The DOI matches its Crossref record; 20 of the 20 references it cites were found in a registry or an index.
Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Nonparametric Statistics for the Behavioral Sciences
Guitton, H., & Siegel, S. (1958) · Revue économique · doi:10.2307/3498751 · Cited by 35,245
Hypervariable ‘minisatellite’ regions in human DNA
Jeffreys, A. J., Wilson, V., & Thein, S. L. (1985) · Nature · doi:10.1038/314067a0 · Cited by 3,741
Self-citationSlipped-strand mispairing: a major mechanism for DNA sequence evolution.
(1987) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040442 · Cited by 2,245
Individual-specific ‘fingerprints’ of human DNA
Jeffreys, A. J., Wilson, V., & Thein, S. L. (1985) · Nature · doi:10.1038/316076a0 · Cited by 2,150
Self-citationVariable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping
Nakamura, Y., Leppert, M., O'Connell, P., Wolff, R., Holm, T., Culver, M., Martin, C., Fujimoto, E., Hoff, M., Kumlin, E., et al. (1987) · Science · doi:10.1126/science.3029872 · Cited by 1,654
Ohta, T., & Kimura, M. (1973) · Genetical Research · doi:10.1017/s0016672300012994 · Cited by 1,176
Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue
Capon, D. J., Chen, E. Y., Levinson, A. D., Seeburg, P. H., & Goeddel, D. V. (1983) · Nature · doi:10.1038/302033a0 · Cited by 997
Positive identification of an immigration test-case using human DNA fingerprints
Jeffreys, A. J., Brookfield, J. F. Y., & Semeonoff, R. (1985) · Nature · doi:10.1038/317818a0 · Cited by 594
Self-citationCharacterization of a panel of highly variable minisatellites cloned from human DNA
WONG, Z., WILSON, V., PATEL, I., POVEY, S., & JEFFREYS, A. J. (1987) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1987.tb01062.x · Cited by 522
Self-citationBell, G. I., Selby, M. J., & Rutter, W. J. (1982) · Nature · doi:10.1038/295031a0 · Cited by 520
Cited by
Brook, J. D., McCurrach, M. E., Harley, H. G., Buckler, A. J., Church, D., Aburatani, H., Hunter, K., Stanton, V. P., Thirion, J.-P., Hudson, T., et al. (1992) · Cell · doi:10.1016/0092-8674(92)90154-5 · Cited by 2,777
Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Pieretti, M., Sutcliffe, J. S., Richards, S., Verkert, A. J. M. H., Holden, J. J. A., Fenwick, R. G., Warren, S. T., et al. (1991) · Cell · doi:10.1016/0092-8674(91)90283-5 · Cited by 2,080
Boerwinkle, E., Leffert, C. C., Lin, J., Lackner, C., Chiesa, G., & Hobbs, H. H. (1992) · Journal of Clinical Investigation · doi:10.1172/jci115855 · Cited by 962
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland
Hästbacka, J., de la Chapelle, A., Kaitila, I., Sistonen, P., Weaver, A., & Lander, E. (1992) · Nature Genetics · doi:10.1038/ng1192-204 · Cited by 558
Innerarity, T., Mahley, R., Weisgraber, K., Bersot, T., Krauss, R., Vega, G., Grundy, S., Friedl, W., Davignon, J., & McCarthy, B. (1990) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)42605-7 · Cited by 352
Metadata
- Authors
- Jeffreys, A. J., Royle, N. J., Wilson, V., & Wong, Z.
- Venue
- Nature
- Published
- 1988-03
- Volume
- 332
- Issue
- 6161
- Pages
- 278-281
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2088073190
- Cited by
- 759
- References
- 20
- FWCI
- 38.71
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. https://app.cochat.ai/papers/10.1038/332278a0
- The paper
- Jeffreys, A. J., Royle, N. J., Wilson, V., & Wong, Z. (1988). Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. Nature. https://doi.org/10.1038/332278a0
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.