Megalizzi D - Search Results

1

Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from ADH1B, CYP1A2 and MTHFR.

Barati S, Fabrizio C, Strafella C, Cascella R, Caputo V, Megalizzi D, Peconi C, Mela J, Colantoni L, Caltagirone C, Termine A, Giardina E. Barati S, et al. Among authors: megalizzi d. Genes (Basel). 2022 Aug 22;13(8):1498. doi: 10.3390/genes13081498. Genes (Basel). 2022. PMID: 36011409 Free PMC article. Review.

2

Age and Sex Modulate SARS-CoV-2 Viral Load Kinetics: A Longitudinal Analysis of 1735 Subjects.

Caputo V, Termine A, Fabrizio C, Calvino G, Luzzi L, Fusco C, Ingrascì A, Peconi C, D'Alessio R, Mihali S, Trastulli G, Megalizzi D, Cascella R, Rossini A, Salvia A, Strafella C, Giardina E. Caputo V, et al. Among authors: megalizzi d, d alessio r. J Pers Med. 2021 Sep 2;11(9):882. doi: 10.3390/jpm11090882. J Pers Med. 2021. PMID: 34575659 Free PMC article.

3

Identification of Genetic Networks Reveals Complex Associations and Risk Trajectory Linking Mild Cognitive Impairment to Alzheimer's Disease.

Strafella C, Caputo V, Termine A, Fabrizio C, Calvino G, Megalizzi D, Ruffo P, Toppi E, Banaj N, Bassi A, Bossù P, Caltagirone C, Spalletta G, Giardina E, Cascella R. Strafella C, et al. Among authors: megalizzi d. Front Aging Neurosci. 2022 Feb 17;14:821789. doi: 10.3389/fnagi.2022.821789. eCollection 2022. Front Aging Neurosci. 2022. PMID: 35250545 Free PMC article.

4

WARE: Wet AMD Risk-Evaluation Tool as a Clinical Decision-Support System Integrating Genetic and Non-Genetic Factors.

Fabrizio C, Termine A, Caputo V, Megalizzi D, Zampatti S, Falsini B, Cusumano A, Eandi CM, Ricci F, Giardina E, Strafella C, Cascella R. Fabrizio C, et al. Among authors: megalizzi d. J Pers Med. 2022 Jun 24;12(7):1034. doi: 10.3390/jpm12071034. J Pers Med. 2022. PMID: 35887531 Free PMC article.

5

Update on the Molecular Aspects and Methods Underlying the Complex Architecture of FSHD.

Caputo V, Megalizzi D, Fabrizio C, Termine A, Colantoni L, Caltagirone C, Giardina E, Cascella R, Strafella C. Caputo V, et al. Among authors: megalizzi d. Cells. 2022 Aug 29;11(17):2687. doi: 10.3390/cells11172687. Cells. 2022. PMID: 36078093 Free PMC article. Review.

6

D4Z4 Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients.

Caputo V, Megalizzi D, Fabrizio C, Termine A, Colantoni L, Bax C, Gimenez J, Monforte M, Tasca G, Ricci E, Caltagirone C, Giardina E, Cascella R, Strafella C. Caputo V, et al. Among authors: megalizzi d. Cells. 2022 Dec 18;11(24):4114. doi: 10.3390/cells11244114. Cells. 2022. PMID: 36552879 Free PMC article.

7

Analysis of Genetic Variants Associated with COVID-19 Outcome Highlights Different Distributions among Populations.

Fabrizio C, Termine A, Caputo V, Megalizzi D, Calvino G, Trastulli G, Ingrascì A, Ferrante S, Peconi C, Rossini A, Salvia A, Caltagirone C, Strafella C, Giardina E, Cascella R. Fabrizio C, et al. Among authors: megalizzi d. J Pers Med. 2022 Nov 5;12(11):1851. doi: 10.3390/jpm12111851. J Pers Med. 2022. PMID: 36579599 Free PMC article.

8

Epigenetic profiling of the D4Z4 locus: Optimization of the protocol for studying DNA methylation at single CpG site level.

Megalizzi D, Trastulli G, Caputo V, Colantoni L, Caltagirone C, Strafella C, Cascella R, Giardina E. Megalizzi D, et al. Electrophoresis. 2023 Oct;44(19-20):1588-1594. doi: 10.1002/elps.202300058. Epub 2023 Aug 11. Electrophoresis. 2023. PMID: 37565369

9

Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD.

Strafella C, Caputo V, Bortolani S, Torchia E, Megalizzi D, Trastulli G, Monforte M, Colantoni L, Caltagirone C, Ricci E, Tasca G, Cascella R, Giardina E. Strafella C, et al. Among authors: megalizzi d. Front Genet. 2023 Aug 22;14:1235589. doi: 10.3389/fgene.2023.1235589. eCollection 2023. Front Genet. 2023. PMID: 37674478 Free PMC article.

10

Innovations in Medicine: Exploring ChatGPT's Impact on Rare Disorder Management.

Zampatti S, Peconi C, Megalizzi D, Calvino G, Trastulli G, Cascella R, Strafella C, Caltagirone C, Giardina E. Zampatti S, et al. Among authors: megalizzi d. Genes (Basel). 2024 Mar 28;15(4):421. doi: 10.3390/genes15040421. Genes (Basel). 2024. PMID: 38674356 Free PMC article. Review.

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