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1.
Natural language processing to identify lupus nephritis phenotype in electronic health records.
BMC Med Inform Decis Mak
; 22(Suppl 2): 348, 2024 Mar 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-38433189
2.
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Circulation
; 145(12): 877-891, 2022 03 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-34930020
3.
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.
Am J Hum Genet
; 106(5): 707-716, 2020 05 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32386537
4.
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC Med Inform Decis Mak
; 22(1): 23, 2022 01 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-35090449
5.
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.
Circulation
; 142(17): 1633-1646, 2020 10 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-32981348
6.
Identifying sub-phenotypes of acute kidney injury using structured and unstructured electronic health record data with memory networks.
J Biomed Inform
; 102: 103361, 2020 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31911172
7.
Probing the Virtual Proteome to Identify Novel Disease Biomarkers.
Circulation
; 138(22): 2469-2481, 2018 11 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-30571344
8.
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.
Circulation
; 138(17): 1839-1849, 2018 10 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-29703846
9.
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.
BMC Med
; 17(1): 135, 2019 07 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-31311600
10.
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.
Circ Res
; 120(2): 341-353, 2017 Jan 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-27899403
11.
Developing a FHIR-based EHR phenotyping framework: A case study for identification of patients with obesity and multiple comorbidities from discharge summaries.
J Biomed Inform
; 99: 103310, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31622801
12.
Facilitating phenotype transfer using a common data model.
J Biomed Inform
; 96: 103253, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31325501
13.
Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network.
J Biomed Inform
; 99: 103293, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31542521
14.
Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.
Am J Hum Genet
; 97(4): 512-20, 2015 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-26365338
15.
Identification of Four Novel Loci in Asthma in European American and African American Populations.
Am J Respir Crit Care Med
; 195(4): 456-463, 2017 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-27611488
16.
Adverse events after surgery for nonmalignant colon polyps are common and associated with increased length of stay and costs.
Gastrointest Endosc
; 84(2): 296-303.e1, 2016 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-26828760
17.
Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic association studies.
BMC Infect Dis
; 16(1): 684, 2016 11 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-27855652
18.
Developing a data element repository to support EHR-driven phenotype algorithm authoring and execution.
J Biomed Inform
; 62: 232-42, 2016 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-27392645
19.
Factors Associated With Long-Term Weight Loss Following Bariatric Surgery Using 2 Methods for Repeated Measures Analysis.
Am J Epidemiol
; 182(3): 235-43, 2015 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-26093003
20.
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
Hum Genet
; 133(1): 95-109, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24026423