The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
Human SNP variability and mutation rate are higher in regions of high recombination
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Citations
Cites
(1993) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040023 · Cited by 11,229
The hitch-hiking effect of a favourable gene
Smith, J. M., & Haigh, J. (1974) · Genetical Research · doi:10.1017/s0016672300014634 · Cited by 3,415
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
The International SNP Map Working Group, Laboratories:, C. S. H., Sachidanandam, R., Weissman, D., Schmidt, S. C., Kakol, J. M., Stein, L. D., National Center for Biotechnology Information:, Marth, G., Sherry, S., et al. (2001) · Nature · doi:10.1038/35057149 · Cited by 2,977
The hitch-hiking effect of a favourable gene
MAYNARD, J., & HAIGH, J. (2007) · Genetics Research · doi:10.1017/s0016672308009579 · Cited by 2,643
Levels of naturally occurring DNA polymorphism correlate with recombination rates in D. melanogaster
Begun, D. J., & Aquadro, C. F. (1992) · Nature · doi:10.1038/356519a0 · Cited by 953
Isochores and the evolutionary genomics of vertebrates
Bernardi, G. (2000) · Gene · doi:10.1016/s0378-1119(99)00485-0 · Cited by 569
Duret, L., & Mouchiroud, D. (2000) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a026239 · Cited by 513
Deleterious background selection with recombination.
Hudson, R. R., & Kaplan, N. L. (1995) · Genetics · doi:10.1093/genetics/141.4.1605 · Cited by 448
The effect of background selection against deleterious mutations on weakly selected, linked variants
Charlesworth, B. (1994) · Genetical Research · doi:10.1017/s0016672300032365 · Cited by 366
Single nucleotide polymorphisms and recombination rate in humans
Nachman, M. W. (2001) · Trends in Genetics · doi:10.1016/s0168-9525(01)02409-x · Cited by 311
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
Initial sequence of the chimpanzee genome and comparison with the human genome
The Chimpanzee Sequencing and Analysis Consortium (2005) · Nature · doi:10.1038/nature04072 · Cited by 2,459
Determinants of genetic diversity
Ellegren, H., & Galtier, N. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.58 · Cited by 874
Chromatin organization is a major influence on regional mutation rates in human cancer cells
Schuster-Böckler, B., & Lehner, B. (2012) · Nature · doi:10.1038/nature11273 · Cited by 657
Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation
Michaelson, J. J., Shi, Y., Gujral, M., Zheng, H., Malhotra, D., Jin, X., Jian, M., Liu, G., Greer, D., Bhandari, A., et al. (2012) · Cell · doi:10.1016/j.cell.2012.11.019 · Cited by 544
Metadata
- Authors
- Lercher, M. J., & Hurst, L. D.
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 2002-07
- Volume
- 18
- Issue
- 7
- Pages
- 337-340
- ISSN
- 0168-9525 (ISSN-L)
- OpenAlex
- W2034078054
- Cited by
- 364
- References
- 36
- FWCI
- 2.24
- 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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- CoChat. (2026). Citation check: Human SNP variability and mutation rate are higher in regions of high recombination. https://app.cochat.ai/papers/10.1016/s0168-9525(02)02669-0
- The paper
- Lercher, M. J., & Hurst, L. D. (2002). Human SNP variability and mutation rate are higher in regions of high recombination. Trends in Genetics. https://doi.org/10.1016/s0168-9525(02)02669-0
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.
