Rosanna Asselta
Rosanna Asselta
Associate professor of Medical Genetics, Humanitas University & IRCCS Istituto Clinico Humanitas
Geverifieerd e-mailadres voor hunimed.eu
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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
11382009
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
7862020
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
5782014
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
5662015
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
3732014
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
2962014
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
2831998
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
2812016
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
1982016
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
TMPRSS2, 2020
1762020
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
1632017
The molecular basis of quantitative fibrinogen disorders
R Asselta, S Duga, ML Tenchini
Journal of Thrombosis and Haemostasis 4 (10), 2115-2129, 2006
1632006
Genetic diagnosis of haemophilia and other inherited bleeding disorders
F Peyvandi, G Jayandharan, M Chandy, A Srivastava, SM Nakaya, ...
Haemophilia 12, 82-89, 2006
1562006
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
1502000
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
1382000
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
1202016
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
1172013
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
1112020
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
1092017
Factor V deficiency
R Asselta, F Peyvandi
Thieme 35 (4), 382-389, 2009
1022009
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Artikelen 1–20