Andrea Freschi
Overview
Explore the profile of Andrea Freschi including associated specialties, affiliations and a list of published articles.
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17
Citations
222
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Recent Articles
1.
Pagan E, Ruggeri M, Bianco N, Bucci E, Graffeo R, Borner M, et al.
Breast
. 2024 Jul;
77:103765.
PMID: 39002281
Purpose: Although younger age has been negatively associated with persistence to adjuvant endocrine therapy (ET), factors contributing to non-persistence remain poorly understood. We assessed factors associated with non-persistence to ET...
2.
Ribi K, Pagan E, Sala I, Ruggeri M, Bianco N, Bucci E, et al.
J Cancer Surviv
. 2022 Jun;
17(6):1847-1858.
PMID: 35689003
Purpose: Despite extensive research on cancer and work-related outcomes, evidence from longitudinal cohort studies is limited, especially in young women with breast cancer (BC). We aimed to investigate employment trajectories...
3.
Freschi A, Del Prete R, Pignata L, Cecere F, Manfrevola F, Mattia M, et al.
Hum Mol Genet
. 2021 Jun;
30(16):1509-1520.
PMID: 34132339
The reciprocal parent of origin-specific expression of H19 and IGF2 is controlled by the H19/IGF2:IG-DMR (IC1), whose maternal allele is unmethylated and acts as a CTCF-dependent insulator. In humans, internal...
4.
Pace M, Colombi I, Falappa M, Freschi A, Bandarabadi M, Armirotti A, et al.
Hum Mol Genet
. 2020 May;
29(12):2051-2064.
PMID: 32426821
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder that is characterized by metabolic alteration and sleep abnormalities mostly related to rapid eye movement (REM) sleep disturbances. The disease is caused by...
5.
Pace M, Falappa M, Freschi A, Balzani E, Berteotti C, Lo Martire V, et al.
JCI Insight
. 2020 May;
5(12).
PMID: 32365348
Imprinted genes are highly expressed in the hypothalamus; however, whether specific imprinted genes affect hypothalamic neuromodulators and their functions is unknown. It has been suggested that Prader-Willi syndrome (PWS), a...
6.
Valente F, Sparago A, Freschi A, Hill-Harfe K, Maas S, Frints S, et al.
Genet Med
. 2019 Jan;
21(8):1808-1820.
PMID: 30635621
Purpose: Beckwith-Wiedemann syndrome (BWS) is a developmental disorder caused by dysregulation of the imprinted gene cluster of chromosome 11p15.5 and often associated with loss of methylation (LOM) of the imprinting...
7.
Freschi A, Hur S, Valente F, Ideraabdullah F, Sparago A, Gentile M, et al.
PLoS Genet
. 2018 Feb;
14(2):e1007243.
PMID: 29470501
Differential DNA methylation defects of H19/IGF2 are associated with congenital growth disorders characterized by opposite clinical pictures. Due to structural differences between human and mouse, the mechanisms by which mutations...
8.
Baglivo I, Pirone L, Pedone E, Pitzer J, Muscariello L, Marino M, et al.
Sci Rep
. 2017 Nov;
7(1):15805.
PMID: 29150637
Mesorhizobium loti contains ten genes coding for proteins sharing high amino acid sequence identity with members of the Ros/MucR transcription factor family. Five of these Ros/MucR family members from Mesorhizobium...
9.
Hur S, Freschi A, Ideraabdullah F, Thorvaldsen J, Luense L, Weller A, et al.
Proc Natl Acad Sci U S A
. 2016 Sep;
113(39):10938-43.
PMID: 27621468
Genomic imprinting affects a subset of genes in mammals, such that they are expressed in a monoallelic, parent-of-origin-specific manner. These genes are regulated by imprinting control regions (ICRs), cis-regulatory elements...
10.
Boonen S, Freschi A, Christensen R, Valente F, Lildballe D, Perone L, et al.
Clin Epigenetics
. 2016 Jun;
8:69.
PMID: 27313795
Background: The overgrowth-associated Beckwith-Wiedemann syndrome (BWS) and the undergrowth-associated Silver-Russell syndrome (SRS) are characterized by heterogeneous molecular defects affecting a large imprinted gene cluster at chromosome 11p15.5-p15.4. While maternal and...