Author details

Full Name

Wei-Qi Wei

Affiliation

Vanderbilt University Medical Center

ORCID

Career Start Year

2004

Papers

132

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
38041473	Developing and evaluating pediatric phecodes (Peds-Phecodes) for high-throughput phenotyping using electronic health records.	J Am Med Inform Assoc	2024
36005898	Scanning the medical phenome to identify new diagnoses after recovery from COVID-19 in a US cohort.	J Am Med Inform Assoc	2023
37662324	Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics.	medRxiv	2023
37662278	Developing and Evaluating Pediatric Phecodes (Peds-Phecodes) for High-Throughput Phenotyping Using Electronic Health Records.	medRxiv	2023
37550754	Clinical diagnoses associated with a positive antinuclear antibody test in patients with and without autoimmune disease.	BMC Rheumatol	2023
37745051	Drug repurposing for Alzheimer's disease from 2012-2022-a 10-year literature review.	Front Pharmacol	2023
37883979	Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.	Am J Hum Genet	2023
37882666	Association between <i>APOL1</i> risk variants and the occurrence of sepsis in Black patients hospitalized with infections: a retrospective cohort study.	Elife	2023
37689782	Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.	Nat Commun	2023
37503019	Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets.	Res Sq	2023
38036523	Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease.	Nat Commun	2023
37218289	De-black-boxing health AI: demonstrating reproducible machine learning computable phenotypes using the N3C-RECOVER Long COVID model in the All of Us data repository.	J Am Med Inform Assoc	2023
37181728	A metadata framework for computational phenotypes.	JAMIA Open	2023
37246632	Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.	Genet Med	2023
36820914	Machine Learning to Predict Interstage Mortality Following Single Ventricle Palliation: A NPC-QIC Database Analysis.	Pediatr Cardiol	2023
36621880	Returning integrated genomic risk and clinical recommendations: The eMERGE study.	Genet Med	2023
36785842	Identifying environmental risk factors for post-acute sequelae of SARS-CoV-2 infection: An EHR-based cohort study from the recover program.	Environ Adv	2023
36474423	Characterizing variability of electronic health record-driven phenotype definitions.	J Am Med Inform Assoc	2023
36747677	Association between <i>APOL1</i> risk variants and the occurrence of sepsis in Black patients hospitalized with infections: a retrospective cohort study.	medRxiv	2023
36846987	Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.	J Am Heart Assoc	2023
36645160	The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach.	Clin Transl Sci	2023
36540998	Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.	Pac Symp Biocomput	2023
36540997	Predictive models for abdominal aortic aneurysms using polygenic scores and PheWAS-derived risk factors.	Pac Symp Biocomput	2023
36711487	Association Between Genetically Predicted Expression of TPMT and Azathioprine Adverse Events.	Res Sq	2023
36935011	Representing and utilizing clinical textual data for real world studies: An OHDSI approach.	J Biomed Inform	2023
36737471	Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.	Sci Rep	2023
36765713	Correlates of Taxane-Induced Neuropathy, an Electronic Health Record Based Observational Study.	Cancers (Basel)	2023
36706849	Evaluating and mitigating bias in machine learning models for cardiovascular disease prediction.	J Biomed Inform	2023
36451277	Evaluating resources composing the PheMAP knowledge base to enhance high-throughput phenotyping.	J Am Med Inform Assoc	2023
36383166	Utilization of electronic health record data to evaluate the association of urban environment with systemic lupus erythematosus symptoms.	Rheumatology (Oxford)	2023
34625956	Identifying Potential Therapeutic Applications and Diagnostic Harms of Increased Bilirubin Concentrations: A Clinical and Genetic Approach.	Clin Pharmacol Ther	2022
35437716	Integration of Omics and Phenotypic Data for Precision Medicine.	Methods Mol Biol	2022
35765100	Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.	Genome Med	2022
35701404	Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.	Nat Commun	2022
35724382	Race, Genotype, and Azathioprine Discontinuation : A Cohort Study.	Ann Intern Med	2022
35594287	Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.	PLoS One	2022
35487368	Novel Analysis Methods to Mine Immune-Mediated Phenotypes and Find Genetic Variation Within the Electronic Health Record (Roadmap for Phenotype to Genotype: Immunogenomics).	J Allergy Clin Immunol Pract	2022
35590255	Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach.	BMC Genomics	2022
36372681	Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.	Obesity (Silver Spring)	2022
36167494	Genome-wide association analyses of common infections in a large practice-based biobank.	BMC Genomics	2022
36263067	Identifying Contextual and Spatial Risk Factors for Post-Acute Sequelae of SARS-CoV-2 Infection: An EHR-based Cohort Study from the RECOVER Program.	medRxiv	2022
35013250	Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.	Nat Commun	2022
35090449	Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.	BMC Med Inform Decis Mak	2022
35308936	Mapping the Read2/CTV3 controlled clinical terminologies to Phecodes in UK Biobank primary care electronic health records: implementation and evaluation.	AMIA Annu Symp Proc	2022
35118815	Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity.	Clin Transl Sci	2022
34930020	Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.	Circulation	2022
34380996	Genetic association of primary nonresponse to anti-TNFÎ± therapy in patients with inflammatory bowel disease.	Pharmacogenet Genomics	2022
34582038	TPMT and NUDT15 Variants Predict Discontinuation of Azathioprine for Myelotoxicity in Patients with Inflammatory Disease: Real-World Clinical Results.	Clin Pharmacol Ther	2022
32961010	Precision Medicine, AI, and the Future of Personalized Health Care.	Clin Transl Sci	2021
33712848	DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.	J Am Med Inform Assoc	2021

1 - 50 of 132

Zhaoyi Chen

University of Florida

Career Start Year 2017

Number of shared co-authors 8

Brett K Beaulieu-Jones

University of Chicago

Career Start Year 2016

Number of shared co-authors 12

Simon Lin

The Abigail Wexner Research Institute, Nationwide Children's Hospital

Career Start Year 2015

Number of shared co-authors 1

Kenney Ng

Center for Computational Health

Career Start Year 2014

Number of shared co-authors 8

Jacqueline Kirby

Vanderbilt University School of Medicine

Career Start Year 2014

Number of shared co-authors 55

Benjamin S Glicksberg

Hasso Plattner Institute for Digital Health, Icahn School of Medicine at Mount Sinai

Career Start Year 2013

Number of shared co-authors 18

Stephen B Ellis

Icahn School of Medicine at Mount Sinai

Career Start Year 2013

Number of shared co-authors 55

Yue Yu

Health Sciences Mayo Clinic

Career Start Year 2012

Number of shared co-authors 15

Omri Gottesman

Icahn School of Medicine at Mount Sinai

Career Start Year 2011

Number of shared co-authors 129

Mary Regina Boland

University of Pennsylvania

Career Start Year 2011

Number of shared co-authors 13

Victor M Castro

Center for Quantitative Health, Massachusetts General Hospital

Career Start Year 2010

Number of shared co-authors 17

Chuan Hong

Harvard Medical School, USA Duke University

Career Start Year 2009

Number of shared co-authors 11

Jihoon Kim

university of california san diego

Career Start Year 2009

Number of shared co-authors 2

Nicholas P Tatonetti

Columbia Universtiy College of Physicians and Surgeons

Career Start Year 2009

Number of shared co-authors 38

Terrie Kitchner

Center for Precision Medicine Research, Marshfield Clinic Research Institute

Career Start Year 2007

Number of shared co-authors 89

Paul Avillach

Harvard Medical School

Career Start Year 2007

Number of shared co-authors 12

Joel T Dudley

Institute for Next Generation Healthcare

Career Start Year 2006

Number of shared co-authors 15

Jessica D Tenenbaum

Duke University

Career Start Year 2006

Number of shared co-authors 8

Janey Wang

Vanderbilt University Medical Center

Career Start Year 2005

Number of shared co-authors 14

Shyam Visweswaran

University of Pittsburgh

Career Start Year 2003

Number of shared co-authors 18

Gil Alterovitz

Brigham and Women's Hospital

Career Start Year 2002

Number of shared co-authors 25

Nigam H Shah

Stanford University

Career Start Year 2002

Number of shared co-authors 26

Richard J B Dobson

Institute of Psychiatry, King's College London

Career Start Year 2002

Number of shared co-authors 9

Assaf Gottlieb

Center for Precision Health, University of Texas Health Science Center at Houston

Career Start Year 2002

Number of shared co-authors 2

Griffin M Weber

Harvard Medical School

Career Start Year 2001

Number of shared co-authors 14

Antoine Neuraz

INSERM UMR 3, Universite Paris Cite, Imagine Institute

Career Start Year 1994

Number of shared co-authors 4

Atul J Butte

Bakar Computational Health Sciences Institute, University of California san francisco

Career Start Year 1993

Number of shared co-authors 18

Isaac S Kohane

Harvard Medical School

Career Start Year 1983

Number of shared co-authors 70

Geoffrey S Ginsburg

National Institutes of Health

Career Start Year 1981

Number of shared co-authors 33

Yves A Lussier

Center for Biomedical Informatics and Biostatistics, University of Arizona

Career Start Year 1971

Number of shared co-authors 10

row(s) 1 - 30 of 30

Joshua C Denny

Vanderbilt University

Co-authored papers 54

QiPing Feng

Vanderbilt University Medical Center

Co-authored papers 53

Charles M Stein

Vanderbilt University School of Medicine

Co-authored papers 32

Dan M Roden

Vanderbilt University Medical Center

Co-authored papers 28

Gail P Jarvik

University of Washington Medical Center

Co-authored papers 27

Iftikhar J Kullo

Mayo Clinic

Co-authored papers 26

Hakon Hakonarson

The Center for Applied Genomics, Children's Hospital of Philadelphia

Co-authored papers 20

Lisa Bastarache

Vanderbilt University Medical Center

Co-authored papers 17

Jonathan D Mosley

Vanderbilt University Medical Center

Co-authored papers 17

Jennifer A Pacheco

University of Pennsylvania

Co-authored papers 15

Bahram Namjou

Cincinnati Children's Hospital

Co-authored papers 15

David R Crosslin

University of Washington Medical Center

Co-authored papers 15

Christopher G Chute

Brown University, Brown University Warren Alpert Medical School, Dartmouth-Hitchcock Medical Center, Harvard School of Public Health, Johns Hopkins Medicine, Mayo Clinic Minnesota

Co-authored papers 15

Robert J Carroll

Vanderbilt University Medical Center

Co-authored papers 14

Eric B Larson

University of Washington

Co-authored papers 13

Marylyn D Ritchie

Center for Systems Genomics, Pennsylvania State University, University Park

Co-authored papers 13

Nancy J Cox

Vanderbilt University Medical Center