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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:

Tandem repeats mediating genetic plasticity in health and disease
Anthony J. Hannan
Nature Reviews Genetics (2018) Vol. 19, Iss. 5, pp. 286-298
Closed Access | Times Cited: 382

Showing 1-25 of 382 citing articles:

30 years of repeat expansion disorders: What have we learned and what are the remaining challenges?
Christel Depienne, Jean‐Louis Mandel
The American Journal of Human Genetics (2021) Vol. 108, Iss. 5, pp. 764-785
Open Access | Times Cited: 304
ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions
Egor Dolzhenko, Viraj Deshpande, Felix Schlesinger, et al.
Bioinformatics (2019) Vol. 35, Iss. 22, pp. 4754-4756
Open Access | Times Cited: 278
Molecular mechanisms underlying nucleotide repeat expansion disorders
Indranil Malik, Chase P. Kelley, Eric T. Wang, et al.
Nature Reviews Molecular Cell Biology (2021) Vol. 22, Iss. 9, pp. 589-607
Open Access | Times Cited: 263
Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVAS
Haloom Rafehi, David J. Szmulewicz, Mark F. Bennett, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 1, pp. 151-165
Open Access | Times Cited: 219
Profiling the genome-wide landscape of tandem repeat expansions
Nima Mousavi, Sharona Shleizer-Burko, Richard Yanicky, et al.
Nucleic Acids Research (2019) Vol. 47, Iss. 15, pp. e90-e90
Open Access | Times Cited: 207
Epigenetic Modifications in Stress Response Genes Associated With Childhood Trauma
Shui Jiang, Lynne‐Marie Postovit, Annamaria Cattaneo, et al.
Frontiers in Psychiatry (2019) Vol. 10
Open Access | Times Cited: 201
Genome-wide detection of tandem DNA repeats that are expanded in autism
Brett Trost, Worrawat Engchuan, Charlotte Nguyen, et al.
Nature (2020) Vol. 586, Iss. 7827, pp. 80-86
Open Access | Times Cited: 196
Pangenomics Comes of Age: From Bacteria to Plant and Animal Applications
Agnieszka A. Golicz, Philipp E. Bayer, Prem L. Bhalla, et al.
Trends in Genetics (2019) Vol. 36, Iss. 2, pp. 132-145
Open Access | Times Cited: 192
ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing data
Egor Dolzhenko, Mark F. Bennett, Phillip A. Richmond, et al.
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 160
Patterns of de novo tandem repeat mutations and their role in autism
Ileena Mitra, Bonnie Huang, Nima Mousavi, et al.
Nature (2021) Vol. 589, Iss. 7841, pp. 246-250
Open Access | Times Cited: 152
An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics
Sanjog R. Chintalaphani, Sandy S. Pineda, Ira W. Deveson, et al.
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 128
Short tandem repeats bind transcription factors to tune eukaryotic gene expression
Connor A. Horton, Amr M. Alexandari, Michael G.B. Hayes, et al.
Science (2023) Vol. 381, Iss. 6664
Open Access | Times Cited: 112
Truvari: refined structural variant comparison preserves allelic diversity
Adam C. English, Vipin K. Menon, Richard A. Gibbs, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 111
Variant calling and benchmarking in an era of complete human genome sequences
Nathan D. Olson, Justin Wagner, Nathan Dwarshuis, et al.
Nature Reviews Genetics (2023) Vol. 24, Iss. 7, pp. 464-483
Closed Access | Times Cited: 81
Repetitive DNA sequence detection and its role in the human genome
Xingyu Liao, Wufei Zhu, Juexiao Zhou, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 68
Characterization and visualization of tandem repeats at genome scale
Egor Dolzhenko, Adam C. English, Harriet Dashnow, et al.
Nature Biotechnology (2024) Vol. 42, Iss. 10, pp. 1606-1614
Closed Access | Times Cited: 49
Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications
Indhu‐Shree Rajan‐Babu, Egor Dolzhenko, Michael A. Eberle, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 7, pp. 476-499
Closed Access | Times Cited: 28
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation
Jonas A. Gustafson, Sophia B Gibson, Nikhita Damaraju, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 26
Analysis and benchmarking of small and large genomic variants across tandem repeats
Adam C. English, Egor Dolzhenko, Helyaneh Ziaei Jam, et al.
Nature Biotechnology (2024)
Closed Access | Times Cited: 26
Polygenic burden of short tandem repeat expansions promotes risk for Alzheimer’s disease
Michael H. Guo, Wan‐Ping Lee, Badri N. Vardarajan, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing Data
Rick M. Tankard, Mark F. Bennett, Peter Degorski, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 6, pp. 858-873
Open Access | Times Cited: 115
Characterization of a Human-Specific Tandem Repeat Associated with Bipolar Disorder and Schizophrenia
Janet Song, Craig B. Lowe, David M. Kingsley
The American Journal of Human Genetics (2018) Vol. 103, Iss. 3, pp. 421-430
Open Access | Times Cited: 100
The genetics of intellectual disability: advancing technology and gene editing
Muhammad Ilyas, Asif Mir, Stéphanie Efthymiou, et al.
F1000Research (2020) Vol. 9, pp. 22-22
Open Access | Times Cited: 92
Role of Rad51 and DNA repair in cancer: A molecular perspective
Erik Laurini, Domenico Marson, Alice Fermeglia, et al.
Pharmacology & Therapeutics (2020) Vol. 208, pp. 107492-107492
Open Access | Times Cited: 88
The Role of Noncoding Variants in Heritable Disease
Juliet D. French, Stacey L. Edwards
Trends in Genetics (2020) Vol. 36, Iss. 11, pp. 880-891
Closed Access | Times Cited: 88
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