Yongjin Yoo - Publications

2013-2018 Biomedical Science Seoual National University 
 2018- Institute for Stem Cell Biology and Regenerative Medicine Stanford University, Palo Alto, CA 
Neural stem cells, Microglia, Reprogramming

19 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Mader MM, Napole A, Wu D, Atkins M, Scavetti A, Shibuya Y, Foltz A, Hahn O, Yoo Y, Danziger R, Tan C, Wyss-Coray T, Steinman L, Wernig M. Myeloid cell replacement is neuroprotective in chronic experimental autoimmune encephalomyelitis. Nature Neuroscience. PMID 38514857 DOI: 10.1038/s41593-024-01609-3  0.54
2023 Susanto TT, Hung V, Levine AG, Kerr CH, Yoo Y, Chen Y, Oses-Prieto JA, Fromm L, Fujii K, Wernig M, Burlingame AL, Ruggero D, Barna M. RAPIDASH: A tag-free enrichment of ribosome-associated proteins reveals compositional dynamics in embryonic tissues and stimulated macrophages. Biorxiv : the Preprint Server For Biology. PMID 38106052 DOI: 10.1101/2023.12.07.570613  0.51
2023 Guo MG, Reynolds DL, Ang CE, Liu Y, Zhao Y, Donohue LKH, Siprashvili Z, Yang X, Yoo Y, Mondal S, Hong A, Kain J, Meservey L, Fabo T, Elfaki I, et al. Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases. Nature Genetics. PMID 37857935 DOI: 10.1038/s41588-023-01533-5  0.534
2023 Yoo Y, Neumayer G, Shibuya Y, Mader MM, Wernig M. A cell therapy approach to restore microglial Trem2 function in a mouse model of Alzheimer's disease. Cell Stem Cell. 30: 1392. PMID 37802040 DOI: 10.1016/j.stem.2023.08.011  0.514
2023 Yoo Y, Neumayer G, Shibuya Y, Marc-Daniel Mader M, Wernig M. A cell therapy approach to restore microglial Trem2 function in a mouse model of Alzheimer's disease. Cell Stem Cell. 30: 1043-1053.e6. PMID 37541210 DOI: 10.1016/j.stem.2023.07.006  0.557
2023 Mader MM, Napole A, Wu D, Shibuya Y, Scavetti A, Foltz A, Atkins M, Hahn O, Yoo Y, Danziger R, Tan C, Wyss-Coray T, Steinman L, Wernig M. Augmentation of a neuroprotective myeloid state by hematopoietic cell transplantation. Biorxiv : the Preprint Server For Biology. PMID 36945385 DOI: 10.1101/2023.03.10.532123  0.543
2022 Shibuya Y, Kumar KK, Mader MM, Yoo Y, Ayala LA, Zhou M, Mohr MA, Neumayer G, Kumar I, Yamamoto R, Marcoux P, Liou B, Bennett FC, Nakauchi H, Sun Y, et al. Treatment of a genetic brain disease by CNS-wide microglia replacement. Science Translational Medicine. 14: eabl9945. PMID 35294256 DOI: 10.1126/scitranslmed.abl9945  0.628
2021 Yoo Y, Park SY, Jo EB, Choi M, Lee KW, Hong D, Lee S, Lee CR, Lee Y, Um JY, Park JB, Seo SW, Choi YL, Kim S, Lee SG, et al. Overexpression of Replication-Dependent Histone Signifies a Subset of Dedifferentiated Liposarcoma with Increased Aggressiveness. Cancers. 13. PMID 34206586 DOI: 10.3390/cancers13133122  0.619
2020 Lee Y, Park S, Lee JS, Kim SY, Cho J, Yoo Y, Lee S, Yoo T, Lee M, Seo J, Lee J, Kneissl J, Lee J, Jeon H, Jeon EY, et al. Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population. Scientific Reports. 10: 1413. PMID 31996704 DOI: 10.1038/S41598-020-58101-8  0.654
2019 Salpietro V, Dixon CL, Guo H, Bello OD, Vandrovcova J, Efthymiou S, Maroofian R, Heimer G, Burglen L, Valence S, Torti E, Hacke M, Rankin J, Tariq H, Colin E, ... ... Yoo Y, et al. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. Nature Communications. 10: 3094. PMID 31300657 DOI: 10.1038/S41467-019-10910-W  0.468
2019 Shashi V, Geist J, Lee Y, Yoo Y, Shin U, Schoch K, Sullivan J, Stong N, Smith E, Jasien J, Kranz P, Lee Y, Shin YB, Wright NT, et al. Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis. Human Mutation. PMID 31264822 DOI: 10.1002/Humu.23760  0.447
2018 Chowdhury T, Yoo Y, Seo Y, Dho YS, Kim S, Choi A, Choi M, Park SH, Park CK, Lee SH, Lee JY. Genomic analysis of synchronous intracranial meningiomas with different histological grades. Journal of Neuro-Oncology. PMID 29423538 DOI: 10.1007/S11060-018-2772-1  0.442
2018 Yoo Y, Cho J, Choi M. Reply to "A novel mutation in the TM6 domain of GABBR2 leads to a Rett-like phenotype". Annals of Neurology. PMID 29377213 DOI: 10.1002/Ana.25154  0.434
2018 Johannesen KM, Gardella E, Linnankivi T, Courage C, de Saint Martin A, Lehesjoki AE, Mignot C, Afenjar A, Lesca G, Abi-Warde MT, Chelly J, Piton A, Merritt JL, Rodan LH, Tan WH, ... ... Yoo Y, et al. Defining the phenotypic spectrum of SLC6A1 mutations. Epilepsia. PMID 29315614 DOI: 10.1111/Epi.13986  0.481
2017 Yoo Y, Jung J, Lee YN, Lee Y, Cho H, Na E, Hong J, Kim E, Lee JS, Lee JS, Hong C, Park SY, Wie J, Miller K, Shur N, et al. GABBR2 mutations determine phenotype in Rett syndrome and epileptic encephalopathy. Annals of Neurology. PMID 28856709 DOI: 10.1002/Ana.25032  0.457
2016 Ko JM, Cho JS, Yoo Y, Seo J, Choi M, Chae JH, Lee HR, Cho TJ. Wiedemann-Steiner Syndrome With 2 Novel KMT2A Mutations: Variable Severity in Psychomotor Development and Musculoskeletal Manifestation. Journal of Child Neurology. PMID 27777327 DOI: 10.1177/0883073816674095  0.497
2016 Lee JS, Yoo Y, Lim BC, Kim KJ, Song J, Choi M, Chae JH. GM3 synthase deficiency due to ST3GAL5 variants in two Korean female siblings: Masquerading as Rett syndrome-like phenotype. American Journal of Medical Genetics. Part A. PMID 27232954 DOI: 10.1002/Ajmg.A.37773  0.495
2015 Seo J, Choi IH, Lee JS, Yoo Y, Kim NK, Choi M, Ko JM, Shin YB. Rare cases of congenital arthrogryposis multiplex caused by novel recurrent CHRNG mutations. Journal of Human Genetics. 60: 213-5. PMID 25608830 DOI: 10.1038/Jhg.2015.2  0.506
2015 Shirane S, Araki M, Morishita S, Edahiro Y, Takei H, Yoo Y, Choi M, Sunami Y, Hironaka Y, Noguchi M, Koike M, Noda N, Ohsaka A, Komatsu N. JAK2, CALR, and MPL mutation spectrum in Japanese patients with myeloproliferative neoplasms. Haematologica. 100: e46-8. PMID 25398833 DOI: 10.3324/Haematol.2014.115113  0.449
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