MAGRI, Chiara
MAGRI, Chiara
Dipartimento di Medicina Molecolare e Traslazionale
"GenotypeColour": colour visualisation of SNPs and CNVs
2009-01-01 Barlati, Sergio; Chiesa, S; Magri, Chiara
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
A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme
2018-01-01 Magri, Chiara; Giacopuzzi, Edoardo; LA VIA, Luca; Bonini, Daniela; Ravasio, Viola; Elhussiny, MOHAMMED ELHUSSINY ALI; Orizio, Flavia; Gangemi, Fabrizio; Valsecchi, Paolo; Bresciani, Roberto; Barbon, Alessandro; Vita, Antonio; Gennarelli, Massimo
Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles
2021-01-01 Magri, C.; Giacopuzzi, E.; Sacco, C.; Bocchio-Chiavetto, L.; Minelli, A.; Gennarelli, M.
Analysis of Citalopram response heterogeneity among STAR*D patients using in-silico methods
2019-01-01 Shoaib, Muhammad; Giacopuzzi, Edoardo; Magri, Chiara; Vitali, Erika; Minelli, Alessandra; Gennarelli, Massimo
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder.
2011-01-01 Bertolin, C; Magri, Chiara; Barlati, Sergio; Vettori, A; Perini, Gi; Peruzzi, P; Mostacciuolo, Ml; Vazza, G.
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
Assessment of haptoglobin alleles in autism spectrum disorders
2020-01-01 Cupaioli, F. A.; Mosca, E.; Magri, C.; Gennarelli, M.; Moscatelli, M.; Raggi, M. E.; Landini, M.; Galluccio, N.; Villa, L.; Bonfanti, A.; Renieri, A.; Fallerini, C.; Minelli, A.; Marabotti, A.; Milanesi, L.; Fasano, A.; Mezzelani, A.
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia
2009-01-01 Iatropoulos, P; Gardella, Rita; Valsecchi, Paolo; Magri, Chiara; Ratti, C; Podavini, D; Rossi, G; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio
Association study between HTR2A rs6313 polymorphism and early response to risperidone and olanzapine in schizophrenia patients
2020-01-01 Maffioletti, E.; Valsecchi, P.; Minelli, A.; Magri, C.; Bonvicini, C.; Barlati, S.; Sacchetti, E.; Vita, A.; Gennarelli, M.
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4
2006-01-01 Magri, Chiara; Gardella, Rita; Imperadori, L; Podavini, D; Iatropoulos, P; Barlati, Sergio; Valsecchi, Paolo; Bonvicini, C; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, S.
Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial)
2021-01-01 Minelli, A.; Barlati, S.; Vitali, E.; Bignotti, S.; Dattilo, V.; Tura, G. B.; Maffioletti, E.; Giacopuzzi, E.; Santoro, V.; Perusi, G.; Cobelli, C.; Magri, C.; Bonizzato, S.; Bocchio-Chiavetto, L.; Spina, E.; Vita, A.; Gennarelli, M.
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections.
2013-01-01 Darrell L., Dinwiddie; Stephen F., Kingsmore; Sonia, Caracciolo; Giuseppe, Rossi; Moratto, Daniele; Cinzia, Mazza; Cristiano, Sabelli; Rosa, Bacchetta; Laura, Passerini; Magri, Chiara; Callum J., Bell; Neil A., Miller; Shannon L., Hateley; Carol J., Saunders; Lu, Zhang; Gary P., Schroth; Barlati, Sergio; Badolato, Raffaele
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
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| "GenotypeColour": colour visualisation of SNPs and CNVs | 1-gen-2009 | Barlati, Sergio; Chiesa, S; Magri, Chiara | |
| 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 | |
| A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme | 1-gen-2018 | Magri, Chiara; Giacopuzzi, Edoardo; LA VIA, Luca; Bonini, Daniela; Ravasio, Viola; Elhussiny, MOHAMMED ELHUSSINY ALI; Orizio, Flavia; Gangemi, Fabrizio; Valsecchi, Paolo; Bresciani, Roberto; Barbon, Alessandro; Vita, Antonio; Gennarelli, Massimo | |
| Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles | 1-gen-2021 | Magri, C.; Giacopuzzi, E.; Sacco, C.; Bocchio-Chiavetto, L.; Minelli, A.; Gennarelli, M. | |
| Analysis of Citalopram response heterogeneity among STAR*D patients using in-silico methods | 1-gen-2019 | Shoaib, Muhammad; Giacopuzzi, Edoardo; Magri, Chiara; Vitali, Erika; Minelli, Alessandra; Gennarelli, Massimo | |
| Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. | 1-gen-2011 | Bertolin, C; Magri, Chiara; Barlati, Sergio; Vettori, A; Perini, Gi; Peruzzi, P; Mostacciuolo, Ml; Vazza, G. | |
| 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 | |
| Assessment of haptoglobin alleles in autism spectrum disorders | 1-gen-2020 | Cupaioli, F. A.; Mosca, E.; Magri, C.; Gennarelli, M.; Moscatelli, M.; Raggi, M. E.; Landini, M.; Galluccio, N.; Villa, L.; Bonfanti, A.; Renieri, A.; Fallerini, C.; Minelli, A.; Marabotti, A.; Milanesi, L.; Fasano, A.; Mezzelani, A. | |
| Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia | 1-gen-2009 | Iatropoulos, P; Gardella, Rita; Valsecchi, Paolo; Magri, Chiara; Ratti, C; Podavini, D; Rossi, G; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio | |
| Association study between HTR2A rs6313 polymorphism and early response to risperidone and olanzapine in schizophrenia patients | 1-gen-2020 | Maffioletti, E.; Valsecchi, P.; Minelli, A.; Magri, C.; Bonvicini, C.; Barlati, S.; Sacchetti, E.; Vita, A.; Gennarelli, M. | |
| Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 | 1-gen-2006 | Magri, Chiara; Gardella, Rita; Imperadori, L; Podavini, D; Iatropoulos, P; Barlati, Sergio; Valsecchi, Paolo; Bonvicini, C; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, S. | |
| Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial) | 1-gen-2021 | Minelli, A.; Barlati, S.; Vitali, E.; Bignotti, S.; Dattilo, V.; Tura, G. B.; Maffioletti, E.; Giacopuzzi, E.; Santoro, V.; Perusi, G.; Cobelli, C.; Magri, C.; Bonizzato, S.; Bocchio-Chiavetto, L.; Spina, E.; Vita, A.; Gennarelli, M. | |
| Combined DOCK8 and CLEC7A mutations causing immunodeficiency in three brothers with diarrhea, eczema and infections. | 1-gen-2013 | Darrell L., Dinwiddie; Stephen F., Kingsmore; Sonia, Caracciolo; Giuseppe, Rossi; Moratto, Daniele; Cinzia, Mazza; Cristiano, Sabelli; Rosa, Bacchetta; Laura, Passerini; Magri, Chiara; Callum J., Bell; Neil A., Miller; Shannon L., Hateley; Carol J., Saunders; Lu, Zhang; Gary P., Schroth; Barlati, Sergio; Badolato, Raffaele | |
| 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 |