Abnormal dendrite and spine morphology in primary visual cortex in the CGG knock-in mouse model of the fragile X premutation

Molecular Pathogenesis of Fragile X-Associated Tremor/Ataxia Syndrome

(2016) Christopher Raske et al.   JOURNAL OF INVESTIGATIVE MEDICINE

Mouse Models of Fragile X-Associated Tremor Ataxia

(2016) Robert F. Berman et al.   JOURNAL OF INVESTIGATIVE MEDICINE

Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation

(2011) Kirin Basuta et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in mice

(2011) Michael R. Hunsaker et al.   BEHAVIOURAL BRAIN RESEARCH

Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairments

(2011) Naomi J. Goodrich-Hunsaker et al.   BRAIN AND COGNITION

CGG repeat in the FMR1 gene: size matters

(2011) R Willemsen et al.   CLINICAL GENETICS

Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task

(2011) Naomi J. Goodrich-Hunsaker et al.   Frontiers in Human Neuroscience

Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder

(2011) Weerasak Chonchaiya et al.   HUMAN GENETICS

A mouse model of the fragile X premutation: Effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis

(2011) Mei Qin et al.   NEUROBIOLOGY OF DISEASE

Subregion-specific dendritic spine abnormalities in the hippocampus of Fmr1 KO mice

(2011) Josien Levenga et al.   NEUROBIOLOGY OF LEARNING AND MEMORY

Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation

(2010) Michael R. Hunsaker et al.   BEHAVIOURAL BRAIN RESEARCH

Mapping self-reports of working memory deficits to executive dysfunction in Fragile X Mental Retardation 1 (FMR1) gene premutation carriers asymptomatic for FXTAS

(2010) Cary S. Kogan et al.   BRAIN AND COGNITION

Ubiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation

(2010) H. Jürgen Wenzel et al.   BRAIN RESEARCH

Developmental characteristics of dendritic spines in the dentate gyrus of Fmr1 knockout mice

(2010) Aaron W. Grossman et al.   BRAIN RESEARCH

Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients

(2010) Chantal Sellier et al.   EMBO JOURNAL

FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: Insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States

(2010) Feras M Hantash et al.   GENETICS IN MEDICINE

Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development

(2010) Christopher L. Cunningham et al.   HUMAN MOLECULAR GENETICS

Progressive spatial processing deficits in a mouse model of the fragile X premutation.

(2009) Michael R. Hunsaker et al.   BEHAVIORAL NEUROSCIENCE

The perception of biological and mechanical motion in female fragile X premutation carriers

(2009) Szabolcs Kéri et al.   BRAIN AND COGNITION

Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration

(2009) Y. Chen et al.   HUMAN MOLECULAR GENETICS

A Review of Fragile X Premutation Disorders

(2009) James A. Bourgeois et al.   JOURNAL OF CLINICAL PSYCHIATRY

A Quantitative ELISA Assay for the Fragile X Mental Retardation 1 Protein

(2009) Christine Iwahashi et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Testing for Fragile X Gene Mutations Throughout the Life Span

(2008) Randi J. Hagerman   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome

(2008) Judith R. Brouwer et al.   JOURNAL OF NEUROCHEMISTRY

Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice

(2008) Femke M.S. de Vrij et al.   NEUROBIOLOGY OF DISEASE

Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function

(2008) Gary J. Bassell et al.   NEURON