The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Molecular-evolutionary mechanisms for genomic disorders
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Citations
Cites
A 1.5 million–base pair inversion polymorphism in families with Williams-Beuren syndrome
Osborne, L. R., Li, M., Pober, B., Chitayat, D., Bodurtha, J., Mandel, A., Costa, T., Grebe, T., Cox, S., Tsui, L.-C., et al. (2001) · Nature Genetics · doi:10.1038/ng753 · Cited by 344
Cited by
Diagnostic genome profiling in mental retardation
de Vries, B. B. A., Pfundt, R., Leisink, M., Koolen, D. A., Vissers, L. E. L. M., Janssen, I. M., Reijmersdal, S. V., Nillesen, W. M., Huys, E. H. L. P. G., Leeuw, N. D., et al. (2005) · The American Journal of Human Genetics · doi:10.1086/491719 · Cited by 605
The MECP2 duplication syndrome
Ramocki, M. B., Tavyev, Y. J., & Peters, S. U. (2010) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.33184 · Cited by 300
Lineage-Specific Gene Duplication and Loss in Human and Great Ape Evolution
Fortna, A., Kim, Y., MacLaren, E., Marshall, K., Hahn, G., Meltesen, L., Brenton, M., Hink, R., Burgers, S., Hernandez-Boussard, T., et al. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020207 · Cited by 276
On the origin of new genes in Drosophila
Zhou, Q., Zhang, G., Zhang, Y., Xu, S., Zhao, R., Zhan, Z., Li, X., Ding, Y., Yang, S., & Wang, W. (2008) · Genome Research · doi:10.1101/gr.076588.108 · Cited by 257
van der Zee, J., Rademakers, R., Engelborghs, S., Gijselinck, I., Bogaerts, V., Vandenberghe, R., Santens, P., Caekebeke, J., De Pooter, T., Peeters, K., et al. (2006) · Brain · doi:10.1093/brain/awl029 · Cited by 90
Metadata
- Authors
- Stankiewicz, P., & Lupski, J. R.
- Venue
- Current Opinion in Genetics & Development
- Publisher
- Elsevier BV
- Published
- 2002-06
- Volume
- 12
- Issue
- 3
- Pages
- 312-319
- ISSN
- 0959-437X (ISSN-L)
- OpenAlex
- W2050441340
- Cited by
- 159
- References
- 1
- FWCI
- 1.58
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
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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: Molecular-evolutionary mechanisms for genomic disorders. https://app.cochat.ai/papers/10.1016/s0959-437x(02)00304-0
- The paper
- Stankiewicz, P., & Lupski, J. R. (2002). Molecular-evolutionary mechanisms for genomic disorders. Current Opinion in Genetics & Development. https://doi.org/10.1016/s0959-437x(02)00304-0
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.
