TRAVERSA, Michele
TRAVERSA, Michele
Dipartimento di Medicina Molecolare e Traslazionale
A genome-wide pharmacogenomic study of patients with schizophrenia suggests that GRM7 mediates the effects of risperidone on positive symptoms
2013-01-01 Magri, Chiara; Minelli, Alessandra; Traversa, Michele; Valsecchi, Paolo; Scassellati, C.; Sacchetti, Emilio; Gennarelli, Massimo
Analysis of Copy Number Variations in Schizophrenia Italian Patients
2009-01-01 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
2010-01-01 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
2010-01-01 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.
2013-01-01 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
2017-01-01 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.
2012-01-01 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.
2015-01-01 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.
2014-01-01 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
2011-01-01 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
2012-01-01 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
2017-01-01 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.
2012-01-01 Piovani, Giovanna; Magri, Chiara; Savio, Giulia; Traversa, Michele; Salvi, Alessandro; DE PETRO, Giuseppina; Barlati, Sergio
Genome wide study of Italian schizophrenia patients
2011-01-01 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
2012-01-01 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
2009-01-01 Magri, Chiara; Pilotta, A.; Piovani, Giovanna; Traversa, Michele; Buzi, F.; Barlati, Sergio
Identification and molecular characterization of cryptic chromosomal rearrangements in mental retardation patients.
2012-01-01 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
2012-01-01 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
2015-01-01 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
2010-01-01 Magri, Chiara; Sacchetti, Emilio; Traversa, Michele; Valsecchi, Paolo; Gardella, Rita; Bonvicini, C; Minelli, Alessandra; Gennarelli, Massimo; Barlati, Sergio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 |