The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy
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Citations
Cites
Valentine, M. T., Fordyce, P. M., Krzysiak, T. C., Gilbert, S. P., & Block, S. M. (2006) · Nature Cell Biology · doi:10.1038/ncb1394 · Cited by 260
Cited by
Poirier, K., Lebrun, N., Broix, L., Tian, G., Saillour, Y., Boscheron, C., Parrini, E., Valence, S., Pierre, B. S., Oger, M., et al. (2013) · Nature Genetics · doi:10.1038/ng.2613 · Cited by 494
New developments in clinical aspects of lymphatic disease
Mortimer, P. S., & Rockson, S. G. (2014) · Journal of Clinical Investigation · doi:10.1172/jci71608 · Cited by 357
Self-citationGenetics of lymphatic anomalies
Brouillard, P., Boon, L., & Vikkula, M. (2014) · Journal of Clinical Investigation · doi:10.1172/jci71614 · Cited by 355
Self-citationLymphatic Vessel Network Structure and Physiology
Breslin, J. W., Yang, Y., Scallan, J. P., Sweat, R. S., Adderley, S. P., & Murfee, W. L. (2018) · Comprehensive Physiology · doi:10.1002/cphy.c180015 · Cited by 341
Primary cilia influence progenitor function during cortical development
Zaidi, D., Chinnappa, K., & Francis, F. (2022) · Cells · doi:10.3390/cells11182895 · Cited by 19
Metadata
- Authors
- Ostergaard, P., Simpson, M. A., Mendola, A., Vasudevan, P., Connell, F. C., van Impel, A., Moore, A. T., Loeys, B. L., Ghalamkarpour, A., Onoufriadis, A., Martinez-Corral, I., Devery, S., Leroy, J. G., van Laer, L., Singer, A., Bialer, M. G., McEntagart, M., Quarrell, O., Brice, G., Trembath, R. C., Schulte-Merker, S., Makinen, T., Vikkula, M., Mortimer, P. S., Mansour, S., & Jeffery, S.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2012-02
- Volume
- 90
- Issue
- 2
- Pages
- 356-362
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W2015220157
- Cited by
- 203
- References
- 1
- FWCI
- 5.51
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy. https://app.cochat.ai/papers/10.1016/j.ajhg.2011.12.018
- The paper
- Ostergaard, P., Simpson, M. A., Mendola, A., Vasudevan, P., Connell, F. C., van Impel, A., Moore, A. T., Loeys, B. L., Ghalamkarpour, A., Onoufriadis, A., Martinez-Corral, I., Devery, S., Leroy, J. G., van Laer, L., Singer, A., Bialer, M. G., McEntagart, M., Quarrell, O., Brice, G., . . . Jeffery, S. (2012). Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy. The American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2011.12.018
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.
