The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
Satokata, I., & Maas, R. (1994) · Nature Genetics · doi:10.1038/ng0494-348 · Cited by 1,275
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
Satokata, I., Ma, L., Ohshima, H., Bei, M., Woo, I., Nishizawa, K., Maeda, T., Takano, Y., Uchiyama, M., Heaney, S., et al. (2000) · Nature Genetics · doi:10.1038/74231 · Cited by 737
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
Vastardis, H., Karimbux, N., Guthua, S. W., Seidman, J. G., & Seidman, C. E. (1996) · Nature Genetics · doi:10.1038/ng0896-417 · Cited by 721
Classification and birth prevalence of orofacial clefts
Tolarová, M. M., & Cervenka, J. (1998) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19980113)75:2<126::aid-ajmg2>3.3.co;2-f · Cited by 477
The many faces and factors oforofacial clefts
Schutte, B. C. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.10.1853 · Cited by 326
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
Wilkie, A. O. M., Tang, Z., Elanko, N., Walsh, S., Twigg, S. R. F., Hurst, J. A., Wall, S. A., Chrzanowska, K. H., & Maxson, R. E. (2000) · Nature Genetics · doi:10.1038/74224 · Cited by 315
Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans
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., et al. (1998) · The American Journal of Human Genetics · doi:10.1086/301956 · Cited by 304
Clinical and Epidemiologic Studies of Cleft Lip and Palate in the Philippines
Murray, J. C., Daack‐Hirsch, S., Buetow, K. H., Munger, R. G., Espina, L., Paglinawan, N., Villanueva, E., Rary, J., Magee, K. S., & Magee, W. P. (1997) · The Cleft Palate-Craniofacial Journal · doi:10.1597/1545-1569(1997)034<0007:caesoc>2.3.co;2 · Cited by 156
Haploinsufficiency ofMSX1: a Mechanism for Selective Tooth Agenesis
Hu, G., Vastardis, H., Bendall, A. J., Wang, Z., Logan, M. P. O., Zhang, H., Nelson, C., Stein, S., Greenfield, N. J., Seidman, C. E., et al. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.10.6044 · Cited by 86
Structure and sequence of the human homeobox gene HOX7
Hewitt, J., Clark, L. N., Ivens, A. C., & Williamson, R. (1991) · Genomics · doi:10.1016/0888-7543(91)90074-o · Cited by 74
Cited by
Cranial neural crest and the building of the vertebrate head
Santagati, F., & Rijli, F. M. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1221 · Cited by 461
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
Wilkie, A. O. M., Tang, Z., Elanko, N., Walsh, S., Twigg, S. R. F., Hurst, J. A., Wall, S. A., Chrzanowska, K. H., & Maxson, R. E. (2000) · Nature Genetics · doi:10.1038/74224 · Cited by 315
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
Msx 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
Ectodermal dysplasias: a new clinical-genetic classification
Priolo, M., & Laganà, C. (2001) · Journal of Medical Genetics · doi:10.1136/jmg.38.9.579 · Cited by 197
Metadata
- Authors
- van den Boogaard, M.-J. H., Dorland, M., Beemer, F. A., & van Amstel, H. K. P.
- Venue
- Nature Genetics
- Published
- 2000-04
- Volume
- 24
- Issue
- 4
- Pages
- 342-343
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2172122920
- Cited by
- 587
- References
- 10
- FWCI
- 11.15
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. https://app.cochat.ai/papers/10.1038/74155
- The paper
- van den Boogaard, M.-J. H., Dorland, M., Beemer, F. A., & van Amstel, H. K. P. (2000). MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nature Genetics. https://doi.org/10.1038/74155
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.
