The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
Fine-scale recombination rate differences between sexes, populations and individuals
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Citations
Cites
Maximum Likelihood from Incomplete Data Via the EM Algorithm
Dempster, A. P., Laird, N. M., & Rubin, D. B. (1977) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1977.tb01600.x · Cited by 50,444
A haplotype map of the human genome
The International HapMap Consortium (2005) · Nature · doi:10.1038/nature04226 · Cited by 5,858
Genomic Control for Association Studies
Devlin, B., & Roeder, K. (1999) · Biometrics · doi:10.1111/j.0006-341x.1999.00997.x · Cited by 3,162
Drive Against Hotspot Motifs in Primates Implicates the PRDM9 Gene in Meiotic Recombination
Myers, S., Bowden, R., Tumian, A., Bontrop, R. E., Freeman, C., MacFie, T. S., McVean, G., & Donnelly, P. (2010) · Science · doi:10.1126/science.1182363 · Cited by 683
Prdm9 Controls Activation of Mammalian Recombination Hotspots
Parvanov, E. D., Petkov, P. M., & Paigen, K. (2010) · Science · doi:10.1126/science.1181495 · Cited by 610
Parental origin of sequence variants associated with complex diseases
DIAGRAM Consortium, Kong, A., Steinthorsdottir, V., Masson, G., Thorleifsson, G., Sulem, P., Besenbacher, S., Jonasdottir, A., Sigurdsson, A., Kristinsson, K. T., et al. (2009) · Nature · doi:10.1038/nature08625 · Cited by 553
Self-citationDetection of sharing by descent, long-range phasing and haplotype imputation
Kong, A., Masson, G., Frigge, M. L., Gylfason, A., Zusmanovich, P., Thorleifsson, G., Olason, P. I., Ingason, A., Steinberg, S., Rafnar, T., et al. (2008) · Nature Genetics · doi:10.1038/ng.216 · Cited by 447
Self-citationBasonuclin-2 requirements for zebrafish adult pigment pattern development and female fertility
Lang, M. R., Patterson, L. B., Gordon, T. N., Johnson, S. L., & Parichy, D. M. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000744 · Cited by 86
Research works printed but not linked: 10
- McVean, G. A. et al. The fine-scale structure of recombination rate variation in the human genome. Science 304, 581–584 (2004) · DOI · Paper page
- Myers, S., Bottolo, L., Freeman, C., McVean, G. & Donnelly, P. A fine-scale map of recombination rates and hotspots across the human genome. Science 310, 321–324 (2005) · DOI · Paper page
- Myers, S., Freeman, C., Auton, A., Donnelly, P. & McVean, G. A common sequence motif associated with recombination hot spots and genome instability in humans. Nature Genet. 40, 1124–1129 (2008) · DOI · Paper page
- Baudat, F. et al. PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice. Science 327, 836–840 (2010) · DOI · Paper page
- O’Reilly, P. F., Birney, E. & Balding, D. J. Confounding between recombination and selection, and the Ped/Pop method for detecting selection. Genome Res. 18, 1304–1313 (2008) · DOI
- Kong, A. et al. A high-resolution recombination map of the human genome. Nature Genet. 31, 241–247 (2002) · DOI · Paper page
- Broman, K. W., Murray, J. C., Sheffield, V. C., White, R. L. & Weber, J. L. Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am. J. Hum. Genet. 63, 861–869 (1998) · DOI · Paper page
- Kong, A. et al. Sequence variants in the RNF212 gene associate with genome-wide recombination rate. Science 319, 1398–1401 (2008) · DOI · Paper page
- Akey, J. M. Constructing genomic maps of positive selection in humans: where do we go from here? Genome Res. 19, 711–722 (2009) · DOI · Paper page
- Stefansson, H. et al. A common inversion under selection in Europeans. Nature Genet. 37, 129–137 (2005) · DOI · Paper page
Cited by
A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline
Jonsson, T., Atwal, J. K., Steinberg, S., Snaedal, J., Jonsson, P. V., Bjornsson, S., Stefansson, H., Sulem, P., Gudbjartsson, D., Maloney, J., et al. (2012) · Nature · doi:10.1038/nature11283 · Cited by 1,738
Self-citationThe evolution of lncRNA repertoires and expression patterns in tetrapods
Necsulea, A., Soumillon, M., Warnefors, M., Liechti, A., Daish, T., Zeller, U., Baker, J. C., Grützner, F., & Kaessmann, H. (2014) · Nature · doi:10.1038/nature12943 · Cited by 984
Determinants of genetic diversity
Ellegren, H., & Galtier, N. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.58 · Cited by 874
A genetic atlas of human admixture history
Hellenthal, G., Busby, G. B. J., Band, G., Wilson, J. F., Capelli, C., Falush, D., & Myers, S. (2014) · Science · doi:10.1126/science.1243518 · Cited by 798
Major Histocompatibility Complex Genomics and Human Disease
Trowsdale, J., & Knight, J. C. (2013) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-091212-153455 · Cited by 759
Metadata
- Authors
- Kong, A., Thorleifsson, G., Gudbjartsson, D. F., Masson, G., Sigurdsson, A., Jonasdottir, A., Walters, G. B., Jonasdottir, A., Gylfason, A., Kristinsson, K. T., Gudjonsson, S. A., Frigge, M. L., Helgason, A., Thorsteinsdottir, U., & Stefansson, K.
- Venue
- Nature
- Published
- 2010-10
- Volume
- 467
- Issue
- 7319
- Pages
- 1099-1103
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2029983700
- Cited by
- 582
- References
- 8
- FWCI
- 20.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
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- CoChat. (2026). Citation check: Fine-scale recombination rate differences between sexes, populations and individuals. https://app.cochat.ai/papers/10.1038/nature09525
- The paper
- Kong, A., Thorleifsson, G., Gudbjartsson, D. F., Masson, G., Sigurdsson, A., Jonasdottir, A., Walters, G. B., Jonasdottir, A., Gylfason, A., Kristinsson, K. T., Gudjonsson, S. A., Frigge, M. L., Helgason, A., Thorsteinsdottir, U., & Stefansson, K. (2010). Fine-scale recombination rate differences between sexes, populations and individuals. Nature. https://doi.org/10.1038/nature09525
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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.
