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Autore Titolo [ Tipo] Anno Filtri: First Letter Of Last Name è B and Autore is Biino, Ginevra [Clear All Filters]
Alteration of liver enzymes is a feature of the MYH9-related disease syndrome. PLoS One 2012;7(4):e35986.
. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. Am J Hum Genet 2018;103(5):691-706.
. Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hum Mol Genet 2015;24(19):5655-64.
. Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nat Genet 2018;50(6):834-848.
. Genome-wide association study identifies 74 loci associated with educational attainment. Nature 2016;533(7604):539-42.
. A genome-wide association study of corneal astigmatism: The CREAM Consortium. Mol Vis 2018;24:127-142.
. Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways. J Med Genet 2011;48(6):369-74.
. Influence of age, sex and ethnicity on platelet count in five Italian geographic isolates: mild thrombocytopenia may be physiological. Br J Haematol 2012;157(3):384-7.
. Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders. Blood 2014;124(6):e4-e10.
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