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Article

Sex differences in the prevalence of genetic mutations in FTD and ALS: A meta-analysis.

Neurology - 10 Oct 2017

Curtis Ashley F, Masellis Mario, Hsiung Ging-Yuek Robin, Moineddin Rahim, Zhang Kathy, Au Bonnie, Millett Geneva, Mackenzie Ian, Rogaeva Ekaterina, Tierney Mary C

Abstract excerpt

OBJECTIVE: To conduct a meta-analysis that investigates sex differences in the prevalence of mutations in the 3 most common genes that cause amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD)-chromosome 9 open reading frame 72 (C9orf72), progranulin (GRN), or microtubule-associated protein tau (MAPT)-in patients clinically diagnosed with these conditions. METHODS: MEDLINE, EMBASE, and PsycINFO...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 28916533
DOI: 10.1212/WNL.0000000000004494
PMCID: PMC5634668

Genes

GRN
MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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