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Youna Hu

Showing results (11-20 of 17) with videos related to

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Plos Genetics|July 13, 2018
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Plos Genetics|September 14, 2018
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Plos Genetics|August 6, 2016
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration LociSamuel E Jones, Jessica Tyrrell, Andrew R Wood, et al.
The New England Journal of Medicine|September 7, 2017
Genetic Associations with Gestational Duration and Spontaneous Preterm BirthGe Zhang, Bjarke Feenstra, Jonas Bacelis, 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.
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.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Plos Genetics|July 13, 2018
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Plos Genetics|September 14, 2018
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Plos Genetics|August 6, 2016
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration LociSamuel E Jones, Jessica Tyrrell, Andrew R Wood, et al.
The New England Journal of Medicine|September 7, 2017
Genetic Associations with Gestational Duration and Spontaneous Preterm BirthGe Zhang, Bjarke Feenstra, Jonas Bacelis, 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.
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.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Pageof 2