Author

Maria Fuciarelli

University of Rome Tor Vergata

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetic & Genomic Medicine· 4

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:differential expression· 2 Assay:DNA methylation· 2 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2

Frequent Co-Authors

Antonella De LilloiD· 4 shared Renato A PolimantiiD· 4 shared Flavio De AngelisiD· 3 shared Dario ManfellottoiD· 2 shared Gita A. PathakiD· 2 shared Marco Di Girolamo· 2 shared Marco LuigettiiD· 2 shared Sabrina Frusconi· 2 shared

Activity by Year

2019-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Antonella De LilloORCID

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4 papers

Recent·Most cited

Epigenomic profiles of African American Transthyretin Val122Ile carriers reveals putatively dysregulated amyloid mechanisms

Gita A. Pathak, Frank R. Wendt, Antonella De Lillo, Yaira Z. Nuñez, Aranyak Goswami, Flavio De Angelis, Maria Fuciarelli, Henry R. Kranzler, Joel E. Gelernter, Renato A Polimanti

This study identifies epigenomic changes in African American Transthyretin Val122Ile carriers linked to heart disease and outpatient surgeries, revealing dysregulated amyloid mechanisms.

Circulation Genomic and Precision Medicine · Jan 11, 2021Peer-reviewedGenetic & Genomic Medicine

Epigenetic profiling of Italian patients identified methylation sites associated with hereditary Transthyretin amyloidosis

Antonella De Lillo, Gita A. Pathak, Flavio De Angelis, Marco Di Girolamo, Marco Luigetti, Mario Sabatelli, Federico Perfetto, Sabrina Frusconi, Dario Manfellotto, Maria Fuciarelli, Renato A Polimanti

The paper identifies methylation sites associated with hereditary Transthyretin amyloidosis through an epigenome-wide association study.

Clinical Epigenetics · Nov 17, 2020Peer-reviewedGenetic & Genomic Medicine

Inter-population differences of allele frequency and regulome tagging are associated with the heterogeneity of loci identified by cross-ancestry genome-wide association studies

Antonella De Lillo, Salvatore D’Antona, Maria Fuciarelli, Renato A Polimanti

The paper identifies allele frequency and regulome tagging differences between UKB and 1KG populations for GWAS loci, showing population-specific associations and potential biases.

medRxiv · Sep 13, 2020 · PreprintGenetic & Genomic Medicine

Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and senile systemic amyloidoses

Antonella De Lillo, Flavio De Angelis, Marco Di Girolamo, Marco Luigetti, Sabrina Frusconi, Dario Manfellotto, Maria Fuciarelli, Renato A Polimanti

This study identifies novel associations between TTR and RBP4 gene variants and multiple phenotypes related to hereditary and senile systemic amyloidoses in a large cohort.

Human Genetics · Oct 28, 2019Peer-reviewedGenetic & Genomic Medicine