C9ORF72Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
C9ORF72Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease
Authors
Keywords
-
Journal
ANNALS OF HUMAN GENETICS
Volume 77, Issue 5, Pages 351-363
Publisher
Wiley
Online
2013-07-12
DOI
10.1111/ahg.12033
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- C9orf72 repeat expansions are a rare genetic cause of parkinsonism
- (2013) Suzanne Lesage et al. BRAIN
- The Disease-associated r(GGGGCC)nRepeat from theC9orf72Gene Forms Tract Length-dependent Uni- and Multimolecular RNA G-quadruplex Structures
- (2013) Kaalak Reddy et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS
- (2013) Peter E.A. Ash et al. NEURON
- The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS
- (2013) K. Mori et al. SCIENCE
- C9orf72 Hexanucleotide Repeat Expansions as the Causative Mutation for Chromosome 9p21–Linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
- (2012) Hussein Daoud et al. ARCHIVES OF NEUROLOGY
- Investigation of C9orf72 in 4 Neurodegenerative Disorders
- (2012) Zhengrui Xi et al. ARCHIVES OF NEUROLOGY
- Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
- (2012) A. Chio et al. BRAIN
- Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72
- (2012) Johnathan Cooper-Knock et al. BRAIN
- The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions
- (2012) Javier Simón-Sánchez et al. BRAIN
- Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
- (2012) Bradley F. Boeve et al. BRAIN
- Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
- (2012) C. J. Mahoney et al. BRAIN
- Analysis of theC9orf72Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide
- (2012) Alberto García-Redondo et al. HUMAN MUTATION
- A Pan-European Study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
- (2012) Julie van der Zee et al. HUMAN MUTATION
- Phenotype difference between ALS patients with expanded repeats inC9ORF72and patients with mutations in other ALS-related genes
- (2012) Stéphanie Millecamps et al. JOURNAL OF MEDICAL GENETICS
- Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72
- (2012) T. Konno et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
- (2012) Susan Byrne et al. LANCET 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
- C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population
- (2012) Mario Sabatelli et al. NEUROBIOLOGY OF AGING
- Screening for C9ORF72 repeat expansion in FTLD
- (2012) Raffaele Ferrari et al. NEUROBIOLOGY OF AGING
- High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients
- (2012) Kin Y. Mok et al. NEUROBIOLOGY OF AGING
- Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis
- (2012) Kotaro Ogaki et al. NEUROBIOLOGY OF AGING
- C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect
- (2012) Antonia Ratti et al. NEUROBIOLOGY OF AGING
- Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease
- (2012) Sara Rollinson et al. NEUROBIOLOGY OF AGING
- Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype
- (2012) Nicola J. Rutherford et al. NEUROBIOLOGY OF AGING
- Parkinson disease is not associated with C9ORF72 repeat expansions
- (2012) Matthew B. Harms et al. NEUROBIOLOGY OF AGING
- Screening for C9orf72 repeat expansions in parkinsonian syndromes
- (2012) Tu-Hsueh Yeh et al. NEUROBIOLOGY OF AGING
- Investigation of C9orf72 repeat expansions in Parkinson's disease
- (2012) Hussein Daoud et al. NEUROBIOLOGY OF AGING
- C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts
- (2012) C. Dobson-Stone et al. NEUROLOGY
- Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases
- (2012) W. van Rheenen et al. NEUROLOGY
- Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome
- (2012) Mariely DeJesus-Hernandez et al. PARKINSONISM & RELATED DISORDERS
- C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes
- (2012) Pietro Fratta et al. Scientific Reports
- Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
- (2011) Michael A. van Es et al. ANNALS OF NEUROLOGY
- A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
- (2011) Ilse Gijselinck et al. LANCET NEUROLOGY
- Mutational analysis of the VCP gene in Parkinson's disease
- (2011) Elisa Majounie et al. NEUROBIOLOGY OF AGING
- The chromosome 9 ALS and FTD locus is probably derived from a single founder
- (2011) Kin Mok et al. NEUROBIOLOGY OF AGING
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- Valosin-containing protein mutation and Parkinson’s disease
- (2011) Nora Chan et al. PARKINSONISM & RELATED DISORDERS
- Genome-Wide Association Study Confirms SNPs inSNCAand theMAPTRegion as Common Risk Factors for Parkinson Disease
- (2010) Todd L. Edwards et al. ANNALS OF HUMAN GENETICS
- Angiostatins decrease in the kidney of newborn piglets after hypoxia-reoxygenation
- (2010) Marwan Emara et al. EUROPEAN JOURNAL OF PHARMACOLOGY
- Advances in understanding the molecular basis of FXTAS
- (2010) D. Garcia-Arocena et al. HUMAN MOLECULAR GENETICS
- TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
- (2010) C. Lagier-Tourenne et al. HUMAN MOLECULAR GENETICS
- Consensus Statement of the Movement Disorder Society on Tremor
- (2010) Günther Deuschl et al. MOVEMENT DISORDERS
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
- (2010) Janel O. Johnson et al. NEURON
- Cyanobacterial neurotoxin BMAA in ALS and Alzheimer’s disease
- (2009) J. Pablo et al. ACTA NEUROLOGICA SCANDINAVICA
- The Combination of Dopa-Responsive Parkinsonian Syndrome and Motor Neuron Disease
- (2009) Elmar Hans Pinkhardt et al. Neurodegenerative Diseases
- Amyotrophic lateral sclerosis
- (2009) Lokesh C Wijesekera et al. Orphanet Journal of Rare Diseases
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now