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Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization StudyWhole-genome sequencing identifies EN1 as a determinant of bone density and fracture.Whole-genome sequence-based analysis of thyroid function.An atlas of genetic influences on human blood metabolites.Allelic variation in TLR4 is linked to susceptibility to Salmonella enterica serovar Typhimurium infection in chickensPathway analysis for genetic association studies: to do, or not to do? That is the question.Assay for estimating total bacterial load: relative qPCR normalisation of bacterial load with associated clinical implications.Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens.A Mendelian randomization study of the effect of type-2 diabetes on coronary heart disease.Sequencing of the Dutch elm disease fungus genome using the Roche/454 GS-FLX Titanium System in a comparison of multiple genomics core facilities.Duplex PCR methods for the molecular detection of Escherichia fergusonii isolates from broiler chickens.Mendelian randomisation applied to drug development in cardiovascular disease: a review.A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects.Erratum: Whole-genome sequence-based analysis of thyroid functionCorrection: Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens.Correction: Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study.Correction: Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens.Pathogenic and multidrug-resistant Escherichia fergusonii from broiler chicken.Software Application Profiles: useful and novel software for epidemiological data analysis.Exome-wide rare variant analyses of two bone mineral density phenotypes: the challenges of analyzing rare genetic variation.Loss of heterozygosity and transcriptome analyses of a 1.2 Mb candidate ovarian cancer tumor suppressor locus region at 17q25.1-q25.2.An Atlas of Human and Murine Genetic Influences on OsteoporosisGenetically Decreased Circulating Vascular Endothelial Growth Factor and Osteoporosis Outcomes: A Mendelian Randomization Study
P50
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P50
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Vincenzo Forgetta
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P106
P21
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P496
0000-0002-6061-4720