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DIPARTIMENTO DI RICERCA TRASLAZIONALE E DELLE NUOVE TECNOLOGIE IN MEDICINA E CHIRURGIA  

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Titolo Data di pubblicazione Autore(i) File
DNA Methylation Biomarkers for Young Children with Idiopathic Autism Spectrum Disorder: A Systematic Review 1-gen-2023 Stoccoro, Andrea; Conti, Eugenia; Scaffei, Elena; Calderoni, Sara; Coppedè, Fabio; Migliore, Lucia; Battini, Roberta
Editorial: Role of genetics, epigenetics, and environmental factors in human complex diseases from the mitochondrial point of view 1-gen-2023 Stoccoro, Andrea; Smith, Adam R; Coppedè, Fabio
Epigenetics of Thymic Epithelial Tumors 1-gen-2023 Nicolì, Vanessa; Coppedè, Fabio
Genes and the Environment in Cancer: Focus on Environmentally Induced DNA Methylation Changes 1-gen-2023 Coppedè, Fabio
Le modificazioni epigenetiche. Un aspetto a lungo ignorato negli studi atti a valutare le interazioni geni-ambiente nella malattia di Alzheimer 1-gen-2023 Coppedè, Fabio
Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders 1-gen-2023 Lintas, Carla; Cassano, Ilaria; Azzarà, Alessia; Stigliano, Maria Grazia; Gregorj, Chiara; Sacco, Roberto; Stoccoro, Andrea; Coppedè, Fabio; Gurrieri, Fiorella
Prenatal Environmental Stressors and DNA Methylation Levels in Placenta and Peripheral Tissues of Mothers and Neonates Evaluated by Applying Artificial Neural Networks 1-gen-2023 Stoccoro, Andrea; Nicolì, Vanessa; Coppedè, Fabio; Grossi, Enzo; Fedrizzi, Giorgio; Menotta, Simonetta; Lorenzoni, Francesca; Caretto, Marta; Carmignani, Arianna; Pistolesi, Sabina; Burgio, Ernesto; Fanos, Vassilios; Migliore, Lucia
Somatic mutations of thymic epithelial tumors with myasthenia gravis 1-gen-2023 Pardini, E.; Cucchiara, F.; Palumbo, S.; Tarrini, G.; Di Vita, A.; Coppede, F.; Nicoli, V.; Guida, M.; Maestri, M.; Ricciardi, R.; Aprile, V.; Ambrogi, M. C.; Barachini, S.; Lucchi, M.; Petrini, I.
A perspective on diet, epigenetics and complex diseases: where is the field headed next? 1-gen-2022 Coppedè, Fabio; Franzago, Marica; Giardina, Emiliano; Nigro, Cristiana Lo; Matullo, Giuseppe; Moltrasio, Chiara; Nacmias, Benedetta; Pileggi, Silvana; Sirchia, Silvia Maria; Stoccoro, Andrea; Storlazzi, Clelia Tiziana; Stuppia, Liborio; Tricarico, Rossella; Merla, Giuseppe
Artificial neural networks reveal sex differences in gene methylation, and connections between maternal risk factors and symptom severity in autism spectrum disorder 1-gen-2022 Stoccoro, Andrea; Gallo, Roberta; Calderoni, Sara; Cagiano, Romina; Muratori, Filippo; Migliore, Lucia; Grossi, Enzo; Coppedè, Fabio
Association between MTHFR C677T and A1298C gene polymorphisms and maternal risk for Down syndrome A protocol for systematic review and/or meta-analysis 1-gen-2022 Ginani, C. T. A.; da Luz, J. R. D.; Silva, S. V. E.; Coppede', F.; Almeida, M. D. G.
Correlation among maternal risk factors, gene methylation and disease severity in females with autism spectrum disorder 1-gen-2022 Gallo, Roberta; Stoccoro, Andrea; Cagiano, Romina; Nicolì, Vanessa; Ricciardi, Rosanna; Tancredi, Raffaella; Trovato, Rosanna; Santorelli, Filippo Maria; Calderoni, Sara; Muratori, Filippo; Migliore, Lucia; Coppedè, Fabio
DNA methylation as a powerful tool to investigate the biology and pathology of aging 1-gen-2022 Coppedè, Fabio
Editorial: Epigenetics of Neurodevelopmental, Neuromuscular and Neurodegenerative Disorders 1-gen-2022 Coppedè, Fabio; Cereda, Cristina; Lintas, Carla; Stoccoro, Andrea
Editorial: Shared Genetic Risk Factors Among Psychiatric Diseases and Other Medical Diseases and Traits 1-gen-2022 Lori, A.; Coppede', F.; Pellegrini, S.
Gene-environment interactions in Alzheimer disease: the emerging role of epigenetics 1-gen-2022 Migliore, Lucia; Coppedè, Fabio
Increase in Mitochondrial D-Loop Region Methylation Levels in Mild Cognitive Impairment Individuals 1-gen-2022 Stoccoro, Andrea; Baldacci, Filippo; Ceravolo, Roberto; Giampietri, Linda; Tognoni, Gloria; Siciliano, Gabriele; Migliore, Lucia; Coppedè, Fabio
Precision Nutrition from the View of Genetics and Epigenetics 1-gen-2022 Migliore, L.; Coppedè, Fabio.
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis 1-gen-2022 Nicolì, V.; Tabano, S. M.; Colapietro, P.; Maestri, M.; Ricciardi, R.; Stoccoro, A.; Fontana, L.; Guida, M.; Miozzo, M.; Coppede', F.; Migliore, L.
Targeting the epigenome to treat neurodegenerative diseases or delay their onset: A perspective 1-gen-2022 Coppede', F.