| Enzyme-replacement therapy in life-threatening hypophosphatasia MP Whyte, CR Greenberg, NJ Salman, MB Bober, WH McAlister, ... New England Journal of Medicine 366 (10), 904-913, 2012 | 573 | 2012 |
| Bisphosphonate-induced osteopetrosis MP Whyte, D Wenkert, KL Clements, WH McAlister, S Mumm New England Journal of Medicine 349 (5), 457-463, 2003 | 523 | 2003 |
| Risk of subsequent fracture after prior fracture among older women A Balasubramanian, J Zhang, L Chen, D Wenkert, SG Daigle, A Grauer, ... Osteoporosis international 30, 79-92, 2019 | 301 | 2019 |
| Hypophosphatasia: validation and expansion of the clinical nosology for children from 25 years experience with 173 pediatric patients MP Whyte, F Zhang, D Wenkert, WH McAlister, KE Mack, MC Benigno, ... Bone 75, 229-239, 2015 | 255 | 2015 |
| Fracture prediction and the definition of osteoporosis in children and adolescents: the ISCD 2007 Pediatric Official Positions F Rauch, H Plotkin, L DiMeglio, RH Engelbert, RC Henderson, C Munns, ... Journal of Clinical Densitometry 11 (1), 22-28, 2008 | 177 | 2008 |
| Hypophosphatasia: nonlethal disease despite skeletal presentation in utero (17 new cases and literature review) D Wenkert, WH McAlister, SP Coburn, JA Zerega, LM Ryan, KL Ericson, ... Journal of Bone and Mineral Research 26 (10), 2389-2398, 2011 | 142 | 2011 |
| Infantile hypophosphatasia: transplantation therapy trial using bone fragments and cultured osteoblasts RA Cahill, D Wenkert, SA Perlman, A Steele, SP Coburn, WH McAlister, ... The Journal of Clinical Endocrinology & Metabolism 92 (8), 2923-2930, 2007 | 130 | 2007 |
| Bisphosphonate‐induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceases MP Whyte, WH McAlister, DV Novack, KL Clements, PL Schoenecker, ... Journal of Bone and Mineral Research 23 (10), 1698-1707, 2008 | 110 | 2008 |
| Timing of the appearance of macronuclear-specific histone variant hv1 and gene expression in developing new macronuclei of Tetrahymena thermophila. D Wenkert, CD Allis The Journal of cell biology 98 (6), 2107-2117, 1984 | 108 | 1984 |
| Deactivating Germline Mutations in LEMD3 Cause Osteopoikilosis and Buschke‐Ollendorff Syndrome, but Not Sporadic Melorheostosis S Mumm, D Wenkert, X Zhang, WH McAlister, RJ Mier, MP Whyte Journal of Bone and Mineral Research 22 (2), 243-250, 2007 | 97 | 2007 |
| Herpes zoster reactivation in patients with rheumatoid arthritis: analysis of disease characteristics and disease‐modifying antirheumatic drugs DA Pappas, MM Hooper, JM Kremer, G Reed, Y Shan, D Wenkert, ... Arthritis care & research 67 (12), 1671-1678, 2015 | 88 | 2015 |
| Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasia MP Whyte, D Wenkert, WH McAlister, MZ Mughal, AJ Freemont, ... Journal of Bone and Mineral Research 24 (8), 1493-1505, 2009 | 72 | 2009 |
| Hypophosphatasia: natural history study of 101 affected children investigated at one research center MP Whyte, D Wenkert, F Zhang Bone 93, 125-138, 2016 | 65 | 2016 |
| Rheumatoid arthritis disease activity and disability affect the risk of serious infection events in RADIUS 1 A Weaver, O Troum, M Hooper, AS Koenig, S Chaudhari, JY Feng, ... The Journal of Rheumatology 40 (8), 1275-1281, 2013 | 63 | 2013 |
| Congenital insensitivity to pain: fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium … V Phatarakijnirund, S Mumm, WH McAlister, DV Novack, D Wenkert, ... Bone 84, 289-298, 2016 | 59 | 2016 |
| Fibrodysplasia ossificans progressiva: Middle‐age onset of heterotopic ossification from a unique missense mutation (c.974G > C, p.G325A) in ACVR1 MP Whyte, D Wenkert, JL Demertzis, EF DiCarlo, E Westenberg, S Mumm Journal of Bone and Mineral Research 27 (3), 729-737, 2012 | 58 | 2012 |
| Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis? CL Heike, ML Cunningham, RD Steiner, D Wenkert, RL Hornung, ... American Journal of Medical Genetics Part A 139 (2), 67-77, 2005 | 57 | 2005 |
| Camurati‐Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand MP Whyte, WG Totty, DV Novack, X Zhang, D Wenkert, S Mumm Journal of Bone and Mineral Research 26 (5), 920-933, 2011 | 54 | 2011 |
| Multicentric carpotarsal osteolysis syndrome is caused by only a few domain‐specific mutations in MAFB, a negative regulator of RANKL‐induced osteoclastogenesis S Mumm, M Huskey, S Duan, D Wenkert, KL Madson, GS Gottesman, ... American journal of medical genetics Part A 164 (9), 2287-2293, 2014 | 48 | 2014 |
| Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers‐Schönberg disease (chloride channel 7 deficiency osteopetrosis) among the … MP Whyte, LG Kempa, WH McAlister, F Zhang, S Mumm, D Wenkert Journal of Bone and Mineral Research 25 (11), 2515-2526, 2010 | 48 | 2010 |
