The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
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Citations
Cites
Geisterfer-Lowrance, A. A. T., Kass, S., Tanigawa, G., Vosberg, H.-P., McKenna, W., Seidman, C. E., & Seidman, J. G. (1990) · Cell · doi:10.1016/0092-8674(90)90274-i · Cited by 1,380
Self-citation
Cited by
Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy
Hinson, J. T., Chopra, A., Nafissi, N., Polacheck, W. J., Benson, C. C., Swist, S., Gorham, J., Yang, L., Schafer, S., Sheng, C. C., et al. (2015) · Science · doi:10.1126/science.aaa5458 · Cited by 638
Self-citationCrilley, J. G., Boehm, E. A., Blair, E., Rajagopalan, B., Blamire, A. M., Styles, P., McKenna, W. J., Östman-Smith, I., Clarke, K., & Watkins, H. (2003) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(02)03009-7 · Cited by 438
Self-citationIdentifying Sarcomere Gene Mutations in Hypertrophic Cardiomyopathy: A Personal History
Seidman, C. E., & Seidman, J. G. (2011) · Circulation Research · doi:10.1161/circresaha.110.223834 · Cited by 271
Self-citationMutation Type Is Not Clinically Useful in Predicting Prognosis in Hypertrophic Cardiomyopathy
Landstrom, A. P., & Ackerman, M. J. (2010) · Circulation · doi:10.1161/circulationaha.110.954446 · Cited by 146
CUDA, G., FANANAPAZIR, L., EPSTEIN, N. D., & SELLERS, J. R. (1997) · Journal of Muscle Research & Cell Motility · doi:10.1023/a:1018613907574 · Cited by 137
Metadata
- Authors
- Watkins, H., Conner, D., Thierfelder, L., Jarcho, J. A., MacRae, C., McKenna, W. J., Maron, B. J., Seidman, J. G., & Seidman, C. E.
- Venue
- Nature Genetics
- Published
- 1995-12
- Volume
- 11
- Issue
- 4
- Pages
- 434-437
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2034972644
- Cited by
- 590
- References
- 1
- FWCI
- 29.53
- Type
- journal article
- Language
- en
- Open access
- closed
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. https://app.cochat.ai/papers/10.1038/ng1295-434
- The paper
- Watkins, H., Conner, D., Thierfelder, L., Jarcho, J. A., MacRae, C., McKenna, W. J., Maron, B. J., Seidman, J. G., & Seidman, C. E. (1995). Mutations in the cardiac myosin binding protein–C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nature Genetics. https://doi.org/10.1038/ng1295-434
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.
