Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

KLICK Syndrome Linked to a POMP Mutation Has Features Suggestive of an Autoinflammatory Keratinization Disease
Takuya Takeichi, Masashi Akiyama
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 16

Showing 16 citing articles:

Nagoya Journal of Medical Science

JAMA (1964) Vol. 188, Iss. 11, pp. 234-234
Open Access | Times Cited: 177
Diseases categorized as autoinflammatory keratinization diseases (AiKDs), and their pathologies and treatments.
Masashi Akiyama
PubMed (2024) Vol. 86, Iss. 1, pp. 1-15
Closed Access | Times Cited: 3
Chaperone-mediated assembly of the proteasome core particle – recent developments and structural insights
Helena M. Schnell, Richard M. Walsh, Shaun Rawson, et al.
Journal of Cell Science (2022) Vol. 135, Iss. 8
Open Access | Times Cited: 13
Autoinflammatory keratinization diseases
Masashi Akiyama
Dermatologica Sinica (2022) Vol. 40, Iss. 4, pp. 197-203
Open Access | Times Cited: 10
Autoinflammatory Keratinization Diseases—The Concept, Pathophysiology, and Clinical Implications
Leszek Blicharz, Joanna Czuwara, Lidia Rudnicka, et al.
Clinical Reviews in Allergy & Immunology (2023) Vol. 65, Iss. 3, pp. 377-402
Open Access | Times Cited: 5
Human filaggrin monomer does not seem to be a proteasome target
Julie Briot, Eric Arbey, Dominique Goudounèche, et al.
Experimental Dermatology (2023) Vol. 33, Iss. 1
Open Access | Times Cited: 4
Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation
Andrea Meinhardt, Paula C. Ramos, R. Jürgen Dohmen, et al.
Journal of Clinical Immunology (2021) Vol. 41, Iss. 7, pp. 1664-1667
Open Access | Times Cited: 10
Inherited ichthyosis as a paradigm of rare skin disorders: Genomic medicine, pathogenesis, and management
Jason S. Park, Amir Hossein Saeidian, Leila Youssefian, et al.
Journal of the American Academy of Dermatology (2022) Vol. 89, Iss. 6, pp. 1215-1226
Closed Access | Times Cited: 6
In silico analysis of the profilaggrin sequence indicates alterations in the stability, degradation route, and intracellular protein fate in filaggrin null mutation carriers
Argho Aninda Paul, Natalia A. Szulc, Adrian Kobiela, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 3
Congenital Ichthyosis: Clinical and Genetic Characteristics of the Disease
Nikolay N. Murashkin, Karine O. Avetisyan, Roman A. Ivanov, et al.
Вопросы современной педиатрии (2022) Vol. 21, Iss. 5, pp. 362-377
Open Access | Times Cited: 5
Trastornos autoinflamatorios de la queratinización
A. Peña-Rosado, Nuria Martí, V. Expósito‐Serrano, et al.
Actas Dermo-Sifiliográficas (2021) Vol. 112, Iss. 10, pp. 891-900
Open Access | Times Cited: 5
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Syndrome – An Unusual Presentation
Shahzer Tauseef, Ayesha Sharmeen, Mohammad Adil, et al.
Indian Journal of Postgraduate Dermatology (2024) Vol. 2, pp. 114-117
Closed Access
Inherited Disorders of Cornification
Vinzenz Oji, Kira Süßmuth, Dieter Metze, et al.
(2024), pp. 1-108
Closed Access
GEN POMP: acerca de su participación en los mecanismos de autoinmunidad e inflamación
Luis Alberto Aparicio Vera, I. Herrera
Revista Paraguaya de Reumatología (2024) Vol. 10, Iss. 1, pp. 30-36
Open Access
Autoinflammatory Keratinization Diseases
A. Peña-Rosado, Nuria Martí, V. Expósito‐Serrano, et al.
Actas Dermo-Sifiliográficas (2021) Vol. 112, Iss. 10, pp. 891-900
Open Access | Times Cited: 1
In silico analysis of the profilaggrin sequence indicates alterations in the stability, degradation route, and intracellular protein fate in filaggrin null mutation carriers
Argho Aninda Paul, Natalia A. Szulc, Adrian Kobiela, et al.
Research Square (Research Square) (2022)
Open Access
Page 1

Scroll to top