Karen Sophia Park (Stephen H Tsang)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 7

Top Topics

Intellectual Disability

Diabetic Retinopathy

Top Venues

Ophthalmic genetics

Cold Spring Harbor molecular case studies

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Joshua J Wang, Karen Sophia Park, Narayan Dhimal, Shichen Shen, Xixiang Tang, Jun Qu, Sarah X Zhang
Proteomic Analysis of Retinal Mitochondria-Associated ER Membranes Identified Novel Proteins of Retinal Degeneration in Long-Term Diabetes. Cells 11 (18) (2022)
Amy Reilein, Helen V Kogan, Rachel Misner, Karen Sophia Park, Daniel Kalderon
Adult stem cells and niche cells segregate gradually from common precursors that build the adult Drosophila ovary during pupal development. eLife 10 (2021)
Thiago Cabral, Jose Ronaldo Lima de Carvalho, Joonpyo Kim, Jin Kyun Oh, Sarah R Levi, Karen Sophia Park, Jimmy K Duong, Junhyung Park, Katherine Boudreault, Rubens Belfort, Stephen H Tsang
Comparative Analysis of Functional and Structural Decline in Retinitis Pigmentosas. International journal of molecular sciences 21 (8) (2020)
Ruben Jauregui, Karen Sophia Park, Stephen H Tsang
Two-year progression analysis of RPE65 autosomal dominant retinitis pigmentosa. Ophthalmic genetics 39 (4) (2019)
Galaxy Y Cho, Kyle Bolo, Karen Sophia Park, Jesse D Sengillo, Karen Sophia Park
Attenuation of Inherited and Acquired Retinal Degeneration Progression with Gene-based Techniques. Molecular diagnosis & therapy 23 (1) (2019)
Sara D Ragi, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, Karen Sophia Park, Vinit B Mahajan, Irene H Maumenee, Stephen H Tsang
Compound heterozygous novel frameshift variants in the PROM1 gene result in Leber congenital amaurosis. Cold Spring Harbor molecular case studies 5 (6) (2019)
Xuan Cui, Ruben Jauregui, Karen Sophia Park, Stephen H Tsang
Multimodal characterization of a novel mutation causing vitamin B6-responsive gyrate atrophy. Ophthalmic genetics 39 (4) (2018)