The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1
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Citations
Cites
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The I.M.A.G.E. Consortium: An Integrated Molecular Analysis of Genomes and Their Expression
Lennon, G., Auffray, C., Polymeropoulos, M., & Soares, M. B. (1996) · Genomics · doi:10.1006/geno.1996.0177 · Cited by 1,123
A Common Language for Physical Mapping of the Human Genome
Olson, M., Hood, L., Cantor, C., & Botstein, D. (1989) · Science · doi:10.1126/science.2781285 · Cited by 857
Meindl, A., Dry, K., Herrmann, K., Manson, E., Ciccodicola, A., Edgar, A., Carvalho, M. R. S., Achatz, H., Hellebrand, H., Lennon, A., et al. (1996) · Nature Genetics · doi:10.1038/ng0596-35 · Cited by 482
Károlyi, L., Konrad, M., Köckerling, A., et al. (1997) · Human Molecular Genetics · doi:10.1093/hmg/6.1.17 · Cited by 191
Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis
Konrad, M. (1996) · Human Molecular Genetics · doi:10.1093/hmg/5.3.367 · Cited by 138
Antignac, C., Arduy, C. H., Beckmann, J. S., Benessy, F., Gros, F., Medhioub, M., Hildebrandt, F., Dufier, J., Kleinknecht, C., Broyer, M., et al. (1993) · Nature Genetics · doi:10.1038/ng0493-342 · Cited by 124
Self-citationMedhioub, M., Chérif, D., Benessy, F., Silbermann, F., Gübler, M.-C., Paslier, D. L., Cohen, O., Weissenbach, J., Beckmann, J. S., & Antignac, C. (1994) · Genomics · doi:10.1006/geno.1994.1387 · Cited by 33
Konrad, M., Saunier, S., Silbermann, F., Benessy, F., Paslier, D. L., Weissenbach, J., Broyer, M., Gübler, M.-C., & Antignac, C. (1995) · Genomics · doi:10.1006/geno.1995.1272 · Cited by 14
Cited by
Hildebrandt, F., Benzing, T., & Katsanis, N. (2011) · New England Journal of Medicine · doi:10.1056/nejmra1010172 · Cited by 1,331
Self-citationThe 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
Wilson, P. D. (2004) · New England Journal of Medicine · doi:10.1056/nejmra022161 · Cited by 916
Copy number variations and clinical cytogenetic diagnosis of constitutional disorders
Lee, C., Iafrate, A. J., & Brothman, A. R. (2007) · Nature Genetics · doi:10.1038/ng2092 · Cited by 388
Open Sesame: How Transition Fibers and the Transition Zone Control Ciliary Composition
Garcia-Gonzalo, F. R., & Reiter, J. F. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028134 · Cited by 290
Metadata
- Authors
- Hildebrandt, F., Otto, E., Rensing, C., Nothwang, H. G., Vollmer, M., Adolphs, J., Hanusch, H., & Brandis, M.
- Venue
- Nature Genetics
- Published
- 1997-10
- Volume
- 17
- Issue
- 2
- Pages
- 149-153
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2044949852
- Cited by
- 353
- References
- 9
- FWCI
- 7.12
- 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: A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1. https://app.cochat.ai/papers/10.1038/ng1097-149
- The paper
- Hildebrandt, F., Otto, E., Rensing, C., Nothwang, H. G., Vollmer, M., Adolphs, J., Hanusch, H., & Brandis, M. (1997). A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1. Nature Genetics. https://doi.org/10.1038/ng1097-149
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.
