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Christopher T Johansen

Showing results (11-20 of 22) with videos related to

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Blood|June 19, 2010
Genetic variation in hyaluronan metabolism loci is associated with plasma plasminogen activator inhibitor-1 concentrationMatthew B Lanktree, Christopher T Johansen, Sonia S Anand, et al.
Journal of Lipid Research|February 8, 2014
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemiasChristopher T Johansen, Joseph B Dubé, Melissa N Loyzer, et al.
Nature Medicine|June 14, 2011
The transcription factor cyclic AMP-responsive element-binding protein H regulates triglyceride metabolismJung Hoon Lee, Petros Giannikopoulos, Stephen A Duncan, et al.
Circulation. Cardiovascular Genetics|November 22, 2014
Common low-density lipoprotein receptor p.G116S variant has a large effect on plasma low-density lipoprotein cholesterol in circumpolar inuit populationsJoseph B Dubé, Jian Wang, Henian Cao, et al.
Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, et al.
Atherosclerosis|May 17, 2016
Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distributionAniruddh P Patel, Gina M Peloso, James P Pirruccello, et al.
The Canadian Journal of Cardiology|April 30, 2013
Western Database of Lipid Variants (WDLV): a catalogue of genetic variants in monogenic dyslipidemiasJennifer Fu, Samantha Kwok, Leah Sinai, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 21, 2011
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, 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.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Blood|June 19, 2010
Genetic variation in hyaluronan metabolism loci is associated with plasma plasminogen activator inhibitor-1 concentrationMatthew B Lanktree, Christopher T Johansen, Sonia S Anand, et al.
Journal of Lipid Research|February 8, 2014
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemiasChristopher T Johansen, Joseph B Dubé, Melissa N Loyzer, et al.
Nature Medicine|June 14, 2011
The transcription factor cyclic AMP-responsive element-binding protein H regulates triglyceride metabolismJung Hoon Lee, Petros Giannikopoulos, Stephen A Duncan, et al.
Circulation. Cardiovascular Genetics|November 22, 2014
Common low-density lipoprotein receptor p.G116S variant has a large effect on plasma low-density lipoprotein cholesterol in circumpolar inuit populationsJoseph B Dubé, Jian Wang, Henian Cao, et al.
Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, et al.
Atherosclerosis|May 17, 2016
Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distributionAniruddh P Patel, Gina M Peloso, James P Pirruccello, et al.
The Canadian Journal of Cardiology|April 30, 2013
Western Database of Lipid Variants (WDLV): a catalogue of genetic variants in monogenic dyslipidemiasJennifer Fu, Samantha Kwok, Leah Sinai, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 21, 2011
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, 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.
Pageof 3