Trisomy Screening

Trisomy Screening is a prenatal cytogenetic method that identifies fetal chromosomal abnormalities by detecting the presence of an extra chromosome, most commonly chromosome 21, 18, or 13, through non-invasive or invasive diagnostic techniques.

736

Publications

38.3K

Citations

3.2K

Authors

1.1K

Institutions

Publications per year

2017–2026

92

Authors

3.2K

  1. KH
    K. H. Nicolaides

    Harris Birthright Research Centre for Fetal Medicine, United Kingdom

    101 publications · 10.4K citations

    57

    h-index

  2. KS
    Kevin Spencer

    Harold Wood Hospital, United Kingdom

    40 publications · 4K citations

    30

    h-index

  3. RJ
    R. J. M. Snijders

    Harris Birthright Research Centre for Fetal Medicine, United Kingdom

    21 publications · 3.1K citations

    20

    h-index

  4. AS
    Argyro Syngelaki

    King's College Hospital, United Kingdom

    17 publications · 2K citations

    16

    h-index

  5. TY
    Tak Yeung Leung

    Chinese University of Hong Kong, Hong Kong SAR China

    17 publications · 849 citations

    14

    h-index

1–5 of 3.2K

Venues

  1. Ultrasound in Obstetrics and Gynecology

    93 publications · 8.3K citations

    49

    h-index

  2. Prenatal Diagnosis

    121 publications · 5.5K citations

    41

    h-index

  3. American Journal of Obstetrics and Gynecology

    AJOG · 39 publications · 3.4K citations

    26

    h-index

  4. PubMed

    Repository · 41 publications · 1.4K citations

    21

    h-index

  5. Fetal Diagnosis and Therapy

    35 publications · 1.1K citations

    17

    h-index

1–5