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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:

What’s Wrong in a Jump? Prediction and Validation of Splice Site Variants
Giulia Riolo, Silvia Cantara, Claudia Ricci
Methods and Protocols (2021) Vol. 4, Iss. 3, pp. 62-62
Open Access | Times Cited: 23

Showing 23 citing articles:

CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods
Shantanu Jain, Constantina Bakolitsa, Steven E. Brenner, et al.
Genome biology (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 37
In silico methods for predicting functional synonymous variants
Brian Lin, Upendra Katneni, Katarzyna I. Jankowska, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 12
Characterization of a novel GRHL2 mutation reveals molecular mechanisms underlying autosomal dominant hearing loss (DFNA28): insights from structural and functional studies
Dominika Oziębło, Natalia Bałdyga, Marcin L. Leja, et al.
Human Molecular Genetics (2025)
Closed Access
Deep learning-based prediction of tissue-specific splice sites in the human neural retina
Tabea Riepe, Suzanne E. de Bruijn, Susanne Roosing, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
From gene to dose: Long-read sequencing and *-allele tools to refine phenotype predictions of CYP2C19
Lonneke J. Graansma, Qinglian Zhai, Loes Busscher, et al.
Frontiers in Pharmacology (2023) Vol. 14
Open Access | Times Cited: 6
Pathogenicity of Intronic and Synonymous Variants of ATP7B in Wilson Disease
Wan‐Qing Xu, Rou‐Min Wang, Yi Dong, et al.
Journal of Molecular Diagnostics (2022) Vol. 25, Iss. 1, pp. 57-67
Open Access | Times Cited: 9
The Effect of Alternative Splicing Sites on Mirtron Formation and Arm Selection of Precursor microRNAs
L. Gál, Anita Schamberger, Gerda Wachtl, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 14, pp. 7643-7643
Open Access | Times Cited: 1
Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss
Valeriia Yu. Danilchenko, Marina V. Zytsar, Ekaterina A. Maslova, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 21, pp. 13453-13453
Open Access | Times Cited: 7
Mosaic variegated aneuploidy syndrome 2 with biallelic novel CEP57 splice site variation in Indian siblings: Expanding the clinical and molecular spectrum
Nitika Langeh, Sumedha Saluja, A.S. Ethayathulla, et al.
Clinical Genetics (2023) Vol. 103, Iss. 4, pp. 478-483
Closed Access | Times Cited: 3
Characterization of peripheral white blood cells transcriptome to unravel the regulatory signatures of bovine subclinical mastitis resistance
Jinyan Yang, Yongjie Tang, Xueqin Liu, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 5
A noncanonical splicing variant c.875-5 T > G in von Willebrand factor causes in-frame exon skipping and type 2A von Willebrand disease
Qian Liang, Ziqi Zhang, Biying Ding, et al.
Thrombosis Research (2024) Vol. 236, pp. 51-60
Closed Access
Applications of AI in Biomedical Genomics and Pharmaceuticals
Mayyas Al‐Remawi, Rami A. Abdel Rahem
(2024), pp. 1-5
Closed Access
Characterization and Engineered U1 snRNA Rescue of Splicing Variants in a Turkish Neurodevelopmental Disease Cohort
Ece Sönmezler, Cristiana Stuani, Semra Hız Kurul, et al.
Human Mutation (2024) Vol. 2024, pp. 1-17
Open Access
7p22.3 microdeletion: a case study of a patient with congenital heart defect, neurodevelopmental delay and epilepsy
Liliya Skvortsova, Anastassiya Perfilyeva, Kira Bespalova, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
Sudden Cardiac Death and Channelopathies: What Lies Behind the Clinical Significance of Rare Splice-Site Alterations in the Genes Involved?
Mauro Pesaresi, Alessia Bernini Di Michele, Filomena Melchionda, et al.
Genes (2024) Vol. 15, Iss. 10, pp. 1272-1272
Open Access
Generation of Transcript Length Variants and Reprogramming of mRNA Splicing During Atherosclerosis Progression in ApoE-Deficient Mice
Miguel Hueso, Adrián Mallén, Estanis Navarro
Biomedicines (2024) Vol. 12, Iss. 12, pp. 2703-2703
Open Access
EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome
Laura Machado Lara Carvalho, Jessica Rzasa, Jennifer Kerkhof, et al.
Molecular Neurobiology (2024)
Closed Access
A Machine Learning Approach to Identify Potential miRNA-Gene Regulatory Network Contributing to the Pathogenesis of SARS-CoV-2 Infection
Rajesh Das, Vigneshwar Suriya Prakash Sinnarasan, Dahrii Paul, et al.
Biochemical Genetics (2023) Vol. 62, Iss. 2, pp. 987-1006
Closed Access | Times Cited: 1
Intron retention coupled with nonsense-mediated decay is involved in cellulase biosynthesis in cellulolytic fungi
Yichen Gao, Aiping Pang, Leyao Ma, et al.
Biotechnology for Biofuels and Bioproducts (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Novel variant in HHAT as a cause of different sex development with partial gonadal dysgenesis associated with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs: Case report
Noelia Baz-Redón, Laura Soler-Colomer, Mónica Fernández‐Cancio, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 2
VIsoQLR: an interactive tool for the detection, quantification and fine-tuning of isoforms using long-read sequencing
Gonzalo Núñez‐Moreno, Alejandra Tamayo, Carolina Ruiz‐Sánchez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Methods to Evaluate the Effects of Synonymous Variants
Brian Lin, Katarzyna I. Jankowska, Douglas Meyer, et al.
Springer eBooks (2022), pp. 133-168
Closed Access | Times Cited: 1
Intron Retention Coupled with Nonsense-Mediated Decay is Involved in Cellulase Biosynthesis in Cellulolytic Fungi
Yichen Gao, Aiping Pang, Leyao Ma, et al.
Research Square (Research Square) (2022)
Closed Access
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