Lista de obras -

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

artículo científico publicado en 2021

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Associations Between Alcohol Intake and Genetic Predisposition with Atrial Fibrillation Risk in a National Biobank

artículo científico publicado en 2020

Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium

artículo científico publicado en 2014

Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Common variants at 12q14 and 12q24 are associated with hippocampal volume

artículo científico publicado en 2012

Deep learning enables genetic analysis of the human thoracic aorta

artículo científico publicado en 2021

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

artículo científico publicado en 2017

Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease

artículo científico publicado en 2016

Frequency of Cardiac Rhythm Abnormalities in a Half Million Adults

artículo científico publicado en 2018

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genetic Determinants of Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation

artículo científico publicado en 2020

Genetic Predisposition, Clinical Risk Factor Burden, and Lifetime Risk of Atrial Fibrillation.

artículo científico publicado en 2017

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

article by Amit V Khera et al published September 2018 in Nature Genetics

Heritability of Atrial Fibrillation

artículo científico publicado en 2017

Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels

artículo científico publicado en 2011

Initial Precipitants and Recurrence of Atrial Fibrillation

artículo científico publicado en 2020

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank

artículo científico publicado en 2019

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

Multi-ethnic genome-wide association study for atrial fibrillation

article

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2018

PLD3 variants in population studies

artículo científico publicado en 2015

Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery

scientific article published on 11 November 2018

Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease

artículo científico publicado en 2015

Predicting stroke through genetic risk functions: the CHARGE Risk Score Project

artículo científico publicado en 2014

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

artículo científico publicado en 2016

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

artículo científico publicado en 2019

Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies

artículo científico publicado en 2016

Titin Truncating Variants in Adults Without Known Congestive Heart Failure

scientific article published on 01 March 2020

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

artículo científico publicado en 2019

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

artículo científico publicado en 2019

Lista de obras de

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Associations Between Alcohol Intake and Genetic Predisposition with Atrial Fibrillation Risk in a National Biobank

Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium

Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Common variants at 12q14 and 12q24 are associated with hippocampal volume

Deep learning enables genetic analysis of the human thoracic aorta

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease

Frequency of Cardiac Rhythm Abnormalities in a Half Million Adults

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

Genetic Determinants of Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation

Genetic Predisposition, Clinical Risk Factor Burden, and Lifetime Risk of Atrial Fibrillation.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

Heritability of Atrial Fibrillation

Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels

Initial Precipitants and Recurrence of Atrial Fibrillation

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

Multi-ethnic genome-wide association study for atrial fibrillation

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

PLD3 variants in population studies

Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery

Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease

Predicting stroke through genetic risk functions: the CHARGE Risk Score Project

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies

Titin Truncating Variants in Adults Without Known Congestive Heart Failure

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations