C. Mallet

Functional analysis of endoglin mutations from hereditary hemorrhagic telangiectasia type 1 patients reveals different mechanisms for endoglin loss of function

C. Mallet, Khadija Lamribet, Sophie Giraud et al. · Human Molecular Genetics · 2014 · 76 citations

Engineering, Genetics, Pathology +19

Angiotensin I-converting enzyme gene polymorphism modulates the consequences of in utero growth retardation on plasma insulin in young adults.

François Cambien, Juliane Léger, C. Mallet et al. · Diabetes · 1998 · 47 citations

Angiotensin II type‐I receptor and ACE polymorphisms and risk of myocardial infarction in men and women

Frank Kee, Caroline Morrison, Odette Poirier et al. · European Journal of Clinical Investigation · 2000 · 28 citations

HLA CLASS II POLYMORPHISM AND IDDM SUSCEPTIBILITY IN THE GREEK POPULATION

I Khalil, M. Spyropoulou, C. Mallet et al. · International Journal of Immunogenetics · 1993 · 21 citations

Erythema multiforme is associated to HLA‐Aw33 and DRw53

V. Lepage, Corinne Douay, C. Mallet et al. · Tissue Antigens · 1988 · 15 citations