Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

HMS faculty, help us improve the algorithms in Profiles by uploading your CV!

Michael Aaron Levine, Ph.D.


Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Ralph D, Levine MA, Richard G, Morrow MM, Flynn EK, Uitto J, Li Q. Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratoderma. Hum Mutat. 2022 Sep; 43(9):1183-1200. PMID: 35475527; PMCID: PMC9357117.
    Citations:    Fields:    
  2. Hawkes CP, Al Jubeh JM, Li D, Tucker SE, Rajiyah T, Levine MA. Novel PTH Gene Mutations Causing Isolated Hypoparathyroidism. J Clin Endocrinol Metab. 2022 05 17; 107(6):e2449-e2458. PMID: 35165722; PMCID: PMC9113798.
    Citations:    Fields:    Translation:Humans
  3. Ralph D, Nitschke Y, Levine MA, Caffet M, Wurst T, Saeidian AH, Youssefian L, Vahidnezhad H, Terry SF, Rutsch F, Uitto J, Li Q. ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification. PLoS Genet. 2022 04; 18(4):e1010192. PMID: 35482848; PMCID: PMC9089899.
    Citations:    Fields:    Translation:Humans
  4. Ramirez-Suarez KI, Cohen SA, Barrera CA, Levine MA, Goldberg DJ, Otero HJ. Longitudinal assessment of vascular calcification in generalized arterial calcification of infancy. Pediatr Radiol. 2022 Apr 19. PMID: 35438330.
    Citations:    Fields:    
  5. London S, Levine MA, Li D, Spiegel R, Lebel A, Halevy R, Tenenbaum-Rakover Y. Hypocalcemia as the Initial Presentation of Type 2 Bartter Syndrome: A Family Report. J Clin Endocrinol Metab. 2022 03 24; 107(4):e1679-e1688. PMID: 34751387.
    Citations:    Fields:    Translation:Humans
  6. Levine MA, Mandeville JB, Calabro F, Izquierdo-Garcia D, Chonde DB, Chen KT, Hong I, Price JC, Luna B, Catana C. Assessment of motion and model bias on the detection of dopamine response to behavioral challenge. J Cereb Blood Flow Metab. 2022 07; 42(7):1309-1321. PMID: 35118904; PMCID: PMC9207487.
    Citations:    Fields:    Translation:Humans
  7. Stoffers AJ, Weber DR, Levine MA. An Update on Vitamin D Deficiency in the twenty-first century: nature and nurture. Curr Opin Endocrinol Diabetes Obes. 2022 02 01; 29(1):36-43. PMID: 34839324; PMCID: PMC8849548.
    Citations: 2     Fields:    Translation:Humans
  8. Mandeville JB, Levine MA, Arsenault JT, Vanduffel W, Rosen BR, Sander CY. A reference tissue forward model for improved PET accuracy using within-scan displacement studies. J Cereb Blood Flow Metab. 2022 06; 42(6):1007-1019. PMID: 34894821; PMCID: PMC9125481.
    Citations:    Fields:    Translation:Animals
  9. Gittoes N, Rejnmark L, Ing SW, Brandi ML, Björnsdottir S, Hahner S, Hofbauer LC, Houillier P, Khan AA, Levine MA, Mannstadt M, Shoback DM, Vokes TJ, Zhang P, Marelli C, Germak J, Clarke BL. The PARADIGHM (physicians advancing disease knowledge in hypoparathyroidism) registry for patients with chronic hypoparathyroidism: study protocol and interim baseline patient characteristics. BMC Endocr Disord. 2021 Nov 20; 21(1):232. PMID: 34801015; PMCID: PMC8606089.
    Citations:    Fields:    Translation:Humans
  10. Danzig J, Li D, Jan de Beur S, Levine MA. High-throughput Molecular Analysis of Pseudohypoparathyroidism 1b Patients Reveals Novel Genetic and Epigenetic Defects. J Clin Endocrinol Metab. 2021 10 21; 106(11):e4603-e4620. PMID: 34157100; PMCID: PMC8677598.
    Citations: 4     Fields:    Translation:HumansCells
  11. Lenherr-Taube N, Young EJ, Furman M, Elia Y, Assor E, Chitayat D, Uster T, Kirwin S, Robbins K, Vinette KMB, Daneman A, Marshall CR, Collins C, Thummel K, Sochett E, Levine MA. Mild Idiopathic Infantile Hypercalcemia-Part 1: Biochemical and Genetic Findings. J Clin Endocrinol Metab. 2021 09 27; 106(10):2915-2937. PMID: 34125233; PMCID: PMC8475208.
    Citations: 1     Fields:    Translation:Humans
  12. Lenherr-Taube N, Furman M, Assor E, Elia Y, Collins C, Thummel K, Levine MA, Sochett E. Mild Idiopathic Infantile Hypercalcemia-Part 2: A Longitudinal Observational Study. J Clin Endocrinol Metab. 2021 09 27; 106(10):2938-2948. PMID: 34139759; PMCID: PMC8475233.
    Citations: 1     Fields:    Translation:Humans
  13. Catana C, Laforest R, An H, Boada F, Cao T, Faul D, Jakoby B, Jansen FP, Kemp BJ, Kinahan PE, Larson P, Levine MA, Maniawski P, Mawlawi O, McConathy JE, McMillan AB, Price JC, Rajagopal A, Sunderland J, Veit-Haibach P, Wangerin KA, Ying C, Hope TA. A Path to Qualification of PET/MRI Scanners for Multicenter Brain Imaging Studies: Evaluation of MRI-Based Attenuation Correction Methods Using a Patient Phantom. J Nucl Med. 2022 04; 63(4):615-621. PMID: 34301784; PMCID: PMC8973286.
    Citations: 1     Fields:    Translation:Humans
  14. Hawkes CP, Levine MA. A painting of the Christ Child with bowed legs: Rickets in the Renaissance. Am J Med Genet C Semin Med Genet. 2021 06; 187(2):216-218. PMID: 33982432; PMCID: PMC8882043.
    Citations: 1     Fields:    Translation:Humans
  15. Ferreira CR, Kavanagh D, Oheim R, Zimmerman K, Stürznickel J, Li X, Stabach P, Rettig RL, Calderone L, MacKichan C, Wang A, Hutchinson HA, Nelson T, Tommasini SM, von Kroge S, Fiedler IA, Lester ER, Moeckel GW, Busse B, Schinke T, Carpenter TO, Levine MA, Horowitz MC, Braddock DT. Response of the ENPP1-Deficient Skeletal Phenotype to Oral Phosphate Supplementation and/or Enzyme Replacement Therapy: Comparative Studies in Humans and Mice. J Bone Miner Res. 2021 05; 36(5):942-955. PMID: 33465815; PMCID: PMC8739051.
    Citations: 1     Fields:    Translation:HumansAnimals
  16. Kalantar-Zadeh K, Ganz T, Trumbo H, Seid MH, Goodnough LT, Levine MA. Parenteral iron therapy and phosphorus homeostasis: A review. Am J Hematol. 2021 05 01; 96(5):606-616. PMID: 33471363; PMCID: PMC8248123.
    Citations: 4     Fields:    Translation:Humans
  17. Hawkes CP, Roy SM, Dekelbab B, Frazier B, Grover M, Haidet J, Listman J, Madsen S, Roan M, Rodd C, Sopher A, Tebben P, Levine MA. Hypercalcemia in Children Using the Ketogenic Diet: A Multicenter Study. J Clin Endocrinol Metab. 2021 01 23; 106(2):e485-e495. PMID: 33124662; PMCID: PMC7823241.
    Citations: 3     Fields:    Translation:Humans
  18. Hawkes CP, Shulman DI, Levine MA. Recombinant human parathyroid hormone (1-84) is effective in CASR-associated hypoparathyroidism. Eur J Endocrinol. 2020 Dec; 183(6):K13-K21. PMID: 33112267; PMCID: PMC7853300.
    Citations: 1     Fields:    Translation:Humans
  19. Espiard S, Drougat L, Settas N, Haydar S, Bathon K, London E, Levy I, Faucz FR, Calebiro D, Bertherat J, Li D, Levine MA, Stratakis CA. PRKACB variants in skeletal disease or adrenocortical hyperplasia: effects on protein kinase A. Endocr Relat Cancer. 2020 11; 27(11):647-656. PMID: 33055300.
    Citations: 2     Fields:    Translation:HumansAnimals
  20. Ferreira CR, Hackbarth ME, Ziegler SG, Pan KS, Roberts MS, Rosing DR, Whelpley MS, Bryant JC, Macnamara EF, Wang S, Müller K, Hartley IR, Chew EY, Corden TE, Jacobsen CM, Holm IA, Rutsch F, Dikoglu E, Chen MY, Mughal MZ, Levine MA, Gafni RI, Gahl WA. Prospective phenotyping of long-term survivors of generalized arterial calcification of infancy (GACI). Genet Med. 2021 02; 23(2):396-407. PMID: 33005041; PMCID: PMC7867608.
    Citations: 12     Fields:    Translation:Humans
  21. Hanley PC, Kanwar HS, Martineau C, Levine MA. Short Stature is Progressive in Patients with Heterozygous NPR2 Mutations. J Clin Endocrinol Metab. 2020 10 01; 105(10). PMID: 32720985.
    Citations: 5     Fields:    Translation:HumansCells
  22. Li D, Bupp C, March ME, Hakonarson H, Levine MA. Intragenic Deletions of GNAS in Pseudohypoparathyroidism Type 1A Identify a New Region Affecting Methylation of Exon A/B. J Clin Endocrinol Metab. 2020 09 01; 105(9). PMID: 32436958; PMCID: PMC7947960.
    Citations: 3     Fields:    Translation:HumansCells
  23. Mantovani G, Bastepe M, Monk D, de Sanctis L, Thiele S, Ahmed SF, Bufo R, Choplin T, De Filippo G, Devernois G, Eggermann T, Elli FM, Garcia Ramirez A, Germain-Lee EL, Groussin L, Hamdy NAT, Hanna P, Hiort O, Jüppner H, Kamenický P, Knight N, Le Norcy E, Lecumberri B, Levine MA, Mäkitie O, Martin R, Martos-Moreno GÁ, Minagawa M, Murray P, Pereda A, Pignolo R, Rejnmark L, Rodado R, Rothenbuhler A, Saraff V, Shoemaker AH, Shore EM, Silve C, Turan S, Woods P, Zillikens MC, Perez de Nanclares G, Linglart A. Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients. Horm Res Paediatr. 2020; 93(3):182-196. PMID: 32756064; PMCID: PMC8140671.
    Citations: 9     Fields:    Translation:Humans
  24. Gordon RJ, Li D, Doyle D, Zaritsky J, Levine MA. Digenic Heterozygous Mutations in SLC34A3 and SLC34A1 Cause Dominant Hypophosphatemic Rickets with Hypercalciuria. J Clin Endocrinol Metab. 2020 07 01; 105(7). PMID: 32311027; PMCID: PMC7448300.
    Citations: 8     Fields:    Translation:Humans
  25. Levine MA. Diagnosis and Management of Vitamin D Dependent Rickets. Front Pediatr. 2020; 8:315. PMID: 32596195; PMCID: PMC7303887.
    Citations: 12     
  26. Casella A, Long C, Zhou J, Lai M, O'Lear L, Caplan I, Levine MA, Roizen JD. Differential Frequency of CYP2R1 Variants Across Populations Reveals Pathway Selection for Vitamin D Homeostasis. J Clin Endocrinol Metab. 2020 05 01; 105(5). PMID: 32115644; PMCID: PMC7096315.
    Citations:    Fields:    Translation:HumansCells
  27. Rampp RD, Mancilla EE, Adzick NS, Levine MA, Kelz RR, Fraker DL, Iyer P, Lindeman BM, Mejia VA, Chen H, Wachtel H. Single Gland, Ectopic Location: Adenomas are Common Causes of Primary Hyperparathyroidism in Children and Adolescents. World J Surg. 2020 05; 44(5):1518-1525. PMID: 31900569.
    Citations: 4     Fields:    Translation:Humans
  28. Bamba V, Levine MA. Long-acting Growth Hormone Therapy: A REAL3 Alternative to Daily Growth Hormone Treatment? J Clin Endocrinol Metab. 2020 04 01; 105(4). PMID: 32055832.
    Citations: 1     Fields:    Translation:Humans
  29. Roizen JD, Levine MA. Vitamin D Therapy and the Era of Precision Medicine. J Clin Endocrinol Metab. 2020 03 01; 105(3). PMID: 31665328.
    Citations: 1     Fields:    Translation:Humans
  30. Modarressi T, Levine MA, Khan AN. Response to Letter to the Editor: "Gestational Gigantomastia Complicated by PTHrP-Mediated Hypercalcemia". J Clin Endocrinol Metab. 2019 11 01; 104(11):5100-5101. PMID: 30977835.
    Citations:    Fields:    Translation:Humans
  31. Mannstadt M, Clarke BL, Bilezikian JP, Bone H, Denham D, Levine MA, Peacock M, Rothman J, Shoback DM, Warren ML, Watts NB, Lee HM, Sherry N, Vokes TJ. Safety and Efficacy of 5 Years of Treatment With Recombinant Human Parathyroid Hormone in Adults With Hypoparathyroidism. J Clin Endocrinol Metab. 2019 11 01; 104(11):5136-5147. PMID: 31369089; PMCID: PMC6760337.
    Citations: 11     Fields:    Translation:Humans
  32. Ehrenkranz J, Levine MA. Bones and Joints: The Effects of Cannabinoids on the Skeleton. J Clin Endocrinol Metab. 2019 10 01; 104(10):4683-4694. PMID: 31393556.
    Citations: 9     Fields:    Translation:HumansAnimals
  33. Li D, March ME, Gutierrez-Uzquiza A, Kao C, Seiler C, Pinto E, Matsuoka LS, Battig MR, Bhoj EJ, Wenger TL, Tian L, Robinson N, Wang T, Liu Y, Weinstein BM, Swift M, Jung HM, Kaminski CN, Chiavacci R, Perkins JA, Levine MA, Sleiman PMA, Hicks PJ, Strausbaugh JT, Belasco JB, Dori Y, Hakonarson H. ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor. Nat Med. 2019 07; 25(7):1116-1122. PMID: 31263281.
    Citations: 34     Fields:    Translation:HumansAnimalsCells
  34. Roizen JD, Levine MA. Response to: Obesity and Vitamin D Metabolism Modifications. J Bone Miner Res. 2019 07; 34(7):1384. PMID: 31141223.
    Citations:    Fields:    Translation:Humans
  35. Gordon RJ, Levine MA. Burosumab treatment of children with X-linked hypophosphataemic rickets. Lancet. 2019 06 15; 393(10189):2364-2366. PMID: 31104830.
    Citations: 4     Fields:    Translation:Humans
  36. Youssefian L, Vahidnezhad H, Saeidian AH, Pajouhanfar S, Sotoudeh S, Mansouri P, Amirkashani D, Zeinali S, Levine MA, Peris K, Colombo R, Uitto J. Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations. J Hepatol. 2019 08; 71(2):366-370. PMID: 30954460.
    Citations: 12     Fields:    Translation:Humans
  37. Roizen JD, Long C, Casella A, O'Lear L, Caplan I, Lai M, Sasson I, Singh R, Makowski AJ, Simmons R, Levine MA. Obesity Decreases Hepatic 25-Hydroxylase Activity Causing Low Serum 25-Hydroxyvitamin D. J Bone Miner Res. 2019 06; 34(6):1068-1073. PMID: 30790351; PMCID: PMC6663580.
    Citations: 26     Fields:    Translation:Animals
  38. Levine MA. The Coming of Age of Hypoparathyroidism: Novel Insights into Causation, Innovative Options for Management. Endocrinol Metab Clin North Am. 2018 12; 47(4):xv-xvi. PMID: 30390823; PMCID: PMC7294790.
    Citations:    Fields:    Translation:Humans
  39. Li D, Gordon CT, Oufadem M, Amiel J, Kanwar HS, Bakay M, Wang T, Hakonarson H, Levine MA. Heterozygous Mutations in TBX1 as a Cause of Isolated Hypoparathyroidism. J Clin Endocrinol Metab. 2018 11 01; 103(11):4023-4032. PMID: 30137364; PMCID: PMC6194809.
    Citations: 5     Fields:    Translation:HumansCells
  40. Gordon RJ, Levine MA. Genetic Disorders of Parathyroid Development and Function. Endocrinol Metab Clin North Am. 2018 12; 47(4):809-823. PMID: 30390815.
    Citations: 11     Fields:    Translation:Humans
  41. Linglart A, Levine MA, Jüppner H. Pseudohypoparathyroidism. Endocrinol Metab Clin North Am. 2018 12; 47(4):865-888. PMID: 30390819; PMCID: PMC7305568.
    Citations: 14     Fields:    Translation:Humans
  42. Li D, Wenger TL, Seiler C, March ME, Gutierrez-Uzquiza A, Kao C, Bhoj E, Tian L, Rosenbach M, Liu Y, Robinson N, Behr M, Chiavacci R, Hou C, Wang T, Bakay M, Pellegrino da Silva R, Perkins JA, Sleiman P, Levine MA, Hicks PJ, Itkin M, Dori Y, Hakonarson H. Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly. Hum Mol Genet. 2018 09 15; 27(18):3233-3245. PMID: 29905864; PMCID: PMC7190898.
    Citations: 13     Fields:    Translation:HumansAnimalsCells
  43. Modarressi T, Levine MA, Tchou J, Khan AN. Gestational Gigantomastia Complicated by PTHrP-Mediated Hypercalcemia. J Clin Endocrinol Metab. 2018 09 01; 103(9):3124-3130. PMID: 30032172.
    Citations: 4     Fields:    Translation:Humans
  44. Li Q, Huang J, Pinkerton AB, Millan JL, van Zelst BD, Levine MA, Sundberg JP, Uitto J. Inhibition of Tissue-Nonspecific Alkaline Phosphatase Attenuates Ectopic Mineralization in the Abcc6-/- Mouse Model of PXE but Not in the Enpp1 Mutant Mouse Models of GACI. J Invest Dermatol. 2019 02; 139(2):360-368. PMID: 30130617; PMCID: PMC6342656.
    Citations: 24     Fields:    Translation:HumansAnimals
  45. Mantovani G, Bastepe M, Monk D, de Sanctis L, Thiele S, Usardi A, Ahmed SF, Bufo R, Choplin T, De Filippo G, Devernois G, Eggermann T, Elli FM, Freson K, García Ramirez A, Germain-Lee EL, Groussin L, Hamdy N, Hanna P, Hiort O, Jüppner H, Kamenický P, Knight N, Kottler ML, Le Norcy E, Lecumberri B, Levine MA, Mäkitie O, Martin R, Martos-Moreno GÁ, Minagawa M, Murray P, Pereda A, Pignolo R, Rejnmark L, Rodado R, Rothenbuhler A, Saraff V, Shoemaker AH, Shore EM, Silve C, Turan S, Woods P, Zillikens MC, Perez de Nanclares G, Linglart A. Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement. Nat Rev Endocrinol. 2018 08; 14(8):476-500. PMID: 29959430; PMCID: PMC6541219.
    Citations: 64     Fields:    Translation:HumansPHPublic Health
  46. Roizen JD, Casella A, Lai M, Long C, Tara Z, Caplan I, O'Lear L, Levine MA. Decreased Serum 25-Hydroxyvitamin D in Aging Male Mice Is Associated With Reduced Hepatic Cyp2r1 Abundance. Endocrinology. 2018 08 01; 159(8):3083-3089. PMID: 29955863; PMCID: PMC6693043.
    Citations: 5     Fields:    Translation:Animals
  47. Wang L, Jia H, Tower RJ, Levine MA, Qin L. Analysis of short-term treatment with the phosphodiesterase type 5 inhibitor tadalafil on long bone development in young rats. Am J Physiol Endocrinol Metab. 2018 10 01; 315(4):E446-E453. PMID: 29920215; PMCID: PMC6230700.
    Citations: 2     Fields:    Translation:AnimalsCells
  48. Roizen JD, Li D, O'Lear L, Javaid MK, Shaw NJ, Ebeling PR, Nguyen HH, Rodda CP, Thummel KE, Thacher TD, Hakonarson H, Levine MA. CYP3A4 mutation causes vitamin D-dependent rickets type 3. J Clin Invest. 2018 05 01; 128(5):1913-1918. PMID: 29461981; PMCID: PMC5919884.
    Citations: 27     Fields:    Translation:HumansCells
  49. Chen KT, Salcedo S, Chonde DB, Izquierdo-Garcia D, Levine MA, Price JC, Dickerson BC, Catana C. MR-assisted PET motion correction in simultaneous PET/MRI studies of dementia subjects. J Magn Reson Imaging. 2018 11; 48(5):1288-1296. PMID: 29517819.
    Citations: 13     Fields:    Translation:Humans
  50. Vokes TJ, Mannstadt M, Levine MA, Clarke BL, Lakatos P, Chen K, Piccolo R, Krasner A, Shoback DM, Bilezikian JP. Recombinant Human Parathyroid Hormone Effect on Health-Related Quality of Life in Adults With Chronic Hypoparathyroidism. J Clin Endocrinol Metab. 2018 02 01; 103(2):722-731. PMID: 29099947; PMCID: PMC6458961.
    Citations: 21     Fields:    Translation:Humans
  51. Wu CC, Econs MJ, DiMeglio LA, Insogna KL, Levine MA, Orchard PJ, Miller WP, Petryk A, Rush ET, Shoback DM, Ward LM, Polgreen LE. Diagnosis and Management of Osteopetrosis: Consensus Guidelines From the Osteopetrosis Working Group. J Clin Endocrinol Metab. 2017 09 01; 102(9):3111-3123. PMID: 28655174.
    Citations: 48     Fields:    Translation:Humans
  52. Chandra A, Wang L, Young T, Zhong L, Tseng WJ, Levine MA, Cengel K, Liu XS, Zhang Y, Pignolo RJ, Qin L. Proteasome inhibitor bortezomib is a novel therapeutic agent for focal radiation-induced osteoporosis. FASEB J. 2018 01; 32(1):52-62. PMID: 28860152; PMCID: PMC5731129.
    Citations: 12     Fields:    Translation:HumansAnimalsCellsPHPublic Health
  53. McCormack SE, Li D, Kim YJ, Lee JY, Kim SH, Rapaport R, Levine MA. Digenic Inheritance of PROKR2 and WDR11 Mutations in Pituitary Stalk Interruption Syndrome. J Clin Endocrinol Metab. 2017 07 01; 102(7):2501-2507. PMID: 28453858; PMCID: PMC5505202.
    Citations: 14     Fields:    Translation:Humans
  54. Li D, Streeten EA, Chan A, Lwin W, Tian L, Pellegrino da Silva R, Kim CE, Anderson MS, Hakonarson H, Levine MA. Exome Sequencing Reveals Mutations in AIRE as a Cause of Isolated Hypoparathyroidism. J Clin Endocrinol Metab. 2017 05 01; 102(5):1726-1733. PMID: 28323927; PMCID: PMC5443324.
    Citations: 11     Fields:    Translation:Humans
  55. Hawkes CP, Li D, Hakonarson H, Meyers KE, Thummel KE, Levine MA. CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations. J Clin Endocrinol Metab. 2017 05 01; 102(5):1440-1446. PMID: 28324001; PMCID: PMC5443336.
    Citations: 23     Fields:    Translation:Humans
  56. Ackermann AM, Levine MA. Compound heterozygous mutations in COL1A1 associated with an atypical form of type I osteogenesis imperfecta. Am J Med Genet A. 2017 Jul; 173(7):1907-1912. PMID: 28436160.
    Citations: 5     Fields:    
  57. Abraham MB, Li D, Tang D, O'Connell SM, McKenzie F, Lim EM, Hakonarson H, Levine MA, Choong CS. Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene. Int J Pediatr Endocrinol. 2017; 2017:1. PMID: 28138333; PMCID: PMC5264330.
    Citations: 7     
  58. Dhir G, Li D, Hakonarson H, Levine MA. Late-onset hereditary hypophosphatemic rickets with hypercalciuria (HHRH) due to mutation of SLC34A3/NPT2c. Bone. 2017 04; 97:15-19. PMID: 27939817.
    Citations: 13     Fields:    Translation:Humans
  59. Chandra A, Lin T, Young T, Tong W, Ma X, Tseng WJ, Kramer I, Kneissel M, Levine MA, Zhang Y, Cengel K, Liu XS, Qin L. Suppression of Sclerostin Alleviates Radiation-Induced Bone Loss by Protecting Bone-Forming Cells and Their Progenitors Through Distinct Mechanisms. J Bone Miner Res. 2017 Feb; 32(2):360-372. PMID: 27635523; PMCID: PMC5476363.
    Citations: 43     Fields:    Translation:AnimalsCellsPHPublic Health
  60. Hysinger EB, Roizen JD, Mentch FD, Vazquez L, Connolly JJ, Bradfield JP, Almoguera B, Sleiman PM, Allen JL, Levine MA, Hakonarson H. Mendelian randomization analysis demonstrates that low vitamin D is unlikely causative for pediatric asthma. J Allergy Clin Immunol. 2016 12; 138(6):1747-1749.e4. PMID: 27554823; PMCID: PMC5526345.
    Citations: 10     Fields:    Translation:Humans
  61. Thacher TD, Levine MA. CYP2R1 mutations causing vitamin D-deficiency rickets. J Steroid Biochem Mol Biol. 2017 10; 173:333-336. PMID: 27473561.
    Citations: 20     Fields:    Translation:HumansAnimals
  62. Bowen SL, Fuin N, Levine MA, Catana C. Transmission imaging for integrated PET-MR systems. Phys Med Biol. 2016 08 07; 61(15):5547-68. PMID: 27384608.
    Citations: 7     Fields:    Translation:Humans
  63. Li D, Tian L, Hou C, Kim CE, Hakonarson H, Levine MA. Association of Mutations in SLC12A1 Encoding the NKCC2 Cotransporter With Neonatal Primary Hyperparathyroidism. J Clin Endocrinol Metab. 2016 05; 101(5):2196-200. PMID: 26963954; PMCID: PMC4870850.
    Citations: 11     Fields:    Translation:Humans
  64. Clarke BL, Brown EM, Collins MT, Jüppner H, Lakatos P, Levine MA, Mannstadt MM, Bilezikian JP, Romanischen AF, Thakker RV. Epidemiology and Diagnosis of Hypoparathyroidism. J Clin Endocrinol Metab. 2016 Jun; 101(6):2284-99. PMID: 26943720; PMCID: PMC5393595.
    Citations: 57     Fields:    Translation:Humans
  65. Servaes S, Brown SD, Choudhary AK, Christian CW, Done SL, Hayes LL, Levine MA, Moreno JA, Palusci VJ, Shore RM, Slovis TL. The etiology and significance of fractures in infants and young children: a critical multidisciplinary review. Pediatr Radiol. 2016 May; 46(5):591-600. PMID: 26886911.
    Citations: 16     Fields:    Translation:Humans
  66. Mancilla EE, Levine MA, Adzick NS. Outcomes of minimally invasive parathyroidectomy in pediatric patients with primary hyperparathyroidism owing to parathyroid adenoma: A single institution experience. J Pediatr Surg. 2017 Jan; 52(1):188-191. PMID: 26898682; PMCID: PMC4974154.
    Citations: 7     Fields:    Translation:Humans
  67. Prentice-Mott HV, Meroz Y, Carlson A, Levine MA, Davidson MW, Irimia D, Charras GT, Mahadevan L, Shah JV. Directional memory arises from long-lived cytoskeletal asymmetries in polarized chemotactic cells. Proc Natl Acad Sci U S A. 2016 Feb 02; 113(5):1267-72. PMID: 26764383; PMCID: PMC4747767.
    Citations: 28     Fields:    Translation:HumansCells
  68. Li Q, Kingman J, Sundberg JP, Levine MA, Uitto J. Dual Effects of Bisphosphonates on Ectopic Skin and Vascular Soft Tissue Mineralization versus Bone Microarchitecture in a Mouse Model of Generalized Arterial Calcification of Infancy. J Invest Dermatol. 2016 Jan; 136(1):275-283. PMID: 26763447; PMCID: PMC4731049.
    Citations: 21     Fields:    Translation:Animals
  69. Roizen JD, Danzig J, Groleau V, McCormack S, Casella A, Harrington J, Sochett E, Tershakovec A, Zemel BS, Stallings VA, Levine MA. Resting Energy Expenditure Is Decreased in Pseudohypoparathyroidism Type 1A. J Clin Endocrinol Metab. 2016 Mar; 101(3):880-8. PMID: 26709970; PMCID: PMC4803160.
    Citations: 20     Fields:    Translation:Humans
  70. Weber DR, Coughlin C, Brodsky JL, Lindstrom K, Ficicioglu C, Kaplan P, Freehauf CL, Levine MA. Low bone mineral density is a common finding in patients with homocystinuria. Mol Genet Metab. 2016 Mar; 117(3):351-4. PMID: 26689745; PMCID: PMC4788514.
    Citations: 7     Fields:    Translation:Humans
  71. Lin T, Tong W, Chandra A, Hsu SY, Jia H, Zhu J, Tseng WJ, Levine MA, Zhang Y, Yan SG, Liu XS, Sun D, Young W, Qin L. A comprehensive study of long-term skeletal changes after spinal cord injury in adult rats. Bone Res. 2015; 3:15028. PMID: 26528401; PMCID: PMC4621491.
    Citations: 13     
  72. Noyes JJ, Levine MA, Belasco JB, Mostoufi-Moab S. Premature Epiphyseal Closure of the Lower Extremities Contributing to Short Stature after cis-Retinoic Acid Therapy in Medulloblastoma: A Case Report. Horm Res Paediatr. 2016; 85(1):69-73. PMID: 26457578.
    Citations: 5     Fields:    Translation:Humans
  73. George S, Weber DR, Kaplan P, Hummel K, Monk HM, Levine MA. Short-Term Safety of Zoledronic Acid in Young Patients With Bone Disorders: An Extensive Institutional Experience. J Clin Endocrinol Metab. 2015 Nov; 100(11):4163-71. PMID: 26308295; PMCID: PMC4702447.
    Citations: 15     Fields:    Translation:Humans
  74. Hawkes CP, Schnellbacher S, Singh RJ, Levine MA. 25-Hydroxyvitamin D Can Interfere With a Common Assay for 1,25-Dihydroxyvitamin D in Vitamin D Intoxication. J Clin Endocrinol Metab. 2015 Aug; 100(8):2883-9. PMID: 26120794; PMCID: PMC4524983.
    Citations: 6     Fields:    Translation:Humans
  75. Gerstner ER, Ye X, Duda DG, Levine MA, Mikkelsen T, Kaley TJ, Olson JJ, Nabors BL, Ahluwalia MS, Wen PY, Jain RK, Batchelor TT, Grossman S. A phase I study of cediranib in combination with cilengitide in patients with recurrent glioblastoma. Neuro Oncol. 2015 Oct; 17(10):1386-92. PMID: 26008604; PMCID: PMC4578584.
    Citations: 27     Fields:    Translation:HumansCTClinical Trials
  76. Thacher TD, Fischer PR, Singh RJ, Roizen J, Levine MA. CYP2R1 Mutations Impair Generation of 25-hydroxyvitamin D and Cause an Atypical Form of Vitamin D Deficiency. J Clin Endocrinol Metab. 2015 Jul; 100(7):E1005-13. PMID: 25942481; PMCID: PMC4490307.
    Citations: 30     Fields:    Translation:HumansCells
  77. Mancilla EE, Brodsky JL, Mehta S, Pignolo RJ, Levine MA. Teriparatide as a systemic treatment for lower extremity nonunion fractures: a case series. Endocr Pract. 2015 Feb; 21(2):136-42. PMID: 25297667.
    Citations: 10     Fields:    Translation:Humans
  78. Levine MA. Pathological calcification and the mystery of Lot's wife. Cell Cycle. 2015; 14(21):3354-5. PMID: 26375426; PMCID: PMC4825569.
    Citations:    Fields:    Translation:Humans
  79. Roizen J, Levine MA. A meta-analysis comparing the biochemistry of primary hyperparathyroidism in youths to the biochemistry of primary hyperparathyroidism in adults. J Clin Endocrinol Metab. 2014 Dec; 99(12):4555-64. PMID: 25181388; PMCID: PMC4255125.
    Citations: 10     Fields:    Translation:Humans
  80. Li D, Opas EE, Tuluc F, Metzger DL, Hou C, Hakonarson H, Levine MA. Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization. J Clin Endocrinol Metab. 2014 Sep; 99(9):E1774-83. PMID: 24823460; PMCID: PMC4154081.
    Citations: 38     Fields:    Translation:Humans
  81. Li D, Weber DR, Deardorff MA, Hakonarson H, Levine MA. Exome sequencing reveals a nonsense mutation in MMP13 as a new cause of autosomal recessive metaphyseal anadysplasia. Eur J Hum Genet. 2015 Feb; 23(2):264-6. PMID: 24781753.
    Citations: 5     Fields:    Translation:Humans
  82. Dasgupta D, Wee MJ, Reyes M, Li Y, Simm PJ, Sharma A, Schlingmann KP, Janner M, Biggin A, Lazier J, Gessner M, Chrysis D, Tuchman S, Baluarte HJ, Levine MA, Tiosano D, Insogna K, Hanley DA, Carpenter TO, Ichikawa S, Hoppe B, Konrad M, Sävendahl L, Munns CF, Lee H, Jüppner H, Bergwitz C. Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis. J Am Soc Nephrol. 2014 Oct; 25(10):2366-75. PMID: 24700880.
    Citations: 57     Fields:    Translation:Humans
  83. Hawkes CP, Levine MA. Ketotic hypercalcemia: a case series and description of a novel entity. J Clin Endocrinol Metab. 2014 May; 99(5):1531-6. PMID: 24606099; PMCID: PMC4010709.
    Citations: 5     Fields:    Translation:Humans
  84. Gannon AW, Monk HM, Levine MA. Cinacalcet monotherapy in neonatal severe hyperparathyroidism: a case study and review. J Clin Endocrinol Metab. 2014 Jan; 99(1):7-11. PMID: 24203066; PMCID: PMC3879678.
    Citations: 28     Fields:    Translation:Humans
  85. Roizen JD, Shah V, Levine MA, Carlow DC. Determination of reference intervals for serum total calcium in the vitamin D-replete pediatric population. J Clin Endocrinol Metab. 2013 Dec; 98(12):E1946-50. PMID: 24217904; PMCID: PMC3849669.
    Citations: 6     Fields:    Translation:Humans
  86. Lietman SA, Levine MA. Fibrous dysplasia. Pediatr Endocrinol Rev. 2013 Jun; 10 Suppl 2:389-96. PMID: 23858622.
    Citations: 9     Fields:    Translation:Humans
  87. Stanescu DE, Levine MA. 50 years ago in the Journal of Pediatrics: metabolic studies in a patient with idiopathic hypercalcemia of infancy. J Pediatr. 2013 Apr; 162(4):752. PMID: 23527844.
    Citations:    Fields:    Translation:Humans
  88. Levine MA. Assessing bone health in children and adolescents. Indian J Endocrinol Metab. 2012 Dec; 16(Suppl 2):S205-12. PMID: 23565379.
    Citations: 18     
  89. Levine MA. An update on the clinical and molecular characteristics of pseudohypoparathyroidism. Curr Opin Endocrinol Diabetes Obes. 2012 Dec; 19(6):443-51. PMID: 23076042.
    Citations: 30     Fields:    Translation:HumansAnimalsCells
  90. Shepherd JA, Fan B, Lu Y, Wu XP, Wacker WK, Ergun DL, Levine MA. A multinational study to develop universal standardization of whole-body bone density and composition using GE Healthcare Lunar and Hologic DXA systems. J Bone Miner Res. 2012 Oct; 27(10):2208-16. PMID: 22623101.
    Citations: 53     Fields:    Translation:Humans
  91. Roizen J, Levine MA. Primary hyperparathyroidism in children and adolescents. J Chin Med Assoc. 2012 Sep; 75(9):425-34. PMID: 22989537.
    Citations: 30     Fields:    Translation:Humans
  92. Fan C, Gaivin RJ, Marth TA, Willard B, Levine MA, Lietman SA. Cloning and characterization of the human SH3BP2 promoter. Biochem Biophys Res Commun. 2012 Aug 17; 425(1):25-32. PMID: 22820184.
    Citations: 1     Fields:    Translation:HumansAnimalsCells
  93. Reichenberger EJ, Levine MA, Olsen BR, Papadaki ME, Lietman SA. The role of SH3BP2 in the pathophysiology of cherubism. Orphanet J Rare Dis. 2012 May 24; 7 Suppl 1:S5. PMID: 22640988.
    Citations: 28     Fields:    Translation:HumansAnimalsCells
  94. Papadaki ME, Lietman SA, Levine MA, Olsen BR, Kaban LB, Reichenberger EJ. Cherubism: best clinical practice. Orphanet J Rare Dis. 2012 May 24; 7 Suppl 1:S6. PMID: 22640403.
    Citations: 44     Fields:    Translation:Humans
  95. Imteyaz H, Karnsakul W, Levine MA, Burrows PE, Benson J, Hsu S, Schwarz KB. Unusual case of hypothyroidism in an infant with hepatic hemangioma. J Pediatr Gastroenterol Nutr. 2012 May; 54(5):692-5. PMID: 21716131.
    Citations: 2     Fields:    Translation:Humans
  96. Punn A, Chen J, Delidaki M, Tang J, Liapakis G, Lehnert H, Levine MA, Grammatopoulos DK. Mapping structural determinants within third intracellular loop that direct signaling specificity of type 1 corticotropin-releasing hormone receptor. J Biol Chem. 2012 Mar 16; 287(12):8974-85. PMID: 22247544.
    Citations: 8     Fields:    Translation:HumansCells
  97. Doyle D, Kirwin SM, Sol-Church K, Levine MA. A novel mutation in the GCM2 gene causing severe congenital isolated hypoparathyroidism. J Pediatr Endocrinol Metab. 2012; 25(7-8):741-6. PMID: 23155703.
    Citations: 6     Fields:    Translation:HumansCells
  98. Kelly A, Levine MA. Hypocalcemia in the critically ill patient. J Intensive Care Med. 2013 May-Jun; 28(3):166-77. PMID: 21841146.
    Citations: 37     Fields:    Translation:Humans
  99. Sanchez J, Perera E, Jan de Beur S, Ding C, Dang A, Berkovitz GD, Levine MA. Madelung-like deformity in pseudohypoparathyroidism type 1b. J Clin Endocrinol Metab. 2011 Sep; 96(9):E1507-11. PMID: 21752878; PMCID: PMC3167675.
    Citations: 15     Fields:    Translation:HumansCells
  100. Huso DL, Edie S, Levine MA, Schwindinger W, Wang Y, Jüppner H, Germain-Lee EL. Heterotopic ossifications in a mouse model of albright hereditary osteodystrophy. PLoS One. 2011; 6(6):e21755. PMID: 21747923.
    Citations: 17     Fields:    Translation:HumansAnimalsCells
  101. Schilling S, Wood JN, Levine MA, Langdon D, Christian CW. Vitamin D status in abused and nonabused children younger than 2 years old with fractures. Pediatrics. 2011 May; 127(5):835-41. PMID: 21482609.
    Citations: 20     Fields:    Translation:Humans
  102. Kawamoto T, Fan C, Gaivin RJ, Levine MA, Lietman SA. Decreased SH3BP2 inhibits osteoclast differentiation and function. J Orthop Res. 2011 Oct; 29(10):1521-7. PMID: 21448930.
    Citations: 3     Fields:    Translation:AnimalsCells
  103. Jap TS, Chiu CY, Niu DM, Levine MA. Three novel mutations in the PHEX gene in Chinese subjects with hypophosphatemic rickets extends genotypic variability. Calcif Tissue Int. 2011 May; 88(5):370-7. PMID: 21293852; PMCID: PMC3075400.
    Citations: 2     Fields:    Translation:Humans
  104. Lietman SA, Yin L, Levine MA. SH3BP2 mutations potentiate osteoclastogenesis via PLC?. J Orthop Res. 2010 Nov; 28(11):1425-30. PMID: 20872577.
    Citations: 5     Fields:    Translation:AnimalsCells
  105. Thacher TD, Fischer PR, Obadofin MO, Levine MA, Singh RJ, Pettifor JM. Comparison of metabolism of vitamins D2 and D3 in children with nutritional rickets. J Bone Miner Res. 2010 Sep; 25(9):1988-95. PMID: 20499377.
    Citations: 23     Fields:    Translation:Humans
  106. Lietman SA, Germain-Lee EL, Levine MA. Hypercalcemia in children and adolescents. Curr Opin Pediatr. 2010 Aug; 22(4):508-15. PMID: 20601885.
    Citations: 29     Fields:    Translation:HumansCells
  107. Long DN, Levine MA, Germain-Lee EL. Bone mineral density in pseudohypoparathyroidism type 1a. J Clin Endocrinol Metab. 2010 Sep; 95(9):4465-75. PMID: 20610593; PMCID: PMC2936057.
    Citations: 10     Fields:    Translation:Humans
  108. Tencza AL, Ichikawa S, Dang A, Kenagy D, McCarthy E, Econs MJ, Levine MA. Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/type IIc sodium-phosphate cotransporter: presentation as hypercalciuria and nephrolithiasis. J Clin Endocrinol Metab. 2009 Nov; 94(11):4433-8. PMID: 19820004; PMCID: PMC2775650.
    Citations: 23     Fields:    Translation:Humans
  109. Crane JL, Shamblott MJ, Axelman J, Hsu S, Levine MA, Germain-Lee EL. Imprinting status of Galpha(s), NESP55, and XLalphas in cell cultures derived from human embryonic germ cells: GNAS imprinting in human embryonic germ cells. Clin Transl Sci. 2009 Oct; 2(5):355-60. PMID: 20443919.
    Citations: 4     Fields:    Translation:HumansCells
  110. Lietman SA, Tenenbaum-Rakover Y, Jap TS, Yi-Chi W, De-Ming Y, Ding C, Kussiny N, Levine MA. A novel loss-of-function mutation, Gln459Arg, of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia. J Clin Endocrinol Metab. 2009 Nov; 94(11):4372-9. PMID: 19789209; PMCID: PMC2775658.
    Citations: 17     Fields:    Translation:HumansCells
  111. Markovic D, Lehnert H, Levine MA, Grammatopoulos DK. Structural determinants critical for localization and signaling within the seventh transmembrane domain of the type 1 corticotropin releasing hormone receptor: lessons from the receptor variant R1d. Mol Endocrinol. 2008 Nov; 22(11):2505-19. PMID: 18772229.
    Citations: 18     Fields:    Translation:HumansCells
  112. Lietman SA, Yin L, Levine MA. SH3BP2 is an activator of NFAT activity and osteoclastogenesis. Biochem Biophys Res Commun. 2008 Jul 11; 371(4):644-8. PMID: 18440306.
    Citations: 18     Fields:    Translation:HumansAnimalsCells
  113. Maret A, Ding C, Kornfield SL, Levine MA. Analysis of the GCM2 gene in isolated hypoparathyroidism: a molecular and biochemical study. J Clin Endocrinol Metab. 2008 Apr; 93(4):1426-32. PMID: 18182452.
    Citations: 17     Fields:    Translation:HumansCells
  114. Lietman SA, Goldfarb J, Desai N, Levine MA. Preimplantation genetic diagnosis for severe albright hereditary osteodystrophy. J Clin Endocrinol Metab. 2008 Mar; 93(3):901-4. PMID: 18089698; PMCID: PMC2266954.
    Citations: 6     Fields:    Translation:Humans
  115. Teli T, Markovic D, Hewitt ME, Levine MA, Hillhouse EW, Grammatopoulos DK. Structural domains determining signalling characteristics of the CRH-receptor type 1 variant R1beta and response to PKC phosphorylation. Cell Signal. 2008 Jan; 20(1):40-9. PMID: 17913459.
    Citations: 14     Fields:    Translation:HumansAnimalsCells
  116. Lietman SA, Schwindinger WF, Levine MA. Genetic and molecular aspects of McCune-Albright syndrome. Pediatr Endocrinol Rev. 2007 Aug; 4 Suppl 4:380-5. PMID: 17982384.
    Citations: 4     Fields:    Translation:Humans
  117. Lietman SA, Prescott NL, Hicks DG, Westra WH, Levine MA. SH3BP2 is rarely mutated in exon 9 in giant cell lesions outside cherubism. Clin Orthop Relat Res. 2007 Jun; 459:22-7. PMID: 17545756.
    Citations: 4     Fields:    Translation:Humans
  118. Long DN, McGuire S, Levine MA, Weinstein LS, Germain-Lee EL. Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity. J Clin Endocrinol Metab. 2007 Mar; 92(3):1073-9. PMID: 17164301.
    Citations: 71     Fields:    Translation:Humans
  119. Henrich LM, Rogol AD, D'Amour P, Levine MA, Hanks JB, Bruns DE. Persistent hypercalcemia after parathyroidectomy in an adolescent and effect of treatment with cinacalcet HCl. Clin Chem. 2006 Dec; 52(12):2286-93. PMID: 17105782.
    Citations: 3     Fields:    Translation:Humans
  120. Punn A, Levine MA, Grammatopoulos DK. Identification of signaling molecules mediating corticotropin-releasing hormone-R1alpha-mitogen-activated protein kinase (MAPK) interactions: the critical role of phosphatidylinositol 3-kinase in regulating ERK1/2 but not p38 MAPK activation. Mol Endocrinol. 2006 Dec; 20(12):3179-95. PMID: 16959871.
    Citations: 29     Fields:    Translation:HumansCells
  121. Markovic D, Papadopoulou N, Teli T, Randeva H, Levine MA, Hillhouse EW, Grammatopoulos DK. Differential responses of corticotropin-releasing hormone receptor type 1 variants to protein kinase C phosphorylation. J Pharmacol Exp Ther. 2006 Dec; 319(3):1032-42. PMID: 16956982.
    Citations: 15     Fields:    Translation:HumansAnimalsCells
  122. Lietman SA, Kalinchinko N, Deng X, Kohanski R, Levine MA. Identification of a novel mutation of SH3BP2 in cherubism and demonstration that SH3BP2 mutations lead to increased NFAT activation. Hum Mutat. 2006 Jul; 27(7):717-8. PMID: 16786512.
    Citations: 14     Fields:    Translation:HumansCells
  123. Young JH, Chang YP, Kim JD, Chretien JP, Klag MJ, Levine MA, Ruff CB, Wang NY, Chakravarti A. Differential susceptibility to hypertension is due to selection during the out-of-Africa expansion. PLoS Genet. 2005 Dec; 1(6):e82. PMID: 16429165; PMCID: PMC1342636.
    Citations: 103     Fields:    Translation:Humans
  124. Lietman SA, Ding C, Levine MA. A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia. J Bone Joint Surg Am. 2005 Nov; 87(11):2489-94. PMID: 16264125.
    Citations: 18     Fields:    Translation:HumansCells
  125. Germain-Lee EL, Schwindinger W, Crane JL, Zewdu R, Zweifel LS, Wand G, Huso DL, Saji M, Ringel MD, Levine MA. A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene. Endocrinology. 2005 Nov; 146(11):4697-709. PMID: 16099856.
    Citations: 53     Fields:    Translation:HumansAnimals
  126. Lietman SA, Ding C, Cooke DW, Levine MA. Reduction in Gsalpha induces osteogenic differentiation in human mesenchymal stem cells. Clin Orthop Relat Res. 2005 May; (434):231-8. PMID: 15864058.
    Citations: 17     Fields:    Translation:HumansCells
  127. Miller RG, Chretien KC, Meoni LA, Liu YP, Klag MJ, Levine MA. Comparison of intravenous pamidronate to standard therapy for osteoporosis: use in patients unable to take oral bisphosphonates. J Clin Rheumatol. 2005 Feb; 11(1):2-7. PMID: 16357689.
    Citations: 1     Fields:    Translation:Humans
  128. Kern LM, Powe NR, Levine MA, Fitzpatrick AL, Harris TB, Robbins J, Fried LP. Association between screening for osteoporosis and the incidence of hip fracture. Ann Intern Med. 2005 Feb 01; 142(3):173-81. PMID: 15684205.
    Citations: 32     Fields:    Translation:HumansPHPublic Health
  129. Teli T, Markovic D, Levine MA, Hillhouse EW, Grammatopoulos DK. Regulation of corticotropin-releasing hormone receptor type 1alpha signaling: structural determinants for G protein-coupled receptor kinase-mediated phosphorylation and agonist-mediated desensitization. Mol Endocrinol. 2005 Feb; 19(2):474-90. PMID: 15498832.
    Citations: 33     Fields:    Translation:HumansAnimalsCells
  130. Nesbit MA, Bowl MR, Harding B, Ali A, Ayala A, Crowe C, Dobbie A, Hampson G, Holdaway I, Levine MA, McWilliams R, Rigden S, Sampson J, Williams AJ, Thakker RV. Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome. J Biol Chem. 2004 May 21; 279(21):22624-34. PMID: 14985365.
    Citations: 53     Fields:    Translation:HumansAnimalsCells
  131. Maret A, Bourdeau I, Ding C, Kadkol SS, Westra WH, Levine MA. Expression of GCMB by intrathymic parathyroid hormone-secreting adenomas indicates their parathyroid cell origin. J Clin Endocrinol Metab. 2004 Jan; 89(1):8-12. PMID: 14715818.
    Citations: 7     Fields:    Translation:HumansAnimals
  132. Papadopoulou N, Chen J, Randeva HS, Levine MA, Hillhouse EW, Grammatopoulos DK. Protein kinase A-induced negative regulation of the corticotropin-releasing hormone R1alpha receptor-extracellularly regulated kinase signal transduction pathway: the critical role of Ser301 for signaling switch and selectivity. Mol Endocrinol. 2004 Mar; 18(3):624-39. PMID: 14657255.
    Citations: 22     Fields:    Translation:HumansCells
  133. Mahadevia PJ, Sosa JA, Levine MA, Zeiger MA, Powe NR. Clinical management of primary hyperparathyroidism and thresholds for surgical referral: a national study examining concordance between practice patterns and consensus panel recommendations. Endocr Pract. 2003 Nov-Dec; 9(6):494-503. PMID: 14715476.
    Citations: 5     Fields:    Translation:Humans
  134. Germain-Lee EL, Groman J, Crane JL, Jan de Beur SM, Levine MA. Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance. J Clin Endocrinol Metab. 2003 Sep; 88(9):4059-69. PMID: 12970262.
    Citations: 35     Fields:    Translation:Humans
  135. Jan de Beur S, Ding C, Germain-Lee E, Cho J, Maret A, Levine MA. Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1. Am J Hum Genet. 2003 Aug; 73(2):314-22. PMID: 12858292; PMCID: PMC1180370.
    Citations: 16     Fields:    Translation:HumansCells
  136. Levine MA. Biochemical markers of bone metabolism: application to understanding bone remodeling in children and adolescents. J Pediatr Endocrinol Metab. 2003 May; 16 Suppl 3:661-72. PMID: 12795369.
    Citations: 1     Fields:    Translation:HumansCells
  137. Jan De Beur SM, O'Connell JR, Peila R, Cho J, Deng Z, Kam S, Levine MA. The pseudohypoparathyroidism type lb locus is linked to a region including GNAS1 at 20q13.3. J Bone Miner Res. 2003 Mar; 18(3):424-33. PMID: 12619926.
    Citations: 7     Fields:    Translation:HumansCells
  138. Carakushansky M, Whatmore AJ, Clayton PE, Shalet SM, Gleeson HK, Price DA, Levine MA, Salvatori R. A new missense mutation in the growth hormone-releasing hormone receptor gene in familial isolated GH deficiency. Eur J Endocrinol. 2003 Jan; 148(1):25-30. PMID: 12534354.
    Citations: 12     Fields:    Translation:Humans
  139. Levine MA. Normal mineral homeostasis. Interplay of parathyroid hormone and vitamin D. Endocr Dev. 2003; 6:14-33. PMID: 12964423.
    Citations: 9     Fields:    Translation:HumansAnimals
  140. Rodgers BD, Weber GM, Kelley KM, Levine MA. Prolonged fasting and cortisol reduce myostatin mRNA levels in tilapia larvae; short-term fasting elevates. Am J Physiol Regul Integr Comp Physiol. 2003 May; 284(5):R1277-86. PMID: 12676749.
    Citations: 12     Fields:    Translation:Animals
  141. Hsu SC, Levine MA. Primary hyperparathyroidism in children and adolescents: the Johns Hopkins Children's Center experience 1984-2001. J Bone Miner Res. 2002 Nov; 17 Suppl 2:N44-50. PMID: 12412777.
    Citations: 20     Fields:    Translation:Humans
  142. Germain-Lee EL, Ding CL, Deng Z, Crane JL, Saji M, Ringel MD, Levine MA. Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a. Biochem Biophys Res Commun. 2002 Aug 09; 296(1):67-72. PMID: 12147228.
    Citations: 44     Fields:    Translation:HumansCells
  143. De Beur SM, Finnegan RB, Vassiliadis J, Cook B, Barberio D, Estes S, Manavalan P, Petroziello J, Madden SL, Cho JY, Kumar R, Levine MA, Schiavi SC. Tumors associated with oncogenic osteomalacia express genes important in bone and mineral metabolism. J Bone Miner Res. 2002 Jun; 17(6):1102-10. PMID: 12054166.
    Citations: 59     Fields:    Translation:HumansCells
  144. Jan de Beur SM, Levine MA. Molecular pathogenesis of hypophosphatemic rickets. J Clin Endocrinol Metab. 2002 Jun; 87(6):2467-73. PMID: 12050201.
    Citations: 19     Fields:    Translation:Humans
  145. Jan de Beur SM, Streeten EA, Civelek AC, McCarthy EF, Uribe L, Marx SJ, Onobrakpeya O, Raisz LG, Watts NB, Sharon M, Levine MA. Localisation of mesenchymal tumours by somatostatin receptor imaging. Lancet. 2002 Mar 02; 359(9308):761-3. PMID: 11888589.
    Citations: 45     Fields:    Translation:Humans
  146. Emala CW, McQuitty CK, Eleff SM, Hopkins-Price P, Lawyer C, Hoh J, Ott J, Levine MA, Hirshman CA. Asthma, allergy, and airway hyperresponsiveness are not linked to the beta(2)-adrenoceptor gene. Chest. 2002 Mar; 121(3):722-31. PMID: 11888952.
    Citations:    Fields:    Translation:Humans
  147. Salvatori R, Fan X, Mullis PE, Haile A, Levine MA. Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding site. Mol Endocrinol. 2002 Mar; 16(3):450-8. PMID: 11875102.
    Citations: 13     Fields:    Translation:HumansAnimalsCells
  148. Shore EM, Ahn J, Jan de Beur S, Li M, Xu M, Gardner RJ, Zasloff MA, Whyte MP, Levine MA, Kaplan FS. Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia. N Engl J Med. 2002 Jan 10; 346(2):99-106. PMID: 11784876.
    Citations: 80     Fields:    Translation:HumansCells
Local representatives can answer questions about the Profiles website or help with editing a profile or issues with profile data. For assistance with this profile: HMS/HSDM faculty should contact contactcatalyst.harvard.edu. For faculty or fellow appointment updates and changes, please ask your appointing department to contact HMS. For fellow personal and demographic information, contact HMS Human Resources at human_resourceshms.harvard.edu. For faculty personal and demographic information, contact HMS Office for Faculty Affairs at facappthms.harvard.edu.
Levine's Networks
Click the
buttons for more information and interactive visualizations!
Concepts (614)
Co-Authors (25)
Similar People (60)
Same Department 
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.