Rosanna Asselta
Rosanna Asselta
Humanitas University
Email verificata su hunimed.eu
Titolo
Citata da
Citata da
Anno
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
10992009
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
5252014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, PA Merlini, A Kiezun, ...
Nature 518 (7537), 102-106, 2015
5102015
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
3482014
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
2821998
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
2662014
Genomewide association study of severe Covid-19 with respiratory failure
D Ellinghaus, F Degenhardt, L Bujanda, M Buti, A Albillos, P Invernizzi, ...
The New England journal of medicine, 2020
2232020
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
1572016
The molecular basis of quantitative fibrinogen disorders
R Asselta, S Duga, ML Tenchini
Journal of Thrombosis and Haemostasis 4 (10), 2115-2129, 2006
1502006
Genetic diagnosis of haemophilia and other inherited bleeding disorders
F Peyvandi, G Jayandharan, M Chandy, A Srivastava, SM Nakaya, ...
Haemophilia 12, 82-89, 2006
1472006
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
1462000
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
1392017
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
1342000
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
1072013
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
992016
Inherited defects of coagulation factor V: the hemorrhagic side
R Asselta, ML Tenchini, S Duga
Journal of Thrombosis and Haemostasis 4 (1), 26-34, 2006
992006
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies
TL Assimes, H Hólm, S Kathiresan, MP Reilly, G Thorleifsson, BF Voight, ...
Journal of the American College of Cardiology 56 (19), 1552-1563, 2010
982010
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
972016
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients
EM Paraboschi, G Soldà, D Gemmati, E Orioli, G Zeri, MD Benedetti, ...
International journal of molecular sciences 12 (12), 8695-8712, 2011
932011
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs
R Asselta, S Duga, S Spena, E Santagostino, F Peyvandi, G Piseddu, ...
Blood, The Journal of the American Society of Hematology 98 (13), 3685-3692, 2001
932001
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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