The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Single nucleotide polymorphisms and recombination rate in humans
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Citations
Cites
The sequence of the human genome
Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) · Science · doi:10.1126/science.1058040 · Cited by 13,909
The hitch-hiking effect of a favourable gene
Smith, J. M., & Haigh, J. (1974) · Genetical Research · doi:10.1017/s0016672300014634 · Cited by 3,415
Clark, A. G., Weiss, K. M., Nickerson, D. A., Taylor, S. L., Buchanan, A., Stengård, J., Salomaa, V., Vartiainen, E., Perola, M., Boerwinkle, E., et al. (1998) · The American Journal of Human Genetics · doi:10.1086/301977 · Cited by 435
Wiehe, T. (1998) · Theoretical Population Biology · doi:10.1006/tpbi.1997.1346 · Cited by 77
Cited by
Initial sequencing and comparative analysis of the mouse genome
Mouse Genome Sequencing Consortium (2002) · Nature · doi:10.1038/nature01262 · Cited by 7,187
The power and promise of population genomics: from genotyping to genome typing
Luikart, G., England, P. R., Tallmon, D., Jordan, S., & Taberlet, P. (2003) · Nature Reviews Genetics · doi:10.1038/nrg1226 · Cited by 1,365
Determinants of genetic diversity
Ellegren, H., & Galtier, N. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.58 · Cited by 874
Forces shaping the fastest evolving regions in the human genome
Pollard, K. S., Salama, S. R., King, B., Kern, A. D., Dreszer, T., Katzman, S., Siepel, A., Pedersen, J. S., Bejerano, G., Baertsch, R., et al. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020168 · Cited by 511
The Signature of Positive Selection at Randomly Chosen Loci
Przeworski, M. (2002) · Genetics · doi:10.1093/genetics/160.3.1179 · Cited by 503
Metadata
- Authors
- Nachman, M. W.
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 2001-09
- Volume
- 17
- Issue
- 9
- Pages
- 481-485
- ISSN
- 0168-9525 (ISSN-L)
- OpenAlex
- W2102668767
- Cited by
- 311
- References
- 4
- FWCI
- 1.85
- Type
- journal article
- Language
- en
- Open access
- closed
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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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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
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- CoChat. (2026). Citation check: Single nucleotide polymorphisms and recombination rate in humans. https://app.cochat.ai/papers/10.1016/s0168-9525(01)02409-x
- The paper
- Nachman, M. W. (2001). Single nucleotide polymorphisms and recombination rate in humans. Trends in Genetics. https://doi.org/10.1016/s0168-9525(01)02409-x
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.
