BRAF/NRAS mutation frequencies among primary tumors and metastases in patients with melanoma M Colombino, M Capone, A Lissia, A Cossu, C Rubino, V De Giorgi, ... Journal of Clinical Oncology 30, 2522-2529, 2012 | 553 | 2012 |
Fragile X syndrome without CCG amplification has an FMR1 deletion AK Gedeon, E Baker, H Robinson, MW Partington, B Gross, A Manca, ... Nature genetics 1 (5), 341-344, 1992 | 268 | 1992 |
A microdeletion of less than 250 kb, including the proximal part of the FMR-1 gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome D Wöhrle, D Kotzot, MC Hirst, A Manca, B Korn, A Schmidt, G Barbi, ... American journal of human genetics 51 (2), 299, 1992 | 201 | 1992 |
A microdeletion of less than 250 kb, including the proximal part of the FMR-1 gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome D Wöhrle, D Kotzot, MC Hirst, A Manca, B Korn, A Schmidt, G Barbi, ... American journal of human genetics 51 (2), 299, 1992 | 201 | 1992 |
Alternative splicing in the fragile X gene FMR1 AJMH Verkerk, E de Graaff, K De Boulle, EE Eichler, DS Konecki, ... Human molecular genetics 2 (4), 399-404, 1993 | 199 | 1993 |
A strategy for the selection of transcribed sequences in the Xq28 region B Korn, Z Sedlacek, A Manca, P Kioschis, D Konecki, H Lehrach, ... Human molecular genetics 1 (4), 235-242, 1992 | 185 | 1992 |
Enhanced expression of the murine FMR1 gene during germ cell proliferation suggests a special function in both the male and the female gonad D Bächner, A Manca, P Stelnbach, D Wöhrle, W Just, W Vogel, ... Human Molecular Genetics 2 (12), 2043-2050, 1993 | 149 | 1993 |
Multiple molecular pathways in melanomagenesis: characterization of therapeutic targets G Palmieri, MN Ombra, M Colombino, M Casula, MC Sini, A Manca, ... Frontiers in oncology 5, 183, 2015 | 118 | 2015 |
Identification of a novel candidate gene, CASC2, in a region of common allelic loss at chromosome 10q26 in human endometrial cancer P Baldinu, A Cossu, A Manca, MP Satta, MC Sini, C Rozzo, S Dessole, ... Human mutation 23 (4), 318-326, 2004 | 100 | 2004 |
Olfactory epithelium histopathological findings in long-term coronavirus disease 2019 related anosmia LA Vaira, C Hopkins, A Sandison, A Manca, N Machouchas, D Turilli, ... The Journal of Laryngology & Otology 134 (12), 1123-1127, 2020 | 84 | 2020 |
Molecular pathways in melanomagenesis: what we learned from next-generation sequencing approaches G Palmieri, M Colombino, M Casula, A Manca, M Mandalà, A Cossu, ... Current oncology reports 20, 1-16, 2018 | 67 | 2018 |
Analysis of candidate genes through a proteomics-based approach in primary cell lines from malignant melanomas and their metastases F Carta, PP Demuro, C Zanini, A Santona, D Castiglia, S D'Atri, ... Melanoma research 15 (4), 235-244, 2005 | 67 | 2005 |
BRAF Gene Is Somatically Mutated but Does Not Make a Major Contribution to Malignant Melanoma Susceptibility: The Italian Melanoma Intergroup Study M Casula, M Colombino, MP Satta, A Cossu, PA Ascierto, ... Journal of clinical oncology 22 (2), 286-292, 2004 | 65 | 2004 |
Prognostic impact of KRAS, NRAS, BRAF, and PIK3CA mutations in primary colorectal carcinomas: a population-based study G Palomba, V Doneddu, A Cossu, P Paliogiannis, A Manca, M Casula, ... Journal of translational medicine 14, 1-11, 2016 | 64 | 2016 |
Enhanced Fmr–1 expression in testis D Bächner, P Steinbach, D Wöhrle, W Just, W Vogel, H Hameister, ... Nature genetics 4 (2), 115-116, 1993 | 63 | 1993 |
Genetic alterations in main candidate genes during melanoma progression MC Sini, V Doneddu, P Paliogiannis, M Casula, M Colombino, A Manca, ... Oncotarget 9 (9), 8531, 2018 | 61 | 2018 |
Long non-coding RNA CASC2 in human cancer G Palmieri, P Paliogiannis, MC Sini, A Manca, G Palomba, V Doneddu, ... Critical Reviews in Oncology/Hematology 111, 31-38, 2017 | 61 | 2017 |
CASC2a gene is down-regulated in endometrial cancer P Baldinu, A Cossu, A Manca, MP Satta, MC Sini, G Palomba, S Dessole, ... Anticancer research 27 (1A), 235-243, 2007 | 59 | 2007 |
Molecular alterations at chromosome 9p21 in melanocytic naevi and melanoma MC Sini, A Manca, A Cossu, M Budroni, G Botti, PA Ascierto, F Cremona, ... British Journal of Dermatology 158 (2), 243-250, 2008 | 56 | 2008 |
Chromosomal abnormalities and microsatellite instability in sporadic endometrial cancer R Muresu, MC Sini, A Cossu, S Tore, P Baldinu, A Manca, M Pisano, ... European Journal of Cancer 38 (13), 1802-1809, 2002 | 55 | 2002 |