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ArticlesPeer ReviewedFull Text
Investigating the Epigenetic Landscape of Major Depressive Disorder: A Genome-Wide Meta-Analysis of DNA Methylation Data, Including New Insights into Stochastic Epigenetic Mutations and Epivariations
Author / Creator:Baldrighi, Giulia Nicole ; Cavagnola, Rebecca ; Calzari, Luciano ; Sacco, Davide ; Costantino, Lucy ; Ferrara, Fulvio ; Gentilini, Davide
Publisher:Switzerland: MDPI AG
Journal title:Biomedicines, 2024-09, Vol.12 (10), p.2181
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Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia
Author / Creator:Azzolini, Claudio ; Donati, Simone ; Micheloni, Giovanni ; Moretti, Vittoria ; Valli, Roberto ; Acquati, Francesco ; Costantino, Lucy ; Ferrara, Fulvio ; Borroni, Davide ; Premi, Elias ; Testa, Francesco ; Simonelli, Francesca ; Porta, Giovanni
Publisher:United States: Hindawi
Journal title:Journal of ophthalmology, 2021-12, Vol.2021, p.1-10
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ArticlesPeer ReviewedFull Text
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis
Author / Creator:Straniero, Letizia ; Soldà, Giulia ; Costantino, Lucy ; Seia, Manuela ; Melotti, Paola ; Colombo, Carla ; Asselta, Rosanna ; Duga, Stefano
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2016-12, Vol.61 (12), p.977-984
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ArticlesPeer ReviewedFull Text
OTX Genes in Adult Tissues
Author / Creator:Terrinoni, Alessandro ; Micheloni, Giovanni ; Moretti, Vittoria ; Caporali, Sabrina ; Bernardini, Sergio ; Minieri, Marilena ; Pieri, Massimo ; Giaroni, Cristina ; Acquati, Francesco ; Costantino, Lucy ; Ferrara, Fulvio ; Valli, Roberto ; Porta, Giovanni
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2023-12, Vol.24 (23), p.16962
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ArticlesPeer ReviewedFull Text
IOTX/I Genes in Adult Tissues
Author / Creator:Terrinoni, Alessandro ; Micheloni, Giovanni ; Moretti, Vittoria ; Caporali, Sabrina ; Bernardini, Sergio ; Minieri, Marilena ; Pieri, Massimo ; Giaroni, Cristina ; Acquati, Francesco ; Costantino, Lucy ; Ferrara, Fulvio ; Valli, Roberto ; Porta, Giovanni
Publisher:MDPI AG
Journal title:International journal of molecular sciences, 2023-11, Vol.24 (23)
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ArticlesPeer ReviewedFull Text
The Brain–Gut Axis, an Important Player in Alzheimer and Parkinson Disease: A Narrative Review
Author / Creator:Caradonna, Eugenio ; Nemni, Raffaello ; Bifone, Angelo ; Gandolfo, Patrizia ; Costantino, Lucy ; Giordano, Luca ; Mormone, Elisabetta ; Macula, Anna ; Cuomo, Mariarosa ; Difruscolo, Rossana ; Vanoli, Camilla ; Vanoli, Emilio ; Ferrara, Fulvio
Publisher:Switzerland: MDPI AG
Journal title:Journal of clinical medicine, 2024-07, Vol.13 (14), p.4130
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ArticlesPeer ReviewedFull Text
A new approach to study stochastic epigenetic mutations in sperm methylome of Vietnam war veterans directly exposed to Agent Orange
Author / Creator:Corsaro, Luigi ; Sacco, Davide ; Corbetta, Carlo ; Gentilini, Davide ; Faversani, Alice ; Ferrara, Fulvio ; Costantino, Lucy
Publisher:England: Oxford University Press
Journal title:Environmental epigenetics, 2024, Vol.10 (1), p.dvae020
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ArticlesPeer ReviewedFull Text
Characterization of a New Variant in IARHGAP31/I Probably Involved in Adams–Oliver Syndrome in a Family with a Variable Phenotypic Spectrum
Author / Creator:Santaniello, Carlo ; Faversani, Alice ; Corsaro, Luigi ; Melloni, Giulia ; Motta, Silvia ; Mandorino, Elena ; Sacco, Davide ; Stioui, Sabine ; Ferrara, Fulvio ; Barteselli, Davide ; De Vita, Dario ; Manuelli, Debora ; Costantino, Lucy
Publisher:MDPI AG
Journal title:Genes, 2024-05, Vol.15 (5)
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ArticlesPeer ReviewedFull Text
Characterization of a New Variant in ARHGAP31 Probably Involved in Adams–Oliver Syndrome in a Family with a Variable Phenotypic Spectrum
Author / Creator:Santaniello, Carlo ; Faversani, Alice ; Corsaro, Luigi ; Melloni, Giulia ; Motta, Silvia ; Mandorino, Elena ; Sacco, Davide ; Stioui, Sabine ; Ferrara, Fulvio ; Barteselli, Davide ; De Vita, Dario ; Manuelli, Debora ; Costantino, Lucy
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-04, Vol.15 (5), p.536
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ArticlesPeer ReviewedFull Text
Exploring the complexities of epigenetics in multiple sclerosis: A study involving meta-analysis of DNA methylation profiles, epigenetic drift, and rare epivariations
Author / Creator:Baldrighi, Giulia Nicole ; Cavagnola, Rebecca ; Sacco, Davide ; Costantino, Lucy ; Bernardinelli, Luisa ; Gentilini, Davide
Publisher:London, England: SAGE Publications
Journal title:Multiple sclerosis journal - experimental, translational and clinical, 2024-10, Vol.10 (4), p.20552173241296726
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ArticlesPeer ReviewedFull Text
Occurrence of L1M Elements in Chromosomal Rearrangements Associated to Chronic Myeloid Leukemia (CML): Insights from Patient-Specific Breakpoints Characterization
Author / Creator:L’Abbate, Alberto ; Moretti, Vittoria ; Pungolino, Ester ; Micheloni, Giovanni ; Valli, Roberto ; Frattini, Annalisa ; Barcella, Matteo ; Acquati, Francesco ; Reinbold, Rolland A ; Costantino, Lucy ; Ferrara, Fulvio ; Trojani, Alessandra ; Ventura, Mario ; Porta, Giovanni ; Cairoli, Roberto
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2023-06, Vol.14 (7), p.1351
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ArticlesPeer ReviewedFull Text
Fine Characterization of the Recurrent c.1584+18672A>G Deep-Intronic Mutation in the Cystic Fibrosis Transmembrane Conductance Regulator Gene
Author / Creator:Costantino, Lucy ; Rusconi, Damiana ; Soldà, Giulia ; Seia, Manuela ; Paracchini, Valentina ; Porcaro, Luigi ; Asselta, Rosanna ; Colombo, Carla ; Duga, Stefano
Publisher:United States: American Thoracic Society
Journal title:American journal of respiratory cell and molecular biology, 2013-05, Vol.48 (5), p.619-625
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ArticlesPeer ReviewedFull Text
Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3)
Author / Creator:Degiorgio, Dario ; Colombo, Carla ; Seia, Manuela ; Porcaro, Luigi ; Costantino, Lucy ; Zazzeron, Laura ; Bordo, Domenico ; Coviello, Domenico A
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2007-12, Vol.15 (12), p.1230-1238
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ArticlesPeer ReviewedFull Text
Two ABCB4 point mutations of strategic NBD-motifs do not prevent protein targeting to the plasma membrane but promote MDR3 dysfunction
Author / Creator:Degiorgio, Dario ; Corsetto, Paola A ; Rizzo, Angela M ; Colombo, Carla ; Seia, Manuela ; Costantino, Lucy ; Montorfano, Gigliola ; Tomaiuolo, Rossella ; Bordo, Domenico ; Sansanelli, Serena ; Li, Min ; Tavian, Daniela ; Rastaldi, Maria P ; Coviello, Domenico A
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2014-05, Vol.22 (5), p.633-639
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Investigating the Epigenetic Landscape of Major Depressive Disorder: A Genome-Wide Meta-Analysis of DNA Methylation Data, Including New Insights into Stochastic Epigenetic Mutations and Epivariations

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Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia

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Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis

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OTX Genes in Adult Tissues

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IOTX/I Genes in Adult Tissues

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The Brain–Gut Axis, an Important Player in Alzheimer and Parkinson Disease: A Narrative Review

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A new approach to study stochastic epigenetic mutations in sperm methylome of Vietnam war veterans directly exposed to Agent Orange

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Characterization of a New Variant in IARHGAP31/I Probably Involved in Adams–Oliver Syndrome in a Family with a Variable Phenotypic Spectrum

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Characterization of a New Variant in ARHGAP31 Probably Involved in Adams–Oliver Syndrome in a Family with a Variable Phenotypic Spectrum

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Exploring the complexities of epigenetics in multiple sclerosis: A study involving meta-analysis of DNA methylation profiles, epigenetic drift, and rare epivariations

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Occurrence of L1M Elements in Chromosomal Rearrangements Associated to Chronic Myeloid Leukemia (CML): Insights from Patient-Specific Breakpoints Characterization

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Fine Characterization of the Recurrent c.1584+18672A>G Deep-Intronic Mutation in the Cystic Fibrosis Transmembrane Conductance Regulator Gene

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Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3)

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Two ABCB4 point mutations of strategic NBD-motifs do not prevent protein targeting to the plasma membrane but promote MDR3 dysfunction

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