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Stefan Coassin

Showing results (31-40 of 82) with videos related to

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Diabetes Care|May 20, 2008
Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMIAnita Brandstätter, Stefan Kiechl, Barbara Kollerits, et al.
Atherosclerosis|January 8, 2010
Sex and age interaction with genetic association of atherogenic uric acid concentrationsAnita Brandstätter, Claudia Lamina, Stefan Kiechl, et al.
Genome Biology|June 26, 2024
Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a modelSilvia Di Maio, Peter Zöscher, Hansi Weissensteiner, et al.
Plos One|April 29, 2020
A genome-wide analysis of DNA methylation identifies a novel association signal for Lp(a) concentrations in the LPA promoterStefan Coassin, Natascha Hermann-Kleiter, Margot Haun, et al.
Genome Medicine|August 23, 2020
Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individualsSilvia Di Maio, Rebecca Grüneis, Gertraud Streiter, et al.
Obesity (Silver Spring, Md.)|February 2, 2008
INSIG2 polymorphism is neither associated with BMI nor with phenotypes of lipoprotein metabolismEva Boes, Barbara Kollerits, Iris M Heid, et al.
Cardiovascular Research|July 27, 2021
The size of apolipoprotein (a) is an independent determinant of the reduction in lipoprotein (a) induced by PCSK9 inhibitorsValentin Blanchard, Kévin Chemello, Tim Hollstein, et al.
Plos Genetics|December 21, 2010
Investigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working populationStefan Coassin, Martina Schweiger, Anita Kloss-Brandstätter, et al.
Atherosclerosis|February 22, 2023
KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association studyJohanna F Schachtl-Riess, Sebastian Schönherr, Claudia Lamina, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 27, 2020
The <i>TMEM189</i> gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogensErnst R Werner, Markus A Keller, Sabrina Sailer, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

Sort By:
Pageof 9
Diabetes Care|May 20, 2008
Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMIAnita Brandstätter, Stefan Kiechl, Barbara Kollerits, et al.
Atherosclerosis|January 8, 2010
Sex and age interaction with genetic association of atherogenic uric acid concentrationsAnita Brandstätter, Claudia Lamina, Stefan Kiechl, et al.
Genome Biology|June 26, 2024
Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a modelSilvia Di Maio, Peter Zöscher, Hansi Weissensteiner, et al.
Plos One|April 29, 2020
A genome-wide analysis of DNA methylation identifies a novel association signal for Lp(a) concentrations in the LPA promoterStefan Coassin, Natascha Hermann-Kleiter, Margot Haun, et al.
Genome Medicine|August 23, 2020
Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individualsSilvia Di Maio, Rebecca Grüneis, Gertraud Streiter, et al.
Obesity (Silver Spring, Md.)|February 2, 2008
INSIG2 polymorphism is neither associated with BMI nor with phenotypes of lipoprotein metabolismEva Boes, Barbara Kollerits, Iris M Heid, et al.
Cardiovascular Research|July 27, 2021
The size of apolipoprotein (a) is an independent determinant of the reduction in lipoprotein (a) induced by PCSK9 inhibitorsValentin Blanchard, Kévin Chemello, Tim Hollstein, et al.
Plos Genetics|December 21, 2010
Investigation and functional characterization of rare genetic variants in the adipose triglyceride lipase in a large healthy working populationStefan Coassin, Martina Schweiger, Anita Kloss-Brandstätter, et al.
Atherosclerosis|February 22, 2023
KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association studyJohanna F Schachtl-Riess, Sebastian Schönherr, Claudia Lamina, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 27, 2020
The <i>TMEM189</i> gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogensErnst R Werner, Markus A Keller, Sabrina Sailer, et al.
Pageof 9