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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:

Contribution of fibroblasts to tunnel formation and inflammation in hidradenitis suppurativa/ acne inversa
John W. Frew, Kristina Navrazhina, Meaghan Marohn, et al.
Experimental Dermatology (2019) Vol. 28, Iss. 8, pp. 886-891
Open Access | Times Cited: 50

Showing 1-25 of 50 citing articles:

Hidradenitis Suppurativa: A Systematic Review Integrating Inflammatory Pathways Into a Cohesive Pathogenic Model
Allard R.J.V. Vossen, Hessel H. van der Zee, Errol P. Prens
Frontiers in Immunology (2018) Vol. 9
Open Access | Times Cited: 198
Hidradenitis Suppurativa
James P. Pham, John W. Frew
Dermatologic Clinics (2025) Vol. 43, Iss. 2, pp. 179-191
Closed Access | Times Cited: 3
Unravelling the complex pathogenesis of hidradenitis suppurativa
John W. Frew
British Journal of Dermatology (2025) Vol. 192, Iss. Supplement_1, pp. i3-i14
Open Access | Times Cited: 2
Epithelialized tunnels are a source of inflammation in hidradenitis suppurativa
Kristina Navrazhina, John W. Frew, Patricia Gilleaudeau, et al.
Journal of Allergy and Clinical Immunology (2021) Vol. 147, Iss. 6, pp. 2213-2224
Open Access | Times Cited: 92
Hidradenitis suppurativa is an autoinflammatory keratinization disease: A review of the clinical, histologic, and molecular evidence
John W. Frew
JAAD International (2020) Vol. 1, Iss. 1, pp. 62-72
Open Access | Times Cited: 70
Interleukin‐17RA blockade by brodalumab decreases inflammatory pathways in hidradenitis suppurativa skin and serum
Kristina Navrazhina, John W. Frew, David Grand, et al.
British Journal of Dermatology (2022) Vol. 187, Iss. 2, pp. 223-233
Open Access | Times Cited: 36
Tertiary lymphoid structures sustain cutaneous B cell activity in hidradenitis suppurativa
Margaret M. Lowe, Jarish N. Cohen, Madison I. Moss, et al.
JCI Insight (2023)
Open Access | Times Cited: 13
Skin immune-mesenchymal interplay within tertiarylymphoid structures promotes autoimmunepathogenesis in hidradenitis suppurativa
Wei-Wen Yu, John Barrett, Jie Tong, et al.
Immunity (2024) Vol. 57, Iss. 12, pp. 2827-2842.e5
Closed Access | Times Cited: 5
Hidradenitis Suppurativa Tunnels: Unveiling a Unique Disease Entity
Nicole Vecin, Nathan C. Balukoff, Marita Yaghi, et al.
JID Innovations (2025) Vol. 5, Iss. 3, pp. 100350-100350
Open Access
Plant-Based Foods for Chronic Skin Diseases: A Focus on the Mediterranean Diet
Giuseppe Annunziata, Ludovica Verde, Alexander Zink, et al.
Current Nutrition Reports (2025) Vol. 14, Iss. 1
Open Access
Skin Deep and Beyond: Unravelling B Cell Extracellular Matrix Interactions in Cutaneous Immunity and Disease
R. Diehl, Stefanie Hübner, Saskia Lehr, et al.
Experimental Dermatology (2025) Vol. 34, Iss. 3
Open Access
Increased expression profile of NCSTN, Notch and PI3K/AKT3 in hidradenitis suppurativa
Schapoor Hessam, Thilo Gambichler, Marina Skrygan, et al.
Journal of the European Academy of Dermatology and Venereology (2020) Vol. 35, Iss. 1, pp. 203-210
Open Access | Times Cited: 32
Methylated miRNAsmay serve as potential biomarkers and therapeutic targets for hidradenitis suppurativa
Uppala Radhakrishna, Uppala Ratnamala, Devendrasinh Jhala, et al.
Journal of the European Academy of Dermatology and Venereology (2022) Vol. 36, Iss. 11, pp. 2199-2213
Closed Access | Times Cited: 21
Tunnels in Hidradenitis Suppurativa: Active Inflammatory Entities with Specific Molecular and Genetic Profiles – A Narrative Review
Piotr Krajewski, Jacek C. Szepietowski, A. Martorell
Dermatology (2023) Vol. 239, Iss. 3, pp. 323-327
Open Access | Times Cited: 12
Epigenetic switch reshapes epithelial progenitor cell signatures and drives inflammatory pathogenesis in hidradenitis suppurativa
Lin Jin, Yunjia Chen, Suhail Muzaffar, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 49
Open Access | Times Cited: 12
Role of the Complement Pathway in Inflammatory Skin Diseases: A Focus on Hidradenitis Suppurativa
Mondana Ghias, Michael J. Hyde, Lewis E. Tomalin, et al.
Journal of Investigative Dermatology (2019) Vol. 140, Iss. 3, pp. 531-536.e1
Open Access | Times Cited: 32
Histologic progression of acne inversa/hidradenitis suppurativa: Implications for future investigations and therapeutic intervention
Robert W. Dunstan, K. Salte, Viktor Todorović, et al.
Experimental Dermatology (2020) Vol. 30, Iss. 6, pp. 820-830
Open Access | Times Cited: 29
Autoimmune, Autoinflammatory Disease and Cutaneous Malignancy Associations with Hidradenitis Suppurativa: A Cross-Sectional Study
Hilliard T. Brydges, Ogechukwu C. Onuh, Rebecca Friedman, et al.
American Journal of Clinical Dermatology (2024) Vol. 25, Iss. 3, pp. 473-484
Closed Access | Times Cited: 3
The sclerotic component of metabolic syndrome: Fibroblast activities may be the central common denominator driving organ function loss and death
Alexander Lynge Reese‐Petersen, Signe Holm Nielsen, Jannie Marie Bülow Sand, et al.
Diabetes Obesity and Metabolism (2024) Vol. 26, Iss. 7, pp. 2554-2566
Closed Access | Times Cited: 3
Integrating complement into the molecular pathogenesis of Hidradenitis Suppurativa
David Grand, Kristina Navrazhina, John W. Frew
Experimental Dermatology (2019) Vol. 29, Iss. 1, pp. 86-92
Open Access | Times Cited: 28
The most recent advances in understanding and managing hidradenitis suppurativa
Shanthi Narla, Alexis B. Lyons, Iltefat Hamzavi
F1000Research (2020) Vol. 9, pp. 1049-1049
Open Access | Times Cited: 26
Beyond antibodies: B cells in Hidradenitis Suppurativa: Bystanders, contributors or therapeutic targets?
John W. Frew, David Grand, Kristina Navrazhina, et al.
Experimental Dermatology (2020) Vol. 29, Iss. 5, pp. 509-515
Open Access | Times Cited: 25
Mechanical forces and Hidradenitis Suppurativa
Jurr Boer, Gregor B. E. Jemec
Experimental Dermatology (2020) Vol. 30, Iss. 2, pp. 212-215
Closed Access | Times Cited: 25
Insights into the Pathogenesis of HS and Therapeutical Approaches
Elia Rosi, Maria Thais Fastame, Ilaria Scandagli, et al.
Biomedicines (2021) Vol. 9, Iss. 9, pp. 1168-1168
Open Access | Times Cited: 22
Human dermal fibroblast subpopulations and epithelial mesenchymal transition signals in hidradenitis suppurativa tunnels are normalized by spleen tyrosine kinase antagonism in vivo
Akshay Flora, Rebecca Jepsen, Emily Kozera, et al.
PLoS ONE (2023) Vol. 18, Iss. 11, pp. e0282763-e0282763
Open Access | Times Cited: 8
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