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 | 1946 | 2020 |
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 | 726 | 2021 |
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 | 461 | 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 | 193 | 2013 |
Severe Covid-19 GWAS Group. Genomewide association study of severe Covid-19 with respiratory failure D Ellinghaus, F Degenhardt, L Bujanda, M Buti, A Albillos, P Invernizzi, ... N Engl j Med 383 (16), 1522-1534, 2020 | 135 | 2020 |
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 | 121 | 2017 |
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 | 117 | 2011 |
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules M Stravalaci, I Pagani, EM Paraboschi, M Pedotti, A Doni, F Scavello, ... Nature immunology 23 (2), 275-286, 2022 | 110 | 2022 |
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 Soldà, R Asselta International journal of molecular sciences 18 (3), 576, 2017 | 97 | 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), 6424, 2015 | 75 | 2015 |
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 | 75 | 2012 |
Detailed stratified GWAS analysis for severe COVID-19 in four European populations F Degenhardt, D Ellinghaus, S Juzenas, J Lerga-Jaso, M Wendorff, ... Human molecular genetics 31 (23), 3945-3966, 2022 | 68* | 2022 |
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 Soldà, C Cantoni, D Supino, L Piccio, ... Human molecular genetics 28 (9), 1414-1428, 2019 | 64 | 2019 |
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 | 52 | 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 | 50 | 2018 |
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 | 46 | 2017 |
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 | 44 | 2018 |
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion F Marasca, S Sinha, R Vadalà, B Polimeni, V Ranzani, EM Paraboschi, ... Nature Genetics 54 (2), 180-193, 2022 | 41 | 2022 |
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 | 36 | 2014 |
X chromosome contribution to the genetic architecture of primary biliary cholangitis R Asselta, EM Paraboschi, A Gerussi, HJ Cordell, GF Mells, RN Sandford, ... Gastroenterology 160 (7), 2483-2495. e26, 2021 | 35 | 2021 |