Atm Deficiency

ATM Deficiency is a genetic disorder characterized by mutations in the ATM gene, which disrupts the kinase-mediated signaling pathway essential for DNA double-strand break repair and cell cycle checkpoint control.

491

Publications

44.2K

Citations

3K

Authors

872

Institutions

Publications per year

2017–2026

94

Variants

Ataxia-telangiectasia Mutated Deficiency

Authors

3K

  1. MF
    Martin F. Lavin

    The University of Queensland, Australia

    19 publications · 5.6K citations

    18

    h-index

  2. YS
    Yosef Shiloh

    Tel Aviv University, Israel

    17 publications · 6.4K citations

    17

    h-index

  3. RA
    Richard A. Gatti

    University of California, Los Angeles, United States

    17 publications · 3.8K citations

    16

    h-index

  4. CB
    Carrolee Barlow

    Salk Institute for Biological Studies, United States

    18 publications · 3.1K citations

    15

    h-index

  5. AW
    Anthony Wynshaw‐Boris

    University of California San Diego, United States

    17 publications · 3K citations

    14

    h-index

1–5 of 3K

Venues

  1. Proceedings of the National Academy of Sciences

    PNAS · 27 publications · 3.8K citations

    27

    h-index

  2. PubMed

    Repository · 26 publications · 2.7K citations

    22

    h-index

  3. Journal of Biological Chemistry

    JBC · 20 publications · 3.6K citations

    20

    h-index

  4. PLoS ONE

    18 publications · 618 citations

    15

    h-index

  5. Human Molecular Genetics

    16 publications · 1.3K citations

    15

    h-index

1–5