The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes
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Citations
Cites
Characterization of single-nucleotide polymorphisms in coding regions of human genes
Cargill, M., Altshuler, D., Ireland, J., Sklar, P., Ardlie, K., Patil, N., Lane, C. R., Lim, E. P., Kalyanaraman, N., Nemesh, J., et al. (1999) · Nature Genetics · doi:10.1038/10290 · Cited by 1,547
Krawczak, M., Reiss, J., & Cooper, D. (1992) · Human Genetics · doi:10.1007/bf00210743 · Cited by 1,324
Hentze, M. W., & Kulozik, A. E. (1999) · Cell · doi:10.1016/s0092-8674(00)80542-5 · Cited by 809
INTERRELATIONSHIPS OF THE PATHWAYS OF mRNA DECAY AND TRANSLATION IN EUKARYOTIC CELLS
Jacobson, A., & Peltz, S. W. (1996) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.65.070196.003401 · Cited by 662
(2014) · Identity · doi:10.2307/j.ctt9qdsck.5 · Cited by 651
D’Souza, I., Poorkaj, P., Hong, M., Nochlin, D., Lee, V. M.-Y., Bird, T. D., & Schellenberg, G. D. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.10.5598 · Cited by 515
Identification of functional exonic splicing enhancer motifs recognized by individual SR proteins
Liu, H.-X., Zhang, M., & Krainer, A. R. (1998) · Genes & Development · doi:10.1101/gad.12.13.1998 · Cited by 510
Self-citationThe role of exon sequences in splice site selection.
Watakabe, A., Tanaka, K., & Shimura, Y. (1993) · Genes & Development · doi:10.1101/gad.7.3.407 · Cited by 361
Ars, E. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.2.237 · Cited by 358
Single-nucleotide polymorphisms can cause different structural folds of mRNA
Shen, L. X., Basilion, J. P., & Stanton, V. P. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.14.7871 · Cited by 317
Cited by
Listening to silence and understanding nonsense: exonic mutations that affect splicing
Cartegni, L., Chew, S. L., & Krainer, A. R. (2002) · Nature Reviews Genetics · doi:10.1038/nrg775 · Cited by 2,209
Self-citationESEfinder: a web resource to identify exonic splicing enhancers
Cartegni, L. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg616 · Cited by 1,603
Self-citationA genomic view of alternative splicing
Modrek, B., & Lee, C. (2002) · Nature Genetics · doi:10.1038/ng0102-13 · Cited by 1,302
Pre-mRNA splicing and human disease
Faustino, N. A., & Cooper, T. A. (2003) · Genes & Development · doi:10.1101/gad.1048803 · Cited by 1,256
Duan, J. (2003) · Human Molecular Genetics · doi:10.1093/hmg/12.3.205 · Cited by 930
Metadata
- Authors
- Liu, H.-X., Cartegni, L., Zhang, M. Q., & Krainer, A. R.
- Venue
- Nature Genetics
- Published
- 2001-01
- Volume
- 27
- Issue
- 1
- Pages
- 55-58
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2100008304
- Cited by
- 477
- References
- 29
- FWCI
- 19.76
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes. https://app.cochat.ai/papers/10.1038/83762
- The paper
- Liu, H.-X., Cartegni, L., Zhang, M. Q., & Krainer, A. R. (2001). A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes. Nature Genetics. https://doi.org/10.1038/83762
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
