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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:

Ectopic expression of Snord115 in choroid plexus interferes with editing but not splicing of 5-Ht2c receptor pre-mRNA in mice
Carsten A. Raabe, Reinhard Voß, Delf-Magnus Kummerfeld, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Functional diversity of small nucleolar RNAs
Tomaž Bratkovič, Janja Božič, Boris Rogelj
Nucleic Acids Research (2019) Vol. 48, Iss. 4, pp. 1627-1651
Open Access | Times Cited: 196
Small nucleolar RNAs: continuing identification of novel members and increasing diversity of their molecular mechanisms of action
Danny Bergeron, Étienne Fafard-Couture, Michelle S. Scott
Biochemical Society Transactions (2020) Vol. 48, Iss. 2, pp. 645-656
Open Access | Times Cited: 50
Small nucleolar RNAs in plasma extracellular vesicles and their discriminatory power as diagnostic biomarkers of Alzheimer's disease
Nicholas F. Fitz, Jiebiao Wang, M. Ilyas Kamboh, et al.
Neurobiology of Disease (2021) Vol. 159, pp. 105481-105481
Open Access | Times Cited: 33
Reassessment of the involvement of Snord115 in the serotonin 2c receptor pathway in a genetically relevant mouse model
Jade Hebras, Virginie Marty, Jean Personnaz, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 37
The role of OncoSnoRNAs and Ribosomal RNA 2’-O-methylation in Cancer
Daniela Barros‐Silva, Jonathan Klavert, Guido Jenster, et al.
RNA Biology (2021) Vol. 18, Iss. sup1, pp. 61-74
Open Access | Times Cited: 32
The emerging diagnostic and therapeutic roles of small nucleolar RNAs in lung diseases
Xiaoying Liu, Md Khadem Ali, Lan Zhao, et al.
Biomedicine & Pharmacotherapy (2023) Vol. 161, pp. 114519-114519
Open Access | Times Cited: 11
SNORA69 is up-regulated in the lateral habenula of individuals with major depressive disorder
Rixing Lin, Haruka Mitsuhashi, Laura M. Fiori, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Epigenetics in Prader-Willi Syndrome
Aron Judd P. Mendiola, Janine M. LaSalle
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 26
Phylogenetic and Molecular Analyses Identify SNORD116 Targets Involved in the Prader–Willi Syndrome
Laeya Baldini, A. Edwards Robert, Bruno Charpentier, et al.
Molecular Biology and Evolution (2021) Vol. 39, Iss. 1
Open Access | Times Cited: 23
A Comprehensive Review of Genetically Engineered Mouse Models for Prader-Willi Syndrome Research
Delf-Magnus Kummerfeld, Carsten A. Raabe, Juergen Brosius, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 7, pp. 3613-3613
Open Access | Times Cited: 17
Roles of SNORD115 and SNORD116 ncRNA clusters during neuronal differentiation
Aleksandra Helwak, Tomasz W. Turowski, Christos Spanos, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Novel Insights into the Role of UBE3A in Regulating Apoptosis and Proliferation
Lilach Simchi, Julia Panov, Olla Morsy, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 5, pp. 1573-1573
Open Access | Times Cited: 17
Specific ZNF274 binding interference atSNORD116activates the maternal transcripts in Prader-Willi syndrome neurons
Maéva Langouët, Dea Gorka, Clarisse Orniacki, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 19, pp. 3285-3295
Open Access | Times Cited: 16
DeletingSnord115genes in mice remodels monoaminergic systems activity in the brain toward cortico-subcortical imbalances
Virginie Marty, Jasmine Jade Butler, Basile Coutens, et al.
Human Molecular Genetics (2022) Vol. 32, Iss. 2, pp. 244-261
Closed Access | Times Cited: 7
Reference Genes across Nine Brain Areas of Wild Type and Prader-Willi Syndrome Mice: Assessing Differences in Igfbp7, Pcsk1, Nhlh2 and Nlgn3 Expression
Delf-Magnus Kummerfeld, Boris V. Skryabin, Juergen Brosius, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 15, pp. 8729-8729
Open Access | Times Cited: 5
Elevated exposures to persistent endocrine disrupting compounds impact the sperm methylome in regions associated with autism spectrum disorder
Angela G. Maggio, Henry T. Shu, Benjamin I. Laufer, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 5
Control of Ca2+signals by astrocyte nanoscale morphology at tripartite synapses
Audrey Denizot, Misa Arizono, Valentin U. Nägerl, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 6
Gene Cascade Finder: A tool for identification of gene cascades and its application in Caenorhabditis elegans
Yusuke Nomoto, Yukihiko Kubota, Yuto Ohnishi, et al.
PLoS ONE (2019) Vol. 14, Iss. 9, pp. e0215187-e0215187
Open Access | Times Cited: 5
Natural copy number differences of tandemly repeated small nucleolar RNAs in the Prader-Willi syndrome genomic region regulate individual behavioral responses in mammals
Maryam Keshavarz, Rebecca Krebs-Wheaton, Peter Refki, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2018)
Open Access | Times Cited: 5
Expression of Concern: Natural copy number variation of tandemly repeated regulatory SNORD RNAs leads to individual phenotypic differences in mice
Maryam Keshavarz, Yoland Savriama, Peter Refki, et al.
Molecular Ecology (2021) Vol. 30, Iss. 19, pp. 4708-4722
Open Access | Times Cited: 5
Epigenetic Regulation Disturbances on Gene Expression in Imprinting Diseases
Zaletaev Dv, М. В. Немцова, V. V. Strelnikov
Molecular Biology (2022) Vol. 56, Iss. 1, pp. 1-28
Closed Access | Times Cited: 3
Impact of exposures to persistent endocrine disrupting compounds on the sperm methylome in regions associated with neurodevelopmental disorders
Angela G. Maggio, Henry T. Shu, Benjamin I. Laufer, et al.
Research Square (Research Square) (2021)
Open Access | Times Cited: 3
The Neurobiology of Prader-Willi Syndrome
Deepan Singh
Cambridge University Press eBooks (2022), pp. 154-170
Closed Access | Times Cited: 2
Copy number variation in small nucleolar RNAs regulates personality behavior
Maryam Keshavarz, Rebecca Krebs-Wheaton, Peter Refki, et al.
MPG.PuRe (Max Planck Society) (2018), pp. 476010
Open Access | Times Cited: 2
Molecular Genetic Findings in Prader-Willi Syndrome
Stefan Stamm, Merlin G. Butler
Springer eBooks (2022), pp. 51-73
Closed Access | Times Cited: 1
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