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Wei-Qi Wei · SciRah

Researcher profile · Semantic Scholar

Wei-Qi Wei

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Wei-Qi Wei — researcher profile on SciRah

h-index: 40
Works: 180
Citations: 10K

Most-cited papers

Precision Medicine, AI, and the Future of Personalized Health Care
Kevin B. Johnson, Wei-Qi Wei, D. Weeraratne, M. Frisse +4 more
2020Clinical and Translational Science1,398 citations Open access
Semantic Scholar
The power of genetic diversity in genome-wide association studies of lipids
Sarah E. Graham, S. Clarke, Kuan-Han H. Wu, S. Kanoni +496 more
2021Nature826 citations Open access
Semantic Scholar
Mapping ICD-10 and ICD-10-CM Codes to Phecodes: Workflow Development and Initial Evaluation
Patrick Wu, A. Gifford, Xiangrui Meng, Xue Li +8 more
2019JMIR Medical Informatics485 citations Open access
Semantic Scholar
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.
Minta Thomas, L. Sakoda, M. Hoffmeister, E. Rosenthal +93 more
2020American Journal of Human Genetics176 citations Open access
Semantic Scholar
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations
T. Ge, M. Irvin, Amit Patki, V. Srinivasasainagendra +44 more
2022Genome Medicine141 citations Open access
Semantic Scholar
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.
O. Dikilitas, D. Schaid, M. Kosel, Robert J. Carroll +18 more
2020American Journal of Human Genetics130 citations Open access
Semantic Scholar
Association of genetic variation with cirrhosis: a multi-trait genome-wide association and gene-environment interaction study
C. Emdin, Mary E. Haas, Veeral H. Ajmera, Tracey G. Simon +11 more
2020Gastroenterology113 citations Open access
Semantic Scholar
Returning integrated genomic risk and clinical recommendations: the eMERGE study
Jodell E. Linder, Aimee Allworth, Harris T. Bland, P. Caraballo +102 more
2023Genetics in Medicine106 citations Open access
Semantic Scholar
Phenome-wide Mendelian-randomization study of genetically determined vitamin D on multiple health outcomes using the UK Biobank study
Xiangrui Meng, Xue Li, M. Timofeeva, Ya-Zhou He +13 more
2019International Journal of Epidemiology70 citations Open access
Semantic Scholar
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, M. McNulty, Atlas Khan +76 more
2023Nature Communications61 citations Open access
Semantic Scholar
Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension
Patrick Wu, Qi-Ping Feng, V. Kerchberger, Scott D. Nelson +9 more
2022Nature Communications58 citations Open access
Semantic Scholar
Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy
Kristi Krebs, Jonas Bovijn, Neil S. Zheng, M. Lepamets +65 more
2020American Journal of Human Genetics47 citations Open access
Semantic Scholar
Drug repurposing for Alzheimer’s disease from 2012–2022—a 10-year literature review
Monika E. Grabowska, Annabelle Huang, Zhe-Xing Wen, Bing-Shan Li +1 more
2023Frontiers in Pharmacology46 citations Open access
Semantic Scholar
PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records
Neil S. Zheng, Qi-Ping Feng, V. Kerchberger, Juan Zhao +6 more
2020J. Am. Medical Informatics Assoc.39 citations Open access
Semantic Scholar
Race, Genotype, and Azathioprine Discontinuation: A Cohort Study
A. Dickson, Laura L. Daniel, E. Jackson, J. Zanussi +13 more
2022Annals of Internal Medicine31 citations Open access
Semantic Scholar
Associations of Genetically Predicted Lipoprotein (a) Levels with Cardiovascular Traits in Individuals of European and African Ancestry
Benjamin A. Satterfield, O. Dikilitas, M. Safarova, S. Clarke +18 more
2021Circulation Genomic and Precision Medicine30 citations Open access
Semantic Scholar
Arrhythmia variant associations and reclassifications in the eMERGE-III sequencing study
A. Glazer, Giovanni E. Davogustto, C. Shaffer, Carlos G. Vanoye +46 more
2021medRxiv29 citations Open access
Semantic Scholar
A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19
Neil S. Zheng, Jeremy L. Warner, Travis J. Osterman, Q. Wells +11 more
2020Journal of Biomedical Informatics28 citations Open access
Semantic Scholar
Clinical diagnoses associated with a positive antinuclear antibody test in patients with and without autoimmune disease
J. Zanussi, Juan Zhao, Wei-Qi Wei, G. Karakoc +5 more
2023BMC Rheumatology27 citations Open access
Semantic Scholar
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study
Yao Hu, M. Graff, J. Haessler, S. Buyske +49 more
2020PLoS Genetics26 citations Open access
Semantic Scholar
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR
M. S. Safarova, Benjamin A. Satterfield, Xiao Fan, E. Austin +28 more
2019npj Genomic Medicine26 citations Open access
Semantic Scholar
TPMT and NUDT15 Variants Predict Discontinuation of Azathioprine for Myelotoxicity in Patients with Inflammatory Disease: Real-World Clinical Results
A. Dickson, Laura L. Daniel, J. Zanussi, W. Plummer +12 more
2021Clinical pharmacology and therapy25 citations Open access
Semantic Scholar
A 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
Ge Liu, Mingjian Shi, J. Mosley, Chun-Hua Weng +13 more
2021JAMA Network Open25 citations Open access
Semantic Scholar
Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms
Milton D. Pividori, Su-Mei Lu, Bing-Lan Li, Chun Su +13 more
2021bioRxiv24 citations Open access
Semantic Scholar
A Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults
Q. Wells, M. Bagheri, A. Aday, D. Gupta +9 more
2021Circulation Genomic and Precision Medicine23 citations Open access
Semantic Scholar
A unified framework identifies novel links between plasma lipids and diseases from electronic medical records across large-scale cohorts
Y. Veturi, A. Lucas, Y. Bradford, Daniel Hui +19 more
2021Nature Genetics22 citations Open access
Semantic Scholar
Genomic considerations for FHIR®; eMERGE implementation lessons
M. Murugan, L. Babb, C. O. Taylor, Luke V. Rasmussen +22 more
2021Journal of Biomedical Informatics21 citations Open access
Semantic Scholar
Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways.
A. Bajaj, Andrea Ihegword, Cheng-Xiang Qiu, Aeron M. Small +16 more
2020Kidney International21 citations Open access
Semantic Scholar
Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies
Danqing Xu, Chen Wang, Atlas Khan, N. Shang +10 more
2021npj Digital Medicine18 citations Open access
Semantic Scholar
DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions
Patrick Wu, Scott D. Nelson, Juan Zhao, C. Stone +10 more
2021J. Am. Medical Informatics Assoc.18 citations Open access
Semantic Scholar
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network
J. Pacheco, Luke V. Rasmussen, Ken Wiley, T. Person +35 more
2023Scientific Reports17 citations Open access
Semantic Scholar
Genome-wide approach to measure variant-based heritability of drug outcome phenotypes
Ayesha Muhammad, Ida Aka, K. Birdwell, A. Gordon +4 more
2021Clinical pharmacology and therapy17 citations Open access
Semantic Scholar
Pharmacogenetics of Hypoglycemia Associated with Sulfonylurea Therapy in Usual Clinical Care
S. Mitchell, Daniel A. Carranza Leon, Sandip Chaugai, V. Kawai +3 more
2020The Pharmacogenomics Journal17 citations Open access
Semantic Scholar
Characterizing variability of electronic health record-driven phenotype definitions
P. Brandt, A. Kho, Yuan Luo, J. Pacheco +21 more
2022J. Am. Medical Informatics Assoc.16 citations
Semantic Scholar
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
E. Pfaff, A. Girvin, M. Crosskey, Srushti Gangireddy +10 more
2023J. Am. Medical Informatics Assoc.15 citations Open access
Semantic Scholar
Education and Electronic Medical Records and Genomics Network, Challenges and Lessons Learned from a Large-Scale Clinical Trial Using Polygenic Risk Scores
John J. Connolly, E. Berner, Maureen E. Smith, Samuel Lévy +31 more
2023Genetics in Medicine15 citations Open access
Semantic Scholar
Integration of Omics and Phenotypic Data for Precision Medicine.
Juan Zhao, Qi-Ping Feng, Wei-Qi Wei
2022Methods in molecular biology14 citations
Semantic Scholar
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders
Xinyuan Zhang, A. Lucas, Y. Veturi, T. Drivas +16 more
2022Nature Communications14 citations Open access
Semantic Scholar
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female‐Specific Health Conditions
B. Xiao, D. Velez Edwards, A. Lucas, T. Drivas +12 more
2023Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease12 citations Open access
Semantic Scholar
Author Correction: The power of genetic diversity in genome-wide association studies of lipids
Sarah E. Graham, S. Clarke, Kuan-Han H. Wu, S. Kanoni +496 more
2023Nature12 citations Open access
Semantic Scholar
The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach
Ge Liu, Lan Jiang, V. Kerchberger, A. Oeser +10 more
2023Clinical and Translational Science12 citations Open access
Semantic Scholar
Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease
C. Emdin, Mary E. Haas, A. Khera, K. Aragam +38 more
2021PLoS Genetics12 citations Open access
Semantic Scholar
ConceptWAS: A high-throughput method for early identification of COVID-19 presenting symptoms and characteristics from clinical notes
Juan Zhao, Monika E. Grabowska, V. Kerchberger, Joshua C. Smith +6 more
2021Journal of Biomedical Informatics12 citations Open access
Semantic Scholar
Readiness for PENicillin allergy testing: Perception of Allergy Label (PEN-PAL) Survey
David T. Coleman, C. Stone, Wei-Qi Wei, E. Phillips
2020Journal of Allergy and Clinical Immunology: In Practice12 citations Open access
Semantic Scholar
Penicillin allergy labels drive perioperative prophylactic antibiotic selection in orthopedic procedures
David T. Coleman, C. Stone, Wei-Qi Wei, E. Phillips
2020Journal of Allergy and Clinical Immunology: In Practice12 citations Open access
Semantic Scholar
Phenotyping coronavirus disease 2019 during a global health pandemic: Lessons learned from the characterization of an early cohort
Sarah Delozier, S. Bland, M. McPheeters, Q. Wells +9 more
2021Journal of Biomedical Informatics11 citations Open access
Semantic Scholar
Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Jodell E. Linder, Ran Tao, Wendy K. Chung, K. Kiryluk +32 more
2023American Journal of Human Genetics10 citations Open access
Semantic Scholar
Identifying environmental risk factors for post-acute sequelae of SARS-CoV-2 infection: An EHR-based cohort study from the recover program
Yong-Kang Zhang, Hui Hu, Vasilios Fokaidis, Colby Lewis V +13 more
2023Environmental Advances10 citations Open access
Semantic Scholar
Genome-wide association analyses of common infections in a large practice-based biobank
Lan Jiang, V. Kerchberger, C. Shaffer, A. Dickson +8 more
2022BMC Genomics9 citations Open access
Semantic Scholar
High-throughput framework for genetic analyses of adverse drug reactions using electronic health records
Neil S. Zheng, C. Stone, Lan Jiang, C. Shaffer +9 more
2021PLoS Genetics9 citations Open access
Semantic Scholar

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