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Youna Hu

Showing results (1-10 of 17) with videos related to

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Statistics in Medicine|February 25, 2012
Sample size determination for quadratic inference functions in longitudinal design with dichotomous outcomesYouna Hu, Peter X-K Song
American Journal of Human Genetics|November 12, 2013
Accurate local-ancestry inference in exome-sequenced admixed individuals via off-target sequence readsYouna Hu, Cristen Willer, Xiaowei Zhan, et al.
Bioinformatics (Oxford, England)|May 7, 2016
RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence dataXiaowei Zhan, Youna Hu, Bingshan Li, et al.
Clinical Transplantation|January 6, 2010
Transition from donor candidates to live kidney donors: the impact of race and undiagnosed medical disease statesSilas P Norman, Peter X K Song, Youna Hu, et al.
Nature Communications|February 3, 2016
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning personYouna Hu, Alena Shmygelska, David Tran, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 23, 2011
Fluid overload at initiation of renal replacement therapy is associated with lack of renal recovery in patients with acute kidney injuryMichael Heung, Dawn F Wolfgram, Mallika Kommareddi, et al.
Pain|July 26, 2016
Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locusAmy V Jones, James R F Hockley, Craig Hyde, et al.
Human Molecular Genetics|February 16, 2017
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition lociAmy V Jones, Mera Tilley, Alex Gutteridge, et al.
American Journal of Human Genetics|April 2, 2013
The benefits of using genetic information to design prevention trialsYouna Hu, Li Li, Margaret G Ehm, et al.
American Journal of Human Genetics|December 3, 2013
Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetesKirk E Lohmueller, Thomas Sparsø, Qibin Li, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Statistics in Medicine|February 25, 2012
Sample size determination for quadratic inference functions in longitudinal design with dichotomous outcomesYouna Hu, Peter X-K Song
American Journal of Human Genetics|November 12, 2013
Accurate local-ancestry inference in exome-sequenced admixed individuals via off-target sequence readsYouna Hu, Cristen Willer, Xiaowei Zhan, et al.
Bioinformatics (Oxford, England)|May 7, 2016
RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence dataXiaowei Zhan, Youna Hu, Bingshan Li, et al.
Clinical Transplantation|January 6, 2010
Transition from donor candidates to live kidney donors: the impact of race and undiagnosed medical disease statesSilas P Norman, Peter X K Song, Youna Hu, et al.
Nature Communications|February 3, 2016
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning personYouna Hu, Alena Shmygelska, David Tran, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 23, 2011
Fluid overload at initiation of renal replacement therapy is associated with lack of renal recovery in patients with acute kidney injuryMichael Heung, Dawn F Wolfgram, Mallika Kommareddi, et al.
Pain|July 26, 2016
Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locusAmy V Jones, James R F Hockley, Craig Hyde, et al.
Human Molecular Genetics|February 16, 2017
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition lociAmy V Jones, Mera Tilley, Alex Gutteridge, et al.
American Journal of Human Genetics|April 2, 2013
The benefits of using genetic information to design prevention trialsYouna Hu, Li Li, Margaret G Ehm, et al.
American Journal of Human Genetics|December 3, 2013
Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetesKirk E Lohmueller, Thomas Sparsø, Qibin Li, et al.
Pageof 2