Prenatal Molecular Testing

Prenatal Molecular Testing is a molecular diagnostic methodology that involves the analysis of fetal nucleic acids obtained from maternal blood, amniotic fluid, or chorionic villi to detect genetic abnormalities and inherited disorders before birth.

3K

Publications

165.5K

Citations

13.6K

Authors

2.9K

Institutions

Publications per year

2017–2026

606

Authors

13.6K

  1. KH
    K. H. Nicolaides

    Harris Birthright Research Centre for Fetal Medicine, United Kingdom

    68 publications · 7.2K citations

    43

    h-index

  2. RW
    Rossa W. K. Chiu

    Chinese University of Hong Kong, Hong Kong SAR China

    51 publications · 9.5K citations

    39

    h-index

  3. YM
    Yuk Ming Dennis Lo

    Chinese University of Hong Kong, Hong Kong SAR China

    54 publications · 16K citations

    39

    h-index

  4. TK
    Tze Kin Lau

    Chinese University of Hong Kong, Hong Kong SAR China

    43 publications · 12.8K citations

    37

    h-index

  5. DW
    Diana W. Bianchi

    Tufts Medical Center, United States

    52 publications · 5.2K citations

    33

    h-index

1–5 of 13.6K

Venues

  1. Prenatal Diagnosis

    524 publications · 23.5K citations

    74

    h-index

  2. Clinical Chemistry

    113 publications · 9.7K citations

    53

    h-index

  3. American Journal of Obstetrics and Gynecology

    AJOG · 141 publications · 8.2K citations

    47

    h-index

  4. The Lancet

    54 publications · 8K citations

    40

    h-index

  5. Obstetrics and Gynecology

    74 publications · 5.2K citations

    39

    h-index

1–5