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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: 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

Showing 1-25 of 278 citing articles:

High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
Marta Byrska-Bishop, Uday S. Evani, Xuefang Zhao, et al.
Cell (2022) Vol. 185, Iss. 18, pp. 3426-3440.e19
Open Access | Times Cited: 645
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
Pangenome Graphs
Jordan M. Eizenga, Adam M. Novak, Jonas A. Sibbesen, et al.
Annual Review of Genomics and Human Genetics (2020) Vol. 21, Iss. 1, pp. 139-162
Open Access | Times Cited: 213
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
Henrik Stranneheim, Kristina Lagerstedt‐Robinson, Måns Magnusson, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 199
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
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease
Galen E.B. Wright, Jennifer A. Collins, Chris Kay, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1116-1126
Open Access | Times Cited: 175
Targeted long-read sequencing identifies missing disease-causing variation
Danny E. Miller, Arvis Sulovari, Tianyun Wang, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1436-1449
Open Access | Times Cited: 169
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
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
Paragraph: a graph-based structural variant genotyper for short-read sequence data
Sai Chen, Peter Krusche, Egor Dolzhenko, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 148
GraphAligner: rapid and versatile sequence-to-graph alignment
Mikko Rautiainen, Tobias Marschall
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 144
Repeat expansions confer WRN dependence in microsatellite-unstable cancers
Niek van Wietmarschen, Sriram Sridharan, William J. Nathan, et al.
Nature (2020) Vol. 586, Iss. 7828, pp. 292-298
Open Access | Times Cited: 142
Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study
Kristina Ibáñez, James M. Polke, R. Tanner Hagelstrom, et al.
The Lancet Neurology (2022) Vol. 21, Iss. 3, pp. 234-245
Open Access | Times Cited: 122
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
Best practices for the interpretation and reporting of clinical whole genome sequencing
Christina Austin‐Tse, Vaidehi Jobanputra, Denise Perry, et al.
npj Genomic Medicine (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 99
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
Integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genes
Jack Humphrey, Sanan Venkatesh, Rahat Hasan, et al.
Nature Neuroscience (2022) Vol. 26, Iss. 1, pp. 150-162
Open Access | Times Cited: 79
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
Structurally divergent and recurrently mutated regions of primate genomes
Yafei Mao, William T. Harvey, David Porubský, et al.
Cell (2024) Vol. 187, Iss. 6, pp. 1547-1562.e13
Open Access | Times Cited: 41
Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4
Zhongbo Chen, Emil K. Gustavsson, Hannah Macpherson, et al.
Movement Disorders (2024) Vol. 39, Iss. 3, pp. 486-497
Open Access | Times Cited: 31
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
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