Vittoria Disciglio

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FOXO3 on the Road to Longevity: Lessons From SNPs and Chromatin Hubs

C. Simone, V. Disciglio, P. Sanese, 2019, Computational and structural biotechnology journal.

Epigenetic and Copy Number Variation Analysis in Retinoblastoma by MS-MLPA

T. Hadjistilianou, M. C. Epistolato, S. Lazzi, 2012, Pathology & Oncology Research.

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

P. Elliott, M. Jarvelin, C. Gieger, 2011, Nature.

Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation

J. Crolla, A. Collins, B. Gener, 2012, European journal of medical genetics.

Targeting SMYD3 to Sensitize Homologous Recombination-Proficient Tumors to PARP-Mediated Synthetic Lethality

M. Bartolini, G. Giannelli, L. Ottini, 2020, iScience.

Investigation of modifier genes within copy number variations in Rett syndrome

J. LaSalle, A. Renieri, M. Mucciolo, 2011, Journal of Human Genetics.

Investigation of modifier genes within copy number variations in Rett syndrome

J. LaSalle, A. Renieri, M. Mucciolo, 2011, Journal of Human Genetics.

Periventricular heterotopia with white matter abnormalities associated with 6p25 deletion

R. Guerrini, O. Zuffardi, A. Renieri, 2012, American journal of medical genetics. Part A.

From Genetics to Histomolecular Characterization: An Insight into Colorectal Carcinogenesis in Lynch Syndrome

A. Pisani, G. Ingravallo, C. Simone, 2021, International journal of molecular sciences.

APC Splicing Mutations Leading to In-Frame Exon 12 or Exon 13 Skipping Are Rare Events in FAP Pathogenesis and Define the Clinical Outcome

C. Simone, V. Disciglio, P. Sanese, 2021, Genes.

APC Splicing Mutations Leading to In-Frame Exon Skipping are Rare Events in FAP Pathogenesis and Define the Clinical Outcome

C. Simone, V. Disciglio, P. Sanese, 2021 .

FOXO3a from the Nucleus to the Mitochondria: A Round Trip in Cellular Stress Response

C. Simone, V. Disciglio, C. Fasano, 2019, Cells.

Whole exome sequencing and single nucleotide polymorphism array analyses to identify germline alterations in genes associated with testosterone metabolism in a patient with androgen insensitivity syndrome and early-onset colorectal cancer

G. Valle, L. De Cecco, S. Canevari, 2016, Chinese journal of cancer.

Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome

M. Fichera, C. Romano, A. Fryer, 2014, American journal of medical genetics. Part A.

c-MYC Protein Stability Is Sustained by MAPKs in Colorectal Cancer

G. Giannelli, A. Valentini, C. Simone, 2022, Cancers.

p53 Arg72Pro and MDM2 309 SNPs in hereditary retinoblastoma

A. Acquaviva, T. Hadjistilianou, M. C. Epistolato, 2011, Journal of Human Genetics.

p 53 Arg 72 Pro and MDM 2 309 SNPs in hereditary retinoblastoma

T. Hadjistilianou, M. C. Epistolato, D. Giachino, 2014 .

iPS cells to model CDKL5-related disorders

M. C. Epistolato, J. Ellis, A. Renieri, 2011, European Journal of Human Genetics.

Pharmacological targeting of the novel β-catenin chromatin-associated kinase p38α in colorectal cancer stem cell tumorspheres and organoids

G. Stassi, G. Giannelli, G. Ingravallo, 2021, Cell Death & Disease.

A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma

S. Manoukian, A. Ferrari, B. Pasini, 2014, BMC Medical Genetics.

A Low Glycemic Index Mediterranean Diet Combined with Aerobic Physical Activity Rearranges the Gut Microbiota Signature in NAFLD Patients

G. Giannelli, C. Bonfiglio, M. De Angelis, 2022, Nutrients.

Identification of a gene expression driven progression pathway in myxoid liposarcoma

L. De Cecco, S. Canevari, P. Casali, 2014, OncoTarget.

Identification of a gene expression driven progression pathway in myxoid liposarcoma

L. De Cecco, S. Canevari, P. Casali, 2014, Oncotarget.

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

L. Coin, C. Gieger, R. Pfundt, 2011, Nature.

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

P. Elliott, M. Jarvelin, C. Gieger, 2021 .

Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome

M. Fichera, C. Romano, A. Fryer, 2014, American journal of medical genetics. Part A.

Tumor Testing and Genetic Analysis to Identify Lynch Syndrome Patients in an Italian Colorectal Cancer Cohort

A. Valentini, A. L. Buonadonna, P. Sanese, 2023, Cancers.

SMYD3 Modulates AMPK-mTOR Signaling Balance in Cancer Cell Response to DNA Damage

G. Varchi, P. Sanese, C. Fasano, 2023, Cells.

Classic Galactosemia: Clinical and Computational Characterization of a Novel GALT Missense Variant (p.A303D) and a Literature Review

A. L. Buonadonna, P. Sanese, C. Fasano, 2023, International Journal of Molecular Sciences.

Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end

C. Simone, V. Disciglio, A. Stella, 2019, Journal of Medical Genetics.

Characterization of a rare variant (c.2635-2A>G) of the MSH2 gene in a family with Lynch syndrome

A. Di Carlo, M. Caruso, A. Valentini, 2018, The International journal of biological markers.

Understanding the Genetic Landscape of Pancreatic Ductal Adenocarcinoma to Support Personalized Medicine: A Systematic Review

P. Sanese, C. Fasano, G. Forte, 2023, Cancers.

Identification and Somatic Characterization of the Germline PTEN Promoter Variant rs34149102 in a Family with Gastrointestinal and Breast Tumors

A. Valentini, C. Simone, V. Disciglio, 2022, Genes.

The novel SMYD3 inhibitor EM127 impairs DNA repair response to chemotherapy-induced DNA damage and reverses cancer chemoresistance

M. Naldi, G. Varchi, C. Ferroni, 2024, Journal of experimental & clinical cancer research : CR.

In Silico Deciphering of the Potential Impact of Variants of Uncertain Significance in Hereditary Colorectal Cancer Syndromes

P. Sanese, C. Fasano, G. Forte, 2024, Cells.

Methyltransferases in cancer drug resistance: Unlocking the potential of targeting SMYD3 to sensitize cancer cells.

P. Sanese, C. Fasano, G. Forte, 2024, Biochimica et biophysica acta. Reviews on cancer.

The chromatin remodeling factors EP300 and TRRAP are novel SMYD3 interactors involved in the emerging ‘nonmutational epigenetic reprogramming’ cancer hallmark

P. Sanese, C. Fasano, G. Forte, 2023, Computational and structural biotechnology journal.

SMYD3 Modulates the HGF/MET Signaling Pathway in Gastric Cancer

G. Varchi, P. Sanese, C. Fasano, 2023, Cells.