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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:

Immune Skew of Circulating Follicular Helper T Cells Associates With Myasthenia Gravis Severity
Shinji Ashida, Hirofumi Ochi, Mio Hamatani, et al.
Neurology Neuroimmunology & Neuroinflammation (2021) Vol. 8, Iss. 2
Open Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

Myasthenia Gravis: Epidemiology, Pathophysiology and Clinical Manifestations
Laura Dresser, Richard Wlodarski, Kourosh Rezania, et al.
Journal of Clinical Medicine (2021) Vol. 10, Iss. 11, pp. 2235-2235
Open Access | Times Cited: 273
T follicular helper cells in autoimmune diseases
Xindi Wei, Xiaoyin Niu
Journal of Autoimmunity (2022) Vol. 134, pp. 102976-102976
Closed Access | Times Cited: 61
The CXCL13/CXCR5 Immune Axis in Health and Disease—Implications for Intrathecal B Cell Activities in Neuroinflammation
Christine Harrer, Ferdinand Otto, Richard Friedrich Radlberger, et al.
Cells (2022) Vol. 11, Iss. 17, pp. 2649-2649
Open Access | Times Cited: 25
Peripheral immune landscape for hypercytokinemia in myasthenic crisis utilizing single-cell transcriptomics
Huahua Zhong, Xiao Huan, Rui Zhao, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 14
Antibody Therapies in Autoimmune Neuromuscular Junction Disorders: Approach to Myasthenic Crisis and Chronic Management
Fiammetta Vanoli, Renato Mantegazza
Neurotherapeutics (2022) Vol. 19, Iss. 3, pp. 897-910
Open Access | Times Cited: 22
CXCR3-Expressing T Cells in Infections and Autoimmunity
Artem Rubinstein, I. V. Kudryavtsev, N. A. Аrsentieva, et al.
Frontiers in Bioscience-Landmark (2024) Vol. 29, Iss. 8
Open Access | Times Cited: 4
Myasthenia gravis in 2025: five new things and four hopes for the future
Sophie Binks, I. M. Morse, Mohammad Ashraghi, et al.
Journal of Neurology (2025) Vol. 272, Iss. 3
Open Access
Peripheral immune profiling highlights a dynamic role of low-density granulocytes in myasthenia gravis
Shu Zhang, Wen Qi, Shengyao Su, et al.
Journal of Autoimmunity (2025) Vol. 152, pp. 103395-103395
Closed Access
Phenotypic and functional dysregulations of CD8 + T Cells in myasthenia gravis
Chang Liu, Hao Zhang, Yu-Yao Zhai, et al.
Clinical and Experimental Medicine (2025) Vol. 25, Iss. 1
Open Access
Myasthenia Gravis, Immunology of
Robert P. Lisak
Elsevier eBooks (2025)
Closed Access
Novel pathophysiological insights in autoimmune myasthenia gravis
Gianvito Masi, Kevin C. O’Connor
Current Opinion in Neurology (2022)
Open Access | Times Cited: 18
Current Biomarker Strategies in Autoimmune Neuromuscular Diseases
Menekse Oeztuerk, Antonia Henes, Christina B. Schroeter, et al.
Cells (2023) Vol. 12, Iss. 20, pp. 2456-2456
Open Access | Times Cited: 9
The CXCL13/CXCR5-chemokine axis in neuroinflammation: evidence of CXCR5+CD4 T cell recruitment to CSF
Christine Harrer, Ferdinand Otto, Georg Pilz, et al.
Fluids and Barriers of the CNS (2021) Vol. 18, Iss. 1
Open Access | Times Cited: 20
B-cell immune dysregulation with low soluble CD22 levels in refractory seronegative myasthenia gravis
Yuumi Okuzono, Shuuichi Miyakawa, Tatsuo Itou, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 2
IL-6 receptor antibody treatment improves muscle weakness in experimental autoimmune myasthenia gravis mouse model
Shota Miyake, Kenichi Serizawa, Shinichi Onishi, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access | Times Cited: 2
Towards personalized management of myasthenia gravis phenotypes: From the role of multi-omics to the emerging biomarkers and therapeutic targets
Carmela Rita Balistreri, Claudia Vinciguerra, Daniele Magro, et al.
Autoimmunity Reviews (2024) Vol. 23, Iss. 12, pp. 103669-103669
Closed Access | Times Cited: 2
Thymoma patients with or without myasthenia gravis have increased Th17 cells, IL-17 production and ICOS expression
Merve Çebi, Arman Çakar, Eren Erdoğdu, et al.
Journal of Neuroimmunology (2023) Vol. 381, pp. 578129-578129
Closed Access | Times Cited: 5
Dysregulated Long Non-coding RNAs in Myasthenia Gravis- A Mini-Review
Liying Sun, X. Ye, Linlin Wang, et al.
Current Molecular Medicine (2024) Vol. 25, Iss. 1, pp. 2-12
Closed Access | Times Cited: 1
In vitro modulation of T cells in myasthenia gravis by low‐dose IL‐2
Merve Çebi, Arman Çakar, Hacer Durmuş, et al.
European Journal of Immunology (2024) Vol. 54, Iss. 11
Closed Access | Times Cited: 1
Single-cell mapping reveals dysregulation of immune cell populations and VISTA+ monocytes in myasthenia gravis
Rui Fan, Wenjun Que, Zhuoting Liu, et al.
Clinical Immunology (2022) Vol. 245, pp. 109184-109184
Closed Access | Times Cited: 7
Circulating plasmablasts and follicular helper T-cell subsets are associated with antibody-positive autoimmune epilepsy
Atsushi Hara, Norio Chihara, Ritsu Akatani, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 6
Role of soluble forms of follicular helper T-cell membrane molecules in the pathogenesis of myasthenia gravis
Hiroyuki Akamine, Akiyuki Uzawa, Yuta Kojima, et al.
Journal of Neuroimmunology (2023) Vol. 375, pp. 578014-578014
Closed Access | Times Cited: 3
Diabetes mellitus aggravates humoral immune response in myasthenia gravis by promoting differentiation and activation of circulating Tfh cells
Tao Li, Chunlin Yang, Tong Du, et al.
Clinical Immunology (2022) Vol. 245, pp. 109141-109141
Closed Access | Times Cited: 5
The differentiation courses of the Tfh cells: a new perspective on autoimmune disease pathogenesis and treatment
Qingya Yang, Fang Zhang, Hongyi Chen, et al.
Bioscience Reports (2023) Vol. 44, Iss. 1
Open Access | Times Cited: 2
Nomogram for the acute exacerbation of acetylcholine receptor antibody-positive generalized myasthenia gravis
Jiaxin Chen, Shiyin Li, Feng Li, et al.
Neurological Sciences (2022) Vol. 44, Iss. 3, pp. 1049-1057
Closed Access | Times Cited: 3
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