Universal Newborn Screening

Universal Newborn Screening is a standardized public health program that systematically applies genetic and biochemical testing to all newborns within a defined population to enable early detection, diagnosis, and intervention for a predefined panel of heritable disorders, thereby distinguishing it from targeted or selective newborn screening approaches.

380

Publications

21.8K

Citations

1.9K

Authors

772

Institutions

Publications per year

2017–2026

111

Variants

Nbs

Authors

1.9K

  1. BL
    Bradford L. Therrell

    The University of Texas at San Antonio Health Science Center, United States

    10 publications · 535 citations

    10

    h-index

  2. SD
    Scott D. Grosse

    National Center on Birth Defects and Developmental Disabilities, United States

    10 publications · 628 citations

    10

    h-index

  3. KR
    Karl R. White

    Utah State University, United States

    7 publications · 424 citations

    7

    h-index

  4. CD
    Carmencita D. Padilla

    University of the Philippines Manila, Philippines

    6 publications · 337 citations

    6

    h-index

  5. CK
    Colin Kennedy

    University of Southampton, United Kingdom

    6 publications · 907 citations

    6

    h-index

1–5 of 1.9K

Venues

  1. PEDIATRICS

    35 publications · 3.8K citations

    27

    h-index

  2. Journal of Inherited Metabolic Disease

    JIMD · 17 publications · 1.3K citations

    16

    h-index

  3. PubMed

    Repository · 27 publications · 1.2K citations

    16

    h-index

  4. International Journal of Neonatal Screening

    IJNS · 16 publications · 474 citations

    15

    h-index

  5. Genetics in Medicine

    GIM · 16 publications · 708 citations

    13

    h-index

1–5