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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:

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

Showing 1-25 of 115 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
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 2, pp. 267-282
Open Access | Times Cited: 271
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
The Genetics of Epilepsy
Piero Perucca, Melanie Bahlo, Samuel F. Berkovic
Annual Review of Genomics and Human Genetics (2020) Vol. 21, Iss. 1, pp. 205-230
Open Access | Times Cited: 172
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
Genetic Testing in Neurodevelopmental Disorders
Juliann M. Savatt, Scott M. Myers
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 152
Mitochondrial disease in adults: recent advances and future promise
Yi Shiau Ng, Laurence A. Bindoff, Gráinne S. Gorman, et al.
The Lancet Neurology (2021) Vol. 20, Iss. 7, pp. 573-584
Open Access | Times Cited: 150
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
Comprehensive genetic diagnosis of tandem repeat expansion disorders with programmable targeted nanopore sequencing
Igor Stevanovski, Sanjog R. Chintalaphani, Hasindu Gamaarachchi, et al.
Science Advances (2022) Vol. 8, Iss. 9
Open Access | Times Cited: 130
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
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
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3
Rahel T. Florian, Florian Kraft, Elsa Leitão, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 137
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Mark Corbett, Thessa Kroes, Liana Veneziano, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 124
CYLD is a causative gene for frontotemporal dementia – amyotrophic lateral sclerosis
Carol Dobson‐Stone, Marianne Hallupp, Hamideh Shahheydari, et al.
Brain (2020) Vol. 143, Iss. 3, pp. 783-799
Open Access | Times Cited: 71
Straglr: discovering and genotyping tandem repeat expansions using whole genome long-read sequences
Readman Chiu, Indhu‐Shree Rajan‐Babu, Jan M. Friedman, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 67
Progressive myoclonus epilepsies—Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes
Carolina Courage, Karen Oliver, Eon Joo Park, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 4, pp. 722-738
Open Access | Times Cited: 66
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
The performance of genome sequencing as a first-tier test for neurodevelopmental disorders
Bart van der Sanden, Gaby Schobers, Jordi Corominas Galbany, et al.
European Journal of Human Genetics (2022) Vol. 31, Iss. 1, pp. 81-88
Open Access | Times Cited: 56
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
Polymorphic short tandem repeats make widespread contributions to blood and serum traits
Jonathan Margoliash, Shai Fuchs, Yang Li, et al.
Cell Genomics (2023) Vol. 3, Iss. 12, pp. 100458-100458
Open Access | Times Cited: 26
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