Associated Papers
Plasminogen missense variants and their involvement in cardiovascular and inflammatory disease.
Brito-Robinson T et al.
Frontiers in Cardiovascular Medicine, 2024
Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine.
Zhou Y et al.
Science Advances, 2021
34516913 (PubMed )
Supplement: sciadv.abi6856_tables_s1_to_s8.zip › sciadv.abi6856_Table_S6.xlsx › Sheet1
Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor.
Loules G et al.
Journal of Clinical Medicine, 2020
33114181 (PubMed )
Supplement: jcm-09-03402-s001.zip › jcm-959403-supplementary.xlsx › Table_S2
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
Sadovnick AD et al.
G3 (bethesda, Md.), 2016
27194806 (PubMed )
Supplement: supp_g3.116.030841_TableS5.pdf
Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.
Seddon JM et al.
Nature Genetics, 2013
24036952 (PubMed )
Supplement: NIHMS512112-supplement-2.xlsx › Supplementary_Table_2B
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