Oil Spill Identification and Monitoring from Sentinel-1 Sar Satellite Earth Observations: a Machine Learning Approach von Stefania Magrì, Tomaso Vairo, Andrea Reverberi, Bruno Fabiano

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Modelling rainfall-induced landslides at a regional scale, a machine learning based approach von Magrì, Stefania, Solimano, Monica, Delogu, Fabio, Del Giudice, Tania, Quagliati, Mauro, Cicoria, Michele, Silvestro, Francesco

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Application of machine learning techniques to derive sea water turbidity from Sentinel-2 imagery von Magrì, Stefania, Ottaviani, Ennio, Prampolini, Enrico, Besio, Giovanni, Fabiano, Bruno, Federici, Bianca

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Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48 von Magri, Stefania, Nanetti, Lorenzo, Gellera, Cinzia, Sarto, Elisa, Rizzo, Elena, Mongelli, Alessia, Ricci, Benedetta, Fancellu, Roberto, Sambati, Luisa, Cortelli, Pietro, Brusco, Alfredo, Bruzzone, Maria Grazia, Mariotti, Caterina, Di Bella, Daniela, Taroni, Franco

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Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28 von Taroni, Franco, Di Bella, Daniela, Lazzaro, Federico, Brusco, Alfredo, Plumari, Massimo, Battaglia, Giorgio, Pastore, Annalisa, Finardi, Adele, Cagnoli, Claudia, Tempia, Filippo, Frontali, Marina, Veneziano, Liana, Sacco, Tiziana, Boda, Enrica, Brussino, Alessandro, Bonn, Florian, Castellotti, Barbara, Baratta, Silvia, Mariotti, Caterina, Gellera, Cinzia, Fracasso, Valentina, Magri, Stefania, Langer, Thomas, Plevani, Paolo, Di Donato, Stefano, Muzi-Falconi, Marco

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A Dynamic Approach to Natech Risk Assessment Applied to an LPG Storage Facility in a Landslides Sensitive Italian Area von Tomaso Vairo, Stefania Magri, Gabriele Mercurio, Margherita Pettinato, Maria Bolla, Bruno Fabiano

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Understanding the Vulnerability of Complex Systems. An Integrated Approach von Tomaso Vairo, Agostino Bruzzone, Stefania Magri, Andrea P. Reverberi, Bruno Fabiano

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Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotype von Gatti, Marta, Magri, Stefania, Di Bella, Daniela, Sarto, Elisa, Taroni, Franco, Mariotti, Caterina, Nanetti, Lorenzo

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DNAJB2‐related Charcot‐Marie‐Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening von Saveri, Paola, Magri, Stefania, Maderna, Emanuela, Balistreri, Francesca, Lombardi, Raffaella, Ciano, Claudia, Moda, Fabio, Garavaglia, Barbara, Reale, Chiara, Lauria Pinter, Giuseppe, Taroni, Franco, Pareyson, Davide, Pisciotta, Chiara

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Hypomyelinating leukodystrophies in adults: Clinical and genetic features von Di Bella, Daniela, Magri, Stefania, Benzoni, Chiara, Farina, Laura, Maccagnano, Carmelo, Sarto, Elisa, Moscatelli, Marco, Baratta, Silvia, Ciano, Claudia, Piacentini, Sylvie H. M. J., Draghi, Lara, Mauro, Elena, Pareyson, Davide, Gellera, Cinzia, Taroni, Franco, Salsano, Ettore

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HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature von DiFrancesco, Jacopo C., Castellotti, Barbara, Milanesi, Raffaella, Ragona, Francesca, Freri, Elena, Canafoglia, Laura, Franceschetti, Silvana, Ferrarese, Carlo, Magri, Stefania, Taroni, Franco, Costa, Cinzia, Labate, Angelo, Gambardella, Antonio, Solazzi, Roberta, Binda, Anna, Rivolta, Ilaria, Di Gennaro, Giancarlo, Casciato, Sara, D’Incerti, Ludovico, Barbuti, Andrea, DiFrancesco, Dario, Granata, Tiziana, Gellera, Cinzia

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Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing von Almomani, Rowida, Marchi, Margherita, Sopacua, Maurice, Lindsey, Patrick, Salvi, Erika, Koning, Bart de, Santoro, Silvia, Magri, Stefania, Smeets, Hubert J M, Martinelli Boneschi, Filippo, Malik, Rayaz R, Ziegler, Dan, Hoeijmakers, Janneke G J, Bönhof, Gidon, Dib-Hajj, Sulayman, Waxman, Stephen G, Merkies, Ingemar S J, Lauria, Giuseppe, Faber, Catharina G, Gerrits, Monique M

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Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disorders von Cozzi, Marta, Magri, Stefania, Tedesco, Barbara, Patelli, Guglielmo, Ferrari, Veronica, Casarotto, Elena, Chierichetti, Marta, Pramaggiore, Paola, Cornaggia, Laura, Piccolella, Margherita, Galbiati, Mariarita, Rusmini, Paola, Crippa, Valeria, Mandrioli, Jessica, Pareyson, Davide, Pisciotta, Chiara, D’Arrigo, Stefano, Ratti, Antonia, Nanetti, Lorenzo, Mariotti, Caterina, Sarto, Elisa, Pensato, Viviana, Gellera, Cinzia, Di Bella, Daniela, Cristofani, Riccardo M., Taroni, Franco, Poletti, Angelo

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ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype von Nanetti, Lorenzo, Sarto, Elisa, Castaldo, Anna, Magri, Stefania, Mongelli, Alessia, Rossi Sebastiano, Davide, Canafoglia, Laura, Grisoli, Marina, Malaguti, Chiara, Rivieri, Francesca, D’Amico, Maria Chiara, Di Bella, Daniela, Franceschetti, Silvana, Mariotti, Caterina, Taroni, Franco

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Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian population von Mongelli, Alessia, Magri, Stefania, Salvatore, Elena, Rizzo, Elena, De Rosa, Anna, Fico, Tommasina, Gatti, Marta, Gellera, Cinzia, Taroni, Franco, Mariotti, Caterina, Nanetti, Lorenzo

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Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A gene von Santangelo, Serena, Bossolasco, Patrizia, Magri, Stefania, Colombrita, Claudia, Invernizzi, Sabrina, Gellera, Cinzia, Nanetti, Lorenzo, Di Bella, Daniela, Silani, Vincenzo, Taroni, Franco, Ratti, Antonia

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Hazardous Spray Release from a Pipeline under Maintenance: Causes and Lessons Learned by a Combined Accident Analysis Perspective von Tomaso Vairo, Stefania Magrì, Andrea P. Reverberi, Bruno Fabiano

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Multifaceted and Age-Dependent Phenotypes Associated With Biallelic PNPLA6 Gene Variants: Eight Novel Cases and Review of the Literature von Nanetti, Lorenzo, Di Bella, Daniela, Magri, Stefania, Fichera, Mario, Sarto, Elisa, Castaldo, Anna, Mongelli, Alessia, Baratta, Silvia, Fenu, Silvia, Moscatelli, Marco, Bonati, Maria Teresa, Martinuzzi, Andrea, Mariotti, Caterina, Taroni, Franco

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Correction: Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing von Almomani, Rowida, Marchi, Margherita, Sopacua, Maurice, Lindsey, Patrick, Salvi, Erika, de Koning, Bart, Santoro, Silvia, Magri, Stefania, Smeets, Hubert J M, Boneschi, Filippo Martinelli, Malik, Rayaz A, Ziegler, Dan, Hoeijmakers, Janneke G J, Bönhof, Gidon, Dib-Hajj, Sulayman, Waxman, Stephen G, Merkies, Ingemar S J, Lauria, Giuseppe, Faber, Catharina G, Gerrits, Monique M

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Next‐generation sequencing in pediatric‐onset epilepsies: Analysis with target panels and personalized therapeutic approach von Castellotti, Barbara, Ragona, Francesca, Freri, Elena, Messina, Giuliana, Magri, Stefania, Previtali, Roberto, Solazzi, Roberta, Franceschetti, Silvana, Taroni, Franco, Canafoglia, Laura, Gellera, Cinzia, Granata, Tiziana, DiFrancesco, Jacopo C.

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