The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection
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Citations
Cites
Sun, C., Skaletsky, H., Rozen, S., Gromoll, J., Nieschlag, E., Oates, R., & Page, D. C. (2000) · Human Molecular Genetics · doi:10.1093/oxfordjournals.hmg.a018920 · Cited by 247
Self-citation
Cited by
Krausz, C., Hoefsloot, L., Simoni, M., & Tüttelmann, F. (2014) · Andrology · doi:10.1111/j.2047-2927.2013.00173.x · Cited by 423
Chang, C.-H., & Larracuente, A. M. (2019) · Genetics · doi:10.1534/genetics.118.301765 · Cited by 141
Y-chromosomal STR haplotypes in Kalmyk population samples
Roewer, L., Krüger, C., Willuweit, S., Nagy, M., Rodig, H., Kokshunova, L., Rothämel, T., Kravchenko, S., Jobling, M. A., Stoneking, M., et al. (2007) · Forensic Science International · doi:10.1016/j.forsciint.2006.11.013 · Cited by 29
Metadata
- Authors
- 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., van der Veen, F., Page, D. C., & Rozen, S.
- Venue
- Nature Genetics
- Published
- 2003-10-05
- Volume
- 35
- Issue
- 3
- Pages
- 247-251
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2019491357
- Cited by
- 425
- References
- 1
- FWCI
- 14.40
- 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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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. https://app.cochat.ai/papers/10.1038/ng1250
- The paper
- 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., van der Veen, F., Page, D. C., & Rozen, S. (2003). Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. Nature Genetics. https://doi.org/10.1038/ng1250
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.
