Neul, Jeffrey L.

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

Chao, H.-T., Chen, H., Samaco, R. C., Xue, M., Chahrour, M., Yoo, J., Neul, J. L., Gong, S., Lu, H.-C., Heintz, N., et al. (2010) · Nature

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 1,168

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

Preclinical research in Rett syndrome: setting the foundation for translational success

Katz, D. M., Berger-Sweeney, J. E., Eubanks, J. H., Justice, M. J., Neul, J. L., Pozzo-Miller, L., Blue, M. E., Christian, D., Crawley, J. N., Giustetto, M., et al. (2012) · Disease Models & Mechanisms

Genetics and Neurodevelopmental DisordersAnimal testing and alternatives

Cited by 206

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

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome

Veeraragavan, S., Wan, Y.-W., Connolly, D. R., Hamilton, S. M., Ward, C. S., Soriano, S., Pitcher, M. R., McGraw, C. M., Huang, S. G., Green, J. R., et al. (2016) · Human Molecular Genetics

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 59

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

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

MeCP2 prevents against sustained ketamine-induced synaptic depression at inhibitory synapses

Piazza, M. K., Weit, A. R., Kavalali, E. T., Neul, J. L., & Monteggia, L. M. (2025) · iScience

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 3