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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:

Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing
Michael Krawczak, Nick Thomas, Bernd Hundrieser, et al.
Human Mutation (2006) Vol. 28, Iss. 2, pp. 150-158
Open Access | Times Cited: 351

Showing 1-25 of 351 citing articles:

Mechanisms and Regulation of Alternative Pre-mRNA Splicing
Yeon Lee, Donald C. Rio
Annual Review of Biochemistry (2015) Vol. 84, Iss. 1, pp. 291-323
Open Access | Times Cited: 1144
Splicing in disease: disruption of the splicing code and the decoding machinery
Guey‐Shin Wang, Thomas A. Cooper
Nature Reviews Genetics (2007) Vol. 8, Iss. 10, pp. 749-761
Closed Access | Times Cited: 1011
Splicing mutations in human genetic disorders: examples, detection, and confirmation
Anna Abramowicz, Monika Goś
Journal of Applied Genetics (2018) Vol. 59, Iss. 3, pp. 253-268
Open Access | Times Cited: 535
ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms
Yoshihiro Onouchi, Tomohiko Gunji, Jane C. Burns, et al.
Nature Genetics (2007) Vol. 40, Iss. 1, pp. 35-42
Open Access | Times Cited: 480
Aberrant RNA splicing in cancer; expression changes and driver mutations of splicing factor genes
Anita Sveen, Sami Kilpinen, Anja Ruusulehto, et al.
Oncogene (2015) Vol. 35, Iss. 19, pp. 2413-2427
Open Access | Times Cited: 441
Pre-mRNA splicing in disease and therapeutics
Ravi K. Singh, Thomas A. Cooper
Trends in Molecular Medicine (2012) Vol. 18, Iss. 8, pp. 472-482
Open Access | Times Cited: 413
The pathobiology of splicing
Amanda J. Ward, Thomas A. Cooper
The Journal of Pathology (2009) Vol. 220, Iss. 2, pp. 152-163
Open Access | Times Cited: 405
CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency
Menno C. van Zelm, Julie Smet, Brigitte Adams, et al.
Journal of Clinical Investigation (2010) Vol. 120, Iss. 4, pp. 1265-1274
Open Access | Times Cited: 379
Deep intronic mutations and human disease
Rita Vaz‐Drago, Noélia Custódio, Maria Carmo‐Fonseca
Human Genetics (2017) Vol. 136, Iss. 9, pp. 1093-1111
Closed Access | Times Cited: 379
Differential GC Content between Exons and Introns Establishes Distinct Strategies of Splice-Site Recognition
Maayan Amit, Maya Donyo, Dror Hollander, et al.
Cell Reports (2012) Vol. 1, Iss. 5, pp. 543-556
Open Access | Times Cited: 282
Alternative splicing as a source of phenotypic diversity
Charlotte Wright, Christopher W. J. Smith, Chris D. Jiggins
Nature Reviews Genetics (2022) Vol. 23, Iss. 11, pp. 697-710
Closed Access | Times Cited: 250
Pick one, but be quick: 5′ splice sites and the problems of too many choices
Xavier Roca, Adrian R. Krainer, Ian C. Eperon
Genes & Development (2013) Vol. 27, Iss. 2, pp. 129-144
Open Access | Times Cited: 209
Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes
D.N. Cooper
Human Genomics (2010) Vol. 4, Iss. 5, pp. 284-284
Open Access | Times Cited: 218
Aberrant 3′ splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization
Igor Vořechovský
Nucleic Acids Research (2006) Vol. 34, Iss. 16, pp. 4630-4641
Open Access | Times Cited: 201
The functional consequences of intron retention: Alternative splicing coupled to NMD as a regulator of gene expression
Ying Ge, Bo Porse
BioEssays (2013) Vol. 36, Iss. 3, pp. 236-243
Closed Access | Times Cited: 196
Aberrant 5′ splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization
Emanuele Buratti, Martin Chivers, Jana Královičová, et al.
Nucleic Acids Research (2007) Vol. 35, Iss. 13, pp. 4250-4263
Open Access | Times Cited: 179
Loss of exon identity is a common mechanism of human inherited disease
Timothy Sterne-Weiler, Jonathan M. Howard, Matthew Mort, et al.
Genome Research (2011) Vol. 21, Iss. 10, pp. 1563-1571
Open Access | Times Cited: 172
Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
D.N. Cooper, Jian–Min Chen, Edward V. Ball, et al.
Human Mutation (2010) Vol. 31, Iss. 6, pp. 631-655
Open Access | Times Cited: 172
Evaluation of in silico splice tools for decision-making in molecular diagnosis
Claude Houdayer, Catherine Dehainault, Christophe Mattler, et al.
Human Mutation (2008) Vol. 29, Iss. 7, pp. 975-982
Open Access | Times Cited: 160
A large fraction of unclassified variants of the mismatch repair genesMLH1andMSH2is associated with splicing defects
Isabelle Tournier, Myriam Vézain, Alexandra Martins, et al.
Human Mutation (2008) Vol. 29, Iss. 12, pp. 1412-1424
Open Access | Times Cited: 160
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing
Matthew Mort, Timothy Sterne-Weiler, Biao Li, et al.
Genome biology (2014) Vol. 15, Iss. 1
Open Access | Times Cited: 153
DGAT1 mutation is linked to a congenital diarrheal disorder
Joel T. Haas, Harland S. Winter, Elaine T. Lim, et al.
Journal of Clinical Investigation (2012) Vol. 122, Iss. 12, pp. 4680-4684
Open Access | Times Cited: 150
Genetics and immunopathology of chronic granulomatous disease
Marie José Stasia, Xing Jun Li
Seminars in Immunopathology (2008) Vol. 30, Iss. 3, pp. 209-235
Closed Access | Times Cited: 145
Variation Interpretation Predictors: Principles, Types, Performance, and Choice
Abhishek Niroula, Mauno Vihinen
Human Mutation (2016) Vol. 37, Iss. 6, pp. 579-597
Open Access | Times Cited: 124
Exon identity crisis: disease-causing mutations that disrupt the splicing code
Timothy Sterne-Weiler, Jeremy R. Sanford
Genome biology (2014) Vol. 15, Iss. 1, pp. 201-201
Open Access | Times Cited: 120
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