FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States

Effects of STX209 (Arbaclofen) on Neurobehavioral Function in Children and Adults with Fragile X Syndrome: A Randomized, Controlled, Phase 2 Trial

(2012) E. M. Berry-Kravis et al.   Science Translational Medicine

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

FMR1 gray-zone alleles: Association with Parkinson's disease in women?

(2011) Deborah A. Hall et al.   MOVEMENT DISORDERS

Parents' Decisions to Screen Newborns for FMR1 Gene Expansions in a Pilot Research Project

(2011) D. Skinner et al.   PEDIATRICS

Open-label add-on treatment trial of minocycline in fragile X syndrome

(2010) Carlo Paribello et al.   BMC Neurology

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

Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: Implications for fragile X syndrome carrier and newborn screening

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

Commentary on population screening for fragile X syndrome

(2010) Bradford Coffee   GENETICS IN MEDICINE

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

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio

(2010) David Eugeny Godler et al.   HUMAN MOLECULAR GENETICS

A Simple, High-Throughput Assay for Fragile X Expanded Alleles Using Triple Repeat Primed PCR and Capillary Electrophoresis

(2010) Elaine Lyon et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

An Information-Rich CGG Repeat Primed PCR That Detects the Full Range of Fragile X Expanded Alleles and Minimizes the Need for Southern Blot Analysis

(2010) Liangjing Chen et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization

(2010) Lisa Cordeiro et al.   Journal of Neurodevelopmental Disorders

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

(2009) Bradford Coffee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Fragile X carrier screening and FMR1 allele distribution in the Japanese population

(2009) Susumu Otsuka et al.   BRAIN & DEVELOPMENT

Screening and instability ofFMR1alleles in a prospective sample of 24,449 mother–newborn pairs from the general population

(2009) S Lévesque et al.   CLINICAL GENETICS

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

(2009) DZ Loesch et al.   CLINICAL GENETICS

Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families

(2009) Laia Rodriguez-Revenga et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study

(2009) Sylvia Metcalfe et al.   GENETICS IN MEDICINE

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

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

A pilot open label, single dose trial of fenobam in adults with fragile X syndrome

(2009) E Berry-Kravis et al.   JOURNAL OF MEDICAL GENETICS

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

Evidence of depressive symptoms in fragile-X syndrome premutated females

(2009) Laia Rodriguez-Revenga et al.   PSYCHIATRIC GENETICS

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