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European Journal of Human Genetics : EJHG|May 5, 2018
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selectionDragana Vuckovic, Massimo Mezzavilla, Massimiliano Cocca, et al.Plos One|February 28, 2009
High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysisGiorgio Pistis, Ignazio Piras, Nicola Pirastu, et al.American Journal of Human Genetics|May 13, 2003
Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolateFernando Gianfrancesco, Teresa Esposito, Maria Neve Ombra, et al.Plos One|May 5, 2012
Alteration of liver enzymes is a feature of the MYH9-related disease syndromeAlessandro Pecci, Ginevra Biino, Tiziana Fierro, et al.Bone|December 17, 2009
Genetic architecture of hand quantitative ultrasound measures: a population-based study in a Sardinian genetic isolateGinevra Biino, Laura Casula, Francesca de Terlizzi, et al.BMC Medical Genetics|September 1, 2009
Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populationsEvelina Mocci, Maria P Concas, Manuela Fanciulli, et al.Human Genetics|June 3, 2019
Estimation of metabolic syndrome heritability in three large populations including full pedigree and genomic informationFrancesca Graziano, Ginevra Biino, Maria Teresa Bonati, et al.Plos Genetics|February 2, 2011
Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasisSilvia Tore, Stefania Casula, Giuseppina Casu, et al.Journal of Medical Genetics|April 16, 2011
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathwaysGiorgia Girotto, Nicola Pirastu, Rossella Sorice, et al.Human Molecular Genetics|July 19, 2015
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and lossDragana Vuckovic, Sally Dawson, Deborah I Scheffer, et al.Pageof 7