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Publications by Randi Hagerman
AGG Interruptions Within the Maternal FMR1 Gene Reduce the Risk of Offspring With Fragile X Syndrome
Genetics in Medicine
Medicine
Genetics
Developmental Profiles of Infants With an FMR1 Premutation
Journal of Neurodevelopmental Disorders
Pediatrics
Cognitive Neuroscience
Perinatology
Neurology
Forensic Medicine
Child Health
Pathology
Cognitive Deficits and Associated ERP N400 Abnormalities in FXTAS With Parkinsonism
Frontiers in Genetics
Genetics
Molecular Medicine
Mavoglurant in Fragile X Syndrome: Results of Two Open-Label, Extension Trials in Adults and Adolescents
Scientific Reports
Multidisciplinary
Electrocortical Changes Associated With Minocycline Treatment in Fragile X Syndrome
Journal of Psychopharmacology
Medicine
Psychiatry
Mental Health
Pharmacology
Altered Redox Mitochondrial Biology in the Neurodegenerative Disorder Fragile X-Tremor/Ataxia Syndrome: Use of Antioxidants in Precision Medicine
Molecular Medicine
Molecular Medicine
Genetics
Molecular Biology
Immune Dysregulation as a Cause of Autoinflammation in Fragile X Premutation Carriers: Link Between FMRI CGG Repeat Number and Decreased Cytokine Responses
PLoS ONE
Multidisciplinary
Clinical Report
Journal of Developmental and Behavioral Pediatrics
Developmental
Mental Health
Child Health
Educational Psychology
Perinatology
Psychiatry
Pediatrics
Unstable Mutations in the FMR1 Gene and the Phenotypes
Advances in Experimental Medicine and Biology
Biochemistry
Medicine
Genetics
Molecular Biology
Modulation of the GABAergic Pathway for the Treatment of Fragile X Syndrome
Neuropsychiatric Disease and Treatment
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