Jacqueline A. Cutler

Cellular and molecular basis of von Willebrand disease: studies on blood outgrowth endothelial cells

Richard Starke, Koralia Paschalaki, C. Dyer et al. · Blood · 2013 · 100 citations · Full text

Medicine, Cell Biology, Pathology +14

The identification and classification of 41 novel mutations in the factor VIII gene (F8C)

Jacqueline A. Cutler, Mike Mitchell, Mark P. Smith et al. · Human Mutation · 2002 · 39 citations · Full text

Medicine, Genetics, Molecular Genetics +17

A multi‐center evaluation of TECHNOSCREEN® ADAMTS‐13 activity assay as a screening tool for detecting deficiency of ADAMTS‐13

Gary Moore, Daniëlle Meijer, Margaret A. Griffiths et al. · Journal of Thrombosis and Haemostasis · 2020 · 32 citations

Medicine, Molecular Medicine, Pathology +10

Eighteen unrelated patients with factor XI deficiency, four novel mutations and a 100% detection rate by denaturing high‐performance liquid chromatography

Michael Mitchell, Purvee Harrington, Jacqueline A. Cutler et al. · British Journal of Haematology · 2003 · 31 citations

Medicine, Genetics, Molecular Genetics +17

Recommendations for clinical laboratory testing of activated protein C resistance; communication from the SSC of the ISTH

Gary Moore, Elizabeth M. Van Cott, Jacqueline A. Cutler et al. · Journal of Thrombosis and Haemostasis · 2019 · 30 citations · Full text

Life Sciences, Immunology, Clinical Immunology +7