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.

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Showing 1-25 of 63 citing articles:

FlyBase: updates to the Drosophila genes and genomes database
Arzu Öztürk-Çolak, Steven J Marygold, Giulia Antonazzo, et al.
Genetics (2024) Vol. 227, Iss. 1
Open Access | Times Cited: 141

Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans
Shinya Yamamoto, Oguz Kanca, Michael F. Wangler, et al.
Nature Reviews Genetics (2023) Vol. 25, Iss. 1, pp. 46-60
Closed Access | Times Cited: 42

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases
Paul C. Marcogliese, Samantha L. Deal, Jonathan C. Andrews, et al.
Cell Reports (2022) Vol. 38, Iss. 11, pp. 110517-110517
Open Access | Times Cited: 39

Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation
Hyunglok Chung, Qi Ye, Ye-Jin Park, et al.
Cell Metabolism (2023) Vol. 35, Iss. 5, pp. 855-874.e5
Open Access | Times Cited: 34

Sphingolipids in neurodegenerative diseases
Xueyang Pan, Debdeep Dutta, Shenzhao Lu, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 24

Tau is required for glial lipid droplet formation and resistance to neuronal oxidative stress
Lindsey D. Goodman, Isha Ralhan, Xin Li, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 10, pp. 1918-1933
Closed Access | Times Cited: 11

De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms
Ali Hosseini Bereshneh, Jonathan C. Andrews, Daniel F. Eberl, et al.
The American Journal of Human Genetics (2025)
Closed Access | Times Cited: 1

Drosophila melanogaster as a versatile model organism to study genetic epilepsies: An overview
Florian P. Fischer, Robin A. Karge, Yvonne G. Weber, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 21

Bi-allelic variants in INTS11 are associated with a complex neurological disorder
Burak Tepe, Erica L. Macke, Marcello Niceta, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 5, pp. 774-789
Open Access | Times Cited: 20

A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels
Debdeep Dutta, Oguz Kanca, Seul Kee Byeon, et al.
Nature Metabolism (2023) Vol. 5, Iss. 9, pp. 1595-1614
Open Access | Times Cited: 11

Unilateral ephaptic program underlying sweetness dominance
MinHyuk Lee, Seon Yeong Kim, Taeim Park, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 10

Deterministic Genetic Barcoding for Multiplexed Behavioral and Single-Cell Transcriptomic Studies
Jorge Blanco Mendana, Margaret Donovan, Lindsey Gengelbach O'Brien, et al.
(2025)
Open Access

An evolutionarily conserved cation channel tunes the sensitivity of gustatory neurons to ephaptic inhibition in Drosophila
MinHyuk Lee, Seong-min Kim, Taeim Park, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 3
Open Access

Deterministic genetic barcoding for multiplexed behavioral and single-cell transcriptomic studies
Jorge Blanco Mendana, Margaret Donovan, Lindsey Gengelbach O'Brien, et al.
eLife (2025) Vol. 12
Open Access

Diversity of Drosophila egg patterning: The missing tools to explore embryonic axis formation
Helen L. Stott, Nir Yakoby
Frontiers in Cell and Developmental Biology (2025) Vol. 13
Open Access

Effects of Lithium on Mortality and Metabolite Profiles in Drosophila Lithium-Inducible SLC6 Transporter Mutants
Junko Kasuya, Karina Kruth, Dong-Keun Lee, et al.
Environmental Toxicology and Pharmacology (2025), pp. 104684-104684
Closed Access

The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability
Yan Huang, Gabrielle Lemire, Lauren C. Briere, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 10, pp. 1923-1931
Open Access | Times Cited: 15

Hox gene–specific cellular targeting using split intein Trojan exons
Fengqiu Diao, Deeptha Vasudevan, Ellie S. Heckscher, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 17
Open Access | Times Cited: 3

Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila
Jenny Zhe Liao, Hyunglok Chung, Claire R. Y. Shih, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3

α-Synuclein pathology in Drosophila melanogaster is exacerbated by haploinsufficiency of Rop: connecting STXBP1 encephalopathy with α-synucleinopathies
Taro Matsuoka, Hideki Yoshida, Takashi Kasai, et al.
Human Molecular Genetics (2024) Vol. 33, Iss. 15, pp. 1328-1338
Closed Access | Times Cited: 3

Harnessing Simple Animal Models to Decode Sleep Mysteries
Seithikurippu R. Pandi‐Perumal, Konda Mani Saravanan, Sayan Paul, et al.
Molecular Biotechnology (2024)
Closed Access | Times Cited: 3

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