Publications by authors named "Nadia Passon"

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Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance.
Federica Baldan, Eliana Demori, Chiara Gnan, Nadia Passon, Giuseppe Damante

Gene· January 2025

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A bird's eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases.
Jessica Zucco, Federica Baldan, Lorenzo Allegri, Elisa Bregant, Nadia Passon

J Hum Genet· June 2024

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Novel IGFALS mutations with predicted pathogenetic effects by the analysis of AlphaFold structure.
Alessandra Franzoni, Federica Baldan, Nadia Passon, Catia Mio, Daniela Driul

Endocrine· February 2023

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Dystonic tremor and blepharospasm in a patient with deletion of 18q.
Yan Tereshko, Enrico Belgrado, Christian Lettieri, Nadia Passon, Giuseppe Damante

Clin Neurol Neurosurg· January 2023

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A novel de novo HDAC8 missense mutation causing Cornelia de Lange syndrome.
Catia Mio, Nadia Passon, Federico Fogolari, Claudia Cesario, Antonio Novelli

Mol Genet Genomic Med· September 2021

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NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome.
Elena Cavaliere, Anna Jolanda Gortan, Nadia Passon, Dora Fabbro, Dario Marin

Clin Genet· July 2021

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A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver-Russell syndrome phenotype.
Catia Mio, Lorenzo Allegri, Nadia Passon, Elisa Bregant, Eliana Demori

Eur J Hum Genet· March 2021

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CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers.
Catia Mio, Nadia Passon, Federica Baldan, Elisa Bregant, Elisabetta Monaco

Eur J Med Genet· April 2020

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Quantitative PCR evaluation of deletions/duplications identified by array CGH.
Federica Baldan, Nadia Passon, Silvia Burra, Eliana Demori, Patrizia Dello Russo

Mol Cell Probes· August 2019

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Evaluation of somatic genomic imbalances in thyroid carcinomas of follicular origin by CGH-based approaches.
Federica Baldan, Catia Mio, Lorenzo Allegri, Nadia Passon, Saverio M Lepore

Minerva Endocrinol· September 2018

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Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder.
Federica Baldan, Chiara Gnan, Alessandra Franzoni, Lucia Ferino, Lorenzo Allegri, Nadia Passon

Cytogenet Genome Res· July 2018

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Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with Epilepsy.
Chiara Gnan, Alessandra Franzoni, Federica Baldan, Nadia Passon, Giuseppe Damante

Mol Syndromol· March 2017

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Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical Findings.
Patrizia Dello Russo, Eliana Demori, Annalisa Sechi, Nadia Passon, Daniela Romagno

Cytogenet Genome Res· January 2017

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Somatic amplifications and deletions in genome of papillary thyroid carcinomas.
Nadia Passon, Elisa Bregant, Marialuisa Sponziello, Maria Dima, Francesca Rosignolo

Endocrine· November 2015

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Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff disease: functional characterization of 9 novel sequence variants.
Stefania Zampieri, Silvia Cattarossi, Ana Maria Oller Ramirez, Camillo Rosano, Charles Marques Lourenco, Nadia Passon

PLoS One· March 2013

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A new germline VHL gene mutation in three patients with apparently sporadic pheochromocytoma.
Angela V D'Elia, Franco Grimaldi, Stefano Pizzolitto, Giovanna De Maglio, Elisa Bregant, Nadia Passon

Clin Endocrinol (Oxf)· March 2013

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The PARP inhibitor PJ34 modifies proliferation, NIS expression and epigenetic marks in thyroid cancer cell lines.
Elisa Lavarone, Cinzia Puppin, Nadia Passon, Sebastiano Filetti, Diego Russo

Mol Cell Endocrinol· January 2013

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Cyclic AMP-response element modulator inhibits the promoter activity of the sodium iodide symporter gene in thyroid cancer cells.
Nadia Passon, Cinzia Puppin, Elisa Lavarone, Elisa Bregant, Alessandra Franzoni

Thyroid· May 2012

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Expression of Dicer and Drosha in triple-negative breast cancer.
Nadia Passon, Anna Gerometta, Cinzia Puppin, Elisa Lavarone, Fabio Puglisi

J Clin Pathol· April 2012

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Histone post-translational modifications associated to BAALC expression in leukemic cells.
Alessandra Franzoni, Nadia Passon, Dora Fabbro, Mario Tiribelli, Daniela Damiani

Biochem Biophys Res Commun· January 2012

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Levels of histone acetylation in thyroid tumors.
Cinzia Puppin, Nadia Passon, Elisa Lavarone, Carla Di Loreto, Francesco Frasca

Biochem Biophys Res Commun· August 2011

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In thyroid cancer cell lines expression of periostin gene is controlled by p73 and is not related to epigenetic marks of active transcription.
Cinzia Puppin, Nadia Passon, Francesco Frasca, Riccardo Vigneri, Federica Tomay

Cell Oncol (Dordr)· April 2011

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Nucleophosmin delocalization in thyroid tumour cells.
Annalisa Pianta, Cinzia Puppin, Nadia Passon, Alessandra Franzoni, Milena Romanello

Endocr Pathol· March 2011

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Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells.
Cinzia Puppin, Nadia Passon, Alessandra Franzoni, Diego Russo, Giuseppe Damante

Oncol Rep· February 2011

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Quick MLPA test for quantification of SMN1 and SMN2 copy numbers.
Nadia Passon, Giorgia Dubsky de Wittenau, Irena Jurman, Slobodanka Radovic, Elisa Bregant

Mol Cell Probes· October 2010

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