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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 26-50 of 382 citing articles:

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS
André B. P. Kuilenburg, Maja Tarailo‐Graovac, Phillip A. Richmond, et al.
New England Journal of Medicine (2019) Vol. 380, Iss. 15, pp. 1433-1441
Open Access | Times Cited: 86
Keeping ribosomal DNA intact: a repeating challenge
Daniël O. Warmerdam, Rob M.F. Wolthuis
Chromosome Research (2018) Vol. 27, Iss. 1-2, pp. 57-72
Open Access | Times Cited: 84
Abnormal brain development in child and adolescent carriers of mutant huntingtin
Ellen van der Plas, Douglas R. Langbehn, Amy L. Conrad, et al.
Neurology (2019) Vol. 93, Iss. 10
Open Access | Times Cited: 84
New pathologic mechanisms in nucleotide repeat expansion disorders
Caitlin M. Rodriguez, Peter K. Todd
Neurobiology of Disease (2019) Vol. 130, pp. 104515-104515
Open Access | Times Cited: 77
Forensic Autosomal Short Tandem Repeats and Their Potential Association With Phenotype
Nicole Wyner, Mark Barash, Dennis McNevin
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 73
Environmental exposures associated with elevated risk for autism spectrum disorder may augment the burden of deleterious de novo mutations among probands
Kealan Pugsley, Stephen W. Scherer, Mark A. Bellgrove, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 1, pp. 710-730
Open Access | Times Cited: 73
Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences
Terence Gall-Duncan, Nozomu Sato, Ryan K. C. Yuen, et al.
Genome Research (2021) Vol. 32, Iss. 1, pp. 1-27
Open Access | Times Cited: 64
Recurrent repeat expansions in human cancer genomes
Graham S. Erwin, Gamze Gürsoy, Rashid Al-Abri, et al.
Nature (2022) Vol. 613, Iss. 7942, pp. 96-102
Open Access | Times Cited: 50
STRling: a k-mer counting approach that detects short tandem repeat expansions at known and novel loci
Harriet Dashnow, Brent S. Pedersen, Laurel Hiatt, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 42
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
A deep population reference panel of tandem repeat variation
Helyaneh Ziaei Jam, Yang Li, Ross DeVito, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 41
Mutation and selection processes regulating short tandem repeats give rise to genetic and phenotypic diversity across species
Max A. Verbiest, Mikhail O. Maksimov, Jin Ye, et al.
Journal of Evolutionary Biology (2022) Vol. 36, Iss. 2, pp. 321-336
Open Access | Times Cited: 39
Native functions of short tandem repeats
Shannon E. Wright, Peter K. Todd
eLife (2023) Vol. 12
Open Access | Times Cited: 28
A genome-wide spectrum of tandem repeat expansions in 338,963 humans
Ya Cui, Wenbin Ye, Jason Sheng Li, et al.
Cell (2024) Vol. 187, Iss. 9, pp. 2336-2341.e5
Open Access | Times Cited: 16
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease
Riccardo Currò, Natalia Dominik, Stefano Facchini, et al.
Brain (2024) Vol. 147, Iss. 5, pp. 1887-1898
Open Access | Times Cited: 12
Neurological disorders caused by novel non-coding repeat expansions: clinical features and differential diagnosis
Elisa Vegezzi, Hiroyuki Ishiura, D. Cristopher Bragg, et al.
The Lancet Neurology (2024) Vol. 23, Iss. 7, pp. 725-739
Closed Access | Times Cited: 12
Single-molecule RNA sizing enables quantitative analysis of alternative transcription termination
Gerardo Patiño-Guillén, Jovan Pešović, Marko Panić, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9
NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION
Arne De Roeck, Wouter De Coster, Liene Bossaerts, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 75
A reference haplotype panel for genome-wide imputation of short tandem repeats
Shubham Saini, Ileena Mitra, Nima Mousavi, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 71
A New Census of Protein Tandem Repeats and Their Relationship with Intrinsic Disorder
Matteo Delucchi, Elke Schaper, Oxana Sachenkova, et al.
Genes (2020) Vol. 11, Iss. 4, pp. 407-407
Open Access | Times Cited: 65
A native function for RAN translation and CGG repeats in regulating fragile X protein synthesis
Caitlin M. Rodriguez, Shannon E. Wright, Michael G. Kearse, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 3, pp. 386-397
Open Access | Times Cited: 60
DNA polymerase stalling at structured DNA constrains the expansion of short tandem repeats
Pierre Murat, Guillaume Guilbaud, Julian E. Sale
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 54
Amino acid homorepeats in proteins
Sreenivas Chavali, Anjali Kumari Singh, Balaji Santhanam, et al.
Nature Reviews Chemistry (2020) Vol. 4, Iss. 8, pp. 420-434
Closed Access | Times Cited: 53
Mutation–selection balance and compensatory mechanisms in tumour evolution
Erez Persi, Yuri I. Wolf, D. Horn, et al.
Nature Reviews Genetics (2020) Vol. 22, Iss. 4, pp. 251-262
Open Access | Times Cited: 52
What is the Pathogenic CAG Expansion Length in Huntington’s Disease?
Jasmine Donaldson, Sophie Powell, Nadia Rickards, et al.
Journal of Huntington s Disease (2021) Vol. 10, Iss. 1, pp. 175-202
Open Access | Times Cited: 46

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