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Author Details

Frederick E Dewey
2006
72
41
PMIDPaper TitleJournal TitlePublished Year
35671065Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac Hypertrophy.Circ Genom Precis Med2022
34646007Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.Genet Med2021
31118516Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.Nature2019
31042164Cyclin-dependent kinase inhibitor 2B regulates efferocytosis and atherosclerosis.J Clin Invest2019
31235787Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure.Nat Commun2019
31216868Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.Circulation2019
29631995Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With Adults.Circ Genom Precis Med2018
28726809Genomic diagnostics within a medically underserved population: efficacy and implications.Genet Med2018
30029678Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease.Genome Med2018
30354297Loss-of-Function ABCC8 Mutations in Pulmonary Arterial Hypertension.Circ Genom Precis Med2018
30353015Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide.Sci Rep2018
30061737Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.Nat Genet2018
30535219Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.JAMA2018
29899519Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.Nat Commun2018
30275531Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.Nat Genet2018
30646163Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.JAMA Netw Open2018
29562163A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease.N Engl J Med2018
29261187Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.Genet Med2018
29218864APPLICATIONS OF GENETICS, GENOMICS AND BIOINFORMATICS IN DRUG DISCOVERY.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing2018
29290336Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.Am J Hum Genet2018
29545597Rare variants in drug target genes contributing to complex diseases, phenome-wide.Sci Rep2018
29727688Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes.Am J Hum Genet2018
28166213Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.Nat Genet2017
28506971Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.Circ Res2017
28538136Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease.N Engl J Med2017
28977528MAPPIN: a method for annotating, predicting pathogenicity and mode of inheritance for nonsynonymous variants.Nucleic Acids Research2017
28471438Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.Genet Med2017
28267856Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.JAMA2017
27897004IDENTIFYING GENETIC ASSOCIATIONS WITH VARIABILITY IN METABOLIC HEALTH AND BLOOD COUNT LABORATORY VALUES: DIVING INTO THE QUANTITATIVE TRAITS BY LEVERAGING LONGITUDINAL DATA FROM AN EHR.Pac Symp Biocomput2017
27578142Corrigendum to Baseline Undertreatment of Adults with Newly Diagnosed Familial Hypercholesterolemia by Genomic Sequencing [J Clin Lipidol 10 (2016) 692-693].J Clin Lipidol2016
27247418Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation.Proc Natl Acad Sci U S A2016
26933753Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease.N Engl J Med2016
26776183INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES.Pac Symp Biocomput2016
26382196CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data.Bioinformatics2016
28008010Genetic identification of familial hypercholesterolemia within a single U.S. health care system.Science2016
28008009Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study.Science2016
27681629Early somatic mosaicism is a rare cause of long-QT syndrome.Proc Natl Acad Sci U S A2016
27959690Variants in ANGPTL4 and the Risk of Coronary Artery Disease.N Engl J Med2016
26448358Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data.PLoS Genet2015
26653627Systems Genomics Identifies a Key Role for Hypocretin/Orexin Receptor-2 in Human Heart Failure.J Am Coll Cardiol2015
26166063Family History of Hypertrophic or Dilated Cardiomyopathy from Family History Section.Current Sports Medicine Reports2015
24702692Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertension.Am J Respir Crit Care Med2014
24531546Cyclin-dependent kinase inhibitor 2B regulates efferocytosis and atherosclerosis.J Clin Invest2014
25027152Interpreting whole-genome sequencing--reply.JAMA2014
24618965Clinical interpretation and implications of whole-genome sequencing.JAMA2014
24973560Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing.Heart Rhythm2014
23392791Validation of a cardiopulmonary exercise test score in heart failure.Circ Heart Fail2013
22715280Systems-based approaches to cardiovascular biomarker discovery.Circ Cardiovasc Genet2012
22354974DNA sequencing: clinical applications of new DNA sequencing technologies.Circulation2012
22424236Personal omics profiling reveals dynamic molecular and medical phenotypes.Cell2012
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