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Author Details
Full Name
Chunhua Weng
Affiliation
Columbia University Irving Medical Center
ORCID
Career Start Year
2002
Papers
293
H Index
36
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36255273
Clinical and temporal characterization of COVID-19 subgroups using patient vector embeddings of electronic health records.
J Am Med Inform Assoc
2023
37615994
The suitability of UMLS and SNOMED-CT for encoding outcome concepts.
J Am Med Inform Assoc
2023
37546941
Natural Language Processing Can Automate Extraction of Barrett's Esophagus Endoscopy Quality Metrics.
medRxiv
2023
37986722
Enhancing Phenotype Recognition in Clinical Notes Using Large Language Models: PhenoBCBERT and PhenoGPT.
ArXiv
2023
37830010
Uncovering key clinical trial features influencing recruitment.
J Clin Transl Sci
2023
37221382
AI-generated text may have a role in evidence-based medicine.
Nat Med
2023
37090575
Associations of Antihypertensive Medication Consumption and Drug-Drug Interaction with Statin and Metformin with Reduced Alzheimer's Disease and Related Dementias Risk among Hypertensive Patients with Mild Cognitive Impairment using High Volume Claims Data.
Res Sq
2023
37350899
Principal Investigators' Perceptions on Factors Associated with Successful Recruitment in Clinical Trials.
AMIA Jt Summits Transl Sci Proc
2023
37350872
Hierarchical Concept Relations Improve Detection of Off-Label Drug Use in Electronic Health Records Data.
AMIA Jt Summits Transl Sci Proc
2023
37350869
Can Race-sensitive Biomedical Embeddings Improve Healthcare Predictive Models?
AMIA Jt Summits Transl Sci Proc
2023
37214819
Polygenic risk affects the penetrance of monogenic kidney disease.
medRxiv
2023
37181728
A metadata framework for computational phenotypes.
JAMIA Open
2023
37141977
A data-driven approach to optimizing clinical study eligibility criteria.
J Biomed Inform
2023
37203669
A Model for Multi-Institutional Clinical Data Repository.
Stud Health Technol Inform
2023
37203581
How Good Is ChatGPT for Medication Evidence Synthesis?
Stud Health Technol Inform
2023
37028392
Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.
Am J Hum Genet
2023
36921288
EvidenceMap: a three-level knowledge representation for medical evidence computation and comprehension.
J Am Med Inform Assoc
2023
36474423
Characterizing variability of electronic health record-driven phenotype definitions.
J Am Med Inform Assoc
2023
36846987
Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.
J Am Heart Assoc
2023
36746961
Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.
Nat Commun
2023
36737471
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.
Sci Rep
2023
36638583
Clinical research staff perceptions on a natural language processing-driven tool for eligibility prescreening: An iterative usability assessment.
Int J Med Inform
2023
36302597
Genomic Disorders in CKD across the Lifespan.
J Am Soc Nephrol
2023
35228896
Angiogenin promotes angiogenesis via the endonucleolytic decay of miR-141 in colorectal cancer.
Mol Ther Nucleic Acids
2022
35710995
Genome-wide polygenic score to predict chronic kidney disease across ancestries.
Nat Med
2022
35612103
Data-Driven Modeling of Randomized Controlled Trial Outcomes.
Stud Health Technol Inform
2022
35673202
Towards Better Diagnosis Prediction Using Bidirectional Recurrent Neural Networks.
Stud Health Technol Inform
2022
35673090
A Sample Size Extractor for RCT Reports.
Stud Health Technol Inform
2022
35673085
Representation and Normalization of Complex Interventions for Evidence Computing.
Stud Health Technol Inform
2022
35673024
Interactive Similarity-Based Search of Clinical Trials.
Stud Health Technol Inform
2022
35673021
Evaluation of Criteria2Query: Towards Augmented Intelligence for Cohort Identification.
Stud Health Technol Inform
2022
35673015
Extending PICO with Observation Normalization for Evidence Computing.
Stud Health Technol Inform
2022
35672961
Harmonization of Measurement Codes for Concept-Oriented Lab Data Retrieval.
Stud Health Technol Inform
2022
35701404
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.
Nat Commun
2022
35396996
Assessing socioeconomic bias in machine learning algorithms in health care: a case study of the HOUSES index.
J Am Med Inform Assoc
2022
35463945
Characterization and Function of the Interaction of Angiogenin With Alpha-Actinin 2.
Front Mol Biosci
2022
35426943
Combining human and machine intelligence for clinical trial eligibility querying.
J Am Med Inform Assoc
2022
35663114
A machine learning approach to identifying delirium from electronic health records.
JAMIA Open
2022
35486806
Risk Factors Associated With SARS-CoV-2 Breakthrough Infections in Fully mRNA-Vaccinated Individuals: Retrospective Analysis.
JMIR Public Health Surveill
2022
35485600
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
J Am Med Inform Assoc
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
35998640
OARD: Open annotations for rare diseases and their phenotypes based on real-world data.
Am J Hum Genet
2022
36068551
A comparative study of pre-trained language models for named entity recognition in clinical trial eligibility criteria from multiple corpora.
BMC Med Inform Decis Mak
2022
36173371
An interactive fitness-for-use data completeness tool to assess activity tracker data.
J Am Med Inform Assoc
2022
36014850
Impaired Amino Acid Metabolism and Its Correlation with Diabetic Kidney Disease Progression in Type 2 Diabetes Mellitus.
Nutrients
2022
36257483
Deep learning for rare disease: A scoping review.
J Biomed Inform
2022
36157500
Corrigendum to "Lipopolysaccharide-induced podocyte injury is regulated by calcineurin/NFAT and TLR4/MyD88/NF-κB signaling pathways through Angiopoietin-like protein 4" [Genes & Diseases 9(2022) 443-455].
Genes Dis
2022
36283581
Ontology-based categorization of clinical studies by their conditions.
J Biomed Inform
2022
35189334
Leveraging electronic health record data for clinical trial planning by assessing eligibility criteria's impact on patient count and safety.
J Biomed Inform
2022
1 - 50 of 293
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row(s) 1 - 30 of 30
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Columbia University
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Co-authored papers
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Co-authored papers
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Krzysztof Kiryluk
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Co-authored papers
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Wei-Qi Wei
Vanderbilt University Medical Center
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David R Crosslin
University of Washington Medical Center
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Kai Wang
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9
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
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Stephen B Johnson
New York University Grossman School of Medicine
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Eric B Larson
University of Washington
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Marc S Williams
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