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Albert V Smith

Showing results (151-160 of 271) with videos related to

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Nature Genetics|September 28, 2023
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcificationMaryam Kavousi, Maxime M Bos, Hanna J Barnes, et al.
American Journal of Human Genetics|February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksGina M Peloso, Paul L Auer, Joshua C Bis, et al.
American Journal of Human Genetics|December 27, 2016
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in ErythropoiesisFrank J A van Rooij, Rehan Qayyum, Albert V Smith, et al.
Plos Genetics|September 27, 2013
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrationsConall M O'Seaghdha, Hongsheng Wu, Qiong Yang, et al.
Circulation. Genomic and Precision Medicine|May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR IntervalHonghuang Lin, Jessica van Setten, Albert V Smith, et al.
Nature Human Behaviour|August 4, 2022
Rare genetic variants explain missing heritability in smokingSeon-Kyeong Jang, Luke Evans, Allison Fialkowski, 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.
Kidney International|December 11, 2014
Genome-wide association study of kidney function decline in individuals of European descentMathias Gorski, Adrienne Tin, Maija Garnaas, et al.
American Journal of Human Genetics|October 2, 2012
Discovery and fine mapping of serum protein loci through transethnic meta-analysisNora Franceschini, Frank J A van Rooij, Bram P Prins, et al.
Journal of Medical Genetics|April 3, 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsElisabeth M van Leeuwen, Aniko Sabo, Joshua C Bis, et al.
Pageof 28

Showing results (151-160 of 271) with videos related to

Sort By:
Pageof 28
Nature Genetics|September 28, 2023
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcificationMaryam Kavousi, Maxime M Bos, Hanna J Barnes, et al.
American Journal of Human Genetics|February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksGina M Peloso, Paul L Auer, Joshua C Bis, et al.
American Journal of Human Genetics|December 27, 2016
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in ErythropoiesisFrank J A van Rooij, Rehan Qayyum, Albert V Smith, et al.
Plos Genetics|September 27, 2013
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrationsConall M O'Seaghdha, Hongsheng Wu, Qiong Yang, et al.
Circulation. Genomic and Precision Medicine|May 12, 2018
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR IntervalHonghuang Lin, Jessica van Setten, Albert V Smith, et al.
Nature Human Behaviour|August 4, 2022
Rare genetic variants explain missing heritability in smokingSeon-Kyeong Jang, Luke Evans, Allison Fialkowski, 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.
Kidney International|December 11, 2014
Genome-wide association study of kidney function decline in individuals of European descentMathias Gorski, Adrienne Tin, Maija Garnaas, et al.
American Journal of Human Genetics|October 2, 2012
Discovery and fine mapping of serum protein loci through transethnic meta-analysisNora Franceschini, Frank J A van Rooij, Bram P Prins, et al.
Journal of Medical Genetics|April 3, 2016
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsElisabeth M van Leeuwen, Aniko Sabo, Joshua C Bis, et al.
Pageof 28