The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
The origin of human aneuploidy: where we have been, where we are going
Open accessAbstract
Aneuploidy is the most common chromosome abnormality in humans, and is the leading genetic cause of miscarriage and congenital birth defects. Since the identification of the first human aneuploid conditions nearly a half-century ago, a great deal of information has accrued on its origin and etiology. We know that most aneuploidy derives from errors in maternal meiosis I, that maternal age is a risk factor for most, if not all, human trisomies, and that alterations in recombination are an important contributor to meiotic non-disjunction. In this review, we summarize some of the data that have led to these conclusions, and discuss some of the approaches now being used to address the underlying causes of meiotic non-disjunction in humans.
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Citations
Cites
To err (meiotically) is human: the genesis of human aneuploidy
Hassold, T., & Hunt, P. (2001) · Nature Reviews Genetics · doi:10.1038/35066065 · Cited by 2,441
Self-citation(1959) · PubMed · Cited by 820
Bisphenol A Exposure Causes Meiotic Aneuploidy in the Female Mouse
Hunt, P. A., Koehler, K. E., Susiarjo, M., Hodges, C. A., Ilagan, A., Voigt, R. C., Thomas, S., Thomas, B. F., & Hassold, T. J. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00189-1 · Cited by 636
Self-citationCritical roles for Dicer in the female germline
Murchison, E. P., Stein, P., Xuan, Z., Pan, H., Zhang, M. Q., Schultz, R. M., & Hannon, G. J. (2007) · Genes & Development · doi:10.1101/gad.1521307 · Cited by 497
THE SOMATIC CHROMOSOMES IN MONGOLISM
JACOBS, P. (1959) · The Lancet · doi:10.1016/s0140-6736(59)91892-6 · Cited by 387
Female Germ Cell Aneuploidy and Embryo Death in Mice Lacking the Meiosis-Specific Protein SCP3
Yuan, L., Liu, J.-G., Hoja, M.-R., Wilbertz, J., Nordqvist, K., & Höög, C. (2002) · Science · doi:10.1126/science.1070594 · Cited by 341
Derivation of male germ cells from bone marrow stem cells
Nayernia, K., Lee, J. H., Drusenheimer, N., Nolte, J., Wulf, G. G., Dressel, R., Gromoll, J., & Engel, W. (2006) · Laboratory Investigation · doi:10.1038/labinvest.3700429 · Cited by 334
Hodges, C. A., Revenkova, E., Jessberger, R., Hassold, T. J., & Hunt, P. A. (2005) · Nature Genetics · doi:10.1038/ng1672 · Cited by 315
Self-citationTrisomy Recurrence: A Reconsideration Based on North American Data
Warburton, D., Dallaire, L., Thangavelu, M., Ross, L., Levin, B., & Kline, J. (2004) · The American Journal of Human Genetics · doi:10.1086/423331 · Cited by 249
Lenzi, M. L., Smith, J., Snowden, T., Kim, M., Fishel, R., Poulos, B. K., & Cohen, P. E. (2005) · The American Journal of Human Genetics · doi:10.1086/427268 · Cited by 236
Cited by
The effect of sperm DNA fragmentation on miscarriage rates: a systematic review and meta-analysis
Robinson, L., Gallos, I. D., Conner, S. J., Rajkhowa, M., Miller, D., Lewis, S., Kirkman-Brown, J., & Coomarasamy, A. (2012) · Human Reproduction · doi:10.1093/humrep/des261 · Cited by 629
Stingele, S., Stoehr, G., Peplowska, K., Cox, J., Mann, M., & Storchova, Z. (2012) · Molecular Systems Biology · doi:10.1038/msb.2012.40 · Cited by 468
Mechanisms of oocyte aneuploidy associated with advanced maternal age
Mikwar, M., MacFarlane, A. J., & Marchetti, F. (2020) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2020.108320 · Cited by 308
Genome analyses of single human oocytes
Hou, Y., Fan, W., Yan, L., Li, R., Lian, Y., Huang, J., Li, J., Xu, L., Tang, F., Xie, X. S., et al. (2013) · Cell · doi:10.1016/j.cell.2013.11.040 · Cited by 302
The origin and impact of embryonic aneuploidy
Fragouli, E., Alfarawati, S., Spath, K., Jaroudi, S., Sarasa, J., Enciso, M., & Wells, D. (2013) · Human Genetics · doi:10.1007/s00439-013-1309-0 · Cited by 290
Metadata
- Authors
- Hassold, T., Hall, H., & Hunt, P.
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-07-31
- Volume
- 16
- Issue
- R2
- Pages
- R203-R208
- ISSN
- 0964-6906 (ISSN-L)
- 1460-2083
- OpenAlex
- W2160473082
- Cited by
- 649
- References
- 23
- FWCI
- 13.39
- Type
- journal article
- Language
- en
- Open access
- bronze
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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