Seizures in Fragile X Syndrome: Associations and Longitudinal Analysis of a Large Clinic-Based Cohort

Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures

(2019) Markus Zweier et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The co-occurrence of epilepsy and autism: A systematic review

(2019) Sara Lukmanji et al.   EPILEPSY & BEHAVIOR

Fragile Females: Case Series of Epilepsy in Girls With FMR1 Disruption

(2019) Kenneth A. Myers et al.   PEDIATRICS

Aberrant RNA translation in fragile X syndrome: From FMRP mechanisms to emerging therapeutic strategies

(2018) Anwesha Banerjee et al.   BRAIN RESEARCH

EEG endophenotypes in autism spectrum disorder

(2018) Jamie K. Capal et al.   EPILEPSY & BEHAVIOR

FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome

(2017) Stephanie L. Sherman et al.   PEDIATRICS

Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment

(2017) Walter E. Kaufmann et al.   PEDIATRICS

Characterization, treatment patterns, and patient-related outcomes of patients with Fragile X syndrome in Germany: final results of the observational EXPLAIN-FXS study

(2016) Frank Haessler et al.   BMC Psychiatry

Premature mortality in autism spectrum disorder

(2016) Tatja Hirvikoski et al.   BRITISH JOURNAL OF PSYCHIATRY

Epileptic Electroencephalography Profile Associates with Attention Problems in Children with Fragile X Syndrome: Review and Case Series

(2016) Benjamin Cowley et al.   Frontiers in Human Neuroscience

Surgical treatment for medically refractory focal epilepsy in a patient with fragile X syndrome

(2015) Cynthia Kenmuir et al.   BRAIN & DEVELOPMENT

Clinical characteristics of children and young adults with co-occurring autism spectrum disorder and epilepsy

(2015) Christelle M. El Achkar et al.   EPILEPSY & BEHAVIOR

Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back

(2015) Christina Gross et al.   Neurotherapeutics

Independent role for presynaptic FMRP revealed by anFMR1missense mutation associated with intellectual disability and seizures

(2015) Leila K. Myrick et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

EEG abnormalities and seizures in genetically diagnosed Fragile X syndrome

(2014) Takijah T. Heard et al.   INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE

Fragile X Syndrome: A Review of Associated Medical Problems

(2014) S. A. Kidd et al.   PEDIATRICS

Phosphorylation of FMRP and alterations of FMRP complex underlie enhanced mLTD in adult rats triggered by early life seizures

(2013) Paul B. Bernard et al.   NEUROBIOLOGY OF DISEASE

The trouble with spines in fragile X syndrome: density, maturity and plasticity

(2012) C.X. He et al.   NEUROSCIENCE

Mortality in Individuals With Autism, With and Without Epilepsy

(2011) Jane Pickett et al.   JOURNAL OF CHILD NEUROLOGY

Autism and epilepsy: Historical perspective

(2010) Roberto Tuchman et al.   BRAIN & DEVELOPMENT

Autism and autistic epileptiform regression with occipital spikes

(2010) Ruth Nass et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Status epilepticus in fragile X syndrome

(2010) Magali Gauthey et al.   EPILEPSIA

Electroencephalogram Discharges in Atypical Cognitive Development

(2010) Richard E. Frye et al.   JOURNAL OF CHILD NEUROLOGY

Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA

(2009) Bradford Coffee 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

Advances in autism genetics: on the threshold of a new neurobiology

(2008) Brett S. Abrahams et al.   NATURE REVIEWS GENETICS

Advances in the Treatment of Fragile X Syndrome

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