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Benjamin A Satterfield

Showing results (21-30 of 27) with videos related to

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Scientific Reports|October 29, 2023
Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infectionKathleen Ferar, Taryn O Hall, Dana C Crawford, et al.
Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, 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 Communications|November 14, 2022
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failureMichael G Levin, Noah L Tsao, Pankhuri Singhal, et al.
Nature Communications|October 16, 2021
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Scientific Reports|October 29, 2023
Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infectionKathleen Ferar, Taryn O Hall, Dana C Crawford, et al.
Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, 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 Communications|November 14, 2022
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failureMichael G Levin, Noah L Tsao, Pankhuri Singhal, et al.
Nature Communications|October 16, 2021
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.
Pageof 3