Single-nucleotide Variant Correction
Single-Nucleotide Variant Correction is a genome editing technique that precisely modifies individual nucleotides in DNA to correct pathogenic point mutations without inducing double-strand breaks, thereby enabling the targeted restoration of normal gene function.
9
Publications
674
Citations
80
Authors
38
Institutions
Publications per year
2017–2026
3
Parents
9
Francisco J. Sánchez‐Rivera, Bianca J. Diaz, Edward R. Kastenhuber et al. · Nature Biotechnology · 2022 · 129 citations · Full text
Shimmer: detection of genetic alterations in tumors using next-generation sequence data
Nancy F. Hansen, Jared J. Gartner, Mei Lan et al. · Bioinformatics · 2013 · 68 citations · Full text
Hiroshi Ochiai, Tatsuo Miyamoto, Akinori Kanai et al. · Proceedings of the National Academy of Sciences · 2013 · 64 citations · Full text
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80
Memorial Sloan Kettering Cancer Center, United States
1 publications · 129 citations
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1
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Memorial Sloan Kettering Cancer Center, United States
1 publications · 129 citations
1
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1–5 of 80
38
National Human Genome Research Institute
Bethesda, United States
1 h-index
5 publications
340 citations
National Institute of Technology, Tokyo College
Hachiōji, Japan
1 h-index
1 publications
64 citations
Shanghai Medical College of Fudan University
Shanghai, China
1 h-index
1 publications
55 citations
Memorial Sloan Kettering Cancer Center
New York, United States
1 h-index
16 publications
2.1K citations
Tianjin Normal University
Tianjin, China
1 h-index
1 publications
55 citations
Stanford Medicine
Stanford, United States
1 h-index
1 publications
21 citations
Intelligent Synthetic Biology Center
Daejeon, South Korea
1 h-index
2 publications
110 citations
National Cancer Center
Goyang-si, South Korea
1 h-index
1 publications
73 citations
1–8 of 38
PNAS · 2 publications · 284 citations
2
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1 publications · 21 citations
1
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JMD · 1 publications · 73 citations
1
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1 publications · 32 citations
1
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1 publications · 12 citations
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