TitleDistinguished Emeritus Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address6701 FANNIN
Houston, TX 77030
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    Other Positions
    TitleDistinguished Emeritus Professor
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Neurology

    Collapse Research 
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    P01HD024234     (GLAZE, DANIEL G.)May 1, 1988 - Aug 31, 1999
    Role: Principal Investigator

    R01HL062404     (GLAZE, DANIEL G.)Sep 20, 1999 - Jul 31, 2005
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    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. Ak M, Suter B, Akturk Z, Harris H, Bowyer K, Mignon L, Pasupuleti S, Glaze DG, Pehlivan D. Exploring the characteristics and most bothersome symptoms in MECP2 duplication syndrome to pave the path toward developing parent-oriented outcome measures. Mol Genet Genomic Med. 2022 Jun 15; e1989. PMID: 35702943.
      Citations:    Fields:    
    2. Duis J, Pullen LC, Picone M, Friedman N, Hawkins S, Sannar E, Pfalzer AC, Shelton AR, Singh D, Zee PC, Glaze DG, Revana A. Diagnosis and management of sleep disorders in Prader-Willi syndrome. J Clin Sleep Med. 2022 06 01; 18(6):1687-1696. PMID: 35172921.
      Citations:    Fields:    Translation:Humans
    3. Buchanan CB, Stallworth JL, Joy AE, Dixon RE, Scott AE, Beisang AA, Benke TA, Glaze DG, Haas RH, Heydemann PT, Jones MD, Lane JB, Lieberman DN, Marsh ED, Neul JL, Peters SU, Ryther RC, Skinner SA, Standridge SM, Kaufmann WE, Percy AK. Anxiety-like behavior and anxiolytic treatment in the Rett syndrome natural history study. J Neurodev Disord. 2022 May 14; 14(1):31. PMID: 35568815.
      Citations:    Fields:    Translation:Humans
    4. Duis J, Nespeca M, Summers J, Bird L, Bindels-de Heus KGCB, Valstar MJ, de Wit MY, Navis C, Ten Hooven-Radstaake M, van Iperen-Kolk BM, Ernst S, Dendrinos M, Katz T, Diaz-Medina G, Katyayan A, Nangia S, Thibert R, Glaze D, Keary C, Pelc K, Simon N, Sadhwani A, Heussler H, Wheeler A, Woeber C, DeRamus M, Thomas A, Kertcher E, DeValk L, Kalemeris K, Arps K, Baym C, Harris N, Gorham JP, Bohnsack BL, Chambers RC, Harris S, Chambers HG, Okoniewski K, Jalazo ER, Berent A, Bacino CA, Williams C, Anderson A. A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome. Mol Genet Genomic Med. 2022 03; 10(3):e1843. PMID: 35150089.
      Citations: 1     Fields:    Translation:Humans
    5. Neul JL, Percy AK, Benke TA, Berry-Kravis EM, Glaze DG, Peters SU, Jones NE, Youakim JM. Design and outcome measures of LAVENDER, a phase 3 study of trofinetide for Rett syndrome. Contemp Clin Trials. 2022 03; 114:106704. PMID: 35149233.
      Citations:    Fields:    Translation:HumansCTClinical Trials
    6. Revana A, Vecchio J, Guffey D, Minard CG, Glaze DG. Clinical application of home sleep apnea testing in children: a prospective pilot study. J Clin Sleep Med. 2022 Feb 01; 18(2):533-540. PMID: 34534072.
      Citations:    Fields:    Translation:Humans
    7. Patel VP, Patroneva A, Glaze DG, Davis Ms K, Merikle E, Revana A. Establishing the content validity of the Epworth Sleepiness Scale for Children and Adolescents in Prader-Willi syndrome. J Clin Sleep Med. 2022 Feb 01; 18(2):485-496. PMID: 34437052.
      Citations:    Fields:    Translation:Humans
    8. Motil KJ, Geerts S, Annese F, Neul JL, Benke T, Marsh E, Lieberman D, Skinner SA, Glaze DG, Heydemann P, Beisang A, Standridge S, Ryther R, Lane JB, Edwards L, Percy AK. Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome. J Pediatr. 2022 05; 244:169-177.e3. PMID: 35063470.
      Citations:    Fields:    Translation:Humans
    9. Veatch OJ, Malow BA, Lee HS, Knight A, Barrish JO, Neul JL, Lane JB, Skinner SA, Kaufmann WE, Miller JL, Driscoll DJ, Bird LM, Butler MG, Dykens EM, Gold JA, Kimonis V, Bacino CA, Tan WH, Kothare SV, Peters SU, Percy AK, Glaze DG. Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes. Pediatr Neurol. 2021 10; 123:30-37. PMID: 34388423.
      Citations: 1     Fields:    Translation:Humans
    10. Ahmad SF, Buckley AW, Glaze DG. Neurology of Sleep. Neurol Clin. 2021 08; 39(3):867-882. PMID: 34215391.
      Citations: 1     Fields:    Translation:Humans
    11. Thapa S, Venkatachalam A, Khan N, Naqvi M, Balderas M, Runge JK, Haag A, Hoch KM, Glaze DG, Luna RA, Motil KJ. Assessment of the gut bacterial microbiome and metabolome of girls and women with Rett Syndrome. PLoS One. 2021; 16(5):e0251231. PMID: 33956889.
      Citations: 2     Fields:    Translation:Humans
    12. Motil KJ, Khan N, Coon JL, Barrish JO, Suter B, Pehlivan D, Schultz RJ, Glaze DG. Gastrointestinal Health Questionnaire for Rett Syndrome: Tool Development. J Pediatr Gastroenterol Nutr. 2021 03 01; 72(3):354-360. PMID: 32969958.
      Citations: 1     Fields:    Translation:Humans
    13. Peters SU, Fu C, Marsh ED, Benke TA, Suter B, Skinner SA, Lieberman DN, Standridge S, Jones M, Beisang A, Feyma T, Heydeman P, Ryther R, Glaze DG, Percy AK, Neul JL. Phenotypic features in MECP2 duplication syndrome: Effects of age. Am J Med Genet A. 2021 02; 185(2):362-369. PMID: 33170557.
      Citations: 2     Fields:    Translation:Humans
    14. Raspa M, Bann CM, Gwaltney A, Benke TA, Fu C, Glaze DG, Haas R, Heydemann P, Jones M, Kaufmann WE, Lieberman D, Marsh E, Peters S, Ryther R, Standridge S, Skinner SA, Percy AK, Neul JL. A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical Trials. Am J Intellect Dev Disabil. 2020 11 01; 125(6):493-509. PMID: 33211820.
      Citations: 4     Fields:    Translation:Humans
    15. Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, Standridge S, Lane J, Dinkel T, Jones M, Hale K, Suter B, Glaze D, Neul J, Percy A, Benke T. Multisystem comorbidities in classic Rett syndrome: a scoping review. BMJ Paediatr Open. 2020; 4(1):e000731. PMID: 33024833.
      Citations: 6     Fields:    
    16. Young DR, Suter B, Levine JT, Glaze DG, Layne CS. Characteristic behaviors associated with gait of individuals with Rett syndrome. Disabil Rehabil. 2022 04; 44(8):1508-1515. PMID: 32931336.
      Citations:    Fields:    Translation:Humans
    17. Fu C, Armstrong D, Marsh E, Lieberman D, Motil K, Witt R, Standridge S, Nues P, Lane J, Dinkel T, Coenraads M, von Hehn J, Jones M, Hale K, Suter B, Glaze D, Neul J, Percy A, Benke T. Consensus guidelines on managing Rett syndrome across the lifespan. BMJ Paediatr Open. 2020; 4(1):e000717. PMID: 32984552.
      Citations: 3     Fields:    
    18. Musso MF, Lindsey HM, Wilde EA, Hunter JV, Glaze DG, Goodrich-Hunsaker NJ, Wu TC, Black G, Biekman B, Zhang W, Zhu H, Anand GS, Friedman EM. Volumetric brain magnetic resonance imaging analysis in children with obstructive sleep apnea. Int J Pediatr Otorhinolaryngol. 2020 Nov; 138:110369. PMID: 32927352.
      Citations: 2     Fields:    Translation:Humans
    19. Neul JL, Skinner SA, Annese F, Lane J, Heydemann P, Jones M, Kaufmann WE, Glaze DG, Percy AK. Metabolic Signatures Differentiate Rett Syndrome From Unaffected Siblings. Front Integr Neurosci. 2020; 14:7. PMID: 32161522.
      Citations: 10     
    20. Layne CS, Young DR, Lee BC, Glaze DG, Schwabe A, Suter B. Kinematics associated with treadmill walking in Rett syndrome. Disabil Rehabil. 2021 06; 43(11):1585-1593. PMID: 31613656.
      Citations:    Fields:    Translation:Humans
    21. Kaplan K, McCool C, Lupski JR, Glaze D, Potocki L. Objective measures of sleep disturbances in children with Potocki-Lupski syndrome. Am J Med Genet A. 2019 10; 179(10):1982-1986. PMID: 31342617.
      Citations:    Fields:    Translation:Humans
    22. Motil KJ, Lane JB, Barrish JO, Annese F, Geerts S, McNair L, Skinner SA, Neul JL, Glaze DG, Percy AK. Biliary Tract Disease in Girls and Young Women With Rett Syndrome. J Pediatr Gastroenterol Nutr. 2019 06; 68(6):799-805. PMID: 30664568.
      Citations: 5     Fields:    Translation:Humans
    23. Stallworth JL, Dy ME, Buchanan CB, Chen CF, Scott AE, Glaze DG, Lane JB, Lieberman DN, Oberman LM, Skinner SA, Tierney AE, Cutter GR, Percy AK, Neul JL, Kaufmann WE. Hand stereotypies: Lessons from the Rett Syndrome Natural History Study. Neurology. 2019 05 28; 92(22):e2594-e2603. PMID: 31053667.
      Citations: 2     Fields:    Translation:HumansCTClinical Trials
    24. Stowe RC, Glaze DG. Electroencephalographic Patterns During Routine Polysomnography in Childhood and Association With Future Epilepsy Diagnosis. J Clin Sleep Med. 2019 04 15; 15(4):553-562. PMID: 30952213.
      Citations: 1     Fields:    Translation:Humans
    25. Glaze DG, Neul JL, Kaufmann WE, Berry-Kravis E, Condon S, Stoms G, Oosterholt S, Della Pasqua O, Glass L, Jones NE, Percy AK. Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome. Neurology. 2019 04 16; 92(16):e1912-e1925. PMID: 30918097.
      Citations: 19     Fields:    Translation:HumansCTClinical Trials
    26. Peters SU, Fu C, Suter B, Marsh E, Benke TA, Skinner SA, Lieberman DN, Standridge S, Jones M, Beisang A, Feyma T, Heydeman P, Ryther R, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. Clin Genet. 2019 05; 95(5):575-581. PMID: 30788845.
      Citations: 9     Fields:    Translation:HumansCells
    27. Marafi D, Suter B, Schultz R, Glaze D, Pavlik VN, Goldman AM. Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 2019 01 08; 92(2):e108-e114. PMID: 30552298.
      Citations: 8     Fields:    Translation:Humans
    28. Neul JL, Benke TA, Marsh ED, Skinner SA, Merritt J, Lieberman DN, Standridge S, Feyma T, Heydemann P, Peters S, Ryther R, Jones M, Suter B, Kaufmann WE, Glaze DG, Percy AK. The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2. Am J Med Genet B Neuropsychiatr Genet. 2019 01; 180(1):55-67. PMID: 30536762.
      Citations: 11     Fields:    Translation:Humans
    29. Buchanan CB, Stallworth JL, Scott AE, Glaze DG, Lane JB, Skinner SA, Tierney AE, Percy AK, Neul JL, Kaufmann WE. Behavioral profiles in Rett syndrome: Data from the natural history study. Brain Dev. 2019 Feb; 41(2):123-134. PMID: 30217666.
      Citations: 9     Fields:    Translation:Humans
    30. Zaghlula M, Glaze DG, Enns GM, Potocki L, Schwabe AL, Suter B. Current clinical evidence does not support a link between TBL1XR1 and Rett syndrome: Description of one patient with Rett features and a novel mutation in TBL1XR1, and a review of TBL1XR1 phenotypes. Am J Med Genet A. 2018 07; 176(7):1683-1687. PMID: 29777588.
      Citations: 6     Fields:    Translation:Humans
    31. Tarquinio DC, Hou W, Neul JL, Berkmen GK, Drummond J, Aronoff E, Harris J, Lane JB, Kaufmann WE, Motil KJ, Glaze DG, Skinner SA, Percy AK. The course of awake breathing disturbances across the lifespan in Rett syndrome. Brain Dev. 2018 Aug; 40(7):515-529. PMID: 29657083.
      Citations: 20     Fields:    Translation:Humans
    32. Layne CS, Lee BC, Young DR, Glaze DG, Schwabe A, Suter B. Temporal Gait Measures Associated With Overground and Treadmill Walking in Rett Syndrome. J Child Neurol. 2018 Jan 01; 883073818780471. PMID: 29926771.
      Citations: 1     Fields:    
    33. Glaze DG, Neul JL, Percy A, Feyma T, Beisang A, Yaroshinsky A, Stoms G, Zuchero D, Horrigan J, Glass L, Jones NE. A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome. Pediatr Neurol. 2017 Nov; 76:37-46. PMID: 28964591.
      Citations: 20     Fields:    Translation:HumansCTClinical Trials
    34. Lane JB, Salter AR, Jones NE, Cutter G, Horrigan J, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Assessment of Caregiver Inventory for Rett Syndrome. J Autism Dev Disord. 2017 Apr; 47(4):1102-1112. PMID: 28132121.
      Citations: 5     Fields:    Translation:Humans
    35. Killian JT, Lane JB, Lee HS, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors. Pediatr Neurol. 2017 05; 70:20-25. PMID: 28347601.
      Citations: 12     Fields:    Translation:Humans
    36. Tarquinio DC, Hou W, Berg A, Kaufmann WE, Lane JB, Skinner SA, Motil KJ, Neul JL, Percy AK, Glaze DG. Longitudinal course of epilepsy in Rett syndrome and related disorders. Brain. 2017 02; 140(2):306-318. PMID: 28007990.
      Citations: 34     Fields:    Translation:Humans
    37. Ward CS, Huang TW, Herrera JA, Samaco RC, Pitcher MR, Herron A, Skinner SA, Kaufmann WE, Glaze DG, Percy AK, Neul JL. Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome. PLoS One. 2016; 11(11):e0165550. PMID: 27828991.
      Citations: 6     Fields:    Translation:HumansAnimals
    38. Scheimann AO, Miller J, Glaze DG. Laparoscopic sleeve gastrectomy in children and adolescents with Prader-Willi syndrome: a matched control study. Surg Obes Relat Dis. 2017 02; 13(2):366. PMID: 27692916.
      Citations: 5     Fields:    Translation:Humans
    39. Sajan SA, Jhangiani SN, Muzny DM, Gibbs RA, Lupski JR, Glaze DG, Kaufmann WE, Skinner SA, Annese F, Friez MJ, Lane J, Percy AK, Neul JL. Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2. Genet Med. 2017 01; 19(1):13-19. PMID: 27171548.
      Citations: 34     Fields:    Translation:HumansCells
    40. Killian JT, Lane JB, Lee HS, Pelham JH, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK. Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors. Pediatr Neurol. 2016 05; 58:67-74. PMID: 26995066.
      Citations: 10     Fields:    Translation:Humans
    41. Tarquinio DC, Hou W, Neul JL, Kaufmann WE, Glaze DG, Motil KJ, Skinner SA, Lee HS, Percy AK. The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders. Pediatr Neurol. 2015 Nov; 53(5):402-11. PMID: 26278631.
      Citations: 31     Fields:    Translation:Humans
    42. Neul JL, Glaze DG, Percy AK, Feyma T, Beisang A, Dinh T, Suter B, Anagnostou E, Snape M, Horrigan J, Jones NE. Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale. J Child Neurol. 2015 Nov; 30(13):1743-8. PMID: 25895911.
      Citations: 19     Fields:    Translation:HumansCTClinical Trials
    43. Herrera JA, Ward CS, Pitcher MR, Percy AK, Skinner S, Kaufmann WE, Glaze DG, Wehrens XH, Neul JL. Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs. Dis Model Mech. 2015 Apr; 8(4):363-71. PMID: 25713300.
      Citations: 7     Fields:    Translation:Animals
    44. Tarquinio DC, Hou W, Neul JL, Lane JB, Barnes KV, O'Leary HM, Bruck NM, Kaufmann WE, Motil KJ, Glaze DG, Skinner SA, Annese F, Baggett L, Barrish JO, Geerts SP, Percy AK. Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis. Pediatr Neurol. 2015 Jun; 52(6):585-91.e2. PMID: 25801175.
      Citations: 18     Fields:    Translation:Humans
    45. Motil KJ, Barrish JO, Neul JL, Glaze DG. Low bone mineral mass is associated with decreased bone formation and diet in girls with Rett syndrome. J Pediatr Gastroenterol Nutr. 2014 Sep; 59(3):386-92. PMID: 25144778.
      Citations: 4     Fields:    Translation:Humans
    46. Killian JT, Lane JB, Cutter GR, Skinner SA, Kaufmann WE, Tarquinio DC, Glaze DG, Motil KJ, Neul JL, Percy AK. Pubertal development in Rett syndrome deviates from typical females. Pediatr Neurol. 2014 Dec; 51(6):769-75. PMID: 25283752.
      Citations: 11     Fields:    Translation:HumansCTClinical Trials
    47. Neul JL, Lane JB, Lee HS, Geerts S, Barrish JO, Annese F, Baggett LM, Barnes K, Skinner SA, Motil KJ, Glaze DG, Kaufmann WE, Percy AK. Developmental delay in Rett syndrome: data from the natural history study. J Neurodev Disord. 2014; 6(1):20. PMID: 25071871.
      Citations: 57     Fields:    
    48. Patriquin MA, Mellman TA, Glaze DG, Alfano CA. Polysomnographic sleep characteristics of generally-anxious and healthy children assessed in the home environment. J Affect Disord. 2014 Jun; 161:79-83. PMID: 24751311.
      Citations: 10     Fields:    Translation:Humans
    49. Suter B, Treadwell-Deering D, Zoghbi HY, Glaze DG, Neul JL. Brief report: MECP2 mutations in people without Rett syndrome. J Autism Dev Disord. 2014 Mar; 44(3):703-11. PMID: 23921973.
      Citations: 12     Fields:    Translation:Humans
    50. Cuddapah VA, Pillai RB, Shekar KV, Lane JB, Motil KJ, Skinner SA, Tarquinio DC, Glaze DG, McGwin G, Kaufmann WE, Percy AK, Neul JL, Olsen ML. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. J Med Genet. 2014 Mar; 51(3):152-8. PMID: 24399845.
      Citations: 111     Fields:    Translation:Humans
    51. Chapleau CA, Lane J, Kirwin SM, Schanen C, Vinette KM, Stubbolo D, MacLeod P, Glaze DG, Motil KJ, Neul JL, Skinner SA, Kaufmann WE, Percy AK. Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome. Am J Med Genet A. 2013 Jul; 161A(7):1638-46. PMID: 23696494.
      Citations: 1     Fields:    Translation:Humans
    52. Malow BA, Byars K, Johnson K, Weiss S, Bernal P, Goldman SE, Panzer R, Coury DL, Glaze DG. A practice pathway for the identification, evaluation, and management of insomnia in children and adolescents with autism spectrum disorders. Pediatrics. 2012 Nov; 130 Suppl 2:S106-24. PMID: 23118242.
      Citations: 53     Fields:    Translation:Humans
    53. Tarquinio DC, Motil KJ, Hou W, Lee HS, Glaze DG, Skinner SA, Neul JL, Annese F, McNair L, Barrish JO, Geerts SP, Lane JB, Percy AK. Growth failure and outcome in Rett syndrome: specific growth references. Neurology. 2012 Oct 16; 79(16):1653-61. PMID: 23035069.
      Citations: 42     Fields:    Translation:Humans
    54. Motil KJ, Caeg E, Barrish JO, Geerts S, Lane JB, Percy AK, Annese F, McNair L, Skinner SA, Lee HS, Neul JL, Glaze DG. Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome. J Pediatr Gastroenterol Nutr. 2012 Sep; 55(3):292-8. PMID: 22331013.
      Citations: 61     Fields:    Translation:Humans
    55. Foster SB, Lu M, Glaze DG, Reuben JM, Harris LL, Cohen EN, Lee BN, Zhao E, Paul ME, Schwarzwald H, McMullen-Jackson C, Clark C, Armstrong FD, Brouwers PY, Miller TL, Colin AA, Scott GB, Shahzeidi S, Willen EJ, Asthana D, Lipshultz SE, Thompson BW, Shearer WT. Associations of cytokines, sleep patterns, and neurocognitive function in youth with HIV infection. Clin Immunol. 2012 Jul; 144(1):13-23. PMID: 22659030.
      Citations: 17     Fields:    Translation:HumansCells
    56. Motil KJ, Barrish JO, Lane J, Geerts SP, Annese F, McNair L, Percy AK, Skinner SA, Neul JL, Glaze DG. Vitamin D deficiency is prevalent in girls and women with Rett syndrome. J Pediatr Gastroenterol Nutr. 2011 Nov; 53(5):569-74. PMID: 21637127.
      Citations: 17     Fields:    Translation:Humans
    57. Bird LM, Tan WH, Bacino CA, Peters SU, Skinner SA, Anselm I, Barbieri-Welge R, Bauer-Carlin A, Gentile JK, Glaze DG, Horowitz LT, Mohan KN, Nespeca MP, Sahoo T, Sarco D, Waisbren SE, Beaudet AL. A therapeutic trial of pro-methylation dietary supplements in Angelman syndrome. Am J Med Genet A. 2011 Dec; 155A(12):2956-63. PMID: 22002941.
      Citations: 18     Fields:    Translation:HumansCellsCTClinical Trials
    58. Tan WH, Bacino CA, Skinner SA, Anselm I, Barbieri-Welge R, Bauer-Carlin A, Beaudet AL, Bichell TJ, Gentile JK, Glaze DG, Horowitz LT, Kothare SV, Lee HS, Nespeca MP, Peters SU, Sahoo T, Sarco D, Waisbren SE, Bird LM. Angelman syndrome: Mutations influence features in early childhood. Am J Med Genet A. 2011 Jan; 155A(1):81-90. PMID: 21204213.
      Citations: 43     Fields:    Translation:HumansCells
    59. Percy AK, Neul JL, Glaze DG, Motil KJ, Skinner SA, Khwaja O, Lee HS, Lane JB, Barrish JO, Annese F, McNair L, Graham J, Barnes K. Rett syndrome diagnostic criteria: lessons from the Natural History Study. Ann Neurol. 2010 Dec; 68(6):951-5. PMID: 21104896.
      Citations: 54     Fields:    Translation:Humans
    60. Neul JL, Kaufmann WE, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, Leonard H, Bailey ME, Schanen NC, Zappella M, Renieri A, Huppke P, Percy AK. Rett syndrome: revised diagnostic criteria and nomenclature. Ann Neurol. 2010 Dec; 68(6):944-50. PMID: 21154482.
      Citations: 414     Fields:    Translation:HumansAnimals
    61. Peters SU, Bird LM, Kimonis V, Glaze DG, Shinawi LM, Bichell TJ, Barbieri-Welge R, Nespeca M, Anselm I, Waisbren S, Sanborn E, Sun Q, O'Brien WE, Beaudet AL, Bacino CA. Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid. Am J Med Genet A. 2010 Aug; 152A(8):1994-2001. PMID: 20635355.
      Citations: 19     Fields:    Translation:HumansCells
    62. Percy AK, Lee HS, Neul JL, Lane JB, Skinner SA, Geerts SP, Annese F, Graham J, McNair L, Motil KJ, Barrish JO, Glaze DG. Profiling scoliosis in Rett syndrome. Pediatr Res. 2010 Apr; 67(4):435-9. PMID: 20032810.
      Citations: 25     Fields:    Translation:Humans
    63. Glaze DG, Percy AK, Skinner S, Motil KJ, Neul JL, Barrish JO, Lane JB, Geerts SP, Annese F, Graham J, McNair L, Lee HS. Epilepsy and the natural history of Rett syndrome. Neurology. 2010 Mar 16; 74(11):909-12. PMID: 20231667.
      Citations: 69     Fields:    Translation:Humans
    64. Kirby RS, Lane JB, Childers J, Skinner SA, Annese F, Barrish JO, Glaze DG, Macleod P, Percy AK. Longevity in Rett syndrome: analysis of the North American Database. J Pediatr. 2010 Jan; 156(1):135-138.e1. PMID: 19772971.
      Citations: 27     Fields:    Translation:Humans
    65. Samaco RC, Mandel-Brehm C, Chao HT, Ward CS, Fyffe-Maricich SL, Ren J, Hyland K, Thaller C, Maricich SM, Humphreys P, Greer JJ, Percy A, Glaze DG, Zoghbi HY, Neul JL. Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities. Proc Natl Acad Sci U S A. 2009 Dec 22; 106(51):21966-71. PMID: 20007372.
      Citations: 120     Fields:    Translation:AnimalsCells
    66. Ramocki MB, Peters SU, Tavyev YJ, Zhang F, Carvalho CM, Schaaf CP, Richman R, Fang P, Glaze DG, Lupski JR, Zoghbi HY. Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome. Ann Neurol. 2009 Dec; 66(6):771-82. PMID: 20035514.
      Citations: 138     Fields:    Translation:HumansCells
    67. Motil KJ, Morrissey M, Caeg E, Barrish JO, Glaze DG. Gastrostomy placement improves height and weight gain in girls with Rett syndrome. J Pediatr Gastroenterol Nutr. 2009 Aug; 49(2):237-42. PMID: 19525868.
      Citations: 12     Fields:    Translation:Humans
    68. Glaze DG, Percy AK, Motil KJ, Lane JB, Isaacs JS, Schultz RJ, Barrish JO, Neul JL, O'Brien WE, Smith EO. A study of the treatment of Rett syndrome with folate and betaine. J Child Neurol. 2009 May; 24(5):551-6. PMID: 19225139.
      Citations: 15     Fields:    Translation:Humans
    69. Motil KJ, Ellis KJ, Barrish JO, Caeg E, Glaze DG. Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome. Pediatr Res. 2008 Oct; 64(4):435-9. PMID: 18535484.
      Citations: 20     Fields:    Translation:Humans
    70. Hopkins B, Glaze D. Disorders of arousal in children. Pediatr Ann. 2008 Jul; 37(7):481-7. PMID: 18710138.
      Citations:    Fields:    Translation:Humans
    71. Huckeba W, Chapieski L, Hiscock M, Glaze D. Arithmetic performance in children with Tourette syndrome: relative contribution of cognitive and attentional factors. J Clin Exp Neuropsychol. 2008 May; 30(4):410-20. PMID: 18938679.
      Citations: 5     Fields:    Translation:Humans
    72. Williams K, Scheimann A, Sutton V, Hayslett E, Glaze DG. Sleepiness and sleep disordered breathing in Prader-Willi syndrome: relationship to genotype, growth hormone therapy, and body composition. J Clin Sleep Med. 2008 Apr 15; 4(2):111-8. PMID: 18468308.
      Citations: 22     Fields:    Translation:Humans
    73. Percy AK, Lane JB, Childers J, Skinner S, Annese F, Barrish J, Caeg E, Glaze DG, MacLeod P. Rett syndrome: North American database. J Child Neurol. 2007 Dec; 22(12):1338-41. PMID: 18174548.
      Citations: 32     Fields:    Translation:Humans
    74. Potocki L, Bi W, Treadwell-Deering D, Carvalho CM, Eifert A, Friedman EM, Glaze D, Krull K, Lee JA, Lewis RA, Mendoza-Londono R, Robbins-Furman P, Shaw C, Shi X, Weissenberger G, Withers M, Yatsenko SA, Zackai EH, Stankiewicz P, Lupski JR. Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype. Am J Hum Genet. 2007 Apr; 80(4):633-49. PMID: 17357070.
      Citations: 141     Fields:    Translation:HumansCells
    75. del Gaudio D, Fang P, Scaglia F, Ward PA, Craigen WJ, Glaze DG, Neul JL, Patel A, Lee JA, Irons M, Berry SA, Pursley AA, Grebe TA, Freedenberg D, Martin RA, Hsich GE, Khera JR, Friedman NR, Zoghbi HY, Eng CM, Lupski JR, Beaudet AL, Cheung SW, Roa BB. Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males. Genet Med. 2006 Dec; 8(12):784-92. PMID: 17172942.
      Citations: 121     Fields:    Translation:HumansCells
    76. Mindell JA, Emslie G, Blumer J, Genel M, Glaze D, Ivanenko A, Johnson K, Rosen C, Steinberg F, Roth T, Banas B. Pharmacologic management of insomnia in children and adolescents: consensus statement. Pediatrics. 2006 Jun; 117(6):e1223-32. PMID: 16740821.
      Citations: 37     Fields:    Translation:Humans
    77. Motil KJ, Schultz RJ, Abrams S, Ellis KJ, Glaze DG. Fractional calcium absorption is increased in girls with Rett syndrome. J Pediatr Gastroenterol Nutr. 2006 Apr; 42(4):419-26. PMID: 16641581.
      Citations: 13     Fields:    Translation:Humans
    78. Goldman AM, Potocki L, Walz K, Lynch JK, Glaze DG, Lupski JR, Noebels JL. Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]. J Child Neurol. 2006 Feb; 21(2):93-8. PMID: 16566870.
      Citations: 13     Fields:    Translation:HumansCells
    79. Yatsenko SA, Treadwell-Deering D, Krull K, Lewis RA, Glaze D, Stankiewicz P, Lupski JR, Potocki L. Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications. Am J Med Genet A. 2005 Oct 01; 138A(2):175-80. PMID: 16152635.
      Citations: 9     Fields:    Translation:HumansCells
    80. Glaze DG. Neurophysiology of Rett syndrome. J Child Neurol. 2005 Sep; 20(9):740-6. PMID: 16225829.
      Citations: 43     Fields:    Translation:Humans
    81. Glaze DG. Evidence based sleep medicine--is pediatric sleep medicine ready? J Clin Sleep Med. 2005 Jul 15; 1(3):255-6. PMID: 17566184.
      Citations:    Fields:    Translation:Humans
    82. Stewart MG, Glaze DG, Friedman EM, Smith EO, Bautista M. Quality of life and sleep study findings after adenotonsillectomy in children with obstructive sleep apnea. Arch Otolaryngol Head Neck Surg. 2005 Apr; 131(4):308-14. PMID: 15837898.
      Citations: 14     Fields:    Translation:Humans
    83. Owens JA, Babcock D, Blumer J, Chervin R, Ferber R, Goetting M, Glaze D, Ivanenko A, Mindell J, Rappley M, Rosen C, Sheldon S. The use of pharmacotherapy in the treatment of pediatric insomnia in primary care: rational approaches. A consensus meeting summary. J Clin Sleep Med. 2005 Jan 15; 1(1):49-59. PMID: 17561616.
      Citations: 24     Fields:    Translation:HumansPHPublic Health
    84. Glaze DG. Childhood insomnia: why Chris can't sleep. Pediatr Clin North Am. 2004 Feb; 51(1):33-50, vi. PMID: 15008581.
      Citations: 8     Fields:    Translation:Humans
    85. Glaze DG. Rett syndrome: of girls and mice--lessons for regression in autism. Ment Retard Dev Disabil Res Rev. 2004; 10(2):154-8. PMID: 15362175.
      Citations: 16     Fields:    Translation:HumansAnimalsCells
    86. Culhane-Shelburne K, Chapieski L, Hiscock M, Glaze D. Executive functions in children with frontal and temporal lobe epilepsy. J Int Neuropsychol Soc. 2002 Jul; 8(5):623-32. PMID: 12164672.
      Citations: 14     Fields:    Translation:HumansCTClinical Trials
    87. Glaze DG. Neurophysiology of Rett syndrome. Ment Retard Dev Disabil Res Rev. 2002; 8(2):66-71. PMID: 12112729.
      Citations: 9     Fields:    Translation:Humans
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