The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Testing for heterogeneity of recombination fraction values in Human Genetics
Abstract
SUMMARY: A method is described for the detection of heterogeneity of recombination fraction values in human data. It uses a comparison of likelihood values. It is applied to the data on elliptocytosis and rhesus previously considered by Morton (1956), together with some new data reported by Bannerman & Renwick (1962). Morton's conclusion that there exists heterogeneity is supported by the new test. The data appear to be best explained by the hypothesis that the families divide themselves into two groups. In the first group, which amounts to something between 20 and 90 % of the whole, the locus for elliptocytosis is closely linked with that for rhesus, the recombination fraction being between 0.01 and 0.1. In the remaining families the two loci are unlinked.
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Cites
Mahalanobis, P. C. (1954) · Dialectica · doi:10.1111/j.1746-8361.1954.tb01124.x · Cited by 1,717
Sequential tests for the detection of linkage.
Morton, N. E. (1955) · Europe PMC (PubMed Central) · Cited by 1,585
Consistency in Statistical Inference and Decision
Smith, C. A. B. (1961) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1961.tb00388.x · Cited by 557
Self-citationThe detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.
(1956) · Europe PMC (PubMed Central) · Cited by 436
Likelihood Inference and Time Series
Barnard, G. A., Jenkins, G. M., & Winsten, C. B. (1962) · Journal of the Royal Statistical Society. Series A (General) · doi:10.2307/2982406 · Cited by 206
GENETICAL LINKAGE BETWEEN THE ABO AND NAIL‐PATELLA LOCI
Renwick, J. H., & Lawler, S. D. (1955) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1955.tb01356.x · Cited by 166
Cited by
Germline p16 mutations in familial melanoma
Hussussian, C. J., Struewing, J. P., Goldstein, A. M., Higgins, P. A. T., Ally, D. S., Sheahan, M. D., Clark, W. H., Tucker, M. A., & Dracopoli, N. C. (1994) · Nature Genetics · doi:10.1038/ng0994-15 · Cited by 977
Localization of an ataxia-telangiectasia gene to chromosome 11q22–23
Gatti, R. A., Berkel, I., Boder, E., Braedt, G., Charmley, P., Concannon, P., Ersoy, F., Foroud, T., Jaspers, N. G. J., Lange, K., et al. (1988) · Nature · doi:10.1038/336577a0 · Cited by 686
Department of Obstetrics and Gynecology
(2015) · Juntendo Medical Journal · doi:10.14789/jmj.61.322 · Cited by 365
Evidence for a Susceptibility Gene for Autism on Chromosome 2 and for Genetic Heterogeneity
Buxbaum, J. D., Silverman, J. M., Smith, C. J., Kilifarski, M., Reichert, J., Hollander, E., Lawlor, B. A., Fitzgerald, M., Greenberg, D. A., & Davis, K. L. (2001) · The American Journal of Human Genetics · doi:10.1086/320588 · Cited by 321
Self-citationReplication of Linkage Studies of Complex Traits: An Examination of Variation in Location Estimates
Roberts, S. B., MacLean, C. J., Neale, M. C., Eaves, L. J., & Kendler, K. S. (1999) · The American Journal of Human Genetics · doi:10.1086/302528 · Cited by 274
Metadata
- Authors
- SMITH, C. A. B.
- Venue
- Annals of Human Genetics
- Publisher
- Wiley
- Published
- 1963-11
- Volume
- 27
- Issue
- 2
- Pages
- 175-182
- ISSN
- 0003-4800 (ISSN-L)
- 1469-1809
- OpenAlex
- W1989432434
- Cited by
- 297
- References
- 6
- FWCI
- 1.30
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
