Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development

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Multi-ethnic genome-wide association study for atrial fibrillation

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A Missense Variant in PLEC Increases Risk of Atrial Fibrillation

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Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

(2017) Manuel A Ferreira et al.   NATURE GENETICS

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

(2017) Ingrid E Christophersen et al.   NATURE GENETICS

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

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Integrating molecular QTL data into genome-wide genetic association analysis: Probabilistic assessment of enrichment and colocalization

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Phenome-wide heritability analysis of the UK Biobank

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Association Between Heart Rate at Rest and Incident Atrial Fibrillation (from the Copenhagen Electrocardiographic Study)

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EHRA/HRS/APHRS/SOLAECE expert consensus on atrial cardiomyopathies: definition, characterization, and clinical implication

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Guidance for the utility of linear models in meta-analysis of genetic association studies of binary phenotypes

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The Geisinger MyCode community health initiative: an electronic health record–linked biobank for precision medicine research

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miR-208b upregulation interferes with calcium handling in HL-1 atrial myocytes: Implications in human chronic atrial fibrillation

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Epigenetic and genetic components of height regulation

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GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach

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P-wave duration and the risk of atrial fibrillation: Results from the Copenhagen ECG Study

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Genetic studies of body mass index yield new insights for obesity biology

(2015) Adam E. Locke et al.   NATURE

Gene expression analysis identifies global gene dosage sensitivity in cancer

(2015) Rudolf S N Fehrmann et al.   NATURE GENETICS

Large-scale whole-genome sequencing of the Icelandic population

(2015) Daniel F Gudbjartsson et al.   NATURE GENETICS

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

(2015) Brendan K Bulik-Sullivan et al.   NATURE GENETICS

Efficient Bayesian mixed-model analysis increases association power in large cohorts

(2015) Po-Ru Loh et al.   NATURE GENETICS

The anatomical distribution of genetic associations

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DGIdb 2.0: mining clinically relevant drug–gene interactions

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The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

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UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age

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Recommended Joint and Meta-Analysis Strategies for Case-Control Association Testing of Single Low-Count Variants

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Risk of atrial fibrillation as a function of the electrocardiographic PR interval: Results from the Copenhagen ECG Study

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J-Shaped Association Between QTc Interval Duration and the Risk of Atrial Fibrillation

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Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data

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Heavy and light roles: myosin in the morphogenesis of the heart

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Cohort Profile: The HUNT Study, Norway

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Familial Aggregation of Lone Atrial Fibrillation in Young Persons

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Hypertrophic cardiomyopathy

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Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

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Ectopic and reentrant activation patterns in the posterior left atrium during stretch-related atrial fibrillation

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Dose-dependent augmentation of cardiac systolic function with the selective cardiac myosin activator, omecamtiv mecarbil: a first-in-man study

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A rare variant in MYH6 is associated with high risk of sick sinus syndrome

(2011) Hilma Holm et al.   NATURE GENETICS

KEGG for integration and interpretation of large-scale molecular data sets

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

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Association Between Familial Atrial Fibrillation and Risk of New-Onset Atrial Fibrillation

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Ca2+-independent positive molecular inotropy for failing rabbit and human cardiac muscle by α-myosin motor gene transfer

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Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

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Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions

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Detection of sharing by descent, long-range phasing and haplotype imputation

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