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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:

RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins
Fengbiao Mao, Luoyuan Xiao, Xianfeng Li, et al.
Nucleic Acids Research (2015) Vol. 44, Iss. D1, pp. D154-D163
Open Access | Times Cited: 57

Showing 1-25 of 57 citing articles:

The Translational Landscape of the Human Heart
Sebastiaan van Heesch, Franziska Witte, Valentin Schneider-Lunitz, et al.
Cell (2019) Vol. 178, Iss. 1, pp. 242-260.e29
Open Access | Times Cited: 515
Role of m6A RNA methylation in cardiovascular disease (Review)
Yuhan Qin, Linqing Li, Erfei Luo, et al.
International Journal of Molecular Medicine (2020) Vol. 46, Iss. 6, pp. 1958-1972
Open Access | Times Cited: 230
m6AVar: a database of functional variants involved in m6A modification
Yueyuan Zheng, Peng Nie, Di Peng, et al.
Nucleic Acids Research (2017) Vol. 46, Iss. D1, pp. D139-D145
Open Access | Times Cited: 174
RMVar: an updated database of functional variants involved in RNA modifications
Xiaotong Luo, Huiqin Li, Jiaqi Liang, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D1405-D1412
Open Access | Times Cited: 147
VarCards: an integrated genetic and clinical database for coding variants in the human genome
Jinchen Li, Leisheng Shi, Kun Zhang, et al.
Nucleic Acids Research (2017) Vol. 46, Iss. D1, pp. D1039-D1048
Open Access | Times Cited: 162
POSTAR: a platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins
Boqin Hu, Yucheng Yang, Yiming Huang, et al.
Nucleic Acids Research (2016) Vol. 45, Iss. D1, pp. D104-D114
Open Access | Times Cited: 161
RMDisease: a database of genetic variants that affect RNA modifications, with implications for epitranscriptome pathogenesis
Kunqi Chen, Bowen Song, Yujiao Tang, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D1396-D1404
Open Access | Times Cited: 77
Genetic Regulation of SMC Gene Expression and Splicing Predict Causal CAD Genes
Rédouane Aherrahrou, Dillon Lue, R. Noah Perry, et al.
Circulation Research (2023) Vol. 132, Iss. 3, pp. 323-338
Open Access | Times Cited: 30
Gain-of-Function Mutations: An Emerging Advantage for Cancer Biology
Yongsheng Li, Yunpeng Zhang, Xia Li, et al.
Trends in Biochemical Sciences (2019) Vol. 44, Iss. 8, pp. 659-674
Open Access | Times Cited: 57
Examination of the associations between m6A-associated single-nucleotide polymorphisms and blood pressure
Xingbo Mo, Shu‐Feng Lei, Yonghong Zhang, et al.
Hypertension Research (2019) Vol. 42, Iss. 10, pp. 1582-1589
Closed Access | Times Cited: 52
Structural visualization of key steps in nucleosome reorganization by human FACT
Kouta Mayanagi, Kazumi Saikusa, Naoyuki Miyazaki, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 50
CircleBase: an integrated resource and analysis platform for human eccDNAs
Xiaolu Zhao, Leisheng Shi, Shasha Ruan, et al.
Nucleic Acids Research (2021) Vol. 50, Iss. D1, pp. D72-D82
Open Access | Times Cited: 34
Genome-wide identification of RNA modification-related single nucleotide polymorphisms associated with rheumatoid arthritis
Mimi Wang, Jingyun Wu, Shu‐Feng Lei, et al.
BMC Genomics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 14
Detection of M 6 A-associated SNPs as Potential Functional Variants for Coronary Artery Disease
Xingbo Mo, Shu‐Feng Lei, Yonghong Zhang, et al.
Epigenomics (2018) Vol. 10, Iss. 10, pp. 1279-1287
Closed Access | Times Cited: 44
OncoBase: a platform for decoding regulatory somatic mutations in human cancers
Xianfeng Li, Leisheng Shi, Yan Wang, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. D1, pp. D1044-D1055
Open Access | Times Cited: 42
Prevalence and architecture of posttranscriptionally impaired synonymous mutations in 8,320 genomes across 22 cancer types
Huajing Teng, Wenqing Wei, Qinglan Li, et al.
Nucleic Acids Research (2020) Vol. 48, Iss. 3, pp. 1192-1205
Open Access | Times Cited: 35
In silico genome‐wide identification of m6A‐associated SNPs as potential functional variants for periodontitis
Weimin Lin, Hao Xu, Yunshu Wu, et al.
Journal of Cellular Physiology (2019) Vol. 235, Iss. 2, pp. 900-908
Closed Access | Times Cited: 30
AI-Driver: an ensemble method for identifying driver mutations in personal cancer genomes
Haoxuan Wang, Tao Wang, Xiaolu Zhao, et al.
NAR Genomics and Bioinformatics (2020) Vol. 2, Iss. 4
Open Access | Times Cited: 29
Integration Analysis of m6A-SNPs and eQTLs Associated With Sepsis Reveals Platelet Degranulation and Staphylococcus aureus Infection are Mediated by m6A mRNA Methylation
Xuri Sun, Yishuang Dai, Guoliang Tan, et al.
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 28
Genome-wide identification of m6A-associated SNPs as potential functional variants for bone mineral density
Xingbo Mo, Y. H. Zhang, Shu‐Feng Lei
Osteoporosis International (2018) Vol. 29, Iss. 9, pp. 2029-2039
Closed Access | Times Cited: 30
Genome-wide enrichment of m6A-associated single-nucleotide polymorphisms in the lipid loci
Xingbo Mo, Shu‐Feng Lei, Yonghong Zhang, et al.
The Pharmacogenomics Journal (2018) Vol. 19, Iss. 4, pp. 347-357
Closed Access | Times Cited: 29
Genetic variants in N6-methyladenosine are associated with bladder cancer risk in the Chinese population
Hanting Liu, Jingjing Gu, Yu Jin, et al.
Archives of Toxicology (2020) Vol. 95, Iss. 1, pp. 299-309
Closed Access | Times Cited: 24
Transcriptomic signatures and repurposing drugs for COVID-19 patients: findings of bioinformatics analyses
Guobing� Li, Shasha Ruan, Xiaolu Zhao, et al.
Computational and Structural Biotechnology Journal (2020) Vol. 19, pp. 1-15
Open Access | Times Cited: 21
Exploring Common Therapeutic Targets for Neurodegenerative Disorders Using Transcriptome Study
S. Akila Parvathy Dharshini, Sherlyn Jemimah, Y‐h. Taguchi, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 17
Identification of candidate causal variants and target genes at 41 breast cancer risk loci through differential allelic expression analysis
Joana M. Xavier, Ramiro Magno, Roslin Russell, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
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