H. Ireland

Pleiotropic effects of antithrombin strand 1C substitution mutations.

David A. Lane, R.J. Olds, J. Conard et al. · Journal of Clinical Investigation · 1992 · 95 citations · Full text

Genetics, Immunology, Molecular Biology +23

Protein S deficiency: a database of mutations. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Sophie Gandrille, Delphine Borgel, H. Ireland et al. · PubMed · 1997 · 76 citations

Thrombosis, Blood Platelet, Medicine +9

Protein S Deficiency: A Database of Mutations

Sophie Gandrille, Delphine Borgel, H. Ireland et al. · Thrombosis and Haemostasis · 1997 · 71 citations

Genetic Disorder, Genetics, Protein S Deficiency +5

A comparative evaluation of assays for markers of activated coagulation and/or fibrinolysis: thrombin–antithrombin complex, D‐dimer and fibrinogen/fibrin fragment E antigen

M Boisclair, David A. Lane, J Wilde et al. · British Journal of Haematology · 1990 · 70 citations

EPCR Ser219Gly: Elevated sEPCR, prothrombin F1+2, risk for coronary heart disease, and increased sEPCR shedding in vitro

H. Ireland, Constantine James Konstantoulas, Emma Hawe et al. · Atherosclerosis · 2005 · 67 citations · Full text

Thrombosis, Prothrombin F1+2, Epcr Ser219gly +12