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Author Details

Todd L Edwards
Vanderbilt University Medical Center
2004
164
44
PMIDPaper TitleJournal TitlePublished Year
36824881Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia.medRxiv2023
37945903Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.Nat Genet2023
37642233Uterine leiomyomata and keloids fibrosis origins: a mini-review of fibroproliferative diseases.Am J Physiol Cell Physiol2023
37461445Glycoprotein VI is Critical for the Detection and Progression of Abdominal Aortic Aneurysms.bioRxiv2023
37353859Variant-based heritability assessment of dexmedetomidine and fentanyl clearance in pediatric patients.Clin Transl Sci2023
37016918Association of genetically-predicted placental gene expression with adult blood pressure traits.J Hypertens2023
37040736Challenges and Opportunities for Data Science in Women's Health.Annu Rev Biomed Data Sci2023
37399599A genetically supported drug repurposing pipeline for diabetes treatment using electronic health records.EBioMedicine2023
36718908Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents.J Am Heart Assoc2023
36472455Interactive network-based clustering and investigation of multimorbidity association matrices with associationSubgraphs.Bioinformatics2023
36609580Genetically-predicted placental gene expression is associated with birthweight and adult body mass index.Sci Rep2023
36540997Predictive models for abdominal aortic aneurysms using polygenic scores and PheWAS-derived risk factors.Pac Symp Biocomput2023
36872133Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry.Eur Urol2023
34957589Population pharmacokinetic analysis of dexmedetomidine in children using real-world data from electronic health records and remnant specimens.Br J Clin Pharmacol2022
35652341Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.Hypertension2022
35500537Using Mendelian randomisation to identify opportunities for type 2 diabetes prevention by repurposing medications used for lipid management.EBioMedicine2022
35522175Blood Pressure Polygenic Scores Are Associated With Apparent Treatment-Resistant Hypertension.Circ Genom Precis Med2022
35654975A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.Nat Genet2022
36314129Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses.Circulation2022
35988586Association between nitric oxide synthase 3 genetic variant and acute kidney injury following pediatric cardiac surgery.Am Heart J2022
35886906Large-Scale Multi-Omics Studies Provide New Insights into Blood Pressure Regulation.Int J Mol Sci2022
36344332Translational opportunities emerge from genetic influences on health.Trends Mol Med2022
35226188Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.Hum Genet2022
35013250Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.Nat Commun2022
34877660Effect of CYP3A5 and CYP3A4 Genetic Variants on Fentanyl Pharmacokinetics in a Pediatric Population.Clin Pharmacol Ther2022
35199555Diastolic Blood Pressure Alleles Improve Congenital Heart Defect Repair Outcomes.Circ Res2022
34986912Impact of obesity on post-operative arrhythmias after congenital heart surgery in children and young adults.Cardiol Young2022
33190990Blunted PTH response to vitamin D insufficiency/deficiency and colorectal neoplasia risk.Clin Nutr2021
33853351Association Between Genetic Variation in Blood Pressure and Increased Lifetime Risk of Peripheral Artery Disease.Arterioscler Thromb Vasc Biol2021
33813844Relationship Between Blood Pressure and Incident Cardiovascular Disease: Linear and Nonlinear Mendelian Randomization Analyses.Hypertension2021
33534346Associations of biogeographic ancestry with hypertension traits.J Hypertens2021
33727701Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2021
33837377Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19.Nat Med2021
34302236Evidence that geographic variation in genetic ancestry associates with uterine fibroids.Hum Genet2021
34148359Association of Apparent Treatment-Resistant Hypertension With Differential Risk of End-Stage Kidney Disease Across Racial Groups in the Million Veteran Program.Hypertension2021
33432171Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.Nat Med2021
32372017The polygenic architecture of left ventricular mass mirrors the clinical epidemiology.Sci Rep2020
32051193Mendelian Randomization of Circulating Polyunsaturated Fatty Acids and Colorectal Cancer Risk.Cancer Epidemiol Biomarkers Prev2020
33230300Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2020
32709459Equity in Health: Consideration of Race and Ethnicity in Precision Medicine.Trends Genet2020
32706693Information Loss in Harmonizing Granular Race and Ethnicity Data: Descriptive Study of Standards.J Med Internet Res2020
32981348Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.Circulation2020
30528449Incidence and effect of early postoperative ventricular arrhythmias after congenital heart surgery.Heart Rhythm2019
31543516Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial.Br J Cancer2019
31480066Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids.Hum Hered2019
31337231Association of <i>APOL1</i> Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program.Circulation2019
31249589A <i>Trans</i>-Ethnic Genome-Wide Association Study of Uterine Fibroids.Front Genet2019
30988330Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.Sci Rep2019
31152163A catalog of genetic loci associated with kidney function from analyses of a million individuals.Nat Genet2019
31001917Evaluation of vitamin D biosynthesis and pathway target genes reveals UGT2A1/2 and EGFR polymorphisms associated with epithelial ovarian cancer in African American Women.Cancer Med2019
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Collaborators

Digna R Velez Edwards
Vanderbilt University Medical Center
Co-authored papers 66
Ruth J F Loos
Co-authored papers 25
Joshua C Denny
Vanderbilt University
Co-authored papers 23
Erwin P Bottinger
Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers 23
Xiuqing Guo
Co-authored papers 20
Yingchang Lu
Co-authored papers 20
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers 20
Dan M Roden
Vanderbilt University Medical Center
Co-authored papers 19
Jerome I Rotter
Co-authored papers 19
Myriam Fornage
Co-authored papers 19
Kent D Taylor
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Wei Zheng
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Sharon L R Kardia
School of Public Health, University of Michigan ann arbor
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Bruce M Psaty
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Yongmei Liu
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Mike A Nalls
Center for Alzheimer's and Related Dementias, National Institutes of Health
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Tamara B Harris
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VA Boston Healthcare System
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Vilmundur Gudnason
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Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
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Paul Elliott
Co-authored papers 16
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 15
David R Crosslin
University of Washington Medical Center
Co-authored papers 15
Tõnu Esko
Co-authored papers 15
Alexander P Reiner
Co-authored papers 15
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 15
Paul M Ridker
Co-authored papers 14
Jennifer A Smith
Co-authored papers 14
John Danesh
Co-authored papers 14
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