Maurizio Margaglione

Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family

Robin Foà, M. Margaglione, R. Foà, 2012, European journal of haematology.

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.

M. Margaglione, E. Grandone, R. Santacroce, 2005, Blood.

Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology.

Marco Seri, Roberto Ravazzolo, Alessandro Ferraris, 2002, Clinical chemistry.

In vitro residual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU.

Nenad Blau, M. Margaglione, N. Blau, 2016, Gene.

Mutation of the angiopoietin‐1 gene (ANGPT1) associates with a new type of hereditary angioedema

M. Margaglione, M. Cicardi, V. Bafunno, 2017, The Journal of allergy and clinical immunology.

Insight into the nature of the CRP-coronary event association using Mendelian randomization.

Juan P Casas, Elena Tremoli, Teake Kooistra, 2006, International journal of epidemiology.