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Identification of a founder BRCA2 mutation in Sardinia.
Pisano M, Cossu A, Persico I, Palmieri G, Angius A, Casu G, Palomba G, Sarobba MG, Rocca PC, Dedola MF, Olmeo N, Pasca A, Budroni M, Marras V, Pisano A, Farris A, Massarelli G, Pirastu M, Tanda F. Pisano M, et al. Among authors: persico i. Br J Cancer. 2000 Feb;82(3):553-9. doi: 10.1054/bjoc.1999.0963. Br J Cancer. 2000. PMID: 10682665 Free PMC article.
BRCA1 and BRCA2 germline mutations in Sardinian breast cancer families and their implications for genetic counseling.
Palmieri G, Palomba G, Cossu A, Pisano M, Dedola MF, Sarobba MG, Farris A, Olmeo N, Contu A, Pasca A, Satta MP, Persico I, Carboni AA, Cossu-Rocca P, Contini M, Mangion J, Stratton MR, Tanda F. Palmieri G, et al. Among authors: persico i. Ann Oncol. 2002 Dec;13(12):1899-907. doi: 10.1093/annonc/mdf326. Ann Oncol. 2002. PMID: 12453858 Free article.
Molecular basis of open-angle glaucoma in Italy.
Angius A, Pisano M, Sanca A, Casu G, Persico I, Pitzalis S, De Gioia E, Grignolo FM, Loi A, Sole G, Cao A, Spinelli P, Ghillotti G, Bonomi L, Fossarello M, Serra A, Gandolfi S, Alberti G, Maraini G, Serru A, Orzalesi N, Pirastu M. Angius A, et al. Among authors: persico i. Acta Ophthalmol Scand Suppl. 1998;(227):16-7. doi: 10.1111/j.1600-0420.1998.tb00865.x. Acta Ophthalmol Scand Suppl. 1998. PMID: 9972327
Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis.
Tore S, Casula S, Casu G, Concas MP, Pistidda P, Persico I, Sassu A, Maestrale GB, Mele C, Caruso MR, Bonerba B, Usai P, Deiana I, Thornton T, Pirastu M, Forabosco P. Tore S, et al. Among authors: persico i. PLoS Genet. 2011 Jan 20;7(1):e1001281. doi: 10.1371/journal.pgen.1001281. PLoS Genet. 2011. PMID: 21283782 Free PMC article.
A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia.
Falchi M, Forabosco P, Mocci E, Borlino CC, Picciau A, Virdis E, Persico I, Parracciani D, Angius A, Pirastu M. Falchi M, et al. Among authors: persico i. Am J Hum Genet. 2004 Dec;75(6):1015-31. doi: 10.1086/426155. Epub 2004 Oct 11. Am J Hum Genet. 2004. PMID: 15478097 Free PMC article.
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome.
Angius A, Cossu S, Uva P, Oppo M, Onano S, Persico I, Fotia G, Atzeni R, Cuccuru G, Asunis M, Cucca F, Pruna D, Crisponi L. Angius A, et al. Among authors: persico i. Clin Genet. 2018 Jun;93(6):1245-1247. doi: 10.1111/cge.13162. Epub 2018 Feb 5. Clin Genet. 2018. PMID: 29399786
41 results