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

av Tattini Lorenzo, Torcini Alessandro, Olmi Simona
Publicerad 2011-07-01

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

av Torcini, Alessandro, Tattini, Lorenzo, Olmi, Simona
Publicerad 2011

Detection of Genomic Structural Variants from Next-Generation Sequencing Data

av Tattini, Lorenzo, D’Aurizio, Romina, Magi, Alberto
I publikationen Front Bioeng Biotechnol (2015)

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

av Magi, Alberto, Tattini, Lorenzo, Benelli, Matteo, Giusti, Betti, Abbate, Rosanna, Ruffo, Stefano
Publicerad 2012

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

av D'Aurizio, Romina, Pippucci, Tommaso, Tattini, Lorenzo, Giusti, Betti, Pellegrini, Marco, Magi, Alberto
I publikationen Nucleic Acids Res (2016)

Accurate Tracking of the Mutational Landscape of Diploid Hybrid Genomes

av Tattini, Lorenzo, Tellini, Nicolò, Mozzachiodi, Simone, D’Angiolo, Melania, Loeillet, Sophie, Nicolas, Alain, Liti, Gianni
I publikationen Mol Biol Evol (2019)

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

av Merello, Elisa, Tattini, Lorenzo, Magi, Alberto, Accogli, Andrea, Piatelli, Gianluca, Pavanello, Marco, Tortora, Domenico, Cama, Armando, Kibar, Zoha, Capra, Valeria, De Marco, Patrizia
I publikationen Eur J Hum Genet (2017)

Characterization and identification of hidden rare variants in the human genome

av Magi, Alberto, D’Aurizio, Romina, Palombo, Flavia, Cifola, Ingrid, Tattini, Lorenzo, Semeraro, Roberto, Pippucci, Tommaso, Giusti, Betti, Romeo, Giovanni, Abbate, Rosanna, Gensini, Gian Franco
I publikationen BMC Genomics (2015)

Genome-wide copy number analysis in pediatric glioblastoma multiforme

av 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
Publicerad 2014

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

av 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
Publicerad 2013

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

av 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
I publikationen Lancet Neurol (2015)