Spinelli R - Search Results

1

Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism.

Proverbio MC, Mangano E, Gessi A, Bordoni R, Spinelli R, Asselta R, Valin PS, Di Candia S, Zamproni I, Diceglie C, Mora S, Caruso-Nicoletti M, Salvatoni A, De Bellis G, Battaglia C. Proverbio MC, et al. Among authors: spinelli r. PLoS One. 2013 Jul 15;8(7):e68740. doi: 10.1371/journal.pone.0068740. Print 2013. PLoS One. 2013. PMID: 23869231 Free PMC article.

2

Algorithm for automatic genotype calling of single nucleotide polymorphisms using the full course of TaqMan real-time data.

Callegaro A, Spinelli R, Beltrame L, Bicciato S, Caristina L, Censuales S, De Bellis G, Battaglia C. Callegaro A, et al. Among authors: spinelli r. Nucleic Acids Res. 2006 Apr 14;34(7):e56. doi: 10.1093/nar/gkl185. Nucleic Acids Res. 2006. PMID: 16617143 Free PMC article.

3

A computational procedure to identify significant overlap of differentially expressed and genomic imbalanced regions in cancer datasets.

Bicciato S, Spinelli R, Zampieri M, Mangano E, Ferrari F, Beltrame L, Cifola I, Peano C, Solari A, Battaglia C. Bicciato S, et al. Among authors: spinelli r. Nucleic Acids Res. 2009 Aug;37(15):5057-70. doi: 10.1093/nar/gkp520. Epub 2009 Jun 19. Nucleic Acids Res. 2009. PMID: 19542187 Free PMC article.

4

Candidate Genes and MiRNAs Linked to the Inverse Relationship Between Cancer and Alzheimer's Disease: Insights From Data Mining and Enrichment Analysis.

Battaglia C, Venturin M, Sojic A, Jesuthasan N, Orro A, Spinelli R, Musicco M, De Bellis G, Adorni F. Battaglia C, et al. Among authors: spinelli r. Front Genet. 2019 Sep 24;10:846. doi: 10.3389/fgene.2019.00846. eCollection 2019. Front Genet. 2019. PMID: 31608105 Free PMC article.

5

DNA copy-number abnormalities do not occur in infant ALL with t(4;11)/MLL-AF4.

Bardini M, Spinelli R, Bungaro S, Mangano E, Corral L, Cifola I, Fazio G, Giordan M, Basso G, De Rossi G, Biondi A, Battaglia C, Cazzaniga G. Bardini M, et al. Among authors: spinelli r. Leukemia. 2010 Jan;24(1):169-76. doi: 10.1038/leu.2009.203. Epub 2009 Nov 12. Leukemia. 2010. PMID: 19907438

6

Genome-wide screening of copy number alterations and LOH events in renal cell carcinomas and integration with gene expression profile.

Cifola I, Spinelli R, Beltrame L, Peano C, Fasoli E, Ferrero S, Bosari S, Signorini S, Rocco F, Perego R, Proserpio V, Raimondo F, Mocarelli P, Battaglia C. Cifola I, et al. Among authors: spinelli r. Mol Cancer. 2008 Jan 14;7:6. doi: 10.1186/1476-4598-7-6. Mol Cancer. 2008. PMID: 18194544 Free PMC article.

7

CEQer: a graphical tool for copy number and allelic imbalance detection from whole-exome sequencing data.

Piazza R, Magistroni V, Pirola A, Redaelli S, Spinelli R, Redaelli S, Galbiati M, Valletta S, Giudici G, Cazzaniga G, Gambacorti-Passerini C. Piazza R, et al. Among authors: spinelli r. PLoS One. 2013 Oct 4;8(10):e74825. doi: 10.1371/journal.pone.0074825. eCollection 2013. PLoS One. 2013. PMID: 24124457 Free PMC article.

8

Recurrent ETNK1 mutations in atypical chronic myeloid leukemia.

Gambacorti-Passerini CB, Donadoni C, Parmiani A, Pirola A, Redaelli S, Signore G, Piazza V, Malcovati L, Fontana D, Spinelli R, Magistroni V, Gaipa G, Peronaci M, Morotti A, Panuzzo C, Saglio G, Usala E, Kim DW, Rea D, Zervakis K, Viniou N, Symeonidis A, Becker H, Boultwood J, Campiotti L, Carrabba M, Elli E, Bignell GR, Papaemmanuil E, Campbell PJ, Cazzola M, Piazza R. Gambacorti-Passerini CB, et al. Among authors: spinelli r. Blood. 2015 Jan 15;125(3):499-503. doi: 10.1182/blood-2014-06-579466. Epub 2014 Oct 24. Blood. 2015. PMID: 25343957 Free article.

9

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.

Piazza R, Valletta S, Winkelmann N, Redaelli S, Spinelli R, Pirola A, Antolini L, Mologni L, Donadoni C, Papaemmanuil E, Schnittger S, Kim DW, Boultwood J, Rossi F, Gaipa G, De Martini GP, di Celle PF, Jang HG, Fantin V, Bignell GR, Magistroni V, Haferlach T, Pogliani EM, Campbell PJ, Chase AJ, Tapper WJ, Cross NC, Gambacorti-Passerini C. Piazza R, et al. Among authors: spinelli r. Nat Genet. 2013 Jan;45(1):18-24. doi: 10.1038/ng.2495. Epub 2012 Dec 9. Nat Genet. 2013. PMID: 23222956 Free PMC article.

10

Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases.

Spinelli R, Pirola A, Redaelli S, Sharma N, Raman H, Valletta S, Magistroni V, Piazza R, Gambacorti-Passerini C. Spinelli R, et al. Mol Genet Genomic Med. 2013 Nov;1(4):246-59. doi: 10.1002/mgg3.23. Epub 2013 Jul 7. Mol Genet Genomic Med. 2013. PMID: 24498620 Free PMC article.

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