Yu Fan

chinese center for disease control and prevention

H指数:13

被引数:504

个人简介

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教育背景

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工作经历

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荣誉奖项

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Features and a specific pattern of cerebral perfusion in patients with Lewy body dementia: Diagnostic ability and clinical correlations

路易体痴呆患者脑灌注的特征及特定模式：诊断能力与临床相关性

Translational Psychiatry

IF6.2

2026-09-210

OAAI

Human pulmonary infection by Brucella suis vaccine strain S2 revealed by genome sequencing in China

Emerging Microbes & Infections

IF0

2026-07-290

Systematic proteomics reveals plasma NEFL as a robust predictor and pathological associate in C9ORF72-related neurodegeneration

系统性蛋白质组学揭示血浆NEFL作为C9ORF72相关神经退行性疾病的强预测因子和病理相关物

Frontiers in Aging Neuroscience

IF4.5

2026-04-210

OAAI

Re-evaluating Dystonia-Linked Gene Variants in a Large European Parkinson's Disease Cohort

MOVEMENT DISORDERS

IF7.6

2026-01-010

PRE

Population-level insights into repeat-associated ataxias from UK Biobank whole-genome sequencing

基于英国生物银行全基因组测序的重复相关共济失调的群体水平见解

Brain

IF11.7

2025-10-310

PRE

Further Investigation of Catechol-O-Methyltransferase Gene and Parkinson's Disease Susceptibility in the UK Biobank Cohort

进一步研究儿茶酚-O-甲基转移酶基因与英国生物银行队列中帕金森病的易感性

Movement Disorders

IF7.6

2025-10-270

PRE

Association of Non-Coding Repeat Expansions with Parkinson's Disease Risk: Evidence from a UK Biobank-Based Whole-Genome Sequencing Study

非编码重复扩展与帕金森病风险的相关性：来自基于英国生物银行全基因组测序研究的证据

Movement Disorders

IF7.6

2025-10-110

PRE

Reply to “Prevalence of NOTCH2NLC and FMR1 Repeat Expansions in Atypical Parkinsonism Compared to Asymptomatic Elderly Individuals”

回复：“与非典型帕金森病患者相比，NOTCH2NLC和FMR1重复扩展在无症状老年人中的患病率”

Movement Disorders

IF7.6

2025-09-240

PRE

Genetic analysis of the ATP11B gene in Chinese Han population with cerebral small vessel disease

BMC GENOMICS

IF3.7

2022-12-121

OAAI

Human blood metabolites and lacunar stroke: A Mendelian randomization study

INTERNATIONAL JOURNAL OF STROKE

IF8.7

2022-12-0516

PRE

CHCHD2 p.Thr61Ile knock-in mice exhibit motor defects and neuropathological features of Parkinson's disease

BRAIN PATHOLOGY

IF6.2

2022-11-0211

OAAI

Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22

FRONTIERS IN MOLECULAR NEUROSCIENCE

IF3.8

2022-06-236

OAAI

GIPC1 CGG Repeat Expansion Is Associated with Movement Disorders

ANNALS OF NEUROLOGY

IF7.7

2022-03-0820

PRE

NOTCH2NLC-related疾病: 不断扩大的频谱和基因型-表型相关性

JOURNAL OF MEDICAL GENETICS

IF3.7

2021-10-2119

PRE

Deciphering Neurodegenerative Diseases Using Long-Read Sequencing

NEUROLOGY

IF8.5

2021-08-3112

OAAI

Reply to NOTCH2NLC Intermediate-Length Repeat Expansions Are Associated with Parkinson Disease

ANNALS OF NEUROLOGY

IF7.7

2021-01-110

PRE

NOTCH2NLCIntermediate-Length Repeat Expansions Are Associated with Parkinson Disease

ANNALS OF NEUROLOGY

IF7.7

2020-10-1957

PREAI

α-Synuclein in Parkinson's Disease: Does a Prion-Like Mechanism of Propagation from Periphery to the Brain Play a Role?

NEUROSCIENTIST

IF3.9

2020-07-307

PREAI

ARSA gene variants and Parkinson's disease

BRAIN

IF11.7

2020-05-216

OAAI

No biallelic intronic AAGGG repeat expansion in RFC1 was found in patients with late-onset ataxia and MSA

PARKINSONISM & RELATED DISORDERS

IF3.4

2020-04-0134

PREAI

Yu Fan

个人简介

教育背景

工作经历

荣誉奖项

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