Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Current studies regarding the secondary use of electronic health records (EHR) predominantly rely on domain expertise and existing medical knowledge. A powerful representation approach can unleash the potential of discovering new medical patterns underlying the EHR. Here, we introduce an unsupervised method for embedding high-dimensional EHR data at the patient level to characterize heterogeneity in complex diseases and identify novel disease patterns linked to disparities in clinical outcomes. We applied this approach to 34,851 unique medical codes across 1,046,649 longitudinal patient events, including 102,740 patients in the Electronic Medical Records and GEnomics (eMERGE) Network. The model achieved strong predictive performance in predicting future disease (median AUROC = 0.87 within one year) and bulk phenotyping (median AUROC = 0.84). Notably, these patient embeddings revealed diverse comorbidity profiles and health outcomes, including distinct subtypes and progression patterns in colorectal cancer and systemic lupus erythematosus.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12354887 | PMC |
http://dx.doi.org/10.1038/s41746-025-01872-z | DOI Listing |