The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and 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 maintains differential methylation at the Igf2/H19 locus
Schoenherr, C. J., Levorse, J. M., & Tilghman, S. M. (2003) · Nature Genetics · doi:10.1038/ng1057 · Cited by 320
Cited by
A decade of exploring the cancer epigenome—biological and translational implications
Baylin, S. B., & Jones, P. A. (2011) · Nature Reviews Cancer · doi:10.1038/nrc3130 · Cited by 2,871
Phenotypic plasticity and the epigenetics of human disease
Feinberg, A. P. (2007) · Nature · doi:10.1038/nature05919 · Cited by 1,613
Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome
Cooper, W. N., Luharia, A., Evans, G. A., Raza, H., Haire, A. C., Grundy, R., Bowdin, S. C., Riccio, A., Sebastio, G., Bliek, J., et al. (2005) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201463 · Cited by 304
Self-citationWeksberg, R., Shuman, C., & Smith, A. C. (2005) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.30058 · Cited by 307
Temple, I. K., Shrubb, V, Lever, M., Bullman, H., & Mackay, D. J. G. (2007) · Journal of Medical Genetics · doi:10.1136/jmg.2007.050807 · Cited by 63
Metadata
- Authors
- Sparago, A., Cerrato, F., Vernucci, M., Ferrero, G. B., Silengo, M. C., & Riccio, A.
- Venue
- Nature Genetics
- Published
- 2004-08-15
- Volume
- 36
- Issue
- 9
- Pages
- 958-960
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1975680353
- Cited by
- 371
- References
- 2
- FWCI
- 11.95
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome. https://app.cochat.ai/papers/10.1038/ng1410
- The paper
- Sparago, A., Cerrato, F., Vernucci, M., Ferrero, G. B., Silengo, M. C., & Riccio, A. (2004). Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome. Nature Genetics. https://doi.org/10.1038/ng1410
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.
