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:

Common and rare genetic variants of complement components in human disease
Elena Goicoechea de Jorge, Alberto López‐Lera, Rafael Bayarri‐Olmos, et al.
Molecular Immunology (2018) Vol. 102, pp. 42-57
Open Access | Times Cited: 20

Showing 20 citing articles:

Therapeutic Targeting of the Complement System: From Rare Diseases to Pandemics
Peter Garred, Andrea J. Tenner, Tom Eirik Mollnes
Pharmacological Reviews (2021) Vol. 73, Iss. 2, pp. 792-827
Open Access | Times Cited: 137

Transcriptomic and proteomic retinal pigment epithelium signatures of age-related macular degeneration
Anne Senabouth, Maciej Daniszewski, Grace E. Lidgerwood, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 47

The Factor H protein family: The switchers of the complement alternative pathway
Laura Lucientes, Bárbara Márquez‐Tirado, Elena Goicoechea de Jorge
Immunological Reviews (2022) Vol. 313, Iss. 1, pp. 25-45
Open Access | Times Cited: 44

Update on C3 Glomerulopathy: A Complement-Mediated Disease
Fernando Caravaca‐Fontán, Laura Lucientes, Teresa Cavero, et al.
˜The œNephron journals/Nephron journals (2020) Vol. 144, Iss. 6, pp. 272-280
Open Access | Times Cited: 58

Deep longitudinal multiomics profiling reveals two biological seasonal patterns in California
M. Reza Sailani, Ahmed A. Metwally, Wenyu Zhou, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 55

Mutations in the alternative complement pathway in multiple myeloma patients with carfilzomib-induced thrombotic microangiopathy
Maria Moscvin, Christine‐Ivy Liacos, Tianzeng Chen, et al.
Blood Cancer Journal (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 17

Soluble Membrane Attack Complex: Biochemistry and Immunobiology
Scott R. Barnum, Doryen Bubeck, Theresa N. Schein
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 49

Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci
Chris Pappas, Moussa A. Zouache, Stacie Matthews, et al.
Human Genomics (2021) Vol. 15, Iss. 1
Open Access | Times Cited: 29

Complement alternative pathway determines disease susceptibility and severity in antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis
Laura Lucientes, Gema Fernández‐Juárez, Bárbara Márquez‐Tirado, et al.
Kidney International (2023) Vol. 105, Iss. 1, pp. 177-188
Open Access | Times Cited: 10

Macular retinal thickness differs markedly in age-related macular degeneration driven by risk polymorphisms on chromosomes 1 and 10
Moussa A. Zouache, Alex Bennion, Jill L. Hageman, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 26

Common Genetic Variants in the Complement System and their Potential Link with Disease Susceptibility and Outcome of Invasive Bacterial Infection
Bryan van den Broek, Michiel van der Flier, Ronald de Groot, et al.
Journal of Innate Immunity (2019) Vol. 12, Iss. 2, pp. 131-141
Open Access | Times Cited: 19

Evaluating the clinical utility of measuring levels of factor H and the related proteins
Pratiti Banerjee, Bert R.J. Veuskens, Elena Goicoechea de Jorge, et al.
Molecular Immunology (2022) Vol. 151, pp. 166-182
Open Access | Times Cited: 10

Diabetes affects endothelial cell function and alters fibrin clot formation in a microvascular flow model: A pilot study
Lorenz Jenny, Andreas Melmer, Markus Laimer, et al.
Diabetes and Vascular Disease Research (2020) Vol. 17, Iss. 1, pp. 147916412090304-147916412090304
Open Access | Times Cited: 10

Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis
Martin Kerick, Marialbert Acosta‐Herrera, Carmen Pilar Simeón‐Aznar, et al.
npj Genomic Medicine (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 6

Combining SPR with atomic-force microscopy enables single-molecule insights into activation and suppression of the complement cascade
Elisavet Makou, Richard G. Bailey, Heather J. Johnston, et al.
Journal of Biological Chemistry (2019) Vol. 294, Iss. 52, pp. 20148-20163
Open Access | Times Cited: 4

Sex-Dependent Association Study of Complement C4 Gene with Treatment-Resistant Schizophrenia and Hospitalization Frequency
Kowsar Teymouri, Mahbod Ebrahimi, Cheng C. Chen, et al.
Psychiatry Research (2024) Vol. 342, pp. 116202-116202
Open Access

Contribution of functional and quantitative genetic variants of Complement Factor H and Factor H-Related (FHR) proteins on renal pathology
Irene Gómez Delgado, Pilar Sánchez‐Corral
Nefrología (English Edition) (2022) Vol. 42, Iss. 3, pp. 280-289
Open Access | Times Cited: 2

Synergistic impact of three complement polymorphisms in the donor, not the recipient, on long-term kidney allograft survival
Felix Poppelaars, Mariana Gaya da Costa, Bernardo Faria, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access

Gene Influencing in COVID-19 Infection, Disease Severity and its Pharmacotherapy
Sougata Sarkar, Shreyashi Dasgupta, Vartika Srivastava, et al.
International Journal of Current Research and Review (2021), pp. 86-96
Open Access

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