721 results on '"Carrell, David"'
Search Results
2. Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection
3. Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection
4. Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network
5. Patient characteristics, pain treatment patterns, and incidence of total joint replacement in a US population with osteoarthritis
6. Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions
7. Development of a machine learning model to predict mild cognitive impairment using natural language processing in the absence of screening
8. Development and validation of a natural language processing algorithm using electronic health record data to identify patients with breast cancer with low social support.
9. The FDA Sentinel Real World Evidence Data Enterprise (RWE‐DE).
10. Protocol for Designing a Model to Predict the Likelihood of Psychosis From Electronic Health Records Using Natural Language Processing and Machine Learning.
11. Neptune: an environment for the delivery of genomic medicine
12. Validation of Acute Pancreatitis Among Adults in an Integrated Healthcare System
13. Validation of acute pancreatitis among adults in an integrated healthcare system
14. A general framework for developing computable clinical phenotype algorithms.
15. Genetic studies of plasma analytes identify novel potential biomarkers for several complex traits
16. Finding uncoded anaphylaxis in electronic health records to estimate the sensitivity of International Classification of Diseases, Tenth Revision, Clinical Modification codes.
17. Medical records-based chronic kidney disease phenotype for clinical care and “big data” observational and genetic studies
18. Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics
19. Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort
20. Primary Care Opioid Taper Plans Are Associated with Sustained Opioid Dose Reduction
21. Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization
22. Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network
23. Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network
24. Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting
25. Facilitating phenotype transfer using a common data model
26. Association Between Endoscopist Personality and Rate of Adenoma Detection
27. The Authors Respond
28. Toward personalizing treatment for depression: predicting diagnosis and severity.
29. Data-driven automated classification algorithms for acute health conditions: applying PheNorm to COVID-19 disease.
30. Physician characteristics associated with higher adenoma detection rate
31. Improving BP control through electronic communications: an economic evaluation.
32. Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data.
33. Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel
34. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
35. Abstract 14663: High Rate of Arrhythmia Diagnoses Following Return of Pathogenic/likely Pathogenic Variants in an Unselected Population
36. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
37. Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
38. Optimizing annotation resources for natural language de-identification via a game theoretic framework
39. The phenotypic legacy of admixture between modern humans and Neandertals
40. Using natural language processing to identify problem usage of prescription opioids
41. GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network
42. Using natural language processing to extract mammographic findings
43. Automated Prediction of Risk for Problem Opioid Use in a Primary Care Setting
44. Characterizing variability of electronic health record-driven phenotype definitions
45. Prevalence of Behavioral Health Conditions Across Frequency of Cannabis Use Among Adult Primary Care Patients in Washington State
46. Using Natural Language Processing of Free-Text Radiology Reports to Identify Type 1 Modic Endplate Changes
47. Genome-wide association study identifies four novel loci associated with Alzheimer’s endophenotypes and disease modifiers
48. Identifying gene–gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts
49. Improving Methods of Identifying Anaphylaxis for Medical Product Safety Surveillance Using Natural Language Processing and Machine Learning
50. Design patterns for the development of electronic health record-driven phenotype extraction algorithms
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