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Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations.
Mocci E, Concas MP, Fanciulli M, Pirastu N, Adamo M, Cabras V, Fraumene C, Persico I, Sassu A, Picciau A, Prodi DA, Serra D, Biino G, Pirastu M, Angius A. Mocci E, et al. Among authors: persico i. BMC Med Genet. 2009 Aug 28;10:81. doi: 10.1186/1471-2350-10-81. BMC Med Genet. 2009. PMID: 19715579 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.
A strategy analysis for genetic association studies with known inbreeding.
Cabras S, Castellanos ME, Biino G, Persico I, Sassu A, Casula L, Del Giacco S, Bertolino F, Pirastu M, Pirastu N. Cabras S, et al. Among authors: persico i. BMC Genet. 2011 Jul 18;12:63. doi: 10.1186/1471-2156-12-63. BMC Genet. 2011. PMID: 21767363 Free PMC article.
EDA2R is associated with androgenetic alopecia.
Prodi DA, Pirastu N, Maninchedda G, Sassu A, Picciau A, Palmas MA, Mossa A, Persico I, Adamo M, Angius A, Pirastu M. Prodi DA, et al. Among authors: persico i. J Invest Dermatol. 2008 Sep;128(9):2268-70. doi: 10.1038/jid.2008.60. Epub 2008 Apr 3. J Invest Dermatol. 2008. PMID: 18385763 Free article.
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.
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report.
Alves RM, Uva P, Veiga MF, Oppo M, Zschaber FCR, Porcu G, Porto HP, Persico I, Onano S, Cuccuru G, Atzeni R, Vieira LCN, Pires MVA, Cucca F, Toralles MBP, Angius A, Crisponi L. Alves RM, et al. Among authors: persico i. BMC Med Genet. 2019 Jan 14;20(1):16. doi: 10.1186/s12881-019-0745-7. BMC Med Genet. 2019. PMID: 30642272 Free PMC article.
41 results