Jeffrey Neul
Affiliations: | Baylor College of Medicine, Houston, TX | ||
| Neurosciences | University of California, San Diego, La Jolla, CA |
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| Kennedy M, Glass L, Glaze DG, et al. (2024) Development of trofinetide for the treatment of Rett syndrome: from bench to bedside. Frontiers in Pharmacology. 14: 1341746 |
| Collins BE, Neul JL. (2022) Rett Syndrome and Duplication Syndrome: Disorders of MeCP2 Dosage. Neuropsychiatric Disease and Treatment. 18: 2813-2835 |
| Erickson KR, Farmer R, Merritt JK, et al. (2022) Behavioral and brain anatomical analysis of Foxg1 heterozygous mice. Plos One. 17: e0266861 |
| McKnight D, Bean L, Karbassi I, et al. (2021) Recommendations by the ClinGen Rett/Angelman-like expert panel for gene-specific variant interpretation methods. Human Mutation |
| Collins BE, Merritt JK, Erickson KR, et al. (2021) Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndrome. Genes, Brain, and Behavior. e12739 |
| Ward CS, Huang TW, Herrera JA, et al. (2020) Loss of MeCP2 Function Across Several Neuronal Populations Impairs Breathing Response to Acute Hypoxia. Frontiers in Neurology. 11: 593554 |
| Dong HW, Erickson K, Lee JR, et al. (2020) Detection of neurophysiological features in female R255X MeCP2 mutation mice. Neurobiology of Disease. 105083 |
| Peters SU, Fu C, Neul JL, et al. (2020) Cortisol profiles and clinical severity in MECP2 duplication syndrome. Journal of Neurodevelopmental Disorders. 12: 19 |
| Merritt JK, Collins BE, Erickson KR, et al. (2020) Pharmacological readthrough of R294X Mecp2 in a novel mouse model of Rett Syndrome. Human Molecular Genetics |
| Herrera JA, Ward CS, Wehrens XH, et al. (2016) Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesis. Human Molecular Genetics. 25: 4983-4995 |