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Anne Tybjaerg-Hansen

Showing results (131-140 of 144) with videos related to

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Circulation Research|November 23, 2021
Posttranscriptional Regulation of the Human LDL Receptor by the U2-SpliceosomePaolo Zanoni, Grigorios Panteloglou, Alaa Othman, et al.
Nature Genetics|September 5, 2017
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart diseaseWei Zhao, Asif Rasheed, Emmi Tikkanen, et al.
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
American Journal of Human Genetics|May 30, 2017
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric TraitsIoanna Tachmazidou, Dániel Süveges, Josine L Min, et al.
Journal of the American College of Cardiology|August 7, 2013
Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization studyMichael V Holmes, Tabassome Simon, Holly J Exeter, et al.
Circulation. Cardiovascular Genetics|December 27, 2011
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studiesJoanne M Murabito, Charles C White, Maryam Kavousi, et al.
Lancet (London, England)|May 22, 2012
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyBenjamin F Voight, Gina M Peloso, Marju Orho-Melander, et al.
Lancet (London, England)|September 29, 2014
HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trialsDaniel I Swerdlow, David Preiss, Karoline B Kuchenbaecker, et al.
Nature Genetics|October 31, 2017
Exome-wide association study of plasma lipids in >300,000 individualsDajiang J Liu, Gina M Peloso, Haojie Yu, et al.
Nature|February 2, 2017
Rare and low-frequency coding variants alter human adult heightEirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.
Pageof 15

Showing results (131-140 of 144) with videos related to

Sort By:
Pageof 15
Circulation Research|November 23, 2021
Posttranscriptional Regulation of the Human LDL Receptor by the U2-SpliceosomePaolo Zanoni, Grigorios Panteloglou, Alaa Othman, et al.
Nature Genetics|September 5, 2017
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart diseaseWei Zhao, Asif Rasheed, Emmi Tikkanen, et al.
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
American Journal of Human Genetics|May 30, 2017
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric TraitsIoanna Tachmazidou, Dániel Süveges, Josine L Min, et al.
Journal of the American College of Cardiology|August 7, 2013
Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization studyMichael V Holmes, Tabassome Simon, Holly J Exeter, et al.
Circulation. Cardiovascular Genetics|December 27, 2011
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studiesJoanne M Murabito, Charles C White, Maryam Kavousi, et al.
Lancet (London, England)|May 22, 2012
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyBenjamin F Voight, Gina M Peloso, Marju Orho-Melander, et al.
Lancet (London, England)|September 29, 2014
HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trialsDaniel I Swerdlow, David Preiss, Karoline B Kuchenbaecker, et al.
Nature Genetics|October 31, 2017
Exome-wide association study of plasma lipids in >300,000 individualsDajiang J Liu, Gina M Peloso, Haojie Yu, et al.
Nature|February 2, 2017
Rare and low-frequency coding variants alter human adult heightEirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.
Pageof 15