Werner Syndrome

Werner Syndrome is a rare autosomal recessive disorder belonging to the class of human diseases characterized by premature aging and caused by mutations in the WRN gene, which encodes a DNA helicase involved in DNA repair and genomic stability.

713

Publications

47.1K

Citations

2.7K

Authors

797

Institutions

Publications per year

2017–2026

76

Variants

Adult Progeria

Authors

2.7K

  1. VA
    Vilhelm A. Bohr

    National Institute on Aging, United States

    62 publications · 5.4K citations

    38

    h-index

  2. JO
    Junko Oshima

    University of Washington, United States

    51 publications · 6.6K citations

    36

    h-index

  3. GM
    George M. Martin

    University of Washington, United States

    39 publications · 6.1K citations

    32

    h-index

  4. MG
    Makoto Goto

    Otsuka (Japan), Japan

    39 publications · 2.9K citations

    26

    h-index

  5. RM
    Robert M. Brosh

    National Institute on Aging, United States

    28 publications · 2.6K citations

    24

    h-index

1–5 of 2.7K

Venues

  1. Journal of Biological Chemistry

    JBC · 58 publications · 6.3K citations

    40

    h-index

  2. Nucleic Acids Research

    38 publications · 2.6K citations

    28

    h-index

  3. PubMed

    Repository · 43 publications · 2.1K citations

    24

    h-index

  4. Proceedings of the National Academy of Sciences

    PNAS · 21 publications · 3.8K citations

    20

    h-index

  5. Human Genetics

    20 publications · 1.7K citations

    18

    h-index

1–5