R. Spinelli

发表

FusionAnalyser: a new graphical, event-driven tool for fusion rearrangements discovery

S. Redaelli, C. Gambacorti-Passerini, R. Piazza, 2012, Nucleic acids research.

Candidate Genes and MiRNAs Linked to the Inverse Relationship Between Cancer and Alzheimer’s Disease: Insights From Data Mining and Enrichment Analysis

Nithiya Jesuthasan, C. Battaglia, G. De Bellis, 2019, Front. Genet..

CEQer: A Graphical Tool for Copy Number and Allelic Imbalance Detection from Whole-Exome Sequencing Data

S. Redaelli, C. Gambacorti-Passerini, R. Piazza, 2013, PloS one.

A COMPUTATIONAL PROCEDURE FOR THE INTEGRATIVE ANALYSIS OF GENOMIC DATA AT THE SINGLE SAMPLE LEVEL

C. Peano, D. Basso, S. Bicciato, 2007 .

Gene expression signature of non-involved lung tissue associated with survival in lung adenocarcinoma patients.

Roberta Spinelli, Rocco Piazza, Federico Ambrogi, 2013, Carcinogenesis.

Read-through transcripts in normal human lung parenchyma are down-regulated in lung adenocarcinoma

T. Dragani, M. Incarbone, F. Colombo, 2016, Oncotarget.

Whole-Exome Sequencing Data – Identifying Somatic Mutations

A. Mogavero, C. Gambacorti-Passerini, R. Piazza, 2014 .

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

Roberta Spinelli, Rocco Piazza, Torsten Haferlach, 2012, Nature Genetics.

Erratum: OncoScore: a novel, Internet-based tool to assess the oncogenic potential of genes

Nitesh Sharma, Luca De Sano, Alessandra Pirola, 2017, Scientific Reports.

OncoScore: a novel, Internet-based tool to assess the oncogenic potential of genes

Luca De Sano, Alessandra Pirola, Daniele Ramazzotti, 2016, Scientific Reports.

Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases

Nitesh D. Sharma, S. Redaelli, C. Gambacorti-Passerini, 2013, Molecular genetics & genomic medicine.

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

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

Genome-wide screening of copy number alterations and LOH events in renal cell carcinomas and integration with gene expression profile

Stefano Ferrero, Roberta Spinelli, Paolo Mocarelli, 2008, Molecular Cancer.

Acquisition of different carbapenem resistance mechanisms by an epidemic clonal lineage of Pseudomonas aeruginosa.

G. Rossolini, R. Spinelli, V. Dubois, 2008, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

Recurrent ETNK1 mutations in atypical chronic myeloid leukemia.

P. Campbell, G. Bignell, M. Cazzola, 2015, Blood.

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.

Cell-mediated immunity in breast cancer patients.

P. Ferrari, A. Nicolini, A. Carpi, 1996, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Integrated Analysis of Whole-Exome Sequencing and Micrornas Expression in Blast Crisis Transformation of Chronic Myeloid Leukemia

Nitesh D. Sharma, D. Perrotti, C. Gambacorti-Passerini, 2012 .

A Bioinformatics Procedure to Identify and Annotate Somatic Mutations in Whole-Exome Sequencing Data

Roberta Spinelli, Rocco Piazza, Carlo Gambacorti Passerini, 2011, CIBB.

Locally Adaptive Statistical Procedures for the Integrative Analysis on Genomic and Transcriptional Data

Roberta Spinelli, Dario Basso, Silvio Bicciato, 2007, WILF.

Oncoscore, a Novel, Internet-Based Tool to Assess the Oncogenic Potential of Genes Can Differentiate Between CP-CML and BC-CML Associated Genes, and Between CP-CML Patients with Good and Bad Prognosis

Luca De Sano, Nitesh D. Sharma, C. Gambacorti-Passerini, 2016 .

Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases

Nitesh D. Sharma, S. Redaelli, C. Gambacorti-Passerini, 2013, Molecular genetics & genomic medicine.