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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:

Genome-wide characterization of human minisatellite VNTRs: population-specific alleles and gene expression differences
Marzieh Eslami Rasekh, Yözen Hernández, Samantha D. Drinan, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 8, pp. 4308-4324
Open Access | Times Cited: 24

Showing 24 citing articles:

Characterization of genome-wide STR variation in 6487 human genomes
Yirong Shi, Yiwei Niu, Peng Zhang, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 41
Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer
Ronen E. Mukamel, Robert E. Handsaker, Maxwell A. Sherman, et al.
Cell (2023) Vol. 186, Iss. 17, pp. 3659-3673.e23
Open Access | Times Cited: 25
The motif composition of variable number tandem repeats impacts gene expression
Tsung-Yu Lu, Paulina N. Smaruj, Geoffrey Fudenberg, et al.
Genome Research (2023) Vol. 33, Iss. 4, pp. 511-524
Open Access | Times Cited: 19
Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humans
Kohei Hamanaka, Daisuke Yamauchi, Eriko Koshimizu, et al.
Genome Research (2023) Vol. 33, Iss. 3, pp. 435-447
Open Access | Times Cited: 16
A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traits
Paras Garg, Bharati Jadhav, William Lee, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 6, pp. 1065-1076
Open Access | Times Cited: 21
Mutation protocols share with sexual reproduction the physiological role of producing genetic variation within ‘constraints that deconstrain’
David G. King
The Journal of Physiology (2024) Vol. 602, Iss. 11, pp. 2615-2626
Open Access | Times Cited: 4
Whole Genome Variable Number Tandem Repeat Analysis in Alzheimer Disease
Alesha Heath, M. Windy McNerney, Jerome A. Yesavage
Neurology Genetics (2025) Vol. 11, Iss. 2
Closed Access
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
Analysis of targeted and whole genome sequencing of PacBio HiFi reads for a comprehensive genotyping of gene-proximal and phenotype-associated Variable Number Tandem Repeats
Sara Javadzadeh, Aaron W. Adamson, Jonghun Park, et al.
PLoS Computational Biology (2025) Vol. 21, Iss. 4, pp. e1012885-e1012885
Open 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
Characterising tandem repeat complexities across long-read sequencing platforms with TREAT and otter
Niccolo Tesí, Alex Salazar, Yaran Zhang, et al.
Genome Research (2024) Vol. 34, Iss. 11, pp. 1942-1953
Open Access | Times Cited: 3
Revisiting tandem repeats in psychiatric disorders from perspectives of genetics, physiology, and brain evolution
Xiao Xiao, Chuyi Zhang, Zhuohua Zhang, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 1, pp. 466-475
Closed Access | Times Cited: 16
Serotonin transporter functional polymorphisms potentially increase risk of schizophrenia separately and as a haplotype
Rana Ghamari, Fatemeh Yazarlou, Zahra Khosravizadeh, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 9
A Study of Association of the MIR137 VNTR rs58335419 with Schizophrenia
Г. И. Коровайцева, И. В. Олейчик, Т. В. Лежейко, et al.
Russian Journal of Genetics (2024) Vol. 60, Iss. 2, pp. 192-198
Closed Access | Times Cited: 1
A study of association of the VNTR MIR-137 rs58335419 with schizophrenia
Г. И. Коровайцева, И. В. Олейчик, Т. В. Лежейко, et al.
Генетика (2024) Vol. 60, Iss. 2, pp. 63-69
Closed Access
Repeats in Genomes
Laxmi Kata, Gourab Das
Elsevier eBooks (2024)
Closed Access
Biomarkers from Medicinal Plants
Amit Kumar Pradhan, Umakanta Chowra, Manabendra Nath, et al.
(2024), pp. 205-239
Closed Access
Genome-wide investigation of VNTR motif polymorphisms in 8,222 genomes: Implications for biological regulation and human traits
Sijia Zhang, Song Qiao, Peng Zhang, et al.
Cell Genomics (2024) Vol. 4, Iss. 12, pp. 100699-100699
Open Access
The motif composition of variable-number tandem repeats impacts gene expression
Tsung-Yu Lu, Paulina N. Smaruj, Geoffrey Fudenberg, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 2
Repeat polymorphisms in non-coding DNA underlie top genetic risk loci for glaucoma and colorectal cancer
Ronen E. Mukamel, Robert E. Handsaker, Maxwell A. Sherman, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 2
Optimization of MLVA loci combination using metaheuristic methods
G. Ng, Kim Loon Ang, Shing Chiang Tan, et al.
Journal of Intelligent & Fuzzy Systems (2023) Vol. 45, Iss. 6, pp. 12123-12142
Closed Access
Differential Impact of VNTR Polymorphism in the CBS Gene on Gastric and Breast Cancers Risk
Sayedeh Zeinab Sajjadi, Zeinab Alizadeh, Mehdi Moghanibashi, et al.
Indian Journal of Clinical Biochemistry (2023) Vol. 40, Iss. 1, pp. 67-73
Closed Access
Structural variants in the bovine genome
Young-Lim Lee
(2022)
Open Access
A phenome-wide association study identifies effects of copy number variation of VNTRs and multicopy genes on multiple human traits
Paras Garg, Bharati Jadhav, William Lee, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
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