The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort studyPaula D. James, David Lillicrap, Georges E. Rivard et al.|Blood|2006Cited by 351
Founder von Willebrand factor haplotype associated with type 1 von Willebrand diseaseLee A. O’Brien, David Lillicrap, Paula D. James et al.|Blood|2003Cited by 97
Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian Type 1 VWD StudyPaula James, David Lillicrap, Andrew D. Paterson et al.|Journal of Thrombosis and Haemostasis|2006Cited by 86
A novel type 2A (Group II) von Willebrand disease mutation (L1503Q) associated with loss of the highest molecular weight von Willebrand factor multimersLee A. O’Brien, David Lillicrap, Jeffrey J. Sutherland et al.|Journal of Thrombosis and Haemostasis|2004Cited by 26
ADAMTS13 cleavage efficiency is altered by mutagenic and, to a lesser extent, polymorphic sequence changes in the A1 and A2 domains of von Willebrand factorCynthia M. Pruss, David Lillicrap, Colleen Notley et al.|British Journal of Haematology|2008Cited by 20