The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
Imprinting in Prader–Willi and Angelman syndromes
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Citations
Cites
Role for DNA methylation in genomic imprinting
Li, E., Beard, C., & Jaenisch, R. (1993) · Nature · doi:10.1038/366362a0 · Cited by 1,964
Role for DNA methylation in genomic imprinting
Li, E., Beard, C., & Jaenisch, R. (1994) · Trends in Genetics · doi:10.1016/0168-9525(94)90228-3 · Cited by 1,691
UBE3A/E6-AP mutations cause Angelman syndrome
Kishino, T., Lalande, M., & Wagstaff, J. (1997) · Nature Genetics · doi:10.1038/ng0197-70 · Cited by 1,298
Brockdorff, N., Ashworth, A., Kay, G. F., McCabe, V. M., Norris, D. P., Cooper, P. J., Swift, S., & Rastan, S. (1992) · Cell · doi:10.1016/0092-8674(92)90519-i · Cited by 1,026
Protein ubiquitination involving an E1–E2–E3 enzyme ubiquitin thioester cascade
Scheffner, M., Nuber, U., & Huibregtse, J. M. (1995) · Nature · doi:10.1038/373081a0 · Cited by 1,016
A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase.
Huibregtse, J. M., Scheffner, M., Beaudenon, S., & Howley, P. M. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.7.2563 · Cited by 1,013
Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome
Nicholls, R. D., Knoll, J. H. M., Butler, M. G., Karam, S., & Lalande, M. (1989) · Nature · doi:10.1038/342281a0 · Cited by 879
Self-citationDe novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
Matsuura, T., Sutcliffe, J. S., Fang, P., Galjaard, R.-J., Jiang, Y.-H., Benton, C. S., Rommens, J. M., & Beaudet, A. L. (1997) · Nature Genetics · doi:10.1038/ng0197-74 · Cited by 856
STOGER, R. (1993) · Cell · doi:10.1016/0092-8674(93)90160-r · Cited by 598
Buiting, K., Saitoh, S., Gross, S., Dittrich, B., Schwartz, S., Nicholls, R. D., & Horsthemke, B. (1995) · Nature Genetics · doi:10.1038/ng0495-395 · Cited by 596
Self-citation
Cited by
Epigenetics in human disease and prospects for epigenetic therapy
Egger, G., Liang, G., Aparicio, A., & Jones, P. A. (2004) · Nature · doi:10.1038/nature02625 · Cited by 3,232
Genome Organization, Function, and Imprinting in Prader-Willi and Angelman Syndromes
Nicholls, R. D., & Knepper, J. L. (2001) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.2.1.153 · Cited by 625
Self-citationCavaillé, J., Buiting, K., Kiefmann, M., Lalande, M., Brannan, C. I., Horsthemke, B., Bachellerie, J.-P., Brosius, J., & Hüttenhofer, A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250426397 · Cited by 601
Self-citationSmilinich, 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-citationGenomic Imprinting: Implications for Human Disease
Falls, J. G., Pulford, D. J., Wylie, A. A., & Jirtle, R. L. (1999) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)65309-6 · Cited by 359
Metadata
- Authors
- Nicholls, R. D., Saitoh, S., & Horsthemke, B.
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 1998-05
- Volume
- 14
- Issue
- 5
- Pages
- 194-200
- ISSN
- 0168-9525 (ISSN-L)
- OpenAlex
- W2045857484
- Cited by
- 450
- References
- 58
- FWCI
- 4.92
- 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.
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- CoChat. (2026). Citation check: Imprinting in Prader–Willi and Angelman syndromes. https://app.cochat.ai/papers/10.1016/s0168-9525(98)01432-2
- The paper
- Nicholls, R. D., Saitoh, S., & Horsthemke, B. (1998). Imprinting in Prader–Willi and Angelman syndromes. Trends in Genetics. https://doi.org/10.1016/s0168-9525(98)01432-2
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.
