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Science (New York, N.Y.)
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October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene <i>LDLR</i>
Daniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
The Journal of Clinical Investigation
|
January 5, 2016
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene
Joshua W Knowles, Weijia Xie, Zhongyang Zhang, et al.
Plos Genetics
|
September 22, 2011
Phased whole-genome genetic risk in a family quartet using a major allele reference sequence
Frederick E Dewey, Rong Chen, Sergio P Cordero, et al.
Journal of the American Heart Association
|
April 29, 2023
Contemporary Homozygous Familial Hypercholesterolemia in the United States: Insights From the CASCADE FH Registry
Marina Cuchel, Paul C Lee, Lisa C Hudgins, et al.
Journal of the American College of Cardiology
|
August 4, 2018
Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel
Amy C Sturm, Joshua W Knowles, Samuel S Gidding, et al.
The New England Journal of Medicine
|
January 12, 2022
Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting
John E Gorzynski, Sneha D Goenka, Kishwar Shafin, et al.
The Journal of Clinical Investigation
|
March 24, 2015
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene
Joshua W Knowles, Weijia Xie, Zhongyang Zhang, et al.
Diabetes
|
March 10, 2011
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
Aldi T Kraja, Dhananjay Vaidya, James S Pankow, et al.
Diabetes
|
December 4, 2013
Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity
Antigone S Dimas, Vasiliki Lagou, Adam Barker, et al.
Diabetes
|
February 27, 2010
Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans
Erik Ingelsson, Claudia Langenberg, Marie-France Hivert, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 188) with videos related to
Sort By:
Page
of 19
Science (New York, N.Y.)
|
October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene <i>LDLR</i>
Daniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
The Journal of Clinical Investigation
|
January 5, 2016
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene
Joshua W Knowles, Weijia Xie, Zhongyang Zhang, et al.
Plos Genetics
|
September 22, 2011
Phased whole-genome genetic risk in a family quartet using a major allele reference sequence
Frederick E Dewey, Rong Chen, Sergio P Cordero, et al.
Journal of the American Heart Association
|
April 29, 2023
Contemporary Homozygous Familial Hypercholesterolemia in the United States: Insights From the CASCADE FH Registry
Marina Cuchel, Paul C Lee, Lisa C Hudgins, et al.
Journal of the American College of Cardiology
|
August 4, 2018
Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel
Amy C Sturm, Joshua W Knowles, Samuel S Gidding, et al.
The New England Journal of Medicine
|
January 12, 2022
Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting
John E Gorzynski, Sneha D Goenka, Kishwar Shafin, et al.
The Journal of Clinical Investigation
|
March 24, 2015
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene
Joshua W Knowles, Weijia Xie, Zhongyang Zhang, et al.
Diabetes
|
March 10, 2011
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
Aldi T Kraja, Dhananjay Vaidya, James S Pankow, et al.
Diabetes
|
December 4, 2013
Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity
Antigone S Dimas, Vasiliki Lagou, Adam Barker, et al.
Diabetes
|
February 27, 2010
Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans
Erik Ingelsson, Claudia Langenberg, Marie-France Hivert, et al.
Page
of 19