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Author Details

QiPing Feng
Vanderbilt University Medical Center
2008
74
21
PMIDPaper TitleJournal TitlePublished Year
38041473Developing and evaluating pediatric phecodes (Peds-Phecodes) for high-throughput phenotyping using electronic health records.J Am Med Inform Assoc2024
36711487Association Between Genetically Predicted Expression of TPMT and Azathioprine Adverse Events.Res Sq2023
37662278Developing and Evaluating Pediatric Phecodes (Peds-Phecodes) for High-Throughput Phenotyping Using Electronic Health Records.medRxiv2023
37550754Clinical diagnoses associated with a positive antinuclear antibody test in patients with and without autoimmune disease.BMC Rheumatol2023
37882666Association between <i>APOL1</i> risk variants and the occurrence of sepsis in Black patients hospitalized with infections: a retrospective cohort study.Elife2023
37689782Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.Nat Commun2023
37503019Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets.Res Sq2023
38036523Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease.Nat Commun2023
37461512Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets.medRxiv2023
36747677Association between <i>APOL1</i> risk variants and the occurrence of sepsis in Black patients hospitalized with infections: a retrospective cohort study.medRxiv2023
36645160The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach.Clin Transl Sci2023
34625956Identifying Potential Therapeutic Applications and Diagnostic Harms of Increased Bilirubin Concentrations: A Clinical and Genetic Approach.Clin Pharmacol Ther2022
35437716Integration of Omics and Phenotypic Data for Precision Medicine.Methods Mol Biol2022
35724382Race, Genotype, and Azathioprine Discontinuation : A Cohort Study.Ann Intern Med2022
35967117Phenome-Wide Association Study of <i>UMOD</i> Gene Variants and Differential Associations With Clinical Outcomes Across Populations in the Million Veteran Program a Multiethnic Biobank.Kidney Int Rep2022
36167494Genome-wide association analyses of common infections in a large practice-based biobank.BMC Genomics2022
35013250Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.Nat Commun2022
35308936Mapping the Read2/CTV3 controlled clinical terminologies to Phecodes in UK Biobank primary care electronic health records: implementation and evaluation.AMIA Annu Symp Proc2022
35118815Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity.Clin Transl Sci2022
34582038TPMT and NUDT15 Variants Predict Discontinuation of Azathioprine for Myelotoxicity in Patients with Inflammatory Disease: Real-World Clinical Results.Clin Pharmacol Ther2022
32964493Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.Genet Epidemiol2021
33712848DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.J Am Med Inform Assoc2021
33822779Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.PLoS Genet2021
33774203ConceptWAS: A high-throughput method for early identification of COVID-19 presenting symptoms and characteristics from clinical notes.J Biomed Inform2021
34097045A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes.JAMA Netw Open2021
34061827High-throughput framework for genetic analyses of adverse drug reactions using electronic health records.PLoS Genet2021
33977795Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis.Lupus2021
34140684A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts.Nat Genet2021
34282949Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry.Circ Genom Precis Med2021
33407432Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort.BMC Med Genomics2021
33310085Association of Genetic Variation With Cirrhosis: A Multi-Trait Genome-Wide Association and Gene-Environment Interaction Study.Gastroenterology2021
33309899A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19.J Biomed Inform2021
32226016Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.PLoS Genet2020
32054992Combining clinical and candidate gene data into a risk score for azathioprine-associated leukopenia in routine clinical practice.Pharmacogenomics J2020
33200151ConceptWAS: a high-throughput method for early identification of COVID-19 presenting symptoms.medRxiv2020
32247630Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways.Kidney Int2020
32307929Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.Arthritis Rheumatol2020
32386537Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.Am J Hum Genet2020
30679510Learning from Longitudinal Data in Electronic Health Record and Genetic Data to Improve Cardiovascular Event Prediction.Sci Rep2019
30223305Co-Prescription of Strong CYP1A2 Inhibitors and the Risk of Tizanidine-Associated Hypotension: A Retrospective Cohort Study.Clin Pharmacol Ther2019
31234639Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects.Circulation2019
31509211A Genetic Approach to the Association Between PCSK9 and Sepsis.JAMA Netw Open2019
31445983Detecting time-evolving phenotypic topics via tensor factorization on electronic health records: Cardiovascular disease case study.J Biomed Inform2019
30774981A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>.NPJ Genom Med2019
30759150Using topic modeling via non-negative matrix factorization to identify relationships between genetic variants and disease phenotypes: A case study of Lipoprotein(a) (LPA).PLoS One2019
30657536Association Between Low-Density Lipoprotein Cholesterol Levels and Risk for Sepsis Among Patients Admitted to the Hospital With Infection.JAMA Netw Open2019
29590070Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.Science2018
30166544A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.Nat Commun2018
30153257Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational study using electronic health records.PLoS Med2018
29703846LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.Circulation2018
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Collaborators

Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers 53
Charles M Stein
Vanderbilt University School of Medicine
Co-authored papers 29
Joshua C Denny
Vanderbilt University
Co-authored papers 24
Dan M Roden
Vanderbilt University Medical Center
Co-authored papers 17
Russell A Wilke
University of South Dakota Sanford School of Medicine
Co-authored papers 15
Alyson L Dickson
Vanderbilt University Medical Center
Co-authored papers 12
Nancy J Cox
Vanderbilt University Medical Center
Co-authored papers 11
Jonathan D Mosley
Vanderbilt University Medical Center
Co-authored papers 11
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 11
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 10
Ronald M Krauss
Co-authored papers 10
Eric B Larson
University of Washington
Co-authored papers 8
Vern Eric Kerchberger
Vanderbilt University Medical Center
Co-authored papers 8
Christian M Shaffer
Vanderbilt University
Co-authored papers 8
Lisa Bastarache
Vanderbilt University Medical Center
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Josh F Peterson
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Scott J Hebbring
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Daniel J Schaid
Mayo Clinic
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Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
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Bahram Namjou
Cincinnati Children's Hospital
Co-authored papers 6
Richard M Weinshilboum
Mayo Clinic
Co-authored papers 6
Monika E Grabowska
Vanderbilt University Medical Center
Co-authored papers 6
Quinn S Wells
Vanderbilt University Medical Center
Co-authored papers 5
Patrick M A Sleiman
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 5
Jerome I Rotter
Co-authored papers 5
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 5
David R Crosslin
University of Washington Medical Center
Co-authored papers 5
Adam S Gordon
Northwestern University Feinberg School of Medicine.
Co-authored papers 5
Sara L Van Driest
National Institutes of Health
Co-authored papers 5
Robert J Carroll
Vanderbilt University Medical Center
Co-authored papers 4
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