Published in PLoS One on March 27, 2014
Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J Thromb Haemost (2006) 4.58
Epidemiological investigation of the prevalence of von Willebrand's disease. Blood (1987) 3.24
Prevalence of von Willebrand disease in children: a multiethnic study. J Pediatr (1993) 1.60
Generation and validation of the Condensed MCMDM-1VWD Bleeding Questionnaire for von Willebrand disease. J Thromb Haemost (2008) 1.59
An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary. J Thromb Haemost (2008) 1.51
Prevalence and spectrum of von Willebrand disease from western India. Indian J Med Res (2005) 1.43
Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction. Biochemistry (1991) 1.22
Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaire. J Thromb Haemost (2010) 1.21
Factor VIII and von Willebrand factor interaction: biological, clinical and therapeutic importance. Haemophilia (2009) 1.15
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients. Blood Cells Mol Dis (2003) 1.11
Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene. Thromb Haemost (2009) 1.01
Genetic defects in von Willebrand disease type 3 in Indian and Greek patients. Blood Cells Mol Dis (2008) 0.95
The prevalence of symptomatic von Willebrand disease in primary care practice. J Thromb Haemost (2009) 0.94
Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I. Am J Hum Genet (1992) 0.94
Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients. Thromb Haemost (2012) 0.90
Molecular characterization of Iranian patients with type 3 von Willebrand disease. Haemophilia (2009) 0.89
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin. Thromb Haemost (1998) 0.89
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease. Thromb Haemost (2000) 0.88
Genetic heterogeneity of severe von Willebrand disease type III in the German population. Hum Genet (1994) 0.88
The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles: a rebuttal. J Thromb Haemost (2013) 0.87
Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients. Thromb Haemost (2013) 0.86
Homozygous gene conversion in von Willebrand factor gene as a cause of type 3 von Willebrand disease and predisposition to inhibitor development. Blood (2001) 0.85
A novel Alu-mediated 61-kb deletion of the von Willebrand factor (VWF) gene whose breakpoints co-locate with putative matrix attachment regions. Blood Cells Mol Dis (2006) 0.84
High-throughput molecular diagnosis of von Willebrand disease by next generation sequencing methods. Haematologica (2012) 0.84
Characterisation of mutations and molecular studies of type 2 von Willebrand disease. Thromb Haemost (2012) 0.82
An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE). Ann Hematol (2013) 0.81
Gene conversions are a common cause of von Willebrand disease. Br J Haematol (2005) 0.80
Von Willebrand factor 1 and factor 2 alleles (intron 40) are suitable markers for carrier detection in von Willebrand disease families in the Indian population. Acta Haematol (2006) 0.80
Molecular characterization, recombinant protein expression, and mRNA analysis of type 3 von Willebrand disease: Studies of an Italian cohort of 10 patients. Am J Hematol (2012) 0.79
A stop codon in a patient with severe type III von Willebrand disease. Blood (1991) 0.78
Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation. Hum Genet (1989) 0.78
Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor gene. Br J Haematol (2000) 0.77
VWF pseudogene: Mimics, masks and spoils. Clin Chim Acta (2010) 0.77