The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans
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Citations
Cites
Strain-Dependent Epithelial Defects in Mice Lacking the EGF Receptor
Sibilia, M., & Wagner, E. F. (1995) · Science · doi:10.1126/science.7618085 · Cited by 1,002
Cited by
TLR4 mutations are associated with endotoxin hyporesponsiveness in humans
Arbour, N. C., Lorenz, E., Schutte, B. C., Zabner, J., Kline, J. N., Jones, M., Frees, K., Watt, J. L., & Schwartz, D. A. (2000) · Nature Genetics · doi:10.1038/76048 · Cited by 2,024
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
van den Boogaard, M.-J. H., Dorland, M., Beemer, F. A., & van Amstel, H. K. P. (2000) · Nature Genetics · doi:10.1038/74155 · Cited by 587
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate
Jezewski, P. A., Vieira, A. R., Nishimura, C., Ludwig, B., Johnson, M., O’Brien, S. E., Daack-Hirsch, S., Schultz, R. E., Weber, A., Nepomucena, B., et al. (2003) · Journal of Medical Genetics · doi:10.1136/jmg.40.6.399 · Cited by 304
Self-citationMsx homeobox gene family and craniofacial development
ALAPPAT, S., ZHANG, Z. Y., & CHEN, Y. P. (2003) · Cell Research · doi:10.1038/sj.cr.7290185 · Cited by 278
Miettinen, P. J., Chin, J. R., Shum, L., Slavkin, H. C., Shuler, C. F., Derynck, R., & Werb, Z. (1999) · Nature Genetics · doi:10.1038/8773 · Cited by 272
Metadata
- Authors
- Lidral, A. C., Romitti, P. A., Basart, A. M., Doetschman, T., Leysens, N. J., Daack-Hirsch, S., Semina, E. V., Johnson, L. R., Machida, J., Burds, A., Parnell, T. J., Rubenstein, J. L. R., & Murray, J. C.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 1998-08
- Volume
- 63
- Issue
- 2
- Pages
- 557-568
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W1965222408
- Cited by
- 304
- References
- 1
- FWCI
- 5.31
- Type
- journal article
- Language
- en
- Open access
- bronze
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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: Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans. https://app.cochat.ai/papers/10.1086/301956
- The paper
- Lidral, A. C., Romitti, P. A., Basart, A. M., Doetschman, T., Leysens, N. J., Daack-Hirsch, S., Semina, E. V., Johnson, L. R., Machida, J., Burds, A., Parnell, T. J., Rubenstein, J. L. R., & Murray, J. C. (1998). Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans. The American Journal of Human Genetics. https://doi.org/10.1086/301956
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.
