The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Mutations in the RNA Component of RNase MRP Cause a Pleiotropic Human Disease, Cartilage-Hair Hypoplasia
Open accessOverview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Beighton, P., & Beighton, G. (1997) · The Person Behind the Syndrome · doi:10.1007/978-1-4471-0925-9_118 · Cited by 3,159
The RNA moiety of ribonuclease P is the catalytic subunit of the enzyme
Guerrier-Takada, C., Gardiner, K., Marsh, T., Pace, N., & Altman, S. (1983) · Cell · doi:10.1016/0092-8674(83)90117-4 · Cited by 2,684
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland
Hästbacka, J., de la Chapelle, A., Kaitila, I., Sistonen, P., Weaver, A., & Lander, E. (1992) · Nature Genetics · doi:10.1038/ng1192-204 · Cited by 558
Self-citationSURVEY AND SUMMARY Transcription by RNA polymerases I and III
Paule, M. R. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.6.1283 · Cited by 502
Function and synthesis of small nucleolar RNAs
Tollervey, D., & Kiss, T. (1997) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(97)80005-1 · Cited by 467
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy
Pelin, K., Hilpelä, P., Donner, K., Sewry, C., Akkari, P. A., Wilton, S. D., Wattanasirichaigoon, D., Bang, M.-L., Centner, T., Hanefeld, F., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.5.2305 · Cited by 338
Self-citationA mammalian Mitochondrial RNA Processing Activity Contains Nucleus-Encoded RNA
Chang, D. D., & Clayton, D. A. (1987) · Science · doi:10.1126/science.2434997 · Cited by 317
A novel endoribonuclease cleaves at a priming site of mouse mitochondrial DNA replication.
Chang, D. D., & Clayton, D. A. (1987) · The EMBO Journal · doi:10.1002/j.1460-2075.1987.tb04770.x · Cited by 249
Linkage disequilibrium mapping in isolated populations: The example of Finland revisited
de la Chapelle, A., & Wright, F. A. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.21.12416 · Cited by 243
Self-citationThe RNA of RNase MRP is required for normal processing of ribosomal RNA.
Chu, S., Archer, R. H., Zengel, J. M., & Lindahl, L. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.2.659 · Cited by 218
Cited by
RNA regulation: A new genetics?
Mattick, J. S. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1321 · Cited by 765
Rapid evolution of noncoding RNAs: lack of conservation does not mean lack of function
Pang, K. C., Frith, M. C., & Mattick, J. S. (2006) · Trends in Genetics · doi:10.1016/j.tig.2005.10.003 · Cited by 656
Signaling to p53: ribosomal proteins find their way
Zhang, Y., & Lu, H. (2009) · Cancer Cell · doi:10.1016/j.ccr.2009.09.024 · Cited by 591
Telomeric and extra-telomeric roles for telomerase and the telomere-binding proteins
Martínez, P., & Blasco, M. A. (2011) · Nature Reviews Cancer · doi:10.1038/nrc3025 · Cited by 468
Biogenesis of small nucleolar ribonucleoproteins
Filipowicz, W., & Pogačić, V. (2002) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(02)00334-4 · Cited by 394
Metadata
- Authors
- Ridanpää, M., van Eenennaam, H., Pelin, K., Chadwick, R., Johnson, C., Yuan, B., vanVenrooij, W., Pruijn, G., Salmela, R., Rockas, S., Mäkitie, O., Kaitila, I., & de la Chapelle, A.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2001-01
- Volume
- 104
- Issue
- 2
- Pages
- 195-203
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2022605680
- Cited by
- 517
- References
- 26
- FWCI
- 12.60
- Type
- journal article
- Language
- en
- Open access
- bronze
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.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Mutations in the RNA Component of RNase MRP Cause a Pleiotropic Human Disease, Cartilage-Hair Hypoplasia. https://app.cochat.ai/papers/10.1016/s0092-8674(01)00205-7
- The paper
- Ridanpää, M., van Eenennaam, H., Pelin, K., Chadwick, R., Johnson, C., Yuan, B., vanVenrooij, W., Pruijn, G., Salmela, R., Rockas, S., Mäkitie, O., Kaitila, I., & de la Chapelle, A. (2001). Mutations in the RNA Component of RNase MRP Cause a Pleiotropic Human Disease, Cartilage-Hair Hypoplasia. Cell. https://doi.org/10.1016/s0092-8674(01)00205-7
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.
