The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome
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Citations
Cites
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
Bell, A. C., & Felsenfeld, G. (2000) · Nature · doi:10.1038/35013100 · Cited by 1,746
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
Hark, A. T., Schoenherr, C. J., Katz, D. J., Ingram, R. S., Levorse, J. M., & Tilghman, S. M. (2000) · Nature · doi:10.1038/35013106 · Cited by 1,547
Zhang, P., Liégeois, N. J., Wong, C., Finegold, M., Hou, H., Thompson, J. C., Silverman, A., Harper, J. W., DePinho, R. A., & Elledge, S. J. (1997) · Nature · doi:10.1038/387151a0 · Cited by 749
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
Ogawa, O., Eccles, M. R., Szeto, J., McNoe, L. A., Yun, K., Maw, M. A., Smith, P. J., & Reeve, A. E. (1993) · Nature · doi:10.1038/362749a0 · Cited by 707
Yan, Y., Frisén, J., Lee, M. H., Massagué, J., & Barbacid, M. (1997) · Genes & Development · doi:10.1101/gad.11.8.973 · Cited by 493
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
Henry, I., Bonaiti-Pellié, C., Chehensse, V., Beldjord, C., Schwartz, C., Utermann, G., & Junien, C. (1991) · Nature · doi:10.1038/351665a0 · Cited by 421
Smilinich, N. J., Day, C. D., Fitzpatrick, G. V., Caldwell, G. M., Lossie, A. C., Cooper, P. R., Smallwood, A. C., Joyce, J. A., Schofield, P. N., Reik, W., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.14.8064 · Cited by 408
Self-citationAn imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome
Hatada, I., Ohashi, H., Fukushima, Y., Kaneko, Y., Inoue, M., Komoto, Y., Okada, A., Ohishi, S., Nabetani, A., Morisaki, H., et al. (1996) · Nature Genetics · doi:10.1038/ng1096-171 · Cited by 382
Agathanggelou, A., Honorio, S., Macartney, D. P., Martinez, A., Dallol, A., Rader, J., Fullwood, P., Chauhan, A., Walker, R., Shaw, J. A., et al. (2001) · Oncogene · doi:10.1038/sj.onc.1204175 · Cited by 376
Self-citationSparago, A., Cerrato, F., Vernucci, M., Ferrero, G. B., Silengo, M. C., & Riccio, A. (2004) · Nature Genetics · doi:10.1038/ng1410 · Cited by 371
Self-citation
Cited by
A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations: Table 1
Wilson, J. R. F., Bateman, A. C., Hanson, H., An, Q., Evans, G., Rahman, N., Jones, J. L., & Eccles, D. M. (2010) · Journal of Medical Genetics · doi:10.1136/jmg.2010.078113 · Cited by 122
Self-citationDominant versus recessive: Molecular mechanisms in metabolic disease
Zschocke, J. (2008) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-008-1016-5 · Cited by 33
Metadata
- Authors
- Cooper, W. N., Luharia, A., Evans, G. A., Raza, H., Haire, A. C., Grundy, R., Bowdin, S. C., Riccio, A., Sebastio, G., Bliek, J., Schofield, P. N., Reik, W., Macdonald, F., & Maher, E. R.
- Venue
- European Journal of Human Genetics
- Published
- 2005-07-06
- Volume
- 13
- Issue
- 9
- Pages
- 1025-1032
- ISSN
- 1018-4813 (ISSN-L)
- 1476-5438
- OpenAlex
- W2141480231
- Cited by
- 304
- References
- 39
- FWCI
- 9.92
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome. https://app.cochat.ai/papers/10.1038/sj.ejhg.5201463
- The paper
- Cooper, W. N., Luharia, A., Evans, G. A., Raza, H., Haire, A. C., Grundy, R., Bowdin, S. C., Riccio, A., Sebastio, G., Bliek, J., Schofield, P. N., Reik, W., Macdonald, F., & Maher, E. R. (2005). Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome. European Journal of Human Genetics. https://doi.org/10.1038/sj.ejhg.5201463
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.
