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

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

Autism spectrum disorders and epilepsy: Moving towards a comprehensive approach to treatment

(2010) Roberto Tuchman et al.   BRAIN & DEVELOPMENT

Frequent association of autism spectrum disorder in patients with childhood onset epilepsy

(2010) Muneaki Matsuo et al.   BRAIN & DEVELOPMENT

Epilepsy and autism spectrum disorders: Are there common developmental mechanisms?

(2010) Amy Brooks-Kayal   BRAIN & DEVELOPMENT

Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome

(2010) Weerasak Chonchaiya et al.   HUMAN GENETICS

The role of fragile X mental retardation protein in major mental disorders

(2010) S. Hossein Fatemi et al.   NEUROPHARMACOLOGY

Early onset of neurological symptoms in fragile X premutation carriers exposed to neurotoxins

(2010) Ripon Paul et al.   NEUROTOXICOLOGY

Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: Preliminary data suggest an involvement of epigenetic mechanisms

(2009) Danuta Z. Loesch et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

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

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

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

Broad Clinical Involvement in a Family Affected by the Fragile X Premutation

(2009) Weerasak Chonchaiya et al.   JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS

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

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

Screening for Expanded Alleles of the FMR1 Gene in Blood Spots from Newborn Males in a Spanish Population

(2009) Isabel Fernandez-Carvajal et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Prevalence of Parent-Reported Diagnosis of Autism Spectrum Disorder Among Children in the US, 2007

(2009) M. D. Kogan et al.   PEDIATRICS

Origins of Epilepsy in Fragile X Syndrome

(2009) Paul J. Hagerman et al.   Epilepsy Currents

No Evidence for a Difference in Neuropsychological Profile among Carriers and Noncarriers of the FMR1 Premutation in Adults under the Age of 50

(2008) Jessica Ezzell Hunter et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder

(2008) Catalina García-Nonell et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Co-occurring conditions associated withFMR1gene variations: Findings from a national parent survey

(2008) Donald B. Bailey et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

Advances in the Treatment of Fragile X Syndrome

(2008) R. J. Hagerman et al.   PEDIATRICS

A Rapid Polymerase Chain Reaction-Based Screening Method for Identification of All Expanded Alleles of the Fragile X (FMR1) Gene in Newborn and High-Risk Populations

(2007) Flora Tassone et al.   JOURNAL OF MOLECULAR DIAGNOSTICS