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Decreased brain stiffness in Alzheimer's disease determined by magnetic resonance elastography
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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/archneur.60.8.1119openalex-snapshot
Alzheimer Disease in the US Population
inferredcites →https://doi.org/10.1002/ana.20009openalex-snapshot
Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound‐B
inferredcites →https://doi.org/10.1002/nbm.1189openalex-snapshot
Non‐invasive measurement of brain viscoelasticity using magnetic resonance elastography
inferredcites →https://doi.org/10.1002/nbm.1254openalex-snapshot
In vivo brain viscoelastic properties measured by magnetic resonance elastography
inferredcites →https://doi.org/10.1002/nbm.1602openalex-snapshot
In vivo viscoelastic properties of the brain in normal pressure hydrocephalus
inferredcites →https://doi.org/10.1016/j.actbio.2006.08.007openalex-snapshot
Three-dimensional analysis of shear wave propagation observed by in vivo magnetic resonance elastography of the brain
inferredcites →https://doi.org/10.1016/j.cgh.2007.06.012openalex-snapshot
Assessment of Hepatic Fibrosis With Magnetic Resonance Elastography
inferredcites →https://doi.org/10.1016/j.mri.2010.07.014openalex-snapshot
Convertible pneumatic actuator for magnetic resonance elastography of the brain
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2008.03.013openalex-snapshot
White matter pathology isolates the hippocampal formation in Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neuroimage.2007.08.030openalex-snapshot
Magnetic resonance elastography of the brain
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.02.040openalex-snapshot
The impact of aging and gender on brain viscoelasticity
inferredcites →https://doi.org/10.1016/j.neuroimage.2009.06.018openalex-snapshot
MR-elastography reveals degradation of tissue integrity in multiple sclerosis
inferredcites →https://doi.org/10.1016/s1361-8415(00)00039-6openalex-snapshot
Magnetic resonance elastography: Non-invasive mapping of tissue elasticity
inferredcites →https://doi.org/10.1016/s1474-4422(09)70299-6openalex-snapshot
Hypothetical model of dynamic biomarkers of the Alzheimer's pathological cascade
inferredcites →https://doi.org/10.1073/pnas.0604035103openalex-snapshot
Characterization of the nanoscale properties of individual amyloid fibrils
inferredcites →https://doi.org/10.1073/pnas.0606150103openalex-snapshot
Viscoelastic properties of individual glial cells and neurons in the CNS
inferredcites →https://doi.org/10.1093/brain/awm336openalex-snapshot
11C PiB and structural MRI provide complementary information in imaging of Alzheimer's disease and amnestic mild cognitive impairment
inferredcites →https://doi.org/10.1109/58.883546openalex-snapshot
Evaluation of a material parameter extraction algorithm using MRI-based displacement measurements
inferredcites →https://doi.org/10.1121/1.3180495openalex-snapshot
Theoretical limitations of the elastic wave equation inversion for tissue elastography
inferredcites →https://doi.org/10.1126/science.1072994openalex-snapshot
The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics
inferredcites →https://doi.org/10.1126/science.7569924openalex-snapshot
Magnetic Resonance Elastography by Direct Visualization of Propagating Acoustic Strain Waves
inferredcites →https://doi.org/10.1148/radiology.219.1.r01ap14101openalex-snapshot
Mild Cognitive Impairment and Alzheimer Disease: Regional Diffusivity of Water
inferredcites →https://doi.org/10.1159/000337230openalex-snapshot
Amyloid Oligomers Exacerbate Tau Pathology in a Mouse Model of Tauopathy
inferredcites →https://doi.org/10.1212/wnl.34.7.939openalex-snapshot
Clinical diagnosis of Alzheimer's disease
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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MR elastography derived shear stiffness-a new imaging biomarker for the assessment of early tumor response to chemotherapy
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inferred← citeshttps://doi.org/10.1002/mrm.26006openalex-snapshot
In vivo wideband multifrequency MR elastography of the human brain and liver
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Magnetic resonance elastography of brain: Comparison between anisotropic and isotropic stiffness and its correlation to age
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Uniqueness of the interior plane strain time-harmonic viscoelastic inverse problem
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Tabletop magnetic resonance elastography for the measurement of viscoelastic parameters of small tissue samples
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Brain tissue stiffness is a sensitive marker for acidosis
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Fatty acids as biomodulators of Piezo1 mediated glial mechanosensitivity in Alzheimer's disease
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Brain aging mechanisms with mechanical manifestations
inferred← citeshttps://doi.org/10.1016/j.media.2017.12.005openalex-snapshot
Robust MR elastography stiffness quantification using a localized divergence free finite element reconstruction
inferred← citeshttps://doi.org/10.1016/j.media.2022.102432openalex-snapshot
Mapping heterogenous anisotropic tissue mechanical properties with transverse isotropic nonlinear inversion MR elastography
inferred← citeshttps://doi.org/10.1016/j.mri.2018.08.016openalex-snapshot
Development of a robust diffusion-MR elastography (dMRE) technique to mitigate intravoxel phase dispersion
inferred← citeshttps://doi.org/10.1016/j.mri.2019.03.009openalex-snapshot
Magnetic resonance elastography of the brain: A study of feasibility and reproducibility using an ergonomic pillow-like passive driver
inferred← citeshttps://doi.org/10.1016/j.mri.2026.110703openalex-snapshot
Fast MR elastography via deep learning-based phase interpolation: A technical feasibility study
inferred← citeshttps://doi.org/10.1016/j.mric.2014.05.001openalex-snapshot
Magnetic Resonance Elastography of Liver
inferred← citeshttps://doi.org/10.1016/j.mric.2021.06.011openalex-snapshot
Magnetic Resonance Elastography of the Brain
inferred← citeshttps://doi.org/10.1016/j.mtcomm.2022.103227openalex-snapshot
Brain stiffness in epilepsy’s patients by indentation test
inferred← citeshttps://doi.org/10.1016/j.namjnl.2026.100138openalex-snapshot
Engineering 3D neural models of neurodegeneration: the Neural Microenvironment Design Code (NMDC), design principles, and emerging new approach methodologies
inferred← citeshttps://doi.org/10.1016/j.neulet.2019.134673openalex-snapshot
Mechanical regulation of oligodendrocyte biology
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2018.01.010openalex-snapshot
High-resolution magnetic resonance elastography reveals differences in subcortical gray matter viscoelasticity between young and healthy older adults
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.04.089openalex-snapshot
Local mechanical properties of white matter structures in the human brain
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2013.12.032openalex-snapshot
High-resolution mechanical imaging of the human brain by three-dimensional multifrequency magnetic resonance elastography at 7T
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2015.02.016openalex-snapshot
Measuring the effects of aging and sex on regional brain stiffness with MR elastography in healthy older adults
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.02.059openalex-snapshot
Medial temporal lobe viscoelasticity and relational memory performance
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2016.03.061openalex-snapshot
A biophysical model of brain deformation to simulate and analyze longitudinal MRIs of patients with Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.03.061openalex-snapshot
Aerobic fitness, hippocampal viscoelasticity, and relational memory performance
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2017.10.008openalex-snapshot
MR elastography of the brain and its application in neurological diseases
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.116592openalex-snapshot
Imaging brain function with simultaneous BOLD and viscoelasticity contrast: fMRI/fMRE
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2021.117889openalex-snapshot
Aging brain mechanics: Progress and promise of magnetic resonance elastography
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2022.119590openalex-snapshot
Mapping brain mechanical property maturation from childhood to adulthood
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2024.120662openalex-snapshot
Mouse brain elastography changes with sleep/wake cycles, aging, and Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.neuron.2023.10.005openalex-snapshot
Mechanics in the nervous system: From development to disease
inferred← citeshttps://doi.org/10.1016/j.nicl.2012.09.003openalex-snapshot
Magnetic resonance elastography reveals altered brain viscoelasticity in experimental autoimmune encephalomyelitis
inferred← citeshttps://doi.org/10.1016/j.nicl.2013.09.006openalex-snapshot
Cerebral magnetic resonance elastography in supranuclear palsy and idiopathic Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.nicl.2015.12.007openalex-snapshot
Regional brain stiffness changes across the Alzheimer's disease spectrum
inferred← citeshttps://doi.org/10.1016/j.nicl.2017.12.023openalex-snapshot
Combining viscoelasticity, diffusivity and volume of the hippocampus for the diagnosis of Alzheimer's disease based on magnetic resonance imaging
inferred← citeshttps://doi.org/10.1016/j.nicl.2021.102579openalex-snapshot
MR Elastography demonstrates reduced white matter shear stiffness in early-onset hydrocephalus
inferred← citeshttps://doi.org/10.1016/j.nicl.2023.103327openalex-snapshot
Hippocampal subfield viscoelasticity in amnestic mild cognitive impairment evaluated with MR elastography
inferred← citeshttps://doi.org/10.1016/j.nicl.2023.103328openalex-snapshot
Differential effect of dementia etiology on cortical stiffness as assessed by MR elastography
inferred← citeshttps://doi.org/10.1016/j.nicl.2024.103606openalex-snapshot
Low-frequency MR elastography reveals altered deep gray matter viscoelasticity in multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.nicl.2025.103857openalex-snapshot
Effects of Parkinson’s disease on mechanical and microstructural properties of the brain
inferred← citeshttps://doi.org/10.1016/j.ultrasmedbio.2023.05.004openalex-snapshot
Magnetic Resonance Imaging of Focused Ultrasound Radiation Force Strain Fields for Discrimination of Solid and Liquid Phases
inferred← citeshttps://doi.org/10.1016/j.wneu.2016.12.121openalex-snapshot
Clinical Correlation of Abnormal Findings on Magnetic Resonance Elastography in Idiopathic Normal Pressure Hydrocephalus
inferred← citeshttps://doi.org/10.1016/j.yexcr.2021.112805openalex-snapshot
Vinculin is required for neuronal mechanosensing but not for axon outgrowth
inferred← citeshttps://doi.org/10.1016/j.zemedi.2026.08.001openalex-snapshot
Magnetic resonance elastography of brain tumors
inferred← citeshttps://doi.org/10.1017/cbo9781139939751.020openalex-snapshot
Neuromechanobiology of the brain
inferred← citeshttps://doi.org/10.1021/acsami.4c18174openalex-snapshot
Viscoelastic Mechanics: From Pathology and Cell Fate to Tissue Regeneration Biomaterial Development
inferred← citeshttps://doi.org/10.1021/acschemneuro.8b00366openalex-snapshot
Reduced Extracellular Matrix Stiffness Prompts SH-SY5Y Cell Softening and Actin Turnover To Selectively Increase Aβ(1–42) Endocytosis
inferred← citeshttps://doi.org/10.1021/acschemneuro.9b00401openalex-snapshot
A Soft Mechanical Phenotype of SH-SY5Y Neuroblastoma and Primary Human Neurons Is Resilient to Oligomeric Aβ(1–42) Injury
inferred← citeshttps://doi.org/10.1021/acsmacrolett.1c00276openalex-snapshot
Chemically Triggered Hydrogel Transformations through Covalent Adaptable Networks and Applications in Cell Culture
inferred← citeshttps://doi.org/10.1038/ajg.2016.134openalex-snapshot
Editorial: A New Spin on Magnetic Resonance Elastography
inferred← citeshttps://doi.org/10.1038/ajg.2016.56openalex-snapshot
Magnetic Resonance Elastography for the Evaluation of Liver Fibrosis in Chronic Hepatitis B and C by Using Both Gradient-Recalled Echo and Spin-Echo Echo Planar Imaging: A Prospective Study
inferred← citeshttps://doi.org/10.1038/s41467-020-14787-yopenalex-snapshot
Microglia control vascular architecture via a TGFβ1 dependent paracrine mechanism linked to tissue mechanics
inferred← citeshttps://doi.org/10.1038/s41467-025-61888-7openalex-snapshot
Mechanobiology of the blood-brain barrier during development, disease and ageing
inferred← citeshttps://doi.org/10.1038/s41551-024-01250-2openalex-snapshot
Meta-analysis of the make-up and properties of in vitro models of the healthy and diseased blood–brain barrier
inferred← citeshttps://doi.org/10.1038/s41577-022-00761-wopenalex-snapshot
Tuning immunity through tissue mechanotransduction
inferred← citeshttps://doi.org/10.1038/s41597-025-05968-9openalex-snapshot
MR elastography datasets including phantom, liver, and brain
inferred← citeshttps://doi.org/10.1038/s41598-020-77577-yopenalex-snapshot
In vivo intervertebral disc deformation: intratissue strain patterns within adjacent discs during flexion–extension
inferred← citeshttps://doi.org/10.1038/s41598-020-77888-0openalex-snapshot
Novel tonometer device distinguishes brain stiffness in epilepsy surgery
inferred← citeshttps://doi.org/10.1038/s41598-021-00610-1openalex-snapshot
Peak ependymal cell stretch overlaps with the onset locations of periventricular white matter lesions
inferred← citeshttps://doi.org/10.1038/s41598-022-05262-3openalex-snapshot
Short echo time dual-frequency MR Elastography with Optimal Control RF pulses
inferred← citeshttps://doi.org/10.1038/s41598-024-57250-4openalex-snapshot
Feasibility of assessing non-invasive intracranial compliance using FSI simulation-based and MR elastography-based brain stiffness
inferred← citeshttps://doi.org/10.1038/s41598-024-60968-wopenalex-snapshot
Transfontanellar shear wave elastography of the neonatal brain for quantitative evaluation of white matter damage
inferred← citeshttps://doi.org/10.1038/s42254-022-00543-2openalex-snapshot
Magnetic resonance elastography from fundamental soft-tissue mechanics to diagnostic imaging
inferred← citeshttps://doi.org/10.1039/c5ra25916aopenalex-snapshot
Astrogliosis in a dish: substrate stiffness induces astrogliosis in primary rat astrocytes
inferred← citeshttps://doi.org/10.1039/d4bm00317aopenalex-snapshot
Advances in 3D tissue models for neural engineering: self-assembled versus engineered tissue models
inferred← citeshttps://doi.org/10.1055/s-0034-1399152openalex-snapshot
In Vivo Measurement of Brain Tumor Elasticity Using Intraoperative Shear Wave Elastography
inferred← citeshttps://doi.org/10.1063/1.5024394openalex-snapshot
Perspective: The role of mechanobiology in the etiology of brain metastasis
inferred← citeshttps://doi.org/10.1063/1.5045124openalex-snapshot
Review: Synthetic scaffolds to control the biochemical, mechanical, and geometrical environment of stem cell-derived brain organoids
inferred← citeshttps://doi.org/10.1063/5.0043338openalex-snapshot
Progress in mimicking brain microenvironments to understand and treat neurological disorders
inferred← citeshttps://doi.org/10.1063/5.0160213openalex-snapshot
Supershear Rayleigh wave imaging for quantitative assessment of biomechanical properties of brain using air-coupled optical coherence elastography
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