Elvezia Paraboschi
Elvezia Paraboschi
Humanitas University
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Geciteerd door
Geciteerd door
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
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
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
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients
EM Paraboschi, G Soldą, D Gemmati, E Orioli, G Zeri, MD Benedetti, ...
International journal of molecular sciences 12 (12), 8695-8712, 2011
A frequent oligogenic involvement in congenital hypothyroidism
T de Filippis, G Gelmini, E Paraboschi, MC Vigone, M Di Frenna, F Marelli, ...
Human Molecular Genetics 26 (13), 2507-2514, 2017
Notch1 regulates chemotaxis and proliferation by controlling the CC‐chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia
L Mirandola, M Chiriva‐Internati, D Montagna, F Locatelli, M Zecca, ...
The Journal of pathology 226 (5), 713-722, 2012
The characterization of GSDMB splicing and backsplicing profiles identifies novel isoforms and a circular RNA that are dysregulated in multiple sclerosis
G Cardamone, EM Paraboschi, V Rimoldi, S Duga, G Soldą, R Asselta
International journal of molecular sciences 18 (3), 576, 2017
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering
TP Fraccia, GP Smith, G Zanchetta, E Paraboschi, Y Yi, DM Walba, ...
Nature communications 6 (1), 1-8, 2015
Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis
G Cardamone, EM Paraboschi, G Soldą, C Cantoni, D Supino, L Piccio, ...
Human molecular genetics 28 (9), 1414-1428, 2019
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis
EM Paraboschi, V Rimoldi, G Solda, T Tabaglio, C Dall'Osso, E Saba, ...
Human molecular genetics 23 (25), 6746-6761, 2014
Exploring the global landscape of genetic variation in coagulation factor XI deficiency
R Asselta, EM Paraboschi, V Rimoldi, M Menegatti, F Peyvandi, ...
Blood, The Journal of the American Society of Hematology 130 (4), e1-e6, 2017
Fibrinogen as a pleiotropic protein causing human diseases: the mutational burden of Aα, Bβ, and γ chains
EM Paraboschi, S Duga, R Asselta
International journal of molecular sciences 18 (12), 2711, 2017
Nonenzymatic polymerization into long linear RNA templated by liquid crystal self-assembly
M Todisco, TP Fraccia, GP Smith, A Corno, L Bethge, S Klussmann, ...
ACS nano 12 (10), 9750-9762, 2018
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases
V Tisato, G Zuliani, M Vigliano, G Longo, E Franchini, P Secchiero, ...
PloS one 13 (3), e0193867, 2018
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis
R Cagliani, M Fumagalli, FR Guerini, S Riva, D Galimberti, GP Comi, ...
Human genetics 131 (1), 87-97, 2012
Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern
C Dall'Osso, I Guella, S Duga, N Locatelli, EM Paraboschi, M Spreafico, ...
haematologica 93 (10), 1505-1513, 2008
Meta-analysis of multiple sclerosis microarray data reveals dysregulation in RNA splicing regulatory genes
EM Paraboschi, G Cardamone, V Rimoldi, D Gemmati, M Spreafico, ...
International journal of molecular sciences 16 (10), 23463-23481, 2015
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women
E Biguzzi, F Franchi, B Acaia, W Ossola, U Nava, EM Paraboschi, ...
Haemophilia 20 (6), e377-e383, 2014
Newtonian to non-newtonian fluid transition of a model transient network
G Nava, T Yang, V Vitali, P Minzioni, I Cristiani, F Bragheri, R Osellame, ...
Soft matter 14 (17), 3288-3295, 2018
Interpreting non-coding genetic variation in multiple sclerosis genome-wide associated regions
EM Paraboschi, G Cardamone, G Soldą, S Duga, R Asselta
Frontiers in genetics 9, 647, 2018
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