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Kelsey E Grinde

Showing results (1-10 of 9) with videos related to

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Biorxiv : the Preprint Server for Biology|April 15, 2024
Adjusting for principal components can induce spurious associations in genome-wide association studies in admixed populationsKelsey E Grinde, Brian L Browning, Alexander P Reiner, et al.
Plos Genetics|December 16, 2024
Adjusting for principal components can induce collider bias in genome-wide association studiesKelsey E Grinde, Brian L Browning, Alexander P Reiner, et al.
American Journal of Human Genetics|February 19, 2019
Genome-wide Significance Thresholds for Admixture Mapping StudiesKelsey E Grinde, Lisa A Brown, Alexander P Reiner, et al.
Frontiers in Genetics|September 30, 2017
Illustrating, Quantifying, and Correcting for Bias in Post-hoc Analysis of Gene-Based Rare Variant Tests of AssociationKelsey E Grinde, Jaron Arbet, Alden Green, et al.
Cancer Medicine|September 21, 2022
Genetic ancestry, differential gene expression, and survival in pediatric B-cell acute lymphoblastic leukemiaFreddy A Barragan, Lauren J Mills, Andrew R Raduski, et al.
Genetic Epidemiology|October 29, 2018
Generalizing polygenic risk scores from Europeans to Hispanics/LatinosKelsey E Grinde, Qibin Qi, Timothy A Thornton, et al.
HGG Advances|June 19, 2023
Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populationsAndrea R V R Horimoto, Lisa A Boyken, Elizabeth E Blue, et al.
Journal of Thrombosis and Haemostasis : JTH|January 28, 2020
Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African AmericansLaura M Raffield, Ake T Lu, Mindy D Szeto, et al.
Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Biorxiv : the Preprint Server for Biology|April 15, 2024
Adjusting for principal components can induce spurious associations in genome-wide association studies in admixed populationsKelsey E Grinde, Brian L Browning, Alexander P Reiner, et al.
Plos Genetics|December 16, 2024
Adjusting for principal components can induce collider bias in genome-wide association studiesKelsey E Grinde, Brian L Browning, Alexander P Reiner, et al.
American Journal of Human Genetics|February 19, 2019
Genome-wide Significance Thresholds for Admixture Mapping StudiesKelsey E Grinde, Lisa A Brown, Alexander P Reiner, et al.
Frontiers in Genetics|September 30, 2017
Illustrating, Quantifying, and Correcting for Bias in Post-hoc Analysis of Gene-Based Rare Variant Tests of AssociationKelsey E Grinde, Jaron Arbet, Alden Green, et al.
Cancer Medicine|September 21, 2022
Genetic ancestry, differential gene expression, and survival in pediatric B-cell acute lymphoblastic leukemiaFreddy A Barragan, Lauren J Mills, Andrew R Raduski, et al.
Genetic Epidemiology|October 29, 2018
Generalizing polygenic risk scores from Europeans to Hispanics/LatinosKelsey E Grinde, Qibin Qi, Timothy A Thornton, et al.
HGG Advances|June 19, 2023
Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populationsAndrea R V R Horimoto, Lisa A Boyken, Elizabeth E Blue, et al.
Journal of Thrombosis and Haemostasis : JTH|January 28, 2020
Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome-wide analysis in African AmericansLaura M Raffield, Ake T Lu, Mindy D Szeto, et al.
Ebiomedicine|January 8, 2021
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortiumBridget M Lin, Kelsey E Grinde, Jennifer A Brody, et al.
Pageof 1