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C Denny

Showing results (391-400 of 480) with videos related to

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Journal of the American Medical Informatics Association : JAMIA|August 21, 2018
A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environmentsJennifer A Pacheco, Luke V Rasmussen, Richard C Kiefer, et al.
Nature Communications|February 3, 2016
Joint mouse-human phenome-wide association to test gene function and disease riskXusheng Wang, Ashutosh K Pandey, Megan K Mulligan, et al.
Plos One|December 19, 2013
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS dataJonathan D Mosley, Sara L Van Driest, Emma K Larkin, et al.
Nature Communications|March 6, 2025
Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groupsJeewoo Kim, Ariel Williams, Hannah Noh, et al.
Science (New York, N.Y.)|March 29, 2018
Phenotype risk scores identify patients with unrecognized Mendelian disease patternsLisa Bastarache, Jacob J Hughey, Scott Hebbring, et al.
Blood|August 13, 2015
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemiaSeth E Karol, Wenjian Yang, Sara L Van Driest, et al.
Journal of Pathology Informatics|November 26, 2015
Practical considerations in genomic decision support: The eMERGE experienceTimothy M Herr, Suzette J Bielinski, Erwin Bottinger, et al.
Plos One|December 2, 2014
Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE NetworkJennifer R Malinowski, Joshua C Denny, Suzette J Bielinski, et al.
Pharmacogenetics and Genomics|May 26, 2017
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adultsQuinn S Wells, Olivia J Veatch, Joshua P Fessel, 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 algorithmYoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, et al.
Pageof 48

Showing results (391-400 of 480) with videos related to

Sort By:
Pageof 48
Journal of the American Medical Informatics Association : JAMIA|August 21, 2018
A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environmentsJennifer A Pacheco, Luke V Rasmussen, Richard C Kiefer, et al.
Nature Communications|February 3, 2016
Joint mouse-human phenome-wide association to test gene function and disease riskXusheng Wang, Ashutosh K Pandey, Megan K Mulligan, et al.
Plos One|December 19, 2013
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS dataJonathan D Mosley, Sara L Van Driest, Emma K Larkin, et al.
Nature Communications|March 6, 2025
Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groupsJeewoo Kim, Ariel Williams, Hannah Noh, et al.
Science (New York, N.Y.)|March 29, 2018
Phenotype risk scores identify patients with unrecognized Mendelian disease patternsLisa Bastarache, Jacob J Hughey, Scott Hebbring, et al.
Blood|August 13, 2015
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemiaSeth E Karol, Wenjian Yang, Sara L Van Driest, et al.
Journal of Pathology Informatics|November 26, 2015
Practical considerations in genomic decision support: The eMERGE experienceTimothy M Herr, Suzette J Bielinski, Erwin Bottinger, et al.
Plos One|December 2, 2014
Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE NetworkJennifer R Malinowski, Joshua C Denny, Suzette J Bielinski, et al.
Pharmacogenetics and Genomics|May 26, 2017
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adultsQuinn S Wells, Olivia J Veatch, Joshua P Fessel, 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 algorithmYoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, et al.
Pageof 48