C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson’s disease complicated by psychosis or dementia in a Sardinian population

The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism

(2015) Lucia V. Schottlaender et al.   NEUROBIOLOGY OF AGING

Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansions

(2015) Sonja W. Scholz et al.   NEUROBIOLOGY OF AGING

Absence ofC9ORF72expanded or intermediate repeats in autopsy-confirmed Parkinson's disease

(2014) Karen Nuytemans et al.   MOVEMENT DISORDERS

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease

(2014) J. Theuns et al.   NEUROLOGY

Multiple System Atrophy and Repeat Expansions inC9orf72—Reply

(2014) Jill S. Goldman et al.   JAMA Neurology

“Atypical” atypical parkinsonism: New genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-A diagnostic guide

(2013) Maria Stamelou et al.   MOVEMENT DISORDERS

C9orf72 repeat expansions are restricted to the ALS-FTD spectrum

(2013) Nicola Ticozzi et al.   NEUROBIOLOGY OF AGING

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

(2013) D. J. Hensman Moss et al.   NEUROLOGY

C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

(2013) Bin Jiao et al.   Frontiers in Cellular Neuroscience

Corticobasal and ataxia syndromes widen the spectrum ofC9ORF72hexanucleotide expansion disease

(2012) SG Lindquist et al.   CLINICAL GENETICS

Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?

(2012) Gianluca Floris et al.   JOURNAL OF NEUROLOGY

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

(2012) Elisa Majounie et al.   LANCET NEUROLOGY

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease

(2012) Elisa Majounie et al.   NEUROBIOLOGY OF AGING

Parkinson disease is not associated with C9ORF72 repeat expansions

(2012) Matthew B. Harms et al.   NEUROBIOLOGY OF AGING

Primer3—new capabilities and interfaces

(2012) Andreas Untergasser et al.   NUCLEIC ACIDS RESEARCH

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

(2011) Alan E. Renton et al.   NEURON