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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:

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

Showing 1-25 of 160 citing articles:

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Wouter van Rheenen, Rick A. A. van der Spek, Mark K. Bakker, et al.
Nature Genetics (2021) Vol. 53, Iss. 12, pp. 1636-1648
Open Access | Times Cited: 392
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
A guide for the diagnosis of rare and undiagnosed disease: beyond the exome
Shruti Marwaha, Joshua W. Knowles, Euan A. Ashley
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 228
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
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
Genomic architecture of autism from comprehensive whole-genome sequence annotation
Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan, et al.
Cell (2022) Vol. 185, Iss. 23, pp. 4409-4427.e18
Open Access | Times Cited: 157
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia
David Pellerin, Matt C. Danzi, Carlo Wilke, et al.
New England Journal of Medicine (2022) Vol. 388, Iss. 2, pp. 128-141
Open Access | Times Cited: 156
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14
Haloom Rafehi, Justin Read, David J. Szmulewicz, et al.
The American Journal of Human Genetics (2022) Vol. 110, Iss. 1, pp. 105-119
Open Access | Times Cited: 109
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
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease
Joel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.
The American Journal of Human Genetics (2023) Vol. 111, Iss. 1, pp. 82-95
Open Access | Times Cited: 48
Sequencing and characterizing short tandem repeats in the human genome
Hope A. Tanudisastro, Ira W. Deveson, Harriet Dashnow, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 7, pp. 460-475
Closed Access | Times Cited: 42
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
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
The genetic architecture of ALS
Aleksey Shatunov, Ammar Al‐Chalabi
Neurobiology of Disease (2020) Vol. 147, pp. 105156-105156
Open Access | Times Cited: 78
A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families
Carolin K. Scriba, Sarah J. Beecroft, Joshua S. Clayton, et al.
Brain (2020) Vol. 143, Iss. 10, pp. 2904-2910
Open Access | Times Cited: 75
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
Familial long-read sequencing increases yield of de novo mutations
Michelle D. Noyes, William T. Harvey, David Porubský, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 4, pp. 631-646
Open Access | Times Cited: 61
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
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
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy
Darcy Fehlings, Mehdi Zarrei, Worrawat Engchuan, et al.
Nature Genetics (2024) Vol. 56, Iss. 4, pp. 585-594
Closed Access | Times Cited: 17
Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease
Christopher J. Record, Menelaos Pipis, Mariola Skorupinska, et al.
Brain (2024) Vol. 147, Iss. 9, pp. 3144-3156
Open Access | Times Cited: 13
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
Andrea Cortese, Sarah J. Beecroft, Stefano Facchini, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13
Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions
Lars Mohren, Friedrich Erdlenbruch, Elsa Leitão, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13
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