Flora Peyvandi
TitleCited byYear
Executive summary: heart disease and stroke statistics—2013 update: a report from the American Heart Association
AS Go, D Mozaffarian, VL Roger, EJ Benjamin, JD Berry, WB Borden, ...
Circulation 127 (1), 143-152, 2013
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
H Schunkert, IR König, S Kathiresan, MP Reilly, TL Assimes, H Holm, ...
Nature genetics 43 (4), 333, 2011
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
S Kathiresan, BF Voight, S Purcell, K Musunuru, D Ardissino, ...
Nature genetics 41 (3), 334-341, 2009
Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies
M Scully, BJ Hunt, S Benjamin, R Liesner, P Rose, F Peyvandi, B Cheung, ...
British journal of haematology 158 (3), 323-335, 2012
New susceptibility locus for coronary artery disease on chromosome 3q22. 3
J Erdmann, A Großhennig, PS Braund, IR König, C Hengstenberg, ...
Nature genetics 41 (3), 280, 2009
Recessively inherited coagulation disorders
PM Mannucci, S Duga, F Peyvandi
Blood 104 (5), 1243-1252, 2004
The thrombogram in rare inherited coagulation disorders: its relation to clinical bleeding
R Al Dieri, F Peyvandi, E Santagostino, M Giansily, PM Mannucci, ...
Thrombosis and haemostasis 88 (10), 576-582, 2002
ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases
M Rieger, PM Mannucci, JAK Hovinga, A Herzog, G Gerstenbauer, ...
Blood 106 (4), 1262-1267, 2005
Rare coagulation deficiencies
F Peyvandi, S Duga, S Akhavan, PM Mannucci
Haemophilia 8 (3), 308-321, 2002
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia.
M Lak, M Keihani, F Elahi, F Peyvandi, PM Mannucci
British journal of haematology 107 (1), 204-206, 1999
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders
F Peyvandi, R Palla, M Menegatti, SM Siboni, S Halimeh, B Faeser, ...
Journal of Thrombosis and Haemostasis 10 (4), 615-621, 2012
Rare coagulation disorders
F Peyvandi, PM Mannucci
Thrombosis and haemostasis 82 (10), 1207-1214, 1999
A randomized trial of factor VIII and neutralizing antibodies in hemophilia A
F Peyvandi, PM Mannucci, I Garagiola, A El-Beshlawy, M Elalfy, ...
New England Journal of Medicine 374 (21), 2054-2064, 2016
ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission
F Peyvandi, S Lavoretano, R Palla, HB Feys, K Vanhoorelbeke, ...
haematologica 93 (2), 232-239, 2008
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease
M Lak, F Peyvandi, PM Mannucci
British journal of haematology 111 (4), 1236-1239, 2000
Caplacizumab for acquired thrombotic thrombocytopenic purpura
F Peyvandi, M Scully, JA Kremer Hovinga, S Cataland, P Knöbl, H Wu, ...
New England Journal of Medicine 374 (6), 511-522, 2016
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group
Circulation 107 (8), 1117-1122, 2003
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Myocardial Infarction Genetics Consortium
Nature genetics 41 (3), 334, 2009
Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
G Mariani, FH Herrmann, A Dolce, A Batorova, D Etro, F Peyvandi, K Wulff, ...
Thrombosis and haemostasis 93 (03), 481-487, 2005
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura
LA Lotta, I Garagiola, R Palla, A Cairo, F Peyvandi
Human mutation 31 (1), 11-19, 2010
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