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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:

Benchmarking AlphaMissense pathogenicity predictions against cystic fibrosis variants
Eli Fritz McDonald, Kathryn E. Oliver, Jonathan P. Schlebach, et al.
PLoS ONE (2024) Vol. 19, Iss. 1, pp. e0297560-e0297560
Open Access | Times Cited: 23

Showing 23 citing articles:

Analysis of AlphaMissense data in different protein groups and structural context
Hedvig Tordai, Odalys Torres, Máté Csepi, et al.
Scientific Data (2024) Vol. 11, Iss. 1
Open Access | Times Cited: 21
Genetic variant classification by predicted protein structure: A case study on IRF6
Hemma Murali, Peng Wang, Eric C. Liao, et al.
Computational and Structural Biotechnology Journal (2024) Vol. 23, pp. 892-904
Open Access | Times Cited: 5
Health research in the era of artificial intelligence: Advances in gene-editing study
Mengyao Dai, Xiangyang Li, Qí Zhāng, et al.
Medicine Plus (2024) Vol. 1, Iss. 2, pp. 100027-100027
Open Access | Times Cited: 4
High resolution deep mutational scanning of the melanocortin-4 receptor enables target characterization for drug discovery
Conor J Howard, Nathan S. Abell, Beatriz A. Osuna, et al.
(2025)
Open Access
Predicting the structure-altering mechanisms of disease variants
Matteo Arnaudi, Mattia Utichi, Matteo Tiberti, et al.
Current Opinion in Structural Biology (2025) Vol. 91, pp. 102994-102994
Open Access
A novel seven-tier framework for the classification of MEFV missense variants using adaptive and rigid classifiers
Mustafa Tarık Alay
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
High-resolution deep mutational scanning of the melanocortin-4 receptor enables target characterization for drug discovery
Conor J Howard, Nathan S. Abell, Beatriz A. Osuna, et al.
eLife (2025) Vol. 13
Open Access
Recent developments in cystic fibrosis drug discovery: where are we today?
Miquéias Lopes‐Pacheco, Amanda Winters, JaNise J. Jackson, et al.
Expert Opinion on Drug Discovery (2025)
Closed Access
Detection of protein structural hotspots using AI distillation and explainability: application to the DAX-1 protein
Noé Dumas, Geoffrey Portelli, Ji Yang, et al.
NAR Genomics and Bioinformatics (2025) Vol. 7, Iss. 2
Open Access
Proteostasis landscapes of cystic fibrosis variants reveal drug response vulnerability
Eli Fritz McDonald, Minsoo Kim, John A. Olson rd, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 17
Open Access
Assessment of ability of AlphaMissense to identify variants affecting susceptibility to common disease
David Curtis
European Journal of Human Genetics (2024) Vol. 32, Iss. 11, pp. 1419-1427
Open Access | Times Cited: 3
Assessment of variant effect predictors unveils variants difficulty as a critical performance indicator
Ragousandirane Radjasandirane, Julien Diharce, Jean‐Christophe Gelly, et al.
(2024)
Closed Access | Times Cited: 2
Estimating the Prevalence of GNE Myopathy Using Population Genetic Databases
Alexa Derksen, Rachel Thompson, M. Y. Shaikh, et al.
Human Mutation (2024) Vol. 2024, Iss. 1
Open Access | Times Cited: 2
Cryo-EM structure of the human subcortical maternal complex and the associated discovery of infertility-associated variants
Pengliang Chi, Guojin Ou, Sibei Liu, et al.
Nature Structural & Molecular Biology (2024) Vol. 31, Iss. 11, pp. 1798-1807
Closed Access | Times Cited: 2
High resolution deep mutational scanning of the melanocortin-4 receptor enables target characterization for drug discovery
Conor J Howard, Nathan S. Abell, Beatriz A. Osuna, et al.
(2024)
Open Access | Times Cited: 2
The Folding Pathway of ABC Transporter CFTR: Effective and Robust
Peter van der Sluijs, Hanneke Hoelen, André Schmidt, et al.
Journal of Molecular Biology (2024) Vol. 436, Iss. 14, pp. 168591-168591
Open Access | Times Cited: 1
A case of pachyonychia congenita with a hotspot variant at Arg127 in KRT16: Disease severity assessment using AlphaMissense technology
Tatsuhiro Noda, Takuya Takeichi, Kana Tanahashi, et al.
The Journal of Dermatology (2024) Vol. 51, Iss. 8, pp. 1134-1136
Closed Access | Times Cited: 1
VUStruct: a compute pipeline for high throughput and personalized structural biology
Christopher W. Moth, Jonathan H. Sheehan, Abdullah Al Mamun, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesis
Caroline Caetano da Silva, Claudio Macias-Treviño, Jason W. Mitchell, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 1
Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesis
Caroline Caetano da Silva, Claudio Macias-Treviño, Jason W. Mitchell, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
High resolution deep mutational scanning of the melanocortin-4 receptor enables target characterization for drug discovery
Conor J Howard, Nathan S. Abell, Beatriz A. Osuna, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
High resolution deep mutational scanning of the melanocortin-4 receptor enables target characterization for drug discovery
Conor J Howard, Nathan S. Abell, Beatriz A. Osuna, et al.
(2024)
Open Access
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