1.
A human APOC3 missense variant and monoclonal antibody accelerate apoC-III clearance and lower triglyceride-rich lipoprotein levels
by Khetarpal, Sumeet A
Nature medicine, 2017, Vol.23 (9), p.1086-1094
2.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
by Polfus, Linda M
American journal of human genetics, 2016, Vol.99 (3), p.785-785
3.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
by Polfus, Linda M
American journal of human genetics, 2016, Vol.99 (2), p.481-488
4.
Additive Effect of Polymorphisms in the IL-6, LTA, and TNF-α Genes and Plasma Fatty Acid Level Modulate Risk for the Metabolic Syndrome and Its Components
by Phillips, Catherine M
The journal of clinical endocrinology and metabolism, 2010, Vol.95 (3), p.1386-1394
5.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
by Polfus, Linda M
American journal of human genetics, 2016, Vol.99 (3), p.785-785
6.
Additive Effect of Polymorphisms in the IL-6, LTA, and TNF-α Genes and Plasma Fatty Acid Level Modulate Risk for the Metabolic Syndrome and Its Components
by Phillips, Catherine M
Endocrinology (Philadelphia), 2010, Vol.151 (2), p.840-840
7.
Additive effect of polymorphisms in the IL-6, LTA, and TNF-{alpha} genes and plasma fatty acid level modulate risk for the metabolic syndrome and its components
by Phillips, Catherine M
The journal of clinical endocrinology and metabolism, 2010, Vol.95 (3), p.1386-1394
8.
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
by Voight, Benjamin F, PhD
The Lancet (British edition), 2012, Vol.380 (9841), p.572-580
9.
Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks
by Peloso, Gina M
American journal of human genetics, 2014, Vol.94 (2), p.223-232
10.
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals
by Eicher, John D
American journal of human genetics, 2016, Vol.99 (1), p.40-55
11.
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
by Peloso, Gina M
American journal of human genetics, 2014, Vol.94 (2), p.223-32
