TRAVERSA, Michele

TRAVERSA, Michele  

Dipartimento di Medicina Molecolare e Traslazionale  

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A genome-wide pharmacogenomic study of patients with schizophrenia suggests that GRM7 mediates the effects of risperidone on positive symptoms 1-gen-2013 Magri, Chiara; Minelli, Alessandra; Traversa, Michele; Valsecchi, Paolo; Scassellati, C.; Sacchetti, Emilio; Gennarelli, Massimo
Analysis of Copy Number Variations in Schizophrenia Italian Patients 1-gen-2009 Traversa, Michele; Magri, Chiara; Valsecchi, Paolo; Gardella, Rita; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio
Application of SNP-arrays, FISH and genotypecolour in molecular diagnosis of mental retardation 1-gen-2010 Magri, Chiara; Piovani, Giovanna; Traversa, Michele; Bertini, Valeria; Pilotta, A.; Barlati, Sergio
Application of SNP-Arrays, FISH and GenotypeColour in Molecular Diagnosis of Mental Retardation 1-gen-2010 Magri, Chiara; Piovani, Giovanna; Traversa, Michele; Bertini, Valeria; Pilotta, A.; Barlati, Sergio
Clinical and molecular characterization of 40 patients with classic Ehlers--Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations. 1-gen-2013 Ritelli, Marco Giuseppe; Dordoni, Chiara; Venturini, Marina; Chiarelli, Nicola; Quinzani, Stefano; Traversa, Michele; Zoppi, Nicoletta; Vascellaro, Annalisa; Wischmeijer, A.; Manfredini, E.; Garavelli, L.; CALZAVARA PINTON, Piergiacomo; Colombi, Marina
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 1-gen-2017 Gardella, Rita; Sacchetti, Emilio; Legati, Andrea; Magri, Chiara; Traversa, Michele; Gennarelli, Massimo
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 1-gen-2012 Gardella, Rita; Legati, Andrea; Magri, Chiara; Traversa, Michele; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio
Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role. 1-gen-2015 S., Valbonesi; Magri, Chiara; Traversa, Michele; S. V., Faraone; A., Cattaneo; E., Milanesi; V., Valenti; Gennarelli, Massimo; C., Scassellati
De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. 1-gen-2014 Piovani, Giovanna; Savio, Giulia; Traversa, Michele; Pilotta, A; DE PETRO, Giuseppina; Barlati, Sergio; Magri, Chiara
De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia 1-gen-2011 Magri, Chiara; Piovani, Giovanna; Pilotta, A; Traversa, Michele; Buzi, F; Barlati, Sergio
Detection of high level of autozygosity in a group of Italian schizophrenia patients 1-gen-2012 Traversa, Michele; Magri, Chiara; Gardella, Rita; Valsecchi, Paolo; Sacchetti, Emilio; Gennarelli, Massimo; Barlati, Sergio
Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways 1-gen-2017 Giacopuzzi, Edoardo; Gennarelli, Massimo; Minelli, Alessandra; Gardella, Rita; Valsecchi, Paolo; Traversa, Michele; Bonvicini, Cristian; Vita, Antonio; Sacchetti, Emilio; Magri, Chiara
Genes and MiRNAs in mental retardation patients with cryptic chromosome imbalances detected by SNP-based array analysis. 1-gen-2012 Piovani, Giovanna; Magri, Chiara; Savio, Giulia; Traversa, Michele; Salvi, Alessandro; DE PETRO, Giuseppina; Barlati, Sergio
Genome wide study of Italian schizophrenia patients 1-gen-2011 Magri, Chiara; Traversa, Michele; Gardella, Rita; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio
Genome-Wide pharmacogenomics analysis of early antipsychotic (risperidone) response in patients with schizophrenia 1-gen-2012 Magri, Chiara; Minelli, Alessandra; Traversa, Michele; Valsecchi, Paolo; Congiu, Chiara; Sacchetti, Emilio; Gennarelli, Massimo
Identification and characterization of an Xq26-27 duplication in a male with psycomotor retardation and craniofacial dysmorphisms 1-gen-2009 Magri, Chiara; Pilotta, A.; Piovani, Giovanna; Traversa, Michele; Buzi, F.; Barlati, Sergio
Identification and molecular characterization of cryptic chromosomal rearrangements in mental retardation patients. 1-gen-2012 Savio, Giulia; Piovani, Giovanna; Magri, Chiara; Traversa, Michele; Salvi, Alessandro; DE PETRO, Giuseppina; Barlati, Sergio
Identificazione mediante exome sequencing di una variante del gene RBMXL1 in una famiglia affetta da atassia cerebellare pura 1-gen-2012 Legati, Andrea; Magri, Chiara; Traversa, Michele; Barlati, Sergio; Colombi, Marina; Gardella, Rita
Molecular characterization and transcriptome-wide expression profiling of two patients affected with spondyloepimetaphyseal dysplasia with joint laxity type 1-gen-2015 Ritelli, Marco Giuseppe; Chiarelli, Nicola; Zoppi, Nicoletta; Dordoni, Chiara; Quinzani, Stefano; Traversa, Michele; Venturini, Marina; CALZAVARA PINTON, Piergiacomo; Colombi, Marina
New Copy Number Variations in Schizophrenia 1-gen-2010 Magri, Chiara; Sacchetti, Emilio; Traversa, Michele; Valsecchi, Paolo; Gardella, Rita; Bonvicini, C; Minelli, Alessandra; Gennarelli, Massimo; Barlati, Sergio