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Author Details

Christian M Shaffer
Vanderbilt University
2004
82
34
PMIDPaper TitleJournal TitlePublished Year
36524479Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.Circulation2023
37038246Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.Eur Heart J2023
36645160The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach.Clin Transl Sci2023
34930020Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.Circulation2022
35377938ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia.Blood2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35533259Genome-wide association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopenia.Blood Adv2022
35389944Composite CYP3A phenotypes influence tacrolimus dose-adjusted concentration in lung transplant recipients.Pharmacogenet Genomics2022
35656995Genetic Determinants of Body Mass Index and Fasting Glucose Are Mediators of Grade 1 Diastolic Dysfunction.J Am Heart Assoc2022
36167494Genome-wide association analyses of common infections in a large practice-based biobank.BMC Genomics2022
34994586Common Ancestry-Specific Ion Channel Variants Predispose to Drug-Induced Arrhythmias.Circulation2022
33137338Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.Kidney Int2021
33895829Genetic Thyrotropin Regulation of Atrial Fibrillation Risk Is Mediated Through an Effect on Height.J Clin Endocrinol Metab2021
34495297Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes.JAMA Cardiol2021
34463132Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults.Circ Genom Precis Med2021
34180972Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.JAMA Intern Med2021
34061827High-throughput framework for genetic analyses of adverse drug reactions using electronic health records.PLoS Genet2021
34341450The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene.Sci Rep2021
32372017The polygenic architecture of left ventricular mass mirrors the clinical epidemiology.Sci Rep2020
31685432Heart failure and atrial tachyarrhythmia on abiraterone: A pharmacovigilance study.Arch Cardiovasc Dis2020
32068817Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease.JAMA2020
32586526Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome.J Pediatr2020
32247630Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways.Kidney Int2020
32186652Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis.JAMA Cardiol2020
30527956Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.Lancet Respir Med2019
31486736CYP2C9*2 is associated with indomethacin treatment failure for patent ductus arteriosus.Pharmacogenomics2019
31509211A Genetic Approach to the Association Between PCSK9 and Sepsis.JAMA Netw Open2019
31158526A Rapid Allele-Specific Assay for HLA-A*32:01 to Identify Patients at Risk for Vancomycin-Induced Drug Reaction with Eosinophilia and Systemic Symptoms.J Mol Diagn2019
30924126Genome-Wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol.Clin Pharmacol Ther2019
30776417HLA-A*32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptoms.J Allergy Clin Immunol2019
31152163A catalog of genetic loci associated with kidney function from analyses of a million individuals.Nat Genet2019
30657536Association Between Low-Density Lipoprotein Cholesterol Levels and Risk for Sepsis Among Patients Admitted to the Hospital With Infection.JAMA Netw Open2019
29053189Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission.J Med Virol2018
30166544A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.Nat Commun2018
29892015Multi-ethnic genome-wide association study for atrial fibrillation.Nat Genet2018
29967236Hypogonadism as a Reversible Cause of Torsades de Pointes in Men.Circulation2018
30535219Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.JAMA2018
29703846LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.Circulation2018
29627106Clinical Features Associated With Nascent Left Ventricular Diastolic Dysfunction in a Population Aged 40 to 55 Years.Am J Cardiol2018
28815128A comparative study of different methods for automatic identification of clopidogrel-induced bleedings in electronic health records.AMIA Jt Summits Transl Sci Proc2017
28408648Azithromycin Causes a Novel Proarrhythmic Syndrome.Circ Arrhythm Electrophysiol2017
28209764<i>Kcnj11</i> Ablation Is Associated With Increased Nitro-Oxidative Stress During Ischemia-Reperfusion Injury: Implications for Human Ischemic Cardiomyopathy.Circ Heart Fail2017
28209224Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.J Am Coll Cardiol2017
28207879Comparison of HLA allelic imputation programs.PLoS One2017
28416818Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Nat Genet2017
28416512Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes.Circ Cardiovasc Genet2017
28490672Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants.Sci Transl Med2017
29083408Exome-wide association study of plasma lipids in &gt;300,000 individuals.Nat Genet2017
28542097Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults.Pharmacogenet Genomics2017
28747752Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Nat Genet2017
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Collaborators

Dan M Roden
Vanderbilt University Medical Center
Co-authored papers 56
Joshua C Denny
Vanderbilt University
Co-authored papers 39
Jonathan D Mosley
Vanderbilt University Medical Center
Co-authored papers 29
Quinn S Wells
Vanderbilt University Medical Center
Co-authored papers 21
Peter Weeke
Rigshospitalet, University of Copenhagen
Co-authored papers 19
Sara L Van Driest
National Institutes of Health
Co-authored papers 14
Jason H Karnes
Vanderbilt University Medical Center
Co-authored papers 13
Murray H Brilliant
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Co-authored papers 12
Erwin P Bottinger
Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers 12
Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers 12
Charles M Stein
Vanderbilt University School of Medicine
Co-authored papers 12
Lisa Bastarache
Vanderbilt University Medical Center
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Ruth J F Loos
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Eric Boerwinkle
Baylor College of Medicine
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Iftikhar J Kullo
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Alexander Teumer
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Vilmundur Gudnason
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Daniel I Chasman
Harvard Medical School, Harvard University
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Daniel J Rader
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Paul M Ridker
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Jerome I Rotter
Co-authored papers 9
Uwe V??lker
University Medicine
Co-authored papers 9
Elizabeth J Phillips
Vanderbilt University Medical Center
Co-authored papers 9
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 9
Marju Orho-Melander
Co-authored papers 9
Bruce M Psaty
Co-authored papers 9
Eric B Larson
University of Washington
Co-authored papers 8
Sekar Kathiresan
Co-authored papers 8
Michiaki Kubo
Co-authored papers 8
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 8
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