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Boxun Zhao 赵博洵
Boxun Zhao 赵博洵
Boston Children's Hospital & Harvard Medical School
在 childrens.harvard.edu 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations
Y Dou, X Yang, Z Li, S Wang, Z Zhang, AY Ye, L Yan, C Yang, Q Wu, J Li, ...
Human mutation 38 (8), 1002-1013, 2017
862017
Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals
B Zhao, Q Wu, AY Ye, J Guo, X Zheng, X Yang, L Yan, QR Liu, TM Hyde, ...
PLoS genetics 15 (4), e1008043, 2019
682019
Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals
AY Huang, X Xu, AY Ye, Q Wu, L Yan, B Zhao, X Yang, Y He, S Wang, ...
Cell research 24 (11), 1311-1327, 2014
672014
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior
HK Harris, T Nakayama, J Lai, B Zhao, N Argyrou, CS Gubbels, A Soucy, ...
Genetics in Medicine 23 (6), 1028-1040, 2021
422021
A framework for individualized splice-switching oligonucleotide therapy
J Kim, S Woo, CM de Gusmao, B Zhao, DH Chin, RL DiDonato, ...
Nature 619 (7971), 828-836, 2023
372023
APP gene copy number changes reflect exogenous contamination
J Kim, B Zhao, AY Huang, MB Miller, MA Lodato, CA Walsh, EA Lee
Nature 584 (7821), E20-E28, 2020
182020
Identification and Genotyping of Transposable Element Insertions From Genome Sequencing Data
C Chu, B Zhao, PJ Park, EA Lee
Current Protocols in Human Genetics 107 (1), e102, 2020
142020
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene
B Zhao, JA Madden, J Lin, GT Berry, MH Wojcik, X Zhao, H Brand, ...
European Journal of Human Genetics 30 (9), 1083-1087, 2022
102022
Contribution and therapeutic implications of retroelement insertions in ataxia telangiectasia
B Zhao, MA Nguyen, S Woo, J Kim, WY Timothy, EA Lee
The American Journal of Human Genetics 110 (11), 1976-1982, 2023
52023
Genomic approaches to trace the history of human brain evolution with an emerging opportunity for transposon profiling of ancient humans
Y Wang, B Zhao, J Choi, EA Lee
Mobile DNA 12, 1-19, 2021
52021
Somatic cancer driver mutations are enriched and associated with inflammatory states in Alzheimer’s disease microglia
AY Huang, Z Zhou, M Talukdar, MB Miller, B Chhouk, L Enyenihi, I Rosen, ...
bioRxiv, 2024
32024
Evidence that APP gene copy number changes reflect recombinant vector contamination
J Kim, B Zhao, AY Huang, MB Miller, MA Lodato, CA Walsh, EA Lee
bioRxiv, 706788, 2019
22019
Human cytomegalovirus harnesses host L1 retrotransposon for efficient replication
SY Hwang, H Kim, D Denisko, B Zhao, D Lee, J Jeong, J Kim, K Park, ...
Nature Communications 15 (1), 7640, 2024
2024
51886 Therapeutic opportunities for ASO-based gene restoration in haploinsufficient genodermatoses
J Lai, L Bassini, B Zhao, D Demirbas, T Yu
Journal of the American Academy of Dermatology 91 (3), AB338, 2024
2024
Creation of a custom antisense oligonucleotide (ASO) for a single patient with retinal dystrophy caused by an intronic pseudogene.
EA McCourt, B Zhao, MT Mathias, A Larson, T Yu
Investigative Ophthalmology & Visual Science 65 (7), 5311-5311, 2024
2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders
AS Lee, LJ Ayers, M Kosicki, WM Chan, LN Fozo, BM Pratt, TE Collins, ...
medRxiv, 2023
2023
Method for low frequency somatic cell mutation identification and quantification
L WEI, B ZHAO, Y HUANG, Q WU, Y YE, X ZHENG
US Patent App. 16/616,865, 2023
2023
OP024: Discovery and therapeutic implications of pathogenic retroelements in neurodegenerative diseases
B Zhao, A Larson, C Hu, D Chiabrando, D Chin, E McCourt, F Bertino, ...
Genetics in Medicine 24 (3), S353-S354, 2022
2022
Disruption of RFX family transcription factors causes autism, attention deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior
TW Harris, Holly K., Tojo Nakayama, Jenny Lai, Boxun Zhao, Nikoleta Argyrou ...
medRxiv 2020 (https://doi.org/10.1101/2020.09.09.20187), pp.2020-09., 2020
2020
Somatic LINE-1 retrotransposition in cortical neurons of Rett patients and healthy individuals
B Zhao, Q Wu, AY Ye, J Guo, X Zheng, X Yang, L Yan, QR Liu, TM Hyde, ...
bioRxiv 2018 (https://doi.org/10.1101/506758), p.506758., 2018
2018
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