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Genes, Brain, and Behavior|May 4, 2021
Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndromeBridget E Collins, Jonathan K Merritt, Kirsty R Erickson, et al.Human Molecular Genetics|May 30, 2020
Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndromeJonathan K Merritt, Bridget E Collins, Kirsty R Erickson, et al.Genes|May 25, 2024
Normalized Clinical Severity Scores Reveal a Correlation between X Chromosome Inactivation and Disease Severity in Rett SyndromeJonathan K Merritt, Xiaolan Fang, Raymond C Caylor, et al.Research Square|January 9, 2026
Trajectory of skill acquisition, loss, and regain in females with classic Rett syndromeJeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.Plos One|October 12, 2022
Behavioral and brain anatomical analysis of Foxg1 heterozygous miceKirsty R Erickson, Rebekah Farmer, Jonathan K Merritt, et al.Human Molecular Genetics|January 31, 2015
Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgeneMeagan R Pitcher, José A Herrera, Shelly A Buffington, et al.Human Molecular Genetics|August 13, 2024
Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoformsLadan Kalani, Bo-Hyun Kim, Alberto Ruiz de Chavez, et al.Analytical Chemistry|October 13, 2016
Mass Spectrometry-Based Visualization of Molecules Associated with Human HabitatsDaniel Petras, Louis-Félix Nothias, Robert A Quinn, et al.Pageof 1