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Cardiovascular Diabetology
|
March 15, 2008
Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sample
Salam A Al-Attar, Rebecca L Pollex, Matthew R Ban, et al.
Journal of Lipid Research
|
September 6, 2017
Polygenic determinants in extremes of high-density lipoprotein cholesterol
Jacqueline S Dron, Jian Wang, Cécile Low-Kam, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
October 22, 2016
Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically
Jian Wang, Jacqueline S Dron, Matthew R Ban, 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 populations
Joseph 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 hypertriglyceridemia
Christopher 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 distribution
Aniruddh 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 dyslipidemias
Jennifer 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 hypertriglyceridemia
Christopher 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 hypertriglyceridemia
Christopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
American Journal of Human Genetics
|
December 14, 2011
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone
Lijia Huang, Katarzyna Szymanska, Victor L Jensen, et al.
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of 4
Search research articles
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Showing results (31-40 of 40) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 40 results.
Cardiovascular Diabetology
|
March 15, 2008
Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sample
Salam A Al-Attar, Rebecca L Pollex, Matthew R Ban, et al.
Journal of Lipid Research
|
September 6, 2017
Polygenic determinants in extremes of high-density lipoprotein cholesterol
Jacqueline S Dron, Jian Wang, Cécile Low-Kam, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
October 22, 2016
Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically
Jian Wang, Jacqueline S Dron, Matthew R Ban, 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 populations
Joseph 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 hypertriglyceridemia
Christopher 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 distribution
Aniruddh 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 dyslipidemias
Jennifer 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 hypertriglyceridemia
Christopher 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 hypertriglyceridemia
Christopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
American Journal of Human Genetics
|
December 14, 2011
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone
Lijia Huang, Katarzyna Szymanska, Victor L Jensen, et al.
Page
of 4