The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Segregation at three loci explains familial and population risk in Hirschsprung disease
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Citations
Cites
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PedCheck: A Program for Identification of Genotype Incompatibilities in Linkage Analysis
O'Connell, J. R., & Weeks, D. E. (1998) · The American Journal of Human Genetics · doi:10.1086/301904 · Cited by 2,056
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
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Cited by
Hirschsprung disease, associated syndromes and genetics: a review
Amiel, J., Sproat-Emison, E., Garcia-Barcelo, M., Lantieri, F., Burzynski, G., Borrego, S., Pelet, A., Arnold, S., Miao, X., Griseri, P., et al. (2008) · Journal of Medical Genetics · doi:10.1136/jmg.2007.053959 · Cited by 1,206
Self-citationGenomic views of distant-acting enhancers
Visel, A., Rubin, E. M., & Pennacchio, L. A. (2009) · Nature · doi:10.1038/nature08451 · Cited by 610
Heanue, T. A., & Pachnis, V. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2137 · Cited by 527
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk
Emison, E. S., McCallion, A. S., Kashuk, C. S., Bush, R. T., Grice, E., Lin, S., Portnoy, M. E., Cutler, D. J., Green, E. D., & Chakravarti, A. (2005) · Nature · doi:10.1038/nature03467 · Cited by 462
Self-citationKorbel, J. O., Tirosh-Wagner, T., Urban, A. E., Chen, X.-N., Kasowski, M., Dai, L., Grubert, F., Erdman, C., Gao, M. C., Lange, K., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813248106 · Cited by 399
Metadata
- Authors
- Gabriel, S. B., Salomon, R., Pelet, A., Angrist, M., Amiel, J., Fornage, M., Attié-Bitach, T., Olson, J. M., Hofstra, R., Buys, C., Steffann, J., Munnich, A., Lyonnet, S., & Chakravarti, A.
- Venue
- Nature Genetics
- Published
- 2002-04-15
- Volume
- 31
- Issue
- 1
- Pages
- 89-93
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1983558993
- Cited by
- 275
- References
- 27
- FWCI
- 25.41
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Segregation at three loci explains familial and population risk in Hirschsprung disease. https://app.cochat.ai/papers/10.1038/ng868
- The paper
- Gabriel, S. B., Salomon, R., Pelet, A., Angrist, M., Amiel, J., Fornage, M., Attié-Bitach, T., Olson, J. M., Hofstra, R., Buys, C., Steffann, J., Munnich, A., Lyonnet, S., & Chakravarti, A. (2002). Segregation at three loci explains familial and population risk in Hirschsprung disease. Nature Genetics. https://doi.org/10.1038/ng868
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.
