| Genomewide association study of severe Covid-19 with respiratory failure Severe Covid-19 GWAS Group New England Journal of Medicine 383 (16), 1522-1534, 2020 | 2013 | 2020 |
| Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Heart Attack Risk in Puget Sound. Schwartz Stephen M 20 26 Siscovick David S ... Nature genetics 41 (3), 334-341, 2009 | 1298 | 2009 |
| 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 | 926 | 2016 |
| Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease TG and HDL Working Group of the Exome Sequencing Project, National Heart ... New England Journal of Medicine 371 (1), 22-31, 2014 | 840 | 2014 |
| Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, P Angelica Merlini, ... Nature 518 (7537), 102-106, 2015 | 763 | 2015 |
| Mapping the human genetic architecture of COVID-19 Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ... Nature 600 (7889), 472-477, 2021 | 744 | 2021 |
| Recessively inherited coagulation disorders PM Mannucci, S Duga, F Peyvandi Blood 104 (5), 1243-1252, 2004 | 616 | 2004 |
| 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 | 466 | 2014 |
| ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy R Asselta, EM Paraboschi, A Mantovani, S Duga Aging (albany NY) 12 (11), 10087, 2020 | 460 | 2020 |
| 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 | 416 | 2014 |
| 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 | 400 | 2016 |
| 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 | 381 | 2014 |
| 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 | 369 | 2016 |
| Rare coagulation deficiencies F Peyvandi, S Duga, S Akhavan, PM Mannucci Haemophilia 8 (3), 308-321, 2002 | 314 | 2002 |
| 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 | 250 | 2017 |
| Rare coagulation disorders F Peyvandi, PM Mannucci Thrombosis and haemostasis 82 (10), 1207-1214, 1999 | 235 | 1999 |
| Phenotypic characterization of genetically lowered human lipoprotein (a) levels CA Emdin, AV Khera, P Natarajan, D Klarin, HH Won, GM Peloso, ... Journal of the American College of Cardiology 68 (25), 2761-2772, 2016 | 222 | 2016 |
| The molecular basis of quantitative fibrinogen disorders R Asselta, S Duga, ML Tenchini Journal of Thrombosis and Haemostasis 4 (10), 2115-2129, 2006 | 205 | 2006 |
| Genetic diagnosis of haemophilia and other inherited bleeding disorders F Peyvandi, G Jayandharan, M Chandy, A Srivastava, SM Nakaya, ... Haemophilia 12, 82-89, 2006 | 191 | 2006 |
| Congenital factor XI deficiency: an update S Duga, O Salomon seminars in thrombosis and hemostasis 39 (06), 621-631, 2013 | 187 | 2013 |
Rosanna AsseltaFull professor of Medical Genetics, Humanitas University & IRCCS Istituto Clinico Humanitas在 hunimed.eu 的电子邮件经过验证
