The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Introducing sense into nonsense in treatments of human genetic diseases
Overview
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Citations
Cites
The highways and byways of mRNA decay
Garneau, N. L., Wilusz, J., & Wilusz, C. J. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2104 · Cited by 1,294
Cited by
Nonsense-mediated mRNA decay in humans at a glance
Kurosaki, T., & Maquat, L. E. (2016) · Journal of Cell Science · doi:10.1242/jcs.181008 · Cited by 396
Wang, D., Shukla, C., Liu, X., Schoeb, T. R., Clarke, L. A., Bedwell, D. M., & Keeling, K. M. (2010) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2009.08.002 · Cited by 62
Metadata
- Authors
- Linde, L., & Kerem, B.
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 2008-11
- Volume
- 24
- Issue
- 11
- Pages
- 552-563
- ISSN
- 0168-9525 (ISSN-L)
- OpenAlex
- W2076732344
- Cited by
- 205
- References
- 1
- FWCI
- 0.90
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Introducing sense into nonsense in treatments of human genetic diseases. https://app.cochat.ai/papers/10.1016/j.tig.2008.08.010
- The paper
- Linde, L., & Kerem, B. (2008). Introducing sense into nonsense in treatments of human genetic diseases. Trends in Genetics. https://doi.org/10.1016/j.tig.2008.08.010
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.