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Bioinformatics (Oxford, England)
|
March 2, 2026
Statistical Methods to Harmonize Electronic Health Record Data Across Healthcare Systems: Case Study and Lessons Learned
Xu Shi, Yuqi Zhai, Xianshi Yu, et al.
Plos One
|
May 17, 2023
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
Yoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, et al.
Journal of the American Medical Informatics Association : JAMIA
|
September 6, 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithms
Huan Mo, William K Thompson, Luke V Rasmussen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 21, 2019
Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel
Theodore Chiang, Xiuping Liu, Tsung-Jung Wu, et al.
Journal of Cardiovascular Translational Research
|
July 22, 2015
A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics (eMERGE) Network
Suzette J Bielinski, Jyotishman Pathak, David S Carrell, et al.
International Journal of Biomedical Data Mining
|
April 8, 2016
ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner Workflow
Kenneth M Borthwick, Diane T Smelser, Jonathan A Bock, et al.
American Journal of Human Genetics
|
February 14, 2017
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, et al.
BMC Medicine
|
July 18, 2019
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network
Bahram Namjou, Todd Lingren, Yongbo Huang, et al.
NPJ Digital Medicine
|
April 14, 2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies
Ning Shang, Atlas Khan, Fernanda Polubriaginof, et al.
Frontiers in Genetics
|
September 2, 2014
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index
Robert M Cronin, Julie R Field, Yuki Bradford, et al.
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Showing results (61-70 of 82) with videos related to
Sort By:
Page
of 9
Bioinformatics (Oxford, England)
|
March 2, 2026
Statistical Methods to Harmonize Electronic Health Record Data Across Healthcare Systems: Case Study and Lessons Learned
Xu Shi, Yuqi Zhai, Xianshi Yu, et al.
Plos One
|
May 17, 2023
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
Yoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, et al.
Journal of the American Medical Informatics Association : JAMIA
|
September 6, 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithms
Huan Mo, William K Thompson, Luke V Rasmussen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 21, 2019
Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel
Theodore Chiang, Xiuping Liu, Tsung-Jung Wu, et al.
Journal of Cardiovascular Translational Research
|
July 22, 2015
A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics (eMERGE) Network
Suzette J Bielinski, Jyotishman Pathak, David S Carrell, et al.
International Journal of Biomedical Data Mining
|
April 8, 2016
ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner Workflow
Kenneth M Borthwick, Diane T Smelser, Jonathan A Bock, et al.
American Journal of Human Genetics
|
February 14, 2017
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, et al.
BMC Medicine
|
July 18, 2019
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network
Bahram Namjou, Todd Lingren, Yongbo Huang, et al.
NPJ Digital Medicine
|
April 14, 2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies
Ning Shang, Atlas Khan, Fernanda Polubriaginof, et al.
Frontiers in Genetics
|
September 2, 2014
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index
Robert M Cronin, Julie R Field, Yuki Bradford, et al.
Page
of 9