Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Abnormalities in normal-appearing white matter from which multiple sclerosis lesions arise
Colm Elliott, Parya MomayyezSiahkal, Douglas L. Arnold, et al.
Brain Communications (2021) Vol. 3, Iss. 3
Open Access | Times Cited: 19

Showing 19 citing articles:

Profiling of microglia nodules in multiple sclerosis reveals propensity for lesion formation
Aletta M.R. van den Bosch, Marlijn van der Poel, Nina L. Fransen, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 21
Chronic experimental autoimmune encephalomyelitis is an excellent model to study neuroaxonal degeneration in multiple sclerosis
Rhonda R. Voskuhl, Allan MacKenzie‐Graham
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 23
Micro‐diffusely abnormal white matter: An early multiple sclerosis lesion phase with intensified myelin blistering
Antonio Luchicchi, Gema Muñoz‐Gonzalez, Saar T. Halperin, et al.
Annals of Clinical and Translational Neurology (2024) Vol. 11, Iss. 4, pp. 973-988
Open Access | Times Cited: 5
White Matter Hyperintensities and Microstructural Alterations in Contact Sport Athletes from Adolescence to Early Midlife
Benjamin L. Brett, Andrew P. Klein, Parsia Vazirnia, et al.
Journal of Neurotrauma (2024) Vol. 41, Iss. 19-20, pp. 2307-2322
Closed Access | Times Cited: 5
Pathological ultrastructural alterations of myelinated axons in normal appearing white matter in progressive multiple sclerosis
Wendy Oost, Allard J. Huitema, Kim Kats, et al.
Acta Neuropathologica Communications (2023) Vol. 11, Iss. 1
Open Access | Times Cited: 12
Longitudinal analysis of new multiple sclerosis lesions with magnetization transfer and diffusion tensor imaging
M Gloor, Michaela Andělová, Laura Gaetano, et al.
European Radiology (2023) Vol. 34, Iss. 3, pp. 1680-1691
Open Access | Times Cited: 7
Single-timepoint low-dimensional characterization and classification of acute versus chronic multiple sclerosis lesions using machine learning
Bastien Caba, Alexandre Cafaro, Aurélien Lombard, et al.
NeuroImage (2022) Vol. 265, pp. 119787-119787
Open Access | Times Cited: 9
The Application of Diffusion Kurtosis Imaging on the Heterogeneous White Matter in Relapsing-Remitting Multiple Sclerosis
Qiyuan Zhu, Qiao Zheng, Dan Luo, et al.
Frontiers in Neuroscience (2022) Vol. 16
Open Access | Times Cited: 8
Reconciling lesions, relapses and smouldering associated worsening: A unifying model for multiple sclerosis pathogenesis
Niraj Mistry, Jeremy Hobart, David Rog, et al.
Multiple Sclerosis and Related Disorders (2024) Vol. 88, pp. 105706-105706
Closed Access | Times Cited: 1
New views on the complex interplay between degeneration and autoimmunity in multiple sclerosis
Peter K. Stys, Shigeki Tsutsui, Arie Gafson, et al.
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access | Times Cited: 1
Azetidine-2-Carboxylic Acid-Induced Oligodendrogliopathy: Relevance to the Pathogenesis of Multiple Sclerosis
Raymond A. Sobel, Megan A. Albertelli, Julian R. Hinojoza, et al.
Journal of Neuropathology & Experimental Neurology (2022) Vol. 81, Iss. 6, pp. 414-433
Open Access | Times Cited: 7
Permanent tissue damage in multiple sclerosis lesions is associated with reduced pre-lesion myelin and axon volume fractions
Ian Tagge, Ilana R. Leppert, Dumitru Fetco, et al.
Multiple Sclerosis Journal (2022) Vol. 28, Iss. 13, pp. 2027-2037
Open Access | Times Cited: 6
Characterization of white matter lesions in multiple sclerosis using proton density and T1-relaxation measures
Sagar Buch, Subramanian Karthikeyan, Teresa C. Chen, et al.
Magnetic Resonance Imaging (2023) Vol. 106, pp. 110-118
Closed Access | Times Cited: 3
Low-frequency MR elastography reveals altered deep gray matter viscoelasticity in multiple sclerosis
Christian Kiss, Sebastian Wurth, Bettina Heschl, et al.
NeuroImage Clinical (2024) Vol. 42, pp. 103606-103606
Open Access
Spin-lock based fast whole-brain 3D macromolecular proton fraction mapping of relapsing–remitting multiple sclerosis
Jian Hou, Zongyou Cai, Weitian Chen, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
Natalizumab Treatment for Relapsing Multiple Sclerosis Stabilises Normal-Appearing White Matter Microstructure: A One-Year Prospective Ultra-High-Field Quantitative Imaging Study
Radu Tănăsescu, Olivier Mougin, I‐Jun Chou, et al.
Brain Sciences (2023) Vol. 13, Iss. 10, pp. 1464-1464
Open Access | Times Cited: 1
The profiling and imaging of sterol molecules in the human brain
Lauren Griffiths
(2023)
Open Access
Multiple sclerosis
Nara Miriam Michaelson, Neha Safi, Ulrike W. Kaunzner, et al.
Advances in magnetic resonance technology and applications (2023), pp. 387-403
Closed Access
Low-Frequency Mr Elastography Reveals Deep Gray Matter Degradation in Multiple Sclerosis
Christian Kiss, Sebastian Wurth, Bettina Heschl, et al.
(2023)
Closed Access
Page 1

Scroll to top