The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
Worldwide Distribution of a Common Methylenetetrahydrofolate Reductase Mutation
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Frosst, P., Blom, H. J., Milos, R., Goyette, P., Sheppard, C. A., Matthews, R. G., Boers, G. J. H., den Heijer, M., Kluijtmans, L. A. J., van den Heuve, L. P., et al. (1995) · Nature Genetics · doi:10.1038/ng0595-111 · Cited by 5,653
World distribution of factor V Leiden
Rees, D. C., Cox, M., & Clegg, J. B. (1995) · The Lancet · doi:10.1016/s0140-6736(95)91803-5 · Cited by 1,156
Self-citationGlobal prevalence of putative haemochromatosis mutations.
Merryweather-Clarke, A. T., Pointon, J. J., Shearman, J. D., & Robson, K. J. (1997) · Journal of Medical Genetics · doi:10.1136/jmg.34.4.275 · Cited by 789
POSSIBLE PREVENTION OF NEURAL-TUBE DEFECTS BY PERICONCEPTIONAL VITAMIN SUPPLEMENTATION
Smithells, R. W., Sheppard, S., Schorah, C. J., Seller, M. J., Nevin, N. C., Harris, R., Read, A. P., & Fielding, D. W. (1980) · The Lancet · doi:10.1016/s0140-6736(80)90886-7 · Cited by 658
Global distribution of the CCR5 gene 32-basepair deletion
Martinson, J. J., Chapman, N. H., Rees, D. C., Liu, Y.-T., & Clegg, J. B. (1997) · Nature Genetics · doi:10.1038/ng0597-100 · Cited by 539
Self-citationA methylenetetrahydrofolate reductase polymorphism and the risk of colorectal cancer.
Chen, J., Giovannucci, E. L., Kelsey, K. T., Rimm, E. B., Stampfer, M. J., Colditz, G. A., Spiegelman, D. L., Willett, W. C., & Hunter, D. J. (1996) · PubMed · Cited by 516
Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia.
Engbersen, A. M. T., Franken, D. G., Boers, G. H. J., Stevens, E. M., Trijbels, F. J. M., & Blom, H. J. (1995) · Europe PMC (PubMed Central) · Cited by 422
van der Put, N. (1997) · QJM · doi:10.1093/qjmed/90.2.111 · Cited by 236
Methylenetetrahydrofolate reductase polymorphism and pre-eclampsia.
Sohda, S., Arinami, T., Hamada, H., Yamada, N., Hamaguchi, H., & Kubo, T. (1997) · Journal of Medical Genetics · doi:10.1136/jmg.34.6.525 · Cited by 212
Differences in methylenetetrahydrofolate reductase genotype frequencies, between Whites and Blacks.
Stevenson, R. E., Schwartz, C. E., Du, Y., & Adams, M. J. (1997) · PubMed · Cited by 111
Cited by
The controversy over homocysteine and cardiovascular risk
Ueland, P. M., Refsum, H., Beresford, S. A., & Vollset, S. E. (2000) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/72.2.324 · Cited by 517
Liew, S.-C., & Gupta, E. D. (2015) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2014.10.004 · Cited by 466
Update on Cobalamin, Folate, and Homocysteine
Carmel, R., Green, R., Rosenblatt, D. S., & Watkins, D. (2003) · Hematology · doi:10.1182/asheducation-2003.1.62 · Cited by 391
Aberrations in folate metabolic pathway and altered susceptibility to autism
Mohammad, N. S., Jain, J. M. N., Chintakindi, K. P., Singh, R. P., Naik, U., & Akella, R. R. D. (2009) · Psychiatric Genetics · doi:10.1097/ypg.0b013e32832cebd2 · Cited by 95
Rai, V. (2017) · Molecular Neurobiology · doi:10.1007/s12035-016-9722-8 · Cited by 88
Metadata
- Authors
- Schneider, J. A., Rees, D. C., Liu, Y.-T., & Clegg, J. B.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 1998-05
- Volume
- 62
- Issue
- 5
- Pages
- 1258-1260
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2079919793
- Cited by
- 263
- References
- 12
- FWCI
- 8.39
- Type
- journal article
- Language
- en
- Open access
- bronze
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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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- This page
- CoChat. (2026). Citation check: Worldwide Distribution of a Common Methylenetetrahydrofolate Reductase Mutation. https://app.cochat.ai/papers/10.1086/301836
- The paper
- Schneider, J. A., Rees, D. C., Liu, Y.-T., & Clegg, J. B. (1998). Worldwide Distribution of a Common Methylenetetrahydrofolate Reductase Mutation. The American Journal of Human Genetics. https://doi.org/10.1086/301836
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.
