| Pharmacogenetic profiling in patients with advanced colorectal cancer treated with first-line FOLFOX-4 chemotherapy A Ruzzo, F Graziano, F Loupakis, E Rulli, E Canestrari, D Santini, ... Journal of clinical oncology 25 (10), 1247-1254, 2007 | 379 | 2007 |
| High Concordance of KRAS Status Between Primary Colorectal Tumors and Related Metastatic Sites: Implications for Clinical Practice D Santini, F Loupakis, B Vincenzi, I Floriani, I Stasi, E Canestrari, E Rulli, ... The oncologist 13 (12), 1270-1275, 2008 | 307 | 2008 |
| Pharmacogenetic profiling for cetuximab plus irinotecan therapy in patients with refractory advanced colorectal cancer F Graziano, A Ruzzo, F Loupakis, E Canestrari, D Santini, V Catalano, ... Journal of Clinical Oncology 26 (9), 1427-1434, 2008 | 153 | 2008 |
| Pharmacogenetic profiling in patients with advanced colorectal cancer treated with first-line FOLFIRI chemotherapy A Ruzzo, F Graziano, F Loupakis, D Santini, V Catalano, R Bisonni, ... The pharmacogenomics journal 8 (4), 278-288, 2008 | 129 | 2008 |
| Polymorphisms in genes involved in DNA repair and metabolism of xenobiotics in individual susceptibility to sporadic diffuse gastric cancer A Ruzzo, E Canestrari, P Maltese, F Pizzagalli, F Graziano, D Santini, ... Walter de Gruyter 45 (7), 822-828, 2007 | 76 | 2007 |
| VEGF gene polymorphisms and susceptibility to colorectal cancer disease in Italian population P Maltese, E Canestrari, A Ruzzo, F Graziano, A Falcone, F Loupakis, ... International journal of colorectal disease 24, 165-170, 2009 | 68 | 2009 |
| Molecular epidemiology in 591 Italian probands with nonsyndromic retinitis pigmentosa and usher syndrome L Colombo, PE Maltese, M Castori, S El Shamieh, C Zeitz, I Audo, ... Investigative Ophthalmology & Visual Science 62 (2), 13-13, 2021 | 55 | 2021 |
| Aldo-Keto Reductase 1C1 (AKR1C1) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema S Michelini, P Chiurazzi, V Marino, D Dell’Orco, E Manara, M Baglivo, ... International journal of molecular sciences 21 (17), 6264, 2020 | 48 | 2020 |
| Bacteriophages presence in nature and their role in the natural selection of bacterial populations Z Naureen, A Dautaj, K Anpilogov, G Camilleri, K Dhuli, B Tanzi, ... Acta Bio Medica: Atenei Parmensis 91 (Suppl 13), 2020 | 44 | 2020 |
| Glucocorticoid resistance in Crohn's disease and ulcerative colitis: an association study investigating GR and FKBP5 gene polymorphisms P Maltese, L Palma, C Sfara, P De Rocco, A Latiano, O Palmieri, ... The Pharmacogenomics Journal 12 (5), 432-438, 2012 | 44 | 2012 |
| Mutation profile of BBS genes in patients with Bardet–Biedl syndrome: An Italian study E Manara, S Paolacci, F D’Esposito, A Abeshi, L Ziccardi, B Falsini, ... Italian journal of pediatrics 45, 1-8, 2019 | 41 | 2019 |
| High resolution melting (HRM) analysis for the detection of ER22/23EK, BclI, and N363S polymorphisms of the glucocorticoid receptor gene P Maltese, E Canestrari, L Palma, A Ruzzo, F Corini, M Menotta, ... The Journal of Steroid Biochemistry and Molecular Biology 113 (3-5), 269-274, 2009 | 38 | 2009 |
| Liver-only metastatic colorectal cancer patients and thymidylate synthase polymorphisms for predicting response to 5-fluorouracil-based chemotherapy F Graziano, A Ruzzo, F Loupakis, D Santini, V Catalano, E Canestrari, ... British journal of cancer 99 (5), 716-721, 2008 | 36 | 2008 |
| Increasing evidence of hereditary lymphedema caused by CELSR1 loss‐of‐function variants PE Maltese, S Michelini, M Ricci, S Maitz, A Fiorentino, R Serrani, ... American Journal of Medical Genetics Part A 179 (9), 1718-1724, 2019 | 35 | 2019 |
| FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function D Tavian, S Missaglia, PE Maltese, S Michelini, A Fiorentino, M Ricci, ... Oncotarget 7 (34), 54228, 2016 | 34 | 2016 |
| A novel p.(Glu111Val) missense mutation in GUCA1A associated with cone-rod dystrophy leads to impaired calcium sensing and perturbed second messenger … V Marino, G Dal Cortivo, E Oppici, PE Maltese, F D’Esposito, E Manara, ... Human Molecular Genetics 27 (24), 4204-4217, 2018 | 32 | 2018 |
| Prevalence of mutations in LEP, LEPR, and MC4R genes in individuals with severe obesity B Paolini, PE Maltese, I Del Ciondolo, D Tavian, S Missaglia, C Ciuoli, ... Genet Mol Res 15 (3), 10, 2016 | 31 | 2016 |
| Endogastric capsule for E-cadherin gene (CDH1) promoter hypermethylation assessment in DNA from gastric juice of diffuse gastric cancer patients P Muretto, A Ruzzo, F Pizzagalli, F Graziano, P Maltese, C Zingaretti, ... Annals of oncology 19 (3), 516-519, 2008 | 31 | 2008 |
| Genetic screening in a large cohort of Italian patients affected by primary lymphedema using a next generation sequencing (NGS) approach S Michelini, A Vettori, PE Maltese, M Cardone, A Bruson, A Fiorentino, ... Lymphology 49 (2), 57-72, 2016 | 30 | 2016 |
| Variations in the interleukin-1 receptor antagonist gene impact on survival of patients with advanced colorectal cancer F Graziano, A Ruzzo, E Canestrari, F Loupakis, D Santini, E Rulli, ... The pharmacogenomics journal 9 (1), 78-84, 2009 | 27 | 2009 |
