Publications by authors named "Michele Traversa"

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Cemiplimab in an Elderly Frail Population of Patients With Locally Advanced or Metastatic Cutaneous Squamous Cell Carcinoma: A Single-Center Real-Life Experience From Italy.
Sabino Strippoli, Annarita Fanizzi, Davide Quaresmini, Annalisa Nardone, Andrea Armenio, Michele Traversa

Front Oncol· November 2021

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The Management of Oligoprogression in the Landscape of New Therapies for Metastatic Melanoma.
Michele Guida, Nicola Bartolomeo, Ivana De Risi, Livia Fucci, Andrea Armenio, Michele Traversa

Cancers (Basel)· October 2019

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Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia.
Rita Gardella, Emilio Sacchetti, Andrea Legati, Chiara Magri, Michele Traversa

Psychiatry Res· December 2017

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Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways.
Edoardo Giacopuzzi, Massimo Gennarelli, Alessandra Minelli, Rita Gardella, Paolo Valsecchi, Michele Traversa

PLoS One· September 2017

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Sorafenib induces variations of the DNA methylome in HA22T/VGH human hepatocellular carcinoma-derived cells.
Edoardo Abeni, Alessandro Salvi, Eleonora Marchina, Michele Traversa, Bruna Arici

Int J Oncol· July 2017

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SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement.
Chiara Magri, Eleonora Marchina, Valeria Bertini, Michele Traversa, Giulia Savio

BMC Med Genet· July 2015

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Long-term response of gemcitabine plus docetaxel chemotherapy regimen for extraskeletal osteosarcoma: A case report.
Sabino Strippoli, Michele Traversa, Antonio Cramarossa, Ondina Popescu, Vito Lorusso

Oncol Lett· June 2015

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Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role.
Stefano Valbonesi, Chiara Magri, Michele Traversa, Stephen V Faraone, Annamaria Cattaneo

Psychiatr Genet· April 2015

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Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel mutations.
Marco Ritelli, Nicola Chiarelli, Nicoletta Zoppi, Chiara Dordoni, Stefano Quinzani, Michele Traversa

Mol Genet Metab Rep· March 2015

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De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay.
Giovanna Piovani, Giulia Savio, Michele Traversa, Alba Pilotta, Giuseppina De Petro

Mol Cytogenet· May 2014

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Clinical and molecular characterization of 40 patients with classic Ehlers-Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations.
Marco Ritelli, Chiara Dordoni, Marina Venturini, Nicola Chiarelli, Stefano Quinzani, Michele Traversa

Orphanet J Rare Dis· April 2013

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De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia.
Chiara Magri, Giovanna Piovani, Alba Pilotta, Traversa Michele, Fabio Buzi

Eur J Med Genet· September 2011

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New copy number variations in schizophrenia.
Chiara Magri, Emilio Sacchetti, Michele Traversa, Paolo Valsecchi, Rita Gardella

PLoS One· October 2010

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Evidences for insulator activity of the 5'UTR of the Drosophila melanogaster LTR-retrotransposon ZAM.
Crescenzio Francesco Minervini, Simona Ruggieri, Michele Traversa, Leonardo D'Aiuto, Rene' Massimiliano Marsano

Mol Genet Genomics· May 2010

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