Lista de obras - Vincenzo Forgetta - Dominio Público Uruguay

A Mendelian randomization study of the effect of type-2 diabetes on coronary heart disease

artículo científico publicado en 2015

A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects ⬇️

artículo científico publicado en 2016

Allelic variation in TLR4 is linked to susceptibility to Salmonella enterica serovar Typhimurium infection in chickens

artículo científico publicado en 2003

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on human blood metabolites

artículo científico publicado en 2014

An atlas of genetic influences on osteoporosis in humans and mice

artículo científico publicado en 2018

Assay for estimating total bacterial load: relative qPCR normalisation of bacterial load with associated clinical implications.

artículo científico publicado en 2015

Author Correction: An atlas of genetic influences on osteoporosis in humans and mice

artículo científico publicado en 2019

Correction: Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens

artículo científico publicado en 2016

Correction: Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens

artículo científico publicado en 2015

Correction: Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study

artículo científico publicado en 2016

Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

artículo científico publicado en 2020

Duplex PCR methods for the molecular detection of Escherichia fergusonii isolates from broiler chickens

artículo científico publicado en 2014

Erratum: Whole-genome sequence-based analysis of thyroid function

artículo científico publicado en 2015

Exome-wide rare variant analyses of two bone mineral density phenotypes: the challenges of analyzing rare genetic variation

artículo científico publicado en 2018

Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study

scientific article published on 24 September 2020

Genetically Decreased Circulating Vascular Endothelial Growth Factor and Osteoporosis Outcomes: A Mendelian Randomization Study

scientific article published on 06 January 2020

Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens

artículo científico publicado en 2015

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

artículo científico publicado en 2018

Loss of heterozygosity and transcriptome analyses of a 1.2 Mb candidate ovarian cancer tumor suppressor locus region at 17q25.1-q25.2.

artículo científico publicado en 2005

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

artículo científico publicado en 2017

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

scientific article published on 01 December 2018

Mendelian randomisation applied to drug development in cardiovascular disease: a review.

artículo científico publicado en 2014

Pathogenic and multidrug-resistant Escherichia fergusonii from broiler chicken

artículo científico publicado en 2012

Pathway analysis for genetic association studies: to do, or not to do? That is the question

artículo científico publicado en 2014

Sequencing of the Dutch elm disease fungus genome using the Roche/454 GS-FLX Titanium System in a comparison of multiple genomics core facilities

artículo científico publicado en 2013

Software Application Profiles: useful and novel software for epidemiological data analysis

artículo científico publicado en 2016

Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study

artículo científico publicado en 2015

Whole-genome sequence-based analysis of thyroid function.

artículo científico publicado en 2015

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

artículo científico publicado en 2015

Lista de obras de Vincenzo Forgetta

A Mendelian randomization study of the effect of type-2 diabetes on coronary heart disease

A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects ⬇️

Allelic variation in TLR4 is linked to susceptibility to Salmonella enterica serovar Typhimurium infection in chickens

An Atlas of Human and Murine Genetic Influences on Osteoporosis

An atlas of genetic influences on human blood metabolites

An atlas of genetic influences on osteoporosis in humans and mice

Assay for estimating total bacterial load: relative qPCR normalisation of bacterial load with associated clinical implications.

Author Correction: An atlas of genetic influences on osteoporosis in humans and mice

Correction: Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens

Correction: 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

Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study

Duplex PCR methods for the molecular detection of Escherichia fergusonii isolates from broiler chickens

Erratum: Whole-genome sequence-based analysis of thyroid function

Exome-wide rare variant analyses of two bone mineral density phenotypes: the challenges of analyzing rare genetic variation

Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study

Genetically Decreased Circulating Vascular Endothelial Growth Factor and Osteoporosis Outcomes: A Mendelian Randomization Study

Genomic Comparison of Non-Typhoidal Salmonella enterica Serovars Typhimurium, Enteritidis, Heidelberg, Hadar and Kentucky Isolates from Broiler Chickens

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects

Loss of heterozygosity and transcriptome analyses of a 1.2 Mb candidate ovarian cancer tumor suppressor locus region at 17q25.1-q25.2.

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

Mendelian randomisation applied to drug development in cardiovascular disease: a review.

Pathogenic and multidrug-resistant Escherichia fergusonii from broiler chicken

Pathway analysis for genetic association studies: to do, or not to do? That is the question

Sequencing of the Dutch elm disease fungus genome using the Roche/454 GS-FLX Titanium System in a comparison of multiple genomics core facilities

Software Application Profiles: useful and novel software for epidemiological data analysis

Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study

Whole-genome sequence-based analysis of thyroid function.

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture