| Glioblastoma chemoresistance: the double play by microenvironment and blood-brain barrier M Da Ros, V De Gregorio, AL Iorio, L Giunti, M Guidi, M De Martino, ... International journal of molecular sciences 19 (10), 2879, 2018 | 194 | 2018 |
| Cancer risk associated with STK11/LKB1 germline mutations in Peutz–Jeghers syndrome patients: Results of an Italian multicenter study N Resta, D Pierannunzio, GM Lenato, A Stella, R Capocaccia, R Bagnulo, ... Digestive and Liver Disease 45 (7), 606-611, 2013 | 172 | 2013 |
| The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis V Palazzo, A Provenzano, F Becherucci, G Sansavini, B Mazzinghi, ... Kidney international 91 (5), 1243-1255, 2017 | 118 | 2017 |
| Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppression S Giglio, A Provenzano, B Mazzinghi, F Becherucci, L Giunti, G Sansavini, ... Journal of the American Society of Nephrology 26 (1), 230-236, 2015 | 115 | 2015 |
| Plasmacytoid urothelial carcinoma of the urinary bladder: clinicopathologic, immunohistochemical, ultrastructural, and molecular analysis of a case series MR Raspollini, I Sardi, L Giunti, S Di Lollo, G Baroni, N Stomaci, ... Human pathology 42 (8), 1149-1158, 2011 | 70 | 2011 |
| Ruxolitinib is an effective treatment for CALR-positive patients with myelofibrosis. P Guglielmelli, G Rotunno, C Bogani, C Mannarelli, L Giunti, ... British journal of haematology 173 (6), 2016 | 59 | 2016 |
| Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome L Giunti, V Cetica, U Ricci, S Giglio, I Sardi, M Paglierani, E Andreucci, ... European journal of human genetics 17 (7), 919-927, 2009 | 52 | 2009 |
| Subtyping mtDNA haplogroup H by SNaPshot minisequencing and its application in forensic individual identification P Grignani, G Peloso, A Achilli, C Turchi, A Tagliabracci, M Alù, ... International Journal of Legal Medicine 120, 151-156, 2006 | 52 | 2006 |
| Embryonal tumor with abundant neuropil and true rosettes: morphological, immunohistochemical, ultrastructural and molecular study of a case showing features of … AM Buccoliero, F Castiglione, DR Degl'Innocenti, A Franchi, M Paglierani, ... Neuropathology 30 (1), 84-91, 2010 | 51 | 2010 |
| Pharmacological modulation of blood-brain barrier increases permeability of doxorubicin into the rat brain I Sardi, G la Marca, S Cardellicchio, L Giunti, S Malvagia, L Genitori, ... American journal of cancer research 3 (4), 424, 2013 | 48 | 2013 |
| Anti-miR21 oligonucleotide enhances chemosensitivity of T98G cell line to doxorubicin by inducing apoptosis L Giunti, M da Ros, S Vinci, S Gelmini, AL Iorio, AM Buccoliero, ... American journal of cancer research 5 (1), 231, 2015 | 46 | 2015 |
| Pediatric brain tumors: mutations of two dioxygenases (hABH2 and hABH3) that directly repair alkylation damage V Cetica, L Genitori, L Giunti, M Sanzo, G Bernini, M Massimino, I Sardi Journal of neuro-oncology 94, 195-201, 2009 | 40 | 2009 |
| Pediatric rhabdoid meningioma: a morphological, immunohistochemical, ultrastructural and molecular case study AM Buccoliero, F Castiglione, DR Degl'Innocenti, A Franchi, M Sanzo, ... Neuropathology 31 (1), 59-65, 2011 | 33 | 2011 |
| Delivery of doxorubicin across the blood–brain barrier by ondansetron pretreatment: a study in vitro and in vivo I Sardi, O Fantappiè, G la Marca, MG Giovannini, AL Iorio, M da Ros, ... Cancer letters 353 (2), 242-247, 2014 | 32 | 2014 |
| Infrared fluorescent automated detection of thirteen short tandem repeat polymorphisms and one gender‐determining system of the CODIS core system U Ricci, I Sani, S Guarducci, C Biondi, S Pelagatti, V Lazzerini, ... ELECTROPHORESIS: An International Journal 21 (17), 3564-3570, 2000 | 32 | 2000 |
| Therapeutic implications of novel mutations of the RFX6 gene associated with early-onset diabetes R Artuso, A Provenzano, B Mazzinghi, L Giunti, V Palazzo, E Andreucci, ... The pharmacogenomics journal 15 (1), 49-54, 2015 | 30 | 2015 |
| MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria F Crucianelli, R Tricarico, D Turchetti, G Gorelli, F Gensini, R Sestini, ... Epigenetics 9 (10), 1431-1438, 2014 | 28 | 2014 |
| Genome-wide copy number analysis in pediatric glioblastoma multiforme L Giunti, M Pantaleo, I Sardi, A Provenzano, A Magi, S Cardellicchio, ... American journal of cancer research 4 (3), 293, 2014 | 25 | 2014 |
| Double incompatibility at human alpha fibrinogen and penta E loci in paternity testing AL Nutini, A Mariottini, L Giunti, F Torricelli, U Ricci Croatian Medical Journal 44 (3), 342-346, 2003 | 25 | 2003 |
| Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation L Giunti, S Pelagatti, V Lazzerini, S Guarducci, E Lapi, S Coviello, ... Brain and Development 23, S242-S245, 2001 | 25 | 2001 |
