Minseok Kwon
Overview
Explore the profile of Minseok Kwon including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
12
Citations
650
Followers
0
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Recent Articles
1.
Sung K, Han S, Lee J, Kwon M, Kim D, Oh Y
Anticancer Res
. 2024 Oct;
44(11):5147-5155.
PMID: 39477293
Background/aim: Lung cancer remains a leading cause of cancer-related mortality worldwide, necessitating the development of effective early diagnostic strategies. Despite advancements in imaging and screening technologies, late-stage diagnoses remain common,...
2.
Rodin R, Dou Y, Kwon M, Sherman M, DGama A, Doan R, et al.
Nat Neurosci
. 2023 Aug;
26(10):1833.
PMID: 37644260
No abstract available.
3.
Rodin R, Dou Y, Kwon M, Sherman M, DGama A, Doan R, et al.
Nat Neurosci
. 2021 Mar;
24(4):611.
PMID: 33753946
No abstract available.
4.
Bizzotto S, Dou Y, Ganz J, Doan R, Kwon M, Bohrson C, et al.
Science
. 2021 Mar;
371(6535):1249-1253.
PMID: 33737485
Although cell lineage information is fundamental to understanding organismal development, very little direct information is available for humans. We performed high-depth (250×) whole-genome sequencing of multiple tissues from three individuals...
5.
Rodin R, Dou Y, Kwon M, Sherman M, DGama A, Doan R, et al.
Nat Neurosci
. 2021 Jan;
24(2):176-185.
PMID: 33432195
We characterize the landscape of somatic mutations-mutations occurring after fertilization-in the human brain using ultra-deep (~250×) whole-genome sequencing of prefrontal cortex from 59 donors with autism spectrum disorder (ASD) and...
6.
Kwon M, Lee S, Berselli M, Chu C, Park P
Bioinformatics
. 2021 Jan;
37(2):263-264.
PMID: 33416869
Summary: Despite the improvement in variant detection algorithms, visual inspection of the read-level data remains an essential step for accurate identification of variants in genome analysis. We developed BamSnap, an...
7.
Dou Y, Kwon M, Rodin R, Cortes-Ciriano I, Doan R, Luquette L, et al.
Nat Biotechnol
. 2020 Jan;
38(3):314-319.
PMID: 31907404
Detection of mosaic mutations that arise in normal development is challenging, as such mutations are typically present in only a minute fraction of cells and there is no clear matched...
8.
Bohrson C, Barton A, Lodato M, Rodin R, Luquette L, Viswanadham V, et al.
Nat Genet
. 2019 Mar;
51(4):749-754.
PMID: 30886424
Whole-genome sequencing of DNA from single cells has the potential to reshape our understanding of mutational heterogeneity in normal and diseased tissues. However, a major difficulty is distinguishing amplification artifacts...
9.
Kwon M, Leem S, Yoon J, Park T
BMC Syst Biol
. 2018 Mar;
12(Suppl 2):19.
PMID: 29560826
Background: With the rapid advancement of array-based genotyping techniques, genome-wide association studies (GWAS) have successfully identified common genetic variants associated with common complex diseases. However, it has been shown that...
10.
Lodato M, Rodin R, Bohrson C, Coulter M, Barton A, Kwon M, et al.
Science
. 2017 Dec;
359(6375):555-559.
PMID: 29217584
It has long been hypothesized that aging and neurodegeneration are associated with somatic mutation in neurons; however, methodological hurdles have prevented testing this hypothesis directly. We used single-cell whole-genome sequencing...