Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Links Between the C9orf72 Repeat Expansion and Psychiatric Symptoms.

Current neurology and neuroscience reports - 26 Nov 2019

Silverman Hannah E, Goldman Jill S, Huey Edward D

Abstract excerpt

PURPOSE OF REVIEW: To present recent findings on the links between the C9orf72 expansion and psychiatric impairment. RECENT FINDINGS: Repeat hexanucleotide expansions in the C9orf72 gene are a cause of familial frontotemporal dementia (FTD), amyotrophic lateral sclerosis (ALS), and the mixed phenotype, FTD-ALS. Symptomatic expansion carriers display higher rates of psychotic and other psychiatric symptoms than...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amyotrophic Lateral Sclerosis Research
Share to C9orf72 Protein
Share to DNA Repeat Expansion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Linkage

Share to Heterozygote

Share to Mental Disorders

Share to Parkinson's Disease Mechanisms and Treatments

Share to Phenotype

Source

Identifiers

PMID: 31773397
DOI: 10.1007/s11910-019-1017-9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Links Between the C9orf72 Repeat Expansion and Psychiatric Symptoms.PMID 31773397Read ↗

The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype.Semantic proximity Read ↗

Expanding Clinical Spectrum of C9ORF72 -Related Disorders and Promising Therapeutic StrategiesSemantic proximity Read ↗

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features.Semantic proximity Read ↗

Psychiatric Presentations of C9orf72 Mutation: What Are the Diagnostic Implications for Clinicians?Semantic proximity Read ↗

C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts.Semantic proximity Read ↗

C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role?Semantic proximity Read ↗

Psychosis and hallucinations in frontotemporal dementia with the C9ORF72 mutation: a detailed clinical cohort.Semantic proximity Read ↗

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72Semantic proximity Read ↗

C9ORF72 hexanucleotide repeat number in frontotemporal lobar degeneration: a genotype-phenotype correlation study.Semantic proximity Read ↗

The C9ORF72 expansion mutation: gene structure, phenotypic and diagnostic issues.Semantic proximity Read ↗

Slowly progressive behavioral frontotemporal dementia syndrome in a family co-segregating the C9orf72 expansion and a Synaptophysin mutation.Semantic proximity Read ↗

Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansionSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.