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Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1 I Andolfo, SL Alper, L De Franceschi, C Auriemma, R Russo, L De Falco, ... Blood, The Journal of the American Society of Hematology 121 (19), 3925-3935, 2013 | 329 | 2013 |
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II K Schwarz, A Iolascon, F Verissimo, NS Trede, W Horsley, W Chen, ... Nature genetics 41 (8), 936-940, 2009 | 312 | 2009 |
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 | 271 | 2020 |
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Suppressor of cytokine signaling 3 (SOCS3) expression and hepatitis C virus–related chronic hepatitis: insulin resistance and response to antiviral therapy M Persico, M Capasso, E Persico, M Svelto, R Russo, D Spano, L Croce, ... Hepatology 46 (4), 1009-1015, 2007 | 202 | 2007 |
New insights on hereditary erythrocyte membrane defects I Andolfo, R Russo, A Gambale, A Iolascon Haematologica 101 (11), 1284, 2016 | 196 | 2016 |
Recommendations regarding splenectomy in hereditary hemolytic anemias A Iolascon, I Andolfo, W Barcellini, F Corcione, L Garçon, L De Franceschi, ... haematologica 102 (8), 1304, 2017 | 194 | 2017 |
Association of Toll-like receptor 7 variants with life-threatening COVID-19 disease in males: findings from a nested case-control study C Fallerini, S Daga, S Mantovani, E Benetti, N Picchiotti, D Francisci, ... elife 10, e67569, 2021 | 175 | 2021 |
Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias R Russo, I Andolfo, F Manna, A Gambale, R Marra, BE Rosato, P Caforio, ... American journal of hematology 93 (5), 672-682, 2018 | 139 | 2018 |
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on … M Capasso, SJ Diskin, F Totaro, L Longo, MD Mariano, R Russo, ... Carcinogenesis 34 (3), 605-611, 2013 | 122 | 2013 |
Dysregulation of lipid metabolism and pathological inflammation in patients with COVID-19 M Caterino, M Gelzo, S Sol, R Fedele, A Annunziata, C Calabrese, ... Scientific reports 11 (1), 2941, 2021 | 120 | 2021 |
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis) I Andolfo, R Russo, F Manna, BE Shmukler, A Gambale, G Vitiello, ... American journal of hematology 90 (10), 921-926, 2015 | 97 | 2015 |
Galectin-1 and its involvement in hepatocellular carcinoma aggressiveness D Spano, R Russo, V Di Maso, N Rosso, LM Terracciano, M Roncalli, ... Molecular Medicine 16, 102-115, 2010 | 97 | 2010 |
Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells I Andolfo, L De Falco, R Asci, R Russo, S Colucci, M Gorrese, M Zollo, ... Haematologica 95 (8), 1244, 2010 | 96 | 2010 |
Diagnosis and management of congenital dyserythropoietic anemias A Gambale, A Iolascon, I Andolfo, R Russo Expert review of hematology 9 (3), 283-296, 2016 | 95 | 2016 |
Elevated expression and polymorphisms of SOCS3 influence patient response to antiviral therapy in chronic hepatitis C M Persico, M Capasso, R Russo, E Persico, L Croce, C Tiribelli, ... Gut 57 (4), 507-515, 2008 | 93 | 2008 |
A first update on mapping the human genetic architecture of COVID-19 Writing group lead Andrews Shea J. 6 Kanai Masahiro 3 Cordioli Mattia 7, ... Nature 608 (7921), E1-E10, 2022 | 92 | 2022 |
Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach A Iolascon, MR Esposito, R Russo haematologica 97 (12), 1786, 2012 | 92 | 2012 |