Nigral Iron Deposition Influences Disease Severity by Modulating the Effect of Parkinson’s Disease on Brain Networks
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Ji-Rong Wen | Xiaojun Xu | Tao Guo | J. Pu | Baorong Zhang | T. Guo | Cheng Zhou | Jingjing Wu | Xiaocao Liu | Haoting Wu | Lu-yan Gu | Xueqin Bai | Min-min Zhang | Zhen-zhen Cao | Jingwen Chen | Xiaojun Guan | Baorong Zhang
[1] J. Schweitzer,et al. A Pitx3-deficient developmental mouse model for fine motor, olfactory, and gastrointestinal symptoms of Parkinson’s disease , 2022, Neurobiology of Disease.
[2] Chunhong Hu,et al. Assessing Mild Cognitive Impairment in Parkinson’s Disease by Magnetic Resonance Quantitative Susceptibility Mapping Combined Voxel-Wise and Radiomic Analysis , 2022, European Neurology.
[3] Xiaojun Xu,et al. Substantia nigra iron affects functional connectivity networks modifying working memory performance in younger adults , 2021, The European journal of neuroscience.
[4] Xiaojun Xu,et al. Progressive microstructural alterations in subcortical nuclei in Parkinson's disease: A diffusion magnetic resonance imaging study. , 2021, Parkinsonism & related disorders.
[5] S. Lehéricy,et al. The spatiotemporal changes in dopamine, neuromelanin and iron characterizing Parkinson’s disease , 2021, Brain : a journal of neurology.
[6] R. Barker,et al. Longitudinal changes in movement-related functional MRI activity in Parkinson's disease patients. , 2021, Parkinsonism & related disorders.
[7] Xiaojun Xu,et al. Effects of APOE ε2 on the Fractional Amplitude of Low-Frequency Fluctuation in Mild Cognitive Impairment: A Study Based on the Resting-State Functional MRI , 2021, Frontiers in Aging Neuroscience.
[8] Simon B. Eickhoff,et al. Functional parcellation of human and macaque striatum reveals human-specific connectivity in the dorsal caudate , 2021, NeuroImage.
[9] Ying Wang,et al. Imaging iron and neuromelanin simultaneously using a single 3D gradient echo magnetization transfer sequence: Combining neuromelanin, iron and the nigrosome-1 sign as complementary imaging biomarkers in early stage Parkinson's disease , 2021, NeuroImage.
[10] Chunlei Liu,et al. Asymmetrical nigral iron accumulation in Parkinson’s disease with motor asymmetry: an explorative, longitudinal and test-retest study , 2020, Aging.
[11] R. Cilia,et al. Natural history of motor symptoms in Parkinson’s disease and the long-duration response to levodopa , 2020, Brain : a journal of neurology.
[12] Valerie Treyer,et al. APOE4 moderates effects of cortical iron on synchronized default mode network activity in cognitively healthy old‐aged adults , 2020, Alzheimer's & dementia.
[13] Chunlei Liu,et al. Iron-related nigral degeneration influences functional topology mediated by striatal dysfunction in Parkinson's disease , 2019, Neurobiology of Aging.
[14] Ana M. Daugherty,et al. Genetic predisposition for inflammation exacerbates effects of striatal iron content on cognitive switching ability in healthy aging , 2019, NeuroImage.
[15] Satrajit S. Ghosh,et al. FMRIPrep: a robust preprocessing pipeline for functional MRI , 2018, bioRxiv.
[16] Z. J. Wang,et al. Decreased subregional specificity of the putamen in Parkinson's Disease revealed by dynamic connectivity-derived parcellation , 2018, NeuroImage: Clinical.
[17] Chunlei Liu,et al. Longitudinal atlas for normative human brain development and aging over the lifespan using quantitative susceptibility mapping , 2018, NeuroImage.
[18] Xiaojun Xu,et al. Disrupted Functional Connectivity of Basal Ganglia across Tremor-Dominant and Akinetic/Rigid-Dominant Parkinson’s Disease , 2017, Front. Aging Neurosci..
[19] Xiaojun Xu,et al. Region-Specific Iron Measured by MRI as a Biomarker for Parkinson’s Disease , 2017, Neuroscience Bulletin.
[20] Yuyao Zhang,et al. Joint 2D and 3D phase processing for quantitative susceptibility mapping: application to 2D echo‐planar imaging , 2017, NMR in biomedicine.
[21] Hoi-Chung Leung,et al. Hemispheric Lateralization of Resting-State Functional Connectivity of the Anterior Insula: Association with Age, Gender, and a Novelty-Seeking Trait , 2016, Brain Connect..
[22] A. Lees,et al. Visual dysfunction in Parkinson’s disease , 2016, Brain : a journal of neurology.
[23] A. Lang,et al. Parkinson's disease , 2015, The Lancet.
[24] Qin Chen,et al. Functional connectome assessed using graph theory in drug-naive Parkinson’s disease , 2015, Journal of Neurology.
[25] R. Bhidayasiri,et al. Visual deprivation elicits subclinical postural inflexibilities in early Parkinson's disease , 2015, Journal of the Neurological Sciences.
[26] Jeff H Duyn,et al. The role of iron in brain ageing and neurodegenerative disorders , 2014, The Lancet Neurology.
[27] Nicola Filippini,et al. Functional connectivity in the basal ganglia network differentiates PD patients from controls , 2014, Neurology.
[28] Antonio P Strafella,et al. Uncovering the role of the insula in non-motor symptoms of Parkinson's disease. , 2014, Brain : a journal of neurology.
[29] Xue Xiao,et al. Integrated Laplacian‐based phase unwrapping and background phase removal for quantitative susceptibility mapping , 2014, NMR in biomedicine.
[30] Ester Ato Lozano,et al. Classical and causal inference approaches to statistical mediation analysis. , 2014, Psicothema.
[31] Fenna M. Krienen,et al. Opportunities and limitations of intrinsic functional connectivity MRI , 2013, Nature Neuroscience.
[32] Marshall M Joffe,et al. A review of causal estimation of effects in mediation analyses , 2012, Statistical methods in medical research.
[33] Andreas Schäfer,et al. High resolution magnetic susceptibility mapping of the substantia nigra in Parkinson's disease , 2012, Journal of magnetic resonance imaging : JMRI.
[34] Chunlei Liu,et al. Whole brain susceptibility mapping using compressed sensing , 2012, Magnetic resonance in medicine.
[35] Werner Poewe,et al. A double-blind, delayed-start trial of rasagiline in Parkinson's disease (the ADAGIO study): prespecified and post-hoc analyses of the need for additional therapies, changes in UPDRS scores, and non-motor outcomes , 2011, The Lancet Neurology.
[36] Bing Wu,et al. Quantitative susceptibility mapping of human brain reflects spatial variation in tissue composition , 2011, NeuroImage.
[37] Ying Han,et al. Frequency-dependent changes in the amplitude of low-frequency fluctuations in amnestic mild cognitive impairment: A resting-state fMRI study , 2011, NeuroImage.
[38] Benjamin O. Turner,et al. Cortical and basal ganglia contributions to habit learning and automaticity , 2010, Trends in Cognitive Sciences.
[39] Jean-Philippe Azulay,et al. Role of sensory information in the control of postural orientation in Parkinson's disease , 2010, Journal of the Neurological Sciences.
[40] Stephen M Smith,et al. Correspondence of the brain's functional architecture during activation and rest , 2009, Proceedings of the National Academy of Sciences.
[41] John Hardy,et al. Parkinson's disease , 2009, The Lancet.
[42] G. Wooten,et al. UPDRS activity of daily living score as a marker of Parkinson's disease progression , 2009, Movement disorders : official journal of the Movement Disorder Society.
[43] Brian B. Avants,et al. Symmetric diffeomorphic image registration with cross-correlation: Evaluating automated labeling of elderly and neurodegenerative brain , 2008, Medical Image Anal..
[44] Stephen M. Smith,et al. Investigations into resting-state connectivity using independent component analysis , 2005, Philosophical Transactions of the Royal Society B: Biological Sciences.
[45] Kristopher J Preacher,et al. SPSS and SAS procedures for estimating indirect effects in simple mediation models , 2004, Behavior research methods, instruments, & computers : a journal of the Psychonomic Society, Inc.
[46] L. Butcher,et al. Pars compacta of the substantia nigra modulates motor activity but is not involved importantly in regulating food and water intake , 1980, Naunyn-Schmiedeberg's Archives of Pharmacology.
[47] H. Braak,et al. Staging of brain pathology related to sporadic Parkinson’s disease , 2003, Neurobiology of Aging.
[48] S. West,et al. A comparison of methods to test mediation and other intervening variable effects. , 2002, Psychological methods.
[49] G. Deuschl,et al. Pathophysiology of Parkinson's disease: From clinical neurology to basic neuroscience and back , 2002, Movement disorders : official journal of the Movement Disorder Society.
[50] J. Obeso,et al. Pathophysiology of the basal ganglia in Parkinson's disease , 2000, Trends in Neurosciences.
[51] John Hardy,et al. The A53T α-Synuclein Mutation Increases Iron-Dependent Aggregation and Toxicity , 2000, The Journal of Neuroscience.
[52] L. Petrucelli,et al. The A53T alpha-synuclein mutation increases iron-dependent aggregation and toxicity. , 2000, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[53] Terrence J. Sejnowski,et al. An Information-Maximization Approach to Blind Separation and Blind Deconvolution , 1995, Neural Computation.
[54] P. Ryvlin,et al. Magnetic resonance imaging evidence of decreased putamenal iron content in idiopathic Parkinson's disease. , 1995, Archives of neurology.
[55] P. Boesiger,et al. T2 relaxation time in patients with Parkinson's disease , 1993, Neurology.
[56] J. Hughes,et al. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. , 1992, Journal of neurology, neurosurgery, and psychiatry.
[57] C D Marsden,et al. Alterations in the levels of iron, ferritin and other trace metals in Parkinson's disease and other neurodegenerative diseases affecting the basal ganglia. , 1991, Brain : a journal of neurology.
[58] T. Di Paolo,et al. Decreased dopamine in the retinas of patients with Parkinson's disease. , 1990, Investigative ophthalmology & visual science.
[59] J. D. Hood,et al. Visual control of balance in cerebellar and parkinsonian syndromes. , 1990, Brain : a journal of neurology.
[60] D. A. Kenny,et al. The moderator-mediator variable distinction in social psychological research: conceptual, strategic, and statistical considerations. , 1986, Journal of personality and social psychology.