Mattia Zaghi

Publications
Public outreach and news

Articles

Journal article: BLOOD. 2024;143(26):2810
First-hit SETBP1 mutations cause a myeloproliferative disorder with bone marrow fibrosis. Blood (vol 143, pg 1399, 2024)
Crespiatico I; Zaghi M; Mastini C; D'Aliberti D; Mauri M; Mercado CM; Fontana D; Spinelli S; Crippa V; Inzoli E; Manghisi B; Civettini I; Ramazzotti D; Sangiorgio V; Gengotti M; Brambilla V; Aroldi A; Banfi F; Barone C; Orsenigo R; Riera L; Riminucci M; Corsi A; Breccia M; Morotti A; Cilloni D; Roccaro A; Sacco A; Stagno F; Serafini M; Mottadelli F; Cazzaniga G; Pagni F; Chiarle R; Azzoni E; Sessa A; Gambacorti-Passerini C; Elli EM; Mologni L; Piazza R
Journal article: BLOOD. 2024;143(14):1399-1413
First-hit SETBP1 mutations cause a myeloproliferative disorder with bone marrow fi brosis
Crespiatico I; Zaghi M; Mastini C; D'Aliberti D; Mauri M; Mercado CM; Fontana D; Spinelli S; Crippa V; Inzoli E; Manghisi B; Civettini I; Ramazzotti D; Sangiorgio V; Gengotti M; Brambilla V; Aroldi A; Banfi F; Barone C; Orsenigo R; Riera L; Riminucci M; Corsi A; Breccia M; Morotti A; Cilloni D; Roccaro A; Sacco A; Stagno F; Fini MS; Mottadelli F; Cazzaniga G; Pagni F; Chiarle R; Azzoni E; Sessa A; Gambacorti-Passerini C; Elli EM; Mologni L; Piazza R
Journal article: NATURE COMMUNICATIONS. 2023;14(1):3212
Balanced SET levels favor the correct enhancer repertoire during cell fate acquisition
Zaghi M; Banfi F; Massimino L; Volpin M; Bellini E; Brusco S; Merelli I; Barone C; Bruni M; Bossini L; Lamparelli LA; Pintado L; D'Aliberti D; Spinelli S; Mologni L; Colasante G; Ungaro F; Cioni J-M; Azzoni E; Piazza R; Montini E; Broccoli V; Sessa A
Journal article: MOLECULAR AUTISM. 2023;14(1):20
SETD5 haploinsufficiency affects mitochondrial compartment in neural cells
Zaghi M; Longo F; Massimino L; Rubio A; Bido S; Mazzara PG; Bellini E; Banfi F; Podini P; Maltecca F; Zippo A; Broccoli V; Sessa A
Journal article: SCIENCE ADVANCES. 2022;8(31):eabn3986
A SOX2-engineered epigenetic silencer factor represses the glioblastoma genetic program and restrains tumor development
Benedetti V; Banfi F; Zaghi M; Moll-Diaz R; Massimino L; Argelich L; Bellini E; Bido S; Muggeo S; Ordazzo G; Mastrototaro G; Moneta M; Sessa A; Broccoli V
Journal article: BIOMOLECULES. 2021;11(11):1713
Rare Does Not Mean Worthless: How Rare Diseases Have Shaped Neurodevelopment Research in the NGS Era
Zaghi M; Banfi F; Bellini E; Sessa A
Journal article: NATURE COMMUNICATIONS. 2021;12(1):4050
SETBP1 accumulation induces P53 inhibition and genotoxic stress in neural progenitors underlying neurodegeneration in Schinzel-Giedion syndrome
Banfi F; Rubio A; Zaghi M; Massimino L; Fagnocchi G; Bellini E; Luoni M; Cancellieri C; Bagliani A; Di Resta C; Maffezzini C; Ianielli A; Ferrari M; Piazza R; Mologni L; Broccoli V; Sessa A
Journal article: FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY. 2021;9:641410
TBL1XR1 Ensures Balanced Neural Development Through NCOR Complex-Mediated Regulation of the MAPK Pathway
Mastrototaro G; Zaghi M; Massimino L; Moneta M; Mohammadi N; Banfi F; Bellini E; Indrigo M; Fagnocchi G; Bagliani A; Taverna S; Rohm M; Herzig S; Sessa A
Journal article: NATURE COMMUNICATIONS. 2020;11(1):4178
Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons
Mazzara PG; Muggeo S; Luoni M; Massimino L; Zaghi M; Valverde PT-T; Brusco S; Marzi MJ; Palma C; Colasante G; Iannielli A; Paulis M; Cordiglieri C; Giannelli SG; Podini P; Gellera C; Taroni F; Nicassio F; Rasponi M; Broccoli V
Journal article: NEURON. 2019;104(2):271-289.e13
SETD5 Regulates Chromatin Methylation State and Preserves Global Transcriptional Fidelity during Brain Development and Neuronal Wiring
Sessa A; Fagnocchi L; Mastrototaro G; Massimino L; Zaghi M; Indrigo M; Cattaneo S; Martini D; Gabellini C; Pucci C; Fasciani A; Belli R; Taverna S; Andreazzoli M; Zippo A; Broccoli V
Journal article: FRONTIERS IN GENETICS. 2019;10:1291
H3K36 Methylation in Neural Development and Associated Diseases
Zaghi M; Broccoli V; Sessa A
Journal article: DEVELOPMENTAL BIOLOGY. 2018;434(2):231-248
TBR2 antagonizes retinoic acid dependent neuronal differentiation by repressing Zfp423 during corticogenesis
Massimino L; Flores-Garcia L; Di Stefano B; Colasante G; Icoresi-Mazzeo C; Zaghi M; Hamilton BA; Sessa A
Journal article: JOURNAL OF MOLECULAR NEUROSCIENCE. 2017;61(4):590-602
Epigenetic Mistakes in Neurodevelopmental Disorders
Mastrototaro G; Zaghi M; Sessa A

All other publications

Book chapter: EPIGENETICS IN HUMAN DISEASE. 2024;p. 285-331
Chapter 8 Emerging role of epigenetics in human neurodevelopmental disorders
Mastrototaro G; Sessa A; Zaghi M
Conference publication: BLOOD. 2023;142:4135
First-Hit SETBP1 Mutations Cause a Myeloproliferative Disorder with Bone Marrow Fibrosis
Crespiatico I; Zaghi M; Mastini C; D'Aliberti D; Mauri M; Mercado CM; Fontana D; Spinelli S; Crippa V; Inzoli E; Manghisi B; Civettini I; Ramazzotti D; Lavoro VFI; Gengotti M; Brambilla V; Aroldi A; Banfi F; Barone C; Orsenigo R; Riera L; Riminucci M; Corsi A; Breccia M; Morotti A; Cilloni D; Roccaro A; Sacco A; Stagno F; Serafini M; Mottadelli F; Cazzaniga G; Pagni F; Chiarle R; Azzoni E; Sessa A; Gambacorti-Passerini C; Elli EM; Mologni L; Piazza R
Preprint: BIORXIV. 2022
Balanced SET levels favor the correct enhancer repertoire during cell fate acquisition
Mattia Z; Banfi F; Massimino L; Volpin M; Bellini E; Brusco S; Merelli I; Barone C; Bruni M; Bossini L; Lamparelli LA; Pintado L; D’Aliberti D; Spinelli S; Mologni L; Colasante G; Ungaro F; Cioni J-M; Azzoni E; Piazza R; Montini E; Broccoli V; Sessa A
Conference publication: MOLECULAR THERAPY. 2021;29(4):58-59
A SOX2 Engineered Epigenetic Silencer Factor Represses the Cancer Genetic Program and Eradicate Glioblastoma Development
Broccoli V; Sessa A; Banfi F; Benedetti V; Zaghi M; Massimino L; Bido S; Argelich L; Giannelli S; Niro A
Preprint: BIORXIV. 2019
Somatostatin-Expressing Interneurons Co-Release GABA and Glutamate onto Different Postsynaptic Targets in the Striatum
Cattaneo S; Ripamonti M; Bedogni F; Sessa A; Taverna S
Conference publication: HUMAN GENE THERAPY. 2016;27(11):A49
CRISPRa-mediated overexpression of the voltage-gated channels Kv1.1 and Nav1.1 as a new therapeutic strategy to restore excitation/inhibition balance in epileptic neuronal circuits
Di Berardino C; Colasante G; Lignani G; Massimino L; Sacchetti S; Zaghi M; Benfenati F; Kullmann D; Broccoli V

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