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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 26-50 of 278 citing articles:

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
A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy
Karla P. Figueroa, Caspar Groß, Elena Buena‐Atienza, et al.
Nature Genetics (2024) Vol. 56, Iss. 6, pp. 1080-1089
Closed Access | Times Cited: 25
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
Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis
Emily P. McCann, Lyndal Henden, Jennifer A. Fifita, et al.
Journal of Medical Genetics (2020) Vol. 58, Iss. 2, pp. 87-95
Open Access | Times Cited: 71
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
Ramita Dewan, Ruth Chia, Jinhui Ding, et al.
Neuron (2020) Vol. 109, Iss. 3, pp. 448-460.e4
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
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
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
Genetic variability in sporadic amyotrophic lateral sclerosis
Sien Hilde Van Daele, Matthieu Moisse, Joke J.F.A. van Vugt, et al.
Brain (2023) Vol. 146, Iss. 9, pp. 3760-3769
Open Access | Times Cited: 42
Systematic evaluation of genetic mutations in ALS: a population-based study
Maurizio Grassano, Andrea Calvo, Cristina Moglia, et al.
Journal of Neurology Neurosurgery & Psychiatry (2022) Vol. 93, Iss. 11, pp. 1190-1193
Open Access | Times Cited: 41
Long‐read sequencing for molecular diagnostics in constitutional genetic disorders
Laura K. Conlin, Erfan Aref‐Eshghi, Deborah McEldrew, et al.
Human Mutation (2022) Vol. 43, Iss. 11, pp. 1531-1544
Open Access | Times Cited: 41
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
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
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
Alistair T. Pagnamenta, Carlos Camps, Edoardo Giacopuzzi, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 32
Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases
M. Anwar Iqbal, Ulrich Broeckel, Brynn Levy, et al.
Journal of Molecular Diagnostics (2023) Vol. 25, Iss. 3, pp. 175-188
Open Access | Times Cited: 29
Comprehensive de novo mutation discovery with HiFi long-read sequencing
Erdi Küçük, Bart van der Sanden, Luke O’Gorman, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 28
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
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies
Chelsea Lowther, Elise Valkanas, Jessica L. Giordano, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 9, pp. 1454-1469
Open Access | Times Cited: 25
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
A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus
David Pellerin, Giulia Gobbo, Madeline Couse, et al.
Nature Genetics (2024) Vol. 56, Iss. 7, pp. 1366-1370
Closed Access | Times Cited: 17
Comprehensive genome analysis and variant detection at scale using DRAGEN
Sairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Nature Biotechnology (2024)
Open Access | Times Cited: 17
Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms
Sairam Behera, Severine Catreux, Massimiliano Rossi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 16
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
Diagnostic uplift through the implementation of short tandem repeat analysis using exome sequencing
Jihoon G. Yoon, Seungbok Lee, Jaeso Cho, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 5, pp. 584-587
Open Access | Times Cited: 13
Increased frequency of repeat expansion mutations across different populations
Kristina Ibáñez, Bharati Jadhav, Matteo Zanovello, et al.
Nature Medicine (2024)
Open Access | Times Cited: 12

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