The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort studyPaula D. James, David Lillicrap, Lee A. O’Brien 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
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
A novel type 2A von Willebrand factor mutation located at the last nucleotide of exon 26 (3538G>A) causes skipping of 2 nonadjacent exonsPaula James, David Lillicrap, Lee A. O’Brien et al.|Blood|2004Cited by 19