E. Mangano

发表

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

B. Giusti, R. Abbate, E. Bonora, 2013, Genome Biology.

Strategies for comparing gene expression profiles from different microarray platforms: application to a case-control experiment.

M. Severgnini, C. Peano, L. Milanesi, 2006, Analytical biochemistry.

INTEGRATED GENOMICS ANALYSIS OF GENE AND MICRORNA EXPRESSION PROFILES IN CLEAR CELL RENAL CARCINOMA CELL LINES

C. Battaglia, R. Perego, I. Cifola, 2011 .

Molecular Portrait of Clear Cell Renal Cell Carcinoma: An Integrative Analysis of Gene Expression and Genomic Copy Number Profiling

S. Bicciato, C. Battaglia, R. Perego, 2012 .

A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

M. Filippi, P. D. De Jager, V. Martinelli, 2022, Journal of Neurology.

A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

M. Filippi, P. D. De Jager, V. Martinelli, 2022, Journal of Neurology.

A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

M. Filippi, P. D. De Jager, V. Martinelli, 2022, Journal of Neurology.

Genetic Analysis of Italian Patients with Congenital Hyperinsulinism of Infancy

A. Salvatoni, C. Battaglia, S. Mora, 2013, Hormone Research in Paediatrics.

Whole-exome sequencing of primary plasma cell leukemia discloses heterogeneous mutational patterns

E. Pinatel, A. Neri, V. Simeon, 2015, Oncotarget.

A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort

C. Santoro, M. Eoli, C. Cesaretti, 2022, Cancers.

Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?

C. Battaglia, C. Gelfi, P. Riva, 2020, European Journal of Human Genetics.

Integrative transcriptomic and protein analysis of human bronchial BEAS-2B exposed to seasonal urban particulate matter.

E. Longhin, M. Camatini, C. Battaglia, 2016, Environmental pollution.

DNA copy-number abnormalities do not occur in infant ALL with t(4;11)/MLL-AF4

G. Basso, C. Battaglia, M. Giordan, 2010, Leukemia.

Major Action of Endogenous Lysyl Oxidase in Clear Cell Renal Cell Carcinoma Progression and Collagen Stiffness Revealed by Primary Cell Cultures.

C. Battaglia, G. Bovo, G. Strada, 2016, The American journal of pathology.

Next Generation Sequencing of Pooled Samples: Guideline for Variants’ Filtering

Roberta Bordoni, Lucia Corrado, Filippo Martinelli Boneschi, 2016, Scientific Reports.

Renal cell carcinoma primary cultures maintain genomic and phenotypic profile of parental tumor tissues

E. Fasoli, F. Magni, C. Battaglia, 2011, BMC Cancer.

The glucose and lipid metabolism reprogramming is grade-dependent in clear cell renal cell carcinoma primary cultures and is targetable to modulate cell viability and proliferation

R. Weiss, C. Battaglia, G. Bovo, 2017, Oncotarget.

Comprehensive Genomic Characterization of Cutaneous Malignant Melanoma Cell Lines Derived from Metastatic Lesions by Whole-Exome Sequencing and SNP Array Profiling

C. Consolandi, M. Severgnini, C. Battaglia, 2013, PloS one.

Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population

M. Filippi, V. Martinelli, G. Comi, 2022, Frontiers in Genetics.

Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility.

M. Filippi, U. Dianzani, V. Martinelli, 2021, Journal of genetics and genomics = Yi chuan xue bao.

Whole Genome SNP Genotyping and Exome Sequencing Reveal Novel Genetic Variants and Putative Causative Genes in Congenital Hyperinsulinism

A. Salvatoni, C. Battaglia, G. De Bellis, 2013, PloS one.

Health Risk Assessment for Air Pollutants: Alterations in Lung and Cardiac Gene Expression in Mice Exposed to Milano Winter Fine Particulate Matter (PM2.5)

Cristina Battaglia, Paride Mantecca, Marina Camatini, 2014, PloS one.

Gene expression profiling of A549 cells exposed to Milan PM2.5.

M. Mattioli, E. Longhin, M. Camatini, 2012, Toxicology letters.

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.

L. Gianolli, S. Mora, G. Chiumello, 2009, European journal of endocrinology.

PET/CT in a patient carrying a novel mutation of the HADH gene

S. Mora, G. Chiumello, E. Mangano, 2009 .

INTEGRATE: Model-based multi-omics data integration to characterize multi-level metabolic regulation

L. Alberghina, C. Consolandi, D. Pescini, 2021, bioRxiv.

A Census of Tandemly Repeated Polymorphic Loci in Genic Regions Through the Comparative Integration of Human Genome Assemblies

Sandra D'Alfonso, Giovanni Manzini, Marco Pellegrini, 2018, Front. Genet..

A reliable strategy for single-cell RNA sequencing analysis using cryoconserved primary cortical cells

C. Consolandi, M. Miano, E. Mangano, 2020, Journal of Neuroscience Methods.

New insights into the molecular basis of spinal neurofibromatosis type 1

M. Eoli, C. Cesaretti, F. Natacci, 2023, European Journal of Human Genetics.

The Genome-Wide Impact of Nipblb Loss-of-Function on Zebrafish Gene Expression

C. Consolandi, S. Bicciato, M. Mazzola, 2020, International journal of molecular sciences.

Insights on the molecular mechanisms of cytotoxicity induced by AS1411 linked to folate-functionalized DNA nanocages in cancer cells.

C. Consolandi, M. Severgnini, S. Biocca, 2023, Nanomedicine : nanotechnology, biology, and medicine.

Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes

M. Eoli, C. Cesaretti, F. Natacci, 2024, Human genetics.