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Fuze Zheng

Peking University First Hospital

H指数:8

被引数:177

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A Conserved MicroRNAs Motif Reveals TDP-43 Pathology and MAPK Pathway Activation in Parkinson's Disease

保守的MicroRNAs基序揭示了帕金森病中的TDP-43病理和MAPK通路激活

The FASEB Journal

IF0

2025-10-280

PRE

Association of Diaphragm Involvement Assessed by Ultrasound With Disease Severity in Facioscapulohumeral Muscular Dystrophy

膈肌受累（经超声评估）与面肩肱型肌营养不良症疾病严重程度的关系

cachexia sarcopenia and muscle

IF0

2025-09-120

OAAI

Age at onset mediates genetic impact on disease severity in facioscapulohumeral muscular dystrophy

IF11.7

2024-12-230

PRE

Disease Progression of GNE Myopathy and Its Relationship With Genotype A Retrospective, Observational Study in Chinese Patients

NEUROLOGY-GENETICS

IF3.7

2024-12-010

OAAI

Comprehensive Proteomic Analysis of Dysferlinopathy Unveiling Molecular Mechanisms and Biomarkers Linked to Pathological Progression

CNS NEUROSCIENCE & THERAPEUTICS

IF5

2024-09-300

OAAI

Detection of pTDP-43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis

BRAIN PATHOLOGY

IF6.2

2024-04-111

OAAI

CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy

JOURNAL OF GENETICS AND GENOMICS

IF7.1

2024-02-012

PRE

Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2023-11-165

OAAI

Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

IF8.5

2023-07-189

OAAI

An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1

IF11.7

2023-06-233

PRE

The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2023-01-234

OA

GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy

ANNALS OF NEUROLOGY

IF7.7

2022-07-0228

PRE

Expanding the phenotype and genotype spectra of PLIN4-associated myopathy with rimmed ubiquitin-positive autophagic vacuolation

ACTA NEUROPATHOLOGICA

IF9.3

2022-05-028

PRE

Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population

IF11.7

2022-03-185

OA