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:

miRNA Genetic Variants Alter Their Secondary Structure and Expression in Patients With RASopathies Syndromes
Joseane Biso de Carvalho, Guilherme Loss de Morais, Thays Cristine dos Santos Vieira, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 14

Showing 14 citing articles:

SNPs in miRNAs and Target Sequences: Role in Cancer and Diabetes
Yogita Chhichholiya, Aman Kumar Suryan, Prabhat Suman, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 33

Epigenetic alterations in preeclampsia: a focus on microRNA149 and tetrahydrofolate reductase gene polymorphisms in Egyptian women
Doha El‐Sayed Ellakwa, Laila A. Rashed, Ahmed Abdel-Aziz El-Mandoury, et al.
Irish Journal of Medical Science (1971 -) (2024)
Closed Access | Times Cited: 4

Study the association of microRNA polymorphisms (miR‐146a, miR‐4513) with the risk of coronary heart diseases in Egyptian population
Heba Mohamed Ali, Doha El‐Sayed Ellakwa, Nesma M. Elaraby, et al.
Journal of Biochemical and Molecular Toxicology (2022) Vol. 37, Iss. 3
Closed Access | Times Cited: 13

Identification of circRNA-miRNA-mRNA regulatory network and its role in cardiac hypertrophy
Ke Gong, Kai Yang, Ting Xie, et al.
PLoS ONE (2023) Vol. 18, Iss. 3, pp. e0279638-e0279638
Open Access | Times Cited: 3

Investigating Neuron Degeneration in Huntington’s Disease Using RNA-Seq Based Transcriptome Study
Nela Pragathi Sneha, S. Akila Parvathy Dharshini, Y‐h. Taguchi, et al.
Genes (2023) Vol. 14, Iss. 9, pp. 1801-1801
Open Access | Times Cited: 2

Case report: The cardio-facio-cutaneous syndrome due to a novel germline mutation in MAP2K1: A multifaceted disease with immunodeficiency and short stature
Aleksandra Szczawińska-Popłonyk, Natalia Popłonyk, Marek Niedziela, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 4

Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects
Alberto Brusati, Antonia Ratti, Viviana Pensato, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 4

Human Brain Shows Recurrent Non-Canonical MicroRNA Editing Events Enriched for Seed Sequence with Possible Functional Consequence
Deepanjan Paul, Asgar Hussain Ansari, Megha Lal, et al.
Non-Coding RNA (2020) Vol. 6, Iss. 2, pp. 21-21
Open Access | Times Cited: 5

Biomarker Landscape in RASopathies
Noemi Ferrito, Juan Báez-Flores, Mario Rodríguez-Martín, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 16, pp. 8563-8563
Open Access

Exosomes and miRNAs in Cardiovascular Diseases and Transcatheter Pulmonary Valve Replacement: Advancements, Gaps and Perspectives
Rixin Liang, Naijimuding Abudurexiti, Jiandi Wu, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 24, pp. 13686-13686
Open Access

miR-4477b gene as a novel pathogenic mutation occurring during the transformation of colorectal adenoma into colorectal cancer
Xiaoyu He, Guohua Cheng, Feng Xiao, et al.
Journal of Gastrointestinal Oncology (2021) Vol. 12, Iss. 1, pp. 69-78
Open Access | Times Cited: 3

Next Generation Sequencing
Anchita Prasad, Harshita Bhargava, Ayam Gupta, et al.
Advances in Bioinformatics (2021), pp. 277-302
Closed Access | Times Cited: 3

Analysis of MIR27A (rs11671784) Variant Association with Systemic Lupus Erythematous
Zenat Khired, Shahad W. Kattan, A. Khuzaim Alzahrani, et al.
Life (2023) Vol. 13, Iss. 3, pp. 701-701
Open Access

Pre-micro RNA polymorphism detection in small versus large vessel disease in stroke Egyptian patients
Ekrami A. Hassan, Hala El-Khawas, Hossam Afify, et al.
Metabolic Brain Disease (2021) Vol. 36, Iss. 6, pp. 1361-1367
Closed Access

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