
Variation and impact of polygenic hematological traits in monogenic sickle cell disease
Author(s) -
Thomas Pincez,
Ken Sin Lo,
Anne-Laure Pham Hung D'Alexandry D'Orengiani,
Melanie E. Garrett,
Carlo Brugnara,
Allison AshleyKoch,
Marilyn J. Telen,
Frédéric Galacteros,
Philippe Joly,
Pablo Bartolucci,
Guillaume Lettre
Publication year - 2022
Publication title -
haematologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.782
H-Index - 142
eISSN - 1592-8721
pISSN - 0390-6078
DOI - 10.3324/haematol.2022.281180
Subject(s) - acute chest syndrome , fetal hemoglobin , locus (genetics) , medicine , disease , genotype , epistasis , context (archaeology) , mendelian randomization , genome wide association study , sickle cell anemia , mendelian inheritance , biology , immunology , genetics , single nucleotide polymorphism , gene , pregnancy , genetic variants , paleontology , fetus