Author

Shusheng Liao

Observed names: Shu-Sheng LIAO, Shu-Sheng Liao, Shu-sheng Liao, Shu‐Sheng Liao

Observed institutions: Central South University, Zunyi Medical University, First Affiliated Hospital of Wenzhou Medical University, Liuzhou General Hospital, First Affiliated Hospital of Fujian Medical University, Xiangya Hospital Central South University, Affiliated Hospital of Zunyi Medical College

ORCID: 0000-0001-8685-600X

Observed ORCID: 0000-0001-8685-600X

OpenAlex ID: A5011413852

SUMO-1 Modification on K166 of PolyQ-Expanded aTaxin-3 Strengthens Its Stability and Increases Its Cytotoxicity

2013 · Ya-Fang Zhou, Shu-Sheng Liao, et al. · PLoS ONE · 38

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Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum

2008 · Shu-sheng Liao, Lu Shen, et al. · Journal of the Neurological Sciences · 28

A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease

2009 · Jifeng Guo, Jiaohua Wei, et al. · Neuroscience Letters · 26

Utility of Point-of-Care Lung Ultrasound for Clinical Classification of COVID-19

2020 · Shu-Ting Zhu, Fang-Yi Tao, et al. · Ultrasound in Medicine & Biology · 14

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Clinicopathological and imaging features of struma ovarii: a retrospective study

2025 · Mei Chen, Shusheng Liao, et al. · Frontiers in Oncology · 11

VPS35, the core component of the retromer complex, and Parkinson's disease

2021 · Ai‐Di Luo, Zu‐Cai Xu, et al. · Ibrain · 11

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Assessment of Right Ventricular-Arterial Coupling by Echocardiography in Patients with Right Ventricular Pressure and Volume Overload

2023 · Hui Li, Teng Ye, et al. · Reviews in Cardiovascular Medicine · 10

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Ultrasonographic and clinicopathological features of pelvic yolk sac tumors in women: a single-center retrospective analysis

2024 · Mei Chen, Shengmin Zhang, et al. · Frontiers in Oncology · 7

Progress of non‐motor symptoms in early‐onset Parkinson's disease

2024 · Fanshi Zhang, Aidi Luo, et al. · Ibrain · 6

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Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.

2009 · Juan Du, Lu Shen, et al. · PubMed · 6

Multimodality imaging for the diagnosis of left ventricular apical hypoplasia: A case presentation and review of the literatures

2024 · Shusheng Liao, Peifeng Jin, et al. · Echocardiography · 4

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Opsoclonus-myoclonus syndrome associated with herpes simplex virus infection: a case report

2020 · Ya Chen, Doujia Chen, et al. · International Journal of Neuroscience · 4

The genetic spectrum of LRRK2 variants in Parkinson’s disease: findings from a large Chinese cohort

2026 · Juan Wan, Hongxu Pan, et al. · npj Parkinson s Disease · 3

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Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han

2008 · Jun-Ling Wang, Hong Jiang, et al. · Journal of Genetics · 3

[Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].

2006 · Xing-wang Song, Bei-sha Tang, et al. · PubMed · 3

Abnormal subthalamic nucleus functional connectivity and machine learning classification in Parkinson’s disease: a multisite functional magnetic resonance imaging study

2025 · Bin Qin, Yisi Tang, et al. · Frontiers in Aging Neuroscience · 2

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Benign Brenner tumor of the ovary: two-dimensional and contrast-enhanced ultrasound features—a retrospective study from a single center

2024 · Mei Chen, Shusheng Liao, et al. · Frontiers in Oncology · 2

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Mitral Valve Repair for Isolated Libman-Sacks Endocarditis in a Patient with Primary Antiphospholipid Syndrome

2021 · Teng Ye, Jue Wang, et al. · International Heart Journal · 2

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Case report: Granulomatosis with polyangiitis patient presented with a mass in the aortic root

2024 · Yinyan Teng, Mei Chen, et al. · Frontiers in Immunology · 1

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Successful surgical management of a single coronary artery with giant coronary artery aneurysm with fistula to the right ventricle

2023 · Mei Chen, Jue Wang, et al. · Echocardiography · 1

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Genetic study of a Chinese pedigree with early onset Parkinson’s disease caused by novel compound heterozygous mutations in PARKIN gene

2021 · Li Zhang, Ai‐Di Luo, et al. · Ibrain · 1

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[Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families].

2006 · Xing-Wang Song, Bei-sha Tang, et al. · PubMed · 1

Noninvasive assessment of hemodynamic profile and myocardial mechanics in pulsus alternans patients by multiple echocardiographic methods

2025 · Rongrong Miao, Tingting Wu, et al. · The Ultrasound Journal

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Unveiling the Reason for Syncope Associated With Cardiac Nodules

2025 · Fangdi Zha, Jianfan Wen, et al. · Pacing and Clinical Electrophysiology

Cross-talk between traditional Chinese medicine and Parkinson's disease based on cell autophagy

2023 · Mufei Wang, Hongsong Yu, et al. · Pharmacological Research - Modern Chinese Medicine

Works count: 31

Citation count: 184

H-index: 7

I10-index: 7