Triploidy Detection

Triploidy Detection is a cytogenetic screening methodology within prenatal genetic diagnosis that identifies fetal triploidy by distinguishing the presence of a complete extra set of chromosomes from other aneuploidies through molecular karyotyping or quantitative fluorescent polymerase chain reaction.

106

Publications

4.4K

Citations

498

Authors

180

Institutions

Publications per year

2017–2026

10

Authors

498

  1. KH
    K. H. Nicolaides

    Harris Birthright Research Centre for Fetal Medicine, United Kingdom

    5 publications · 606 citations

    5

    h-index

  2. KM
    Kathy Mann

    Guy's and St Thomas' NHS Foundation Trust, United Kingdom

    3 publications · 206 citations

    3

    h-index

  3. CH
    Charles H. Rodeck

    University College London, United Kingdom

    3 publications · 152 citations

    3

    h-index

  4. CD
    Celia Donaghue

    Guy's and St Thomas' NHS Foundation Trust, United Kingdom

    3 publications · 206 citations

    3

    h-index

  5. CM
    Caroline Mackie Ogilvie

    Guy's and St Thomas' NHS Foundation Trust, United Kingdom

    3 publications · 206 citations

    3

    h-index

1–5 of 498

Venues

  1. Prenatal Diagnosis

    24 publications · 1.4K citations

    19

    h-index

  2. Aquaculture

    10 publications · 469 citations

    10

    h-index

  3. American Journal of Obstetrics and Gynecology

    AJOG · 6 publications · 457 citations

    6

    h-index

  4. PubMed

    Repository · 4 publications · 58 citations

    4

    h-index

  5. Euphytica

    3 publications · 75 citations

    3

    h-index

1–5