GeneBase 1.1: a tool to summarize data from NCBI gene datasets and its application to an update of human gene statistics

por Piovesan, Allison, Caracausi, Maria, Antonaros, Francesca, Pelleri, Maria Chiara, Vitale, Lorenza
Publicado 2016

Identification of minimal eukaryotic introns through GeneBase, a user-friendly tool for parsing the NCBI Gene databank

por Piovesan, Allison, Caracausi, Maria, Ricci, Marco, Strippoli, Pierluigi, Vitale, Lorenza, Pelleri, Maria Chiara
Publicado 2015

Systematic identification of human housekeeping genes possibly useful as references in gene expression studies

por Caracausi, Maria, Piovesan, Allison, Antonaros, Francesca, Strippoli, Pierluigi, Vitale, Lorenza, Pelleri, Maria Chiara
Publicado 2017

A molecular view of the normal human thyroid structure and function reconstructed from its reference transcriptome map

por Vitale, Lorenza, Piovesan, Allison, Antonaros, Francesca, Strippoli, Pierluigi, Pelleri, Maria Chiara, Caracausi, Maria
Publicado 2017

On the length, weight and GC content of the human genome

por Piovesan, Allison, Pelleri, Maria Chiara, Antonaros, Francesca, Strippoli, Pierluigi, Caracausi, Maria, Vitale, Lorenza
Publicado 2019

Dataset of differential gene expression between total normal human thyroid and histologically normal thyroid adjacent to papillary thyroid carcinoma

por Vitale, Lorenza, Piovesan, Allison, Antonaros, Francesca, Strippoli, Pierluigi, Pelleri, Maria Chiara, Caracausi, Maria
Publicado 2019

Human protein-coding genes and gene feature statistics in 2019

por Piovesan, Allison, Antonaros, Francesca, Vitale, Lorenza, Strippoli, Pierluigi, Pelleri, Maria Chiara, Caracausi, Maria
Publicado 2019

Reference quantitative transcriptome dataset for adult Caenorhabditis elegans

por Piovesan, Allison, Antonaros, Francesca, Strippoli, Pierluigi, Vitale, Lorenza, Pelleri, Maria Chiara, Caracausi, Maria
Publicado 2019

Integrated differential transcriptome maps of Acute Megakaryoblastic Leukemia (AMKL) in children with or without Down Syndrome (DS)

por Pelleri, Maria Chiara, Piovesan, Allison, Caracausi, Maria, Berardi, Anna Concetta, Vitale, Lorenza, Strippoli, Pierluigi
Publicado 2014

Integrated Quantitative Transcriptome Maps of Human Trisomy 21 Tissues and Cells

por Pelleri, Maria Chiara, Cattani, Chiara, Vitale, Lorenza, Antonaros, Francesca, Strippoli, Pierluigi, Locatelli, Chiara, Cocchi, Guido, Piovesan, Allison, Caracausi, Maria
Publicado 2018

Structural Characterization of the Highly Restricted Down Syndrome Critical Region on 21q22.13: New KCNJ6 and DSCR4 Transcript Isoforms

por Antonaros, Francesca, Pitocco, Margherita, Abete, Domenico, Vione, Beatrice, Piovesan, Allison, Vitale, Lorenza, Strippoli, Pierluigi, Caracausi, Maria, Pelleri, Maria Chiara
Publicado 2021

Complexity of Bidirectional Transcription and Alternative Splicing at Human RCAN3 Locus

por Facchin, Federica, Vitale, Lorenza, Bianconi, Eva, Piva, Francesco, Frabetti, Flavia, Strippoli, Pierluigi, Casadei, Raffaella, Pelleri, Maria Chiara, Piovesan, Allison, Canaider, Silvia
Publicado 2011

Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells

por Tan, Jennifer Y., Sirey, Tamara, Honti, Frantisek, Graham, Bryony, Piovesan, Allison, Merkenschlager, Matthias, Webber, Caleb, Ponting, Chris P., Marques, Ana C.
Publicado 2015

Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotype

por Pelleri, Maria Chiara, Cicchini, Elena, Locatelli, Chiara, Vitale, Lorenza, Caracausi, Maria, Piovesan, Allison, Rocca, Alessandro, Poletti, Giulia, Seri, Marco, Strippoli, Pierluigi, Cocchi, Guido
Publicado 2016

MTHFR C677T polymorphism analysis: A simple, effective restriction enzyme‐based method improving previous protocols

por Antonaros, Francesca, Olivucci, Giulia, Cicchini, Elena, Ramacieri, Giuseppe, Pelleri, Maria Chiara, Vitale, Lorenza, Strippoli, Pierluigi, Locatelli, Chiara, Cocchi, Guido, Piovesan, Allison, Caracausi, Maria
Publicado 2019

Machine learning based analysis for intellectual disability in Down syndrome

por Baldo, Federico, Piovesan, Allison, Rakvin, Marijana, Ramacieri, Giuseppe, Locatelli, Chiara, Lanfranchi, Silvia, Onnivello, Sara, Pulina, Francesca, Caracausi, Maria, Antonaros, Francesca, Lombardi, Michele, Pelleri, Maria Chiara
Publicado 2023

Partial trisomy 21 map: Ten cases further supporting the highly restricted Down syndrome critical region (HR‐DSCR) on human chromosome 21

por Pelleri, Maria Chiara, Cicchini, Elena, Petersen, Michael B., Tranebjærg, Lisbeth, Mattina, Teresa, Magini, Pamela, Antonaros, Francesca, Caracausi, Maria, Vitale, Lorenza, Locatelli, Chiara, Seri, Marco, Strippoli, Pierluigi, Piovesan, Allison, Cocchi, Guido
Publicado 2019

The transcriptome profile of human trisomy 21 blood cells

por Antonaros, Francesca, Zenatelli, Rossella, Guerri, Giulia, Bertelli, Matteo, Locatelli, Chiara, Vione, Beatrice, Catapano, Francesca, Gori, Alice, Vitale, Lorenza, Pelleri, Maria Chiara, Ramacieri, Giuseppe, Cocchi, Guido, Strippoli, Pierluigi, Caracausi, Maria, Piovesan, Allison
Publicado 2021

Partial trisomy 21 with or without highly restricted Down syndrome critical region (HR-DSCR): report of two new cases and reanalysis of the genotype–phenotype association

por Pelleri, Maria Chiara, Locatelli, Chiara, Mattina, Teresa, Bonaglia, Maria Clara, Piazza, Francesca, Magini, Pamela, Antonaros, Francesca, Ramacieri, Giuseppe, Vione, Beatrice, Vitale, Lorenza, Seri, Marco, Strippoli, Pierluigi, Cocchi, Guido, Piovesan, Allison, Caracausi, Maria
Publicado 2022

Plasma and urinary metabolomic profiles of Down syndrome correlate with alteration of mitochondrial metabolism

por Caracausi, Maria, Ghini, Veronica, Locatelli, Chiara, Mericio, Martina, Piovesan, Allison, Antonaros, Francesca, Pelleri, Maria Chiara, Vitale, Lorenza, Vacca, Rosa Anna, Bedetti, Federica, Mimmi, Maria Chiara, Luchinat, Claudio, Turano, Paola, Strippoli, Pierluigi, Cocchi, Guido
Publicado 2018