Stefano Duga

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Rosanna AsseltaFull professor of Medical Genetics, Humanitas University & IRCCS Istituto Clinico HumanitasEmail verificata su hunimed.eu
Giulia SoldàHumanitas UniversityEmail verificata su hunimed.eu
Flora PeyvandiUniversità degli Studi di MilanoEmail verificata su unimi.it
Elvezia ParaboschiHumanitas UniversityEmail verificata su hunimed.eu
Gianni PezzoliPresident Grigioni Foundation, Director Em. Parkinson Institute Milano ItalyEmail verificata su parkinson.it
Roberto CiliaFondazione IRCCS Istituto Neurologico Carlo BestaEmail verificata su istituto-besta.it
Letizia StranieroHumanitas UniversityEmail verificata su humanitasresearch.it
Alessio Di FonzoIRCCS Foundation Ca’ Granda Ospedale Maggiore Policlinico, Dino Ferrari CenterEmail verificata su policlinico.mi.it
Manuela PlateCentre for Inflammation and Tissue Repair - UCL Respiratory - UCLEmail verificata su ucl.ac.uk
Donato GemmatiUniversity of FerraraEmail verificata su unife.it
Massimo AureliUniversità degli Studi di MilanoEmail verificata su unimi.it
Luigi Ferini StrambiUniversità Vita-salute San RaffaeleEmail verificata su hsr.it
Sonia CacciaAssistant Professor of Molecular Biology, Dpt. of Biomedical and Clinical Sciences "L. SaccoEmail verificata su unimi.it
Massimo LazzeriHumanitas Clinical and Research Hospital - IRCCS - Rozzano (Milano)Email verificata su humanitas.it
Edoardo MonfriniUniversità degli Studi di Milano, Fondazione IRCCS Cà Granda Ospedale Maggiore PoliclinicoEmail verificata su unimi.it
Giorgio GuazzoniHumanitas UniversityEmail verificata su hunimed.eu
Alberto MantovaniDirettore Scientifico, Istituto Clinico Humanitas, Humanitas UniversityEmail verificata su humanitasresearch.it
Raimondo De CristofaroCatholic University School of MedicineEmail verificata su unicatt.it
Matt FarrerUniversity of FloridaEmail verificata su can.ubc.ca
Maurizio A. LeoneIRCCS Casa Sollievo della Sofferenza and Istituto "Mario Negri" IRCCSEmail verificata su iol.it

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Stefano Duga

Full professor of Molecular Biology, Humanitas University, IRCCS Istituto Clinico Humanitas

Email verificata su hunimed.eu - Home page

Post-transcriptional regulation of gene expression Human genetics Neurodegenerative disorders Myocardial infarction


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
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	1932	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
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	907	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	824	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	716	2021
Recessively inherited coagulation disorders PM Mannucci, S Duga, F Peyvandi Blood 104 (5), 1243-1252, 2004	608	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	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	459	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	411	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	397	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	378	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
Rare coagulation deficiencies F Peyvandi, S Duga, S Akhavan, PM Mannucci Haemophilia 8 (3), 308-321, 2002	309	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	245	2017
Rare coagulation disorders F Peyvandi, PM Mannucci Thrombosis and haemostasis 82 (10), 1207-1214, 1999	233	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	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	202	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	185	2013

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