Melanoma genome sequencing reveals frequent PREX2 mutations
Has this study been replicated?
The atlas records 1 replication of this study. Recorded outcomes: 1 failed. The earliest on record is from 2017.
Replications
- Replication Study: Melanoma genome sequencing reveals frequent PREX2 mutations, Horrigan et al. (2017). eLife. Outcome recorded: failed.
resulted in no statistically significant difference in tumor-free survival driven by PREX2 variants
Outcome read from the abstract. View paper
Cite this record
Berger, M. F., Hodis, E., Heffernan, T. P., Deribe, Y. L., Lawrence, M. S., Protopopov, A., Ivanova, E., Watson, I. R., Nickerson, E., Ghosh, P., Zhang, H., Zeid, R., Ren, X., Cibulskis, K., Sivachenko, A. Y., Wagle, N., Sucker, A., Sougnez, C., Onofrio, R., … Garraway, L. A. (2012). Melanoma genome sequencing reveals frequent PREX2 mutations. Nature, 485(7399), 502–506. https://doi.org/10.1038/nature11071
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