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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:

Variable number tandem repeats – Their emerging role in sickness and health
Jack N.G. Marshall, Ana Illera Lopez, Abigail L. Pfaff, et al.
Experimental Biology and Medicine (2021) Vol. 246, Iss. 12, pp. 1368-1376
Open Access | Times Cited: 19

Showing 19 citing articles:

Genetic modifiers of repeat expansion disorders
Sangeerthana Rajagopal, Jasmine Donaldson, Michael Flower, et al.
Emerging Topics in Life Sciences (2023) Vol. 7, Iss. 3, pp. 325-337
Open Access | Times Cited: 19
Deciphering the role of a SINE-VNTR-Alu retrotransposon polymorphism as a biomarker of Parkinson’s disease progression
Alexander Fröhlich, Abigail L. Pfaff, Ben Middlehurst, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 7
Description of a New Simple and Cost-Effective Molecular Testing That Could Simplify MUC1 Variant Detection
Victor Fages, Florentin Bourre, Romain Larrue, et al.
Kidney International Reports (2024) Vol. 9, Iss. 5, pp. 1451-1457
Open Access | Times Cited: 6
A comprehensive tandem repeat catalog of the human genome
Readman Chiu, Indhu‐Shree Rajan‐Babu, Jan M. Friedman, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
Variations and Polymorphisms: The Human Pangenome Project
Shweta Pandey, Sanjiv S. Gambhir, Vipin Kumar Singh, et al.
Elsevier eBooks (2025), pp. 282-294
Closed Access
Modification of Huntington’s disease by short tandem repeats
Eun Pyo Hong, Eliana Marisa Ramos, N. Ahmad Aziz, et al.
Brain Communications (2024) Vol. 6, Iss. 2
Open Access | Times Cited: 3
Non-reference genome transposable elements (TEs) have a significant impact on the progression of the Parkinson’s disease
Sulev Kõks, Abigail L. Pfaff, Lewis M. Singleton, et al.
Experimental Biology and Medicine (2022) Vol. 247, Iss. 18, pp. 1680-1690
Open Access | Times Cited: 11
Expression Quantitative Trait Loci (eQTLs) Associated with Retrotransposons Demonstrate their Modulatory Effect on the Transcriptome
Sulev Kõks, Abigail L. Pfaff, Vivien J. Bubb, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 12, pp. 6319-6319
Open Access | Times Cited: 13
Mismatch repair is a double-edged sword in the battle against microsatellite instability
Carson J. Miller, Karen Usdin
Expert Reviews in Molecular Medicine (2022) Vol. 24
Open Access | Times Cited: 10
On the edge of deletion: Using natural and engineered microhomology to edit the human genome
Gabriel Martínez‐Gálvez, Suji Lee, Ryo Niwa, et al.
Gene and Genome Editing (2024) Vol. 7, pp. 100033-100033
Open Access | Times Cited: 1
Association between PDCD6-VNTR polymorphism and urinary cancer susceptibility
Gi-Eun Yang, Min-Hye Kim, Mi-So Jeong, et al.
Genes & Genomics (2024)
Closed Access | Times Cited: 1
Introduction to genomic and molecular biology
Dhavendra Kumar
Elsevier eBooks (2024), pp. 1-24
Closed Access | Times Cited: 1
Characterisation of retrotransposon insertion polymorphisms in whole genome sequencing data from individuals with amyotrophic lateral sclerosis
Abigail L. Savage, Alfredo Iacoangeli, Gerald G. Schumann, et al.
Gene (2022) Vol. 843, pp. 146799-146799
Open Access | Times Cited: 6
SARS-CoV-2 and human retroelements: a case for molecular mimicry?
Benjamin Koch
BMC Genomic Data (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 5
Behavioral genetics and animal science
Temple Grandin, Mark J. Deesing
Elsevier eBooks (2022), pp. 1-47
Closed Access | Times Cited: 4
Deciphering the role of a SINE-VNTR-Alu retrotransposon polymorphism as a biomarker of Parkinson’s disease progression
Alexander Fröhlich, Abigail L. Pfaff, Ben Middlehurst, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression
Jack N.G. Marshall, Alexander Fröhlich, Li Li, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 2
SARS-CoV-2 and human retroelements: a case for molecular mimicry?
Benjamin Koch
Research Square (Research Square) (2022)
Open Access | Times Cited: 1
TRIB3 promoter 33 bp VNTR is associated with the risk of cerebrovascular disease in type 2 diabetic patients
Jiaqi Lai, Jiaying Ouyang, Weijie Lin, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 1
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