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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:

Rules and tools to predict the splicing effects of exonic and intronic mutations
Kinji Ohno, Jun‐ichi Takeda, Akio Masuda
Wiley Interdisciplinary Reviews - RNA (2017) Vol. 9, Iss. 1
Closed Access | Times Cited: 107

Showing 26-50 of 107 citing articles:

Severe neurocognitive and growth disorders due to variation in THOC2 , an essential component of nuclear mRNA export machinery
Raman Kumar, Alison Gardner, Claire C. Homan, et al.
Human Mutation (2018) Vol. 39, Iss. 8, pp. 1126-1138
Open Access | Times Cited: 20
A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families
Revital Bronstein, Elizabeth E. Capowski, Sudeep Mehrotra, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 6, pp. 967-979
Open Access | Times Cited: 18
Congenital myasthenic syndrome–associated agrin variants affect clustering of acetylcholine receptors in a domain-specific manner
Bisei Ohkawara, Xin‐Ming Shen, Duygu Selcen, et al.
JCI Insight (2020) Vol. 5, Iss. 7
Open Access | Times Cited: 17
Splicing impact of deep exonic missense variants in CAPN3 explored systematically by minigene functional assay
Eugénie Dionnet, Aurélia Defour, Nathalie Da Silva, et al.
Human Mutation (2020) Vol. 41, Iss. 10, pp. 1797-1810
Open Access | Times Cited: 17
Tumor Antigens beyond the Human Exome
Lisabeth Emilius, Franziska Bremm, Amanda Katharina Binder, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4673-4673
Open Access | Times Cited: 2
Assessing the reliability of point mutation as data augmentation for deep learning with genomic data
Hyun‐Jung Lee, Utku Özbulak, Ho-min Park, et al.
BMC Bioinformatics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 2
Context matters: Regulation of splice donor usage
Johannes Ptok, Lisa Müller, Stephan Theiss, et al.
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2019) Vol. 1862, Iss. 11-12, pp. 194391-194391
Closed Access | Times Cited: 16
Hybrid Minigene Assay: An Efficient Tool to Characterize mRNA Splicing Profiles of NF1 Variants
Valeria Morbidoni, Elisa Baschiera, Monica Forzan, et al.
Cancers (2021) Vol. 13, Iss. 5, pp. 999-999
Open Access | Times Cited: 13
Presumed COL4A3/COL4A4 Missense/Synonymous Variants Induce Aberrant Splicing
Haiyue Deng, Yanqin Zhang, Jie Ding, et al.
Frontiers in Medicine (2022) Vol. 9
Open Access | Times Cited: 10
Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotype
Loann Raud, Chandran Ka, Isabelle Gourlaouen, et al.
Transfusion (2019) Vol. 59, Iss. 4, pp. 1367-1375
Closed Access | Times Cited: 15
Functional analysis of novel genetic variants of NKX2‐5 associated with nonsyndromic congenital heart disease
Ritu Dixit, Chitra Narasimhan, Vijayalakshmi I. Balekundri, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 12, pp. 3644-3663
Closed Access | Times Cited: 12
A synonymous UPF3B variant causing a speech disorder implicates NMD as a regulator of neurodevelopmental disorder gene networks
Deepti Domingo, Urwah Nawaz, Mark Corbett, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 15, pp. 2568-2578
Open Access | Times Cited: 12
Clinical Utility of Functional RNA Analysis for the Reclassification of Splicing Gene Variants in Hereditary Cancer
Κωνσταντίνος Αγιαννιτόπουλος, Georgia Pepe, Eirini Papadopoulou, et al.
Cancer Genomics & Proteomics (2021) Vol. 18, Iss. 3, pp. 285-294
Open Access | Times Cited: 11
Rewriting the (tran)script: Application to spinal muscular atrophy
Hasane Ratni, Lutz Mueller, Martin Ebeling
Progress in medicinal chemistry (2019), pp. 119-156
Closed Access | Times Cited: 11
Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1
Tomohiko Inoue, China Nagano, Masafumi Matsuo, et al.
Clinical and Experimental Nephrology (2020) Vol. 24, Iss. 7, pp. 606-612
Open Access | Times Cited: 11
Systematics for types and effects of RNA variations
Mauno Vihinen
RNA Biology (2020) Vol. 18, Iss. 4, pp. 481-498
Open Access | Times Cited: 11
Alternative splicing: An important regulatory mechanism in colorectal carcinoma
Jianyi Wang, Chuhan Wang, Le Li, et al.
Molecular Carcinogenesis (2021) Vol. 60, Iss. 4, pp. 279-293
Closed Access | Times Cited: 10
Variants in the circadian clock genes PER2 and PER3 associate with familial sleep phase disorders
Laura Plavc, Cene Skubic, Leja Dolenc‐Grošelj, et al.
Chronobiology International (2024) Vol. 41, Iss. 5, pp. 757-766
Open Access | Times Cited: 1
Implication of GATA4 synonymous variants in congenital heart disease: A comprehensive in-silico approach
Ritu Dixit, Ashok Kumar, Bhagyalaxmi Mohapatra
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (2018) Vol. 813, pp. 31-38
Closed Access | Times Cited: 11
A computational approach for explaining the effect of the prl gene polymorphism on prolactin structure and biological activity in Japanese quails
Mohammed Baqur S. Al‐Shuhaib, Fadhil R. Al-Kafajy, Ghadeer S. Al-Jashami
Animal Biotechnology (2019) Vol. 32, Iss. 3, pp. 273-281
Closed Access | Times Cited: 10
The computational approach to variant interpretation
Selen Özkan, Natàlia Padilla, Alejandro Moles‐Fernández, et al.
Elsevier eBooks (2021), pp. 89-119
Closed Access | Times Cited: 9
Principles and Practical Considerations for the Analysis of Disease-Associated Alternative Splicing Events Using the Gateway Cloning-Based Minigene Vectors pDESTsplice and pSpliceExpress
Elena Putscher, Michael Hecker, Brit Fitzner, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 10, pp. 5154-5154
Open Access | Times Cited: 9
Discovery of a pre-mRNA structural scaffold as a contributor to the mammalian splicing code
Kaushik Saha, Mike M. Fernandez, Tapan Biswas, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 12, pp. 7103-7121
Open Access | Times Cited: 9
IntSplice2: Prediction of the Splicing Effects of Intronic Single-Nucleotide Variants Using LightGBM Modeling
Jun‐ichi Takeda, Sae Fukami, Akira Tamura, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 9
Activation of cryptic splice sites in three patients with chronic granulomatous disease
Martin de Boer, Karin van Leeuwen, Mathias Hauri‐Hohl, et al.
Molecular Genetics & Genomic Medicine (2019) Vol. 7, Iss. 9
Open Access | Times Cited: 9

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