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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.

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Showing 1-25 of 27 citing articles:

Centers for Mendelian Genomics: A decade of facilitating gene discovery
Samantha Baxter, Jennifer E. Posey, Nicole J. Lake, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 4, pp. 784-797
Open Access | Times Cited: 67
Common Variable Immunodeficiency: More Pathways than Roads to Rome
Xiao Peng, Andrés Caballero-Oteyza, Bodo Grimbacher
Annual Review of Pathology Mechanisms of Disease (2022) Vol. 18, Iss. 1, pp. 283-310
Open Access | Times Cited: 42
Recent advances in elucidating the genetics of common variable immunodeficiency
Vaishali Aggarwal, Aaqib Zaffar Banday, Ankur Kumar Jindal, et al.
Genes & Diseases (2019) Vol. 7, Iss. 1, pp. 26-37
Open Access | Times Cited: 45
Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study
Jessica Rojas‐Restrepo, Andrés Caballero-Oteyza, Katrin Huebscher, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 33
Clinical, Immunological, and Genetic Features in Patients with NFKB1 and NFKB2 Mutations: a Systematic Review
Nazanin Fathi, Matineh Nirouei, Zahra Salimian Rizi, et al.
Journal of Clinical Immunology (2024) Vol. 44, Iss. 7
Closed Access | Times Cited: 4
Beyond monogenetic rare variants: tackling the low rate of genetic diagnoses in predominantly antibody deficiency
Emily S.J. Edwards, Julian J. Bosco, Samar Ojaimi, et al.
Cellular and Molecular Immunology (2020) Vol. 18, Iss. 3, pp. 588-603
Open Access | Times Cited: 29
The pediatric common variable immunodeficiency — from genetics to therapy: a review
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Ewelina Bukowska‐Olech, et al.
European Journal of Pediatrics (2021) Vol. 181, Iss. 4, pp. 1371-1383
Open Access | Times Cited: 25
Screening patients with autoimmune endocrine disorders for cytokine autoantibodies reveals monogenic immune deficiencies
Thea Sjøgren, Eirik Bratland, Ellen C. Røyrvik, et al.
Journal of Autoimmunity (2022) Vol. 133, pp. 102917-102917
Closed Access | Times Cited: 18
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
Thi Thom Mac, Frédéric Castinetti, Céline Bar, et al.
Journal of Neuroendocrinology (2023) Vol. 35, Iss. 6
Open Access | Times Cited: 10
Heterozygous deletion of 10q24.31-q24.33– a new syndrome associated with multiple congenital anomalies: case report and literature review
Anastasiia A. Buianova, Yulia S. Lashkova, T. Kulichenko, et al.
Neurological Research and Practice (2025) Vol. 7, Iss. 1
Open Access
Case Report: Cytomegalovirus Disease Is an Under-Recognized Contributor to Morbidity and Mortality in Common Variable Immunodeficiency
Samantha Chan, Jack Godsell, Miles Horton, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 9
How do nuclear factor kappa B (NF-κB)1 and NF-κB2 defects lead to the incidence of clinical and immunological manifestations of inborn errors of immunity?
Nazanin Fathi, Hanieh Mojtahedi, Marzieh Nasiri, et al.
Expert Review of Clinical Immunology (2023) Vol. 19, Iss. 3, pp. 329-339
Closed Access | Times Cited: 5
Immunogenetic Landscape in Pediatric Common Variable Immunodeficiency
Aleksandra Szczawińska-Popłonyk, Wiktoria Ciesielska, Marta Konarczak, et al.
(2024)
Open Access | Times Cited: 1
Clinical and experimental treatment of primary humoral immunodeficiencies
Anna Szaflarska, Marzena Lenart, Magdalena Rutkowska-Zapała, et al.
Clinical & Experimental Immunology (2024) Vol. 216, Iss. 2, pp. 120-131
Open Access | Times Cited: 1
Intrinsic functional defects in B cells of patients with NFKB2 mutations
Qing Min, Yaxuan Li, Xiaoling Wu, et al.
Clinical & Experimental Immunology (2024)
Closed Access | Times Cited: 1
Disseminated Coccidioidomycosis as the First Presentation of a C-Terminal NFKB2 Pathogenic Variant: A Case Report and Review of the Literature
Samantha Pérez Cavazos, Rodrigo A. De la Cruz Cruz, José Iván Castillo Bejarano, et al.
The Pediatric Infectious Disease Journal (2021) Vol. 41, Iss. 2, pp. 140-144
Closed Access | Times Cited: 6
Cytomegalovirus in primary immunodeficiency
Jack Godsell, Samantha Chan, C Slade, et al.
Current Opinion in Infectious Diseases (2021) Vol. 34, Iss. 6, pp. 663-671
Closed Access | Times Cited: 6
Common variable immunodeficiency, cross currents, and prevailing winds
Neil Romberg, Carole Le Coz
Immunological Reviews (2023) Vol. 322, Iss. 1, pp. 233-243
Closed Access | Times Cited: 2
Defective kinase activity of IKKα leads to combined immunodeficiency and disruption of immune tolerance in humans
Gökhan Cildir, Ümran Aba, Damla Pehlivan, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
A case of novel NFKB2 variant with hypertensive emergency and nephrotic syndrome leading to CKD 5D
Toru Nagata, Kenji Nakagawa, Fumitoshi Tsurumi, et al.
Pediatric Nephrology (2024) Vol. 39, Iss. 9, pp. 2637-2640
Open Access
Defective kinase activity of IKKα leads to combined immunodeficiency and disruption of immune tolerance in humans
Gökhan Cildir, Ümran Aba, Damla Pehlivan, et al.
Research Square (Research Square) (2024)
Closed Access
Immunogenetic Landscape in Pediatric Common Variable Immunodeficiency
Aleksandra Szczawińska-Popłonyk, Wiktoria Ciesielska, Marta Konarczak, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 18, pp. 9999-9999
Open Access
IκBNS expression in B cells is dispensable for IgG responses to T cell-dependent antigens
Sharesta Khoenkhoen, Mónika Ádori, Darío Solís-Sayago, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 2
Identification of novel NFKB1 and ICOS frameshift variants in patients with CVID
Anli Liu, Qiang Liu, Shaoqiu Leng, et al.
Clinical & Experimental Immunology (2022) Vol. 211, Iss. 1, pp. 68-77
Open Access | Times Cited: 2
Centers for Mendelian Genomics: A decade of facilitating gene discovery
Samantha Baxter, Jennifer E. Posey, Nicole J. Lake, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
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