Stefano Duga

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Rosanna AsseltaFull professor of Medical Genetics, Humanitas University & IRCCS Istituto Clinico HumanitasDirección de correo verificada de hunimed.eu
Giulia SoldàHumanitas UniversityDirección de correo verificada de hunimed.eu
Flora PeyvandiUniversità degli Studi di MilanoDirección de correo verificada de unimi.it
Elvezia ParaboschiHumanitas UniversityDirección de correo verificada de hunimed.eu
Gianni PezzoliPresident Grigioni Foundation, Director Em. Parkinson Institute Milano ItalyDirección de correo verificada de parkinson.it
Letizia StranieroHumanitas UniversityDirección de correo verificada de humanitasresearch.it
Roberto CiliaFondazione IRCCS Istituto Neurologico Carlo BestaDirección de correo verificada de istituto-besta.it
Alessio Di FonzoIRCCS Foundation Ca’ Granda Ospedale Maggiore Policlinico, Dino Ferrari CenterDirección de correo verificada de policlinico.mi.it
Manuela PlateCentre for Inflammation and Tissue Repair - UCL Respiratory - UCLDirección de correo verificada de ucl.ac.uk
Massimo AureliUniversità degli Studi di MilanoDirección de correo verificada de unimi.it
Donato GemmatiUniversity of FerraraDirección de correo verificada de unife.it
Sonia CacciaAssistant Professor of Molecular Biology, Dpt. of Biomedical and Clinical Sciences "L. SaccoDirección de correo verificada de unimi.it
Luigi Ferini StrambiUniversità Vita-salute San RaffaeleDirección de correo verificada de hsr.it
Edoardo MonfriniUniversità degli Studi di Milano, Fondazione IRCCS Cà Granda Ospedale Maggiore PoliclinicoDirección de correo verificada de unimi.it
Massimo LazzeriHumanitas Clinical and Research Hospital - IRCCS - Rozzano (Milano)Dirección de correo verificada de humanitas.it
Giorgio GuazzoniHumanitas UniversityDirección de correo verificada de hunimed.eu
Alberto MantovaniDirettore Scientifico, Istituto Clinico Humanitas, Humanitas UniversityDirección de correo verificada de humanitasresearch.it
Raimondo De CristofaroCatholic University School of MedicineDirección de correo verificada de unicatt.it
Matt FarrerUniversity of FloridaDirección de correo verificada de can.ubc.ca
Maurizio A. LeoneIRCCS Casa Sollievo della Sofferenza and Istituto "Mario Negri" IRCCSDirección de correo verificada de iol.it

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Stefano Duga

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

Dirección de correo verificada de hunimed.eu - Página principal

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


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
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	2115	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	1319	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	973	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	866	2014
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	842	2021
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	785	2015
Recessively inherited coagulation disorders PM Mannucci, S Duga, F Peyvandi Blood 104 (5), 1243-1252, 2004	629	2004
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	484	2020
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	481	2014
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	451	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	418	2016
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	408	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	395	2014
Rare coagulation deficiencies F Peyvandi, S Duga, S Akhavan, PM Mannucci Haemophilia 8 (3), 308-321, 2002	318	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	263	2017
Rare coagulation disorders F Peyvandi, PM Mannucci Thrombosis and haemostasis 82 (10), 1207-1214, 1999	240	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	233	2016
The molecular basis of quantitative fibrinogen disorders R Asselta, S Duga, ML Tenchini Journal of Thrombosis and Haemostasis 4 (10), 2115-2129, 2006	212	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	204	2006
Congenital factor XI deficiency: an update S Duga, O Salomon seminars in thrombosis and hemostasis 39 (06), 621-631, 2013	200	2013

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