Coherent periodic activity in excitatory neural networks : the role of network connectivity

Por Tattini Lorenzo, Torcini Alessandro, Olmi Simona
Publicado em 2011-07-01

Coherent periodic activity in excitatory neural networks : the role of network connectivity

Por Torcini, Alessandro, Tattini, Lorenzo, Olmi, Simona
Publicado em 2011

Detection of Genomic Structural Variants from Next-Generation Sequencing Data

Por Tattini, Lorenzo, D’Aurizio, Romina, Magi, Alberto
Publicado no Front Bioeng Biotechnol (2015)

WNP: A Novel Algorithm for Gene Products Annotation from Weighted Functional Networks

Por Magi, Alberto, Tattini, Lorenzo, Benelli, Matteo, Giusti, Betti, Abbate, Rosanna, Ruffo, Stefano
Publicado em 2012

Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2

Por D'Aurizio, Romina, Pippucci, Tommaso, Tattini, Lorenzo, Giusti, Betti, Pellegrini, Marco, Magi, Alberto
Publicado no Nucleic Acids Res (2016)

Accurate Tracking of the Mutational Landscape of Diploid Hybrid Genomes

Por Tattini, Lorenzo, Tellini, Nicolò, Mozzachiodi, Simone, D’Angiolo, Melania, Loeillet, Sophie, Nicolas, Alain, Liti, Gianni
Publicado no Mol Biol Evol (2019)

Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial development

Por Merello, Elisa, Tattini, Lorenzo, Magi, Alberto, Accogli, Andrea, Piatelli, Gianluca, Pavanello, Marco, Tortora, Domenico, Cama, Armando, Kibar, Zoha, Capra, Valeria, De Marco, Patrizia
Publicado no Eur J Hum Genet (2017)

Characterization and identification of hidden rare variants in the human genome

Por Magi, Alberto, D’Aurizio, Romina, Palombo, Flavia, Cifola, Ingrid, Tattini, Lorenzo, Semeraro, Roberto, Pippucci, Tommaso, Giusti, Betti, Romeo, Giovanni, Abbate, Rosanna, Gensini, Gian Franco
Publicado no BMC Genomics (2015)

Genome-wide copy number analysis in pediatric glioblastoma multiforme

Por Giunti, Laura, Pantaleo, Marilena, Sardi, Iacopo, Provenzano, Aldesia, Magi, Alberto, Cardellicchio, Stefania, Castiglione, Francesca, Tattini, Lorenzo, Novara, Francesca, Buccoliero, Anna Maria, de Martino, Maurizio, Genitori, Lorenzo, Zuffardi, Orsetta, Giglio, Sabrina
Publicado em 2014

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

Por Magi, Alberto, Tattini, Lorenzo, Cifola, Ingrid, D’Aurizio, Romina, Benelli, Matteo, Mangano, Eleonora, Battaglia, Cristina, Bonora, Elena, Kurg, Ants, Seri, Marco, Magini, Pamela, Giusti, Betti, Romeo, Giovanni, Pippucci, Tommaso, Bellis, Gianluca De, Abbate, Rosanna, Gensini, Gian Franco
Publicado em 2013

Characterization of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next generation sequencing study

Por Mirzaa, Ghayda, Conti, Valerio, Timms, Andrew E., Smyser, Christopher D., Ahmed, Sarah, Carter, Melissa, Barnett, Sarah, Hufnagel, Robert B., Goldstein, Amy, Narumi-Kishimoto, Yoko, Olds, Carissa, Collins, Sarah, Johnston, Kathreen, Deleuze, Jean-François, Nitschké, Patrick, Friend, Kathryn, Harris, Catharine, Goetsch, Allison, Martin, Beth, Boyle, Evan August, Parrini, Elena, Mei, Davide, Tattini, Lorenzo, Slavotinek, Anne, Blair, Ed, Barnett, Christopher, Shendure, Jay, Chelly, Jamel, Dobyns, William B., Guerrini, Renzo
Publicado no Lancet Neurol (2015)