De Angelis F - Search Results

1

An Atlas of Genetic Correlations and Genetically Informed Associations Linking Psychiatric and Immune-Related Phenotypes.

Tylee DS, Lee YK, Wendt FR, Pathak GA, Levey DF, De Angelis F, Gelernter J, Polimanti R. Tylee DS, et al. Among authors: de angelis f. JAMA Psychiatry. 2022 Jul 1;79(7):667-676. doi: 10.1001/jamapsychiatry.2022.0914. JAMA Psychiatry. 2022. PMID: 35507366 Free PMC article.

2

Phenotype versus genotype methods for copy number variant analysis of glutathione S-transferases M1.

Piacentini S, Polimanti R, De Angelis F, Iorio A, Fuciarelli M. Piacentini S, et al. Among authors: de angelis f. Ann Hum Genet. 2013 Sep;77(5):409-15. doi: 10.1111/ahg.12025. Epub 2013 Jun 3. Ann Hum Genet. 2013. PMID: 23731058

3

Functional variability of glutathione S-transferases in Basque populations.

Iorio A, Piacentini S, Polimanti R, De Angelis F, Calderon R, Fuciarelli M. Iorio A, et al. Among authors: de angelis f. Am J Hum Biol. 2014 May-Jun;26(3):361-6. doi: 10.1002/ajhb.22520. Epub 2014 Feb 17. Am J Hum Biol. 2014. PMID: 24677736

4

Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis.

Iorio A, De Angelis F, Di Girolamo M, Luigetti M, Pradotto LG, Mazzeo A, Frusconi S, My F, Manfellotto D, Fuciarelli M, Polimanti R. Iorio A, et al. Among authors: de angelis f. BMC Genomics. 2017 Mar 23;18(1):254. doi: 10.1186/s12864-017-3646-1. BMC Genomics. 2017. PMID: 28335735 Free PMC article.

5

Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis.

Iorio A, De Lillo A, De Angelis F, Di Girolamo M, Luigetti M, Sabatelli M, Pradotto L, Mauro A, Mazzeo A, Stancanelli C, Perfetto F, Frusconi S, My F, Manfellotto D, Fuciarelli M, Polimanti R. Iorio A, et al. Among authors: de angelis f, de lillo a. Eur J Hum Genet. 2017 Sep;25(9):1055-1060. doi: 10.1038/ejhg.2017.95. Epub 2017 Jun 21. Eur J Hum Genet. 2017. PMID: 28635949 Free PMC article.

6

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

De Lillo A, De Angelis F, Di Girolamo M, Luigetti M, Frusconi S, Manfellotto D, Fuciarelli M, Polimanti R. De Lillo A, et al. Among authors: de angelis f. Hum Genet. 2019 Dec;138(11-12):1331-1340. doi: 10.1007/s00439-019-02078-6. Epub 2019 Oct 29. Hum Genet. 2019. PMID: 31659433

7

ACE2 Netlas: In-silico functional characterization and drug-gene interactions of ACE2 gene network to understand its potential involvement in COVID-19 susceptibility.

Pathak GA, Wendt FR, Goswami A, Angelis F; COVID-19 Human Genetics Initiative; Polimanti R. Pathak GA, et al. Among authors: angelis f. medRxiv [Preprint]. 2020 Oct 28:2020.10.27.20220665. doi: 10.1101/2020.10.27.20220665. medRxiv. 2020. PMID: 33140059 Free PMC article. Updated. Preprint.

8

Host genetic liability for severe COVID-19 overlaps with alcohol drinking behavior and diabetic outcomes in over 1 million participants.

Wendt FR, De Lillo A, Pathak GA, De Angelis F, Polimanti R. Wendt FR, et al. Among authors: de angelis f, de lillo a. medRxiv [Preprint]. 2020 Nov 18:2020.11.08.20227884. doi: 10.1101/2020.11.08.20227884. medRxiv. 2020. PMID: 33200138 Free PMC article. Updated. Preprint.

9

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

De Lillo A, Pathak GA, De Angelis F, Di Girolamo M, Luigetti M, Sabatelli M, Perfetto F, Frusconi S, Manfellotto D, Fuciarelli M, Polimanti R. De Lillo A, et al. Among authors: de angelis f. Clin Epigenetics. 2020 Nov 17;12(1):176. doi: 10.1186/s13148-020-00967-6. Clin Epigenetics. 2020. PMID: 33203445 Free PMC article.

10

Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms.

Pathak GA, Wendt FR, De Lillo A, Nunez YZ, Goswami A, De Angelis F, Fuciarelli M, Kranzler HR, Gelernter J, Polimanti R. Pathak GA, et al. Among authors: de angelis f, de lillo a. Circ Genom Precis Med. 2021 Feb;14(1):e003011. doi: 10.1161/CIRCGEN.120.003011. Epub 2021 Jan 11. Circ Genom Precis Med. 2021. PMID: 33428857 Free PMC article.

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