| Genetic mechanisms of critical illness in COVID-19 E Pairo-Castineira, S Clohisey, L Klaric, AD Bretherick, K Rawlik, D Pasko, ... Nature 591 (7848), 92-98, 2021 | 1299 | 2021 |
| 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 | 716 | 2021 |
| 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 | 328 | 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 | 309 | 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 | 269 | 2020 |
| Whole-genome sequencing reveals host factors underlying critical COVID-19 A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ... Nature 607 (7917), 97-103, 2022 | 220 | 2022 |
| 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 | 191 | 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, 2021 | 171 | 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 | 135 | 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 | 121 | 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 | 118 | 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 | 95 | 2010 |
| 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 |
| Diagnosis and management of congenital dyserythropoietic anemias A Gambale, A Iolascon, I Andolfo, R Russo Expert review of hematology 9 (3), 283-296, 2016 | 91 | 2016 |
| Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach A Iolascon, MR Esposito, R Russo haematologica 97 (12), 1786, 2012 | 90 | 2012 |
achille iolasconAffiliazione Dept of Molecular Medicine and Medical BiotechnologyVerified email at unina.it
