Associated Papers
Large deletions in the F8 gene predict immune tolerance induction failure in people with severe hemophilia A.
Oomen I et al.
Research and Practice in Thrombosis and Haemostasis, 2025
Fc gamma receptors: Their evolution, genomic architecture, genetic variation, and impact on human disease.
Frampton S et al.
Immunological Reviews, 2024
Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome.
Cai R et al.
Frontiers in Cell and Developmental Biology, 2021
Comprehensive Study of Germline Mutations and Double-Hit Events in Esophageal Squamous Cell Cancer.
Zeng B et al.
Frontiers in Oncology, 2021
33889545 (PubMed )
Supplement: Table_3.XLSX › Sheet1
FCGR Genetic Variation in Two Populations From Ecuador Highlands-Extensive Copy-Number Variation, Distinctive Distribution of Functional Polymorphisms, and a Novel, Locally Common, Chimeric FCGR3B/A (CD16B/A) Gene.
Moraru M et al.
Frontiers in Immunology, 2021
34108956 (PubMed )
Supplement: DataSheet_1.xlsx › Table_III._FCGR_functional_SNPs
An HIV Vaccine Protective Allele in FCGR2C Associates With Increased Odds of Perinatal HIV Acquisition.
Ebonwu J et al.
Frontiers in Immunology, 2021
The Human FcγRII (CD32) Family of Leukocyte FcR in Health and Disease.
Anania JC et al.
Frontiers in Immunology, 2019
Extensive Ethnic Variation and Linkage Disequilibrium at the FCGR2/3 Locus: Different Genetic Associations Revealed in Kawasaki Disease.
Nagelkerke SQ et al.
Frontiers in Immunology, 2019
Nonclassical FCGR2C haplotype is associated with protection from red blood cell alloimmunization in sickle cell disease.
Meinderts SM et al.
Blood, 2017
Nonallelic homologous recombination of the FCGR2/3 locus results in copy number variation and novel chimeric FCGR2 genes with aberrant functional expression.
Nagelkerke SQ et al.
Genes and Immunity, 2015
Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus.
Mueller M et al.
American Journal of Human Genetics, 2013
Evolutionary history of copy-number-variable locus for the low-affinity Fcγ receptor: mutation rate, autoimmune disease, and the legacy of helminth infection.
Machado LR et al.
American Journal of Human Genetics, 2012
Unfaithful association of FCGR2B genetic polymorphisms with susceptibility to SLE.
Napolioni V et al.
Autoimmunity, 2009
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