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:

Mechanisms Causing Acantholysis in Pemphigus-Lessons from Human Skin
Desalegn Tadesse Egu, Thomas Schmitt, Jens Waschke
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Meeting report – Desmosome dysfunction and disease: Alpine desmosome disease meeting
Volker Spindler, Brenda Gerull, Kathleen J. Green, et al.
Journal of Cell Science (2023) Vol. 136, Iss. 1
Open Access | Times Cited: 15

Dsg3 epitope-specific signalling in pemphigus
Thomas Schmitt, Christoph Hudemann, Sina Moztarzadeh, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 12

Role of auto-antibodies in the mechanisms of dengue pathogenesis and its progression: a comprehensive review
Tanusree Ghorai, Avipsha Sarkar, Anirban Roy, et al.
Archives of Microbiology (2024) Vol. 206, Iss. 5
Closed Access | Times Cited: 4

EGFR Inhibition by Erlotinib Rescues Desmosome Ultrastructure and Keratin Anchorage and Protects against Pemphigus Vulgaris IgG–Induced Acantholysis in Human Epidermis
Desalegn Tadesse Egu, Thomas Schmitt, Nancy Ernst, et al.
Journal of Investigative Dermatology (2024) Vol. 144, Iss. 11, pp. 2440-2452
Open Access | Times Cited: 4

cAMP: A master regulator of cadherin‐mediated binding in endothelium, epithelium and myocardium
Franziska Vielmuth, Mariya Y. Radeva, Sunil Yeruva, et al.
Acta Physiologica (2023) Vol. 238, Iss. 4
Open Access | Times Cited: 11

The impact of signaling pathways on the desmosome ultrastructure in pemphigus
Thomas Schmitt, Julia Huber, Julia Pircher, et al.
Frontiers in Immunology (2025) Vol. 15
Open Access

Meeting report – Alpine desmosome disease meeting 2024: advances and emerging topics in desmosomes and related diseases
Jens Waschke, Masayuki Amagai, Christoph Becker, et al.
Journal of Cell Science (2025) Vol. 138, Iss. 2
Closed Access

Pemphigus vulgaris autoantibodies induce an ER stress response
Coryn L. Hoffman, Navaneetha Krishnan Bharathan, Yoshitaka SHIBATA, et al.
Journal of Investigative Dermatology (2025)
Open Access

Mouse models of pemphigus: valuable tools to investigate pathomechanisms and novel therapeutic interventions
Shirin Emtenani, Michael Hertl, Enno Schmidt, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 9

Unbiased screening identifies regulators of cell-cell adhesion and treatment options in pemphigus
Henriette Franz, Maitreyi Rathod, Aude Zimmermann, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3

Desmosomal Cadherin Tension Loss in Pemphigus Vulgaris Mediated by the Inhibition of Active RhoA at Cell-Cell Adhesions
Xiaowei Jin, Jordan Rosenbohm, Amir Ostadi Moghaddam, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2

Pemphigus Vulgaris
Nika Kianfar, Maryam Daneshpazhooh, Julia S. Lehman
Mayo Clinic Proceedings (2024) Vol. 99, Iss. 4, pp. 607-609
Open Access | Times Cited: 1

Quantification of Apoptotic Bodies and Correlation of TNF-α & IL-2 Levels with Severity of Pemphigus Vulgaris
Renu Ravikumar, Pratibha Ramani, S Gheena, et al.
Journal of Advanced Oral Research (2024) Vol. 15, Iss. 2, pp. 186-194
Closed Access | Times Cited: 1

HDAC1-mediated regulation of KDM1A in pemphigus vulgaris: unlocking mechanisms on ERK pathway activation and cohesion loss
Mao Luo, Z. M. Jiang, Ping Wang, et al.
Human Molecular Genetics (2024) Vol. 33, Iss. 24, pp. 2133-2144
Closed Access | Times Cited: 1

A Novel In Vivo Active Pemphigus Model Targeting Desmoglein1 and Desmoglein3: A Tool Representing All Pemphigus Variants
Roberta Lotti, Claudio Giacinto Atene, Emma Dorotea Zanfi, et al.
Biology (2023) Vol. 12, Iss. 5, pp. 702-702
Open Access | Times Cited: 3

Interleukin‐37 inhibits desmoglein‐3 endocytosis and keratinocyte dissociation via upregulation of Caveolin‐1 and inhibition of the STAT3 pathway
Junqin Liang, Fengxia Hu, Lidan Mao, et al.
Journal of the European Academy of Dermatology and Venereology (2023) Vol. 37, Iss. 9, pp. 1920-1927
Closed Access | Times Cited: 2

Catalytic antibodies in arrhythmogenic cardiomyopathy patients cleave desmoglein 2 and N-cadherin and impair cardiomyocyte cohesion
Sunil Yeruva, Konstanze Stangner, Anna Jungwirth, et al.
Cellular and Molecular Life Sciences (2023) Vol. 80, Iss. 8
Open Access | Times Cited: 2

Pemphigus: New approaches to diagnosis and disease severity assessment
Nataliа P. Teplyuk, Yuliya V. Колесова, Daria V. Mak, et al.
Russian Journal of Skin and Venereal Diseases (2023) Vol. 26, Iss. 5, pp. 515-526
Open Access | Times Cited: 2

Measurement of pesticides in hair samples from pemphigus foliaceus and pemphigus vulgaris patients in Southeastern Brazil
Leonardo La Serra, Adriana Martinelli Salathiel, Rafael Lanaro, et al.
Anais Brasileiros de Dermatologia (2023) Vol. 98, Iss. 5, pp. 644-650
Open Access | Times Cited: 1

ZNPs reduce epidermal mechanical strain resistance by promoting desmosomal cadherin endocytosis via mTORC1-TFEB-BLOC1S3 axis
Xuan Lai, Menglei Wang, Zhen Zhang, et al.
Journal of Nanobiotechnology (2024) Vol. 22, Iss. 1
Open Access

Pemphigus vulgaris autoantibodies induce an ER stress response
Coryn L Hoffman, Navaneetha Krishnan Bharathan, Yoshitaka SHIBATA, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

Proteomic Analysis Reveals Oxidative Phosphorylation and JAKSTAT Pathways Mediated Pathogenesis of Pemphigus Vulgaris
Yuqi Cheng, Mingming Zhao, CaiHong Zhu, et al.
Experimental Dermatology (2024) Vol. 33, Iss. 10
Closed Access

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