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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:

A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant
Alina Kurolap, Orly Eshach Adiv, Liza Konnikova, et al.
Journal of Clinical Immunology (2019) Vol. 39, Iss. 4, pp. 430-439
Closed Access | Times Cited: 19

Showing 19 citing articles:

Novel Genetic Discoveries in Primary Immunodeficiency Disorders
Margaret Redmond, Rebecca Scherzer, Benjamin T. Prince
Clinical Reviews in Allergy & Immunology (2022) Vol. 63, Iss. 1, pp. 55-74
Open Access | Times Cited: 29
Genetic susceptibility to EBV infection: insights from inborn errors of immunity
Stuart G. Tangye
Human Genetics (2020) Vol. 139, Iss. 6-7, pp. 885-901
Closed Access | Times Cited: 45
Evolution and long‐term outcomes of combined immunodeficiency due to CARMIL2 deficiency
Burcu Kolukısa, Dilek Başer, Bengü Akçam, et al.
Allergy (2021) Vol. 77, Iss. 3, pp. 1004-1019
Open Access | Times Cited: 35
A Novel Pathogenic Variant in CARMIL2 (RLTPR) Causing CARMIL2 Deficiency and EBV-Associated Smooth Muscle Tumors
Jennifer R. Yonkof, Ajay Gupta, Cesar M. Rueda, et al.
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 34
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency
Romain Lévy, Florian Gothe, Mana Momenilandi, et al.
The Journal of Experimental Medicine (2022) Vol. 220, Iss. 2
Open Access | Times Cited: 20
Of Mycelium and Men: Inherent Human Susceptibility to Fungal Diseases
Donald C. Vinh
Pathogens (2023) Vol. 12, Iss. 3, pp. 456-456
Open Access | Times Cited: 8
Epstein–Barr Virus in Inborn Immunodeficiency—More Than Infection
Ciro N. R. Lino, Sujal Ghosh
Cancers (2021) Vol. 13, Iss. 19, pp. 4752-4752
Open Access | Times Cited: 20
Profound immunodeficiency with severe skin disease explained by concomitant novel CARMIL2 and PLEC1 loss-of-function mutations
Maria Elena Maccari, Carsten Speckmann, Maximilian Heeg, et al.
Clinical Immunology (2019) Vol. 208, pp. 108228-108228
Closed Access | Times Cited: 20
Novel CARMIL2 loss-of-function variants are associated with pediatric inflammatory bowel disease
Luca Bosa, Vritika Batura, Davide Colavito, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 15
Atopic manifestations of inborn errors of immunity
Laura Sams, Sonali Wijetilleka, Mark Ponsford, et al.
Current Opinion in Allergy and Clinical Immunology (2023) Vol. 23, Iss. 6, pp. 478-490
Open Access | Times Cited: 4
CARMIL2 Immunodeficiency with Epstein Barr Virus Associated Smooth Muscle Tumor (EBV-SMT). Report of a Case with Comprehensive Review of Literature
Mukul Vij, Meena Sivasankaran, Dhaarani Jayaraman, et al.
Fetal and Pediatric Pathology (2021) Vol. 41, Iss. 6, pp. 1023-1034
Closed Access | Times Cited: 9
Exogenous interleukin-2 can rescue in-vitro T cell activation and proliferation in patients with a novel capping protein regulator and myosin 1 linker 2 mutation
Oded Shamriz, Amos J. Simon, Atar Lev, et al.
Clinical & Experimental Immunology (2020) Vol. 200, Iss. 3, pp. 215-227
Open Access | Times Cited: 9
Case report: Primary immunodeficiency due to a novel mutation in CARMIL2 and its response to combined immunomodulatory therapy
Yu Zhu, Lili Ye, Hua Huang, et al.
Frontiers in Pediatrics (2023) Vol. 10
Open Access | Times Cited: 3
Complex Muco-cutaneous Manifestations of CARMIL2-associated Combined Immunodeficiency: A Novel Presentation of Dysfunctional Epithelial Barriers
Giuseppe Marangi, Simone Garcovich, Gabriele Di Sante, et al.
Acta Dermato Venereologica (2019) Vol. 100, Iss. 1, pp. 1-2
Open Access | Times Cited: 8
CARMIL2‐related immunodeficiency manifesting with photosensitivity
Leila H. Shayegan, Maria C. Garzón, Kimberly D. Morel, et al.
Pediatric Dermatology (2020) Vol. 37, Iss. 4, pp. 695-697
Open Access | Times Cited: 6
Combined immune deficiencies (CIDs)
Capucine Pïcard, Mathieu Fusaro, Sara Kashef, et al.
Elsevier eBooks (2020), pp. 207-268
Closed Access | Times Cited: 2
Novel CARMIL2 (RLTPR) Mutation Presenting with Hyper-IgE and Eosinophilia: A Case Report
Raha Zamani, Samaneh Zoghi, Sepideh Shahkarami, et al.
Endocrine Metabolic & Immune Disorders - Drug Targets (2023) Vol. 24, Iss. 5, pp. 596-605
Closed Access
Therapeutic effects and mechanism of oat β-glucan plus montmorillonite powder on diarrhea in young rats
Shuyang Liu, Hamad Rafique, Liang Zou, et al.
Food Hydrocolloids for Health (2023) Vol. 4, pp. 100169-100169
Open Access
Inborn errors of immunity with implications for food allergy
Tamar Rubin, Catherine A. Biggs, Erika Sifuentes-Rodriguez
Elsevier eBooks (2022), pp. 792-806
Closed Access
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