| 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 |
0.576 |
|
| 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 |
0.548 |
|
| 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 |
0.574 |
|
| 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 |
0.553 |
|
| 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 |
0.592 |
|
| 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 |
0.579 |
|
| 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 |
0.65 |
|
| 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 |
0.639 |
|
| 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 |
0.67 |
|
| 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 |
0.603 |
|
| 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 |
0.445 |
|
| 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 |
0.439 |
|
| 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 |
0.48 |
|
| 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 |
0.496 |
|
| 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 |
0.493 |
|
| 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 |
0.503 |
|
| 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 |
0.448 |
|
| Show low-probability matches. |