The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
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Citations
Cites
Positional Cloning of the Werner's Syndrome Gene
Yu, C.-E., Oshima, J., Fu, Y.-H., Wijsman, E. M., Hisama, F., Alisch, R., Matthews, S., Nakura, J., Miki, T., Ouais, S., et al. (1996) · Science · doi:10.1126/science.272.5259.258 · Cited by 1,722
The Bloom's syndrome gene product is homologous to RecQ helicases
Ellis, N. A., Groden, J., Ye, T.-Z., Straughen, J., Lennon, D. J., Ciocci, S., Proytcheva, M., & German, J. (1995) · Cell · doi:10.1016/0092-8674(95)90105-1 · Cited by 1,403
Gangloff, S., McDonald, J. P., Bendixen, C., Arthur, L., & Rothstein, R. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.12.8391 · Cited by 677
Watt, P. M., Louis, E. J., Borts, R. H., & Hickson, I. D. (1995) · Cell · doi:10.1016/0092-8674(95)90335-6 · Cited by 399
Stewart, E. (1997) · The EMBO Journal · doi:10.1093/emboj/16.10.2682 · Cited by 350
Yamagata, K., Kato, J.-I., Shimamoto, A., Goto, M., Furuichi, Y., & Ikeda, H. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.15.8733 · Cited by 294
Self-citationKitao, S., Ohsugi, I., Ichikawa, K., Goto, M., Furuichi, Y., & Shimamoto, A. (1998) · Genomics · doi:10.1006/geno.1998.5595 · Cited by 249
Self-citationPuranam, K. L., & Blackshear, P. J. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)43957-9 · Cited by 201
Rothmund-Thomson syndrome: Review of the world literature
Vennos, E. M., Collins, M., & James, W. D. (1992) · Journal of the American Academy of Dermatology · doi:10.1016/0190-9622(92)70249-f · Cited by 183
Seki, M., Miyazawa, H., Tada, S., Yanagisawa, J., Yamaoka, T., Hoshino, S.-I., Ozawa, K., Eki, T., Nogami, M., Okumura, K., et al. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.22.4566 · Cited by 145
Cited by
The Bloom's syndrome gene product promotes branch migration of Holliday junctions
Karow, J. K., Constantinou, A., Li, J.-L., West, S. C., & Hickson, I. D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.100448097 · Cited by 502
Recombinational DNA repair and human disease
Thompson, L. H., & Schild, D. (2002) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/s0027-5107(02)00224-5 · Cited by 417
Mullen, J. R., Kaliraman, V., Ibrahim, S. S., & Brill, S. J. (2001) · Genetics · doi:10.1093/genetics/157.1.103 · Cited by 403
Fanconi anaemia and cancer: an intricate relationship
Nalepa, G., & Clapp, D. W. (2018) · Nature Reviews Cancer · doi:10.1038/nrc.2017.116 · Cited by 389
Cancer predisposition caused by elevated mitotic recombination in Bloom mice
Luo, G., Santoro, I. M., McDaniel, L. D., Nishijima, I., Mills, M., Youssoufian, H., Vogel, H., Schultz, R. A., & Bradley, A. (2000) · Nature Genetics · doi:10.1038/82548 · Cited by 372
Metadata
- Authors
- Kitao, S., Shimamoto, A., Goto, M., Miller, R. W., Smithson, W. A., Lindor, N. M., & Furuichi, Y.
- Venue
- Nature Genetics
- Published
- 1999-05
- Volume
- 22
- Issue
- 1
- Pages
- 82-84
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- DOI
- 10.1038/8788
- OpenAlex
- W1935801587
- Cited by
- 666
- References
- 18
- FWCI
- 14.79
- Type
- journal article
- Language
- en
- Open access
- closed
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- This page
- CoChat. (2026). Citation check: Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. https://app.cochat.ai/papers/10.1038/8788
- The paper
- Kitao, S., Shimamoto, A., Goto, M., Miller, R. W., Smithson, W. A., Lindor, N. M., & Furuichi, Y. (1999). Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. Nature Genetics. https://doi.org/10.1038/8788
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.
