Lista de obras - Andrea Ganna - Dominio Público Uruguay

5 year mortality predictors in 498,103 UK Biobank participants: a prospective population-based study

artículo científico publicado en 2015

A first update on mapping the human genetic architecture of COVID-19

artículo científico publicado en 2022

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

artículo científico publicado en 2021

Common variants associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

Correction: Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study

artículo científico publicado en 2017

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

article published in 2017

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

artículo científico publicado en 2018

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

artículo científico publicado en 2018

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study

artículo científico publicado en 2016

Enabling Efficient and Confident Annotation of LC-MS Metabolomics Data through MS1 Spectrum and Time Prediction

artículo científico publicado en 2016

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

artículo científico publicado en 2022

Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations

article

Gene × dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestry

artículo científico publicado en 2015

Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry

artículo científico publicado en 2013

Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity

artículo científico publicado en 2015

Genetic determinants of mortality. Can findings from genome-wide association studies explain variation in human mortality?

artículo científico publicado en 2013

Genetic evidence of assortative mating in humans

article

Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior

artículo científico publicado en 2016

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

artículo científico publicado en 2014

Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance.

artículo científico publicado en 2018

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Heterogeneous Contribution of Microdeletions in the Development of Common Generalized and Focal epilepsies

Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies

artículo científico publicado en 2017

Higher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE Consortium Studies

artículo científico publicado en 2013

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

artículo científico publicado en 2015

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

artículo científico publicado en 2016

Identification of metabolic profiles associated with human exposure to perfluoroalkyl substances

artículo científico publicado en 2018

Improvement of myocardial infarction risk prediction via inflammation-associated metabolite biomarkers

artículo científico publicado en 2017

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

preprint published 25 September 2016

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

artículo científico publicado en 2018

Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior

artículo científico publicado en 2019

Large-scale metabolomic profiling identifies novel biomarkers for incident coronary heart disease

artículo científico publicado en 2014

Large-scale non-targeted metabolomic profiling in three human population-based studies

Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions

artículo científico publicado en 2017

Low-frequency variant functional architectures reveal strength of negative selection across coding and non-coding annotations

Meta-analysis investigating associations between healthy diet and fasting glucose and insulin levels and modification by loci associated with glucose homeostasis in data from 15 cohorts

artículo científico publicado en 2012

Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics ⬇️

artículo científico publicado el 25 de julio de 2013

Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19

Multilocus genetic risk scores for coronary heart disease prediction

artículo científico publicado en 2013

Non-targeted metabolomics combined with genetic analyses identifies bile acid synthesis and phospholipid metabolism as being associated with incident type 2 diabetes

artículo científico publicado en 2016

Nonparametric estimation of the rediscovery rate

artículo científico publicado en 2016

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies

artículo científico publicado en 2019

Prediction impact curve is a new measure integrating intervention effects in the evaluation of risk models

artículo científico publicado en 2015

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

artículo científico publicado en 2018

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

Rediscovery rate estimation for assessing the validation of significant findings in high-throughput studies

artículo científico publicado en 2014

Risk prediction measures for case-cohort and nested case-control designs: an application to cardiovascular disease

artículo científico publicado en 2012

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

artículo científico publicado en 2013

Signals of polygenic adaptation on height have been overestimated due to uncorrected population structure in genome-wide association studies

scholarly article published 25 June 2018

The Swedish Twin Registry: establishment of a biobank and other recent developments

artículo científico publicado en 2012

The impact of rare variation on gene expression across tissues

artículo científico publicado en 2017

The impact of rare variation on gene expression across tissues

article

The metabolic fingerprint of p,p'-DDE and HCB exposure in humans

artículo científico publicado en 2015

The mutational constraint spectrum quantified from variation in 141,456 humans

artículo científico publicado en 2020

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

artículo científico publicado en 2016

Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium

artículo científico publicado en 2015

Utilizing twins as controls for non-twin case-materials in genome wide association studies

artículo científico publicado en 2013

Variant Score Ranker-a web application for intuitive missense variant prioritization

scientific article published on 01 November 2019

[Assessment of job strain and its consequencies in a large public organisation. Findings from the SEMM Study]

article

[Global cardiovascular risk evaluation in primary care]

artículo científico publicado en 2010

Lista de obras de Andrea Ganna

5 year mortality predictors in 498,103 UK Biobank participants: a prospective population-based study

A first update on mapping the human genetic architecture of COVID-19

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

Common variants associated with plasma triglycerides and risk for coronary artery disease

Correction: Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

Discovery and refinement of loci associated with lipid levels

Effect of Insulin Resistance on Monounsaturated Fatty Acid Levels: A Multi-cohort Non-targeted Metabolomics and Mendelian Randomization Study

Enabling Efficient and Confident Annotation of LC-MS Metabolomics Data through MS1 Spectrum and Time Prediction

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations

Gene × dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestry

Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry

Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity

Genetic determinants of mortality. Can findings from genome-wide association studies explain variation in human mortality?

Genetic evidence of assortative mating in humans

Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance.

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Heterogeneous Contribution of Microdeletions in the Development of Common Generalized and Focal epilepsies

Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies

Higher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE Consortium Studies

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

Identification of metabolic profiles associated with human exposure to perfluoroalkyl substances

Improvement of myocardial infarction risk prediction via inflammation-associated metabolite biomarkers

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior

Large-scale metabolomic profiling identifies novel biomarkers for incident coronary heart disease

Large-scale non-targeted metabolomic profiling in three human population-based studies

Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions

Low-frequency variant functional architectures reveal strength of negative selection across coding and non-coding annotations

Meta-analysis investigating associations between healthy diet and fasting glucose and insulin levels and modification by loci associated with glucose homeostasis in data from 15 cohorts

Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics ⬇️

Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19

Multilocus genetic risk scores for coronary heart disease prediction

Non-targeted metabolomics combined with genetic analyses identifies bile acid synthesis and phospholipid metabolism as being associated with incident type 2 diabetes

Nonparametric estimation of the rediscovery rate

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies

Prediction impact curve is a new measure integrating intervention effects in the evaluation of risk models

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

Rediscovery rate estimation for assessing the validation of significant findings in high-throughput studies

Risk prediction measures for case-cohort and nested case-control designs: an application to cardiovascular disease

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

Signals of polygenic adaptation on height have been overestimated due to uncorrected population structure in genome-wide association studies

The Swedish Twin Registry: establishment of a biobank and other recent developments

The impact of rare variation on gene expression across tissues

The impact of rare variation on gene expression across tissues

The metabolic fingerprint of p,p'-DDE and HCB exposure in humans

The mutational constraint spectrum quantified from variation in 141,456 humans

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium

Utilizing twins as controls for non-twin case-materials in genome wide association studies

Variant Score Ranker-a web application for intuitive missense variant prioritization

[Assessment of job strain and its consequencies in a large public organisation. Findings from the SEMM Study]

[Global cardiovascular risk evaluation in primary care]