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Author Details
Full Name
Digna R Velez Edwards
Affiliation
Vanderbilt University Medical Center
ORCID
Career Start Year
2006
Papers
164
H Index
41
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36366911
Tutorial: Using Community Engagement Studios to Enhance Pharmacogenetic Study Design for Maximizing Enrollment of Diverse Children and Pregnant People.
Clin Pharmacol Ther
2023
37547012
PheMIME: An Interactive Web App and Knowledge Base for Phenome-Wide, Multi-Institutional Multimorbidity Analysis.
medRxiv
2023
37693472
Pharmacogenetics of tuberculosis treatment toxicity and effectiveness in a large Brazilian cohort.
medRxiv
2023
37642233
Uterine leiomyomata and keloids fibrosis origins: a mini-review of fibroproliferative diseases.
Am J Physiol Cell Physiol
2023
37256887
Sex modifies the effect of genetic risk scores for polycystic ovary syndrome on metabolic phenotypes.
PLoS Genet
2023
37016918
Association of genetically-predicted placental gene expression with adult blood pressure traits.
J Hypertens
2023
37040736
Challenges and Opportunities for Data Science in Women's Health.
Annu Rev Biomed Data Sci
2023
36520636
Racial/Ethnic and Sex Differences in Somatic Cancer Gene Mutations among Patients with Early-Onset Colorectal Cancer.
Cancer Discov
2023
36721373
Time-Varying Exposures and Miscarriage: A Comparison of Statistical Models Through Simulation.
Am J Epidemiol
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
36472455
Interactive network-based clustering and investigation of multimorbidity association matrices with associationSubgraphs.
Bioinformatics
2023
36846987
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.
J Am Heart Assoc
2023
36609580
Genetically-predicted placental gene expression is associated with birthweight and adult body mass index.
Sci Rep
2023
36540997
Predictive models for abdominal aortic aneurysms using polygenic scores and PheWAS-derived risk factors.
Pac Symp Biocomput
2023
36872475
What knowledge is required for an informed choice related to non-invasive prenatal screening?
J Genet Couns
2023
36824881
Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia.
medRxiv
2023
35226188
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.
Hum Genet
2022
35482220
Racial and Ethnic Variation in Genetic Susceptibility: Are Disparities in Infertility Prevalence and Outcomes more than Black and White?
Reprod Sci
2022
35597276
Maternal alcohol metabolism predicted by alcohol dehydrogenase genotype and the association between alcohol consumption and miscarriage.
Am J Obstet Gynecol
2022
36210504
Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci.
J Natl Cancer Inst
2022
36117404
Periconceptional folic acid supplementation and child asthma: a <i>Right From the Start</i> follow-up study.
J Matern Fetal Neonatal Med
2022
33512511
Determinants of stage at diagnosis of HPV-related cancer including area deprivation and clinical factors.
J Public Health (Oxf)
2022
32673615
Week-by-week alcohol consumption in early pregnancy and spontaneous abortion risk: a prospective cohort study.
Am J Obstet Gynecol
2021
33534346
Associations of biogeographic ancestry with hypertension traits.
J Hypertens
2021
33704461
Fate or coincidence: do COPD and major depression share genetic risk factors?
Hum Mol Genet
2021
33727701
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
2021
34530389
Learning the impact of acute and chronic diseases on forecasting neonatal encephalopathy.
Comput Methods Programs Biomed
2021
34404387
Uterine fibroids and risk of preterm birth by clinical subtypes: a prospective cohort study.
BMC Pregnancy Childbirth
2021
34302236
Evidence that geographic variation in genetic ancestry associates with uterine fibroids.
Hum Genet
2021
34155315
Western-style diet consumption impairs maternal insulin sensitivity and glucose metabolism during pregnancy in a Japanese macaque model.
Sci Rep
2021
34148359
Association of Apparent Treatment-Resistant Hypertension With Differential Risk of End-Stage Kidney Disease Across Racial Groups in the Million Veteran Program.
Hypertension
2021
34140684
A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts.
Nat Genet
2021
34162658
Identification of a Locus Near <i>ULK1</i> Associated With Progression-Free Survival in Ovarian Cancer.
Cancer Epidemiol Biomarkers Prev
2021
33420026
Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics.
Nat Commun
2021
32961557
Characterizing the Clinical and Genetic Spectrum of Polycystic Ovary Syndrome in Electronic Health Records.
J Clin Endocrinol Metab
2021
32289280
A genome-wide association study of polycystic ovary syndrome identified from electronic health records.
Am J Obstet Gynecol
2020
33230300
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
2020
32741603
Association of uterine fibroids with birthweight and gestational age.
Ann Epidemiol
2020
32709459
Equity in Health: Consideration of Race and Ethnicity in Precision Medicine.
Trends Genet
2020
32121581
What Results Should Be Returned from Opportunistic Screening in Translational Research?
J Pers Med
2020
30521025
Gestational Age at Arrest of Development: An Alternative Approach for Assigning Time at Risk in Studies of Time-Varying Exposures and Miscarriage.
Am J Epidemiol
2019
31678588
Deep learning predicts extreme preterm birth from electronic health records.
J Biomed Inform
2019
31437903
Leveraging Electronic Health Records to Learn Progression Path for Severe Maternal Morbidity.
Stud Health Technol Inform
2019
31437902
Learning to Identify Severe Maternal Morbidity from Electronic Health Records.
Stud Health Technol Inform
2019
31548585
Publisher Correction: Shared heritability and functional enrichment across six solid cancers.
Nat Commun
2019
31451708
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
Nat Commun
2019
31194258
Alcohol Use in Pregnancy and Miscarriage: A Systematic Review and Meta-Analysis.
Alcohol Clin Exp Res
2019
31480066
Estimating Uterine Fibroid SNP-Based Heritability in European American Women with Imaging-Confirmed Fibroids.
Hum Hered
2019
31278762
Association between First Trimester Antidepressant Use and Risk of Spontaneous Abortion.
Pharmacotherapy
2019
31249589
A <i>Trans</i>-Ethnic Genome-Wide Association Study of Uterine Fibroids.
Front Genet
2019
1 - 50 of 164
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Collaborators
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Mike A Nalls
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Albert V Smith
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Alexander P Reiner
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Paul M Ridker
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Daniel I Chasman
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