| 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 | 1846 | 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 | 1288 | 2009 |
| 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 | 823 | 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 | 759 | 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 | 712 | 2021 |
| 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 | 464 | 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 | 458 | 2020 |
| 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 | 395 | 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 | 377 | 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 | 363 | 2016 |
| Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome. A Oldani, M Zucconi, R Asselta, M Modugno, MT Bonati, L Dalpra, ... Brain: a journal of neurology 121 (2), 205-223, 1998 | 305 | 1998 |
| ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population E Benetti, R Tita, O Spiga, A Ciolfi, G Birolo, A Bruselles, G Doddato, ... European Journal of Human Genetics 28 (11), 1602-1614, 2020 | 268 | 2020 |
| 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 | 245 | 2017 |
| 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 | 216 | 2016 |
| The molecular basis of quantitative fibrinogen disorders R Asselta, S Duga, ML Tenchini Journal of Thrombosis and Haemostasis 4 (10), 2115-2129, 2006 | 201 | 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 |
| Phase behavior and critical activated dynamics of limited-valence DNA nanostars S Biffi, R Cerbino, F Bomboi, EM Paraboschi, R Asselta, F Sciortino, ... Proceedings of the National Academy of Sciences 110 (39), 15633-15637, 2013 | 189 | 2013 |
| Association of rare and common variation in the lipoprotein lipase gene with coronary artery disease AV Khera, HH Won, GM Peloso, C O’Dushlaine, D Liu, NO Stitziel, ... Jama 317 (9), 937-946, 2017 | 176 | 2017 |
| Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry AJ Lee, Y Wang, RN Alcalay, H Mejia‐Santana, R Saunders‐Pullman, ... Movement Disorders 32 (10), 1432-1438, 2017 | 155 | 2017 |
| 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 | 152 | 2000 |
Stefano DugaFull professor of Molecular Biology, Humanitas University, IRCCS Istituto Clinico HumanitasVerified email at hunimed.eu
