Fragile X Syndrome: The FMR1 CGG Repeat Distribution Among World Populations

Treatment of fragile X-associated tremor ataxia syndrome (FXTAS) and related neurological problems

(2016) Randi Hagerman   Clinical Interventions in Aging

Decreased Fragile X Mental Retardation Protein Expression Underlies Amygdala Dysfunction in Carriers of the Fragile X Premutation

(2011) David Hessl et al.   BIOLOGICAL PSYCHIATRY

CGG repeat in the FMR1 gene: size matters

(2011) R Willemsen et al.   CLINICAL GENETICS

Initiation of Translation of the FMR1 mRNA Occurs Predominantly through 5′-End-Dependent Ribosomal Scanning

(2011) Anna L. Ludwig et al.   JOURNAL OF MOLECULAR BIOLOGY

Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles

(2011) F. Tassone et al.   NUCLEIC ACIDS RESEARCH

Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males

(2010) Stephen C. Collins et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genetic Diversity of the Fragile X Syndrome Gene (FMR1) in a Large Sub-Saharan West African Population

(2010) Emmanuel K. Peprah et al.   ANNALS OF HUMAN GENETICS

Gene Expression Profiling Identifies WNT7A As a Possible Candidate Gene for Decreased Cancer Risk in Fragile X Syndrome Patients

(2010) Mónica Alejandra Rosales-Reynoso et al.   ARCHIVES OF MEDICAL RESEARCH

A systematic review of population screening for fragile X syndrome

(2010) Melissa K Hill et al.   GENETICS IN MEDICINE

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

Mechanisms of trinucleotide repeat instability during human development

(2010) Cynthia T. McMurray   NATURE REVIEWS GENETICS

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

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

Microsatellite repeat instability and neurological disease

(2009) Judith R. Brouwer et al.   BIOESSAYS

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

(2009) Susumu Otsuka et al.   BRAIN & DEVELOPMENT

Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population

(2009) Ali Reza Pouya et al.   European Journal of Medical Genetics

Haplotype and AGG Interspersion Analysis of FMR1 Alleles in a Croatian Population: No Founder Effect Detected in Patients with Fragile X Syndrome

(2009) H. Đokić et al.   HUMAN BIOLOGY

A Review of Fragile X Premutation Disorders

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

The AGG interruption pattern within the CGG repeat of the FMR1 gene among Taiwanese population

(2009) Hua-Hsien Chiu et al.   JOURNAL OF GENETICS

Examination of FMR1 transcript and protein levels among 74 premutation carriers

(2009) Emmanuel Peprah et al.   JOURNAL OF HUMAN GENETICS

The nucleotide binding dynamics of human MSH2–MSH3 are lesion dependent

(2009) Barbara A L Owen et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice

(2009) A. Entezam et al.   NUCLEIC ACIDS RESEARCH

MSH2 ATPase Domain Mutation Affects CTG•CAG Repeat Instability in Transgenic Mice

(2009) Stéphanie Tomé et al.   PLoS Genetics

Genetic variation of theFMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara

(2008) Patricio Barros-Núñez et al.   AMERICAN JOURNAL OF HUMAN BIOLOGY

Reproductive Health of Adolescent Girls Who Carry the FMR1 Premutation

(2008) John J. De Caro et al.   Annals of the New York Academy of Sciences

Reduced Hippocampal Activation During Recall is Associated with Elevated FMR1 mRNA and Psychiatric Symptoms in Men with the Fragile X Premutation

(2008) Kami Koldewyn et al.   Brain Imaging and Behavior

Features of trinucleotide repeat instability in vivo

(2008) Irina V Kovtun et al.   CELL RESEARCH

Clinical significance of tri-nucleotide repeats in Fragile X testing: A clarification of American College of Medical Genetics guidelines

(2008) Kathryn E Kronquist et al.   GENETICS IN MEDICINE

Prevalence of the Fragile X Syndrome Among Estonian Mentally Retarded and the Entire Children's Population

(2008) Helen Puusepp et al.   JOURNAL OF CHILD NEUROLOGY

Fragile X Syndrome in Korea: A Case Series and a Review of the Literature

(2008) Shin-Young Yim et al.   JOURNAL OF KOREAN MEDICAL SCIENCE

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

(2008) Gary J. Bassell et al.   NEURON

Inherited Susceptibility to Common Cancers

(2008) William D. Foulkes   NEW ENGLAND JOURNAL OF MEDICINE