| A dynamic balance between gene activation and repression regulates the shade avoidance response in Arabidopsis G Sessa, M Carabelli, M Sassi, A Ciolfi, M Possenti, F Mittempergher, ... Genes & development 19 (23), 2811-2815, 2005 | 277 | 2005 |
| 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 | 268 | 2020 |
| Canopy shade causes a rapid and transient arrest in leaf development through auxin-induced cytokinin oxidase activity M Carabelli, M Possenti, G Sessa, A Ciolfi, M Sassi, G Morelli, I Ruberti Genes & development 21 (15), 1863-1868, 2007 | 233 | 2007 |
| Plant adaptation to dynamically changing environment: the shade avoidance response I Ruberti, G Sessa, A Ciolfi, M Possenti, M Carabelli, G Morelli Biotechnology advances 30 (5), 1047-1058, 2012 | 223 | 2012 |
| Evaluation of DNA methylation episignatures for diagnosis and phenotype correlations in 42 Mendelian neurodevelopmental disorders E Aref-Eshghi, J Kerkhof, VP Pedro, M Barat-Houari, N Ruiz-Pallares, ... The American Journal of Human Genetics 106 (3), 356-370, 2020 | 204 | 2020 |
| Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome F Kortüm, V Caputo, CK Bauer, L Stella, A Ciolfi, M Alawi, G Bocchinfuso, ... Nature genetics 47 (6), 661-667, 2015 | 204 | 2015 |
| A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function MT Lam, S Coppola, OHF Krumbach, G Prencipe, A Insalaco, C Cifaldi, ... Journal of Experimental Medicine 216 (12), 2778-2799, 2019 | 161 | 2019 |
| The Arabidopsis homeodomain-leucine zipper II gene family: diversity and redundancy AR Ciarbelli, A Ciolfi, S Salvucci, V Ruzza, M Possenti, M Carabelli, ... Plant molecular biology 68, 465-478, 2008 | 150 | 2008 |
| Modeling medulloblastoma in vivo and with human cerebellar organoids C Ballabio, M Anderle, M Gianesello, C Lago, E Miele, M Cardano, ... Nature communications 11 (1), 583, 2020 | 125 | 2020 |
| Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases L Grassi, R Alfonsi, F Francescangeli, M Signore, ML De Angelis, ... Cell death & disease 10 (3), 201, 2019 | 123 | 2019 |
| Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies M Niceta, E Stellacci, KW Gripp, G Zampino, M Kousi, M Anselmi, ... The American Journal of Human Genetics 96 (5), 816-825, 2015 | 123 | 2015 |
| Integrin α7 is a functional marker and potential therapeutic target in glioblastoma TL Haas, MR Sciuto, L Brunetto, C Valvo, M Signore, ME Fiori, ... Cell stem cell 21 (1), 35-50. e9, 2017 | 112 | 2017 |
| Dynamics of the shade-avoidance response in Arabidopsis A Ciolfi, G Sessa, M Sassi, M Possenti, S Salvucci, M Carabelli, G Morelli, ... Plant physiology 163 (1), 331-353, 2013 | 111 | 2013 |
| Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders MA Levy, H McConkey, J Kerkhof, M Barat-Houari, S Bargiacchi, ... Human Genetics and Genomics Advances 3 (1), 2022 | 99 | 2022 |
| Mutations in ZBTB20 cause Primrose syndrome V Cordeddu, B Redeker, E Stellacci, A Jongejan, A Fragale, TEJ Bradley, ... Nature genetics 46 (8), 815-817, 2014 | 99 | 2014 |
| A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome. V Caputo, L Cianetti, M Niceta, C Carta, A Ciolfi, G Bocchinfuso, E Carrani, ... American journal of human genetics 90 (1), 161, 2012 | 92 | 2012 |
| Mutations in KCNK4 that affect gating cause a recognizable neurodevelopmental syndrome CK Bauer, P Calligari, FC Radio, V Caputo, ML Dentici, N Falah, F High, ... The American Journal of Human Genetics 103 (4), 621-630, 2018 | 88 | 2018 |
| Activating mutations affecting the Dbl homology domain of SOS2 cause Noonan syndrome V Cordeddu, JC Yin, C Gunnarsson, C Virtanen, S Drunat, F Lepri, ... Human mutation 36 (11), 1080-1087, 2015 | 86 | 2015 |
| Biallelic mutations in TBCD, encoding the tubulin folding cofactor D, perturb microtubule dynamics and cause early-onset encephalopathy E Flex, M Niceta, S Cecchetti, I Thiffault, MG Au, A Capuano, E Piermarini, ... The American Journal of Human Genetics 99 (4), 962-973, 2016 | 79 | 2016 |
| Enhanced MAPK1 function causes a neurodevelopmental disorder within the RASopathy clinical spectrum M Motta, L Pannone, F Pantaleoni, G Bocchinfuso, FC Radio, S Cecchetti, ... The American Journal of Human Genetics 107 (3), 499-513, 2020 | 68 | 2020 |
