Evidence for the role of FMR1 gray zone alleles as a risk factor for parkinsonism in females

Clinical Phenotype of Adult Fragile X Gray Zone Allele Carriers: a Case Series

(2016) Sarah M. Debrey et al.   CEREBELLUM

The relationship between glucocerebrosidase mutations and Parkinson disease

(2016) Anna Migdalska-Richards et al.   JOURNAL OF NEUROCHEMISTRY

White Matter Changes in Patients with Parkinson's Disease Carrying Small CGG Expansion FMR1 Alleles: A Pilot Study

(2014) Nicholas Trost et al.   Neurodegenerative Diseases

Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms

(2013) Paul Hagerman   ACTA NEUROPATHOLOGICA

Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriers

(2012) Y Liu et al.   CLINICAL GENETICS

New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease

(2012) DZ Loesch et al.   CLINICAL GENETICS

Screening for FMR1 expanded alleles in patients with parkinsonism in mainland China

(2012) Xiong Zhang et al.   NEUROSCIENCE LETTERS

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

(2012) Flora Tassone et al.   Genome Medicine

Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism

(2011) Danuta Z Loesch et al.   GENETICS IN MEDICINE

Fragile X-associated tremor ataxia syndrome in FMR1 gray zone allele carriers

(2011) Deborah Hall et al.   MOVEMENT DISORDERS

FMR1 gene expansion and scans without evidence of dopaminergic deficits in parkinsonism patients

(2010) D.A. Hall et al.   PARKINSONISM & RELATED DISORDERS

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

(2009) DZ Loesch et al.   CLINICAL GENETICS

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

Mitochondria in the aetiology and pathogenesis of Parkinson's disease

(2008) Anthony HV Schapira   LANCET NEUROLOGY

An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1)

(2008) Mahmoud S Khaniani et al.   Molecular Cytogenetics