The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
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Citations
Cites
Bosma, P. J., Chowdhury, J. R., Bakker, C., Gantla, S., de Boer, A., Oostra, B. A., Lindhout, D., Tytgat, G. N. J., Jansen, P. L. M., Elferink, R. P. J. O., et al. (1995) · New England Journal of Medicine · doi:10.1056/nejm199511023331802 · Cited by 1,447
Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups
Edwards, A., Hammond, H. A., Jin, L., Caskey, C. T., & Chakraborty, R. (1992) · Genomics · doi:10.1016/0888-7543(92)90371-x · Cited by 1,426
Reaven, G. M. (1994) · PubMed · Cited by 241
Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
Aono, S., Keino, H., Yamada, Y., Adachi, Y., Nanno, T., Uyama, E., Koiwai, O., & Sato, H. (1995) · The Lancet · doi:10.1016/s0140-6736(95)90702-5 · Cited by 192
Population studies on Gilbert's syndrome.
Owens, D., & Evans, J. (1975) · Journal of Medical Genetics · doi:10.1136/jmg.12.2.152 · Cited by 189
Decreased glucuronidation and increased bioactivation of acetaminophen in Gilbert's syndrome
De Morais, S. M. F., Uetrecht, J. P., & Wells, P. G. (1992) · Gastroenterology · doi:10.1016/0016-5085(92)90106-9 · Cited by 160
Koiwai, O., Nishizawa, M., Hasada, K., et al. (1995) · Human Molecular Genetics · doi:10.1093/hmg/4.7.1183 · Cited by 158
Bailey, A., Robinson, D. A., & Dawson, A. (1977) · The Lancet · doi:10.1016/s0140-6736(77)92226-7 · Cited by 89
Moghrabi, N. N., Clarke, D. J., Boxer, M., et al. (1993) · Genomics · doi:10.1006/geno.1993.1451 · Cited by 83
Alteration of drug metabolism in Gilbert's syndrome.
Carulli, N., de Leòn, M. P., Mauro, E., et al. (1976) · Gut · doi:10.1136/gut.17.8.581 · Cited by 51
Cited by
Human UDP-Glucuronosyltransferases: Metabolism, Expression, and Disease
Tukey, R. H., & Strassburg, C. P. (2000) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.40.1.581 · Cited by 1,523
Innocenti, F., Undevia, S. D., Iyer, L., Xian Chen, P., Das, S., Kocherginsky, M., Karrison, T., Janisch, L., Ramírez, J., Rudin, C. M., et al. (2004) · Journal of Clinical Oncology · doi:10.1200/jco.2004.07.173 · Cited by 964
Beutler, E., Gelbart, T., & Demina, A. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.14.8170 · Cited by 853
UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity
Iyer, L., Das, S., Janisch, L., Wen, M., Ramírez, J., Karrison, T., Fleming, G. F., Vokes, E. E., Schilsky, R. L., & Ratain, M. J. (2002) · The Pharmacogenomics Journal · doi:10.1038/sj.tpj.6500072 · Cited by 720
Iyer, L., King, C. D., Whitington, P. F., Green, M. D., Roy, S. K., Tephly, T. R., Coffman, B. L., & Ratain, M. J. (1998) · Journal of Clinical Investigation · doi:10.1172/jci915 · Cited by 686
Metadata
- Authors
- Monaghan, G., Ryan, M., Hume, R., Burchell, B., & Seddon, R.
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 1996-03
- Volume
- 347
- Issue
- 9001
- Pages
- 578-581
- ISSN
- 0099-5355 (ISSN-L)
- 0140-6736
- OpenAlex
- W2089720722
- Cited by
- 585
- References
- 12
- FWCI
- 27.09
- Type
- journal article
- Language
- en
- Open access
- closed
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- This page
- CoChat. (2026). Citation check: Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome. https://app.cochat.ai/papers/10.1016/s0140-6736(96)91273-8
- The paper
- Monaghan, G., Ryan, M., Hume, R., Burchell, B., & Seddon, R. (1996). Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome. The Lancet. https://doi.org/10.1016/s0140-6736(96)91273-8
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.