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Personal profile

Education/Academic qualification

University of Minnesota

Sep 1 2011Jun 12 2015

Fingerprint The Fingerprint is created by mining the titles and abstracts of the person's research outputs and projects/funding awards to create an index of weighted terms from discipline-specific thesauri.

  • 17 Similar Profiles
Mucopolysaccharidosis I Medicine & Life Sciences
Iduronidase Medicine & Life Sciences
Glycosaminoglycans Chemical Compounds
Brain Chemical Compounds
Neurology Chemical Compounds
Enzyme Replacement Therapy Medicine & Life Sciences
Sandhoff Disease Medicine & Life Sciences
Iduronate Sulfatase Medicine & Life Sciences

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Research Output 2010 2018

6 Citations

Dose-Dependent Prevention of Metabolic and Neurologic Disease in Murine MPS II by ZFN-Mediated In Vivo Genome Editing

Laoharawee, K., DeKelver, R. C., Podetz-Pedersen, K. M., Rohde, M., Sproul, S., Nguyen, H. O., Nguyen, T., St. Martin, S. J., Ou, L., Tom, S., Radeke, R., Meyer, K. E., Holmes, M. C., Whitley, C. B., Wechsler, T. & Mc Ivor, R. S., Apr 4 2018, In : Molecular Therapy. 26, 4, p. 1127-1136 10 p.

Research output: Contribution to journalArticle

Mucopolysaccharidosis II
Zinc Fingers
Metabolic Diseases
Nervous System Diseases
Iduronate Sulfatase

Metabolomics profiling reveals profound metabolic impairments in mice and patients with Sandhoff disease

Ou, L., Przybilla, M. J. & Whitley, C. B., Jan 1 2018, (Accepted/In press) In : Molecular Genetics and Metabolism.

Research output: Contribution to journalArticle

Sandhoff Disease
Metabolomics
Metabolites
Biomarkers
G(M2) Ganglioside
Iduronidase
Mucopolysaccharidosis I
Neurology
Glycosaminoglycans
Lectins

SAAMP 2.0: An algorithm to predict genotype-phenotype correlation of lysosomal storage diseases

Ou, L., Przybilla, M. J. & Whitley, C. B., May 1 2018, In : Clinical Genetics. 93, 5, p. 1008-1014 7 p.

Research output: Contribution to journalArticle

Lysosomal Storage Diseases
Genetic Association Studies
Computational Biology
Iduronate Sulfatase
Mucopolysaccharidosis IV
3 Citations

Phenotype prediction for mucopolysaccharidosis type i by in silico analysis

Ou, L., Przybilla, M. J. & Whitley, C. B., Jul 4 2017, In : Orphanet journal of rare diseases. 12, 1, 125.

Research output: Contribution to journalArticle

Mucopolysaccharidoses
Mucopolysaccharidosis I
Computer Simulation
Single Nucleotide Polymorphism
Phenotype

Activities 2015 2015

  • 1 Types of Award - Prize (including medals and awards)

Doctoral Dissertation Fellowship

Li Ou (Recipient)
Sep 2015Aug 2016

Activity: Other activity typesTypes of Award - Prize (including medals and awards)

Prizes

American Society of Gene and Cell Therapy Travel Award

Li Ou (Recipient), May 2016

Prize: Prize (including medals and awards)

Baosteel Fellowship for Excellent Students

Li Ou (Recipient), 2009

Prize: Prize (including medals and awards)

Students

NIH Lysosomal Disease Network Fellow

Li Ou (Recipient), 2015

Prize: Prize (including medals and awards)

Pediatric Research, Education and Scholarship Symposium Presentation Award

Li Ou (Recipient), Apr 2013

Prize: Prize (including medals and awards)

Sichuan University Freshman Fellowship

Li Ou (Recipient), Sep 2007

Prize: Prize (including medals and awards)