraction
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Differential developmental trajectories of magnetic susceptibility in human brain gray and white matter over the lifespan
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Progression of brain atrophy in the early stages of Parkinson's disease: A longitudinal tensor‐based morphometry study in de novo patients without cognitive impairment
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Region‐specific disturbed iron distribution in early idiopathic P arkinson's disease measured by quantitative susceptibility mapping
inferredcites →https://doi.org/10.1002/jmri.24768openalex-snapshot
Susceptibility-weighted imaging and quantitative susceptibility mapping in the brain
inferredcites →https://doi.org/10.1002/mds.25240openalex-snapshot
Progression of cortical thinning in early Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.26417openalex-snapshot
Quantitative susceptibility mapping of the midbrain in Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.27318openalex-snapshot
Distinct progression pattern of susceptibility MRI in the substantia nigra of Parkinson's patients
inferredcites →https://doi.org/10.1002/mds.27717openalex-snapshot
Voxel‐based quantitative susceptibility mapping in Parkinson's disease with mild cognitive impairment
inferredcites →https://doi.org/10.1002/mds.27730openalex-snapshot
Ventral posterior substantia nigra iron increases over 3 years in Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.28477openalex-snapshot
Visual Dysfunction Predicts Cognitive Impairment and White Matter Degeneration in Parkinson's Disease
inferredcites →https://doi.org/10.1002/mrm.10171openalex-snapshot
Generalized autocalibrating partially parallel acquisitions (GRAPPA)
inferredcites →https://doi.org/10.1002/mrm.28377openalex-snapshot
An optimized and highly repeatable MRI acquisition and processing pipeline for quantitative susceptibility mapping in the head‐and‐neck region
inferredcites →https://doi.org/10.1002/mrm.28563openalex-snapshot
Phase unwrapping with a rapid opensource minimum spanning tree algorithm (ROMEO)
inferredcites →https://doi.org/10.1002/nbm.3064openalex-snapshot
Background field removal by solving the Laplacian boundary value problem
inferredcites →https://doi.org/10.1002/nbm.3489openalex-snapshot
Regionally progressive accumulation of iron in Parkinson's disease as measured by quantitative susceptibility mapping
inferredcites →https://doi.org/10.1002/nbm.3546openalex-snapshot
Contributions to magnetic susceptibility of brain tissue
inferredcites →https://doi.org/10.1007/s00401-022-02488-3openalex-snapshot
Adaptive structural changes in the motor cortex and white matter in Parkinson’s disease
inferredcites →https://doi.org/10.1007/s00415-005-0864-2openalex-snapshot
Longitudinal evaluation of cerebral morphological changes in Parkinson's disease with and without dementia
inferredcites →https://doi.org/10.1007/s00723-017-0877-xopenalex-snapshot
Quantitative Susceptibility Mapping of the Substantia Nigra in Parkinson’s Disease
inferredcites →https://doi.org/10.1007/s11682-018-9922-0openalex-snapshot
Brain degeneration in Parkinson’s disease patients with cognitive decline: a coordinate-based meta-analysis
inferredcites →https://doi.org/10.1016/0022-510x(83)90045-xopenalex-snapshot
Pathological changes in the nucleus of meynert in Alzheimer's and Parkinson's diseases
inferredcites →https://doi.org/10.1016/j.jns.2018.01.008openalex-snapshot
Quantifying iron deposition within the substantia nigra of Parkinson's disease by quantitative susceptibility mapping
inferredcites →https://doi.org/10.1016/j.mri.2015.02.021openalex-snapshot
Quantifying brain iron deposition in patients with Parkinson's disease using quantitative susceptibility mapping, R2 and R2*
inferredcites →https://doi.org/10.1016/j.nbd.2018.11.001openalex-snapshot
Dopaminergic degeneration induces early posterior cortical thinning in Parkinson's disease
inferredcites →https://doi.org/10.1016/j.neuroimage.2011.04.026openalex-snapshot
T 2 *-based fiber orientation mapping
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.neuroimage.2015.07.050openalex-snapshot
Age and sex related differences in subcortical brain iron concentrations among healthy adults
inferredcites →https://doi.org/10.1016/j.neuroimage.2016.05.024openalex-snapshot
High-resolution characterisation of the aging brain using simultaneous quantitative susceptibility mapping (QSM) and R2* measurements at 7 T
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.neuroimage.2018.07.065openalex-snapshot
A robust multi-scale approach to quantitative susceptibility mapping
inferredcites →https://doi.org/10.1016/j.neuroimage.2019.02.016openalex-snapshot
Multi-atlas tool for automated segmentation of brain gray matter nuclei and quantification of their magnetic susceptibility
inferredcites →https://doi.org/10.1016/j.neuroimage.2019.02.019openalex-snapshot
Imaging beta amyloid aggregation and iron accumulation in Alzheimer's disease using quantitative susceptibility mapping MRI
inferredcites →https://doi.org/10.1016/j.neuroimage.2021.118584openalex-snapshot
The effect of beta-amyloid and tau protein aggregations on magnetic susceptibility of anterior hippocampal laminae in Alzheimer's diseases
inferredcites →https://doi.org/10.1016/j.neuroimage.2023.119923openalex-snapshot
Age-dependent changes in brain iron deposition and volume in deep gray matter nuclei using quantitative susceptibility mapping
inferredcites →https://doi.org/10.1016/j.nicl.2016.12.025openalex-snapshot
Longitudinal changes of cortical microstructure in Parkinson's disease assessed with T1 relaxometry
inferredcites →https://doi.org/10.1016/j.nicl.2021.102604openalex-snapshot
In vivo nucleus basalis of Meynert degeneration in mild cognitive impairment with Lewy bodies
inferredcites →https://doi.org/10.1016/j.parkreldis.2017.05.005openalex-snapshot
Brain correlates of progressive olfactory loss in Parkinson's disease
inferredcites →https://doi.org/10.1016/j.parkreldis.2017.08.029openalex-snapshot
Quantitative susceptibility mapping differentiates between parkinsonian disorders
inferredcites →https://doi.org/10.1016/j.parkreldis.2019.05.012openalex-snapshot
Progression of Parkinson's disease patients' subtypes based on cortical thinning: 4-year follow-up
inferredcites →https://doi.org/10.1016/s0378-3758(99)00041-5openalex-snapshot
Resampling-based false discovery rate controlling multiple test procedures for correlated test statistics
inferredcites →https://doi.org/10.1016/s1471-4914(03)00031-5openalex-snapshot
Protein carbonylation in human diseases
inferredcites →https://doi.org/10.1021/acs.jctc.6b01251openalex-snapshot
Computing the Diamagnetic Susceptibility and Diamagnetic Anisotropy of Membrane Proteins from Structural Subunits
inferredcites →https://doi.org/10.1037/0894-4105.20.6.625openalex-snapshot
Overdependence on degraded gist memory in Alzheimer's disease.
inferredcites →https://doi.org/10.1038/s41419-020-2298-2openalex-snapshot
Ferroptosis: past, present and future
inferredcites →https://doi.org/10.1038/s41467-022-32944-3openalex-snapshot
Preclinical and randomized clinical evaluation of the p38α kinase inhibitor neflamapimod for basal forebrain cholinergic degeneration
inferredcites →https://doi.org/10.1056/nejmoa2100708openalex-snapshot
Donanemab in Early Alzheimer’s Disease
inferredcites →https://doi.org/10.1056/nejmoa2212948openalex-snapshot
Lecanemab in Early Alzheimer’s Disease
inferredcites →https://doi.org/10.1089/ars.2012.5036openalex-snapshot
Oxidative DNA Damage and Nucleotide Excision Repair
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/10.1093/brain/awab084openalex-snapshot
Regional brain iron and gene expression provide insights into neurodegeneration in Parkinson’s disease
inferredcites →https://doi.org/10.1093/brain/awr321openalex-snapshot
Severe olfactory dysfunction is a prodromal symptom of dementia associated with Parkinson's disease: a 3 year longitudinal study
inferredcites →https://doi.org/10.1093/brain/awu036openalex-snapshot
Mild cognitive impairment is linked with faster rate of cortical thinning in patients with Parkinson’s disease longitudinally
inferredcites →https://doi.org/10.1093/brain/awv211openalex-snapshot
Baseline and longitudinal grey matter changes in newly diagnosed Parkinson’s disease: ICICLE-PD study
inferredcites →https://doi.org/10.1093/brain/aww278openalex-snapshot
The whole-brain pattern of magnetic susceptibility perturbations in Parkinson’s disease
inferredcites →https://doi.org/10.1093/brain/awy072openalex-snapshot
Nucleus basalis of Meynert degeneration precedes and predicts cognitive impairment in Parkinson’s disease
inferredcites →https://doi.org/10.1093/brain/awy211openalex-snapshot
Can neuroimaging predict dementia in Parkinson’s disease?
inferredcites →https://doi.org/10.1093/braincomms/fcz006openalex-snapshot
Neuroimaging in Parkinson’s disease dementia: connecting the dots
inferredcites →https://doi.org/10.1109/mcse.2016.93openalex-snapshot
MRICloud: Delivering High-Throughput MRI Neuroinformatics as Cloud-Based Software as a Service
inferredcites →https://doi.org/10.1109/tmi.2010.2046908openalex-snapshot
N4ITK: Improved N3 Bias Correction
inferredcites →https://doi.org/10.1111/j.1471-4159.1989.tb07264.xopenalex-snapshot
Increased Nigral Iron Content and Alterations in Other Metal Ions Occurring in Brain in Parkinson's Disease
inferredcites →https://doi.org/10.1111/j.1582-4934.2008.00356.xopenalex-snapshot
A potential pathogenetic role of iron in Alzheimer's disease
inferredcites →https://doi.org/10.1111/jnc.14676openalex-snapshot
l ‐3,4‐dihydroxyphenylalanine ( l ‐DOPA) modulates brain iron, dopaminergic neurodegeneration and motor dysfunction in iron overload and mutant alpha‐synuclein mouse models of Parkinson's disease
inferredcites →https://doi.org/10.1118/1.597854openalex-snapshot
The role of magnetic susceptibility in magnetic resonance imaging: MRI magnetic compatibility of the first and second kinds
inferredcites →https://doi.org/10.1136/jnnp-2018-319592openalex-snapshot
Hippocampal subfield atrophy of CA1 and subicular structures predict progression to dementia in idiopathic Parkinson’s disease
inferredcites →https://doi.org/10.1136/jnnp-2019-322042openalex-snapshot
Brain iron deposition is linked with cognitive severity in Parkinson’s disease
inferredcites →https://doi.org/10.1146/annurev.ne.09.030186.002041openalex-snapshot
Parallel Organization of Functionally Segregated Circuits Linking Basal Ganglia and Cortex
inferredcites →https://doi.org/10.1159/000522329openalex-snapshot
Assessing Mild Cognitive Impairment in Parkinson’s Disease by Magnetic Resonance Quantitative Susceptibility Mapping Combined Voxel-Wise and Radiomic Analysis
inferredcites →https://doi.org/10.1212/cpj.0000000000000719openalex-snapshot
Visual tests predict dementia risk in Parkinson disease
inferredcites →https://doi.org/10.1212/wnl.0000000000000842openalex-snapshot
Predictors of dementia in Parkinson disease
inferredcites →https://doi.org/10.1212/wnl.56.6.730openalex-snapshot
Risk of dementia in Parkinson’s disease
inferredcites →https://doi.org/10.1371/journal.pone.0143923openalex-snapshot
Tracking Parkinson’s Disease over One Year with Multimodal Magnetic Resonance Imaging in a Group of Older Patients with Moderate Disease
inferredcites →https://doi.org/10.1371/journal.pone.0162460openalex-snapshot
Quantitative Susceptibility Mapping in Parkinson's Disease
inferredcites →https://doi.org/10.14283/jpad.2021.16openalex-snapshot
Determinants of Medical Direct Costs of Care among Patients of a Memory Center
inferredcites →https://doi.org/10.1523/jneurosci.1907-15.2016openalex-snapshot
In Vivo MRI Mapping of Brain Iron Deposition across the Adult Lifespan
inferredcites →https://doi.org/10.1523/jneurosci.20-16-06048.2000openalex-snapshot
The A53T alpha-synuclein mutation increases iron-dependent aggregation and toxicity.
inferredcites →https://doi.org/10.18632/aging.103870openalex-snapshot
Asymmetrical nigral iron accumulation in Parkinson’s disease with motor asymmetry: an explorative, longitudinal and test-retest study
inferredcites →https://doi.org/10.21037/qims-20-444openalex-snapshot
Meynert nucleus-related cortical thinning in Parkinson’s disease with mild cognitive impairment
inferredcites →https://doi.org/10.21037/qims-21-87openalex-snapshot
Age-related magnetic susceptibility changes in deep grey matter and cerebral cortex of normal young and middle-aged adults depicted by whole brain analysis
inferredcites →https://doi.org/10.3174/ajnr.a4260openalex-snapshot
Usefulness of Quantitative Susceptibility Mapping for the Diagnosis of Parkinson Disease
inferredcites →https://doi.org/10.3174/ajnr.a4645openalex-snapshot
Lateral Asymmetry and Spatial Difference of Iron Deposition in the Substantia Nigra of Patients with Parkinson Disease Measured with Quantitative Susceptibility Mapping
inferredcites →https://doi.org/10.3233/jad-2010-100354openalex-snapshot
Mitochondrial Iron Metabolism and Its Role in Neurodegeneration
inferredcites →https://doi.org/10.3389/fnagi.2018.00325openalex-snapshot
Differential Progression of Regional Hippocampal Atrophy in Aging and Parkinson’s Disease
inferredcites →https://doi.org/10.3389/fnins.2020.607705openalex-snapshot
Iron Content in Deep Gray Matter as a Function of Age Using Quantitative Susceptibility Mapping: A Multicenter Study
inferredcites →https://doi.org/10.3389/fnins.2021.618435openalex-snapshot
Systematic Review: Quantitative Susceptibility Mapping (QSM) of Brain Iron Profile in Neurodegenerative Diseases

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← backgroundhttps://doi.org/10.5281/zenodo.10436155zenodo-depositor-declared
inferred← citeshttps://doi.org/10.1002/alz.70567openalex-snapshot
Reply: Reconsidering white matter vulnerability and biomarker interpretation across Lewy body dementia subtypes
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Voxel‐Wise Whole‐Brain Analysis in Quantitative Susceptibility Mapping: A Narrative Review
inferred← citeshttps://doi.org/10.1002/mds.30265openalex-snapshot
Substantia Nigra Iron Deposition in Lewy Body Disease: A Magnetic Resonance Imaging and Neuropathology Study
inferred← citeshttps://doi.org/10.1002/mds.30325openalex-snapshot
Impaired Glymphatic Clearance, Measured Using Diffusion Tensor Image Analysis Along the Perivascular Space ( DTI ‐ ALPS) , is Linked to Poor Cognitive Outcomes in Parkinson's Disease
inferred← citeshttps://doi.org/10.1002/mds.70497openalex-snapshot
Longitudinal Iron Changes in the Substantia Nigra of Early‐Stage Parkinson's Disease
inferred← citeshttps://doi.org/10.1007/174_2024_544openalex-snapshot
Imaging of Movement Disorders
inferred← citeshttps://doi.org/10.1007/s00234-026-04133-2openalex-snapshot
7 Tesla MRI with Quantitative Susceptibility Mapping: qualitative grading and quantitative focal measurements of the substantia nigra as a potential biomarker for Parkinson’s disease
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Utilizing combined quantitative multiparametric MRI as potential biomarkers for improved early-stage parkinson’s disease diagnosis
inferred← citeshttps://doi.org/10.1016/j.bbr.2026.116186openalex-snapshot
Impact of obesity-related cerebral iron overload and perfusion alterations on cognition: A multi-parametric MRI study
inferred← citeshttps://doi.org/10.1016/j.ejrad.2025.112074openalex-snapshot
Multiparametric analysis based on 18F-AV133 PET/MR imaging for clinical application in Parkinson’s disease
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Multimodal magnetic resonance imaging studies on non-motor symptoms of Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.jfma.2025.12.005openalex-snapshot
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Vertex-wise biomechanical sensitivity mapping of subcortical structures under atrophy in Parkinson’s disease
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Advances in neuroimaging applications of quantitative susceptibility mapping
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Biomarkers in Parkinson’s Disease
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Neuroimaging of Parkinson's disease by quantitative susceptibility mapping
inferred← citeshttps://doi.org/10.1038/s41467-024-49949-9openalex-snapshot
Neuroimaging and fluid biomarkers in Parkinson’s disease in an era of targeted interventions
inferred← citeshttps://doi.org/10.1038/s41531-025-00931-2openalex-snapshot
Patterns of cerebellar cortex hypermetabolism on motor and cognitive functions in PD
inferred← citeshttps://doi.org/10.1038/s41531-025-01223-5openalex-snapshot
Longitudinal insights from iron accumulation in motor system of prodromal and clinical Parkinson’s disease
inferred← citeshttps://doi.org/10.1093/brain/awaf325openalex-snapshot
Quantitative susceptibility mapping reveals differences between subtypes of Lewy body dementia
inferred← citeshttps://doi.org/10.1093/braincomms/fcaf146openalex-snapshot
Neuroimaging-based data-driven subtypes of spatiotemporal atrophy due to Parkinson’s disease
inferred← citeshttps://doi.org/10.1093/braincomms/fcaf212openalex-snapshot
Early brain iron changes in Parkinson's disease and isolated rapid eye movement sleep behaviour disorder: a four-year longitudinal multimodal quantitative MRI study
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Cerebellar involvement in Parkinson’s disease: Pathophysiology and neuroimaging
inferred← citeshttps://doi.org/10.1109/iccebs58601.2023.10449173openalex-snapshot
Parkinson's Disease Detection by Machine Learning
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Exploring the role of quantitative susceptibility mapping in assessing brain iron deposition in hemodialysis patients
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Differential brain iron deposition in Parkinson’s disease subtypes: a comparative quantitative susceptibility mapping study of tremor-dominant versus postural instability/gait difficulty phenotypes
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Imaging of Cerebral Iron as an Emerging Marker for Brain Aging, Neurodegeneration, and Cerebrovascular Diseases
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Association of Cognitive Behavior and Non-Motor Manifestations in Parkinson’s Disease
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