Sfoglia per Autore
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
Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders.
2013-01-01 Minelli, Alessandra; Maffioletti, Elisabetta; Cloninger, Cr; Magri, Chiara; Sartori, R; Bortolomasi, M; Congiu, Chiara; Bignotti, S; Segala, M; Giacopuzzi, M; Gennarelli, Massimo
Whole exome sequencing of schizophrenia patients with high level of autozygosity.
2014-01-01 Magri, Chiara; Giacopuzzi, Edoardo; Valsecchi, Paolo; Traversa, Michele; Gardella, Rita; Borsani, Giuseppe; Barlati, Sergio; Sacchetti, Emilio; Gennarelli, Massimo
Study of the genetic architecture behind mood disorders by whole exome sequencing on a large Italian pedigree
2014-01-01 Giacopuzzi, Edoardo; Magri, Chiara; Minelli, Alessandra; Valsecchi, Paolo; Monchieri, S.; Borsani, Giuseppe; Sacchetti, Emilio; Gennarelli, Massimo
Whole exome sequencing of schizophrenia patients with high level of autozygosity.
2014-01-01 Magri, Chiara; Giacopuzzi, Edoardo; Valsecchi, Paolo; Traversa, Michele; Gardella, Rita; Borsani, Giuseppe; Barlati, Sergio; Sacchetti, Emilio; Gennarelli, Massimo
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
Whole exome sequencing of schizophrenia patients with high level of autozygosity.
2014-01-01 Magri, Chiara; Giacopuzzi, Edoardo; Valsecchi, Paolo; Traversa, Michele; Gardella, Rita; Borsani, Giuseppe; Barlati, Sergio; Sacchetti, Emilio; Gennarelli, Massimo
SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement
2015-01-01 Magri, Chiara; Marchina, Eleonora; Bertini, Valeria; Traversa, Michele; Savio, Giulia; Pilotta, Alba; Piovani, Giovanna
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder
2015-01-01 de Moor, Marleen H. M; van den Berg, Stéphanie M; Verweij, Karin J. H; Krueger, Robert F; Luciano, Michelle; Arias Vasquez, Alejandro; Matteson, Lindsay K; Derringer, Jaime; Esko, Tõnu; Amin, Najaf; Gordon, Scott D; Hansell, Narelle K; Hart, Amy B; Seppälä, Ilkka; Huffman, Jennifer E; Konte, Bettina; Lahti, Jari; Lee, Minyoung; Miller, Mike; Nutile, Teresa; Tanaka, Toshiko; Teumer, Alexander; Viktorin, Alexander; Wedenoja, Juho; Abecasis, Goncalo R; Adkins, Daniel E; Agrawal, Arpana; Allik, Jüri; Appel, Katja; Bigdeli, Timothy B; Busonero, Fabio; Campbell, Harry; Costa, Paul T; Davey Smith, George; Davies, Gail; de Wit, Harriet; Ding, Jun; Engelhardt, Barbara E; Eriksson, Johan G; Fedko, Iryna O; Ferrucci, Luigi; Franke, Barbara; Giegling, Ina; Grucza, Richard; Hartmann, Annette M; Heath, Andrew C; Heinonen, Kati; Henders, Anjali K; Homuth, Georg; Hottenga, Jouke Jan; Iacono, William G; Janzing, Joost; Jokela, Markus; Karlsson, Robert; Kemp, John P; Kirkpatrick, Matthew G; Latvala, Antti; Lehtimäki, Terho; Liewald, David C; Madden, Pamela A. F; Magri, Chiara; Magnusson, Patrik K. E; Marten, Jonathan; Maschio, Andrea; Medland, Sarah E; Mihailov, Evelin; Milaneschi, Yuri; Montgomery, Grant W; Nauck, Matthias; Ouwens, Klaasjan G; Palotie, Aarno; Pettersson, Erik; Polasek, Ozren; Qian, Yong; Pulkki Råback, Laura; Raitakari, Olli T; Realo, Anu; Rose, Richard J; Ruggiero, Daniela; Schmidt, Carsten O; Slutske, Wendy S; Sorice, Rossella; Starr, John M; St Pourcain, Beate; Sutin, Angelina R; Timpson, Nicholas J; Trochet, Holly; Vermeulen, Sita; Vuoksimaa, Eero; Widen, Elisabeth; Wouda, Jasper; Wright, Margaret J; Zgaga, Lina; Porteous, David; Minelli, Alessandra; Palmer, Abraham A; Rujescu, Dan; Ciullo, Marina; Hayward, Caroline; Rudan, Igor; Metspalu, Andres; Kaprio, Jaakko; Deary, Ian J; Räikkönen, Katri; Wilson, James F; Keltikangas Järvinen, Liisa; Bierut, Laura J; Hettema, John M; Grabe, Hans J; van Duijn, Cornelia M; Evans, David M; Schlessinger, David; Pedersen, Nancy L; Terracciano, Antonio; Mcgue, Matt; Penninx, Brenda W. J. H; Martin, Nicholas G; Boomsma, Dorret I.
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
Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder
2015-01-01 Minelli, Alessandra; Magri, Chiara; Barbon, Alessandro; Bonvicini, Cristian; Segala, Matilde; Congiu, Chiara; Bignotti, Stefano; Milanesi, Elena; Trabucchi, Luigi; Cattane, Nadia; Bortolomasi, Marco; Gennarelli, Massimo
Exome sequencing of schizophrenia patients with high level of homozygosity identifies a homozygous novel mutation that reduces the glutamate acid decarboxylase 67 (GAD67) activity
2016-01-01 Magri, Chiara; Giacopuzzi, Edoardo; Barbon, Alessandro; LA VIA, Luca; Mingardi, J; Congiu, Chiara; Orizio, Flavia; Bresciani, Roberto; Sacchetti, Emilio; Gennarelli, Massimo
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium
2016-01-01 van Den Berg, Stéphanie M; de Moor, Marleen H. M.; Verweij, Karin J. H.; Krueger, Robert F.; Luciano, Michelle; Arias Vasquez, Alejandro; Matteson, Lindsay K.; Derringer, Jaime; Esko, Tõnu; Amin, Najaf; Gordon, Scott D.; Hansell, Narelle K.; Hart, Amy B.; Seppälä, Ilkka; Huffman, Jennifer E.; Konte, Bettina; Lahti, Jari; Lee, Minyoung; Miller, Mike; Nutile, Teresa; Tanaka, Toshiko; Teumer, Alexander; Viktorin, Alexander; Wedenoja, Juho; Abdellaoui, Abdel; Abecasis, Goncalo R.; Adkins, Daniel E.; Agrawal, Arpana; Allik, Jüri; Appel, Katja; Bigdeli, Timothy B.; Busonero, Fabio; Campbell, Harry; Costa, Paul T.; Smith, George Davey; Davies, Gail; de Wit, Harriet; Ding, Jun; Engelhardt, Barbara E.; Eriksson, Johan G.; Fedko, Iryna O.; Ferrucci, Luigi; Franke, Barbara; Giegling, Ina; Grucza, Richard; Hartmann, Annette M.; Heath, Andrew C.; Heinonen, Kati; Henders, Anjali K.; Homuth, Georg; Hottenga, Jouke Jan; Iacono, William G.; Janzing, Joost; Jokela, Markus; Karlsson, Robert; Kemp, John P.; Kirkpatrick, Matthew G.; Latvala, Antti; Lehtimäki, Terho; Liewald, David C.; Madden, Pamela A. F.; Magri, Chiara; Magnusson, Patrik K. E.; Marten, Jonathan; Maschio, Andrea; Mbarek, Hamdi; Medland, Sarah E.; Mihailov, Evelin; Milaneschi, Yuri; Montgomery, Grant W.; Nauck, Matthias; Nivard, Michel G.; Ouwens, Klaasjan G.; Palotie, Aarno; Pettersson, Erik; Polasek, Ozren; Qian, Yong; Pulkki Råback, Laura; Raitakari, Olli T.; Realo, Anu; Rose, Richard J.; Ruggiero, Daniela; Schmidt, Carsten O.; Slutske, Wendy S.; Sorice, Rossella; Starr, John M.; St Pourcain, Beate; Sutin, Angelina R.; Timpson, Nicholas J.; Trochet, Holly; Vermeulen, Sita; Vuoksimaa, Eero; Widen, Elisabeth; Wouda, Jasper; Wright, Margaret J.; Zgaga, Lina; Generation Scotland, Null; Porteous, David; Minelli, Alessandra; Palmer, Abraham A.; Rujescu, Dan; Ciullo, Marina; Hayward, Caroline; Rudan, Igor; Metspalu, Andres; Kaprio, Jaakko; Deary, Ian J.; Räikkönen, Katri; Wilson, James F.; Keltikangas Järvinen, Liisa; Bierut, Laura J.; Hettema, John M.; Grabe, Hans J.; Penninx, Brenda W. J. H.; van Duijn, Cornelia M.; Evans, David M.; Schlessinger, David; Pedersen, Nancy L.; Terracciano, Antonio; Mcgue, Matt; Martin, Nicholas G.; Boomsma, Dorret I.
Genome-wide analysis of RNA-editing levels in human blood identifies interactions with mRNA processing genes and suggests correlation with biological and drug-related variables
2017-01-01 Giacopuzzi, E; Magri, C; Gennarelli, M; Barbon, A
The impairment of GABAergic pathway as one of the driver forces in the etiopathogenesis of schizophrenia: evidence from functional studies and gene-set enrichment analyses
2017-01-01 Magri, Chiara; Giacopuzzi, Edoardo; La Via, L.; Bonini, D.; Ravasio, V.; Elhussiny, M. E. A.; Valsecchi, P.; Bresciani, R.; Barbon, A.; Vita, A.; Gennarelli, M.
New biological pathways for major depression: gene expression decomposition in G x E components
2017-01-01 Sacco, Chiara; Giacopuzzi, E; Gennarelli, M; Magri, C
The effect of childhood trauma on blood transcriptome expression in major depressive disorder
2017-01-01 Minelli, Alessandra; Magri, Chiara; Giacopuzzi, Edoardo; Gennarelli, Massimo
The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis
2017-01-01 Sacchetti, Emilio; Magri, Chiara; Minelli, Alessandra; Valsecchi, Paolo; Traversa, Michele; Calza, Stefano; Vita, Antonio; Gennarelli, Massimo
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
Functional study of a novel homozygous mutation in the GAD1 gene, detected in a patient with schizophrenia.
2017-01-01 Magri, Chiara; Giacopuzzi, Edoardo; Barbon, Alessandro; La Via, Luca; Congiu, Chiara; Orizio, Flavia; Ferraboli, Sergio; Bresciani, Roberto; Borsani, Giuseppe; Sacchetti, Emilio; Gennarelli, Massimo
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders. | 1-gen-2013 | Minelli, Alessandra; Maffioletti, Elisabetta; Cloninger, Cr; Magri, Chiara; Sartori, R; Bortolomasi, M; Congiu, Chiara; Bignotti, S; Segala, M; Giacopuzzi, M; Gennarelli, Massimo | |
| Whole exome sequencing of schizophrenia patients with high level of autozygosity. | 1-gen-2014 | Magri, Chiara; Giacopuzzi, Edoardo; Valsecchi, Paolo; Traversa, Michele; Gardella, Rita; Borsani, Giuseppe; Barlati, Sergio; Sacchetti, Emilio; Gennarelli, Massimo | |
| Study of the genetic architecture behind mood disorders by whole exome sequencing on a large Italian pedigree | 1-gen-2014 | Giacopuzzi, Edoardo; Magri, Chiara; Minelli, Alessandra; Valsecchi, Paolo; Monchieri, S.; Borsani, Giuseppe; Sacchetti, Emilio; Gennarelli, Massimo | |
| Whole exome sequencing of schizophrenia patients with high level of autozygosity. | 1-gen-2014 | Magri, Chiara; Giacopuzzi, Edoardo; Valsecchi, Paolo; Traversa, Michele; Gardella, Rita; Borsani, Giuseppe; Barlati, Sergio; Sacchetti, Emilio; Gennarelli, Massimo | |
| 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 | |
| Whole exome sequencing of schizophrenia patients with high level of autozygosity. | 1-gen-2014 | Magri, Chiara; Giacopuzzi, Edoardo; Valsecchi, Paolo; Traversa, Michele; Gardella, Rita; Borsani, Giuseppe; Barlati, Sergio; Sacchetti, Emilio; Gennarelli, Massimo | |
| SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement | 1-gen-2015 | Magri, Chiara; Marchina, Eleonora; Bertini, Valeria; Traversa, Michele; Savio, Giulia; Pilotta, Alba; Piovani, Giovanna | |
| Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder | 1-gen-2015 | de Moor, Marleen H. M; van den Berg, Stéphanie M; Verweij, Karin J. H; Krueger, Robert F; Luciano, Michelle; Arias Vasquez, Alejandro; Matteson, Lindsay K; Derringer, Jaime; Esko, Tõnu; Amin, Najaf; Gordon, Scott D; Hansell, Narelle K; Hart, Amy B; Seppälä, Ilkka; Huffman, Jennifer E; Konte, Bettina; Lahti, Jari; Lee, Minyoung; Miller, Mike; Nutile, Teresa; Tanaka, Toshiko; Teumer, Alexander; Viktorin, Alexander; Wedenoja, Juho; Abecasis, Goncalo R; Adkins, Daniel E; Agrawal, Arpana; Allik, Jüri; Appel, Katja; Bigdeli, Timothy B; Busonero, Fabio; Campbell, Harry; Costa, Paul T; Davey Smith, George; Davies, Gail; de Wit, Harriet; Ding, Jun; Engelhardt, Barbara E; Eriksson, Johan G; Fedko, Iryna O; Ferrucci, Luigi; Franke, Barbara; Giegling, Ina; Grucza, Richard; Hartmann, Annette M; Heath, Andrew C; Heinonen, Kati; Henders, Anjali K; Homuth, Georg; Hottenga, Jouke Jan; Iacono, William G; Janzing, Joost; Jokela, Markus; Karlsson, Robert; Kemp, John P; Kirkpatrick, Matthew G; Latvala, Antti; Lehtimäki, Terho; Liewald, David C; Madden, Pamela A. F; Magri, Chiara; Magnusson, Patrik K. E; Marten, Jonathan; Maschio, Andrea; Medland, Sarah E; Mihailov, Evelin; Milaneschi, Yuri; Montgomery, Grant W; Nauck, Matthias; Ouwens, Klaasjan G; Palotie, Aarno; Pettersson, Erik; Polasek, Ozren; Qian, Yong; Pulkki Råback, Laura; Raitakari, Olli T; Realo, Anu; Rose, Richard J; Ruggiero, Daniela; Schmidt, Carsten O; Slutske, Wendy S; Sorice, Rossella; Starr, John M; St Pourcain, Beate; Sutin, Angelina R; Timpson, Nicholas J; Trochet, Holly; Vermeulen, Sita; Vuoksimaa, Eero; Widen, Elisabeth; Wouda, Jasper; Wright, Margaret J; Zgaga, Lina; Porteous, David; Minelli, Alessandra; Palmer, Abraham A; Rujescu, Dan; Ciullo, Marina; Hayward, Caroline; Rudan, Igor; Metspalu, Andres; Kaprio, Jaakko; Deary, Ian J; Räikkönen, Katri; Wilson, James F; Keltikangas Järvinen, Liisa; Bierut, Laura J; Hettema, John M; Grabe, Hans J; van Duijn, Cornelia M; Evans, David M; Schlessinger, David; Pedersen, Nancy L; Terracciano, Antonio; Mcgue, Matt; Penninx, Brenda W. J. H; Martin, Nicholas G; Boomsma, Dorret I. | |
| 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 | |
| Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder | 1-gen-2015 | Minelli, Alessandra; Magri, Chiara; Barbon, Alessandro; Bonvicini, Cristian; Segala, Matilde; Congiu, Chiara; Bignotti, Stefano; Milanesi, Elena; Trabucchi, Luigi; Cattane, Nadia; Bortolomasi, Marco; Gennarelli, Massimo | |
| Exome sequencing of schizophrenia patients with high level of homozygosity identifies a homozygous novel mutation that reduces the glutamate acid decarboxylase 67 (GAD67) activity | 1-gen-2016 | Magri, Chiara; Giacopuzzi, Edoardo; Barbon, Alessandro; LA VIA, Luca; Mingardi, J; Congiu, Chiara; Orizio, Flavia; Bresciani, Roberto; Sacchetti, Emilio; Gennarelli, Massimo | |
| Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium | 1-gen-2016 | van Den Berg, Stéphanie M; de Moor, Marleen H. M.; Verweij, Karin J. H.; Krueger, Robert F.; Luciano, Michelle; Arias Vasquez, Alejandro; Matteson, Lindsay K.; Derringer, Jaime; Esko, Tõnu; Amin, Najaf; Gordon, Scott D.; Hansell, Narelle K.; Hart, Amy B.; Seppälä, Ilkka; Huffman, Jennifer E.; Konte, Bettina; Lahti, Jari; Lee, Minyoung; Miller, Mike; Nutile, Teresa; Tanaka, Toshiko; Teumer, Alexander; Viktorin, Alexander; Wedenoja, Juho; Abdellaoui, Abdel; Abecasis, Goncalo R.; Adkins, Daniel E.; Agrawal, Arpana; Allik, Jüri; Appel, Katja; Bigdeli, Timothy B.; Busonero, Fabio; Campbell, Harry; Costa, Paul T.; Smith, George Davey; Davies, Gail; de Wit, Harriet; Ding, Jun; Engelhardt, Barbara E.; Eriksson, Johan G.; Fedko, Iryna O.; Ferrucci, Luigi; Franke, Barbara; Giegling, Ina; Grucza, Richard; Hartmann, Annette M.; Heath, Andrew C.; Heinonen, Kati; Henders, Anjali K.; Homuth, Georg; Hottenga, Jouke Jan; Iacono, William G.; Janzing, Joost; Jokela, Markus; Karlsson, Robert; Kemp, John P.; Kirkpatrick, Matthew G.; Latvala, Antti; Lehtimäki, Terho; Liewald, David C.; Madden, Pamela A. F.; Magri, Chiara; Magnusson, Patrik K. E.; Marten, Jonathan; Maschio, Andrea; Mbarek, Hamdi; Medland, Sarah E.; Mihailov, Evelin; Milaneschi, Yuri; Montgomery, Grant W.; Nauck, Matthias; Nivard, Michel G.; Ouwens, Klaasjan G.; Palotie, Aarno; Pettersson, Erik; Polasek, Ozren; Qian, Yong; Pulkki Råback, Laura; Raitakari, Olli T.; Realo, Anu; Rose, Richard J.; Ruggiero, Daniela; Schmidt, Carsten O.; Slutske, Wendy S.; Sorice, Rossella; Starr, John M.; St Pourcain, Beate; Sutin, Angelina R.; Timpson, Nicholas J.; Trochet, Holly; Vermeulen, Sita; Vuoksimaa, Eero; Widen, Elisabeth; Wouda, Jasper; Wright, Margaret J.; Zgaga, Lina; Generation Scotland, Null; Porteous, David; Minelli, Alessandra; Palmer, Abraham A.; Rujescu, Dan; Ciullo, Marina; Hayward, Caroline; Rudan, Igor; Metspalu, Andres; Kaprio, Jaakko; Deary, Ian J.; Räikkönen, Katri; Wilson, James F.; Keltikangas Järvinen, Liisa; Bierut, Laura J.; Hettema, John M.; Grabe, Hans J.; Penninx, Brenda W. J. H.; van Duijn, Cornelia M.; Evans, David M.; Schlessinger, David; Pedersen, Nancy L.; Terracciano, Antonio; Mcgue, Matt; Martin, Nicholas G.; Boomsma, Dorret I. | |
| Genome-wide analysis of RNA-editing levels in human blood identifies interactions with mRNA processing genes and suggests correlation with biological and drug-related variables | 1-gen-2017 | Giacopuzzi, E; Magri, C; Gennarelli, M; Barbon, A | |
| The impairment of GABAergic pathway as one of the driver forces in the etiopathogenesis of schizophrenia: evidence from functional studies and gene-set enrichment analyses | 1-gen-2017 | Magri, Chiara; Giacopuzzi, Edoardo; La Via, L.; Bonini, D.; Ravasio, V.; Elhussiny, M. E. A.; Valsecchi, P.; Bresciani, R.; Barbon, A.; Vita, A.; Gennarelli, M. | |
| New biological pathways for major depression: gene expression decomposition in G x E components | 1-gen-2017 | Sacco, Chiara; Giacopuzzi, E; Gennarelli, M; Magri, C | |
| The effect of childhood trauma on blood transcriptome expression in major depressive disorder | 1-gen-2017 | Minelli, Alessandra; Magri, Chiara; Giacopuzzi, Edoardo; Gennarelli, Massimo | |
| The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis | 1-gen-2017 | Sacchetti, Emilio; Magri, Chiara; Minelli, Alessandra; Valsecchi, Paolo; Traversa, Michele; Calza, Stefano; Vita, Antonio; Gennarelli, Massimo | |
| 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 | |
| Functional study of a novel homozygous mutation in the GAD1 gene, detected in a patient with schizophrenia. | 1-gen-2017 | Magri, Chiara; Giacopuzzi, Edoardo; Barbon, Alessandro; La Via, Luca; Congiu, Chiara; Orizio, Flavia; Ferraboli, Sergio; Bresciani, Roberto; Borsani, Giuseppe; Sacchetti, Emilio; Gennarelli, Massimo |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile