| A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva EM Shore, M Xu, GJ Feldman, DA Fenstermacher, TJ Cho, IH Choi, ... Nature genetics 38 (5), 525-527, 2006 | 1301 | 2006 |
| Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton LJ Brunet, JA McMahon, AP McMahon, RM Harland Science 280 (5368), 1455-1457, 1998 | 1021 | 1998 |
| Conversion of vascular endothelial cells into multipotent stem-like cells D Medici, EM Shore, VY Lounev, FS Kaplan, R Kalluri, BR Olsen Nature medicine 16 (12), 1400-1406, 2010 | 824 | 2010 |
| Heterotopic ossification FS Kaplan, DL Glaser, N Hebela, EM Shore JAAOS-Journal of the American Academy of Orthopaedic Surgeons 12 (2), 116-125, 2004 | 489 | 2004 |
| Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1 FS Kaplan, M Xu, P Seemann, JM Connor, DL Glaser, L Carroll, P Delai, ... Human mutation 30 (3), 379-390, 2009 | 482 | 2009 |
| Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva AB Shafritz, EM Shore, FH Gannon, MA Zasloff, R Taub, M Muenke, ... New England Journal of Medicine 335 (8), 555-561, 1996 | 440 | 1996 |
| Fibrodysplasia ossificans progressiva FS Kaplan, M Le Merrer, DL Glaser, RJ Pignolo, RE Goldsby, ... Best practice & research Clinical rheumatology 22 (1), 191-205, 2008 | 407 | 2008 |
| Identification of progenitor cells that contribute to heterotopic skeletogenesis VY Lounev, R Ramachandran, MN Wosczyna, M Yamamoto, ... The Journal of Bone and Joint Surgery. American volume. 91 (3), 652, 2009 | 382 | 2009 |
| Identification of a membrane-cytoskeletal complex containing the cell adhesion molecule uvomorulin (E-cadherin), ankyrin, and fodrin in Madin-Darby canine kidney epithelial cells. WJ Nelson, EM Shore, AZ Wang, RW Hammerton The Journal of cell biology 110 (2), 349-357, 1990 | 365 | 1990 |
| Fibrodysplasia ossificans progressiva: clinical and genetic aspects RJ Pignolo, EM Shore, FS Kaplan Orphanet journal of rare diseases 6 (1), 1-6, 2011 | 331 | 2011 |
| Paternally Inherited Inactivating Mutations of the GNAS1 Gene in Progressive Osseous Heteroplasia EM Shore, J Ahn, SJ De Beur, M Li, M Xu, RJMK Gardner, MA Zasloff, ... New England Journal of Medicine 346 (2), 99-106, 2002 | 319 | 2002 |
| Inherited human diseases of heterotopic bone formation EM Shore, FS Kaplan Nature Reviews Rheumatology 6 (9), 518-527, 2010 | 289 | 2010 |
| Biosynthesis of the cell adhesion molecule uvomorulin (E-cadherin) in Madin-Darby canine kidney epithelial cells. EM Shore, WJ Nelson Journal of Biological Chemistry 266 (29), 19672-19680, 1991 | 278 | 1991 |
| Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement G Mantovani, M Bastepe, D Monk, L De Sanctis, S Thiele, A Usardi, ... Nature Reviews Endocrinology 14 (8), 476-500, 2018 | 277 | 2018 |
| The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization Q Shen, SC Little, M Xu, J Haupt, C Ast, T Katagiri, S Mundlos, ... The Journal of clinical investigation 119 (11), 3462-3472, 2009 | 262 | 2009 |
| Progressive osseous heteroplasia FS Kaplan, EM Shore Journal of Bone and Mineral Research 15 (11), 2084-2094, 2000 | 237 | 2000 |
| Early mortality and cardiorespiratory failure in patients with fibrodysplasia ossificans progressiva FS Kaplan, MA Zasloff, JA Kitterman, EM Shore, CC Hong, DM Rocke The Journal of Bone and Joint Surgery. American volume. 92 (3), 686, 2010 | 227 | 2010 |
| Early diagnosis of fibrodysplasia ossificans progressiva FS Kaplan, M Xu, DL Glaser, F Collins, M Connor, J Kitterman, D Sillence, ... Pediatrics 121 (5), e1295-e1300, 2008 | 220 | 2008 |
| Fibrodysplasia ossificans progressiva: diagnosis, management, and therapeutic horizons RJ Pignolo, EM Shore, FS Kaplan Pediatric endocrinology reviews: PER 10 (0 2), 437, 2013 | 214 | 2013 |
| Activation of Hedgehog signaling by loss of GNAS causes heterotopic ossification JB Regard, D Malhotra, J Gvozdenovic-Jeremic, M Josey, M Chen, ... Nature medicine 19 (11), 1505-1512, 2013 | 213 | 2013 |
