I. M. Nesbitt

PPIB Mutations Cause Severe Osteogenesis Imperfecta

Fleur S. van Dijk, I. M. Nesbitt, Eline H. Zwikstra et al. · The American Journal of Human Genetics · 2009 · 296 citations · Full text

Bone Disease, Genetics, Osteoarthritis +6

Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor

Simon Allen, Adel Abuzenadah, Joanna L. Blagg et al. · Blood · 2000 · 72 citations

CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis

Fleur S. van Dijk, I. M. Nesbitt, Peter G. J. Nikkels et al. · European Journal of Human Genetics · 2009 · 54 citations · Full text

Developmental Biology, Orthopaedic Surgery, Crtap Mutations +11

Characterisation of Type 2N von Willebrand Disease Using Phenotypic and Molecular Techniques

I. M. Nesbitt, Anne Goodeve, Andrea M. Guilliatt et al. · Thrombosis and Haemostasis · 1996 · 37 citations

Genetics, Genetic Epidemiology, Immunology +18

The management of von Willebrand's disease-associated gastrointestinal angiodysplasia

Edward S. Morris, K. K. Hampton, I. M. Nesbitt et al. · Blood Coagulation & Fibrinolysis · 2001 · 28 citations

Affected Patients, Thrombosis, Gastrointestinal Angiodysplasia +8