Andrea Freschi

Genoa, 16163, Italy

Last Updated: 09/26/2026

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Found 12 publications

The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model.

The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model.

Journal: Human molecular genetics

Published: March 01, 2021

Loss of Snord116 alters cortical neuronal activity in mice: a preclinical investigation of Prader-Willi syndrome.

Loss of Snord116 alters cortical neuronal activity in mice: a preclinical investigation of Prader-Willi syndrome.

Journal: Human molecular genetics

Published: March 04, 2020

Loss of Snord116 impacts lateral hypothalamus, sleep, and food-related behaviors.

Loss of Snord116 impacts lateral hypothalamus, sleep, and food-related behaviors.

Journal: JCI insight

Published: February 28, 2020

Non-invasive identification of synthetic organic pigments in contemporary art paints by visible-excited spectrofluorimetry and visible reflectance spectroscopy.

Non-invasive identification of synthetic organic pigments in contemporary art paints by visible-excited spectrofluorimetry and visible reflectance spectroscopy.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Published: September 18, 2019

Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus.

Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 09, 2018

Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.

Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.

Journal: PLoS genetics

Published: October 17, 2017

Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability.

Ml proteins from Mesorhizobium loti and MucR from Brucella abortus: an AT-rich core DNA-target site and oligomerization ability.

Journal: Scientific reports

Published: May 31, 2017

Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes.

Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 14, 2016

Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes.

Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes.

Journal: Clinical epigenetics

Published: April 07, 2016

Fetal growth patterns in Beckwith-Wiedemann syndrome.

Fetal growth patterns in Beckwith-Wiedemann syndrome.

Journal: Clinical genetics

Published: December 01, 2015

(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.

(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.

Journal: European journal of human genetics : EJHG

Published: October 27, 2014

A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.

A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.

Journal: Journal of human genetics

Published: October 24, 2014

Showing 1-12 of 12

Last Updated: 09/26/2026