The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development
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Citations
Cites
Lufkin, T., Dierich, A., LeMeur, M., Mark, M., & Chambon, P. (1991) · Cell · doi:10.1016/0092-8674(91)90034-v · Cited by 697
Etchevers, H. C., Vincent, C., Douarin, N. M. L., & F. Couly, G. (2001) · Development · doi:10.1242/dev.128.7.1059 · Cited by 657
Chisaka, O., Musci, T. S., & Capecchi, M. R. (1992) · Nature · doi:10.1038/355516a0 · Cited by 537
Two rhombomeres are altered in Hoxa-1 mutant mice
Mark, M., Lufkin, T., Vonesch, J.-L., Ruberte, E., Olivo, J.-C., Dollé, P., Gorry, P., Lumsden, A., & Chambon, P. (1993) · Development · doi:10.1242/dev.119.2.319 · Cited by 397
Hoxa1 and Hoxb1 synergize in patterning the hindbrain, cranial nerves and second pharyngeal arch
Gavalas, A., Studer, M., Lumsden, A., Rijli, F. M., Krumlauf, R., & Chambon, P. (1998) · Development · doi:10.1242/dev.125.6.1123 · Cited by 325
Murphy, P., & Hill, R. E. (1991) · Development · doi:10.1242/dev.111.1.61 · Cited by 237
Limb malformations and the human HOX genes
Goodman, F. R. (2002) · American Journal of Medical Genetics · doi:10.1002/ajmg.10776 · Cited by 218
Ingram, J. L., Stodgell, C., Hyman, S. L., Figlewicz, D. A., WEITKAMP, L. R., & Rodier, P. M. (2000) · Teratology · doi:10.1002/1096-9926(200012)62:6<393::aid-tera6>3.0.co;2-v · Cited by 169
Shrimpton, A. E., Levinsohn, E. M., Yozawitz, J. M., Packard, D. S., Cady, R. B., Middleton, F. A., Persico, A. M., & Hootnick, D. R. (2004) · The American Journal of Human Genetics · doi:10.1086/422015 · Cited by 87
Generation of a Novel Functional Neuronal Circuit inHoxa1 Mutant Mice
del Toro, E. D., Borday, V., Davenne, M., Neun, R., Rijli, F., & Champagnat, J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-15-05637.2001 · Cited by 82
Cited by
Searching for ways out of the autism maze: genetic, epigenetic and environmental clues
Persico, A. M., & Bourgeron, T. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.05.010 · Cited by 575
Patterning and axon guidance of cranial motor neurons
Guthrie, S. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2254 · Cited by 201
Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist
Lintas, C., & Persico, A. M. (2009) · Journal of Medical Genetics · doi:10.1136/jmg.2008.060871 · Cited by 178
Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia
Lin, Z., Chen, Q., Shi, L., Lee, M., Giehl, K. A., Tang, Z., Wang, H., Zhang, J., Yin, J., Wu, L., et al. (2012) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2012.08.029 · Cited by 79
Mowery, T. M., Wilson, S. M., Kostylev, P. V., Dina, B., Buchholz, J. B., Prieto, A. L., & Garraghty, P. E. (2015) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2014.10.003 · Cited by 29
Metadata
- Authors
- Tischfield, M. A., Bosley, T. M., Salih, M. A. M., Alorainy, I. A., Sener, E. C., Nester, M. J., Oystreck, D. T., Chan, W.-M., Andrews, C., Erickson, R. P., & Engle, E. C.
- Venue
- Nature Genetics
- Published
- 2005-09-11
- Volume
- 37
- Issue
- 10
- Pages
- 1035-1037
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2140566949
- Cited by
- 304
- References
- 13
- FWCI
- 5.88
- 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: Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. https://app.cochat.ai/papers/10.1038/ng1636
- The paper
- Tischfield, M. A., Bosley, T. M., Salih, M. A. M., Alorainy, I. A., Sener, E. C., Nester, M. J., Oystreck, D. T., Chan, W.-M., Andrews, C., Erickson, R. P., & Engle, E. C. (2005). Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Nature Genetics. https://doi.org/10.1038/ng1636
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.
