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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:

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions
Max Schubach, Thorben Maaß, Lusiné Nazaretyan, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. D1, pp. D1143-D1154
Open Access | Times Cited: 92

Showing 1-25 of 92 citing articles:

Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies
Amir Ghaffari Jolfayi, Erfan Kohansal, Serwa Ghasemi, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 6
A Comprehensive Bioinformatics Approach to Analysis of Variants: Variant Calling, Annotation, and Prioritization
Merve Nur Köroğlu, Kaya Bilgüvar
Methods in molecular biology (2025), pp. 207-233
Closed Access
Association of Novel Pathogenic Variant (p. Ile366Asn) in PLA2G6 Gene with Infantile Neuroaxonal Dystrophy
Asma Naseer Cheema, Ruyu Shi, M. Ilyas Kamboh
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 1, pp. 352-352
Open Access
High-coverage whole-genome sequencing of a Jakun individual from the “Orang Asli” Proto-Malay subtribe from Peninsular Malaysia
Wai-Sum Yap, Alvin Cengnata, Woei-Yuh Saw, et al.
Human Genome Variation (2025) Vol. 12, Iss. 1
Open Access
Expanding the Molecular Spectrum of MMP21 Missense Variants: Clinical Insights and Literature Review
Domizia Pasquetti, Paola Tesolin, Federica Perino, et al.
Genes (2025) Vol. 16, Iss. 1, pp. 62-62
Open Access
Introduction to androgenetics: terminology, approaches, and impactful studies across 60 years
Arvand Akbari, Laura Kasak, Maris Laan
Andrology (2025)
Closed Access
Compound Heterozygous p.(R124C) (Classic Lattice Corneal Dystrophy) and p.(R124H) (Granular Corneal Dystrophy Type 2) in TGFBI: Phenotype, Genotype, and Treatment
Ji Sang Min, Tae‐im Kim, Ikhyun Jun, et al.
Genes (2025) Vol. 16, Iss. 1, pp. 76-76
Open Access
Immunotherapy Responsive Recurrent Post-Infectious Ataxia Associated With Recurrent ATP2B2 Gene Variant
J Vanćura, Abhik K. Banerjee, Natalie K. Boyd, et al.
Neurology Genetics (2025) Vol. 11, Iss. 1
Closed Access
A network-based systems genetics framework identifies pathobiology and drug repurposing in Parkinson’s disease
Lijun Dou, Zhenxing Xu, Jielin Xu, et al.
npj Parkinson s Disease (2025) Vol. 11, Iss. 1
Open Access
Evaluating pathogenicity of variants of unknown significance in APP, PSEN1, and PSEN2
Jacob Marsh, Guangming Huang, Kevin M. Bowling, et al.
Neurotherapeutics (2025), pp. e00527-e00527
Open Access
Association Analysis of Rare CNTN5 Variants With Autism Spectrum Disorder in a Japanese Population
Abdul Fuad Hadi, Reza K. Arta, Itaru Kushima, et al.
Neuropsychopharmacology Reports (2025) Vol. 45, Iss. 1
Open Access
Modern Approaches to Protein Constructions: A Comprehensive Review of Computational Tools and Databases for De Novo Protein Design and Engineering
Md. Mojnu Mia, Habiba Sultana, Md. Al Amin, et al.
Engineering Reports (2025) Vol. 7, Iss. 2
Open Access
Genomics of pediatric cardiomyopathy
Teresa M. Lee, Stephanie M. Ware, Alicia M. Kamsheh, et al.
Pediatric Research (2025)
Open Access
Classification and Genotype–Phenotype Relationships of GBA1 Variants: MDSGene Systematic Review
Malco Rossi, Susen Schaake, Tatiana Usnich, et al.
Movement Disorders (2025)
Open Access
Comprehensive functional characterization of Complement factor I rare variant genotypes identified in the SCOPE Geographic Atrophy cohort
Thomas M Hallam, Anneliza Andreadi, Scott J Sharp, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 7, pp. 107452-107452
Open Access | Times Cited: 4
Gastric cancer actionable genomic alterations across diverse populations worldwide and pharmacogenomics strategies based on precision oncology
Gabriela Echeverría‐Garcés, María José Ramos-Medina, Rodrigo Vargas, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 3
The 2024 Nucleic Acids Research database issue and the online molecular biology database collection
Daniel J. Rigden, Xosé M. Fernández
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D1-D9
Open Access | Times Cited: 8
Longitudinal analysis of circulating tumor cell numbers improves tracking metastatic breast cancer progression
Małgorzata Szostakowska-Rodzoś, Anna Fabisiewicz, Maciej Wakuła, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
Whole-exome sequencing study of opioid dependence offers novel insights into the contributions of exome variants
Lu Wang, Yaira Z. Nuñez, Henry R. Kranzler, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 2
Multimodal AI/ML for discovering novel biomarkers and predicting disease using multi-omics profiles of patients with cardiovascular diseases
William DeGroat, Habiba Abdelhalim, Elizabeth Peker, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
A Novel Mutation in the INSR Gene Causes Severe Insulin Resistance and Rabson–Mendenhall Syndrome in a Paraguayan Patient
Maria Natalia Rojas Velazquez, Fabiola Blanco, Ana Ayala‐Lugo, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 6, pp. 3143-3143
Open Access | Times Cited: 1
Risk and Resilience Variants in the Retinoic Acid Metabolic and Developmental Pathways Associated with Risk of FASD Outcomes
Leo McKay, Berardino Petrelli, Molly Pind, et al.
Biomolecules (2024) Vol. 14, Iss. 5, pp. 569-569
Open Access | Times Cited: 1
MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing data
Jordan Rossen, Huwenbo Shi, Benjamin J. Strober, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Discovery of Pathogenic Variants Associated with Idiopathic Recurrent Pregnancy Loss Using Whole-Exome Sequencing
Jeong Yong Lee, JaeWoo Moon, Hae‐Jin Hu, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5447-5447
Open Access | Times Cited: 1
MATR3’s Role beyond the Nuclear Matrix: From Gene Regulation to Its Implications in Amyotrophic Lateral Sclerosis and Other Diseases
Jhune Rizsan Santos, Jeehye Park
Cells (2024) Vol. 13, Iss. 11, pp. 980-980
Open Access | Times Cited: 1
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