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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:

Mouse Models of Primary Sjogren’s Syndrome
Young-Seok Park, Adrienne E. Gauna, Seunghee Cha
Current Pharmaceutical Design (2015) Vol. 21, Iss. 18, pp. 2350-2364
Open Access | Times Cited: 77

Showing 1-25 of 77 citing articles:

Lacrimal gland development: From signaling interactions to regenerative medicine
Ankur Garg, Xin Zhang
Developmental Dynamics (2017) Vol. 246, Iss. 12, pp. 970-980
Open Access | Times Cited: 70
The Multifaceted Roles of B Cells in the Thymus: From Immune Tolerance to Autoimmunity
Justine Castañeda, Yessia Hidalgo, Daniela Sauma, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 41
The NOD Mouse Beyond Autoimmune Diabetes
A. Aubin, Félix Lombard‐Vadnais, Roxanne Collin, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 31
MSC-Derived Small Extracellular Vesicles Attenuate Autoimmune Dacryoadenitis by Promoting M2 Macrophage Polarization and Inducing Tregs via miR-100-5p
Na Li, Zhiqi Gao, Lu Zhao, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 30
Intracrine Regulation of Estrogen and Other Sex Steroid Levels in Endometrium and Non-gynecological Tissues; Pathology, Physiology, and Drug Discovery
Gonda Konings, Linda Stevens Brentjens, Bert Delvoux, et al.
Frontiers in Pharmacology (2018) Vol. 9
Open Access | Times Cited: 55
A new dry eye mouse model produced by exorbital and intraorbital lacrimal gland excision
Katsuhiko Shinomiya, Mayumi Ueta, Shigeru Kinoshita
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 53
Enriching Islet Phospholipids With Eicosapentaenoic Acid Reduces Prostaglandin E2 Signaling and Enhances Diabetic β-Cell Function
Joshua C. Neuman, Michael D. Schaid, Allison L. Brill, et al.
Diabetes (2017) Vol. 66, Iss. 6, pp. 1572-1585
Open Access | Times Cited: 50
Activation of Stimulator of Interferon Genes (STING) and Sjögren Syndrome
Joanna Papinska, Harini Bagavant, Grzegorz B. Gmyrek, et al.
Journal of Dental Research (2018) Vol. 97, Iss. 8, pp. 893-900
Open Access | Times Cited: 48
Human umbilical cord mesenchymal stem cells alleviate ongoing autoimmune dacryoadenitis in rabbits via polarizing macrophages into an anti-inflammatory phenotype
Xiaoxiao Lu, Na Li, Lu Zhao, et al.
Experimental Eye Research (2019) Vol. 191, pp. 107905-107905
Open Access | Times Cited: 44
Mitochondrial double-stranded RNAs as a pivotal mediator in the pathogenesis of Sjӧgren’s syndrome
Jimin Yoon, Min-Seok Lee, Ahsan Ausaf Ali, et al.
Molecular Therapy — Nucleic Acids (2022) Vol. 30, pp. 257-269
Open Access | Times Cited: 26
Chronic Autoimmune Epithelitis in Sjögren’s Syndrome and Primary Biliary Cholangitis: A Comprehensive Review
Carlo Selmi, M. Eric Gershwin
Rheumatology and Therapy (2017) Vol. 4, Iss. 2, pp. 263-279
Open Access | Times Cited: 48
Current and Emerging Evidence for Toll-Like Receptor Activation in Sjögren’s Syndrome
Jeremy Kiripolsky, Jill M. Kramer
Journal of Immunology Research (2018) Vol. 2018, pp. 1-12
Open Access | Times Cited: 45
Rescue of autophagy and lysosome defects in salivary glands of MRL/lpr mice by a therapeutic phosphopeptide
Baihui Li, Fengjuan Wang, Nicolas Schall, et al.
Journal of Autoimmunity (2018) Vol. 90, pp. 132-145
Closed Access | Times Cited: 42
Interleukin-27 Is Essential for Type 1 Diabetes Development and Sjögren Syndrome-like Inflammation
Ashley E. Ciecko, Bardees M. Foda, Jennifer Barr, et al.
Cell Reports (2019) Vol. 29, Iss. 10, pp. 3073-3086.e5
Open Access | Times Cited: 42
Involvement of Aquaporins in the Pathogenesis, Diagnosis and Treatment of Sjögren’s Syndrome
Muhammad Shahnawaz Soyfoo, Clara Chivasso, Jason Perret, et al.
International Journal of Molecular Sciences (2018) Vol. 19, Iss. 11, pp. 3392-3392
Open Access | Times Cited: 40
Human umbilical cord mesenchymal stem cells confer potent immunosuppressive effects in Sjögren’s syndrome by inducing regulatory T cells
Yanying Liu, Chunlei Li, Shiyao Wang, et al.
Modern Rheumatology (2019) Vol. 31, Iss. 1, pp. 186-196
Closed Access | Times Cited: 37
Recent Advances in Mouse Models of Sjögren's Syndrome
Yunzhen Gao, Yan Chen, Zhongjian Zhang, et al.
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 34
Salivary stimulatory and anti-inflammatory effects of aqueous Lilium brownii var. viridulum Baker extract for Sjögren’s syndrome: in vitro and in vivo studies
Na-Yeon Ha, Hae-in Jeong, Mun Seog Chang, et al.
Brazilian Journal of Pharmaceutical Sciences (2025) Vol. 61
Open Access
Contribution of Genetic Factors to Sjögren’s Syndrome and Sjögren’s Syndrome Related Lymphomagenesis
Adrianos Nezos, Clio P. Mavragani
Journal of Immunology Research (2015) Vol. 2015, pp. 1-12
Open Access | Times Cited: 38
Myoepithelial cell-driven acini contraction in response to oxytocin receptor stimulation is impaired in lacrimal glands of Sjögren’s syndrome animal models
Dillon Hawley, Xin Tang, Tatiana Zyrianova, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 36
What can Sjögren's syndrome-like disease in mice contribute to human Sjögren's syndrome?
Ammon B. Peck, Cuong Q. Nguyen
Clinical Immunology (2017) Vol. 182, pp. 14-23
Open Access | Times Cited: 35
Mesenchymal stem cells inhibited the differentiation of MDSCs via COX2/PGE2 in experimental sialadenitis
Jingjing Qi, Xiaojun Tang, Wenchao Li, et al.
Stem Cell Research & Therapy (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 31
Pathophysiologic role of Interleukin-33/ST2 in Sjögren's syndrome
Muhammad Shahnawaz Soyfoo, Charles Nicaise
Autoimmunity Reviews (2021) Vol. 20, Iss. 3, pp. 102756-102756
Open Access | Times Cited: 26
MBD2 acts as a repressor to maintain the homeostasis of the Th1 program in type 1 diabetes by regulating the STAT1-IFN-γ axis
Tiantian Yue, Fei Sun, Faxi Wang, et al.
Cell Death and Differentiation (2021) Vol. 29, Iss. 1, pp. 218-229
Open Access | Times Cited: 25
Myeloid-derived suppressor cells as cellular immunotherapy in transplantation and autoimmune diseases
Jilu Zhang, Alan W. Hodges, Shu‐Hsia Chen, et al.
Cellular Immunology (2021) Vol. 362, pp. 104300-104300
Open Access | Times Cited: 24
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