Detalhe da pesquisa
1.
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
; 25(4): 100006, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36621880
2.
AD-BERT: Using pre-trained language model to predict the progression from mild cognitive impairment to Alzheimer's disease.
J Biomed Inform
; 144: 104442, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37429512
3.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-35090449
4.
Genomic considerations for FHIR®; eMERGE implementation lessons.
J Biomed Inform
; 118: 103795, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33930535
5.
Participant choices for return of genomic results in the eMERGE Network.
Genet Med
; 22(11): 1821-1829, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32669677
6.
Effects of 2 Forms of Practice Facilitation on Cardiovascular Prevention in Primary Care: A Practice-randomized, Comparative Effectiveness Trial.
Med Care
; 58(4): 344-351, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31876643
7.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-31911172
8.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-31622801
9.
Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network.
J Biomed Inform
; 99: 103293, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31542521
10.
Facilitating phenotype transfer using a common data model.
J Biomed Inform
; 96: 103253, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31325501
11.
Developing a portable natural language processing based phenotyping system.
BMC Med Inform Decis Mak
; 19(Suppl 3): 78, 2019 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30943974
12.
Developing a data element repository to support EHR-driven phenotype algorithm authoring and execution.
J Biomed Inform
; 62: 232-42, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27392645
13.
The genomic CDS sandbox: An assessment among domain experts.
J Biomed Inform
; 60: 84-94, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26778834
14.
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Circulation
; 127(13): 1377-85, 2013 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23463857
15.
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
Am J Hum Genet
; 89(4): 529-42, 2011 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21981779
16.
Anatomic and advanced adenoma detection rates as quality metrics determined via natural language processing.
Am J Gastroenterol
; 109(12): 1844-9, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24935271
17.
Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.
Mol Vis
; 20: 1281-95, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25352737
18.
A rural community's involvement in the design and usability testing of a computer-based informed consent process for the Personalized Medicine Research Project.
Am J Med Genet A
; 164A(1): 129-40, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24273095
19.
Design patterns for the development of electronic health record-driven phenotype extraction algorithms.
J Biomed Inform
; 51: 280-6, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24960203
20.
Seamless Integration of Computer-Adaptive Patient Reported Outcomes into an Electronic Health Record.
Appl Clin Inform
; 15(1): 145-154, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38154472