Random X Inactivation

Random X Inactivation is a genetic mechanism in female mammals whereby one of the two X chromosomes is transcriptionally silenced in a cell-specific manner during early embryonic development, with the choice of the inactivated X chromosome occurring randomly and independently in each cell, leading to a mosaic pattern of gene expression across tissues.

265

Publications

18.3K

Citations

1.2K

Authors

460

Institutions

Publications per year

2017–2026

34

Authors

1.2K

  1. JG
    Joost Gribnau

    Erasmus MC, Netherlands

    7 publications · 556 citations

    7

    h-index

  2. NT
    Nobuo Takagi

    Hokkaido University, Japan

    6 publications · 378 citations

    6

    h-index

  3. ÉH
    Édith Heard

    Institut Curie, France

    6 publications · 1.1K citations

    6

    h-index

  4. BC
    B.M. Cattanach

    Mary Lyon Centre at MRC Harwell, United Kingdom

    5 publications · 438 citations

    5

    h-index

  5. NB
    Neil Brockdorff

    University of Oxford, United Kingdom

    5 publications · 830 citations

    5

    h-index

1–5 of 1.2K

Venues

  1. Proceedings of the National Academy of Sciences

    PNAS · 12 publications · 930 citations

    11

    h-index

  2. Genetics Research

    11 publications · 595 citations

    11

    h-index

  3. American Journal of Medical Genetics

    11 publications · 480 citations

    10

    h-index

  4. Development

    11 publications · 734 citations

    10

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  5. Human Genetics

    9 publications · 542 citations

    9

    h-index

1–5