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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:

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS
André B. P. Kuilenburg, Maja Tarailo‐Graovac, Phillip A. Richmond, et al.
New England Journal of Medicine (2019) Vol. 380, Iss. 15, pp. 1433-1441
Open Access | Times Cited: 86

Showing 1-25 of 86 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: 303
On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability
Alexandra N. Khristich, Sergei M. Mirkin
Journal of Biological Chemistry (2020) Vol. 295, Iss. 13, pp. 4134-4170
Open Access | Times Cited: 248
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: 226
An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics
Sanjog R. Chintalaphani, Sandy S. Pineda, Ira W. Deveson, et al.
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 126
From Anti-SARS-CoV-2 Immune Responses to COVID-19 via Molecular Mimicry
Darja Kanduc
Antibodies (2020) Vol. 9, Iss. 3, pp. 33-33
Open Access | Times Cited: 103
The Pleiotropic Effects of Glutamine Metabolism in Cancer
Alex J. Bott, Sara Maimouni, Wei‐Xing Zong
Cancers (2019) Vol. 11, Iss. 6, pp. 770-770
Open Access | Times Cited: 100
Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy
Łukasz J. Sznajder, Maurice S. Swanson
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 13, pp. 3365-3365
Open Access | Times Cited: 93
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: 65
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
How to proceed after “negative” exome: A review on genetic diagnostics, limitations, challenges, and emerging new multiomics techniques
Saskia B. Wortmann, Machteld M. Oud, Mariëlle Alders, et al.
Journal of Inherited Metabolic Disease (2022) Vol. 45, Iss. 4, pp. 663-681
Open Access | Times Cited: 57
Glial Glutamine Homeostasis in Health and Disease
Jens V. Andersen, Arne Schousboe
Neurochemical Research (2022) Vol. 48, Iss. 4, pp. 1100-1128
Closed Access | Times Cited: 46
Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs
Martin Paucar, Daniel Nilsson, Martin Engvall, et al.
Journal of Internal Medicine (2024) Vol. 296, Iss. 3, pp. 234-248
Open Access | Times Cited: 11
The Glutamate/GABA‐Glutamine Cycle: Insights, Updates, and Advances
Jens V. Andersen
Journal of Neurochemistry (2025) Vol. 169, Iss. 3
Open Access | Times Cited: 1
The diagnosis of inborn errors of metabolism by an integrative “multi‐omics” approach: A perspective encompassing genomics, transcriptomics, and proteomics
Sarah L. Stenton, Laura S. Kremer, Robert Kopajtich, et al.
Journal of Inherited Metabolic Disease (2019) Vol. 43, Iss. 1, pp. 25-35
Closed Access | Times Cited: 61
Truncating Variants in RFC1 in Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome
Riccardo Ronco, Cecilia Perini, Riccardo Currò, et al.
Neurology (2022) Vol. 100, Iss. 5
Open Access | Times Cited: 38
GPAD: a natural language processing-based application to extract the gene-disease association discovery information from OMIM
K. M. Tahsin Hassan Rahit, Vladimir Avramović, Jessica X. Chong, et al.
BMC Bioinformatics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 6
A comparison of software for analysis of rare and common short tandem repeat (STR) variation using human genome sequences from clinical and population-based samples
John W. Oketch, Louise V. Wain, Edward J. Hollox
PLoS ONE (2024) Vol. 19, Iss. 4, pp. e0300545-e0300545
Open Access | Times Cited: 6
Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions
Indhu‐Shree Rajan‐Babu, Junran J. Peng, Readman Chiu, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 41
Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency
Denisa Hathazi, Helen Griffin, Matthew J. Jennings, et al.
The EMBO Journal (2020) Vol. 39, Iss. 23
Open Access | Times Cited: 40
Trinucleotide CGG Repeat Diseases: An Expanding Field of Polyglycine Proteins?
Manon Boivin, Nicolas Charlet‐Berguerand
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 27
Acute toxicity of broflanilide on neurosecretory system and locomotory behavior of zebrafish (Danio rerio)
Kai Wang, Chengju Wang, Jiahong Wang, et al.
Chemosphere (2022) Vol. 305, pp. 135426-135426
Closed Access | Times Cited: 23
Advances in the discovery and analyses of human tandem repeats
Mark Chaisson, Arvis Sulovari, Paul N. Valdmanis, et al.
Emerging Topics in Life Sciences (2023) Vol. 7, Iss. 3, pp. 361-381
Open Access | Times Cited: 16
Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwards
Jevin Parmar, Nigel G. Laing, Marina Kennerson, et al.
Journal of Neurology Neurosurgery & Psychiatry (2024) Vol. 95, Iss. 11, pp. 992-1001
Open Access | Times Cited: 5
Advances in repeat expansion diseases and a new concept of repeat motif–phenotype correlation
Hiroyuki Ishiura, Shoji Tsuji
Current Opinion in Genetics & Development (2020) Vol. 65, pp. 176-185
Closed Access | Times Cited: 39
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms
Kym M. Boycott, Philippe M. Campeau, Heather Howley, et al.
The American Journal of Human Genetics (2020) Vol. 106, Iss. 2, pp. 143-152
Open Access | Times Cited: 37
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