Glaze, Daniel G.

Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome

Neul, J. L., Fang, P., Barrish, J., Lane, J., Caeg, E. B., Smith, E. O., Zoghbi, H., Percy, A., & Glaze, D. G. (2008) · Neurology

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 498

Methyl-CpG-binding protein 2 ( MECP2 ) mutation type is associated with disease severity in Rett syndrome

Cuddapah, V. A., Pillai, R. B., Shekar, K. V., Lane, J. B., Motil, K. J., Skinner, S. A., Tarquinio, D. C., Glaze, D. G., McGwin, G., Kaufmann, W. E., et al. (2014) · Journal of Medical Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 311

Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome

Motil, K. J., Caeg, E., Barrish, J. O., Geerts, S., Lane, J. B., Percy, A. K., Annese, F., McNair, L., Skinner, S. A., Lee, H., et al. (2012) · Journal of Pediatric Gastroenterology and Nutrition

Genetics and Neurodevelopmental DisordersChild Nutrition and Feeding Issues

Cited by 210

Rett syndrome diagnostic criteria: Lessons from the Natural History Study

Percy, A. K., Neul, J. L., Glaze, D. G., Motil, K. J., Skinner, S. A., Khwaja, O., Lee, H., Lane, J. B., Barrish, J. O., Annese, F., et al. (2010) · Annals of Neurology

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 144

Associations of cytokines, sleep patterns, and neurocognitive function in youth with HIV infection

Foster, S. B., Lu, M., Glaze, D. G., Reuben, J. M., Harris, L. L., Cohen, E. N., Lee, B.-N., Zhao, E., Paul, M. E., Schwarzwald, H., et al. (2012) · Clinical Immunology

HIV Research and TreatmentHIV-related health complications and treatments

Cited by 49

Abnormal circadian rhythm of melatonin in Smith–Magenis syndrome patients with RAI1 point mutations

Boone, P. M., Reiter, R. J., Glaze, D. G., Tan, D., Lupski, J. R., & Potocki, L. (2011) · American Journal of Medical Genetics Part A

Circadian rhythm and melatoninGenetics and Neurodevelopmental Disorders

Cited by 47

Vitamin D deficiency is prevalent in girls and women with Rett syndrome

Motil, K. J., Barrish, J. O., Lane, J., Geerts, S. P., Annese, F., McNair, L., Percy, A. K., Skinner, S. A., Neul, J. L., & Glaze, D. G. (2011) · Journal of Pediatric Gastroenterology and Nutrition

Vitamin D Research StudiesGenetics and Neurodevelopmental Disorders

Cited by 46