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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:

Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis
Natasha Caminsky, Eliseos J. Mucaki, Peter K. Rogan
F1000Research (2014) Vol. 3, pp. 282-282
Open Access | Times Cited: 89

Showing 26-50 of 89 citing articles:

Role of an SNP in Alternative Splicing of Bovine NCF4 and Mastitis Susceptibility
Zhihua Ju, Changfa Wang, Xiuge Wang, et al.
PLoS ONE (2015) Vol. 10, Iss. 11, pp. e0143705-e0143705
Open Access | Times Cited: 25
Quantitative Analysis of BRCA1 and BRCA2 Germline Splicing Variants Using a Novel RNA-Massively Parallel Sequencing Assay
Suzette Farber-Katz, Vickie Hsuan, Sitao Wu, et al.
Frontiers in Oncology (2018) Vol. 8
Open Access | Times Cited: 24
Clinical and Therapeutic Evaluation of the Ten Most Prevalent CRB1 Mutations
Bruna Lopes da Costa, Masha Kolesnikova, Sarah R. Levi, et al.
Biomedicines (2023) Vol. 11, Iss. 2, pp. 385-385
Open Access | Times Cited: 8
Systematic pan-cancer analysis of somatic allele frequency
Liam F. Spurr, Muzi Li, Nawaf Alomran, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 23
A targeted genome association study examining transient receptor potential ion channels, acetylcholine receptors, and adrenergic receptors in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis
Samantha Johnston, Donald Staines, Anne H. Klein, et al.
BMC Medical Genetics (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 21
DNA methylation in canine brains is related to domestication and dog-breed formation
Ann-Sofie Sundman, Fábio Pértille, Luiz Lehmann Coutinho, et al.
PLoS ONE (2020) Vol. 15, Iss. 10, pp. e0240787-e0240787
Open Access | Times Cited: 19
Association of Messenger RNA Level With Phenotype in Patients With Choroideremia
Lewis E. Fry, Maria I. Patrício, Jonathan Williams, et al.
JAMA Ophthalmology (2019) Vol. 138, Iss. 2, pp. 128-128
Open Access | Times Cited: 19
Ten Novel Mutations in Chinese Patients with Megalencephalic Leukoencephalopathy with Subcortical Cysts and a Long-Term Follow-Up Research
Binbin Cao, Huifang Yan, Mangmang Guo, et al.
PLoS ONE (2016) Vol. 11, Iss. 6, pp. e0157258-e0157258
Open Access | Times Cited: 18
Novel NTRK1 mutations associated with congenital insensitivity to pain with anhidrosis verified by functional studies
Tai‐Seung Nam, Wenting Li, Somy Yoon, et al.
Journal of the Peripheral Nervous System (2017) Vol. 22, Iss. 2, pp. 92-99
Closed Access | Times Cited: 18
A novel ‘splice site’ HCN4 Gene mutation, c.1737 + 1 G > T, causes familial bradycardia, reduced heart rate response, impaired chronotropic competence and increased short-term heart rate variability
Lidia Haţegan, Beáta Csányi, Balázs Ördög, et al.
International Journal of Cardiology (2017) Vol. 241, pp. 364-372
Closed Access | Times Cited: 17
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
Combining genetic constraint with predictions of alternative splicing to prioritize deleterious splicing in rare disease studies
Michael J. Cormier, Brent S. Pedersen, Pınar Bayrak‐Toydemir, et al.
BMC Bioinformatics (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 10
Detection of polymorphism within leptin gene in Egyptian river buffalo and predict its effects on different molecular levels
Karima F. Mahrous, Mohamad M. Aboelenin, Mohamed Rashed, et al.
Journal of Genetic Engineering and Biotechnology (2020) Vol. 18, Iss. 1, pp. 6-6
Open Access | Times Cited: 14
Splicing dysregulation contributes to the pathogenicity of several F9 exonic point variants
Upendra Katneni, Aaron Liss, David D. Holcomb, et al.
Molecular Genetics & Genomic Medicine (2019) Vol. 7, Iss. 8
Open Access | Times Cited: 13
Disrupted minor intron splicing is prevalent in Mendelian disorders
Anouk Olthof, Jeffrey S. Rasmussen, Philippe M. Campeau, et al.
Molecular Genetics & Genomic Medicine (2020) Vol. 8, Iss. 9
Open Access | Times Cited: 12
A proposed molecular mechanism for pathogenesis of severe RNA-viral pulmonary infections
Peter K. Rogan, Eliseos J. Mucaki, Ben C. Shirley
F1000Research (2021) Vol. 9, pp. 943-943
Open Access | Times Cited: 11
Biallelic Novel USP53 Splicing Variant Disrupting the Gene Function that Causes Cholestasis Phenotype and Review of the Literature
Alper Gezdirici, Özlem KALAYCIK ŞENGÜL, Mustafa Doğan, et al.
Molecular Syndromology (2022) Vol. 13, Iss. 6, pp. 471-484
Open Access | Times Cited: 8
Multiplex PCR and NGS-based identification of mRNA splicing variants: Analysis of BRCA1 splicing pattern as a model
J. Hojný, Petra Zemánková, Filip Lhota, et al.
Gene (2017) Vol. 637, pp. 41-49
Closed Access | Times Cited: 11
PAX7 nucleotide variants and the risk of non‐syndromic orofacial clefts in the Polish population
Agnieszka Gaczkowska, Barbara Biedziak, Margareta Budner, et al.
Oral Diseases (2019) Vol. 25, Iss. 6, pp. 1608-1618
Closed Access | Times Cited: 11
Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease
Binbin Cao, Xiaoping Yang, Yinyin Chen, et al.
Metabolic Brain Disease (2017) Vol. 32, Iss. 4, pp. 1123-1131
Closed Access | Times Cited: 10
Variant in the X-chromosome spliceosomal gene GPKOW causes male-lethal microcephaly with intrauterine growth restriction
Renée Carroll, Raman Kumar, Marie Shaw, et al.
European Journal of Human Genetics (2017) Vol. 25, Iss. 9, pp. 1078-1082
Open Access | Times Cited: 10
A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa
Yabin Chen, Li Huang, Xiaodong Jiao, et al.
Human Genomics (2018) Vol. 12, Iss. 1
Open Access | Times Cited: 10
<p>Regulation of alternative splicing in obesity-induced hypertension</p>
Zodwa Dlamini, Rodney Hull, Tshepiso J. Makhafola, et al.
Diabetes Metabolic Syndrome and Obesity (2019) Vol. Volume 12, pp. 1597-1615
Open Access | Times Cited: 10
Functional assessment of somatic STK11 variants identified in primary human non-small cell lung cancers
Liam Donnelly, Tyler Hogan, Sean M. Lenahan, et al.
Carcinogenesis (2021) Vol. 42, Iss. 12, pp. 1428-1438
Open Access | Times Cited: 9
Genome-wide discovery of InDels and validation of PCR-Based InDel markers for earliness in a RIL population and genotypes of lentil (Lens culinaris Medik.)
K.M. Shivaprasad, Muraleedhar S. Aski, Gyan P. Mishra, et al.
PLoS ONE (2024) Vol. 19, Iss. 5, pp. e0302870-e0302870
Open Access | Times Cited: 1

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