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Goo Jun

Showing results (51-60 of 70) with videos related to

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Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.
Bioinformatics (Oxford, England)|August 20, 2013
Imputation of coding variants in African Americans: better performance using data from the exome sequencing projectQing Duan, Eric Yi Liu, Paul L Auer, et al.
Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2017
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigreesGoo Jun, Alisa Manning, Marcio Almeida, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortiumGoo Jun, Adam C English, Ginger A Metcalf, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.
Bioinformatics (Oxford, England)|August 20, 2013
Imputation of coding variants in African Americans: better performance using data from the exome sequencing projectQing Duan, Eric Yi Liu, Paul L Auer, et al.
Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.
Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2017
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigreesGoo Jun, Alisa Manning, Marcio Almeida, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortiumGoo Jun, Adam C English, Ginger A Metcalf, et al.
Pageof 7