The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip
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Citations
Cites
Optical Projection Tomography as a Tool for 3D Microscopy and Gene Expression Studies
Sharpe, J., Ahlgren, U., Perry, P., Hill, B., Ross, A., Hecksher-Sørensen, J., Baldock, R., & Davidson, D. (2002) · Science · doi:10.1126/science.1068206 · Cited by 1,158
Nickerson, D. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.14.2745 · Cited by 931
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
Kondo, S., Schutte, B. C., Richardson, R. J., Bjork, B. C., Knight, A. S., Watanabe, Y., Howard, E., Ferreira de Lima, R. L. L., Daack-Hirsch, S., Sander, A., et al. (2002) · Nature Genetics · doi:10.1038/ng985 · Cited by 897
Self-citationHorvath, S., Xu, X., & Laird, N. M. (2001) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200625 · Cited by 739
Comparative analyses of multi-species sequences from targeted genomic regions
Thomas, J. W., Touchman, J. W., Blakesley, R. W., Bouffard, G. G., Beckstrom-Sternberg, S. M., Margulies, E. H., Blanchette, M., Siepel, A. C., Thomas, P. J., McDowell, J. C., et al. (2003) · Nature · doi:10.1038/nature01858 · Cited by 638
Self-citationDudbridge, F. (2008) · Human Heredity · doi:10.1159/000119108 · Cited by 612
Transcription factor AP-2 essential for cranial closure and craniofacial development
Schorle, H., Meier, P., Buchert, M., Jaenisch, R., & Mitchell, P. J. (1996) · Nature · doi:10.1038/381235a0 · Cited by 610
Interferon Regulatory Factor 6 ( IRF6 ) Gene Variants and the Risk of Isolated Cleft Lip or Palate
Zucchero, T. M., Cooper, M. E., Maher, B. S., Daack-Hirsch, S., Nepomuceno, B., Ribeiro, L., Caprau, D., Christensen, K., Suzuki, Y., Machida, J., et al. (2004) · New England Journal of Medicine · doi:10.1056/nejmoa032909 · Cited by 579
Self-citationGraham, R. R., Kyogoku, C., Sigurdsson, S., Vlasova, I. A., Davies, L. R. L., Baechler, E. C., Plenge, R. M., Koeuth, T., Ortmann, W. A., Hom, G., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701266104 · Cited by 450
Identification and Characterization of Multi-Species Conserved Sequences
Margulies, E. H. (2003) · Genome Research · doi:10.1101/gr.1602203 · Cited by 335
Cited by
Mangold, E., Ludwig, K. U., Birnbaum, S., Baluardo, C., Ferrian, M., Herms, S., Reutter, H., de Assis, N. A., Chawa, T. A., Mattheisen, M., et al. (2010) · Nature Genetics · doi:10.1038/ng.506 · Cited by 431
Self-citationThe Genetics of Transcription Factor DNA Binding Variation
Deplancke, B., Alpern, D., & Gardeux, V. (2016) · Cell · doi:10.1016/j.cell.2016.07.012 · Cited by 390
A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans
Liu, F., van der Lijn, F., Schurmann, C., Zhu, G., Chakravarty, M. M., Hysi, P. G., Wollstein, A., Lao, O., de Bruijne, M., Ikram, M. A., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002932 · Cited by 326
Cranial neural crest cells on the move: Their roles in craniofacial development
Cordero, D. R., Brugmann, S., Chu, Y., Bajpai, R., Jame, M., & Helms, J. A. (2011) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.33702 · Cited by 305
Grant, S. F. A., Wang, K., Zhang, H., Glaberson, W., Annaiah, K., Kim, C. E., Bradfield, J. P., Glessner, J. T., Thomas, K. A., Garris, M., et al. (2009) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2009.06.020 · Cited by 278
Metadata
- Authors
- Program, N. C. S., Rahimov, F., Marazita, M. L., Visel, A., Cooper, M. E., Hitchler, M. J., Rubini, M., Domann, F. E., Govil, M., Christensen, K., Bille, C., Melbye, M., Jugessur, A., Lie, R. T., Wilcox, A. J., Fitzpatrick, D. R., Green, E. D., Mossey, P. A., Little, J., Steegers-Theunissen, R. P., Pennacchio, L. A., Schutte, B. C., & Murray, J. C.
- Venue
- Nature Genetics
- Published
- 2008-10-05
- Volume
- 40
- Issue
- 11
- Pages
- 1341-1347
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1964690949
- Cited by
- 425
- References
- 24
- FWCI
- 19.34
- Type
- journal article
- Language
- en
- Open access
- green
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Cite CoChat for the checks on this page, and the paper for its own findings.
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- CoChat. (2026). Citation check: Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip. https://app.cochat.ai/papers/10.1038/ng.242
- The paper
- Program, N. C. S., Rahimov, F., Marazita, M. L., Visel, A., Cooper, M. E., Hitchler, M. J., Rubini, M., Domann, F. E., Govil, M., Christensen, K., Bille, C., Melbye, M., Jugessur, A., Lie, R. T., Wilcox, A. J., Fitzpatrick, D. R., Green, E. D., Mossey, P. A., Little, J., . . . Murray, J. C. (2008). Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip. Nature Genetics. https://doi.org/10.1038/ng.242
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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.
