The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
A common sequence motif associated with recombination hot spots and genome instability in humans
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Citations
Cites
A second generation human haplotype map of over 3.1 million SNPs
The International HapMap Consortium (2007) · Nature · doi:10.1038/nature06258 · Cited by 4,438
A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome
Myers, S., Bottolo, L., Freeman, C., McVean, G., & Donnelly, P. (2005) · Science · doi:10.1126/science.1117196 · Cited by 1,134
Self-citationJeffreys, A. J., Kauppi, L., & Neumann, R. (2001) · Nature Genetics · doi:10.1038/ng1001-217 · Cited by 835
Human Rad51 Protein Promotes ATP-Dependent Homologous Pairing and Strand Transfer Reactions In Vitro
Baumann, P., Benson, F. E., & West, S. C. (1996) · Cell · doi:10.1016/s0092-8674(00)81394-x · Cited by 689
Coop, G., Wen, X., Ober, C., Pritchard, J. K., & Przeworski, M. (2008) · Science · doi:10.1126/science.1151851 · Cited by 368
Mutational Mechanisms of Williams-Beuren Syndrome Deletions
Bayés, M., Magano, L. F., Rivera, N., Flores, R., & A. Pérez Jurado, L. (2003) · The American Journal of Human Genetics · doi:10.1086/376565 · Cited by 337
Reiter, L. T., Murakami, T., Koeuth, T., Pentao, L., Muzny, D. M., Gibbs, R. A., & Lupski, J. R. (1996) · Nature Genetics · doi:10.1038/ng0396-288 · Cited by 296
Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot
Jeffreys, A. J., & Neumann, R. (2002) · Nature Genetics · doi:10.1038/ng910 · Cited by 233
Jeffreys, A. J., Murray, J., & Neumann, R. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80138-0 · Cited by 216
Minisatellites: Mutability and Genome Architecture
Vergnaud, G., & Denoeud, F. (2000) · Genome Research · doi:10.1101/gr.10.7.899 · Cited by 208
Cited by
A map of human genome variation from population-scale sequencing.
The 1000 Genomes Project Consortium (2010) · Nature · doi:10.1038/nature09534 · Cited by 7,877
Origins and functional impact of copy number variation in the human genome
The Wellcome Trust Case Control Consortium, Conrad, D. F., Pinto, D., Redon, R., Feuk, L., Gokcumen, O., Zhang, Y., Aerts, J., Andrews, T. D., Barnes, C., et al. (2010) · Nature · doi:10.1038/nature08516 · Cited by 1,970
Mechanisms of change in gene copy number
Hastings, P. J., Lupski, J. R., Rosenberg, S. M., & Ira, G. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2593 · Cited by 1,316
Copy number variation in human health, disease, and evolution
Zhang, F., Gu, W., Hurles, M. E., & Lupski, J. R. (2009) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.9.081307.164217 · Cited by 1,207
PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice
Baudat, F., Buard, J., Grey, C., Fledel-Alon, A., Ober, C., Przeworski, M., Coop, G., & de Massy, B. (2010) · Science · doi:10.1126/science.1183439 · Cited by 1,026
Metadata
- Authors
- Myers, S., Freeman, C., Auton, A., Donnelly, P., & McVean, G.
- Venue
- Nature Genetics
- Published
- 2008-08-24
- Volume
- 40
- Issue
- 9
- Pages
- 1124-1129
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2013550946
- Cited by
- 447
- References
- 26
- FWCI
- 16.63
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: A common sequence motif associated with recombination hot spots and genome instability in humans. https://app.cochat.ai/papers/10.1038/ng.213
- The paper
- Myers, S., Freeman, C., Auton, A., Donnelly, P., & McVean, G. (2008). A common sequence motif associated with recombination hot spots and genome instability in humans. Nature Genetics. https://doi.org/10.1038/ng.213
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.
