Yongjin Yoo
Affiliations: | 2013-2018 | Biomedical Science | Seoual National University |
| 2018- | Institute for Stem Cell Biology and Regenerative Medicine | Stanford University, Palo Alto, CA |
Area:
Neural stem cells, Microglia, ReprogrammingGoogle:
"https://scholar.google.com/citations?user=QSvHyfoAAAAJ&hl=en"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Murim Choi | grad student | 2013-2018 | Seoul National Univerity |
| Marius Wernig | post-doc | 2018-2022 | Stanford (Cell Biology Tree) |
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Publications
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| Susanto TT, Hung V, Levine AG, et al. (2023) RAPIDASH: A tag-free enrichment of ribosome-associated proteins reveals compositional dynamics in embryonic tissues and stimulated macrophages. Biorxiv : the Preprint Server For Biology |
| Guo MG, Reynolds DL, Ang CE, et al. (2023) Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases. Nature Genetics |
| Yoo Y, Neumayer G, Shibuya Y, et al. (2023) A cell therapy approach to restore microglial Trem2 function in a mouse model of Alzheimer's disease. Cell Stem Cell. 30: 1392 |
| Yoo Y, Neumayer G, Shibuya Y, et al. (2023) A cell therapy approach to restore microglial Trem2 function in a mouse model of Alzheimer's disease. Cell Stem Cell. 30: 1043-1053.e6 |
| Mader MM, Napole A, Wu D, et al. (2023) Augmentation of a neuroprotective myeloid state by hematopoietic cell transplantation. Biorxiv : the Preprint Server For Biology |
| Shibuya Y, Kumar KK, Mader MM, et al. (2022) Treatment of a genetic brain disease by CNS-wide microglia replacement. Science Translational Medicine. 14: eabl9945 |
| Yoo Y, Park SY, Jo EB, et al. (2021) Overexpression of Replication-Dependent Histone Signifies a Subset of Dedifferentiated Liposarcoma with Increased Aggressiveness. Cancers. 13 |
| Lee Y, Park S, Lee JS, et al. (2020) Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population. Scientific Reports. 10: 1413 |
| Salpietro V, Dixon CL, Guo H, et al. (2019) AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. Nature Communications. 10: 3094 |
| Shashi V, Geist J, Lee Y, et al. (2019) Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis. Human Mutation |