Bayesian networks for probabilistic inference and decision analysis in forensic science

por Taroni, Franco
Publicado 2014

Reply to Budowle, Ge, Chakraborty and Gill-King: use of prior odds for missing persons identifications

por Biedermann, Alex, Taroni, Franco, Margot, Pierre
Publicado 2012

A Bayesian network approach to the database search problem in criminal proceedings

por Biedermann, Alex, Vuille, Joëlle, Taroni, Franco
Publicado 2012

DNA, statistics and the law: a cross-disciplinary approach to forensic inference

por Biedermann, Alex, Vuille, Joëlle, Taroni, Franco
Publicado 2014

Prediction in forensic science: a critical examination of common understandings

por Biedermann, Alex, Bozza, Silvia, Taroni, Franco
Publicado 2015

Evidence, probability and relative plausibility

por Aitken, Colin, Taroni, Franco, Bozza, Silvia
Publicado 2022

Commentary: Likelihood Ratio as Weight of Forensic Evidence: A Closer Look

por Aitken, Colin, Nordgaard, Anders, Taroni, Franco, Biedermann, Alex
Publicado 2018

Are Inconclusive Decisions in Forensic Science as Deficient as They Are Said to Be?

por Biedermann, Alex, Bozza, Silvia, Taroni, Franco, Vuille, Joëlle
Publicado 2019

The role of prior probability in forensic assessments

por Thompson, William C., Vuille, Joëlle, Biedermann, Alex, Taroni, Franco
Publicado 2013

A model-independent redundancy measure for human versus ChatGPT authorship discrimination using a Bayesian probabilistic approach

por Bozza, Silvia, Roten, Claude-Alain, Jover, Antoine, Cammarota, Valentina, Pousaz, Lionel, Taroni, Franco
Publicado 2023

PEX7 Mutations Cause Congenital Cataract Retinopathy and Late-Onset Ataxia and Cognitive Impairment: Report of Two Siblings and Review of the Literature

por Nanetti, Lorenzo, Pensato, Viviana, Leoni, Valerio, Rizzetto, Manuela, Caccia, Claudio, Taroni, Franco, Mariotti, Caterina, Gellera, Cinzia
Publicado 2015

3-Methylglutaconic Aciduria Type I: A Rare Cause of Late-Onset Leukoencephalopathy

por Benzoni, Chiara, Magri, Stefania, Moscatelli, Marco, Fenu, Silvia, Caccia, Claudio, Taroni, Franco, Salsano, Ettore, Di Bella, Daniela
Publicado 2022

Evaluation of Forensic DNA Traces When Propositions of Interest Relate to Activities: Analysis and Discussion of Recurrent Concerns

por Biedermann, Alex, Champod, Christophe, Jackson, Graham, Gill, Peter, Taylor, Duncan, Butler, John, Morling, Niels, Hicks, Tacha, Vuille, Joelle, Taroni, Franco
Publicado 2016

Is the Oxidant/Antioxidant Status Altered in CADASIL Patients?

por Campolo, Jonica, De Maria, Renata, Mariotti, Caterina, Tomasello, Chiara, Parolini, Marina, Frontali, Marina, Inzitari, Domenico, Valenti, Raffaella, Federico, Antonio, Taroni, Franco, Parodi, Oberdan
Publicado 2013

Somatosensory Conduction Pathway in Spastic Paraplegia Type 5

por Vanotti, Alessandra, Nanetti, Lorenzo, Rossi Sebastiano, Davide, Visani, Elisa, Duran, Dunja, Di Bella, Daniela, Sarto, Elisa, Caccia, Claudio, Leoni, Valerio, Taroni, Franco, Mariotti, Caterina
Publicado 2014

Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms

por Pensato, Viviana, Magri, Stefania, Dalla Bella, Eleonora, Tannorella, Pierpaola, Bersano, Enrica, Sorarù, Gianni, Gatti, Marta, Ticozzi, Nicola, Taroni, Franco, Lauria, Giuseppe, Mariotti, Caterina, Gellera, Cinzia
Publicado 2020

Progression of Cerebellar Atrophy in Spinocerebellar Ataxia Type 2 Gene Carriers: A Longitudinal MRI Study in Preclinical and Early Disease Stages

por Nigri, Anna, Sarro, Lidia, Mongelli, Alessia, Pinardi, Chiara, Porcu, Luca, Castaldo, Anna, Ferraro, Stefania, Grisoli, Marina, Bruzzone, Maria Grazia, Gellera, Cinzia, Taroni, Franco, Mariotti, Caterina, Nanetti, Lorenzo
Publicado 2020

DNAJB2‐related Charcot‐Marie‐Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening

por 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
Publicado 2022

Charcot–Marie–Tooth disease type 2F associated with biallelic HSPB1 mutations

por Abati, Elena, Magri, Stefania, Meneri, Megi, Manenti, Giulia, Velardo, Daniele, Balistreri, Francesca, Pisciotta, Chiara, Saveri, Paola, Bresolin, Nereo, Comi, Giacomo Pietro, Ronchi, Dario, Pareyson, Davide, Taroni, Franco, Corti, Stefania
Publicado 2021

Multifaceted and Age-Dependent Phenotypes Associated With Biallelic PNPLA6 Gene Variants: Eight Novel Cases and Review of the Literature

por 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
Publicado 2022