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Ralph B. D'Agostino

Researcher at Wake Forest University

Publications -  1336
Citations -  250792

Ralph B. D'Agostino is an academic researcher from Wake Forest University. The author has contributed to research in topics: Framingham Heart Study & Framingham Risk Score. The author has an hindex of 226, co-authored 1287 publications receiving 229636 citations. Previous affiliations of Ralph B. D'Agostino include VA Boston Healthcare System & University of Illinois at Urbana–Champaign.

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Sex and Age Differences in Lipoprotein Subclasses Measured by Nuclear Magnetic Resonance Spectroscopy: The Framingham Study

TL;DR: Women have a less atherogenic subclass profile than men, even after accounting for differences in lipid concentrations, and women also had a lower-risk subclass profile consisting of larger LDL and HDL particles than men.
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Gender and C-reactive protein: data from the Multiethnic Study of Atherosclerosis (MESA) cohort.

TL;DR: Evaluation of gender-specific CRP cut points to determine cardiovascular risk should be considered and this pattern of higher CRP levels in women was consistent across all ethnic subgroups even after multivariable adjustment.
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Hyperlipidemia in Early Adulthood Increases Long-Term Risk of Coronary Heart Disease

TL;DR: Cumulative exposure to hyperlipidemia in young adulthood increases the subsequent risk of CHD in a dose-dependent fashion and adults with prolonged exposure to even moderate elevations in non–high-density lipoprotein cholesterol have elevated risk for future CHD and may benefit from more aggressive primary prevention.
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Long-term alcohol consumption and the risk of atrial fibrillation in the Framingham Study.

TL;DR: The data indicate little association between long-term moderate alcohol consumption and the risk of AF, but a significantly increased risk ofAF among subjects consuming >36 g/day (approximatively >3 drinks/day).
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Chemokine receptor mutant CX3CR1-M280 has impaired adhesive function and correlates with protection from cardiovascular disease in humans.

TL;DR: In this article, the authors showed that FKN-dependent cell-cell adhesion under conditions of physiologic shear is severely reduced in cells expressing CX3CR1-M280.