Li Ou
ScholarGPS® ID: 15929607120342
Affiliation History
Field
Medicine
Discipline
Pediatrics
Top Specialties
Metabolism | Molecular Genetics | Enzyme | Rare Disease | Enzyme Replacement Therapy | Blood–brain Barrier
Metrics Summary
Publication Count
60
Predicted Citations
783
Predicted h-index
16
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
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Molecular Genetics and Metabolism, volume 141, issue 2, pages 108005- (2024). |
DP-DNA: A Digital Pattern-Aware DNA Encoding Scheme to Improve Encoding Density of DNA Storage (conference) 2023 31st International Symposium on Modeling, Analysis, and Simulation of Computer and Telecommunication Systems (MASCOTS) (2023) Stony Brook, NY, USA |
Scientific Reports, volume 13, issue 1 (2023). |
AAV Engineering for Improving Tropism to the Central Nervous System (journal article) Biology, volume 12, issue 2, pages 186- (2023). |
Identification of a novel fusion Iduronidase with improved activity in the cardiovascular system (journal article) Molecular Genetics and Metabolism Reports, volume 33 (2022). |
rAAV immunogenicity, toxicity, and durability in 255 clinical trials: A meta-analysis (journal article) Frontiers in Immunology, volume 13 (2022). |
HL-DNA: A Hybrid Lossy/Lossless Encoding Scheme to Enhance DNA Storage Density and Robustness for Images (conference) 2022 IEEE 40th International Conference on Computer Design (ICCD) (2022) Olympic Valley, CA, USA |
A versatile toolkit for overcoming AAV immunity (journal article) Frontiers in Immunology, volume 13 (2022). |
Bioinformatics analyses of the brain connectome in MPS I vs control mice: Neural network biomarkers for disease diagnosis (journal article) Molecular Genetics and Metabolism, volume 135, issue 2, pages S77- (2022). |
A questionnaire-based study to comprehensively assess the status quo of rare disease patients and care-givers in China (journal article) Orphanet Journal of Rare Diseases, volume 16, issue 1 (2021). |
Rare disease awareness and perspectives of physicians in China: a questionnaire-based study (journal article) Orphanet Journal of Rare Diseases, volume 16, issue 1 (2021). |
Examination of a blood-brain barrier targeting β-galactosidase-monoclonal antibody fusion protein in a murine model of GM1-gangliosidosis (journal article) Molecular Genetics and Metabolism Reports, volume 27 (2021). |
A comprehensive analysis of rare diseases in China through questionnaire and interviews (journal article) Molecular Genetics and Metabolism, volume 132, issue 2, pages S115- (2021). |
Genotype-phenotype correlation of MPS II: A meta-analysis (journal article) Molecular Genetics and Metabolism, volume 132, issue 2, pages S105- (2021). |
Examination of a blood-brain barrier targeting β-galactosidase-monoclonal antibody fusion protein in a murine model of GM1-gangliosidosis (journal article) Molecular Genetics and Metabolism, volume 132, issue 2, pages S88- (2021). |
PS gene editing with a novel HEXO construct to treat both Tay-Sachs and Sandhoff diseases (journal article) Molecular Genetics and Metabolism, volume 132, issue 2, pages S80-S81 (2021). |
Immunogenicity, genotoxicity, and efficacy of PS gene editing in treating MPS I mice (journal article) Molecular Genetics and Metabolism, volume 132, issue 2, pages S81- (2021). |
Molecular Genetics and Metabolism, volume 132, issue 2, pages S19-S20 (2021). |
The urgent need to empower rare disease organizations in China: an interview-based study (journal article) Orphanet Journal of Rare Diseases, volume 15, issue 1 (2020). |
A Highly Efficacious PS Gene Editing System Corrects Metabolic and Neurological Complications of Mucopolysaccharidosis Type I (journal article) Molecular Therapy, volume 28, issue 6, pages 1442-1454 (2020). |