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Todd Lingren

Showing results (31-40 of 39) with videos related to

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Journal of Biomedical Informatics|July 21, 2019
Facilitating phenotype transfer using a common data modelGeorge Hripcsak, Ning Shang, Peggy L Peissig, et al.
Plos One|July 30, 2016
Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum DisorderTodd Lingren, Pei Chen, Joseph Bochenek, et al.
Journal of the American Medical Informatics Association : JAMIA|September 6, 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithmsHuan Mo, William K Thompson, Luke V Rasmussen, 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 NetworkBahram Namjou, Todd Lingren, Yongbo Huang, et al.
Scientific Reports|February 3, 2023
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE networkJennifer A Pacheco, Luke V Rasmussen, Ken Wiley, et al.
Nature|December 10, 2021
The power of genetic diversity in genome-wide association studies of lipidsSarah E Graham, Shoa L Clarke, Kuan-Han H Wu, et al.
Nature|May 26, 2023
Author Correction: The power of genetic diversity in genome-wide association studies of lipidsSarah E Graham, Shoa L Clarke, Kuan-Han H Wu, et al.
Genome Biology|December 27, 2022
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysisStavroula Kanoni, Sarah E Graham, Yuxuan Wang, et al.
American Journal of Human Genetics|August 5, 2022
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipidsShweta Ramdas, Jonathan Judd, Sarah E Graham, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Journal of Biomedical Informatics|July 21, 2019
Facilitating phenotype transfer using a common data modelGeorge Hripcsak, Ning Shang, Peggy L Peissig, et al.
Plos One|July 30, 2016
Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum DisorderTodd Lingren, Pei Chen, Joseph Bochenek, et al.
Journal of the American Medical Informatics Association : JAMIA|September 6, 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithmsHuan Mo, William K Thompson, Luke V Rasmussen, 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 NetworkBahram Namjou, Todd Lingren, Yongbo Huang, et al.
Scientific Reports|February 3, 2023
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE networkJennifer A Pacheco, Luke V Rasmussen, Ken Wiley, et al.
Nature|December 10, 2021
The power of genetic diversity in genome-wide association studies of lipidsSarah E Graham, Shoa L Clarke, Kuan-Han H Wu, et al.
Nature|May 26, 2023
Author Correction: The power of genetic diversity in genome-wide association studies of lipidsSarah E Graham, Shoa L Clarke, Kuan-Han H Wu, et al.
Genome Biology|December 27, 2022
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysisStavroula Kanoni, Sarah E Graham, Yuxuan Wang, et al.
American Journal of Human Genetics|August 5, 2022
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipidsShweta Ramdas, Jonathan Judd, Sarah E Graham, et al.
Pageof 4