Lane, Jane B.
Civitan International · University of Alabama at Birmingham
6 papers on CoChatORCID 0000-0003-0602-9325
Most cited papers
- Verified
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
- Verified
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
- Verified
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
- Verified
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
- Verified
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
- Verified
Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study
Cutri‐French, C., Armstrong, D., Saby, J., Gorman, C., Lane, J., Fu, C., Peters, S. U., Percy, A., Neul, J. L., & Marsh, E. D. (2020) · Annals of Neurology
Genetics and Neurodevelopmental DisordersEpilepsy research and treatment
Cited by 45
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