Shriners Hospital for Children, St. Louis

Year	Article	Times Cited	Times Cited (no self-citations)
2015	Whyte MP, Zhang F, Wenkert D, McAlister WH, Mack KE, Benigno MC, Coburn SP, Wagy S, Griffin DM, Ericson KL, Mumm S. Hypophosphatasia: validation and expansion of the clinical nosology for children from 25 years experience with 173 pediatric patients. Bone. June 2015;75:229-239.	18	11
2017	Whyte MP. Hypophosphatasia: an overview for 2017. Bone. September 2017;102:15-25.	14	12
2020	Mumm S, Gottesman GS, Wenkert D, Campeau PM, Nenninger A, Huskey M, Bijanki VN, Veis DJ, Barnes AM, Marini JC, Stolina M, Zhang F, McAlister WH, Whyte MP. Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation. Bone. January 2020;130:115047.	2	0
2020	Whyte MP, Amalnath SD, McAlister WH, McKee MD, Veis DJ, Huskey M, Duan S, Bijanki VN, Alur S, Mumm S. Hypophosphatemic osteosclerosis, hyperostosis, and enthesopathy associated with novel homozygous mutations of DMP1 encoding dentin matrix protein 1 and SPP1 encoding osteopontin: the first digenic SIBLING protein osteopathy? Bone. March 2020;132:115190.	1	1
2020	Iwamoto SJ, Rothman MS, Duan S, Baker JC, Mumm S, Whyte MP. Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANK. Bone. April 2020;133:115224.	2	0
2020	Whyte MP, Zhang F, Wenkert D, Mumm S, Berndt TJ, Kumar R. Hyperphosphatemia with low FGF7 and normal FGF23 and sFRP4 levels in the circulation characterizes pediatric hypophosphatasia. Bone. May 2020;134:115300.	1	0
2020	Lin EL, Gottesman GS, McAlister WH, Bijanki VN, Mack KE, Griffin DM, Mumm S, Whyte MP. Healing of vitamin D deficiency rickets complicating hypophosphatasia suggests a role beyond circulating mineral sufficiency for vitamin D in musculoskeletal health. Bone. July 2020;136:115322.	0	0
2020	Whyte MP, Campeau PM, McAlister WH, Roodman GD, Kurihara N, Nenninger A, Duan S, Gottesman GS, Bijanki VN, Sedighi H, Veis DJ, Mumm S. Juvenile Paget's disease from heterozygous mutation of SP7 encoding osterix (specificity protein 7, transcription factor SP7). Bone. August 2020;137:115364.	2	2
2020	Brance ML, Brun LR, Cóccaro NM, Aravena A, Duan S, Mumm S, Whyte MP. High bone mass from mutation of low-density lipoprotein receptor-related protein 6 (LRP6). Bone. December 2020;141:115550.	0	0
2021	Shepherdson JL, Zheng H, Amarillo IE, McAlinden A, Shinawi M. Delineation of the 1q24.3 microdeletion syndrome provides further evidence for the potential role of non-coding RNAs in regulating the skeletal phenotype. Bone. January 2021;142:115705.	0	0
2021	Seefried L, Kishnani PS, Moseley S, Denker AE, Watsky E, Whyte MP, Dahir KM. Pharmacodynamics of asfotase alfa in adults with pediatric-onset hypophosphatasia. Bone. January 2021;142:115664.	1	0
2021	Hensley AP, McAlinden A. The role of microRNAs in bone development. Bone. February 2021;143:115760.	1	1
2021	McAlinden A. Response to letter to the editor. Bone. March 2021;144:115823.	0	0
2021	Whyte MP, Aronson J, McAlister WH, Weinstein RS, Wenkert D, Clements KL, Gottesman GS, Madson KL, Stolina M, Bijanki VN, Plotkin H, Huskey M, Duan S, Mumm S. Coalescing expansile skeletal disease: delineation of an extraordinary osteopathy involving the ifitm5 mutation of osteogenesis imperfecta type V. Bone. April 2021;145:115835.	0	0
2021	Cook FJ, Seagrove-Guffey M, Mumm S, Veis DJ, McAlister WH, Bijanki VN, Wenkert D, Whyte MP. Non-endemic skeletal fluorosis: causes and associated secondary hyperparathyroidism (case report and literature review). Bone. April 2021;145:115839.	1	0
2021	Zarei A, Ballard A, Cox L, Bayguinov P, Harris T, Davis JL, Roper P, Fitzpatrick J, Faccio R, Veis DJ. Osteolineage depletion of mitofusin2 enhances cortical bone formation in female mice. Bone. July 2021;148:115941.	0	0
2021	Whyte MP, May JD, McAlister WH, Burgener K, Cortez SR, Kreienkamp R, Castro O, Verzola R, Zavala AS, McPherson CC, Gottesman GS, Ericson KL, Coburn SP, Arbelaez AM. Vitamin B₆ deficiency with normal plasma levels of pyridoxal 5′-phosphate in perinatal hypophosphatasia. Bone. September 2021;150:116007.	2	1
2021	Zheng H, Liu J, Yu J, McAlinden A. Expression profiling of mitochondria-associated microRNAs during osteogenic differentiation of human MSCs. Bone. October 2021;151:116058.	0	0
2022	Whyte MP, Zhang F, Wenkert D, Mack KE, Bijanki VN, Ericson KL, Coburn SP. Hypophosphatasia: vitamin B₆ status of affected children and adults. Bone. January 2022;154:116204.	0	0
2022	Salles Rosa Neto N, Englert D, McAlister WH, Mumm S, Mills D, Veis DJ, Burshell A, Boyde A, Whyte MP. Periarticular calcifications containing giant pseudo-crystals of francolite in skeletal fluorosis from 1,1-difluoroethane “huffing”. Bone. July 2022;160:116421.	0	0
2023	Whyte MP. Carbonic anhydrase II deficiency. Bone. April 2023;169:116684.	1	1
2023	Craven M, Vajravelu ME, Shekdar KV, Levine MA, Mumm S, Whyte MP, Mancilla EE. Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): clinical characterization and response to bisphosphonate therapy. Bone. May 2023;170:116698.	0	0
2023	Whyte MP. Osteopetrosis: discovery and early history of “marble bone disease”. Bone. June 2023;171:116737.	0	0
2023	Whyte MP, McAlister WH, Dhiman V, Gopinathan NR, Bhadada SK. Drug-induced osteopetrosis. Bone. August 2023;173:116788.	0	0
2016	Millán JL, Whyte MP. Alkaline phosphatase and hypophosphatasia. Calcif Tiss Int. April 2016;98(4):398-416.	23	15
2021	Padidela R, Whyte MP, Glorieux FH, Munns CF, Ward LM, Nilsson O, Portale AA, Simmons JH, Namba N, Cheong HI, Pitukcheewanont P, Sochett E, Högler W, Muroya K, Tanaka H, Gottesman GS, Biggin A, Perwad F, Williams A, Nixon A, Sun W, Chen A, Skrinar A, Imel EA. Patient-reported outcomes from a randomized, active-controlled, open-label, phase 3 trial of burosumab versus conventional therapy in children with x-linked hypophosphatemia. Calcif Tiss Int. May 2021;108(5):622-633.	0	0
2020	Wang C, Xiao J, Nowak K, Gunasekera K, Alippe Y, Speckman S, Yang T, Kress D, Abu‐Amer Y, Hottiger MO, Mbalaviele G. PARP1 hinders histone H2B occupancy at the NFATc1 promoter to restrain osteoclast differentiation. J Bone Miner Res. April 2020;35(4):776-788.	0	0
2020	Smith PS, Gottesman GS, Zhang F, Cook F, Ramirez B, Wenkert D, Wollberg V, Huskey M, Mumm S, Whyte MP. X‐linked hypophosphatemia: uniquely mild disease associated with PHEX 3′‐UTR mutation c.231A>G (a retrospective case–control study). J Bone Miner Res*. May 2020;35(5):920-931.	4	2
2020	di Carlo FS, Pazzaglia L, Mumm S, Benassi MS, De Chiara A, Franchi A, Parafioriti A, Righi A, Esposito T, Whyte MP, Gianfrancesco F. ZNF687 mutations in an extended cohort of neoplastic transformations in Paget's disease of bone: implications for clinical pathology. J Bone Miner Res. October 2020;35(10):1974-1980.	0	0
2021	Whyte MP. Tumor‐induced osteomalacia: treatment progress using burosumab, an anti‐FGF23 monoclonal antibody. J Bone Miner Res. April 2021;36(4):625-626.	0	0
2021	Veis DJ, Cassat JE. Infectious osteomyelitis: marrying bone biology and microbiology to shed new light on a persistent clinical challenge. J Bone Miner Res. April 2021;36(4):636-643.	1	1
2020	Shen H, Yoneda S, Abu‐Amer Y, Guilak F, Gelberman RH. Stem cell‐derived extracellular vesicles attenuate the early inflammatory response after tendon injury and repair. J Orthop Res. January 2020;38(1):117-127.	0	0
2022	Guilak F, Estes BT, Moutos FT. Functional tissue engineering of articular cartilage for biological joint resurfacing: the 2021 Elizabeth Winston Lanier Kappa Delta Award. J Orthop Res. August 2022;40(8):1721-1734.	0	0
2022	Pferdehirt L, Guo P, Lu A, Huard M, Guilak F, Huard J. In vitro analysis of genome-engineered muscle-derived stem cells for autoregulated anti-inflammatory and antifibrotic activity. J Orthop Res. December 2022;40(12):2937-2946.	0	0
2023	Buettmann EG, Chlebek C, Lockard CA, Clayton SW, Lewis KJ, Collins KH. Post or perish? social media strategies for disseminating orthopedic research. J Orthop Res. August 2023;41(8):1643-1652.	0	0
2016	Whyte MP. Hypophosphatasia: aetiology, nosology, pathogenesis, diagnosis and treatment. Nat Rev Endocrinol. April 2016;12(4):233-246.	23	17

Name	Count	Oldest	Newest
Bijanki, Vinieth N.	7	2020	2022
Veis, Deborah J.	7	2020	2022
Mumm, Steven	14	2015	2023
Guilak, Farshid	3	2020	2022
Zhang, Fan	5	2015	2022
Duan, Shenghui	1	2020	2020
Wenkert, Deborah	7	2015	2022
Gottesman, Gary S.	7	2020	2021
Whyte, Michael P.	25	2015	2023