Stefano Duga
Stefano Duga
Full professor of Molecular Biology, Humanitas University, IRCCS Istituto Clinico Humanitas
Verified email at hunimed.eu - Homepage
Title
Cited by
Cited by
Year
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
10932009
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB J°rgensen, S Duga, PA Merlini, A Kiezun, ...
Nature 518 (7537), 102-106, 2015
5042015
Recessively inherited coagulation disorders
PM Mannucci, S Duga, F Peyvandi
Blood 104 (5), 1243-1252, 2004
4882004
Diagnostic yield and clinical utility of sequencing familial hypercholesterolemia genes in patients with severe hypercholesterolemia
AV Khera, HH Won, GM Peloso, KS Lawson, TM Bartz, X Deng, ...
Journal of the American College of Cardiology 67 (22), 2578-2589, 2016
4452016
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
Myocardial Infarction Genetics Consortium Investigators
New England Journal of Medicine 371 (22), 2072-2082, 2014
3462014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
GM Peloso, PL Auer, JC Bis, A Voorman, AC Morrison, NO Stitziel, ...
The American Journal of Human Genetics 94 (2), 223-232, 2014
2622014
Rare coagulation deficiencies
F Peyvandi, S Duga, S Akhavan, PM Mannucci
Haemophilia 8 (3), 308-321, 2002
2532002
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
2422014
Genomewide association study of severe Covid-19 with respiratory failure
D Ellinghaus, F Degenhardt, L Bujanda, M Buti, A Albillos, P Invernizzi, ...
New England Journal of Medicine, 2020
1632020
Survival and dementia in GBA‐associated Parkinson's disease: The mutation matters
R Cilia, S Tunesi, G Marotta, E Cereda, C Siri, S Tesei, AL Zecchinelli, ...
Annals of neurology 80 (5), 662-673, 2016
1502016
The molecular basis of quantitative fibrinogen disorders
R Asselta, S Duga, ML Tenchini
Journal of Thrombosis and Haemostasis 4 (10), 2115-2129, 2006
1492006
cDNA cloning of turtle prion protein
T Simonic, S Duga, B Strumbo, R Asselta, F Ceciliani, S Ronchi
FEBS letters 469 (1), 33-38, 2000
1462000
Genetic diagnosis of haemophilia and other inherited bleeding disorders
F Peyvandi, G Jayandharan, M Chandy, A Srivastava, SM Nakaya, ...
Haemophilia 12, 82-89, 2006
1452006
Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease
TR Webb, J Erdmann, KE Stirrups, NO Stitziel, NGD Masca, H Jansen, ...
Journal of the American College of Cardiology 69 (7), 823-836, 2017
1382017
Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion
S Duga, R Asselta, E Santagostino, S Zeinali, T Simonic, M Malcovati, ...
Blood, The Journal of the American Society of Hematology 95 (4), 1336-1341, 2000
1342000
Congenital factor XI deficiency: an update
S Duga, O Salomon
Seminars in thrombosis and hemostasis 39 (06), 621-631, 2013
1092013
Inherited defects of coagulation factor V: the hemorrhagic side
R Asselta, ML Tenchini, S Duga
Journal of Thrombosis and Haemostasis 4 (1), 26-34, 2006
992006
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
982016
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies
TL Assimes, H Hˇlm, S Kathiresan, MP Reilly, G Thorleifsson, BF Voight, ...
Journal of the American College of Cardiology 56 (19), 1552-1563, 2010
982010
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia
NO Stitziel, SW Fouchier, B Sjouke, GM Peloso, AM Moscoso, PL Auer, ...
Arteriosclerosis, thrombosis, and vascular biology 33 (12), 2909-2914, 2013
972013
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