The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Adjusting the focus on human variation
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Citations
Cites
The hitch-hiking effect of a favourable gene
Smith, J. M., & Haigh, J. (1974) · Genetical Research · doi:10.1017/s0016672300014634 · Cited by 3,415
Mitochondrial DNA and human evolution
Cann, R. L., Stoneking, M., & Wilson, A. C. (1987) · Nature · doi:10.1038/325031a0 · Cited by 3,100
Hudson, R. R., & Kaplan, N. L. (1985) · Genetics · doi:10.1093/genetics/111.1.147 · Cited by 1,555
Self-citationProspects for whole-genome linkage disequilibrium mapping of common disease genes
Kruglyak, L. (1999) · Nature Genetics · doi:10.1038/9642 · Cited by 1,416
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
Detecting Ancient Admixture in Humans Using Sequence Polymorphism Data
Wall, J. D. (2000) · Genetics · doi:10.1093/genetics/154.3.1271 · Cited by 116
Cited by
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
Are Rare Variants Responsible for Susceptibility to Complex Diseases?
Pritchard, J. K. (2001) · The American Journal of Human Genetics · doi:10.1086/321272 · Cited by 1,197
Interrogating a High-Density SNP Map for Signatures of Natural Selection
Akey, J. M., Zhang, G., Zhang, K., Jin, L., & Shriver, M. D. (2002) · Genome Research · doi:10.1101/gr.631202 · Cited by 964
Haplotype Variation and Linkage Disequilibrium in 313 Human Genes
Stephens, J. C., Schneider, J. A., Tanguay, D. A., Choi, J., Acharya, T., Stanley, S. E., Jiang, R., Messer, C. J., Chew, A., Han, J.-H., et al. (2001) · Science · doi:10.1126/science.1059431 · Cited by 873
Constructing genomic maps of positive selection in humans: Where do we go from here?
Akey, J. M. (2009) · Genome Research · doi:10.1101/gr.086652.108 · Cited by 426
Metadata
- Authors
- Przeworski, M., Hudson, R. R., & Di Rienzo, A.
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 2000-07
- Volume
- 16
- Issue
- 7
- Pages
- 296-302
- ISSN
- 0168-9525 (ISSN-L)
- OpenAlex
- W2157793907
- Cited by
- 273
- References
- 6
- FWCI
- 3.51
- 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.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Adjusting the focus on human variation. https://app.cochat.ai/papers/10.1016/s0168-9525(00)02030-8
- The paper
- Przeworski, M., Hudson, R. R., & Di Rienzo, A. (2000). Adjusting the focus on human variation. Trends in Genetics. https://doi.org/10.1016/s0168-9525(00)02030-8
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.
