Rosanna Asselta
Rosanna Asselta
Humanitas University
Verified email at hunimed.eu
TitleCited byYear
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
S Kathiresan, BF Voight, S Purcell, K Musunuru, D Ardissino, ...
Nature genetics 41 (3), 334-341, 2009
8822009
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, 2015
3982015
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
2922014
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
2581998
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
2272014
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
1792009
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
1312000
Genetic diagnosis of haemophilia and other inherited bleeding disorders
F Peyvandi, G Jayandharan, M Chandy, A Srivastava, SM Nakaya, ...
Haemophilia 12, 82-89, 2006
1292006
The molecular basis of quantitative fibrinogen disorders
R Asselta, S Duga, ML Tenchini
Journal of Thrombosis and Haemostasis 4 (10), 2115-2129, 2006
1282006
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 95 (4), 1336-1341, 2000
1282000
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies
TL Assimes, H Hˇlm, S Kathiresan, MP Reilly, G Thorleifsson, BF Voight, ...
Journal of the American College of Cardiology 56 (19), 1552-1563, 2010
952010
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
902017
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 98 (13), 3685-3692, 2001
882001
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
862016
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
852006
Factor V deficiency
R Asselta, F Peyvandi
Seminars in thrombosis and hemostasis 35 (04), 382-389, 2009
832009
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
812013
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing
G Solda, M Robusto, P Primignani, P Castorina, E Benzoni, A Cesarani, ...
Human molecular genetics 21 (3), 577-585, 2011
772011
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients
EM Paraboschi, G SoldÓ, D Gemmati, E Orioli, G Zeri, MD Benedetti, ...
International journal of molecular sciences 12 (12), 8695-8712, 2011
742011
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
672016
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