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Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability.
Sanna S, Li B, Mulas A, Sidore C, Kang HM, Jackson AU, Piras MG, Usala G, Maninchedda G, Sassu A, Serra F, Palmas MA, Wood WH 3rd, Njølstad I, Laakso M, Hveem K, Tuomilehto J, Lakka TA, Rauramaa R, Boehnke M, Cucca F, Uda M, Schlessinger D, Nagaraja R, Abecasis GR. Sanna S, et al. Among authors: maninchedda g. PLoS Genet. 2011 Jul;7(7):e1002198. doi: 10.1371/journal.pgen.1002198. Epub 2011 Jul 28. PLoS Genet. 2011. PMID: 21829380 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: maninchedda g. 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.
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate.
Gianfrancesco F, Esposito T, Ombra MN, Forabosco P, Maninchedda G, Fattorini M, Casula S, Vaccargiu S, Casu G, Cardia F, Deiana I, Melis P, Falchi M, Pirastu M. Gianfrancesco F, et al. Among authors: maninchedda g. Am J Hum Genet. 2003 Jun;72(6):1479-91. doi: 10.1086/375628. Epub 2003 May 9. Am J Hum Genet. 2003. PMID: 12740763 Free PMC article.