Motil, Kathleen J.

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

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

Prevalence of atopic disorders and immunodeficiency in patients with ectodermal dysplasia syndromes

Mark, B. J., Becker, B. A., Halloran, D. R., Bree, A. F., Sindwani, R., Fete, M. D., Motil, K. J., Srun, S. W., & Fete, T. J. (2012) · Annals of Allergy, Asthma & Immunology

dental development and anomaliesImmunodeficiency and Autoimmune Disorders

Cited by 38