MANGANO, ELEONORA
MANGANO, ELEONORA
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes
2024 V. Tritto, P. Bettinaglio, E. Mangano, C. Cesaretti, F. Marasca, C. Castronovo, R. Bordoni, C. Battaglia, V. Saletti, V. Ranzani, B. Bodega, M. Eoli, F. Natacci, P. Riva
New insights into the molecular basis of spinal neurofibromatosis type 1
2023 P. Bettinaglio, E. Mangano, V. Tritto, R. Bordoni, R. Paterra, A. Borghi, M. Volontè, C. Battaglia, V. Saletti, C. Cesaretti, F. Natacci, M.A.B. Melone, M. Eoli, P. Riva
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
2023 R. Paterra, P. Bettinaglio, A. Borghi, E. Mangano, V. Tritto, C. Cesaretti, C. Schettino, R. Bordoni, C. Santoro, S. Avignone, M.E.M. Moscatelli, M. Anna Beatrice Melone, V. Saletti, G. Piluso, F. Natacci, P.V. Riva, M. Eoli
Next generation sequencing of pooled samples : guideline for variants' filtering
2016 S. Anand, E. Mangano, N. Barizzone, R. Bordoni, M. Sorosina, F. Clarelli, L. Corrado, F. Martinelli Boneschi, S. D'Alfonso, G. De Bellis
Whole-exome sequencing of primary plasma cell leukemia discloses heterogeneous mutational patterns
2015 I. Cifola, M. Lionetti, E. Pinatel, K. Todoerti, E. Mangano, A. Pietrelli, S. Fabris, L. Mosca, V. Simeon, M.T. Petrucci, F. Morabito, M. Offidani, F. Di Raimondo, A. Falcone, T. Caravita, C. Battaglia, G. De Bellis, A. Palumbo, P. Musto, A. Neri
Congenital Hyperinsulinism of Infancy (CHI) : hunt for new genes
2014 C. Battaglia, C. Cosentino, M. Proverbio, A. Pietrelli, E. Mangano, R. Bordoni, C. Perego, E. Di Cairano, A. Maggi, L. Tattini, G. De Bellis
Comprehensive genomic characterization of cutaneous malignant melanoma cell lines derived from metastatic lesions by whole-exome sequencing and SNP array profiling
2013 I. Cifola, A. Pietrelli, C. Consolandi, M. Severgnini, E. Mangano, V. Russo, G. De Bellis, C. Battaglia
Integrated genomics analysis of gene and miRNA expression profiles in clear cell renal carcinoma cell lines
2011 V. Tinaglia, I. Cifola, F. Frascati, E. Mangano, M. Biasolo, M.C. Proverbio, S. Bortoluzzi, V. Di Stefano, C. Bianchi, R. Perego, C. Battaglia
Integration of gene and miRNA expression profiles in clear cell renal carcinoma cell lines and relationship with VHL gene status
2010 C. Battaglia, V. Tinaglia, I. Cifola, F. Frascati, E. Mangano, M. Biasiolo, S. Bortoluzzi, S. Bombelli, C. Bianchi, R. Perego
Genomic profiling of chromosomal instability in renal carcinoma primary cultures and cell lines by SNP array technology
2009 E. Mangano
A computational procedure to identify significant overlap of differentially expressed and genomic imbalanced regions in cancer datasets
2009 S. Bicciato, R. Spinelli, M. Zampieri, E. Mangano, F. Ferrari, L. Beltrame, I. Cifola, C. Peano, A. Solari, C. Battaglia
Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography/CT in a patient carrying a novel mutation of the HADH gene
2009 S. Di Candia, A. Gessi, G. Pepe, P. Sogno Valin, E. Mangano, G. Chiumello, L. Gianolli, M.C. Proverbio, S. Mora
A computational procedure to identify significant overlap of differentially expressed and genomic imbalanced regions in cancer datasets
2008 S. Bicciato, R. Spinelli, E. Mangano, F. Ferrari, L. Beltrame, L. Zampieri, I. Cifola, C. Peano, C. Battaglia
Identification of significant overlap of differentially expressed and genomic imbalanced regions in cancer datasets
2008 F. Ferrari, R. Spinelli, E. Mangano, L. Beltrame, M. Zampieri, I. Cifola, C. Peano, S. Bicciato, C. Battaglia
A computational approach to identify whole genome homozygosity mapping across multiple SNP mapping experiments
2008 R. Spinelli, A. Gessi, M. Proverbio, E. Mangano, F. Ferrari, I. Cifola, M. Bardini, G. Cazzaniga, A. Salvatoni, C. Battaglia
Congenital hyperinsulinism of infancy (CHI) : clinical and metabolic evaluation, molecular analysis and phenotype correlation : Institution of the Italian National Registry
2008 M. Bove, P. Sogno Valin, S. Di Candia, I. Zamproni, S. Mora, M.C. Proverbio, E. Mangano, R. Spinelli, C. Battaglia, L. Bosio, M. Caruso, A. Salvatoni, G. Chiumello, A. Gessi
The first mutation in HADHSC gene in a Italian infant with congenital hyperinsulinism
2008 S. Di Candia, M. Bove, P. Sogno Valin, I. Zamproni, S. Mora, M.C. Proverbio, A. Gessi, E. Mangano, R. Spinelli, C. Battaglia, L. Bosio, M. Caruso, A. Salvatoni, G. Chiumello
Defect in β-oxidation SCHAD enzyme in familial congenital hyperinsulinism of infancy (CHI)
2008 A. Gessi, M.C. Proverbio, E. Mangano, R. Spinelli, M. Bove, P. Sogno Valin, S. Di Candia, I. Zamproni, S. Mora, L. Bosio, M. Caruso, A. Salvatoni, G. Chiumello, C. Battaglia
Homozygousity mapping of congenital hyperinsulinism of infancy (CHI) in Italian patients
2008 A. Gessi, M.C. Proverbio, E. Mangano, R. Spinelli, M. Bove, P. Sogno Valin, S. Di Candia, I. Zamproni, S. Mora, L. Bosio, M. Caruso, A. Salvatoni, G. Chiumello, C. Battaglia
Renal cell carcinoma primary cultures as in vitro model to study genomic profile of parental tumor tissues
2008 I. Cifola, C. Bianchi, E. Mangano, S. Bombelli, S. Ferrero, E. Fasoli, P. Brambilla, L. Beltrame, R. Perego, C. Battaglia