The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index.
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
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Cites
Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics
Maquat, L. E. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1310 · Cited by 1,214
Tissue-specific expression and regulation of sexually dimorphic genes in mice
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A Striking Organization of a Large Family of Human Neural Cadherin-like Cell Adhesion Genes
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Cadherin superfamily genes: functions, genomic organization, and neurologic diversity
Yagi, T., & Takeichi, M. (2000) · Genes & Development · doi:10.1101/gad.14.10.1169 · Cited by 637
The cadherin superfamily in neuronal connections and interactions
Takeichi, M. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2043 · Cited by 431
Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F
Ahmed, Z. M., Riazuddin, S., Bernstein, S. L., Ahmed, Z., Khan, S., Griffith, A. J., Morell, R. J., Friedman, T. B., Riazuddin, S., & Wilcox, E. R. (2001) · The American Journal of Human Genetics · doi:10.1086/321277 · Cited by 415
Sex chromosomes and brain gender
Arnold, A. P. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1494 · Cited by 368
Parallel FoxP1 and FoxP2 Expression in Songbird and Human Brain Predicts Functional Interaction
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Self-citationType II Cadherin Ectodomain Structures: Implications for Classical Cadherin Specificity
Patel, S. D., Ciatto, C., Chen, C. P., Bahna, F., Rajebhosale, M., Arkus, N., Schieren, I., Jessell, T. M., Honig, B., Price, S. R., et al. (2006) · Cell · doi:10.1016/j.cell.2005.12.046 · Cited by 293
Mutations of the Ephrin-B1 Gene Cause Craniofrontonasal Syndrome
Wieland, I., Jakubiczka, S., Muschke, P., Cohen, M. Y., Thiele, H., Gerlach, K. L., Adams, R. H., & Wieacker, P. F. (2004) · The American Journal of Human Genetics · doi:10.1086/421532 · Cited by 243
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Betancur, C. (2011) · Brain Research · doi:10.1016/j.brainres.2010.11.078 · Cited by 954
Flavell, S. W., Kim, T.-K., Gray, J. M., Harmin, D. A., Hemberg, M., Hong, E. J., Markenscoff-Papadimitriou, E., Bear, D. M., & Greenberg, M. E. (2008) · Neuron · doi:10.1016/j.neuron.2008.11.029 · Cited by 440
Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence
Moreno-De-Luca, A., Myers, S. M., Challman, T. D., Moreno-De-Luca, D., Evans, D. W., & Ledbetter, D. H. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(13)70011-5 · Cited by 330
Lipedema: An inherited condition
Child, A. H., Gordon, K. D., Sharpe, P., Brice, G., Ostergaard, P., Jeffery, S., & Mortimer, P. S. (2010) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.33313 · Cited by 329
The WAVE regulatory complex links diverse receptors to the actin cytoskeleton
Chen, B., Brinkmann, K., Chen, Z., Pak, C. W., Liao, Y., Shi, S., Henry, L., Grishin, N. V., Bogdan, S., & Rosen, M. K. (2014) · Cell · doi:10.1016/j.cell.2013.11.048 · Cited by 323
Metadata
- Authors
- Dibbens, L. M., Tarpey, P. S., Hynes, K., Bayly, M. A., Scheffer, I. E., Smith, R., Bomar, J., Sutton, E., Vandeleur, L., Shoubridge, C., Edkins, S., Turner, S. J., Stevens, C., O'Meara, S., Tofts, C., Barthorpe, S., Buck, G., Cole, J., Halliday, K., Jones, D., Lee, R., Madison, M., Mironenko, T., Varian, J., West, S., Widaa, S., Wray, P., Teague, J., Dicks, E., Butler, A., Menzies, A., Jenkinson, A., Shepherd, R., Gusella, J. F., Afawi, Z., Mazarib, A., Neufeld, M. Y., Kivity, S., Lev, D., Lerman-Sagie, T., Korczyn, A. D., Derry, C. P., Sutherland, G. R., Friend, K., Shaw, M., Corbett, M., Kim, H.-G., Geschwind, D. H., Thomas, P., Haan, E., Ryan, S., McKee, S., Berkovic, S. F., Futreal, P. A., Stratton, M. R., Mulley, J. C., & Gécz, J.
- Venue
- Nature Genetics
- Published
- 2008-05-11
- Volume
- 40
- Issue
- 6
- Pages
- 776-781
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2011465123
- Cited by
- 451
- References
- 21
- FWCI
- 14.06
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. https://app.cochat.ai/papers/10.1038/ng.149
- The paper
- Dibbens, L. M., Tarpey, P. S., Hynes, K., Bayly, M. A., Scheffer, I. E., Smith, R., Bomar, J., Sutton, E., Vandeleur, L., Shoubridge, C., Edkins, S., Turner, S. J., Stevens, C., O'Meara, S., Tofts, C., Barthorpe, S., Buck, G., Cole, J., Halliday, K., . . . Gécz, J. (2008). X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. Nature Genetics. https://doi.org/10.1038/ng.149
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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.
