| Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes B Lee, M Godfrey, E Vitale, H Hori, MG Mattei, M Sarfarazi, P Tsipouras, ... Nature 352 (6333), 330-334, 1991 | 860 | 1991 |
| Mapping, cloning and genetic characterization of the region containing the Wilson disease gene K Petrukhin, SG Fischer, M Pirastu, RE Tanzi, I Chernov, M Devoto, ... Nature genetics 5 (4), 338-343, 1993 | 622 | 1993 |
| Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5 P Tsipouras, R Del Mastro, M Sarfarazi, B Lee, E Vitale, AH Child, ... New England Journal of Medicine 326 (14), 905-909, 1992 | 297 | 1992 |
| Circulating levels of IL-1 family cytokines and receptors in Alzheimer’s disease: new markers of disease progression? P Italiani, I Puxeddu, S Napoletano, E Scala, D Melillo, S Manocchio, ... Journal of neuroinflammation 15, 1-12, 2018 | 137 | 2018 |
| Repating developmental expression of G-Hox 7, a novel homeobox-containing gene in the chicken HR Suzuki, BJ Padanilam, E Vitale, F Ramirez, M Solursh Developmental biology 148 (1), 375-388, 1991 | 129 | 1991 |
| Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study X Estivill, M Farrall, R Williamson, M Ferrari, M Seia, AM Giunta, G Novelli, ... American journal of human genetics 43 (1), 23, 1988 | 107 | 1988 |
| Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis. WA Horton, MA Machado, J Ellard, D Campbell, J Bartley, F Ramirez, ... Proceedings of the National Academy of Sciences 89 (10), 4583-4587, 1992 | 103 | 1992 |
| Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region. PW Kleyn, CH Wang, LL Lien, E Vitale, J Pan, BM Ross, A Grunn, ... Proceedings of the National Academy of Sciences 90 (14), 6801-6805, 1993 | 83 | 1993 |
| G to T transversion at position+ 5 of a splice donor site causes skipping of the preceding exon in the type III procollagen transcripts of a patient with Ehlers-Danlos syndrome … B Lee, E Vitale, A Superti-Furga, B Steinmann, F Ramirez Journal of Biological Chemistry 266 (8), 5256-5259, 1991 | 81 | 1991 |
| Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene. S Selig, S Bruno, JM Scharf, CH Wang, E Vitale, TC Gilliam, LM Kunkel Proceedings of the National Academy of Sciences 92 (9), 3702-3706, 1995 | 59 | 1995 |
| Genomic Cloning and Characterization of the Human Thrombin Receptor Gene: STRUCTURAL SIMILARITY TO THE PROTEINASE ACTIVATED RECEPTOR-2 GENE (∗) VA Schmidt, E Vitale, WF Bahou Journal of Biological Chemistry 271 (16), 9307-9312, 1996 | 51 | 1996 |
| Role of cytosolic calcium-dependent phospholipase A2 in Alzheimer's disease pathogenesis MT Gentile, MG Reccia, PP Sorrentino, E Vitale, G Sorrentino, AA Puca, ... Molecular neurobiology 45, 596-604, 2012 | 50 | 2012 |
| A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema‐distichiasis syndrome associated with renal disease and diabetes mellitus C Yildirim‐Toruner, K Subramanian, L El Manjra, E Chen, S Goldstein, ... American Journal of Medical Genetics Part A 131 (3), 281-286, 2004 | 50 | 2004 |
| Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations F Gianfrancesco, M Cannella, T Martino, V Maglione, T Esposito, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007 | 45 | 2007 |
| Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12 E Vitale, S Cook, R Sun, C Specchia, K Subramanian, M Rocchi, ... Human molecular genetics 11 (3), 295-300, 2002 | 45 | 2002 |
| Refinement of the spinal muscular atrophy locus by genetic and physical mapping CH Wang, PW Kleyn, E Vitale, BM Ross, L Lien, J Xu, TA Carter, ... American journal of human genetics 56 (1), 202, 1995 | 37 | 1995 |
| Effects of different light quality and biofertilizers on structural and physiological traits of spinach plants L Vitale, E Vitale, G Guercia, M Turano, C Arena Photosynthetica 58 (4), 932-943, 2020 | 34 | 2020 |
| Characterization of the human MSX-1 promoter and an enhancer responsible for retinoic acid induction. R Shen, Y Chen, L Huang, E Vitale, M Solursh Cellular & Molecular Biology Research 40 (4), 297-312, 1994 | 34 | 1994 |
| the International Marfan Syndrome Collaborative Study. Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes … P Tsipouras, R Del Mastro, M Sarfarazi, B Lee, E Vitale, AH Child, ... N Engl J Med 326 (14), 905-909, 1992 | 33 | 1992 |
| Suitability of Solanum lycopersicum L. ‘Microtom’ for growth in Bioregenerative Life Support Systems: exploring the effect of high‐LET ionising radiation on … C Arena, E Vitale, B Hay Mele, PR Cataletto, M Turano, P Simoniello, ... Plant Biology 21 (4), 615-626, 2019 | 32 | 2019 |
Enrico ParanoPrimo Ricercatore, Responsabile IRIB sede di Catania, Consiglio Nazionale delle Ricerche, CNRVerified email at cnr.it
