Genetics of Familial Non-Medullary Thyroid Carcinoma (FNMTC)

por Diquigiovanni, Chiara, Bonora, Elena
Publicado 2021

Omics Technologies Improving Breast Cancer Research and Diagnostics

por Orsini, Arianna, Diquigiovanni, Chiara, Bonora, Elena
Publicado 2023

Calcium and Reactive Oxygen Species Signaling Interplays in Cardiac Physiology and Pathologies

por De Nicolo, Bianca, Cataldi-Stagetti, Erica, Diquigiovanni, Chiara, Bonora, Elena
Publicado 2023

Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family

por Kumar, Abhishek, Bandapalli, Obul Reddy, Paramasivam, Nagarajan, Giangiobbe, Sara, Diquigiovanni, Chiara, Bonora, Elena, Eils, Roland, Schlesner, Matthias, Hemminki, Kari, Försti, Asta
Publicado 2018

Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer

por Srivastava, Aayushi, Giangiobbe, Sara, Skopelitou, Diamanto, Miao, Beiping, Paramasivam, Nagarajan, Diquigiovanni, Chiara, Bonora, Elena, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Publicado 2021

BRAF Exon 15 Mutations in Papillary Carcinoma and Adjacent Thyroid Parenchyma: A Search for the Early Molecular Events Associated with Tumor Development

por Acquaviva, Giorgia, de Biase, Dario, Diquigiovanni, Chiara, Argento, Chiara Maria, De Leo, Antonio, Bonora, Elena, Rhoden, Kerry Jane, Pession, Annalisa, Tallini, Giovanni
Publicado 2020

Novel understanding on genetic mechanisms of enteric neuropathies leading to severe gut dysmotility

por Bianco, Francesca, Lattanzio, Giulia, Lorenzini, Luca, Diquigiovanni, Chiara, Mazzoni, Maurizio, Clavenzani, Paolo, Calzà, Laura, Giardino, Luciana, Sternini, Catia, Bonora, Elena, De Giorgio, Roberto
Publicado 2021

Mutant SPART causes defects in mitochondrial protein import and bioenergetics reversed by Coenzyme Q

por Diquigiovanni, Chiara, Rizzardi, Nicola, Kampmeier, Antje, Liparulo, Irene, Bianco, Francesca, De Nicolo, Bianca, Cataldi-Stagetti, Erica, Cuna, Elisabetta, Severi, Giulia, Seri, Marco, Bertrand, Miriam, Haack, Tobias B., Marina, Adela Della, Braun, Frederik, Fato, Romana, Kuechler, Alma, Bergamini, Christian, Bonora, Elena
Publicado 2023

Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients

por Bonora, Elena, Graziano, Claudio, Minopoli, Fiorella, Bacchelli, Elena, Magini, Pamela, Diquigiovanni, Chiara, Lomartire, Silvia, Bianco, Francesca, Vargiolu, Manuela, Parchi, Piero, Marasco, Elena, Mantovani, Vilma, Rampoldi, Luca, Trudu, Matteo, Parmeggiani, Antonia, Battaglia, Agatino, Mazzone, Luigi, Tortora, Giada, Maestrini, Elena, Seri, Marco, Romeo, Giovanni
Publicado 2014

Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients

por Bonora, Elena, Graziano, Claudio, Minopoli, Fiorella, Bacchelli, Elena, Magini, Pamela, Diquigiovanni, Chiara, Lomartire, Silvia, Bianco, Francesca, Vargiolu, Manuela, Parchi, Piero, Marasco, Elena, Mantovani, Vilma, Rampoldi, Luca, Trudu, Matteo, Parmeggiani, Antonia, Battaglia, Agatino, Mazzone, Luigi, Tortora, Giada, Maestrini, Elena, Seri, Marco, Romeo, Giovanni
Publicado 2014