The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
The rate of spontaneous mutation of a human gene
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Citations
Cites
A Mathematical Theory of Natural and Artificial Selection, Part V: Selection and Mutation
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Self-citation
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Cited by
Duan, D., Goemans, N., Takeda, S., Mercuri, E., & Aartsma-Rus, A. (2021) · Nature Reviews Disease Primers · doi:10.1038/s41572-021-00248-3 · Cited by 1,312
Characterization of the human factor VIII gene
Gitschier, J., Wood, W. I., Goralka, T. M., Wion, K. L., Chen, E. Y., Eaton, D. H., Vehar, G. A., Capon, D. J., & Lawn, R. M. (1984) · Nature · doi:10.1038/312326a0 · Cited by 988
Rate, molecular spectrum, and consequences of human mutation
Lynch, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912629107 · Cited by 792
Variation in genome-wide mutation rates within and between human families
the 1000 Genomes Project (2011) · Nature Genetics · doi:10.1038/ng.862 · Cited by 581
Revising the human mutation rate: implications for understanding human evolution
Scally, A., & Durbin, R. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3295 · Cited by 610
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
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Repping, S., Skaletsky, H., Brown, L., van Daalen, S. K. M., Korver, C. M., Pyntikova, T., Kuroda-Kawaguchi, T., de Vries, J. W. A., Oates, R. D., Silber, S., et al. (2003) · Nature Genetics · doi:10.1038/ng1250 · Cited by 425
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Genotype Versus Phenotype in Families with Androgen Insensitivity Syndrome
Boehmer, A. L. M., Brüggenwirth, H., van Assendelft, C., Otten, B. J., Verleun-Mooijman, M. C. T., Niermeijer, M. F., Brunner, H. G., Rouwé, C. W., Waelkens, J. J., Oostdijk, W., et al. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.9.7825 · Cited by 290
Determinants of Mutation Rate Variation in the Human Germline
Ségurel, L., Wyman, M. J., & Przeworski, M. (2014) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-031714-125740 · Cited by 289
Properties and rates of germline mutations in humans
Campbell, C. D., & Eichler, E. E. (2013) · Trends in Genetics · doi:10.1016/j.tig.2013.04.005 · Cited by 275
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Estimating the human mutation rate using autozygosity in a founder population.
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A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations: Table 1
Wilson, J. R. F., Bateman, A. C., Hanson, H., An, Q., Evans, G., Rahman, N., Jones, J. L., & Eccles, D. M. (2010) · Journal of Medical Genetics · doi:10.1136/jmg.2010.078113 · Cited by 122
An Estimate of the Average Number of Recessive Lethal Mutations Carried by Humans
Gao, Z., Waggoner, D., Stephens, M., Ober, C., & Przeworski, M. (2015) · Genetics · doi:10.1534/genetics.114.173351 · Cited by 109
De Novo Rates and Selection of Schizophrenia-Associated Copy Number Variants
Rees, E., Moskvina, V., Owen, M. J., O'Donovan, M. C., & Kirov, G. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.07.011 · Cited by 94
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Mutation rates and the evolution of germline structure
Scally, A. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0137 · Cited by 58
X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism
Wang, Y., Busin, R., Reeves, C., Bezman, L., Raymond, G., Toomer, C. J., Watkins, P. A., Snowden, A., Moser, A., Naidu, S., et al. (2011) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2011.05.016 · Cited by 58
Aging genomes: A necessary evil in the logic of life
Vijg, J. (2014) · BioEssays · doi:10.1002/bies.201300127 · Cited by 25
Metadata
- Authors
- Haldane, J. B. S.
- Venue
- Journal of Genetics
- Published
- 2004-12
- Volume
- 83
- Issue
- 3
- Pages
- 235-244
- ISSN
- 0022-1333 (ISSN-L)
- 0973-7731
- OpenAlex
- W2030297710
- Cited by
- 472
- References
- 1
- FWCI
- 6.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
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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.
