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Shore, Eileen M., Xu, Meiqi, Feldman, George J., Fenstermacher, David A., Brown, Matthew A., Kaplan, Frederick S., Cho, Tae-Joon, Choi, In Ho, Connor, J. Michael, Delai, Patricia, Zasloff, Michael, Glaser, David L., LeMerrer, Martine, Smith, Roger, Morhart, Rolf, Rogers, John G., Triffitt, James T. and Urtizberea, J. Andoni (2006) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nature Genetics, 38 5: 525-527. doi:10.1038/ng1783 169   319 Cited 333 times in Scopus333 10
Shore, Eileen M., Xu, Meiqi, Feldman, George J., Fenstermacher, David A., Brown, Matthew A., Kaplan, Frederick S. and FOP Int Res Consortium (2007) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527)). Nature Genetics, 39 2: 276-276. doi:10.1038/ng0207-276b 45   6 Cited 3 times in Scopus3 0
Duncan, Emma, Brown, Matthew and Shore, Eileen M. (2014) The revolution in human monogenic disease mapping. Genes, 5 3: 792-803. doi:10.3390/genes5030792 26   0 0