The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
CATSPER2, a human autosomal nonsyndromic male infertility gene
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Citations
Cites
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1
Dgany, O., Avidan, N., Delaunay, J., Krasnov, T., Shalmon, L., Shalev, H., Eidelitz-Markus, T., Kapelushnik, J., Cattan, D., Pariente, A., et al. (2002) · The American Journal of Human Genetics · doi:10.1086/344781 · Cited by 168
Self-citation
Cited by
Control of hyperactivation in sperm
Suarez, S. S. (2008) · Human Reproduction Update · doi:10.1093/humupd/dmn029 · Cited by 584
Hyperactivated sperm motility driven by CatSper2 is required for fertilization
Quill, T. A., Sugden, S. A., Rossi, K. L., Doolittle, L. K., Hammer, R. E., & Garbers, D. L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2136654100 · Cited by 377
Calcium Channels in the Development, Maturation, and Function of Spermatozoa
Darszon, A., Nishigaki, T., Beltran, C., & Treviño, C. L. (2011) · Physiological Reviews · doi:10.1152/physrev.00028.2010 · Cited by 364
Molecular Basis of Human Sperm Capacitation
Puga Molina, L. C., Luque, G. M., Balestrini, P. A., Marín-Briggiler, C. I., Romarowski, A., & Buffone, M. G. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00072 · Cited by 256
Genetic abnormalities leading to qualitative defects of sperm morphology or function
Ray, P. F., Toure, A., Metzler‐Guillemain, C., Mitchell, M. J., Arnoult, C., & Coutton, C. (2017) · Clinical Genetics · doi:10.1111/cge.12905 · Cited by 179
Metadata
- Authors
- Avidan, N., Tamary, H., Dgany, O., Cattan, D., Pariente, A., Thulliez, M., Borot, N., Moati, L., Barthelme, A., Shalmon, L., Krasnov, T., Ben-Asher, E., Olender, T., Khen, M., Yaniv, I., Zaizov, R., Shalev, H., Delaunay, J., Fellous, M., Lancet, D., & Beckmann, J. S.
- Venue
- European Journal of Human Genetics
- Published
- 2003-06-27
- Volume
- 11
- Issue
- 7
- Pages
- 497-502
- ISSN
- 1018-4813 (ISSN-L)
- 1476-5438
- OpenAlex
- W2167121071
- Cited by
- 213
- References
- 1
- FWCI
- 3.71
- 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: CATSPER2, a human autosomal nonsyndromic male infertility gene. https://app.cochat.ai/papers/10.1038/sj.ejhg.5200991
- The paper
- Avidan, N., Tamary, H., Dgany, O., Cattan, D., Pariente, A., Thulliez, M., Borot, N., Moati, L., Barthelme, A., Shalmon, L., Krasnov, T., Ben-Asher, E., Olender, T., Khen, M., Yaniv, I., Zaizov, R., Shalev, H., Delaunay, J., Fellous, M., . . . Beckmann, J. S. (2003). CATSPER2, a human autosomal nonsyndromic male infertility gene. European Journal of Human Genetics. https://doi.org/10.1038/sj.ejhg.5200991
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.
