Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample-Reference-Cited by-同舟云学术

Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample

Published:2014-06 Issue:6 Volume:35 Page:1510.e1-1510.e5
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Fahey Ciara,Byrne Susan,McLaughlin Russell,Kenna Kevin,Shatunov Aleksey,Donohoe Gary,Gill Michael,Al-Chalabi Ammar,Bradley Daniel G.,Hardiman Orla,Corvin Aiden P.,Morris Derek W.

Funder

Science Foundation Ireland

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference24 articles.

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3. Intermediate repeat expansion length in C9orf72 may be pathological in amyotrophic lateral sclerosis;Byrne;Amyotroph. Lateral Scler. Frontotemporal Degener,2013

4. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9orf72 causes chromosome 9p-Linked FTD and ALS;DeJesus-Hernandez;Neuron,2011

5. Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia;Fecto;J. Mol. Neurosci.,2011

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1. Distribution of the C9orf72 hexanucleotide repeat expansion in healthy subjects: a multicenter study promoted by the Italian IRCCS network of neuroscience and neurorehabilitation;Frontiers in Neurology;2024-01-31

2. Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population;Journal of the Neurological Sciences;2022-11

3. C9orf72 hexanucleotide repeat expansion found in suspected spinobulbar muscular atrophy (SBMA);Neurologia i Neurochirurgia Polska;2022-06-30

4. C9orf72-Related Neurodegenerative Diseases: From Clinical Diagnosis to Therapeutic Strategies;Frontiers in Aging Neuroscience;2022-06-10

5. Intermediate lengths of the C9ORF72 hexanucleotide repeat expansion may synergistically contribute to attention deficit hyperactivity disorder in child and his father: case report;Neurocase;2021-03-04