Associated Papers
Genetic and epigenetic dysregulation of CR1 is associated with catastrophic antiphospholipid syndrome.
Ranjan N et al.
Annals of the Rheumatic Diseases, 2025
Genetic and Epigenetic Dysregulation of CR1 is Associated with Catastrophic Antiphospholipid Syndrome (CAPS).
Ranjan N et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
An immunogenomic exome landscape of triple positive primary antiphospholipid patients.
Guffroy A et al.
Genes and Immunity, 2024
Using whole-genome sequencing to characterize clinically significant blood groups among healthy older Australians.
Jadhao S et al.
Blood Advances, 2022
35420653 (PubMed )
Supplement: mmc1.xlsx › Supplementary_table3
RBCeq: A robust and scalable algorithm for accurate genetic blood typing.
Jadhao S et al.
Ebiomedicine, 2022
35033986 (PubMed )
Supplement: mmc2.xlsx › Supplementary_Table11
Integrated genomic analysis reveals mutated ELF3 as a potential gallbladder cancer vaccine candidate.
Pandey A et al.
Nature Communications, 2020
32839463 (PubMed )
Supplement: 41467_2020_17880_MOESM6_ESM.xlsx › Unpaired_Mutations_GBC
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