Associated Papers
Plasminogen missense variants and their involvement in cardiovascular and inflammatory disease.
Brito-Robinson T et al.
Frontiers in Cardiovascular Medicine, 2024
Targeted sequencing of selected functional genes in patients with wild-type transthyretin amyloidosis.
Moreno-Gázquez I et al.
Bmc Research Notes, 2023
Zoobiquity experiments show the importance of the local MMP9-plasminogen axis in inflammatory bowel diseases in both dogs and patients.
Yamasaki T et al.
International Immunology, 2023
Whole-exome sequencing analyses in a Saudi Ischemic Stroke Cohort reveal association signals, and shows polygenic risk scores are related to Modified Rankin Scale Risk.
Alkhamis FA et al.
Functional & Integrative Genomics, 2023
Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine.
Zhou Y et al.
Science Advances, 2021
Functional prediction and comparative population analysis of variants in genes for proteases and innate immunity related to SARS-CoV-2 infection.
Klaassen K et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases, 2020
Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family.
Mescheriakova JY et al.
Multiple Sclerosis (houndmills, Basingstoke, England), 2019
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease.
Vilariño-Güell C et al.
Plos Genetics, 2019
Diagnostic Utility of Complement Serology for Atypical Hemolytic Uremic Syndrome.
Sridharan M et al.
Mayo Clinic Proceedings, 2018
Treatment of plasminogen deficiency patients with fresh frozen plasma.
Kızılocak H et al.
Pediatric Blood & Cancer, 2018
Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency.
Dönmez-Demir B et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2016
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
Sadovnick AD et al.
G3 (bethesda, Md.), 2016
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