Magri C - Search Results

1

Assessment of haptoglobin alleles in autism spectrum disorders.

Cupaioli FA, Mosca E, Magri C, Gennarelli M, Moscatelli M, Raggi ME, Landini M, Galluccio N, Villa L, Bonfanti A, Renieri A, Fallerini C, Minelli A, Marabotti A, Milanesi L, Fasano A, Mezzelani A. Cupaioli FA, et al. Among authors: magri c. Sci Rep. 2020 May 8;10(1):7758. doi: 10.1038/s41598-020-64679-w. Sci Rep. 2020. PMID: 32385356 Free PMC article.

2

Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients.

Magri C, Gardella R, Valsecchi P, Barlati SD, Guizzetti L, Imperadori L, Bonvicini C, Tura GB, Gennarelli M, Sacchetti E, Barlati S. Magri C, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):745-53. doi: 10.1002/ajmg.b.30674. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18163426

3

Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia.

Iatropoulos P, Gardella R, Valsecchi P, Magri C, Ratti C, Podavini D, Rossi G, Gennarelli M, Sacchetti E, Barlati S. Iatropoulos P, et al. Among authors: magri c. Psychiatr Genet. 2009 Oct;19(5):237-43. doi: 10.1097/YPG.0b013e32832cebf7. Psychiatr Genet. 2009. PMID: 19641478

4

New copy number variations in schizophrenia.

Magri C, Sacchetti E, Traversa M, Valsecchi P, Gardella R, Bonvicini C, Minelli A, Gennarelli M, Barlati S. Magri C, et al. PLoS One. 2010 Oct 13;5(10):e13422. doi: 10.1371/journal.pone.0013422. PLoS One. 2010. PMID: 20967226 Free PMC article.

5

Role of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders.

Minelli A, Maffioletti E, Cloninger CR, Magri C, Sartori R, Bortolomasi M, Congiu C, Bignotti S, Segala M, Giacopuzzi M, Gennarelli M. Minelli A, et al. Among authors: magri c. Depress Anxiety. 2013 Dec;30(12):1170-6. doi: 10.1002/da.22158. Epub 2013 Jul 16. Depress Anxiety. 2013. PMID: 23861224

6

Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role.

Valbonesi S, Magri C, Traversa M, Faraone SV, Cattaneo A, Milanesi E, Valenti V, Gennarelli M, Scassellati C. Valbonesi S, et al. Among authors: magri c. Psychiatr Genet. 2015 Apr;25(2):59-70. doi: 10.1097/YPG.0000000000000056. Psychiatr Genet. 2015. PMID: 25370694

7

Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder.

Minelli A, Magri C, Barbon A, Bonvicini C, Segala M, Congiu C, Bignotti S, Milanesi E, Trabucchi L, Cattane N, Bortolomasi M, Gennarelli M. Minelli A, et al. Among authors: magri c. Transl Psychiatry. 2015 Dec 1;5(12):e687. doi: 10.1038/tp.2015.180. Transl Psychiatry. 2015. PMID: 26624926 Free PMC article.

8

The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis.

Sacchetti E, Magri C, Minelli A, Valsecchi P, Traversa M, Calza S, Vita A, Gennarelli M. Sacchetti E, et al. Among authors: magri c. Pharmacogenomics J. 2017 Mar;17(2):146-154. doi: 10.1038/tpj.2015.90. Epub 2016 Feb 9. Pharmacogenomics J. 2017. PMID: 26856250 Clinical Trial.

9

Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia.

Gardella R, Sacchetti E, Legati A, Magri C, Traversa M, Gennarelli M. Gardella R, et al. Among authors: magri c. Psychiatry Res. 2017 Dec;258:598-599. doi: 10.1016/j.psychres.2016.10.057. Epub 2016 Oct 29. Psychiatry Res. 2017. PMID: 28043646 No abstract available.

10

Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways.

Giacopuzzi E, Gennarelli M, Minelli A, Gardella R, Valsecchi P, Traversa M, Bonvicini C, Vita A, Sacchetti E, Magri C. Giacopuzzi E, et al. Among authors: magri c. PLoS One. 2017 Aug 7;12(8):e0182778. doi: 10.1371/journal.pone.0182778. eCollection 2017. PLoS One. 2017. PMID: 28787007 Free PMC article.

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