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

Genetics of frontotemporal dementia in China.

Amyotrophic lateral sclerosis & frontotemporal degeneration - 1 Aug 2021

Jiang Yaling, Jiao Bin, Xiao Xuewen, Shen Lu

Abstract excerpt

Backgbround: Frontotemporal dementia (FTD) is the second most common presenile dementia, characterized by prominent behavioral, language, and cognitive impairment, which has a strong genetic component contributing to its pathogenesis. Due to geographical and ethnic variability, the prevalence of the causative genes of FTD may be different. Methods: To explore the genetics of FTD in the Chinese population, we...

Read the complete abstract on PubMed

Topics

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

Share to Amyotrophic Lateral Sclerosis
Share to Amyotrophic Lateral Sclerosis Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cholinesterase and Neurodegenerative Diseases

Share to Frontotemporal Dementia

Share to Frontotemporal Lobar Degeneration

Share to Mutation

Share to Neurological diseases and metabolism

Source

Identifiers

PMID: 33538206
DOI: 10.1080/21678421.2021.1880596

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetics of frontotemporal dementia in China.PMID 33538206Read ↗

Genetic Spectrum and Clinical Heterogeneity of Chinese Frontotemporal Dementia Patients: Data from PUMCH Dementia Cohort.Semantic proximity Read ↗

Genetic and clinical landscape of Chinese frontotemporal dementia: dominance of TBK1 and OPTN mutations.Semantic proximity Read ↗

The role of genetics in neurodegenerative dementia: a large cohort study in South ChinaSemantic proximity Read ↗

Recent advances in the molecular genetics of frontotemporal lobar degeneration.Semantic proximity Read ↗

Identification and functional characterization of novel variants of MAPT and GRN in Chinese patients with frontotemporal dementia.Semantic proximity Read ↗

Frontotemporal dementia-related gene mutations in clinical dementia patients from a Chinese population.Semantic proximity Read ↗

Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients.Semantic proximity Read ↗

Genetics of Frontotemporal Lobar Degeneration: From the Bench to the Clinic.Semantic proximity Read ↗

Frequency of frontotemporal dementia-related gene variants in Turkey.Semantic proximity Read ↗

Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia.Semantic proximity Read ↗

The Frequency of Genetic Mutations Associated With Behavioral Variant Frontotemporal Dementia in Chinese Han PatientsSemantic proximity Read ↗

Phenotype Heterogeneity and Genotype Correlation of MAPT Mutations in a Chinese PUMCH Cohort.Semantic proximity Read ↗

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