The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.
Ataxia–telangiectasia, an evolving phenotype
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Citations
Cites
DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation
Bakkenist, C. J., & Kastan, M. B. (2003) · Nature · doi:10.1038/nature01368 · Cited by 3,466
The Genetic Basis of Human Cancer
Vogelstein, B., & Kinzler, K. W. (1997) · Cited by 1,120
Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome
Varon, R., Vissinga, C., Platzer, M., Cerosaletti, K. M., Chrzanowska, K. H., Saar, K., Beckmann, G., Seemanová, E., Cooper, P. R., Nowak, N. J., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)81174-5 · Cited by 1,079
Self-citationRequirement of the MRN complex for ATM activation by DNA damage
Uziel, T., Lerenthal, Y., Moyal, L., Andegeko, Y., Mittelman, L., & Shiloh, Y. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg541 · Cited by 1,075
Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity
TAYLOR, A. M. R., HARNDEN, D. G., ARLETT, C. F., HARCOURT, S. A., LEHMANN, A. R., STEVENS, S., & BRIDGES, B. A. (1975) · Nature · doi:10.1038/258427a0 · Cited by 990
Localization of an ataxia-telangiectasia gene to chromosome 11q22–23
Gatti, R. A., Berkel, I., Boder, E., Braedt, G., Charmley, P., Concannon, P., Ersoy, F., Foroud, T., Jaspers, N. G. J., Lange, K., et al. (1988) · Nature · doi:10.1038/336577a0 · Cited by 686
Self-citationSenataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2
Moreira, M.-C., Klur, S., Watanabe, M., Németh, A. H., Ber, I. L., Moniz, J.-C., Tranchant, C., Aubourg, P., Tazir, M., Schöls, L., et al. (2004) · Nature Genetics · doi:10.1038/ng1303 · Cited by 519
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin
Moreira, M.-C., Barbot, C., Tachi, N., Kozuka, N., Uchida, E., Gibson, T., Mendonça, P., Costa, M., Barros, J., Yanagisawa, T., et al. (2001) · Nature Genetics · doi:10.1038/ng1001-189 · Cited by 434
Boder, E., & Sedgwick, R. P. (1958) · PubMed · Cited by 432
Stankovic, T., Kidd, A. M. J., Sutcliffe, A., McGuire, G. M., Robinson, P., Weber, P., Bedenham, T., Bradwell, A. R., Easton, D. F., Lennox, G. G., et al. (1998) · The American Journal of Human Genetics · doi:10.1086/301706 · Cited by 400
Cited by
Ataxia-telangiectasia: from a rare disorder to a paradigm for cell signalling and cancer
Lavin, M. F. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2514 · Cited by 901
The impact of a negligent G2/M checkpoint on genomic instability and cancer induction
Löbrich, M., & Jeggo, P. A. (2007) · Nature Reviews Cancer · doi:10.1038/nrc2248 · Cited by 632
Stiff, T., Walker, S. A., Cerosaletti, K., Goodarzi, A. A., Petermann, E., Concannon, P., O'Driscoll, M., & Jeggo, P. A. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601446 · Cited by 360
The autosomal recessive cerebellar ataxias.
Anheim, M., Tranchant, C., & Koenig, M. (2012) · New England Journal of Medicine · doi:10.1056/nejmra1006610 · Cited by 356
DNA Strand Break Repair and Human Genetic Disease
McKinnon, P. J., & Caldecott, K. W. (2007) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.7.080505.115648 · Cited by 305
Metadata
- Authors
- Chun, H. H., & Gatti, R. A.
- Venue
- DNA Repair
- Publisher
- Elsevier BV
- Published
- 2004-08
- Volume
- 3
- Issue
- 8-9
- Pages
- 1187-1196
- ISSN
- 1568-7856 (ISSN-L)
- 1568-7864
- OpenAlex
- W1988524165
- Cited by
- 428
- References
- 62
- FWCI
- 8.31
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Ataxia–telangiectasia, an evolving phenotype. https://app.cochat.ai/papers/10.1016/j.dnarep.2004.04.010
- The paper
- Chun, H. H., & Gatti, R. A. (2004). Ataxia–telangiectasia, an evolving phenotype. DNA Repair. https://doi.org/10.1016/j.dnarep.2004.04.010
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.
