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Olivier Piguet

brain and mind centre
H指数:77
被引数:2.4万

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Identity-by-descent to resolve reduced penetrance and advance gene discovery in neurodegenerative disease

基于亲缘关系的分析以解决神经退行性疾病中的遗传力降低问题并推动基因发现

Brain
IF11.7
2026-09-250
OAAI
Behavioural and psychological symptom determinants of carer burden across clinical syndromes associated with frontotemporal lobar degeneration and Alzheimer’s disease: a transdiagnostic analysis

额颞叶萎缩和阿尔茨海默病相关临床综合征中行为和心理症状对护理负担的影响因素:一项跨诊断分析

2026-09-120
OA
The International Alliance on Brain Health (IABH): Bridging global efforts toward integrated brain and mental health plans and the promotion of local implementations

国际脑健康联盟(IABH):连接全球努力,推动整合脑健康与心理健康规划及促进地方实施

2026-07-011
PRE
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron disease

LAMA2中的超罕见变异是额颞叶痴呆和运动神经元病的风险因素

2026-05-210
OA
The exposome of brain aging across 34 countries

34个国家的大脑老化暴露组

2026-04-030
PRE
Clinical recognition of frontotemporal dementia with right temporal predominance: a consensus statement from the International Working Group

右颞叶为主的前额叶痴呆的临床识别:国际工作组共识声明

2025-12-120
OAAI
International consensus for the assessment of social cognition in neurocognitive disorders: framework definition and clinical recommendations of the SIGNATURE initiative

神经认知障碍社会认知评估的国际共识:SIGNATURE倡议的框架定义与临床建议

2025-12-060
OAAI
Reference-Group Adjusted Behavioural Dysfunction Questionnaire Score Discriminates Highly Behavioural-Variant Frontotemporal Dementia From Major Depressive Disorder and Alzheimer's Disease Dementia

参考群体调整的行为功能障碍问卷评分可区分高度行为变异性额颞叶痴呆与重度抑郁障碍及阿尔茨海默病痴呆

2025-11-100
OAAI
Comparison of neuron-derived extracellular vesicles miRNA profile between patients with behavioural variant frontotemporal dementia and primary psychiatric disorders

行为变异型额颞叶痴呆患者与原发性精神障碍患者神经元源性外泌体miRNA表达谱的比较

2025-10-020
OAAI
Susceptibility to visual hallucinations in the amyotrophic lateral sclerosis-frontotemporal dementia spectrum: The role of dysfunctional attentional networks

肌萎缩侧索硬化-额颞叶痴呆谱系中视觉幻觉的易感性:功能失调注意网络的调控作用

Cortex
IF3.3
2025-09-270
PRE
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing

通过全基因组测序破译ftld-tdp病理亚型的不同遗传危险因素

2025-04-250
OA