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List of works by Dan Roden

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PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations

scientific article
The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies

scientific article (publication date: 26 January 2011)
ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiolo

scientific article
ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiolo

scientific article published in September 2006
Fulminant Myocarditis with Combination Immune Checkpoint Blockade

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

scientific article
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

scientific article (publication date: October 2013)
Meta-analysis identifies six new susceptibility loci for atrial fibrillation

scientific article published on 29 April 2012
Common variants in KCNN3 are associated with lone atrial fibrillation

scientific article
Implementing genomic medicine in the clinic: the future is here

scientific article published on 10 January 2013
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

scientific article
Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

scientific article
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose

scientific article published on 5 June 2008
Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia

scientific journal article
Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

scientific article
Genetic determinants of response to warfarin during initial anticoagulation

scientific article
ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: A report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiolog

scientific article published on 25 August 2006
Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record

scientific article
Sudden cardiac death prediction and prevention: report from a National Heart, Lung, and Blood Institute and Heart Rhythm Society Workshop

scientific article
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

scientific article
Drug-Induced Long QT Syndrome

scientific article published on December 1, 2010
Identifying genetic risk factors for serious adverse drug reactions: current progress and challenges

scientific article published on November 2007
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

scientific article published on 2 March 2016
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

scientific article
ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death--executive summary: A report of the American College of Cardiology/American Heart Association Task Force and the European S

scientific article published on 01 September 2006
Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation

scientific article published on 31 March 2008
A rare variant in MYH6 is associated with high risk of sick sinus syndrome

scientific article
Metabolic syndrome and risk of development of atrial fibrillation: the Niigata preventive medicine study

scientific article published on 19 February 2008
Drug-induced torsades de pointes and implications for drug development.

scientific article
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

scientific article
Incorporation of pharmacogenomics into routine clinical practice: the Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline development process

scientific article
Inactivating mutations in NPC1L1 and protection from coronary heart disease

scientific article
Principles of human subjects protections applied in an opt-out, de-identified biobank

scientific article
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.

scientific article published on 2 June 2003
Prevention of torsade de pointes in hospital settings: a scientific statement from the American Heart Association and the American College of Cardiology Foundation

scientific article published on 08 February 2010
Calmodulin kinase II and arrhythmias in a mouse model of cardiac hypertrophy

scientific article
Exome-wide association study of plasma lipids in >300,000 individuals

scientific article published on 30 October 2017
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk

scientific article published on 05 March 2013
Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system

scientific journal article
Cardiac ion channels

scientific article
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

scientific article
A calcium sensor in the sodium channel modulates cardiac excitability

scientific article
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study

scientific article published on 05 June 2013
When good drugs go bad.

scientific article
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome

scientific article published on 22 August 2005
Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science

scientific article
The Lambeth Conventions (II): guidelines for the study of animal and human ventricular and supraventricular arrhythmias

scientific article
The genetic basis of variability in drug responses

scientific article
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

scientific article published on 28 November 2016
Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation

scientific article

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