We did a two-stage genome-wide association study on clinical FTD, analysing samples from 3526 patients with FTD and 9402 healthy controls.
Mutations in three genes—MAPT, GRN, and C9orf72—have been associated with FTD. We sought to identify novel genetic risk loci associated with the disorder.
Jun 16, 2014 · We did a two-stage genome-wide association study on clinical FTD, analysing samples from 3526 patients with FTD and 9402 healthy controls. To ...
Mutations in three genes-MAPT, GRN, and C9orf72-have been associated with FTD. We sought to identify novel genetic risk loci associated with the disorder.
Mutations in three genes—MAPT, GRN, and C9orf72—have been associated with FTD. We sought to identify novel genetic risk loci associated with the disorder.
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Aug 31, 2024 · BACKGROUND: Frontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations, ...
Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia · Medicine. Brain : a journal of neurology · 2017.
Sep 2, 2021 · We performed a genome-wide association analysis in which we compared genotype data of 354 FTD patients (8%, N = 28 with pathological C9ORF72 ...
Jun 17, 2024 · Frontotemporal dementia (FTD) is the second most common cause of early-onset dementia after Alzheimer disease (AD). Efforts in the field ...
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