Byungjin Hwang, PhD

Title(s)Postdoctoral Scholar, Medicine
SchoolSchool of Medicine
Address513 Parnassus Avenue, HSE, #901B
San Francisco CA 94143
Phone--
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Mitigation of chromosome loss in clinical CRISPR-Cas9-engineered T cells. bioRxiv. 2023 Mar 22. Tsuchida CA, Brandes N, Bueno R, Trinidad M, Mazumder T, Yu B, Hwang B, Chang C, Liu J, Sun Y, Hopkins CR, Parker KR, Qi Y, Satpathy AT, Stadtmauer EA, Cate JHD, Eyquem J, Fraietta JA, June CH, Chang HY, Ye CJ, Doudna JA. PMID: 36993359; PMCID: PMC10055432.
      View in: PubMed   Mentions:
    2. Pooled screening of CAR T cells identifies diverse immune signaling domains for next-generation immunotherapies. Sci Transl Med. 2022 11 09; 14(670):eabm1463. Goodman DB, Azimi CS, Kearns K, Talbot A, Garakani K, Garcia J, Patel N, Hwang B, Lee D, Park E, Vykunta VS, Shy BR, Ye CJ, Eyquem J, Marson A, Bluestone JA, Roybal KT. PMID: 36350984; PMCID: PMC9939256.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    3. SCITO-seq: single-cell combinatorial indexed cytometry sequencing. Nat Methods. 2021 08; 18(8):903-911. Hwang B, Lee DS, Tamaki W, Sun Y, Ogorodnikov A, Hartoularos GC, Winters A, Yeung BZ, Nazor KL, Song YS, Chow ED, Spitzer MH, Ye CJ. PMID: 34354295; PMCID: PMC8643207.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    4. Author Correction: Single-cell RNA sequencing technologies and bioinformatics pipelines. Exp Mol Med. 2021 May; 53(5):1005. Hwang B, Lee JH, Bang D. PMID: 34045654; PMCID: PMC8178331.
      View in: PubMed   Mentions: 5     Fields:    
    5. Lineage tracing using a Cas9-deaminase barcoding system targeting endogenous L1 elements. Nat Commun. 2019 03 15; 10(1):1234. Hwang B, Lee W, Yum SY, Jeon Y, Cho N, Jang G, Bang D. PMID: 30874552; PMCID: PMC6420643.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    6. Facilitated Large-Scale Sequence Validation Platform Using Tn5-Tagmented Cell Lysates. ACS Synth Biol. 2019 03 15; 8(3):596-600. Hwang B, Heo S, Cho N, Seo H, Bang D. PMID: 30726053.
      View in: PubMed   Mentions: 1     Fields:    Translation:Cells
    7. CRISPR-Cap: multiplexed double-stranded DNA enrichment based on the CRISPR system. Nucleic Acids Res. 2019 01 10; 47(1):e1. Lee J, Lim H, Jang H, Hwang B, Lee JH, Cho J, Lee JH, Bang D. PMID: 30215766; PMCID: PMC6326800.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    8. Single-cell RNA sequencing technologies and bioinformatics pipelines. Exp Mol Med. 2018 08 07; 50(8):1-14. Hwang B, Lee JH, Bang D. PMID: 30089861; PMCID: PMC6082860.
      View in: PubMed   Mentions: 444     Fields:    Translation:HumansAnimals
    9. High-throughput construction of multiple cas9 gene variants via assembly of high-depth tiled and sequence-verified oligonucleotides. Nucleic Acids Res. 2018 05 18; 46(9):e55. Cho N, Seo HN, Ryu T, Kwon E, Huh S, Noh J, Yeom H, Hwang B, Ha H, Lee JH, Kwon S, Bang D. PMID: 29529247; PMCID: PMC5961255.
      View in: PubMed   Mentions: 1     Fields:    
    10. The high frequency of the U2AF1 S34Y mutation and its association with isolated trisomy 8 in myelodysplastic syndrome in Asians, but not in Caucasians. Leuk Res. 2017 10; 61:96-103. Kim SY, Kim K, Hwang B, Im K, Park SN, Kim JA, Hwang SM, Bang D, Lee DS. PMID: 28938223.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    11. Asymmetrical barcode adapter-assisted recovery of duplicate reads and error correction strategy to detect rare mutations in circulating tumor DNA. Sci Rep. 2017 05 02; 7:46678. Ahn J, Hwang B, Young Kim H, Jang H, Kim HP, Han SW, Kim TY, Hyun Lee J, Bang D. PMID: 28462938; PMCID: PMC5411960.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    12. Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing. PLoS One. 2016; 11(12):e0167641. Kim JA, Hwang B, Park SN, Huh S, Im K, Choi S, Chung HY, Huh J, Seo EJ, Lee JH, Bang D, Lee DS. PMID: 27959900; PMCID: PMC5154520.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    13. Toward a new paradigm of DNA writing using a massively parallel sequencing platform and degenerate oligonucleotide. Sci Rep. 2016 11 23; 6:37176. Hwang B, Bang D. PMID: 27876825; PMCID: PMC5120280.
      View in: PubMed   Mentions:    Fields:    
    14. De novo assembly and next-generation sequencing to analyse full-length gene variants from codon-barcoded libraries. Nat Commun. 2015 Sep 21; 6:8351. Cho N, Hwang B, Yoon JK, Park S, Lee J, Seo HN, Lee J, Huh S, Chung J, Bang D. PMID: 26387459; PMCID: PMC4595759.
      View in: PubMed   Mentions: 6     Fields:    Translation:Cells
    15. Genetic testing of Korean familial hypercholesterolemia using whole-exome sequencing. PLoS One. 2015; 10(5):e0126706. Han SM, Hwang B, Park TG, Kim DI, Rhee MY, Lee BK, Ahn YK, Cho BR, Woo J, Hur SH, Jeong JO, Park S, Jang Y, Lee MG, Bang D, Lee JH, Lee SH. PMID: 25962062; PMCID: PMC4427254.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
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