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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:

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

Showing 1-25 of 196 citing articles:

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack Fu, F. Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1320-1331
Open Access | Times Cited: 365
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
Molecular mechanisms underlying nucleotide repeat expansion disorders
Indranil Malik, Chase P. Kelley, Eric T. Wang, et al.
Nature Reviews Molecular Cell Biology (2021) Vol. 22, Iss. 9, pp. 589-607
Open Access | Times Cited: 263
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
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
Patterns of de novo tandem repeat mutations and their role in autism
Ileena Mitra, Bonnie Huang, Nima Mousavi, et al.
Nature (2021) Vol. 589, Iss. 7841, pp. 246-250
Open Access | Times Cited: 152
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
Short tandem repeats bind transcription factors to tune eukaryotic gene expression
Connor A. Horton, Amr M. Alexandari, Michael G.B. Hayes, et al.
Science (2023) Vol. 381, Iss. 6664
Open Access | Times Cited: 112
Genetic correlates of phenotypic heterogeneity in autism
Varun Warrier, Xinhe Zhang, Patrick Reed, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1293-1304
Open Access | Times Cited: 104
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
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
Contribution of autosomal rare and de novo variants to sex differences in autism
Mahmoud Koko, F. Kyle Satterstrom, Varun Warrier, et al.
The American Journal of Human Genetics (2025)
Open Access | Times Cited: 3
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
Genetic Advances in Autism
Anita Thapar, Michael Rutter
Journal of Autism and Developmental Disorders (2020) Vol. 51, Iss. 12, pp. 4321-4332
Open Access | Times Cited: 123
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
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
Genetic contributions to autism spectrum disorder
Alexandra Havdahl, Maria Niarchou, Anna Starnawska, et al.
Psychological Medicine (2021) Vol. 51, Iss. 13, pp. 2260-2273
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
De novo mutations, genetic mosaicism and human disease
Mohiuddin Mohiuddin, R. Frank Kooy, Christopher E. Pearson
Frontiers in Genetics (2022) Vol. 13
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
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
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