Personalized Follow Up and Genetic Diagnosis Update of FMR1-Related Conditions: A Change in Diagnosis, Prognosis and Expectations. [PDF]
Roche-Martínez A +5 more
europepmc +1 more source
Altered ECM deposition and cell adhesion signaling in a human cortical organoid model of fragile X syndrome. [PDF]
Havusha-Laufer S +9 more
europepmc +1 more source
RNA-Based Therapeutics in Genetic Neurodevelopmental Disorders: Bridging Molecular Genetics and Precision Medicine. [PDF]
Focșa IO +11 more
europepmc +1 more source
Genetic Reduction of the Translational Repressors FMRP and 4E-BP2 Preserves Memory in Mouse Models of Alzheimer's Disease. [PDF]
Ribeiro FC +11 more
europepmc +1 more source
Unraveling the Individualized Shared and Distinct Dynamic Functional Connectivity in Idiopathic Autism Spectrum Disorder and Fragile X Syndrome. [PDF]
Pan B +7 more
europepmc +1 more source
HK2 drives synaptic dysfunction in fragile X syndrome via epigenetic regulation of H3K18 lactylation. [PDF]
Luan Y +7 more
europepmc +1 more source
Overlapping Pathways: Autism Spectrum Disorder in Fragile X Carrier States and the Need for Greater Awareness. [PDF]
Fernandez MV +4 more
europepmc +1 more source
Characterizing Populations Based on Proximity to a Fragile X Syndrome Specialty Clinic. [PDF]
Ogunsola HY +7 more
europepmc +1 more source
Exploring the Relationship Between Fragile X Syndrome and Autism: A Bibliometric Analysis of Global Research Trends. [PDF]
Kaplan A, Malik S, Persaud NA, Ganti L.
europepmc +1 more source

