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

Authors

80

  1. FJ
    Francisco J. Sánchez‐Rivera

    Memorial Sloan Kettering Cancer Center, United States

    1 publications · 129 citations

    1

    h-index

  2. SK
    Seokhwi Kim

    Samsung Medical Center, South Korea

    1 publications · 73 citations

    1

    h-index

  3. HS
    Henri Schmidt

    Princeton University, United States

    1 publications · 129 citations

    1

    h-index

  4. TK
    Tadashi Kajii

    Yamaguchi University, Japan

    1 publications · 64 citations

    1

    h-index

  5. DC
    Debyani Chakravarty

    Memorial Sloan Kettering Cancer Center, United States

    1 publications · 129 citations

    1

    h-index

1–5 of 80

Venues

  1. Proceedings of the National Academy of Sciences

    PNAS · 2 publications · 284 citations

    2

    h-index

  2. Blood

    1 publications · 21 citations

    1

    h-index

  3. Journal of Molecular Diagnostics

    JMD · 1 publications · 73 citations

    1

    h-index

  4. PLoS ONE

    1 publications · 32 citations

    1

    h-index

  5. Cold Spring Harbor Protocols

    1 publications · 12 citations

    1

    h-index

1–5