| Intestinal npt2b plays a major role in phosphate absorption and homeostasis Y Sabbagh, SP O'Brien, W Song, JH Boulanger, A Stockmann, C Arbeeny, ... Journal of the American Society of Nephrology 20 (11), 2348-2358, 2009 | 382 | 2009 |
| Repression of osteocyte Wnt/β‐catenin signaling is an early event in the progression of renal osteodystrophy Y Sabbagh, FG Graciolli, S O'Brien, W Tang, LM dos Reis, S Ryan, ... Journal of Bone and Mineral Research 27 (8), 1757-1772, 2012 | 289 | 2012 |
| Hypophosphatemia leads to rickets by impairing caspase-mediated apoptosis of hypertrophic chondrocytes Y Sabbagh, TO Carpenter, MB Demay Proceedings of the National Academy of Sciences 102 (27), 9637-9642, 2005 | 289 | 2005 |
| A novel model of adenine-induced tubulointerstitial nephropathy in mice T Jia, H Olauson, K Lindberg, R Amin, K Edvardsson, B Lindholm, ... BMC nephrology 14, 1-8, 2013 | 211 | 2013 |
| Intestinal phosphate transport Y Sabbagh, H Giral, Y Caldas, M Levi, SC Schiavi Advances in chronic kidney disease 18 (2), 85-90, 2011 | 178 | 2011 |
| Genetic dissection of phosphate-and vitamin D-mediated regulation of circulating Fgf23 concentrations X Yu, Y Sabbagh, SI Davis, MB Demay, KE White Bone 36 (6), 971-977, 2005 | 162 | 2005 |
| The complexity of chronic kidney disease–mineral and bone disorder across stages of chronic kidney disease FG Graciolli, KR Neves, F Barreto, DV Barreto, LM Dos Reis, ME Canziani, ... Kidney international 91 (6), 1436-1446, 2017 | 161 | 2017 |
| Long-term therapeutic effect of vitamin D analog doxercalciferol on diabetic nephropathy: strong synergism with AT1 receptor antagonist Y Zhang, DK Deb, J Kong, G Ning, Y Wang, G Li, Y Chen, Z Zhang, ... American Journal of Physiology-Renal Physiology 297 (3), F791-F801, 2009 | 145 | 2009 |
| Npt2b deletion attenuates hyperphosphatemia associated with CKD SC Schiavi, W Tang, C Bracken, SP O’Brien, W Song, J Boulanger, ... Journal of the American Society of Nephrology 23 (10), 1691-1700, 2012 | 128 | 2012 |
| PHEXdb, a locus‐specific database for mutations causing X‐linked hypophosphatemia Y Sabbagh, AO Jones, HS Tenenhouse Human mutation 16 (1), 1-6, 2000 | 117 | 2000 |
| Erythropoietin stimulates murine and human fibroblast growth factor-23, revealing novel roles for bone and bone marrow EL Clinkenbeard, MR Hanudel, KR Stayrook, HN Appaiah, EG Farrow, ... haematologica 102 (11), e427, 2017 | 110 | 2017 |
| Ontogeny of Phex/PHEX protein expression in mouse embryo and subcellular localization in osteoblasts DL Thompson, Y Sabbagh, HS Tenenhouse, PC Roche, MK Drezner, ... Journal of Bone and Mineral Research 17 (2), 311-320, 2002 | 96 | 2002 |
| Osteoblasts lacking the vitamin D receptor display enhanced osteogenic potential in vitro K Sooy, Y Sabbagh, MB Demay Journal of cellular biochemistry 94 (1), 81-87, 2005 | 95 | 2005 |
| Impaired bone development and increased mesenchymal progenitor cells in calvaria of RB1−/− mice GM Gutierrez, E Kong, Y Sabbagh, NE Brown, JS Lee, MB Demay, ... Proceedings of the National Academy of Sciences 105 (47), 18402-18407, 2008 | 71 | 2008 |
| Impaired bone development and increased mesenchymal progenitor cells in calvaria of RB1−/− mice GM Gutierrez, E Kong, Y Sabbagh, NE Brown, JS Lee, MB Demay, ... Proceedings of the National Academy of Sciences 105 (47), 18402-18407, 2008 | 71 | 2008 |
| Calcium and vitamin D: what is known about the effects on growing bone MB Demay, Y Sabbagh, TO Carpenter Pediatrics 119 (Supplement_2), S141-S144, 2007 | 70 | 2007 |
| Effects of dietary phosphate on adynamic bone disease in rats with chronic kidney disease–role of sclerostin? JC Ferreira, GO Ferrari, KR Neves, RT Cavallari, WV Dominguez, ... PLoS One 8 (11), e79721, 2013 | 67 | 2013 |
| Disease-causing missense mutations in the PHEX gene interfere with membrane targeting of the recombinant protein Y Sabbagh, G Boileau, L DesGroseillers, HS Tenenhouse Human molecular genetics 10 (15), 1539-1546, 2001 | 66 | 2001 |
| Novel phosphate-regulating genes in the pathogenesis of renal phosphate wasting disorders HS Tenenhouse, Y Sabbagh Pflügers Archiv 444, 317-326, 2002 | 65 | 2002 |
| Structure and Function of Disease-Causing Missense Mutations in the PHEX Gene Y Sabbagh, G Boileau, M Campos, AK Carmona, HS Tenenhouse The Journal of Clinical Endocrinology & Metabolism 88 (5), 2213-2222, 2003 | 62 | 2003 |
