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Pei-Chien Tsai

National Chung Hsing University

H指数:20

被引数:1,347

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荣誉奖项

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Clinical and genetic characterization of hereditary spastic paraplegia type 4 in a Taiwanese cohort

台湾队列中遗传性痉挛性截瘫痷4型的临床和遗传特征

PARKINSONISM & RELATED DISORDERS

IF3.4

2026-07-010

PRE

SOD1 mutations in Taiwanese ALS patients: Clinical characteristics, frequency, and a p.T138R founder effect

AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION

IF2.8

2025-12-010

PRE

De novo pathogenic CSF1R variant implicates microglial dysfunction in pathogenesis of febrile infection-related epilepsy syndrome

新发致病性CSF1R变异提示小胶质细胞功能障碍在发热感染相关性癫痫综合征发病机制中的作用

IF6.6

2025-07-050

OA

Exploring Occupational Asthmagen-Related Asthma Phenotypes: A Cluster Analysis and Machine Learning Study

IF12

2024-12-160

PRE

The Oncolytic Avian Reovirus p17 Protein Inhibits Invadopodia Formation in Murine Melanoma Cancer Cells by Suppressing the FAK/Src Pathway and the Formation of theTKs5/NCK1 Complex

IF3.5

2024-07-171

OAAI

Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2024-06-040

OA

Development of Polycistronic Baculovirus Surface Display Vectors to Simultaneously Express Viral Proteins of Porcine Reproductive and Respiratory Syndrome and Analysis of Their Immunogenicity in Swine

IF3.4

2023-10-311

OAAI

Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2023-01-061

OA

Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy

IF11.7

2022-04-1248

OA

Genetic and Functional Analysis of Glycosyltransferase 8 Domain-Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis

NEUROLOGY-GENETICS

IF3.7

2021-12-013

OAAI

Analysis of NOTCH2NLC GGC repeat expansion in Taiwanese patients with amyotrophic lateral sclerosis

NEUROBIOLOGY OF AGING

IF3.5

2021-12-0111

PREAI

Clinical and genetic characterization of adult-onset leukoencephalopathy caused by CSF1R mutations

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2021-10-1515

OA

Rapid progressive ALS in a patient with a DNAJC7 loss-of-function mutation

NEUROLOGY-GENETICS

IF3.7

2020-10-0514

OAAI

Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2020-05-278

OAAI

Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxia

台湾小脑共济失调患者PUM1基因突变研究

PARKINSONISM & RELATED DISORDERS

IF3.4

2019-09-019

PREAI

Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan

NEUROBIOLOGY OF AGING

IF3.5

2018-12-0111

PREAI

Genetic loci determining total immunoglobulin E levels from birth through adulthood

IF12

2018-11-283

PREAI

Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis

NEUROBIOLOGY OF AGING

IF3.5

2018-02-0113

PREAI

Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy

SCIENTIFIC REPORTS

IF3.9

2017-11-1013

OAAI

A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy

复发性WARS突变是常染色体显性远端遗传性运动神经病的新原因

IF11.7

2017-03-2276

OAAI