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Christopher N Foley

Showing results (1-10 of 16) with videos related to

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Annual Review of Genomics and Human Genetics|May 1, 2018
Inferring Causal Relationships Between Risk Factors and Outcomes from Genome-Wide Association Study DataStephen Burgess, Christopher N Foley, Verena Zuber
International Journal of Epidemiology|August 2, 2019
Factorial Mendelian randomization: using genetic variants to assess interactionsJessica M B Rees, Christopher N Foley, Stephen Burgess
International Journal of Epidemiology|May 31, 2018
Modal-based estimation via heterogeneity-penalized weighting: model averaging for consistent and efficient estimation in Mendelian randomization when a plurality of candidate instruments are validStephen Burgess, Verena Zuber, Apostolos Gkatzionis, et al.
Bioinformatics (Oxford, England)|September 11, 2020
MR-Clust: clustering of genetic variants in Mendelian randomization with similar causal estimatesChristopher N Foley, Amy M Mason, Paul D W Kirk, et al.
Nature Communications|January 19, 2020
A robust and efficient method for Mendelian randomization with hundreds of genetic variantsStephen Burgess, Christopher N Foley, Elias Allara, et al.
Wellcome Open Research|January 1, 2021
MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized dataJim R Broadbent, Christopher N Foley, Andrew J Grant, et al.
Nature Communications|February 4, 2021
A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traitsChristopher N Foley, James R Staley, Philip G Breen, et al.
Molecular Psychiatry|March 20, 2019
Shared mechanisms between coronary heart disease and depression: findings from a large UK general population-based cohortGolam M Khandaker, Verena Zuber, Jessica M B Rees, et al.
Nature Communications|August 26, 2024
Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK BiobankRobert F Hillary, Danni A Gadd, Zhana Kuncheva, et al.
Nature|February 24, 2022
Genetic associations of protein-coding variants in human diseaseBenjamin B Sun, Mitja I Kurki, Christopher N Foley, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Annual Review of Genomics and Human Genetics|May 1, 2018
Inferring Causal Relationships Between Risk Factors and Outcomes from Genome-Wide Association Study DataStephen Burgess, Christopher N Foley, Verena Zuber
International Journal of Epidemiology|August 2, 2019
Factorial Mendelian randomization: using genetic variants to assess interactionsJessica M B Rees, Christopher N Foley, Stephen Burgess
International Journal of Epidemiology|May 31, 2018
Modal-based estimation via heterogeneity-penalized weighting: model averaging for consistent and efficient estimation in Mendelian randomization when a plurality of candidate instruments are validStephen Burgess, Verena Zuber, Apostolos Gkatzionis, et al.
Bioinformatics (Oxford, England)|September 11, 2020
MR-Clust: clustering of genetic variants in Mendelian randomization with similar causal estimatesChristopher N Foley, Amy M Mason, Paul D W Kirk, et al.
Nature Communications|January 19, 2020
A robust and efficient method for Mendelian randomization with hundreds of genetic variantsStephen Burgess, Christopher N Foley, Elias Allara, et al.
Wellcome Open Research|January 1, 2021
MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized dataJim R Broadbent, Christopher N Foley, Andrew J Grant, et al.
Nature Communications|February 4, 2021
A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traitsChristopher N Foley, James R Staley, Philip G Breen, et al.
Molecular Psychiatry|March 20, 2019
Shared mechanisms between coronary heart disease and depression: findings from a large UK general population-based cohortGolam M Khandaker, Verena Zuber, Jessica M B Rees, et al.
Nature Communications|August 26, 2024
Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK BiobankRobert F Hillary, Danni A Gadd, Zhana Kuncheva, et al.
Nature|February 24, 2022
Genetic associations of protein-coding variants in human diseaseBenjamin B Sun, Mitja I Kurki, Christopher N Foley, et al.
Pageof 2