Magi A - Search Results

1

Read count approach for DNA copy number variants detection.

Magi A, Tattini L, Pippucci T, Torricelli F, Benelli M. Magi A, et al. Bioinformatics. 2012 Feb 15;28(4):470-8. doi: 10.1093/bioinformatics/btr707. Epub 2011 Dec 23. Bioinformatics. 2012. PMID: 22199393

2

Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data.

Blangiardo M, Toti S, Giusti B, Abbate R, Magi A, Poggi F, Rossi L, Torricelli F, Biggeri A. Blangiardo M, et al. Among authors: magi a. Bioinformatics. 2006 Jan 1;22(1):50-7. doi: 10.1093/bioinformatics/bti750. Epub 2005 Nov 2. Bioinformatics. 2006. PMID: 16267084

3

A shifting level model algorithm that identifies aberrations in array-CGH data.

Magi A, Benelli M, Marseglia G, Nannetti G, Scordo MR, Torricelli F. Magi A, et al. Biostatistics. 2010 Apr;11(2):265-80. doi: 10.1093/biostatistics/kxp051. Epub 2009 Nov 30. Biostatistics. 2010. PMID: 19948744

4

A very fast and accurate method for calling aberrations in array-CGH data.

Benelli M, Marseglia G, Nannetti G, Paravidino R, Zara F, Bricarelli FD, Torricelli F, Magi A. Benelli M, et al. Among authors: magi a. Biostatistics. 2010 Jul;11(3):515-8. doi: 10.1093/biostatistics/kxq008. Epub 2010 Mar 5. Biostatistics. 2010. PMID: 20207682

5

Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm.

Magi A, Benelli M, Yoon S, Roviello F, Torricelli F. Magi A, et al. Nucleic Acids Res. 2011 May;39(10):e65. doi: 10.1093/nar/gkr068. Epub 2011 Feb 14. Nucleic Acids Res. 2011. PMID: 21321017 Free PMC article.

6

Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6.

Donati C, Marseglia G, Magi A, Serratì S, Cencetti F, Bernacchioni C, Nannetti G, Benelli M, Brunelli S, Torricelli F, Cossu G, Bruni P. Donati C, et al. Among authors: magi a. PLoS One. 2011;6(5):e20389. doi: 10.1371/journal.pone.0020389. Epub 2011 May 24. PLoS One. 2011. PMID: 21629665 Free PMC article.

7

EX-HOM (EXome HOMozygosity): a proof of principle.

Pippucci T, Benelli M, Magi A, Martelli PL, Magini P, Torricelli F, Casadio R, Seri M, Romeo G. Pippucci T, et al. Among authors: magi a. Hum Hered. 2011;72(1):45-53. doi: 10.1159/000330164. Epub 2011 Aug 18. Hum Hered. 2011. PMID: 21849793 Free article.

8

Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.

Striano P, Coppola A, Paravidino R, Malacarne M, Gimelli S, Robbiano A, Traverso M, Pezzella M, Belcastro V, Bianchi A, Elia M, Falace A, Gazzerro E, Ferlazzo E, Freri E, Galasso R, Gobbi G, Molinatto C, Cavani S, Zuffardi O, Striano S, Ferrero GB, Silengo M, Cavaliere ML, Benelli M, Magi A, Piccione M, Dagna Bricarelli F, Coviello DA, Fichera M, Minetti C, Zara F. Striano P, et al. Among authors: magi a. Arch Neurol. 2012 Mar;69(3):322-30. doi: 10.1001/archneurol.2011.1999. Epub 2011 Nov 14. Arch Neurol. 2012. PMID: 22083797 Free article. Review.

9

372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.

Marseglia G, Scordo MR, Pescucci C, Nannetti G, Biagini E, Scandurra V, Gerundino F, Magi A, Benelli M, Torricelli F. Marseglia G, et al. Among authors: magi a. Eur J Med Genet. 2012 Mar;55(3):216-21. doi: 10.1016/j.ejmg.2012.01.005. Epub 2012 Jan 25. Eur J Med Genet. 2012. PMID: 22333924

10

WNP: a novel algorithm for gene products annotation from weighted functional networks.

Magi A, Tattini L, Benelli M, Giusti B, Abbate R, Ruffo S. Magi A, et al. PLoS One. 2012;7(6):e38767. doi: 10.1371/journal.pone.0038767. Epub 2012 Jun 28. PLoS One. 2012. PMID: 22761703 Free PMC article.

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