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OpenAlex Citation Counts

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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:

Diffusion tensor imaging findings in the multiple sclerosis patients and their relationships to various aspects of disability
Anna Pokryszko−Dragan, Anna Banaszek, Marta Nowakowska‐Kotas, et al.
Journal of the Neurological Sciences (2018) Vol. 391, pp. 127-133
Closed Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

Disentangling white-matter damage from physiological fibre orientation dispersion in multiple sclerosis
Kasper Winther Andersen, Samo Lasič, Henrik Lundell, et al.
Brain Communications (2020) Vol. 2, Iss. 2
Open Access | Times Cited: 71
Association Between Diffusion Tensor Imaging Measurements and Cognitive Performances in People with Multiple Sclerosis: A Systematic Review and Meta-analysis
Omid Mirmosayyeb, Mohammad Yazdan Panah, Saeed Vaheb, et al.
Multiple Sclerosis and Related Disorders (2025) Vol. 94, pp. 106261-106261
Closed Access | Times Cited: 1
Diffusion tensor imaging and disability progression in multiple sclerosis: A 4‐year follow‐up study
Marcin Kolasa, Ullamari Hakulinen, Antti Brander, et al.
Brain and Behavior (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 46
High serum neurofilament associates with diffuse white matter damage in MS
Maija Saraste, Svetlana Bezukladova, Markus Matilainen, et al.
Neurology Neuroimmunology & Neuroinflammation (2020) Vol. 8, Iss. 1
Open Access | Times Cited: 37
Insights into disseminated MS brain pathology with multimodal diffusion tensor and PET imaging
Svetlana Bezukladova, Jouni Tuisku, Markus Matilainen, et al.
Neurology Neuroimmunology & Neuroinflammation (2020) Vol. 7, Iss. 3
Open Access | Times Cited: 34
Cerebellar Contributions to Motor and Cognitive Control in Multiple Sclerosis✰✰✰
Nora E. Fritz, Erin M. Edwards, Chuyang Ye, et al.
Archives of Physical Medicine and Rehabilitation (2022) Vol. 103, Iss. 8, pp. 1592-1599
Closed Access | Times Cited: 21
Brain connectivity changes underlying depression and fatigue in relapsing-remitting multiple sclerosis: A systematic review
Agniete Kampaite, Rebecka Gustafsson, Elizabeth N. York, et al.
PLoS ONE (2024) Vol. 19, Iss. 3, pp. e0299634-e0299634
Open Access | Times Cited: 4
Myelin Damage in Normal Appearing White Matter Contributes to Impaired Cognitive Processing Speed in Multiple Sclerosis
Shawna Abel, Irene M. Vavasour, Lisa Eunyoung Lee, et al.
Journal of Neuroimaging (2019) Vol. 30, Iss. 2, pp. 205-211
Closed Access | Times Cited: 32
Associations Between Findings From Myelin Water Imaging and Cognitive Performance Among Individuals With Multiple Sclerosis
Shawna Abel, Irene M. Vavasour, Lisa Eunyoung Lee, et al.
JAMA Network Open (2020) Vol. 3, Iss. 9, pp. e2014220-e2014220
Open Access | Times Cited: 30
Multiple sclerosis-related fatigue lacks a unified definition
Iman Adibi, Mehdi Sanayei, Farinaz Tabibian, et al.
Journal of Research in Medical Sciences (2022) Vol. 27, Iss. 1, pp. 24-24
Open Access | Times Cited: 15
Temporal Dynamics of Diffusion Metrics in Early Multiple Sclerosis and Clinically Isolated Syndrome: A 2-Year Follow-Up Tract-Based Spatial Statistics Study
Ruth Schneider, Erhan Genç, Christian Ahlborn, et al.
Frontiers in Neurology (2019) Vol. 10
Open Access | Times Cited: 22
Axonal loss in major sensorimotor tracts is associated with impaired motor performance in minimally disabled multiple sclerosis patients
Myrte Strik, L. Eduardo Cofré Lizama, Camille J. Shanahan, et al.
Brain Communications (2021) Vol. 3, Iss. 2
Open Access | Times Cited: 17
Environmental enrichment reduces restricted repetitive behavior by altering gray matter microstructure
Anna L. Farmer, Marcelo Febo, Bradley J. Wilkes, et al.
PLoS ONE (2024) Vol. 19, Iss. 7, pp. e0307290-e0307290
Open Access | Times Cited: 2
Measurements of the corpus callosum index and fractional anisotropy of the corpus callosum and their cutoff values are useful to assess global brain volume loss in multiple sclerosis
Juichi Fujimori, Kengo Uryu, Kazuo Fujihara, et al.
Multiple Sclerosis and Related Disorders (2020) Vol. 45, pp. 102388-102388
Closed Access | Times Cited: 16
Differential Associations of Mobility With Fronto-Striatal Integrity and Lesion Load in Older Adults With and Without Multiple Sclerosis
Mark E. Wagshul, Frederick W. Foley, Kapil Chaudhary, et al.
Neurorehabilitation and neural repair (2023) Vol. 37, Iss. 4, pp. 205-217
Open Access | Times Cited: 5
Cognitive Contributors of Backward Walking in Persons with Multiple Sclerosis
Taylor N. Takla, Alexis N. Chargo, Ana M. Daugherty, et al.
Multiple Sclerosis International (2023) Vol. 2023, pp. 1-10
Open Access | Times Cited: 5
A Comparison of Magnetic Resonance Imaging Methods to Assess Multiple Sclerosis Lesions: Implications for Patient Characterization and Clinical Trial Design
E. Mark Haacke, Evanthia Bernitsas, Karthik Subramanian, et al.
Diagnostics (2021) Vol. 12, Iss. 1, pp. 77-77
Open Access | Times Cited: 12
Bridging the callosal gap in gait: corpus callosum white matter integrity’s role in lower limb coordination
Sutton B. Richmond, Daniel S. Peterson, Brett W. Fling
Brain Imaging and Behavior (2022) Vol. 16, Iss. 4, pp. 1552-1562
Closed Access | Times Cited: 8
Fractional Anisotropy of Thalamic Nuclei Is Associated With Verticality Misperception After Extra-Thalamic Stroke
Taiza E. G. Santos, Jussara Almeida de Oliveira Baggio, Carlo Rondinoni, et al.
Frontiers in Neurology (2019) Vol. 10
Open Access | Times Cited: 12
Diffusion tensor imaging changes of the cortico-thalamic-striatal tracts correlate with fatigue and disability in people with relapsing-remitting MS
Abdulaziz Alshehri, Nikitas Koussis, Oun Al‐iedani, et al.
European Journal of Radiology (2023) Vol. 170, pp. 111207-111207
Open Access | Times Cited: 4
Using myelin water imaging to link underlying pathology to clinical function in multiple sclerosis: A scoping review
Erin M. Edwards, Wendy Wu, Nora E. Fritz
Multiple Sclerosis and Related Disorders (2022) Vol. 59, pp. 103646-103646
Closed Access | Times Cited: 7
Contribution of Gray Matter Atrophy and White Matter Damage to Cognitive Impairment in Mildly Disabled Relapsing-Remitting Multiple Sclerosis Patients
Ángela Bernabéu, Sandra Morales, Valery Naranjo, et al.
Diagnostics (2021) Vol. 11, Iss. 3, pp. 578-578
Open Access | Times Cited: 8
Correlations between hippocampal functional connectivity, structural changes, and clinical data in patients with relapsing-remitting multiple sclerosis: a case-control study using multimodal magnetic resonance imaging
Xuemei Han, Xinquan Gu, Ying Liu, et al.
Neural Regeneration Research (2021) Vol. 17, Iss. 5, pp. 1115-1115
Open Access | Times Cited: 8
Quantitative evaluation of callosal abnormalities in relapsing-remitting multiple sclerosis using diffusion tensor imaging: A systemic review and meta-analysis
Lu Xu, Sheng‐Hui Chang, Li Yang, et al.
Clinical Neurology and Neurosurgery (2020) Vol. 201, pp. 106442-106442
Closed Access | Times Cited: 8
Apparent diffusion coefficient measurements in normal appearing white matter may support the differential diagnosis between multiple sclerosis lesions and other white matter hyperintensities
Anna Zacharzewska-Gondek, Anna Pokryszko−Dragan, Tomasz Gondek, et al.
Journal of the Neurological Sciences (2018) Vol. 397, pp. 24-30
Closed Access | Times Cited: 4
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