Prenatal Cytogenetics

Prenatal Cytogenetics is a subdiscipline of cytogenetics that involves the analysis of fetal chromosomes, typically obtained through invasive or non-invasive procedures during pregnancy, to detect congenital chromosomal abnormalities and genetic disorders prior to birth.

2K

Publications

96.7K

Citations

7.8K

Authors

1.8K

Institutions

Publications per year

2017–2026

179

Authors

7.8K

  1. CC
    Chih‐Ping Chen

    Mackay Memorial Hospital, Taiwan

    83 publications · 1.7K citations

    21

    h-index

  2. WW
    Wayseen Wang

    Mackay Memorial Hospital, Taiwan

    75 publications · 1.6K citations

    21

    h-index

  3. SC
    Schu‐Rern Chern

    Mackay Memorial Hospital, Taiwan

    74 publications · 1.6K citations

    20

    h-index

  4. KH
    K. H. Nicolaides

    Harris Birthright Research Centre for Fetal Medicine, United Kingdom

    24 publications · 1.9K citations

    19

    h-index

  5. RJ
    Ronald J. Wapner

    Columbia University, United States

    21 publications · 3.2K citations

    18

    h-index

1–5 of 7.8K

Venues

  1. Prenatal Diagnosis

    441 publications · 19.3K citations

    73

    h-index

  2. American Journal of Medical Genetics

    107 publications · 5K citations

    39

    h-index

  3. PubMed

    Repository · 140 publications · 6.1K citations

    37

    h-index

  4. American Journal of Obstetrics and Gynecology

    AJOG · 63 publications · 2.8K citations

    34

    h-index

  5. Human Genetics

    70 publications · 3.9K citations

    34

    h-index

1–5