The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
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Citations
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Basic local alignment search tool
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669
Fast and sensitive silver staining of DNA in polyacrylamide gels
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The tetratricopeptide repeat: a structural motif mediating protein-protein interactions
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Deininger, P. L., & Batzer, M. A. (1999) · Molecular Genetics and Metabolism · doi:10.1006/mgme.1999.2864 · Cited by 909
The Cardinal Manifestations of Bardet–Biedl Syndrome, a Form of Laurence–Moon–Biedl Syndrome
Green, J. S., Parfrey, P. S., Harnett, J. D., Farid, N. R., Cramer, B. C., Johnson, G., Heath, O., McManamon, P. J., O'Leary, E., & Pryse-Phillips, W. (1989) · New England Journal of Medicine · doi:10.1056/nejm198910123211503 · Cited by 555
Lubas, W. A., Frank, D. W., Krause, M., & Hanover, J. A. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.14.9316 · Cited by 551
Protein Family Classification Based on Searching a Database of Blocks
Henikoff, S., & Henikoff, J. G. (1994) · Genomics · doi:10.1006/geno.1994.1018 · Cited by 363
Jacobsen, S. E., Binkowski, K. A., & Olszewski, N. E. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.17.9292 · Cited by 355
Katsanis, N., Beales, P. L., Woods, M. O., Lewis, R. A., Green, J. S., Parfrey, P. S., Ansley, S. J., Davidson, W. S., & Lupski, J. R. (2000) · Nature Genetics · doi:10.1038/79201 · Cited by 325
Mutations in MKKS cause Bardet-Biedl syndrome
Slavotinek, A. M., Stone, E. M., Mykytyn, K., Heckenlively, J. R., Green, J. S., Heon, E., Musarella, M. A., Parfrey, P. S., Sheffield, V. C., & Biesecker, L. G. (2000) · Nature Genetics · doi:10.1038/79116 · Cited by 275
Self-citation
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Goetz, S. C., & Anderson, K. V. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2774 · Cited by 1,824
The Ciliopathies: An Emerging Class of Human Genetic Disorders
Badano, J. L., Mitsuma, N., Beales, P. L., & Katsanis, N. (2006) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.7.080505.115610 · Cited by 1,144
The Human Obesity Gene Map: The 2005 Update
Rankinen, T., Zuberi, A., Chagnon, Y. C., Weisnagel, S. J., Argyropoulos, G., Walts, B., Pérusse, L., & Bouchard, C. (2006) · Obesity · doi:10.1038/oby.2006.71 · Cited by 1,119
Li, J. B., Gerdes, J. M., Haycraft, C. J., Fan, Y., Teslovich, T. M., May-Simera, H., Li, H., Blacque, O. E., Li, L., Leitch, C. C., et al. (2004) · Cell · doi:10.1016/s0092-8674(04)00450-7 · Cited by 760
Ciliopathies: an expanding disease spectrum
Waters, A. M., & Beales, P. L. (2011) · Pediatric Nephrology · doi:10.1007/s00467-010-1731-7 · Cited by 676
Metadata
- Authors
- Mykytyn, K., Braun, T., Carmi, R., Haider, N. B., Searby, C. C., Shastri, M., Beck, G., Wright, A. F., Iannaccone, A., Elbedour, K., Riise, R., Baldi, A., Raas-Rothschild, A., Gorman, S. W., Duhl, D. M., Jacobson, S. G., Casavant, T., Stone, E. M., & Sheffield, V. C.
- Venue
- Nature Genetics
- Published
- 2001-06
- Volume
- 28
- Issue
- 2
- Pages
- 188-191
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1595325053
- Cited by
- 274
- References
- 22
- FWCI
- 12.94
- 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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- This page
- CoChat. (2026). Citation check: Identification of the gene that, when mutated, causes the human obesity syndrome BBS4. https://app.cochat.ai/papers/10.1038/88925
- The paper
- Mykytyn, K., Braun, T., Carmi, R., Haider, N. B., Searby, C. C., Shastri, M., Beck, G., Wright, A. F., Iannaccone, A., Elbedour, K., Riise, R., Baldi, A., Raas-Rothschild, A., Gorman, S. W., Duhl, D. M., Jacobson, S. G., Casavant, T., Stone, E. M., & Sheffield, V. C. (2001). Identification of the gene that, when mutated, causes the human obesity syndrome BBS4. Nature Genetics. https://doi.org/10.1038/88925
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.