Bombay Phenotype

The Bombay Phenotype is a rare genetic blood type characterized by the absence of the H antigen, the foundational carbohydrate structure required for the expression of A and B antigens, due to homozygous mutations in the FUT1 gene, resulting in individuals phenotypically appearing as type O despite potentially harboring ABO alleles.

68

Publications

2.9K

Citations

271

Authors

114

Institutions

Publications per year

2017–2026

6

Variants

Hh Blood GroupOh Phenotype

Authors

271

  1. YK
    Yoshiro Koda

    Kurume University, Japan

    4 publications · 199 citations

    4

    h-index

  2. RO
    Rafaël Oriol

    Inserm, France

    4 publications · 145 citations

    4

    h-index

  3. MS
    Mikiko Soejima

    Kurume University, Japan

    4 publications · 199 citations

    4

    h-index

  4. GG
    G. Gérard

    Hôpital Broussais, France

    3 publications · 82 citations

    3

    h-index

  5. DV
    D Vitrac

    Centre National de la Recherche Scientifique, France

    3 publications · 82 citations

    3

    h-index

1–5 of 271

Venues

  1. Vox Sanguinis

    13 publications · 409 citations

    11

    h-index

  2. Transfusion

    11 publications · 285 citations

    10

    h-index

  3. Asian Journal of Transfusion Science

    AJTS · 5 publications · 103 citations

    5

    h-index

  4. PubMed

    Repository · 4 publications · 110 citations

    4

    h-index

  5. Blood

    4 publications · 226 citations

    4

    h-index

1–5